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2024The Rogdi knockout mouse is a model for Kohlschütter-Tönz syndrome.Jimenez-Armijo A, Morkmued S, Ahumada JT, Kharouf N, de Feraudy Y, Gogl G, Riet F, Niederreither K, Laporte J, Birling MC, Selloum M, Herault Y, Hernandez M, Bloch-Zupan A |
2023A conditional null allele of Dync1h1 enables targeted analyses of dynein roles in neuronal length sensing.Di Pizio A, Marvaldi L, Birling MC, Okladnikov N, Dupuis L, Fainzilber M, Rishal I |
A human dynein heavy chain mutation impacts cortical progenitor cells causing developmental defects, reduced brain size and altered brain architecture.Romero DM, Zaidi D, Cifuentes-Diaz C, Maillard C, Grannec G, Selloum M, Birling MC, Bahi-Buisson N, Francis F |
A systematic review of the development and application of home cage monitoring in laboratory mice and rats.Kahnau P, Mieske P, Wilzopolski J, Kalliokoski O, Mandillo S, Hölter SM, Voikar V, Amfim A, Badurek S, Bartelik A, Caruso A, Čater M, Ey E, Golini E, Jaap A, Hrncic D, Kiryk A, Lang B, Loncarevic-Vasiljkovic N, Meziane H, Radzevičienė A, Rivalan M, Scattoni ML, Torquet N, Trifkovic J, Ulfhake B, Thöne-Reineke C, Diederich K, Lewejohann L, Hohlbaum K |
Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders.Martin Lorenzo S, Muniz Moreno MDM, Atas H, Pellen M, Nalesso V, Raffelsberger W, Prevost G, Lindner L, Birling MC, Menoret S, Tesson L, Negroni L, Concordet JP, Anegon I, Herault Y |
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Oestereicher MA, Wotton JM, Ayabe S, Bou About G, Cheng TK, Choi JH, Clary D, Dew EM, Elfertak L, Guimond A, Haseli Mashhadi H, Heaney JD, Kelsey L, Keskivali-Bond P, Lopez Gomez F, Marschall S, McFarland M, Meziane H, Munoz Fuentes V, Nam KH, Nichtová Z, Pimm D, Bower L, Prochazka J, Rozman J, Santos L, Stewart M, Tanaka N, Ward CS, Willett AME, Wilson R, Braun RE, Dickinson ME, Flenniken AM, Herault Y, Lloyd KCK, Mallon AM, McKerlie C, Murray SA, Nutter LMJ, Sedlacek R, Seong JK, Sorg T, Tamura M, Wells S, Schneltzer E, Fuchs H, Gailus-Durner V, Hrabe de Angelis M, White JK, Spielmann N |
CRISMERE Chromosome Engineering in Mouse and RatLaurence Schaeffer, Loic Lindner, Guillaume Pavlovic, Yann Hérault & Marie-Christine Birling |
Development of HPV16 mouse and dog models for more accurate prediction of human vaccine efficacy.Totain E, Lindner L, Martin N, Misseri Y, Iché A, Birling MC, Sorg T, Herault Y, Bousquet-Melou A, Bouillé P, Duthoit C, Pavlovic G, Boullier S |
Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein.Kretz PF, Wagner C, Mikhaleva A, Montillot C, Hugel S, Morella I, Kannan M, Fischer MC, Milhau M, Yalcin I, Brambilla R, Selloum M, Herault Y, Reymond A, Collins SC, Yalcin B |
Genome-wide screening reveals the genetic basis of mammalian embryonic eye development.Chee JM, Lanoue L, Clary D, Higgins K, Bower L, Flenniken A, Guo R, Adams DJ, Bosch F, Braun RE, Brown SDM, Chin HG, Dickinson ME, Hsu CW, Dobbie M, Gao X, Galande S, Grobler A, Heaney JD, Herault Y, de Angelis MH, Mammano F, Nutter LMJ, Parkinson H, Qin C, Shiroishi T, Sedlacek R, Seong JK, Xu Y, Brooks B, McKerlie C, Lloyd KCK, Westerberg H, Moshiri A |
How much do we know about the function of mammalian genes?Teboul L, Hérault Y, Wells S, Pavlovic G |
IL-3 produced by T cells is crucial for basophil extravasation in hapten-induced allergic contact dermatitis.Hachem CE, Marschall P, Hener P, Karnam A, Bonam SR, Meyer P, Flatter E, Birling MC, Bayry J, Li M |
Increased On-Target Rate and Risk of Concatemerization after CRISPR-Enhanced Targeting in ES CellsValérie Erbs, Romain Lorentz, Benjamin Eisenman, Laurence Schaeffer, Laurence Luppi, Loic Lindner, Yann Hérault, Guillaume Pavlovic, ,Marie Wattenhofer-Donzé and Marie-Christine Birling |
INFRAFRONTIER: mouse model resources for modelling human diseases.Ali Khan A, Valera Vazquez G, Gustems M, Matteoni R, Song F, Gormanns P, Fessele S, Raess M, Hrabĕ de Angelis M |
Prolonged nicotine exposure reduces aversion to the drug in mice by altering nicotinic transmission in the interpeduncular nucleus.Mondoloni S, Nguyen C, Vicq E, Ciscato M, Jehl J, Durand-de Cuttoli R, Torquet N, Tolu S, Pons S, Maskos U, Marti F, Faure P, Mourot A |
Timeline of Developmental Defects Generated upon Genetic Inhibition of the Retinoic Acid Receptor Signaling PathwayMarius Teletin, Manuel Mark, Olivia Wendling, Nadège Vernet, Betty Féret, Muriel Klopfenstein, Yann Herault, Norbert B. Ghyselinck |
2022AAV-delivered diacylglycerol kinase DGKk achieves long-term rescue of fragile X syndrome mouse model.Habbas K, Cakil O, Zámbó B, Tabet R, Riet F, Dembele D, Mandel JL, Hocquemiller M, Laufer R, Piguet F, Moine H |
Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes.Higgins K, Moore BA, Berberovic Z, Adissu HA, Eskandarian M, Flenniken AM, Shao A, Imai DM, Clary D, Lanoue L, Newbigging S, Nutter LMJ, Adams DJ, Bosch F, Braun RE, Brown SDM, Dickinson ME, Dobbie M, Flicek P, Gao X, Galande S, Grobler A, Heaney JD, Herault Y, de Angelis MH, Chin HG, Mammano F, Qin C, Shiroishi T, Sedlacek R, Seong JK, Xu Y, Lloyd KCK, McKerlie C, Moshiri A |
Behavioral Testing Design for Evaluation of Cognitive Disabilities.Riet F, Mittelhaeuser C, Lux A, Bour R, Selloum M, Sorg T, Herault Y, Meziane H |
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathyNadine Spielmann, Gregor Miller, Tudor I. Oprea, Chih-Wei Hsu, Gisela Fobo, Goar Frishman, Corinna Montrone, Hamed Haseli Mashhadi, Jeremy Mason, Violeta Munoz Fuentes, Stefanie Leuchtenberger, Andreas Ruepp, Matias Wagner, Dominik S. Westphal, Cordula Wolf, Agnes Görlach, Adrián Sanz-Moreno, Yi-Li Cho, Raffaele Teperino, Stefan Brandmaier, Sapna Sharma, Isabella Rikarda Galter, Manuela A. Östereicher, Lilly Zapf, Philipp Mayer-Kuckuk, Jan Rozman, Lydia Teboul, Rosie K. A. Bunton-Stasyshyn, Heather Cater, Michelle Stewart, Skevoulla Christou, Henrik Westerberg, Amelia M. Willett, Janine M. Wotton, Willson B. Roper, Audrey E. Christiansen, Christopher S. Ward, Jason D. Heaney, Corey L. Reynolds, Jan Prochazka, Lynette Bower, David Clary, Mohammed Selloum, Ghina Bou About, Olivia Wendling, Hugues Jacobs, Sophie Leblanc, Hamid Meziane, Tania Sorg, Enrique Audain, Arthur Gilly, Nigel W. Rayner, IMPC consortium, Genomics England Research Consortium, Marc-Phillip Hitz, Eleftheria Zeggini, Eckhard Wolf, Radislav Sedlacek, Steven A. Murray, Karen L. Svenson, Robert E. Braun, Jaqueline K. White, Lois Kelsey, Xiang Gao, Toshihiko Shiroishi, Ying Xu, Je Kyung Seong, Fabio Mammano, Glauco P. Tocchini-Valentini, Arthur L. Beaudet, Terrence F. Meehan, Helen Parkinson, Damian Smedley, Ann-Marie Mallon, Sara E. Wells, Harald Grallert, Wolfgang Wurst, Susan Marschall, Helmut Fuchs, Steve D. M. Brown, Ann M. Flenniken, Lauryl M. J. Nutter, Colin McKerlie, Yann Herault, K. C. Kent Lloyd, Mary E. Dickinson, Valerie Gailus-Durner & Martin Hrabe de Angelis |
HRAS germline mutations impair LKB1/AMPK signaling and mitochondrial homeostasis in Costello syndrome models.Dard L, Hubert C, Esteves P, Blanchard W, Bou About G, Baldasseroni L, Dumon E, Angelini C, Delourme M, Guyonnet-Dupérat V, Claverol S, Fontenille L, Kissa K, Séguéla PE, Thambo JB, Nicolas L, Herault Y, Bellance N, Dias Amoedo N, Magdinier F, Sorg T, Lacombe D, Rossignol R |
Keratinocyte-derived cytokine TSLP promotes growth and metastasis of melanoma by regulating the tumor-associated immune microenvironment.Yao W, German B, Chraa D, Braud A, Hugel C, Meyer P, Davidson G, Laurette P, Mengus G, Flatter E, Marschall P, Segaud J, Guivarch M, Hener P, Birling MC, Lipsker D, Davidson I, Li M |
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.Meziane H, Birling MC, Wendling O, Leblanc S, Dubos A, Selloum M, Pavlovic G, Sorg T, Kalscheuer VM, Billuart P, Laumonnier F, Chelly J, van Bokhoven H, Herault Y |
Loss of low-molecular-weight protein tyrosine phosphatase shows limited improvement in glucose tolerance but causes mild cardiac hypertrophy in mice.Jensen-Cody S, Coyne ES, Ding X, Sebin A, Vogel J, Goldstein J, Rosahl TW, Zhou HH, Jacobs H, Champy MF, About GB, Talukdar S, Zhou Y |
The Human SCN9A (R185H) Point Mutation Induces Pain Hypersensitivity and Spontaneous Pain in Mice.Xue Y, Kremer M, Muniz Moreno MDM, Chidiac C, Lorentz R, Birling MC, Barrot M, Herault Y, Gaveriaux-Ruff C |
Ts66Yah, a mouse model of Down syndrome with improved construct and face validity.Duchon A, Del Mar Muñiz Moreno M, Chevalier C, Nalesso V, Andre P, Fructuoso-Castellar M, Mondino M, Po C, Noblet V, Birling MC, Potier MC, Herault Y |
2021A resource of targeted mutant mouse lines for 5,061 genes.Birling MC, Yoshiki A, Adams DJ, Ayabe S, Beaudet AL, Bottomley J, Bradley A, Brown SDM, Bürger A, Bushell W, Chiani F, Chin HG, Christou S, Codner GF, DeMayo FJ, Dickinson ME, Doe B, Donahue LR, Fray MD, Gambadoro A, Gao X, Gertsenstein M, Gomez-Segura A, Goodwin LO, Heaney JD, Hérault Y, de Angelis MH, Jiang ST, Justice MJ, Kasparek P, King RE, Kühn R, Lee H, Lee YJ, Liu Z, Lloyd KCK, Lorenzo I, Mallon AM, McKerlie C, Meehan TF, Fuentes VM, Newman S, Nutter LMJ, Oh GT, Pavlovic G, Ramirez-Solis R, Rosen B, Ryder EJ, Santos LA, Schick J, Seavitt JR, Sedlacek R, Seisenberger C, Seong JK, Skarnes WC, Sorg T, Steel KP, Tamura M, Tocchini-Valentini GP, Wang CL, Wardle-Jones H, Wattenhofer-Donzé M, Wells S, Wiles MV, Willis BJ, Wood JA, Wurst W, Xu Y, Teboul L, Murray SA |
Building the Future Therapies for Down Syndrome: The Third International Conference of the T21 Research SocietyDierssen M.a,b,c · Herault Y.d · Helguera P.e · Martínez de Lagran M.a,c · Vazquez A.b · Christian B.f · Carmona-Iragui M.g,h · Wiseman F.i · Mobley W.j · Fisher E.M.C.k · Brault V.d · Esbensen A.l · Jacola L.M.m · Potier M.C.n · Hamlett E.D.o · Abbeduto L.p · del Hoyo Soriano L.p · Busciglio J.q · Iulita M.F.r · Crispino J.s · Malinge S.t · Barone E.u · Perluigi M.u · Costanzo F.v · Delabar J.M.n · Bartesaghi R.w · Dekker A.D.x · De Deyn P.x,y · Fortea Ormaechea J.g,h · Shaw P.A.z · Haydar T.F.z · Sherman S.L.A · Strydom A.B · Bhattacharyya A.f |
Characterization of the spontaneous degenerative mitral valve disease in FVB mice.Ayme-Dietrich E, Da Silva S, Bouabout GA, Arnoux A, Guyonnet J, Becker G, Monassier L |
Droplet digital PCR or quantitative PCR for in-depth genomic and functional validation of genetically altered rodents.Lindner L, Cayrou P, Rosahl TW, Zhou HH, Birling MC, Herault Y, Pavlovic G |
Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome.Brault V, Nguyen TL, Flores-Gutiérrez J, Iacono G, Birling MC, Lalanne V, Meziane H, Manousopoulou A, Pavlovic G, Lindner L, Selloum M, Sorg T, Yu E, Garbis SD, Hérault Y |
HDAC inhibitor ameliorates behavioral deficits in Mecp2(308/y) mouse model of Rett syndrome.Lebrun N, Delépine C, Selloum M, Meziane H, Nectoux J, Herault Y, Bienvenu T |
High Resolution Episcopic Microscopy for Qualitative and Quantitative Data in Phenotyping Altered Embryos and Adult Mice Using the New "Histo3D" System.Wendling O, Hentsch D, Jacobs H, Lemercier N, Taubert S, Pertuy F, Vonesch JL, Sorg T, Di Michele M, Le Cam L, Rosahl T, Carballo-Jane E, Liu M, Mu J, Mark M, Herault Y |
Importing genetically altered animals: ensuring quality.Birling MC, Fray MD, Kasparek P, Kopkanova J, Massimi M, Matteoni R, Montoliu L, Nutter LMJ, Raspa M, Rozman J, Ryder EJ, Scavizzi F, Voikar V, Wells S, Pavlovic G, Teboul L |
INFRAFRONTIER quality principles in systemic phenotyping.Ehlich H, Cater HL, Flenniken AM, Goncalves Da Cruz I, Mura AM, Ntafis V, Raess M, Selloum M, Stoeger C, Suchanova S, Vuolteenaho R, Brown SDM, Hérault Y, Hinttala R, Hrabě de Angelis M, Kollias G, Kontoyiannis DL, Malissen B, McKerlie C, Sedláček R, Wells SE, Zarubica A, Rozman J, Sorg T |
Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder.Courraud J, Chater-Diehl E, Durand B, Vincent M, Del Mar Muniz Moreno M, Boujelbene I, Drouot N, Genschik L, Schaefer E, Nizon M, Gerard B, Abramowicz M, Cogné B, Bronicki L, Burglen L, Barth M, Charles P, Colin E, Coubes C, David A, Delobel B, Demurger F, Passemard S, Denommé AS, Faivre L, Feger C, Fradin M, Francannet C, Genevieve D, Goldenberg A, Guerrot AM, Isidor B, Johannesen KM, Keren B, Kibæk M, Kuentz P, Mathieu-Dramard M, Demeer B, Metreau J, Steensbjerre Møller R, Moutton S, Pasquier L, Pilekær Sørensen K, Perrin L, Renaud M, Saugier P, Rio M, Svane J, Thevenon J, Tran Mau Them F, Tronhjem CE, Vitobello A, Layet V, Auvin S, Khachnaoui K, Birling MC, Drunat S, Bayat A, Dubourg C, El Chehadeh S, Fagerberg C, Mignot C, Guipponi M, Bienvenu T, Herault Y, Thompson J, Willems M, Mandel JL, Weksberg R, Piton A |
Introduction to mammalian genome special issue: the microbiome in human health and disease.Pavlovic G, Seong JK, Weinstock GM |
Microglia-specific knock-down of Bmal1 improves memory and protects mice from high fat diet-induced obesity.Wang XL, Kooijman S, Gao Y, Tzeplaeff L, Cosquer B, Milanova I, Wolff SEC, Korpel N, Champy MF, Petit-Demoulière B, Goncalves Da Cruz I, Sorg-Guss T, Rensen PCN, Cassel JC, Kalsbeek A, Boutillier AL, Yi CX |
Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models.Duchon A, Del Mar Muniz Moreno M, Martin Lorenzo S, Silva de Souza MP, Chevalier C, Nalesso V, Meziane H, Loureiro de Sousa P, Noblet V, Armspach JP, Brault V, Herault Y |
Pathogenesis of Anorectal Malformations in Retinoic Acid Receptor Knockout Mice Studied by HREM.Mark M, Teletin M, Wendling O, Vonesch JL, Féret B, Hérault Y, Ghyselinck NB |
Reliable and robust droplet digital PCR (ddPCR) and RT-ddPCR protocols for mouse studies.Lindner L, Cayrou P, Jacquot S, Birling MC, Herault Y, Pavlovic G |
SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2.Niewiadomska-Cimicka A, Doussau F, Perot JB, Roux MJ, Keime C, Hache A, Piguet F, Novati A, Weber C, Yalcin B, Meziane H, Champy MF, Grandgirard E, Karam A, Messaddeq N, Eisenmann A, Brouillet E, Nguyen HHP, Flament J, Isope P, Trottier Y |
Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models.Martin Lorenzo S, Nalesso V, Chevalier C, Birling MC, Herault Y |
2020Aggregation and Amyloidogenicity of the Nuclear Coactivator Binding Domain of CREB-Binding Protein.Garcia AM, Giorgiutti C, El Khoury Y, Bauer V, Spiegelhalter C, Leize-Wagner E, Hellwig P, Potier N, Torbeev V |
Antinociceptive Effects of Potent, Selective and Brain Penetrant Muscarinic M4 Positive Allosteric Modulators in Rodent Pain Models.Grauer SM(1), Sanoja R(2), Poulin D(3), Rashid H(3), Jochnowitz N(4), Calhoun M(4), Zwilling D(4), Varty GB(4), Rosahl TW(4), Meziane H(5), Mittlelhaeuser C(5), Mazzola R(4), Morrow J(2), Smith SM(2), Henze D(2), Marcus J(2). |
BAHD1 haploinsufficiency results in anxiety-like phenotypes in male mice.Pourpre R, Naudon L, Meziane H, Lakisic G, Jouneau L, Varet H, Legendre R, Wendling O, Selloum M, Proux C, Coppée JY, Herault Y, Bierne H |
Conditional switching of KIF2A mutation provides new insights into cortical malformations pathogeny.Gilet J(1)(2)(3)(4), Ivanova E(1)(2)(3)(4), Trofimova D(3), Rudolf G(1)(2)(3)(4), Meziane H(4), Broix L(1)(2)(3)(4), Drouot N(1)(2)(3)(4), Courraud J(1)(2)(3)(4), Skory V(1)(2)(3)(4), Voulleminot P(5), Osipenko M(1)(2)(3)(4), Bahi-Buisson N(6), Yalcin B(1)(2)(3)(4), Birling MC(4), Hinckelmann MV(1)(2)(3)(4), Kwok BH(7)(8), Allingham JS(3), Chelly J(1)(2)(3)(4)(5)(9)(10). |
Genetic quality assurance and genetic monitoring of laboratory mice and rats: FELASA Working Group Report.Benavides F, Rülicke T, Prins JB, Bussell J, Scavizzi F, Cinelli P, Herault Y, Wedekind D |
High-throughput discovery of genetic determinants of circadian misalignment.Zhang T(1), Xie P(1), Dong Y(1), Liu Z(1), Zhou F(1), Pan D(1), Huang Z(1), Zhai Q(1), Gu Y(1), Wu Q(2)(3), Tanaka N(4), Obata Y(4), Bradley A(5), Lelliott CJ(5); Sanger Institute Mouse Genetics Project, Nutter LMJ(6), McKerlie C(6), Flenniken AM(6), Champy MF(7), Sorg T(7), Herault Y(7), Angelis MH(8)(9), Durner VG(8), Mallon AM(10), Brown SDM(10), Meehan T(11), Parkinson HE(11), Smedley D(12), Lloyd KCK(13), Yan J(14), Gao X(14), Seong JK(15), Wang CL(16), Sedlacek R(9), Liu Y(17), Rozman J(8)(9)(18), Yang L(1), Xu Y(1)(3). |
Human and mouse essentiality screens as a resource for disease gene discovery.Cacheiro P(1), Muñoz-Fuentes V(2), Murray SA(3), Dickinson ME(4)(5), Bucan M(6), Nutter LMJ(7), Peterson KA(3), Haselimashhadi H(2), Flenniken AM(8), Morgan H(9), Westerberg H(9), Konopka T(1), Hsu CW(4), Christiansen A(4), Lanza DG(5), Beaudet AL(5), Heaney JD(5), Fuchs H(10), Gailus-Durner V(10), Sorg T(11), Prochazka J(12), Novosadova V(12), Lelliott CJ(13), Wardle-Jones H(13), Wells S(9), Teboul L(9), Cater H(9), Stewart M(9), Hough T(9), Wurst W(14)(15)(16), Sedlacek R(12), Adams DJ(13), Seavitt JR(5), Tocchini-Valentini G(17), Mammano F(17), Braun RE(3), McKerlie C(7)(18), Herault Y(19), de Angelis MH(10)(20)(21), Mallon AM(9), Lloyd KCK(22), Brown SDM(9), Parkinson H(2), Meehan TF(2), Smedley D(23); Genomics England Research Consortium; International Mouse Phenotyping Consortium. |
Introduction to Mammalian Genome Special Issue: Epigenetics.Beckers J, Teperino R, Hérault Y, Hrabé de Angelis M |
Modeling Down syndrome in animals from the early stage to the 4.0 models and next.Muñiz Moreno MDM, Brault V, Birling MC, Pavlovic G, Herault Y |
PATHBIO: an international training program for precision mouse phenotyping.Ruberte J, Schofield PN, Brakebusch C, Vogel P, Herault Y, Gracia G, McKerlie C, Hrabĕ de Angelis M, Hagn M, Sundberg JP |
Soft windowing application to improve analysis of high-throughput phenotyping data.Haselimashhadi H, Mason JC, Munoz-Fuentes V, López-Gómez F, Babalola K, Acar EF, Kumar V, White J, Flenniken AM, King R, Straiton E, Seavitt JR, Gaspero A, Garza A, Christianson AE, Hsu CW, Reynolds CL, Lanza DG, Lorenzo I, Green JR, Gallegos JJ, Bohat R, Samaco RC, Veeraragavan S, Kim JK, Miller G, Fuchs H, Garrett L, Becker L, Kang YK, Clary D, Cho SY, Tamura M, Tanaka N, Soo KD, Bezginov A, About GB, Champy MF, Vasseur L, Leblanc S, Meziane H, Selloum M, Reilly PT, Spielmann N, Maier H, Gailus-Durner V, Sorg T, Hiroshi M, Yuichi O, Heaney JD, Dickinson ME, Wolfgang W, Tocchini-Valentini GP, Lloyd KCK, McKerlie C, Seong JK, Yann H, de Angelis MH, Brown SDM, Smedley D, Flicek P, Mallon AM, Parkinson H, Meehan TF |
Variability in Genome Editing Outcomes: Challenges for Research Reproducibility and Clinical Safety.Teboul L, Herault Y, Wells S, Qasim W, Pavlovic G |
2019Cbs overdosage is necessary and sufficient to induce cognitive phenotypes in mouse models of Down syndrome and interacts genetically with Dyrk1a.Marechal D(1)(2)(3)(4), Brault V(1)(2)(3)(4), Leon A(5), Martin D(1)(2)(3)(4), Pereira PL(6), Loaec N(5), Birling MC(7), Friocourt G(5), Blondel M(5), Herault Y(1)(2)(3)(4)(7). |
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.Moore BA(1), Leonard BC(#)(2), Sebbag L(#)(1), Edwards SG(1), Cooper A(1), Imai DM(3), Straiton E(4), Santos L(4), Reilly C(3), Griffey SM(3), Bower L(5), Clary D(5), Mason J(6), Roux MJ(7)(8)(9)(10)(11), Meziane H(7)(8)(9)(10)(11), Herault Y(7)(8)(9)(10)(11); International Mouse Phenotyping Consortium, McKerlie C(12)(13), Flenniken AM(12)(14), Nutter LMJ(12)(13), Berberovic Z(12)(14), Owen C(12)(14), Newbigging S(12)(14), Adissu H(12)(14), Eskandarian M(12)(14), Hsu CW(15), Kalaga S(15), Udensi U(15), Asomugha C(15), Bohat R(16), Gallegos JJ(16), Seavitt JR(16), Heaney JD(16), Beaudet AL(16), Dickinson ME(15)(16), Justice MJ(12)(13)(16), Philip V(17), Kumar V(17), Svenson KL(17), Braun RE(17), Wells S(4), Cater H(4), Stewart M(4), Clementson-Mobbs S(4), Joynson R(4), Gao X(18), Suzuki T(19), Wakana S(19), Smedley D(20), Seong JK(21), Tocchini-Valentini G(22), Moore M(23), Fletcher C(24), Karp N(25), Ramirez-Solis R(25), White JK(17)(25), de Angelis MH(26), Wurst W(26), Thomasy SM(2)(27), Flicek P(6), Parkinson H(6), Brown SDM(4), Meehan TF(6), Nishina PM(17), Murray SA(17), Krebs MP(17), Mallon AM(4), Kent Lloyd KC(5), Murphy CJ(2)(27), Moshiri A(27). |
HENA, heterogeneous network-based data set for Alzheimer's disease.Sugis E(1)(2), Dauvillier J(3), Leontjeva A(4), Adler P(1)(2), Hindie V(5), Moncion T(5), Collura V(5), Daudin R(6)(7), Loe-Mie Y(8), Herault Y(9), Lambert JC(10), Hermjakob H(11), Pupko T(12), Rain JC(5), Xenarios I(13)(14)(15)(16), Vilo J(1)(2), Simonneau M(17)(18), Peterson H(19)(20). |
Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.Qiu Y(1), Arbogast T(2), Lorenzo SM(3), Li H(1), Tang SC(4), Richardson E(2), Hong O(4), Cho S(4), Shanta O(5), Pang T(4), Corsello C(6), Deutsch CK(7), Chevalier C(3), Davis EE(2), Iakoucheva LM(4), Herault Y(3), Katsanis N(2), Messer K(1), Sebat J(8). |
Optimizing PCR for Mouse Genotyping: Recommendations for Reliable, Rapid, Cost Effective, Robust and Adaptable to High-Throughput Genotyping Protocol for Any Type of Mutation.Jacquot S(1), Chartoire N(1), Piguet F(2), Herault Y(1)(3), Pavlovic G(1). |
Severe head dysgenesis resulting from imbalance between anterior and posterior ontogenetic programs.Grall E(1), Gourain V(2), Nair A(1), Martin E(1), Birling MC(3), Freund JN(4), Duluc I(5). |
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals.Giannuzzi G(1), Schmidt PJ(2), Porcu E(3), Willemin G(4), Munson KM(5), Nuttle X(5), Earl R(6), Chrast J(4), Hoekzema K(5), Risso D(5), Mannik K(4), De Nittis P(4), Baratz ED(7); 16p11.2 Consortium, Herault Y(8), Gao X(9), Philpott CC(7), Bernier RA(6), Kutalik Z(10), Fleming MD(2), Eichler EE(11), Reymond A(4). |
The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia.Collins SC(1)(2)(3)(4)(5), Uzquiano A(6)(7)(8), Selloum M(1)(2)(3)(4)(9), Wendling O(1)(2)(3)(4)(9), Gaborit M(1)(2)(3)(4), Osipenko M(1)(2)(3)(4), Birling MC(1)(2)(3)(4)(9), Yalcin B(1)(2)(3)(4), Francis F(6)(7)(8). |
Transgenic mouse models expressing human and macaque prion protein exhibit similar prion susceptibility on a strain-dependent manner.Espinosa JC(1), Comoy EE(2), Marin-Moreno A(3), Aguilar-Calvo P(3), Birling MC(4), Pitarch JL(3), Deslys JP(2), Torres JM(5). |
TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis.Ivanova EL(1)(2)(3)(4), Gilet JG(1)(2)(3)(4), Sulimenko V(5), Duchon A(1)(2)(3)(4), Rudolf G(1)(2)(3)(4), Runge K(1)(2)(3)(4), Collins SC(1)(2)(3)(4)(6), Asselin L(1)(2)(3)(4), Broix L(1)(2)(3)(4), Drouot N(1)(2)(3)(4), Tilly P(1)(2)(3)(4), Nusbaum P(7), Vincent A(1)(2)(4), Magnant W(1)(2)(4), Skory V(1)(2)(3)(4), Birling MC(8), Pavlovic G(8), Godin JD(1)(2)(3)(4), Yalcin B(1)(2)(3)(4), Herault Y(1)(2)(3)(4), Draber P(5), Chelly J(1)(2)(3)(4)(9)(10), Hinckelmann MV(11)(12)(13)(14). |
Ultrasound-Guided Approaches to Improve Orthotopic Mouse Xenograft Models for Hepatocellular Carcinoma.Bou About G(1), Thiebault E(1), Wattenhofer-Donze M(1), Jacobs H(1), Guimond A(1), Sorg T(1), Robinet E(2), Baumert TF(2), Monassier L(1)(3)(4), Herault Y(1)(5)(6). |
2018A new mouse model of ARX dup24 recapitulates the patients' behavioral and fine motor alterations.Dubos A(1)(2)(3)(4), Meziane H(4), Iacono G(5), Curie A(6), Riet F(4), Martin C(7), Loaec N(8), Birling MC(4), Selloum M(4), Normand E(7)(9), Pavlovic G(4), Sorg T(4), Stunnenberg HG(5), Chelly J(1)(2)(3)(10), Humeau Y(7), Friocourt G(8), Herault Y(1)(2)(3)(4). |
A Population Study of Common Ocular Abnormalities in C57BL/6N rd8 Mice.Moore BA(1), Roux MJ(2)(3)(4)(5), Sebbag L(1), Cooper A(1), Edwards SG(1), Leonard BC(1), Imai DM(6), Griffey S(6), Bower L(7), Clary D(7), Lloyd KCK(7)(8), Herault Y(2)(3)(4)(5)(9), Thomasy SM(10)(11), Murphy CJ(10)(11), Moshiri A(11). |
Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A.Nguyen TL(1)(2)(3)(4)(5), Duchon A(1)(2)(3)(4), Manousopoulou A(6), Loaec N(5), Villiers B(5), Pani G(1)(2)(3)(4), Karatas M(7)(8), Mechling AE(8), Harsan LA(7)(8), Limanton E(9), Bazureau JP(9), Carreaux F(9), Garbis SD(10), Meijer L(11), Herault Y(12)(2)(3)(4). |
