L'équipe
  • Chercheurs

    Véronique BRAULT

    Claire GAVERIAUX-RUFF

    Yann HERAULT

    Michel ROUX

  • Post-Doctorants

    Emilie AUDOUARD

    Damien MARECHAL

    Monika RATAJ BANIOWSKA

  • Doctorants

    Laura Joy BOULOS

    Sandra MARTIN LORENZO

    Maria del Mar MUNIZ MORENO

    Thu Lan NGUYEN

    Marion PELLEN

    Laurie-Anne ROECKEL

    Yaping XUE

  • Ingénieurs & Techniciens

    Claire CHEVALIER

    Arnaud DUCHON

    Valérie NALESSO

    Guillaume PANI

    David REISS

Médecine translationnelle et neurogénétique

Physiopathologie des Aneuploidies, gène à effet de dose et Trisomie 21

Publications

Imprimer la liste complète

  • Genome wide conditional mouse knockout resources

    Kaloff C. , Anastassiadis K. , Ayadi A. , R. Baldock4, J. Beig1, M.-C. Birling3, A. Bradley5, S.D.M. Brown6, A. Bürger1, W. Bushell5, F. Chiani7, F.S. Collins8, B. Doe5, J.T. Eppig9, R.H. Finnell10, 11, C. Fletcher12, P. Flicek13, M. Fray6, R.H. Friedel38, 39, A. Gambadoro7, H. Gates6, J. Hansen1, Y. Herault3, 14, 15, 16, 17, G.G. Hicks18, A. Hörlein40, M. Hrabé de Angelis19, V. Iyer5, P.J. de Jong20, G. Koscielny41, 42, R. Kühn1, 43, 44, P. Liu5, K.C.K Lloyd21, R.G. Lopez22, S. Marschall19, S. Martínez22, C. McKerlie23, T. Meehan13, H. von Melchner24, M. Moore25, S.A. Murray9, A. Nagy26, L.M.J. Nutter23, G. Pavlovic3, 14, 15, 16, A. Pombero45, H. Prosser5, R. Ramirez-Solis5, M. Ringwald9, B. Rosen5, 46, N. Rosenthal9, J. Rossant27, 47, P. Ruiz Noppinger28, E. Ryder5, W.C. Skarnes5, J. Schick48, F. Schnütgen24, P. Schofield29, C. Seisenberger1, M. Selloum3, D. Smedley13, 30, E.M. Simpson31, 32, 33, 49, 50, A.F. Stewart2, L. Teboul6, G.P. Tocchini Valentini7, D. Valenzuela34, A.P. West5, W. Wurst

    Drug Discovery Today: Disease Models 12 September 2017 2017;:.

  • 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).

    Nat Genet Aug 2017;49:1231-1238.

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