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Aneuploidy: 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. |