Identification of genes required for eye development by high-throughput screening of mouse knockouts.Moore BA(1), Leonard BC(#)(2), Sebbag L(#)(1), Edwards SG(1), Cooper A(1), Imai DM(3), Straiton E(4), Santos L(4), Reilly C(3), Griffey SM(3), Bower L(5), Clary D(5), Mason J(6), Roux MJ(7)(8)(9)(10)(11), Meziane H(7)(8)(9)(10)(11), Herault Y(7)(8)(9)(10)(11); International Mouse Phenotyping Consortium, McKerlie C(12)(13), Flenniken AM(12)(14), Nutter LMJ(12)(13), Berberovic Z(12)(14), Owen C(12)(14), Newbigging S(12)(14), Adissu H(12)(14), Eskandarian M(12)(14), Hsu CW(15), Kalaga S(15), Udensi U(15), Asomugha C(15), Bohat R(16), Gallegos JJ(16), Seavitt JR(16), Heaney JD(16), Beaudet AL(16), Dickinson ME(15)(16), Justice MJ(12)(13)(16), Philip V(17), Kumar V(17), Svenson KL(17), Braun RE(17), Wells S(4), Cater H(4), Stewart M(4), Clementson-Mobbs S(4), Joynson R(4), Gao X(18), Suzuki T(19), Wakana S(19), Smedley D(20), Seong JK(21), Tocchini-Valentini G(22), Moore M(23), Fletcher C(24), Karp N(25), Ramirez-Solis R(25), White JK(17)(25), de Angelis MH(26), Wurst W(26), Thomasy SM(2)(27), Flicek P(6), Parkinson H(6), Brown SDM(4), Meehan TF(6), Nishina PM(17), Murray SA(17), Krebs MP(17), Mallon AM(4), Lloyd KCK(5), Murphy CJ(2)(27), Moshiri A(27). |
Identification of genetic elements in metabolism by high-throughput mouse phenotyping.Rozman J(1)(2), Rathkolb B(1)(2)(3), Oestereicher MA(1), Schutt C(1), Ravindranath AC(2)(4), Leuchtenberger S(1), Sharma S(2)(5), Kistler M(1), Willershauser M(6)(7)(8), Brommage R(1), Meehan TF(9), Mason J(9), Haselimashhadi H(9); IMPC Consortium, Hough T(10), Mallon AM(10), Wells S(10), Santos L(10), Lelliott CJ(11), White JK(11)(12), Sorg T(13)(14)(15)(16)(17), Champy MF(13)(14)(15)(16)(17), Bower LR(18), Reynolds CL(19), Flenniken AM(20)(21)(22), Murray SA(12), Nutter LMJ(20)(21), Svenson KL(12), West D(23), Tocchini-Valentini GP(24), Beaudet AL(20)(21), Bosch F(25), Braun RB(12), Dobbie MS(26), Gao X(27), Herault Y(13)(14)(15)(16)(17), Moshiri A(28), Moore BA(29), Kent Lloyd KC(18), McKerlie C(20)(21), Masuya H(30), Tanaka N(30), Flicek P(9), Parkinson HE(9), Sedlacek R(31), Seong JK(32), Wang CL(33), Moore M(34), Brown SD(10), Tschop MH(2)(35)(36), Wurst W(37)(38)(39)(40), Klingenspor M(6)(7)(8), Wolf E(2)(3), Beckers J(1)(2)(41), Machicao F(42), Peter A(2)(42)(43), Staiger H(2)(43)(44), Haring HU(2)(42)(43), Grallert H(2)(5)(45), Campillos M(2)(4), Maier H(1), Fuchs H(1), Gailus-Durner V(1), Werner T(46), Hrabe de Angelis M(47)(48)(49). |
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome.Iacono G(1), Dubos A(2)(3)(4)(5), Meziane H(2), Benevento M(6)(7)(8), Habibi E(1), Mandoli A(1), Riet F(2), Selloum M(2), Feil R(9)(10), Zhou H(1)(7), Kleefstra T(7)(8), Kasri NN(6)(7)(8), van Bokhoven H(6)(7)(8), Herault Y(2)(3)(4)(5), Stunnenberg HG(1). |
Ketohexokinase knockout mice, a model for essential fructosuria, exhibit altered fructose metabolism and are protected from diet-induced metabolic defects.Miller CO, Yang X, Lu K, Cao J, Herath K, Rosahl TW, Askew R, Pavlovic G, Zhou G, Li C, Akiyama TE |
Nox4 genetic inhibition in experimental hypertension and metabolic syndrome.Bouabout G(1), Ayme-Dietrich E(2), Jacob H(1), Champy MF(1), Birling MC(1), Pavlovic G(1), Madeira L(2), Fertak LE(1), Petit-Demouliere B(1), Sorg T(1), Herault Y(1), Mudgett J(3), Monassier L(4). |
Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse.Ung DC(1)(2), Iacono G(3), Meziane H(4), Blanchard E(1)(5)(6), Papon MA(1)(2), Selten M(7), van Rhijn JR(7), Montjean R(8)(9)(10)(11), Rucci J(8)(9)(10)(11), Martin S(12), Fleet A(13), Birling MC(4), Marouillat S(1)(2), Roepman R(14)(15), Selloum M(4), Lux A(4), Thepault RA(1)(2), Hamel P(13), Mittal K(16), Vincent JB(16), Dorseuil O(8)(9)(10)(11), Stunnenberg HG(3), Billuart P(8)(9)(10)(11), Nadif Kasri N(7)(14), Herault Y(4)(17)(18)(19)(20), Laumonnier F(1)(2)(6). |
Synaptic dysfunction in amygdala in intellectual disorder models.Aincy M(1), Meziane H(2), Herault Y(3), Humeau Y(4). |
Translating molecular advances in Down syndrome and Fragile X syndrome into therapies.Faundez V(1), De Toma I(2), Bardoni B(3), Bartesaghi R(4), Nizetic D(5), de la Torre R(6), Cohen Kadosh R(7), Herault Y(8), Dierssen M(9), Potier MC(10); Down Syndrome and Other Genetic Developmental Disorders ECNP Network. |
2017A Fast, Easy, and Customizable Eight-Color Flow Cytometric Method for Analysis of the Cellular Content of Bronchoalveolar Lavage Fluid in the Mouse.Daubeuf F(1)(2), Becker J(3), Aguilar-Pimentel JA(4), Ebel C(5), Hrabe de Angelis M(4), Herault Y(3)(5)(6)(7)(8), Frossard N(1)(2). |
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Bowl MR(1), Simon MM(1), Ingham NJ(2)(3), Greenaway S(1), Santos L(1), Cater H(1), Taylor S(1), Mason J(4), Kurbatova N(4), Pearson S(3), Bower LR(5), Clary DA(5), Meziane H(6), Reilly P(6), Minowa O(7), Kelsey L(8)(9)(10); International Mouse Phenotyping Consortium, Tocchini-Valentini GP(11), Gao X(12), Bradley A(3), Skarnes WC(3), Moore M(13), Beaudet AL(14), Justice MJ(8)(9)(10)(14), Seavitt J(14), Dickinson ME(15), Wurst W(16), de Angelis MH(17), Herault Y(6)(18)(19)(20), Wakana S(7), Nutter LMJ(8)(9)(10), Flenniken AM(8)(9)(10), McKerlie C(8)(9)(10), Murray SA(21), Svenson KL(21), Braun RE(21), West DB(22), Lloyd KCK(5), Adams DJ(3), White J(3), Karp N(3), Flicek P(4), Smedley D(23), Meehan TF(4), Parkinson HE(4), Teboul LM(1), Wells S(1), Steel KP(2)(3), Mallon AM(1), Brown SDM(24). |
Atp6ap2 ablation in adult mice impairs viability through multiple organ deficiencies.Wendling O(1), Champy MF(1), Jaubert S(2), Pavlovic G(1), Dubos A(1)(3)(4)(5)(6), Lindner L(1), Jacobs H(1), Mark M(1)(3)(4)(5)(6), Combe R(1), Da Cruz IG(1), Luche H(6), Mudgett JS(7), Rosahl T(7), Sorg T(1), Malissen M(2), Reilly PT(1), Herault Y(8)(9)(10)(11)(12). |
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein.Mariani LL(1)(2), Rivaud-Pechoux S(3), Charles P(1), Ewenczyk C(1), Meneret A(2)(3), Monga BB(4), Fleury MC(5)(6)(7), Hainque E(8)(9)(10), Maisonobe T(11), Degos B(2), Echaniz-Laguna A(5)(12), Renaud M(5)(6)(7), Wirth T(5), Grabli D(2)(9), Brice A(1)(9)(10), Vidailhet M(2)(9)(10), Stoppa-Lyonnet D(13)(14), Dubois-d'Enghien C(13), Le Ber I(2)(9), Koenig M(15), Roze E(2)(9)(10), Tranchant C(5)(6)(7), Durr A(1)(9)(10), Gaymard B(16), Anheim M(17)(18)(19)(20). |
Deciphering the Role of Oncogenic MITFE318K in Senescence Delay and Melanoma Progression.Bonet C(1)(2), Luciani F(3)(4), Ottavi JF(1)(2), Leclerc J(1)(2), Jouenne FM(5), Boncompagni M(1)(2), Bille K(1)(2), Hofman V(2)(6), Bossis G(7), Marco de Donatis G(8), Strub T(9), Cheli Y(1)(2), Ohanna M(1)(2), Luciano F(10), Marchetti S(10), Rocchi S(1)(2), Birling MC(1)(11), Avril MF(12), Poulalhon N(13), Luc T(13), Bertolotto C(1)(2). |
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Meehan TF(1), Conte N(1), West DB(2), Jacobsen JO(3), Mason J(1), Warren J(1), Chen CK(1), Tudose I(1), Relac M(1), Matthews P(1), Karp N(4), Santos L(5), Fiegel T(5), Ring N(5), Westerberg H(5), Greenaway S(5), Sneddon D(5), Morgan H(5), Codner GF(5), Stewart ME(5), Brown J(5), Horner N(5); International Mouse Phenotyping Consortium, Haendel M(6), Washington N(7), Mungall CJ(7), Reynolds CL(8), Gallegos J(8), Gailus-Durner V(9), Sorg T(10)(11)(12)(13), Pavlovic G(10)(11)(12)(13), Bower LR(14), Moore M(15), Morse I(16), Gao X(17), Tocchini-Valentini GP(18), Obata Y(19), Cho SY(20)(21), Seong JK(20)(22), Seavitt J(8), Beaudet AL(8), Dickinson ME(8), Herault Y(10)(11)(12)(13), Wurst W(9), de Angelis MH(9), Lloyd KCK(14), Flenniken AM(23), Nutter LMJ(23), Newbigging S(23), McKerlie C(23), Justice MJ(24), Murray SA(25), Svenson KL(25), Braun RE(25), White JK(4), Bradley A(4), Flicek P(1), Wells S(5), Skarnes WC(4), Adams DJ(4), Parkinson H(1), Mallon AM(5), Brown SDM(5), Smedley D(3). |
Dry ice is a reliable substrate for the distribution of frozen mouse spermatozoa: A multi-centric study.Raspa M(1), Guan M(2), Paoletti R(3), Montoliu L(4), Ayadi A(5), Marschall S(6); EMMA/Infrafrontier Technical Working Group, Fray M(2), Scavizzi F(7). |
Efficient and rapid generation of large genomic variants in rats and mice using CRISMERE.Birling MC(1), Schaeffer L(1), Andre P(1), Lindner L(1), Marechal D(1), Ayadi A(1), Sorg T(1), Pavlovic G(1), Herault Y(1,)(2,)(3,)(4,)(5). |
Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors.Haziza S(1,)(2), Mohan N(1), Loe-Mie Y(2), Lepagnol-Bestel AM(2), Massou S(1), Adam MP(1), Le XL(1), Viard J(2), Plancon C(3), Daudin R(2), Koebel P(4), Dorard E(2), Rose C(2), Hsieh FJ(5), Wu CC(6), Potier B(2), Herault Y(4), Sala C(7), Corvin A(8), Allinquant B(2), Chang HC(5), Treussart F(1), Simonneau M(1,)(2,)(9). |
Integrated transcriptional analysis unveils the dynamics of cellular differentiation in the developing mouse hippocampus.Iacono G(1), Benevento M(2)(3)(4), Dubos A(5), Herault Y(5), van Bokhoven H(2)(3)(4), Nadif Kasri N(2)(3)(4), Stunnenberg HG(6). |
Modeling human disease in rodents by CRISPR/Cas9 genome editing.Birling MC(1), Herault Y(2)(3)(4)(5)(6), Pavlovic G(2). |
Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.Arbogast T(1)(2)(3)(4), Iacono G(5), Chevalier C(1)(2)(3)(4), Afinowi NO(6), Houbaert X(7), van Eede MC(8), Laliberte C(8), Birling MC(9), Linda K(10), Meziane H(9), Selloum M(9), Sorg T(9), Nadif Kasri N(10), Koolen DA(10), Stunnenberg HG(5), Henkelman RM(8), Kopanitsa M(6), Humeau Y(7), De Vries BBA(10), Herault Y(1)(2)(3)(4)(9). |
Non-invasive quantitative imaging of hepatocellular carcinoma growth in mice by micro-CT using liver-targeted iodinated nano-emulsions.Anton N(1)(2), Parlog A(3)(4)(5)(6), Bou About G(3)(4)(5)(6), Attia MF(7)(8)(9)(10), Wattenhofer-Donze M(3)(4)(5)(6), Jacobs H(3)(4)(5)(6), Goncalves I(3)(4)(5)(6), Robinet E(11), Sorg T(3)(4)(5)(6), Vandamme TF(7)(8). |
Prevalence of sexual dimorphism in mammalian phenotypic traits.Karp NA(1)(2), Mason J(3), Beaudet AL(4), Benjamini Y(5), Bower L(6), Braun RE(7), Brown SDM(8), Chesler EJ(7), Dickinson ME(9), Flenniken AM(10), Fuchs H(11), Angelis MH(11)(12)(13), Gao X(14), Guo S(14), Greenaway S(8), Heller R(5), Herault Y(15)(16)(17)(18)(19), Justice MJ(20), Kurbatova N(5), Lelliott CJ(21), Lloyd KCK(6), Mallon AM(8), Mank JE(22), Masuya H(23), McKerlie C(10)(24), Meehan TF(3), Mott RF(25), Murray SA(7), Parkinson H(3), Ramirez-Solis R(21), Santos L(8), Seavitt JR(4), Smedley D(26), Sorg T(15)(16)(17)(18)(19), Speak AO(21), Steel KP(21)(27), Svenson KL(7); International Mouse Phenotyping Consortium, Wakana S(23), West D(28), Wells S(8), Westerberg H(8), Yaacoby S(5), White JK(7)(21). |
RF313, an orally bioavailable neuropeptide FF receptor antagonist, opposes effects of RF-amide-related peptide-3 and opioid-induced hyperalgesia in rodents.Elhabazi K(1), Humbert JP(2), Bertin I(3), Quillet R(4), Utard V(5), Schneider S(6), Schmitt M(7), Bourguignon JJ(8), Laboureyras E(9), Ben Boujema M(10), Simonnet G(11), Ancel C(12), Simonneaux V(13), Beltramo M(14), Bucher B(15), Sorg T(16), Meziane H(17), Schneider E(18), Petit-Demouliere B(19), Ilien B(20), Bihel F(21), Simonin F(22). |
Rodent models in Down syndrome research: impact and future opportunities.Herault Y, Delabar JM, Fisher EMC, Tybulewicz VLJ, Yu E, Brault V |
Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.Sellier C, Buijsen RAM, He F, Natla S, Jung L, Tropel P, Gaucherot A, Jacobs H, Meziane H, Vincent A, Champy MF, Sorg T, Pavlovic G, Wattenhofer-Donze M, Birling MC, Oulad-Abdelghani M, Eberling P, Ruffenach F, Joint M, Anheim M, Martinez-Cerdeno V, Tassone F, Willemsen R, Hukema RK, Viville S, Martinat C, Todd PK, Charlet-Berguerand N |
Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.Sellier C, Buijsen RAM, He F, Natla S, Jung L, Tropel P, Gaucherot A, Jacobs H, Meziane H, Vincent A, Champy MF, Sorg T, Pavlovic G, Wattenhofer-Donze M, Birling MC, Oulad-Abdelghani M, Eberling P, Ruffenach F, Joint M, Anheim M, Martinez-Cerdeno V, Tassone F, Willemsen R, Hukema RK, Viville S, Martinat C, Todd PK, Charlet-Berguerand N |
2016Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes.Delepine C(1), Meziane H(2), Nectoux J(3), Opitz M(1), Smith AB(4), Ballatore C(5), Saillour Y(1), Bennaceur-Griscelli A(6), Chang Q(7), Williams EC(7), Dahan M(8), Duboin A(9), Billuart P(1), Herault Y(2), Bienvenu T(10). |
Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction.Codner GF(1), Lindner L(2), Caulder A(1), Wattenhofer-Donzé M(2), Radage A(1), Mertz A(2), Eisenmann B(2), Mianné J(2), Evans EP(1), Beechey CV(1), Fray MD(1), Birling MC(2), Hérault Y(2), Pavlovic G(3), Teboul L(4). |
Corrigendum: Domains of genome-wide gene expression dysregulation in Down's syndrome.Letourneau A, Santoni FA, Bonilla X, Sailani MR, Gonzalez D, Kind J, Chevalier C, Thurman R, Sandstrom RS, Hibaoui Y, Garieri M, Popadin K, Falconnet E, Gagnebin M, Gehrig C, Vannier A, Guipponi M, Farinelli L, Robyr D, Migliavacca E, Borel C, Deutsch S, Feki A, Stamatoyannopoulos JA, Herault Y, van Steensel B, Guigo R, Antonarakis SE. |
Counterregulation between thymic stromal lymphopoietin- and IL-23-driven immune axes shapes skin inflammation in mice with epidermal barrier defects.Li J(1), Leyva-Castillo JM(1), Hener P(1), Eisenmann A(1), Zaafouri S(2), Jonca N(2), Serre G(2), Birling MC(3), Li M(4). |
DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down Syndrome.Duchon A(1), Herault Y(2). |
E4F1-mediated control of pyruvate dehydrogenase activity is essential for skin homeostasis.Goguet-Rubio P(1), Seyran B(1), Gayte L(1), Bernex F(2), Sutter A(1), Delpech H(3), Linares LK(1), Riscal R(1), Repond C(4), Rodier G(3), Kirsh O(5), Touhami J(6), Noel J(7), Vincent C(8), Pirot N(7), Pavlovic G(9), Herault Y(9), Sitbon M(6), Pellerin L(4), Sardet C(3), Lacroix M(10), Le Cam L(10). |
Epidermal-specific deletion of CD44 reveals a function in keratinocytes in response to mechanical stress.Shatirishvili M(1), Burk AS(2), Franz CM(3), Pace G(1), Kastilan T(1), Breuhahn K(4), Hinterseer E(5), Dierich A(6), Bakiri L(7), Wagner EF(7), Ponta H(1), Hartmann TN(5), Tanaka M(2,)(8), Orian-Rousseau V(1). |
Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability.Meziane H(1), Khelfaoui M(2), Morello N(3), Hiba B(4), Calcagno E(3), Reibel-Foisset S(5), Selloum M(1), Chelly J(6), Humeau Y(7), Riet F(1), Zanni G(8), Herault Y(1), Bienvenu T(9), Giustetto M(3), Billuart P(10). |
High-throughput discovery of novel developmental phenotypes.Dickinson ME, Flenniken AM, Ji X, Teboul L, Wong MD, White JK, Meehan TF, Weninger WJ, Westerberg H, Adissu H, Baker CN, Bower L, Brown JM, Caddle LB, Chiani F, Clary D, Cleak J, Daly MJ, Denegre JM, Doe B, Dolan ME, Edie SM, Fuchs H, Gailus-Durner V, Galli A, Gambadoro A, Gallegos J, Guo S, Horner NR, Hsu CW, Johnson SJ, Kalaga S, Keith LC, Lanoue L, Lawson TN, Lek M, Mark M, Marschall S, Mason J, McElwee ML, Newbigging S, Nutter LM, Peterson KA, Ramirez-Solis R, Rowland DJ, Ryder E, Samocha KE, Seavitt JR, Selloum M, Szoke-Kovacs Z, Tamura M, Trainor AG, Tudose I, Wakana S, Warren J, Wendling O, West DB, Wong L, Yoshiki A; International Mouse Phenotyping Consortium; Jackson Laboratory; Infrastructure Nationale PHENOMIN, Institut Clinique de la Souris (ICS); Charles River Laboratories; MRC Harwell; Toronto Centre for Phenogenomics; Wellcome Trust Sanger Institute; RIKEN BioResource Center, MacArthur DG, Tocchini-Valentini GP, Gao X, Flicek P, Bradley A, Skarnes WC, Justice MJ, Parkinson HE, Moore M, Wells S, Braun RE, Svenson KL, de Angelis MH, Herault Y, Mohun T, Mallon AM, Henkelman RM, Brown SD, Adams DJ, Lloyd KC, McKerlie C, Beaudet AL, Bucan M, Murray SA. |
How Does Circadian Rhythm Impact Salt Sensitivity of Blood Pressure in Mice? A Study in Two Close C57Bl/6 Substrains.Combe R(1), Mudgett J(2), El Fertak L(1), Champy MF(1), Ayme-Dietrich E(3), Petit-Demoulière B(1), Sorg T(1), Herault Y(1), Madwed JB(2), Monassier L(1,)(3). |
Lymphopoiesis in transgenic mice over-expressing Artemis.Rivera-Munoz P(1,)(2), Abramowski V(1,)(2), Jacquot S(3), André P(3), Charrier S(4), Lipson-Ruffert K(5), Fischer A(2,)(6,)(7), Galy A(4), Cavazzana M(2,)(6), de Villartay JP(1,)(2). |
Multimodal imaging of a humanized orthotopic model of hepatocellular carcinoma in immunodeficient mice.Wu T(1,)(2,)(3), Heuillard E(1,)(2,)(4), Lindner V(5), Bou About G(6), Ignat M(7,)(8), Dillenseger JP(2,)(9,)(10,)(11), Anton N(2,)(12), Dalimier E(13), Gossé F(1,)(2), Fouré G(4), Blindauer F(4), Giraudeau C(4), El-Saghire H(1,)(2), Bouhadjar M(4), Calligaro C(4), Sorg T(6), Choquet P(2,)(9,)(10,)(11), Vandamme T(2,)(12), Ferrand C(14,)(15,)(16), Marescaux J(4,)(7,)(8), Baumert TF(1,)(2,)(4,)(7), Diana M(4,)(8), Pessaux P(1,)(2,)(4,)(7,)(8), Robinet E(1,)(2,)(4). |
Physiological Expression of AMPKgamma2RG Mutation Causes Wolff-Parkinson-White Syndrome and Induces Kidney Injury in Mice.Yang X(1), Mudgett J(2), Bou-About G(3), Champy MF(3), Jacobs H(3), Monassier L(4), Pavlovic G(3), Sorg T(3), Herault Y(3), Petit-Demouliere B(3), Lu K(1), Feng W(1), Wang H(5), Ma LJ(1), Askew R(2), Erion MD(1), Kelley DE(1), Myers RW(1), Li C(1), Guan HP(6). |
Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes.Arbogast T(1,)(2,)(3,)(4), Ouagazzal AM(1,)(2,)(3,)(4), Chevalier C(1,)(2,)(3,)(4), Kopanitsa M(5), Afinowi N(5), Migliavacca E(6,)(7), Cowling BS(1,)(2,)(3,)(4), Birling MC(8), Champy MF(8), Reymond A(6), Herault Y(1,)(2,)(3,)(4,)(8). |
Role of the BAHD1 Chromatin-Repressive Complex in Placental Development and Regulation of Steroid Metabolism.Lakisic G(1), Lebreton A(2,)(3,)(4), Pourpre R(1), Wendling O(5), Libertini E(6), Radford EJ(7,)(8), Le Guillou M(9), Champy MF(5), Wattenhofer-Donze M(5), Soubigou G(6), Ait-Si-Ali S(10), Feunteun J(9), Sorg T(5), Coppee JY(6), Ferguson-Smith AC(7), Cossart P(2,)(3,)(4), Bierne H(1). |
The cell proliferation antigen Ki-67 organises heterochromatin.Sobecki M(1)(2), Mrouj K(1)(2), Camasses A(1)(2), Parisis N(1)(2), Nicolas E(3), Lleres D(1)(2), Gerbe F(2)(4)(5), Prieto S(1)(2), Krasinska L(1)(2), David A(2)(4)(5), Eguren M(6), Birling MC(7), Urbach S(2)(4)(5)(8), Hem S(9), Dejardin J(2)(10), Malumbres M(6), Jay P(2)(4)(5), Dulic V(1)(2), Lafontaine DLj(3), Feil R(1)(2), Fisher D(1)(2). |
Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss.Scekic-Zahirovic J(1), Sendscheid O(2), El Oussini H(1), Jambeau M(3), Sun Y(3), Mersmann S(2), Wagner M(2), Dieterlé S(1), Sinniger J(1), Dirrig-Grosch S(1), Drenner K(3), Birling MC(4), Qiu J(5), Zhou Y(5), Li H(5), Fu XD(5), Rouaux C(1), Shelkovnikova T(6), Witting A(7), Ludolph AC(7), Kiefer F(8), Storkebaum E(9), Lagier-Tourenne C(10), Dupuis L(11). |
2015A mu-delta opioid receptor brain atlas reveals neuronal co-occurrence in subcortical networks.Erbs E(1), Faget L, Scherrer G, Matifas A, Filliol D, Vonesch JL, Koch M, Kessler P, Hentsch D, Birling MC, Koutsourakis M, Vasseur L, Veinante P, Kieffer BL, Massotte D. |
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.Hrabe de Angelis M, Nicholson G, Selloum M, White JK, Morgan H, Ramirez-Solis R, Sorg T, Wells S, Fuchs H, Fray M, Adams DJ, Adams NC, Adler T, Aguilar-Pimentel A, Ali-Hadji D, Amann G, AndrE P, Atkins S, Auburtin A, Ayadi A, Becker J, Becker L, Bedu E, Bekeredjian R, Birling MC, Blake A, Bottomley J, Bowl MR, Brault V, Busch DH, Bussell JN, Calzada-Wack J, Cater H, Champy MF, Charles P, Chevalier C, Chiani F, Codner GF, Combe R, Cox R, Dalloneau E, Dierich A, Di Fenza A, Doe B, Duchon A, Eickelberg O, Esapa CT, Fertak LE, Feigel T, Emelyanova I, Estabel J, Favor J, Flenniken A, Gambadoro A, Garrett L, Gates H, Gerdin AK, Gkoutos G, Greenaway S, Glasl L, Goetz P, Da Cruz IG, Gotz A, Graw J, Guimond A, Hans W, Hicks G, Holter SM, Hofler H, Hancock JM, Hoehndorf R, Hough T, Houghton R, Hurt A, Ivandic B, Jacobs H, Jacquot S, Jones N, Karp NA, Katus HA, Kitchen S, Klein-Rodewald T, Klingenspor M, Klopstock T, Lalanne V, Leblanc S, Lengger C, le Marchand E, Ludwig T, Lux A, McKerlie C, Maier H, Mandel JL, Marschall S, Mark M, Melvin DG, Meziane H, Micklich K, Mittelhauser C, Monassier L, Moulaert D, Muller S, Naton B, Neff F, Nolan PM, Nutter LM, Ollert M, Pavlovic G, Pellegata NS, Peter E, Petit-Demouliere B, Pickard A, Podrini C, Potter P, Pouilly L, Puk O, Richardson D, Rousseau S, Quintanilla-Fend L, Quwailid MM, Racz I, Rathkolb B, Riet F, Rossant J, Roux M, Rozman J, Ryder E, Salisbury J, Santos L, Schable KH, Schiller E, Schrewe A, Schulz H, Steinkamp R, Simon M, Stewart M, Stoger C, Stoger T, Sun M, Sunter D, Teboul L, Tilly I, Tocchini-Valentini GP, Tost M, Treise I, Vasseur L, Velot E, Vogt-Weisenhorn D, Wagner C, Walling A, Wattenhofer-Donze M, Weber B, Wendling O, Westerberg H, Willershauser M, Wolf E, Wolter A, Wood J, Wurst W, Yildirim AO, Zeh R, Zimmer A, Zimprich A; EUMODIC Consortium, Holmes C, Steel KP, Herault Y, Gailus-Durner V, Mallon AM, Brown SD. |
An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism.Meziane H(1), Schaller F(2), Bauer S(2), Villard C(3), Matarazzo V(2), Riet F(1), Guillon G(4), Lafitte D(3), Desarmenien MG(4), Tauber M(5), Muscatelli F(6). |
Applying the ARRIVE Guidelines to an In Vivo Database.Karp NA(1), Meehan TF(2), Morgan H(3), Mason JC(2), Blake A(3), Kurbatova N(2), Smedley D(1), Jacobsen J(1), Mott RF(4), Iyer V(5), Matthews P(5), Melvin DG(1), Wells S(3), Flenniken AM(6), Masuya H(7), Wakana S(7), White JK(8), Lloyd KC(9), Reynolds CL(10), Paylor R(11), West DB(12), Svenson KL(13), Chesler EJ(13), de Angelis MH(14), Tocchini-Valentini GP(15), Sorg T(16), Herault Y(16), Parkinson H(2), Mallon AM(3), Brown SD(3). |
Blastocyst genotyping for quality control of mouse mutant archives: an ethical and economical approach.Scavizzi F(1), Ryder E(2), Newman S(2), Raspa M(1), Gleeson D(2), Wardle-Jones H(2), Montoliu L(3,)(4), Fernandez A(3,)(4), Dessain ML(5), Larrigaldie V(5), Khorshidi Z(6), Vuolteenaho R(7), Soininen R(7), André P(8), Jacquot S(8), Hong Y(9), de Angelis MH(9), Ramirez-Solis R(2), Doe B(10). |
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration.Dubos A(1), Castells-Nobau A(2), Meziane H(3), Oortveld MA(2), Houbaert X(4), Iacono G(5), Martin C(4), Mittelhaeuser C(3), Lalanne V(3), Kramer JM(2), Bhukel A(6), Quentin C(7), Slabbert J(8), Verstreken P(8), Sigrist SJ(7), Messaddeq N(9), Birling MC(3), Selloum M(3), Stunnenberg HG(5), Humeau Y(4), Schenck A(10), Herault Y(11). |
Contribution of serotonin to cardiac remodeling associated with hypertensive diastolic ventricular dysfunction in rats.Ayme-Dietrich E(1), Marzak H, Lawson R, Mokni W, Wendling O, Combe R, Becker J, El Fertak L, Champy MF, Matz R, Andriantsitohaina R, Doly S, Boutourlinsky K, Maroteaux L, Monassier L. |
Deletion of the App-Runx1 region in mice models human partial monosomy 21.Arbogast T(1), Raveau M(1), Chevalier C(1), Nalesso V(1), Dembele D(1), Jacobs H(2), Wendling O(2), Roux M(3), Duchon A(1), Herault Y(4). |
INFRAFRONTIER--providing mutant mouse resources as research tools for the international scientific community.INFRAFRONTIER Consortium. |
LXR-Mediated ABCA1 Expression and Function Are Modulated by High Glucose and PRMT2.Hussein MA(1), Shrestha E(1), Ouimet M(2), Barrett TJ(2), Leone S(1), Moore KJ(2), Herault Y(3), Fisher EA(2), Garabedian MJ(1). |
Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region.Brault V(1), Duchon A(1), Romestaing C(2), Sahun I(3), Pothion S(4), Karout M(1), Borel C(5), Dembele D(1), Bizot JC(6), Messaddeq N(1), Sharp AJ(7), Roussel D(2), Antonarakis SE(8), Dierssen M(3), Herault Y(9). |
