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Altered 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). |