Principles and application of LIMS in mouse clinics.Maier H(1), Schutt C(2), Steinkamp R(2), Hurt A(2), Schneltzer E(2), Gormanns P(2), Lengger C(2), Griffiths M(3), Melvin D(3), Agrawal N(3), Alcantara R(3), Evans A(3), Gannon D(3), Holroyd S(3), Kipp C(3), Raj NP(3), Richardson D(3), LeBlanc S(4), Vasseur L(4), Masuya H(5), Kobayashi K(5), Suzuki T(5), Tanaka N(5), Wakana S(5), Walling A(6), Clary D(7), Gallegos J(8), Fuchs H(2), de Angelis MH(9,)(10,)(11), Gailus-Durner V(2). |
Shifting eating to the circadian rest phase misaligns the peripheral clocks with the master SCN clock and leads to a metabolic syndrome.Mukherji A(1), Kobiita A(1), Damara M(1), Misra N(1), Meziane H(2), Champy MF(2), Chambon P(3). |
2014Developmental molecular and functional cerebellar alterations induced by PCP4/PEP19 overexpression: implications for Down syndrome.Mouton-Liger F(1), Sahún I(2), Collin T(3), Lopes Pereira P(4), Masini D(2), Thomas S(1), Paly E(1), Luilier S(5), Même S(6), Jouhault Q(1), Bennaï S(1), Beloeil JC(6), Bizot JC(5), Hérault Y(7), Dierssen M(2), Créau N(8). |
Generation and Use of Transgenic Mice in Drug DiscoveryGuillaume Pavlovic, Véronique Brault, Tania Sorg andYann Hérault |
Hyperactivation of Alk induces neonatal lethality in knock-in AlkF1178L mice.Lopez-Delisle L(1), Pierre-Eugène C, Bloch-Gallego E, Birling MC, Duband JL, Durand E, Bourgeois T, Matrot B, Sorg T, Huerre M, Meziane H, Roux MJ, Champy MF, Gallego J, Delattre O, Janoueix-Lerosey I. |
Impact of temporal variation on design and analysis of mouse knockout phenotyping studies.Karp NA(1), Speak AO(1), White JK(1), Adams DJ(1), Hrabé de Angelis M(2), Hérault Y(3), Mott RF(4). |
Impact of the apolipoprotein E polymorphism, age and sex on neurogenesis in mice: Pathophysiological relevance for Alzheimer's disease?Koutseff A, Mittelhaeuser C, Essabri K, Auwerx J, Meziane H. |
In Vivo 9.4T MRI and1H MRS for Evaluation of Brain Structural and Metabolic Changes in the Ts65Dn Mouse Model for Down SyndromeS. Même1*, N. Joudiou1, N. Yousfi1, F. Szeremeta1, P. Lopes-Pereira2, J. C. Beloeil1,
Y. Herault2,3,4, W. Même1 |
Modeling Copy Number Variations in the MouseYann Hérault, Arnaud Duchon, Damien Maréchal, Véronique Brault. |
Old spontaneously hypertensive rats gather together typical features of human chronic left-ventricular dysfunction with preserved ejection fraction.Marzak H(1), Ayme-Dietrich E, Lawson R, Mokni W, Combe R, Becker J, Fertak LE, Champy MF, Monassier L. |
Proteomic survey reveals altered energetic patterns and metabolic failure prior to retinal degeneration.Griciuc A(1), Roux MJ, Merl J, Giangrande A, Hauck SM, Aron L, Ueffing M. |
Regulator of G-protein signaling 18 controls both platelet generation and function.Delesque-Touchard N(1), Pendaries C(1), Volle-Challier C(1), Millet L(1), Salel V(1), Hervé C(1), Pflieger AM(1), Berthou-Soulie L(2), Prades C(2), Sorg T(3), Herbert JM(1), Savi P(1), Bono F(1). |
Rfx6 maintains the functional identity of adult pancreatic beta cells.Piccand J(1), Strasser P(1), Hodson DJ(2), Meunier A(1), Ye T(1), Keime C(1), Birling MC(3), Rutter GA(2), Gradwohl G(4). |
Skin progenitor cells contribute to bleomycin-induced skin fibrosis.Liu S(1), Herault Y, Pavlovic G, Leask A. |
Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy.Clar J(1), Gri B(1), Calderaro J(2), Birling MC(3), Hérault Y(3), Smit GP(4), Mithieux G(1), Rajas F(1). |
2013A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.Simon MM, Greenaway S, White JK, Fuchs H, Gailus-Durner V, Wells S, Sorg T, Wong K, Bedu E, Cartwright EJ, Dacquin R, Djebali S, Estabel J, Graw J, Ingham NJ, Jackson IJ, Lengeling A, Mandillo S, Marvel J, Meziane H, Preitner F, Puk O, Roux M, Adams DJ, Atkins S, Ayadi A, Becker L, Blake A, Brooker D, Cater H, Champy MF, Combe R, Danecek P, di Fenza A, Gates H, Gerdin AK, Golini E, Hancock JM, Hans W, Holter SM, Hough T, Jurdic P, Keane TM, Morgan H, Muller W, Neff F, Nicholson G, Pasche B, Roberson LA, Rozman J, Sanderson M, Santos L, Selloum M, Shannon C, Southwell A, Tocchini-Valentini GP, Vancollie VE, Westerberg H, Wurst W, Zi M, Yalcin B, Ramirez-Solis R, Steel KP, Mallon AM, de Angelis MH, Herault Y, Brown SD. |
A pathway for unicellular tube extension depending on the lymphatic vessel determinant Prox1 and on osmoregulation.Kolotuev I(1), Hyenne V, Schwab Y, Rodriguez D, Labouesse M. |
Distinct fibroblast lineages determine dermal architecture in skin development and repair.Driskell RR(1), Lichtenberger BM(2), Hoste E(3), Kretzschmar K(2), Simons BD(4), Charalambous M(5), Ferron SR(5), Herault Y(6), Pavlovic G(6), Ferguson-Smith AC(5), Watt FM(7). |
Endogenous mammalian RF-amide peptides, including PrRP, kisspeptin and 26RFa, modulate nociception and morphine analgesia via NPFF receptors.Elhabazi K, Humbert JP, Bertin I, Schmitt M, Bihel F, Bourguignon JJ, Bucher B, Becker JA, Sorg T, Meziane H, Petit-Demoulière B, Ilien B, Simonin F. |
FELASA guidelines for the refinement of methods for genotyping genetically-modified rodents: a report of the Federation of European Laboratory Animal Science Associations Working Group.Bonaparte D(1), Cinelli P, Douni E, Hérault Y, Maas M, Pakarinen P, Poutanen M, Lafuente MS, Scavizzi F; Federation of European Laboratory Animal Science Associations Working Group. |
Repression of Osteoblast Maturation by ERR Accounts for Bone Loss Induced by Estrogen Deficiency.Gallet M, Saïdi S, Haÿ E, Photsavang J, Marty C, Sailland J, Carnesecchi J, Tribollet V, Barenton B, Forcet C, Birling MC, Sorg T, Chassande O, Cohen-Solal M, Vanacker JM. |
Surveying the Down syndrome mouse model resource identifies critical regions responsible for chronic otitis media.Bhutta MF, Cheeseman MT, Herault Y, Yu YE, Brown SD. |
The homeodomain factor Gbx1 is required for locomotion and cell specification in the dorsal spinal cord.Meziane H, Fraulob V, Riet F, Krezel W, Selloum M, Geffarth M, Acampora D, Hérault Y, Simeone A, Brand M, Dollé P, Rhinn M. |
The STRA6 Receptor Is Essential for Retinol-binding Protein-induced Insulin Resistance but Not for Maintaining Vitamin A Homeostasis in Tissues Other Than the Eye.Berry DC, Jacobs H, Marwarha G, Gely-Pernot A, O'Byrne SM, Desantis D, Klopfenstein M, Feret B, Dennefeld C, Blaner WS, Croniger CM, Mark M, Noy N, Ghyselinck NB. |
2012Absence of TI-VAMP/Vamp7 leads to increased anxiety in mice.Danglot L, Zylbersztejn K, Petkovic M, Gauberti M, Meziane H, Combe R, Champy MF, Birling MC, Pavlovic G, Bizot JC, Trovero F, Della Ragione F, Proux-Gillardeaux V, Sorg T, Vivien D, D'Esposito M, Galli T. |
Acoustic Startle Reflex and Prepulse Inhibition.Ouagazzal AM(1), Meziane H(2). |
Activation of nociceptin/orphanin FQ peptide receptors disrupts visual but not auditory sensorimotor gating in BALB/cByJ mice: comparison to dopamine receptor agonists.Ces A, Reiss D, Walter O, Wichmann J, Prinssen EP, Kieffer BL, Ouagazzal AM. |
Estrogen dependent activation function of ER is essential for the sexual behavior of mouse females.Antal MC, Petit-Demoulière B, Meziane H, Chambon P, Krust A. |
Highly-efficient, fluorescent, locus directed cre and FlpO deleter mice on a pure C57BL/6N genetic background.Birling MC, Dierich A, Jacquot S, Hérault Y, Pavlovic G. |
Involvement of neuropeptide FF receptors in neuroadaptive responses to acute and chronic opiate treatments.Elhabazi K, Trigo JM, Mollereau C, Moulédous L, Zajac JM, Bihel F, Schmitt M, Bourguignon JJ, Meziane H, Petit-demoulière B, Bockel F, Maldonado R, Simonin F. |
Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project.Ayadi A, Birling MC, Bottomley J, Bussell J, Fuchs H, Fray M, Gailus-Durner V, Greenaway S, Houghton R, Karp N, Leblanc S, Lengger C, Maier H, Mallon AM, Marschall S, Melvin D, Morgan H, Pavlovic G, Ryder E, Skarnes WC, Selloum M, Ramirez-Solis R, Sorg T, Teboul L, Vasseur L, Walling A, Weaver T, Wells S, White JK, Bradley A, Adams DJ, Steel KP, Hrab? de Angelis M, Brown SD, Herault Y. |
Targeted ultramicrotomy: a valuable tool for correlated light and electron microscopy of small model organisms.Kolotuev I(1), Bumbarger DJ, Labouesse M, Schwab Y. |
The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model.Raveau M(1), Lignon JM, Nalesso V, Duchon A, Groner Y, Sharp AJ, Dembele D, Brault V, Herault Y. |
The mammalian gene function resource: the International Knockout Mouse Consortium.Bradley A(1), Anastassiadis K, Ayadi A, Battey JF, Bell C, Birling MC, Bottomley J, Brown SD, Burger A, Bult CJ, Bushell W, Collins FS, Desaintes C, Doe B, Economides A, Eppig JT, Finnell RH, Fletcher C, Fray M, Frendewey D, Friedel RH, Grosveld FG, Hansen J, Herault Y, Hicks G, Horlein A, Houghton R, Hrabe de Angelis M, Huylebroeck D, Iyer V, de Jong PJ, Kadin JA, Kaloff C, Kennedy K, Koutsourakis M, Lloyd KC, Marschall S, Mason J, McKerlie C, McLeod MP, von Melchner H, Moore M, Mujica AO, Nagy A, Nefedov M, Nutter LM, Pavlovic G, Peterson JL, Pollock J, Ramirez-Solis R, Rancourt DE, Raspa M, Remacle JE, Ringwald M, Rosen B, Rosenthal N, Rossant J, Ruiz Noppinger P, Ryder E, Schick JZ, Schnutgen F, Schofield P, Seisenberger C, Selloum M, Simpson EM, Skarnes WC, Smedley D, Stanford WL, Stewart AF, Stone K, Swan K, Tadepally H, Teboul L, Tocchini-Valentini GP, Valenzuela D, West AP, Yamamura K, Yoshinaga Y, Wurst W. |
The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of Dishevelled.Glasco DM(1), Sittaramane V, Bryant W, Fritzsch B, Sawant A, Paudyal A, Stewart M, Andre P, Cadete Vilhais-Neto G, Yang Y, Song MR, Murdoch JN, Chandrasekhar A. |
2011Characterization and Validation of Cre-Driver Mouse LinesGofflot F, Wendling O, Chartoire N, Birling MC, Warot X, Auwerx J |
Chronic Treatment with a Promnesiant GABA-A 5-Selective Inverse Agonist Increases Immediate Early Genes Expression during Memory Processing in Mice and Rectifies Their Expression Levels in a Down Syndrome Mouse Model.Braudeau J, Dauphinot L, Duchon A, Loistron A, Dodd RH, Hérault Y, Delatour B,
Potier MC. |
Genetic and pharmacological evaluation of cathepsin s in a mouse model of asthma.Deschamps K, Cromlish W, Weicker S, Lamontagne S, Huszar SL, Gauthier JY, Mudgett JS, Guimond A, Romand R, Frossard N, Percival MD, Slipetz D, Tan CM. |
Involvement of retinol dehydrogenase 10 in embryonic patterning and rescue of its loss of function by maternal retinaldehyde treatment.Rhinn M, Schuhbaur B, Niederreither K, Dollé P. |
Mouse Breeding and Colony ManagementAyadi A, Ferrand G, Goncalves da Cruz I, Warot X |
PTBP1 Is Required for Embryonic Development before GastrulationSuckale J., Wendling O., Masjkur J., Jager M., Munster C., Anastassiadis K., Stewart A.F., Solimena M. |
Reduced body weight in male Tspan8-deficient mice.Champy MF, Le Voci L, Selloum M, Peterson LB, Cumiskey AM, Blom D. |
Standardized Post-Mortem Examination and Fixation Procedures for Mutant and Treated MiceAntal M.C., muller S., Wendling O, Herault Y, Mark M. |
TASK-3 as a potential antidepressant target.Gotter AL, Santarelli VP, Doran SM, Tannenbaum PL, Kraus RL, Rosahl TW, Meziane H, Montial M, Reiss DR, Wessner K, McCampbell A, Stevens J, Brunner JI, Fox SV, Uebele VN, Bayliss DA, Winrow CJ, Renger JJ. |
The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndromeDuchon A., Pothion S., Brault V., Sharp A.J., Tybulewicz V.L., Fisher E.M., Herault Y. |
TIF1beta association with HP1 is essential for post-gastrulation development, but not for Sertoli cell functions during spermatogenesisHerzog M., Wendling O., Guillou F., Chambon P., Mark M., Losson R., Cammas F. |
2010Active multilayered capsules for in vivo bone formationFacca S., Cortez C., Mendoza-Palomares C., Messadeq N., Dierich A., Johnston A.P., Mainard D., Voegel J.C., Caruso F., Benkirane-Jessel N. |
Altered lipoprotein metabolism in P2Y(13) knockout miceBlom D., Yamin T.T., Champy M.F., Selloum M., Bedu E., Carballo-Jane E., Gerckens L., Luell S., Meurer R., Chin J., Mudgett J., Puig O. |
beta-Endorphin expression in the mouse retinaGallagher S.K., Witkovsky P., Roux M.J., Low M.J., Otero-Corchon V., Hentges S.T., Vigh J. |
Contribution of gene-modified mice and rats to our understanding of the cardiovascular pharmacology of serotoninMonassier L., Laplante M.A., Ayadi T., Doly S., Maroteaux L. |
Down Syndrome: From Understanding the Neurobiology to TherapyGardiner K., Herault Y., Lott I.T., Antonarakis S.E., Reeves R.H., Dierssen M. |
Enterovirus-related activation of the cardiomyocyte mitochondrial apoptotic pathway in patients with acute myocarditis.Ventéo L, Bourlet T, Renois F, Douche-Aourik F, Mosnier JF, Maison GL, Pluot M, Pozzetto B, Andreoletti L. |
EuroPhenome: a repository for high-throughput mouse phenotyping dataMorgan H., Beck T., Blake A., Gates H., Adams N., Debouzy G., Leblanc S., Lengger C., Maier H., Melvin D., Meziane H., Richardson D., Wells S., White J., Wood J., de Angelis M.H., Brown S.D., Hancock J.M., Mallon A.M. |
Identification of genes and networks driving cardiovascular and metabolic phenotypes in a mouse f2 intercrossDerry J.M., Zhong H., Molony C., Macneil D., Guhathakurta D., Zhang B., Mudgett J., Small K., El Fertak L., Guimond A., Selloum M., Zhao W., Champy M.F., Monassier L., Vogt T., Cully D., Kasarskis A., Schadt E.E. |
Murine neonatal infection provides an efficient model for congenital ocular toxoplasmosisLahmar I., Guinard M., Sauer A., Marcellin L., Abdelrahman T., Roux M., Mousli M., Moussa A., Babba H., Pfaff A.W., Candolfi E. |
Mutations in lama1 disrupt retinal vascular development and inner limiting membrane formationEdwards M.M., Mammadova-Bach E., Alpy F., Klein A., Hicks W.L., Roux M., Simon-Assmann P., Smith R.S., Orend G., Wu J., Peachey N.S., Naggert J.K., Lefebvre O., Nishina P.M. |
Myeloproliferative neoplasm induced by constitutive expression of JAK2V617F in knock-in mice.Marty C, Lacout C, Martin A, Hasan S, Jacquot S, Birling MC, Vainchenker W, Villeval JL. |
Negative control of Smad activity by ectodermin/Tif1gamma patterns the mammalian embryoMorsut L., Yan K.P., Enzo E., Aragona M., Soligo S.M., Wendling O., Mark M., Khetchoumian K., Bressan G., Chambon P., Dupont S., Losson R., Piccolo S. |
Oxidative stress in skeletal muscle stimulates early expression of Rad in a mouse model of amyotrophic lateral sclerosis.Halter B, Gonzalez de Aguilar JL, Rene F, Petri S, Fricker B, Echaniz-Laguna A, Dupuis L, Larmet Y, Loeffler JP. |
PCSK9 is not involved in the degradation of LDL receptors and BACE1 in the adult mouse brain.Liu M, Wu G, Baysarowich J, Kavana M, Addona GH, Bierilo KK, Mudgett JS, Pavlovic G, Sitlani A, Renger JJ, Hubbard BK, Fisher TS, Zerbinatti CV. |
Retinoic acid receptor (RAR)-alpha is not critically required for mediating retinoic acid effects in the developing mouse retinaCammas L., Trensz F., Jellali A., Ghyselinck N.B., Roux M.J., Dolle P. |
The pollutant diethylhexyl phthalate regulates hepatic energy metabolism via species-specific PPARalpha-dependent mechanisms.Feige JN, Gerber A, Casals-Casas C, Yang Q, Winkler C, Bedu E, Bueno M, Gelman L, Auwerx J, Gonzalez FJ, Desvergne B. |
2009Aneuploidy: from a physiological mechanism of variance to Down syndromeDierssen M., Herault Y., Estivill X. |
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndromePereira P.L., Magnol L., Sahun I., Brault V., Duchon A., Prandini P., Gruart A., Bizot J.C., Chadefaux-Vekemans B., Deutsch S., Trovero F., Delgado-Garcia J.M., Antonarakis S.E., Dierssen M., Herault Y. |
A ruthenium-containing organometallic compound reduces tumor growth through induction of the endoplasmic reticulum stress gene CHOP.Meng X, Leyva ML, Jenny M, Gross I, Benosman S, Fricker B, Harlepp S, Hébraud P, Boos A, Wlosik P, Bischoff P, Sirlin C, Pfeffer M, Loeffler JP, Gaiddon C. |
Brain structures implicated in the four-plate test in naive and experienced Swiss mice using injection of diazepam and the 5-HT2A agonist DOI.Petit-Demoulière B, Massé F, Cogrel N, Hascoët M, Bourin M. |
DYRK1A, a novel determinant of the methionine-homocysteine cycle in different mouse models overexpressing this Down-syndrome-associated kinaseNoll C., Planque C., Ripoll C., Guedj F., Diez A., Ducros V., Belin N., Duchon A., Paul J.L., Badel A., de Freminville B., Grattau Y., Blehaut H., Herault Y., Janel N., Delabar J.M. |
Efficient temporally-controlled targeted mutagenesis in smooth muscle cells of the adult mouseWendling O., Bornert J.M., Chambon P., Metzger D. |
EMMA--mouse mutant resources for the international scientific communityWilkinson P., Sengerova J., Matteoni R., Chen C.K., Soulat G., Ureta-Vidal A., Fessele S., Hagn M., Massimi M., Pickford K., Butler R.H., Marschall S., Mallon A.M., Pickard A., Raspa M., Scavizzi F., Fray M., Larrigaldie V., Leyritz J., Birney E., Tocchini-Valentini G.P., Brown S., Herault Y., Montoliu L., de Angelis M.H., Smedley D. |
Fork stalling and template switching as a mechanism for polyalanine tract expansion affecting the DYC mutant of HOXD13, a new murine model of synpolydactylyCocquempot O., Brault V., Babinet C., Herault Y. |
Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal developmentLaffaire J., Rivals I., Dauphinot L., Pasteau F., Wehrle R., Larrat B., Vitalis T., Moldrich R.X., Rossier J., Sinkus R., Herault Y., Dusart I., Potier M.C. |
Heme oxygenase-1 accelerates cutaneous wound healing in miceGrochot-Przeczek A., Lach R., Mis J., Skrzypek K., Gozdecka M., Sroczynska P., Dubiel M., Rutkowski A., Kozakowska M., Zagorska A., Walczynski J., Was H., Kotlinowski J., Drukala J., Kurowski K., Kieda C., Herault Y., Dulak J., Jozkowicz A. |
Identification of the UBP1 locus as a critical blood pressure determinant using a combination of mouse and human genetics.Koutnikova H, Laakso M, Lu L, Combe R, Paananen J, Kuulasmaa T, Kuusisto J, Häring HU, Hansen T, Pedersen O, Smith U, Hanefeld M, Williams RW, Auwerx J. |
Ppargamma2 is a key driver of longevity in the mouseArgmann C., Dobrin R., Heikkinen S., Auburtin A., Pouilly L., Cock T.A., Koutnikova H., Zhu J., Schadt E.E., Auwerx J. |
Proliferation deficits and gene expression dysregulation in Down's syndrome (Ts1Cje) neural progenitor cells cultured from neurospheresMoldrich R.X., Dauphinot L., Laffaire J., Vitalis T., Herault Y., Beart P.M., Rossier J., Vivien D., Gehrig C., Antonarakis S.E., Lyle R., Potier M.C. |
Site-specific recombinases for manipulation of the mouse genomeBirling M.C., Gofflot F., Warot X. |
The Histone Deacetylase SIRT1 Controls Male Fertility in Mice Through Regulation of Hypothalamic-Pituitary Gonadotropin SignalingKolthur-Seetharam U., Teerds K., Rooij D.G., Wendling O., McBurney M., Sassone-Corsi P., Davidson I. |
The Pro12Ala PPARgamma2 Variant Determines Metabolism at the Gene-Environment InterfaceHeikkinen S., Argmann C., Feige J.N., Koutnikova H., Champy M.F., Dali-Youcef N., Schadt E.E., Laakso M., Auwerx J. |
2008Anxiolytic-like effects of DOI microinjections into the hippocampus (but not the amygdala nor the PAG) in the mice four plates test.Masse F, Petit-Demouliere B, Dubois I, Hascoët M, Bourin M. |
Evaluation tools and animal models of peripheral neuropathies.Fricker B, Muller A, René F. |
Factors triggering abolishment of benzodiazepines effects in the Four-Plate Test--retest in mice.Petit-Demoulière B, Hascoët M, Bourin M. |
Genetic background determines metabolic phenotypes in the mouseChampy M.F., Selloum M., Zeitler V., Caradec C., Jung B., Rousseau S., Pouilly L., Sorg T., Auwerx J. |
Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombinationDuchon A., Besson V., Pereira P.L., Magnol L., Herault Y. |
Nociceptin receptor impairs recognition memory via interaction with NMDA receptor-dependent mitogen-activated protein kinase/extracellular signal-regulated kinase signaling in the hippocampusGoeldner C., Reiss D., Wichmann J., Meziane H., Kieffer B.L., Ouagazzal A.M. |
Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory studyMandillo S., Tucci V., Holter S.M., Meziane H., Banchaabouchi M.A., Kallnik M., Lad H.V., Nolan P.M., Ouagazzal A.M., Coghill E.L., Gale K., Golini E., Jacquot S., Krezel W., Parker A., Riet F., Schneider I., Marazziti D., Auwerx J., Brown S.D., Chambon P., Rosenthal N., Tocchini-Valentini G., Wurst W. |
The genetic ablation of SRC-3 protects against obesity and improves insulin sensitivity by reducing the acetylation of PGC-1{alpha}Coste A., Louet J.F., Lagouge M., Lerin C., Antal M.C., Meziane H., Schoonjans K., Puigserver P., O'Malley B.W., Auwerx J. |
Variations in DNA elucidate molecular networks that cause diseaseChen Y., Zhu J., Lum P.Y., Yang X., Pinto S., MacNeil D.J., Zhang C., Lamb J., Edwards S., Sieberts S.K., Leonardson A., Castellini L.W., Wang S., Champy M.F., Zhang B., Emilsson V., Doss S., Ghazalpour A., Horvath S., Drake T.A., Lusis A.J., Schadt E.E. |
2007Absence of dopamine D2 receptors unmasks an inhibitory control over the brain circuitries activated by cocaineWelter M., Vallone D., Samad T.A., Meziane H., Usiello A., Borrelli E. |
Adipose tissue-specific inactivation of the retinoblastoma protein protects against diabesity because of increased energy expenditureDali-Youcef N., Mataki C., Coste A., Messaddeq N., Giroud S., Blanc S., Koehl C., Champy M.F., Chambon P., Fajas L., Metzger D., Schoonjans K., Auwerx J. |
Animal models of anxiety in mice.Bourin M, Petit-Demoulière B, Dhonnchadha BN, Hascöet M. |
Bone Formation Mediated by Synergy-Acting Growth Factors Embedded in a Polyelectrolyte Multilayer FilmDierich A., Le Guen E., Messaddeq N., Stoltz J.F., Netter P., Schaaf P., Voegel J.C., Benkirane-Jessel N. |
Cre/loxP-mediated chromosome engineering of the mouse genomeBrault V., Besson V., Magnol L., Duchon A., Herault Y. |
Estrous cycle effects on behavior of C57BL/6J and BALB/cByJ female mice: implications for phenotyping strategiesMeziane H., Ouagazzal A.M., Aubert L., Wietrzych M., Krezel W. |
Evaluation of glucose homeostasisHeikkinen S, Argmann CA, Champy MF, Auwerx J |
[Functional genomics of the mouse: the European dynamics].Masson R, Sorg T, Warot X. |
Histopathology in mouse metabolic investigationsMark M., Teletin M., Antal C., Wendling O., Auwerx J., Heikkinen S., Khetchoumian K., Argmann C.A., Dgheem M. |
IL-13 induces expression of CD36 in human monocytes through PPARgamma activationBerry A., Balard P., Coste A., Olagnier D., Lagane C., Authier H., Benoit-Vical F., Lepert J.C., Seguela J.P., Magnaval J.F., Chambon P., Metzger D., Desvergne B., Wahli W., Auwerx J., Pipy B. |
Increased peripheral lipid clearance in an animal model of amyotrophic lateral sclerosis.Fergani A, Oudart H, Gonzalez De Aguilar JL, Fricker B, René F, Hocquette JF, Meininger V, Dupuis L, Loeffler JP. |
In Vivo Imaging of Farnesoid X Receptor Activity Reveals the Ileum as the Primary Bile Acid Signaling TissueHouten S.M., Volle D.H., Cummins C.L., Mangelsdorf D.J., Auwerx J. |
KIT is required for hepatic function during mouse post-natal developmentMagnol L., Chevallier M.C., Nalesso V., Retif S., Fuchs H., Klempt M., Pereira P., Riottot M., Andrzejewski S., Doan B.T., Panthier J.J., Puech A., Beloeil J.C., de Angelis M.H., Herault Y. |
LRH-1-mediated glucocorticoid synthesis in enterocytes protects against inflammatory bowel diseaseCoste A., Dubuquoy L., Barnouin R., Annicotte J.S., Magnier B., Notti M., Corazza N., Antal M.C., Metzger D., Desreumaux P., Brunner T., Auwerx J., Schoonjans K. |
LRP1 Functions as an Atheroprotective Integrator of TGFbeta and PDFG Signals in the Vascular Wall: Implications for Marfan SyndromeBoucher P., Li W.P., Matz R.L., Takayama Y., Auwerx J., Anderson R.G., Herz J. |
Malignant transformation of DMBA/TPA-induced papillomas and nevi in the skin of mice selectively lacking retinoid-X-receptor alpha in epidermal keratinocytesIndra A.K., Castaneda E., Antal M.C., Jiang M., Messaddeq N., Meng X., Loehr C.V., Gariglio P., Kato S., Wahli W., Desvergne B., Metzger D., Chambon P. |
Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responsesBesson V., Brault V., Duchon A., Togbe D., Bizot J.C., Quesniaux V.F., Ryffel B., Herault Y. |
Peroxisome Proliferator-Activated Receptor-{alpha} Activation Inhibits Langerhans Cell FunctionDubrac S., Stoitzner P., Pirkebner D., Elentner A., Schoonjans K., Auwerx J., Saeland S., Hengster P., Fritsch P., Romani N., Schmuth M. |
Proteomic shifts in embryonic stem cells with gene dose modifications suggest the presence of balancer proteins in protein regulatory networksMao L., Zabel C., Herrmann M., Nolden T., Mertes F., Magnol L., Chabert C., Hartl D., Herault Y., Delabar J.M., Manke T., Himmelbauer H., Klose J. |
Quantitative ultrasonic tissue characterization as a new tool for continuous monitoring of chronic liver remodelling in miceGuimond A., Teletin M., Garo E., D'Sa A., Selloum M., Champy M.F., Vonesch J.L., Monassier L. |
Studies of the Common DIO2 Thr92Ala Polymorphism and Metabolic Phenotypes in 7342 Danish White SubjectsGrarup N., Andersen M.K., Andreasen C.H., Albrechtsen A., Borch-Johnsen K., Jorgensen T., Auwerx J., Schmitz O., Hansen T., Pedersen O. |
Systematic gene expression mapping clusters nuclear receptors according to their function in the brainGofflot F., Chartoire N., Vasseur L., Heikkinen S., Dembele D., Le Merrer J., Auwerx J. |
Temporal parameters of one-trial tolerance to benzodiazepines in four-plate test-retest.Petit-Demouliere B, Bourin M. |
The small heterodimer partner is a gonadal gatekeeper of sexual maturation in male miceVolle D.H., Duggavathi R., Magnier B.C., Houten S.M., Cummins C.L., Lobaccaro J.M., Verhoeven G., Schoonjans K., Auwerx J. |
Tissue collection for systematic phenotyping in the mouseAntal C., Teletin M., Wendling O., Dgheem M., Auwerx J., Mark M. |
2006Absence of the steroid receptor coactivator-3 induces B-cell lymphomaCoste A., Antal M.C., Chan S., Kastner P., Mark M., O'Malley B.W., Auwerx J. |
ACE inhibition prevents myocardial infarction-induced skeletal muscle mitochondrial dysfunction.Zoll J, Monassier L, Garnier A, N'Guessan B, Mettauer B, Veksler V, Piquard F, Ventura-Clapier R, Geny B. |
A mouse model for human short-stature syndromes identifies Shox2 as an upstream regulator of Runx2 during long-bone developmentCobb J., Dierich A., Huss-Garcia Y., Duboule D. |
Apoptosis and differentiation commitment: novel insights revealed by gene profiling studies in mouse embryonic stem cellsDuval D., Trouillas M., Thibault C., Dembele D., Diemunsch F., Reinhardt B., Mertz A.L., Dierich A., Boeuf H. |
Auditory and visual prepulse inhibition in mice: parametric analysis and strain comparisonsAubert L., Reiss D., Ouagazzal A.M. |
Brg1 is required for murine neural stem cell maintenance and gliogenesisMatsumoto S., Banine F., Struve J., Xing R., Adams C., Liu Y., Metzger D., Chambon P., Rao M.S., Sherman L.S. |
Cardiovascular disorders: insights into in vivo cardiovascular phenotypingMonassier L, Constantinesco A |
Conditional (loxP-flanked) allele for the gene encoding the retinoic acid-synthesizing enzyme retinaldehyde dehydrogenase 2 (RALDH2)Vermot J., Garnier J.M., Dierich A., Niederreither K., Harvey R.P., Chambon P., Dolle P. |
Deletion of peroxisome proliferator-activated receptor-alpha induces an alteration of cardiac functionsLoichot C., Jesel L., Tesse A., Tabernero A., Schoonjans K., Roul G., Carpusca I., Auwerx J., Andriantsitohaina R. |
Dissociation of analgesic and hormonal responses to forced swim stress using opioid receptor knockout miceContet C., Gaveriaux-Ruff C., Matifas A., Caradec C., Champy M.F., Kieffer B.L. |
Dynamic expression of retinoic acid-synthesizing and -metabolizing enzymes in the developing mouse inner earRomand R., Kondo T., Fraulob V., Petkovich M., Dolle P., Hashino E. |
Endocrine functions of bile acidsHouten S.M., Watanabe M., Auwerx J. |
Evaluation of Energy HomeostasisArgmann CA, Champy MF, Auwerx J |
Exploration of metabolic and endocrine function in the mouseChampy MF, Argmann CA, Chambon P, Auwerx J |
Expression analysis of murine genes using in situ hybridization with radioactive and nonradioactively labeled RNA probesChotteau-Lelievre A., Dolle P., Gofflot F. |
Function of retinoid nuclear receptors: lessons from genetic and pharmacological dissections of the retinoic acid signaling pathway during mouse embryogenesis.Mark M(1), Ghyselinck NB, Chambon P. |
Genetic and pharmacological evidence that a retinoic acid cannot be the RXR-activating ligand in mouse epidermis keratinocytesCalleja C., Messaddeq N., Chapellier B., Yang H., Krezel W., Li M., Metzger D., Mascrez B., Ohta K., Kagechika H., Endo Y., Mark M., Ghyselinck N.B., Chambon P. |
Knockin mice expressing fluorescent delta-opioid receptors uncover G protein-coupled receptor dynamics in vivoScherrer G., Tryoen-Toth P., Filliol D., Matifas A., Laustriat D., Cao Y.Q., Basbaum A.I., Dierich A., Vonesh J.L., Gaveriaux-Ruff C., Kieffer B.L. |
Lipid and Bile Acid AnalysisArgmann CA, Houten SM, Champy MF, Auwerx j |
Localized inflammatory skin disease following inducible ablation of I kappa B kinase 2 in murine epidermisStratis A., Pasparakis M., Markur D., Knaup R., Pofahl R., Metzger D., Chambon P., Krieg T., Haase I. |
Mature-onset obesity and insulin resistance in mice deficient in the signaling adapter p62Rodriguez A., Duran A., Selloum M., Champy M.F., Diez-Guerra F.J., Flores J.M., Serrano M., Auwerx J., Diaz-Meco M.T., Moscat J. |
Mice models of hypertensionMonassier L, Combe R, El Fertak L |
Minimizing Variation Due to Genotype and EnvironmentArgmann CA, Auwerx J |
Modeling chromosomes in mouse to explore the function of genes, genomic disorders, and chromosomal organizationBrault V., Pereira P., Duchon A., Herault Y. |
Oncogenic steroid receptor coactivator-3 is a key regulator of the white adipogenic programLouet J.F., Coste A., Amazit L., Tannour-Louet M., Wu R.C., Tsai S.Y., Tsai M.J., Auwerx J., O'Malley B.W. |
PGC1alpha expression is controlled in skeletal muscles by PPARbeta, whose ablation results in fiber-type switching, obesity, and type 2 diabetesSchuler M., Ali F., Chambon C., Duteil D., Bornert J.M., Tardivel A., Desvergne B., Wahli W., Chambon P., Metzger D. |
Receptor protein tyrosine phosphatase gamma is a marker for pyramidal cells and sensory neurons in the nervous system and is not necessary for normal developmentLamprianou S., Vacaresse N., Suzuki Y., Meziane H., Buxbaum J.D., Schlessinger J., Harroch S. |
Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1alphaLagouge M., Argmann C., Gerhart-Hines Z., Meziane H., Lerin C., Daussin F., Messadeq N., Milne J., Lambert P., Elliott P., Geny B., Laakso M., Puigserver P., Auwerx J. |
Retinoic Acid Metabolism and Signaling Pathways in the Adult and Developing Mouse TestisVernet N., Dennefeld C., Rochette-Egly C., Oulad-Abdelghani M., Chambon P., Ghyselinck N.B., Mark M. |
Retinoids and spermatogenesis: Lessons from mutant mice lacking the plasma retinol binding proteinGhyselinck N.B., Vernet N., Dennefeld C., Giese N., Nau H., Chambon P., Viville S., Mark M. |
Retinoid signaling in inner ear developmentRomand R., Dolle P., Hashino E. |
Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death.Andrieu D, Meziane H, Marly F, Angelats C, Fernandez PA, Muscatelli F. |
Skin epidermis lacking the c-myc gene is resistant to Ras-driven tumorigenesis but can reacquire sensitivity upon additional loss of the p21Cip1 geneOskarsson T., Essers M.A., Dubois N., Offner S., Dubey C., Roger C., Metzger D., Chambon P., Hummler E., Beard P., Trumpp A. |
Skin lesion development in a mouse model of incontinentia pigmenti is triggered by NEMO deficiency in epidermal keratinocytes and requires TNF signalingNenci A., Huth M., Funteh A., Schmidt-Supprian M., Bloch W., Metzger D., Chambon P., Rajewsky K., Krieg T., Haase I., Pasparakis M. |
Temporal regulation of Cre recombinase activity in neural stem cellsImayoshi I., Ohtsuka T., Metzger D., Chambon P., Kageyama R. |
Topical vitamin D3 and low-calcemic analogs induce thymic stromal lymphopoietin in mouse keratinocytes and trigger an atopic dermatitisLi M., Hener P., Zhang Z., Kato S., Metzger D., Chambon P. |
Viral-mediated temporally controlled dopamine production in a rat model of Parkinson diseaseLi X.G., Okada T., Kodera M., Nara Y., Takino N., Muramatsu C., Ikeguchi K., Urano F., Ichinose H., Metzger D., Chambon P., Nakano I., Ozawa K., Muramatsu S. |
Visceral obesity is associated with high levels of serum squalenePeltola P., Pihlajamaki J., Koutnikova H., Ruotsalainen E., Salmenniemi U., Vauhkonen I., Kainulainen S., Gylling H., Miettinen T.A., Auwerx J., Laakso M. |
2005Assessment of left ventricular perfusion, volumes, and motion in mice using pinhole gated SPECT.Constantinesco A, Choquet P, Monassier L, Israel-Jost V, Mertz L. |
Contribution of cellular retinol-binding protein type 1 to retinol metabolism during mouse developmentMatt N., Schmidt C.K., Dupe V., Dennefeld C., Nau H., Chambon P., Mark M., Ghyselinck N.B. |
Dorsal pancreas agenesis in retinoic acid-deficient Raldh2 mutant miceMartin M., Gallego-Llamas J., Ribes V., Kedinger M., Niederreither K., Chambon P., Dolle P., Gradwohl G. |
EMPReSS: standardized phenotype screens for functional annotation of the mouse genome.Brown SD, Chambon P, de Angelis MH; Eumorphia Consortium. |
Functional role of RXRs and PPARgamma in mature adipocytesMetzger D., Imai T., Jiang M., Takukawa R., Desvergne B., Wahli W., Chambon P. |
Genomewide production of multipurpose alleles for the functional analysis of the mouse genomeSchnutgen F., De-Zolt S., Van Sloun P., Hollatz M., Hansen J., Altschmied J., Seisenberger C., Ghyselinck N.B., Ruiz P., Chambon P., Wurst W., von Melchner H. |
Impaired expression of the peroxisome proliferator-activated receptor alpha during hepatitis C virus infectionDharancy S., Malapel M., Perlemuter G., Roskams T., Cheng Y., Dubuquoy L., Podevin P., Conti F., Canva V., Philippe D., Gambiez L., Mathurin P., Paris J.C., Schoonjans K., Calmus Y., Pol S., Auwerx J., Desreumaux P. |
Liver receptor homolog 1 contributes to intestinal tumor formation through effects on cell cycle and inflammationSchoonjans K., Dubuquoy L., Mebis J., Fayard E., Wendling O., Haby C., Geboes K., Auwerx J. |
Mouse phenogenomics: the fast track to "systems metabolism"Argmann C.A., Chambon P., Auwerx J. |
Peroxisome proliferator-activated receptor gamma: the more the merrier?Argmann C.A., Cock T.A., Auwerx J. |
Retinoic acid-dependent eye morphogenesis is orchestrated by neural crest cellsMatt N., Dupe V., Garnier J.M., Dennefeld C., Chambon P., Mark M., Ghyselinck N.B. |
TAF10 is required for the establishment of skin barrier function in foetal, but not in adult mouse epidermisIndra A.K., Mohan W.S., Frontini M., Scheer E., Messaddeq N., Metzger D., Tora L. |
Targeted somatic mutagenesis in the mouse epidermisMetzger D., Li M., Chambon P. |
Temporally controlled targeted somatic mutagenesis in skeletal muscles of the mouseSchuler M., Ali F., Metzger E., Chambon P., Metzger D. |
The optomotor response: a robust first-line visual screening method for mice.Abdeljalil J, Hamid M, Abdel-Mouttalib O, Stéphane R, Raymond R, Johan A, José S, Pierre C, Serge P. |
Training and aging modulate the loss-of-balance phenotype observed in a new ENU-induced allele of Otopetrin1Besson V., Nalesso V., Herpin A., Bizot J.C., Messaddeq N., Romand R., Puech A., Blanquet V., Herault Y. |
Working memory deficits in retinoid X receptor gamma-deficient miceWietrzych M., Meziane H., Sutter A., Ghyselinck N., Chapman P.F., Chambon P., Krezel W. |
2004Absence of S6K1 protects against age- and diet-induced obesity while enhancing insulin sensitivityUm S.H., Frigerio F., Watanabe M., Picard F., Joaquin M., Sticker M., Fumagalli S., Allegrini P.R., Kozma S.C., Auwerx J., Thomas G. |
Bile acids lower triglyceride levels via a pathway involving FXR, SHP, and SREBP-1cWatanabe M., Houten S.M., Wang L., Moschetta A., Mangelsdorf D.J., Heyman R.A., Moore D.D., Auwerx J. |
Cardiovascular and survival effects of sympatho-inhibitors in adriamycin-induced cardiomyopathy in rats.Thomas L, Bellmont S, Christen MO, La Roche B, Monassier L. |
Cre-mediated conditional gene targeting to understand liver functionsMetzger D., Chambon P |
Current mouse models for studying cardiac dysfunctions: technical and imaging aspectsMonassier L, Theodoropoulos C, Sandler R, Constantinesco A. |
Disease progression despite early loss of polyglutamine protein expression in SCA7 mouse modelHelmlinger D., Abou-Sleymane G., Yvert G., Rousseau S., Weber C., Trottier Y., Mandel J.L., Devys D. |
Efficient temporally controlled targeted somatic mutagenesis in hepatocytes of the mouseSchuler M., Dierich A., Chambon P., Metzger D. |
Expression of the liver X receptor alpha and beta in embryonic and adult miceAnnicotte J.S., Schoonjans K., Auwerx J. |
Idebenone delays the onset of cardiac functional alteration without correction of Fe-S enzymes deficit in a mouse model for Friedreich ataxiaSeznec H., Simon D., Monassier L., Criqui-Filipe P., Gansmuller A., Rustin P., Koenig M., Puccio H. |
Impaired pancreatic growth, beta cell mass, and beta cell function in E2F1 (-/- )miceFajas L., Annicotte J.S., Miard S., Sarruf D., Watanabe M., Auwerx J. |
Involvement of the serotonin 5-HT2B receptor in cardiac hypertrophy linked to sympathetic stimulation: control of interleukin-6, interleukin-1beta, and tumor necrosis factor-alpha cytokine production by ventricular fibroblastsJaffre F., Callebert J., Sarre A., Etienne N., Nebigil C.G., Launay J.M., Maroteaux L., Monassier L. |
Knockout mouse models in pain researchDierich A., Kieffer B.L. |
Ligand-dependent contribution of RXRbeta to cholesterol homeostasis in Sertoli cellsMascrez B., Ghyselinck N.B., Watanabe M., Annicotte J.S., Chambon P., Auwerx J., Mark M. |
LRH-1: an orphan nuclear receptor involved in development, metabolism and steroidogenesisFayard E., Auwerx J., Schoonjans K. |
Molecular cloning, genomic structure, and expression analysis of the mouse transcriptional intermediary factor 1 gamma geneYan K.P., Dolle P., Mark M., Lerouge T., Wendling O., Chambon P., Losson R. |
Mouse functional genomics requires standardization of mouse handling and housing conditionsChampy M.F., Selloum M., Piard L., Zeitler V., Caradec C., Chambon P., Auwerx J. |
Partially redundant functions of SRC-1 and TIF2 in postnatal survival and male reproductionMark M., Yoshida-Komiya H., Gehin M., Liao L., Tsai M.J., O'Malley B.W., Chambon P., Xu J. |
Peroxisome proliferator-activated receptor gamma is required in mature white and brown adipocytes for their survival in the mouse.Imai T, Takakuwa R, Marchand S, Dentz E, Bornert JM, Messaddeq N, Wendling O, Mark M, Desvergne B, Wahli W, Chambon P, Metzger D. |
Peroxisome proliferator-activated receptor-gamma: too much of a good thing causes harmCock T.A., Houten S.M., Auwerx J. |
PU.1 determines the self-renewal capacity of erythroid progenitor cellsBack J., Dierich A., Bronn C., Kastner P., Chan S. |
Retinal dystrophy resulting from ablation of RXR alpha in the mouse retinal pigment epitheliumMori M., Metzger D., Picaud S., Hindelang C., Simonutti M., Sahel J., Chambon P., Mark M. |
Retinoic acid signalling in the development of branchial archesMark M., Ghyselinck N.B., Chambon P. |
Synergy between LRH-1 and beta-Catenin Induces G(1) Cyclin-Mediated Cell ProliferationBotrugno O.A., Fayard E., Annicotte J.S., Haby C., Brennan T., Wendling O., Tanaka T., Kodama T., Thomas W., Auwerx J., Schoonjans K. |
The European dimension for the mouse genome mutagenesis programAuwerx J., Avner P., Baldock R., Ballabio A., Balling R., Barbacid M., Berns A., Bradley A., Brown S., Carmeliet P., Chambon P., Cox R., Davidson D., Davies K., Duboule D., Forejt J., Granucci F., Hastie N., De Angelis M.H., Jackson I., Kioussis D., Kollias G., Lathrop M., Lendahl U., Malumbres M., Von Melchner H., Muller W., Partanen J., Ricciardi-Castagnoli P., Rigby P., Rosen B., Rosenthal N., Skarnes B., Stewart A.F., Thornton J., Tocchini-Valentini G., Wagner E., Wahli W., Wurst W. |
Tissue-specific and inducible Cre-mediated recombination in the gut epitheliumEl Marjou F., Janssen K.P., Hung-Junn Chang B., Li M., Hindie V., Chan L., Louvard D., Chambon P., Metzger D., Robine S. |
2003A directional strategy for monitoring Cre-mediated recombination at the cellular level in the mouseSchnutgen F., Doerflinger N., Calleja C., Wendling O., Chambon P., Ghyselinck N.B. |
A newborn lethal defect due to inactivation of retinaldehyde dehydrogenase type 3 is prevented by maternal retinoic acid treatmentDupe V., Matt N., Garnier J.M., Chambon P., Mark M., Ghyselinck N.B. |
Compensation by the muscle limits the metabolic consequences of lipodystrophy in PPAR{gamma} hypomorphic miceKoutnikova H., Cock T.A., Watanabe M., Houten S.M., Champy M.F., Dierich A., Auwerx J. |
Functional interaction between PARP-1 and PARP-2 in chromosome stability and embryonic development in mouseMenissier de Murcia J., Ricoul M., Tartier L., Niedergang C., Huber A., Dantzer F., Schreiber V., Ame J.C., Dierich A., LeMeur M., Sabatier L., Chambon P., de Murcia G. |
Genetics of dark skin in miceFitch K.R., McGowan K.A., van Raamsdonk C.D., Fuchs H., Lee D., Puech A., Herault Y., Threadgill D.W., Hrabe de Angelis M., Barsh G.S. |
I(1) imidazoline receptors involved in cardiovascular regulation: where are we and where are we going?Bousquet P, Greney H, Bruban V, Schann S, Ehrhardt JD, Monassier L, Feldman J. |
Knockout mice as model systems for studying nm23/NDP kinase gene functions. Application to the nm23-M1 geneArnaud-Dabernat S., Bourbon P.M., Dierich A., Le Meur M., Daniel J.Y. |
Leptin: cutting the fat off the boneCock T.A., Auwerx J. |
NSD1 is essential for early post-implantation development and has a catalytically active SET domainRayasam G.V., Wendling O., Angrand P.O., Mark M., Niederreither K., Song L., Lerouge T., Hager G.L., Chambon P., Losson R. |
Overexpression of the serotonin 5-HT2B receptor in heart leads to abnormal mitochondrial function and cardiac hypertrophyNebigil C.G., Jaffre F., Messaddeq N., Hickel P., Monassier L., Launay J.M., Maroteaux L. |
Pancreatic-Duodenal Homeobox 1 Regulates Expression of Liver Receptor Homolog 1 during Pancreas DevelopmentAnnicotte J.S., Fayard E., Swift G.H., Selander L., Edlund H., Tanaka T., Kodama T., Schoonjans K., Auwerx J. |
Récepteurs à la Provençale. EMBO workshop on the biology of nuclear receptors.Auwerx J., Drouin J., Laudet V. |
TAF10 (TAF(II)30) is necessary for TFIID stability and early embryogenesis in miceMohan W.S., Scheer E., Wendling O., Metzger D., Tora L. |
2002A conditional floxed (loxP-flanked) allele for the retinoic acid receptor beta (RARbeta) geneChapellier B., Mark M., Bastien J., Dierich A., LeMeur M., Chambon P., Ghyselinck N.B. |
A conditional floxed (loxP-flanked) allele for the retinoic acid receptor gamma (RARgamma) geneChapellier B., Mark M., Garnier J.M., Dierich A., Chambon P., Ghyselinck N.B. |
A Hoxa2 knockin allele that expresses EGFP upon conditional Cre- mediated recombinationPasqualetti M., Ren S.Y., Poulet M., LeMeur M., Dierich A., Rijli F.M. |
A Hoxa2 mutant conditional allele generated by Flp- and Cre-mediated recombinationRen S.Y., Pasqualetti M., Dierich A., Le Meur M., Rijli F.M. |
A nested deletion approach to generate Cre deleter mice with progressive Hox profilesHerault Y., Kmita M., Sawaya C.C., Duboule D. |
Evidence for synergy between alpha(2)-adrenergic and nonadrenergic mechanisms in central blood pressure regulation.Bruban V, Estato V, Schann S, Ehrhardt JD, Monassier L, Renard P, Scalbert E, Feldman J, Bousquet P. |
Evolutionary conserved sequences are required for the insulation of the vertebrate Hoxd complex in neural cellsKmita M., Tarchini B., Duboule D., Herault Y. |
Liver receptor homolog 1 controls the expression of the scavenger receptor class B type ISchoonjans K., Annicotte J.S., Huby T., Botrugno O.A., Fayard E., Ueda Y., Chapman J., Auwerx J. |
Progesterone receptor knockout mice have an improved glucose homeostasis secondary to beta -cell proliferationPicard F., Wanatabe M., Schoonjans K., Lydon J., O'Malley B.W., Auwerx J. |
Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbsKmita M., Fraudeau N., Herault Y., Duboule D. |
Sigma receptors: from discovery to highlights of their implications in the cardiovascular system.Monassier L, Bousquet P. |
SRC-1 and TIF2 control energy balance between white and brown adipose tissuesPicard F., Gehin M., Annicotte J., Rocchi S., Champy M.F., O'Malley B.W., Chambon P., Auwerx J. |
The AF-1 activation-function of ERalpha may be dispensable to mediate the effect of estradiol on endothelial NO production in micePendaries C., Darblade B., Rochaix P., Krust A., Chambon P., Korach K.S., Bayard F., Arnal J.F. |
The function of TIF2/GRIP1 in mouse reproduction is distinct from those of SRC-1 and p/CIPGehin M., Mark M., Dennefeld C., Dierich A., Gronemeyer H., Chambon P. |
The retinoblastoma-histone deacetylase 3 complex inhibits PPARgamma and adipocyte differentiationFajas L., Egler V., Reiter R., Hansen J., Kristiansen K., Debril M.B., Miard S., Auwerx J. |
1999Hox gene expression in limbs: colinearity by opposite regulatory controlsHerault Y., Beckers J., Gerard M., Duboule D. |
1998Engineering chromosomes in mice through targeted meiotic recombination (TAMERE)Herault Y., Rassoulzadegan M., Cuzin F., Duboule D. |
Genetic analysis of a Hoxd-12 regulatory element reveals global versus local modes of controls in the HoxD complexHerault Y., Beckers J., Kondo T., Fraudeau N., Duboule D. |
Genetic control of murine limb morphogenesis: relationships with human syndromes and evolutionary relevanceKondo T., Herault Y., Zakany J., Duboule D. |
1997[Control of limb morphogenesis by the Hox genes]Herault Y., Duboule D. |
[Hox genes and genetic control of limb development]Herault Y., Kondo T., Zakany J., Duboule D. |
Ulnaless (Ul), a regulatory mutation inducing both loss-of-function and gain-of-function of posterior Hoxd genesHerault Y., Fraudeau N., Zakany J., Duboule D. |
1996Function of the Evx-2 gene in the morphogenesis of vertebrate limbsHerault Y., Hraba-Renevey S., van der Hoeven F., Duboule D. |
[Genetic control of limb development]Herault Y., Duboule D. |
1995RNA-dependent DNA binding activity of the Pur factor, potentially involved in DNA replication and gene transcriptionHerault Y., Chatelain G., Brun G., Michel D. |
The expression of the avian clusterin gene can be driven by two alternative promoters with distinct regulatory elementsMichel D., Chatelain G., Herault Y., Brun G. |
1993H-DNA can act as a transcriptional insulatorMichel D., Chatelain G., Herault Y., Harper F., Brun G. |
Serum factors and v-src control two complementary mitogenic pathways in quail neuroretinal cells in cultureGillet G., Michel D., Crisanti P., Guerin M., Herault Y., Pessac B., Calothy G., Brun G., Volovitch M. |
The PUR element stimulates transcription and is a target for single strand-specific binding factors conserved among vertebrate classesHerault Y., Chatelain G., Brun G., Michel D. |
1992The long repetitive polypurine/polypyrimidine sequence (TTCCC)48 forms DNA triplex with PU-PU-PY base triplets in vivoMichel D., Chatelain G., Herault Y., Brun G. |
V-src-induced-transcription of the avian clusterin geneHerault Y., Chatelain G., Brun G., Michel D. |
1991cDNA and predicted amino acid sequences of the human ribosomal protein genes rpS12 and rpL17Herault Y., Michel D., Chatelain G., Brun G. |
