Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

Autor: Hrabe de Angelis, M. (M), Nicholson, G. (G), Selloum, M. (Mohammed), White, J. (J) K. (K), Morgan, H. (H), Ramirez-Solis, R. (R), Sorg, T. (Tania), Wells, S. (S), Fuchs, H. (H), Fray, M. (M), Adams, D. (D) J. (J), Adams, N. (N) C. (C), Adler, T. (T), Aguilar-Pimentel, A. (A), Ali-Hadji, D. (Dalila), Amann, G. (Grégory), Andre, P. (Philippe), Atkins, S. (S), Auburtin, A. (Aurélie), Ayadi, A. (Abdelkader), Becker, J. (Julien), Becker, L. (L), Bedu, E. (Elodie), Bekeredjian, R. (R), Birling, M. (Marie-Christine), Blake, A. (A), Bottomley, J. (J), Bowl, M. (M) R. (R), Brault, V. (Véronique), Busch, D. (D) H. (H), Bussell, J. (J) N. (N), Calzada-Wack, J. (J), Cater, H. (H), Champy, M. (Marie-France), Charles, P. (Philippe), Chevalier, C. (Claire), Chiani, F. (F), Codner, G. (G) F. (F), Combe, R. (R), Cox, R. (R), Dalloneau, E. (E), Dierich, A. (A), Di Fenza, A. (A), Doe, B. (B), Duchon, A. (Arnaud), Eickelberg, O. (O), Esapa, C. (C) T. (T), Fertak, L. (L) E. (E), Feigel, T. (T), Emelyanova, I. (I), Estabel, J. (J), Favor, J. (J), Flenniken, A. (A), Gambadoro, A. (A), Garrett, L. (L), Gates, H. (H), Gerdin, A. (A) K. (K), Gkoutos, G. (G), Greenaway, S. (S), Glasl, L. (L), Goetz, P. (P), Da Cruz, I. (I) G. (G), Gotz, A. (A), Graw, J. (J), Guimond, A. (Alain), Hans, W. (W), Hicks, G. (G), Holter, S. (S) M. (M), Hofler, H. (H), Hancock, J. (J) M. (M), Hoehndorf, R. (R), Hough, T. (T), Houghton, R. (R), Hurt, A. (A), Ivandic, B. (B), Jacobs, H. (Hugues), Jacquot, S. (Sylvie), Jones, N. (N), Karp, N. (N) A. (A), Katus, H. (H) A. (A), Kitchen, S. (S), Klein-Rodewald, T. (T), Klingenspor, M. (M), Klopstock, T. (T), Lalanne, V. (Valérie), Leblanc, S. (Sophie), Lengger, C. (C), le Marchand, E. (Elise), Ludwig, T. (T), Lux, A. (Aline), McKerlie, C. (C), Maier, H. (H), Mandel, J. (Jean-Louis), Marschall, S. (S), Mark, M. (Manuel), Melvin, D. (D) G. (G), Meziane, H. (Hamid), Micklich, K. (K), Mittelhauser, C. (C), Monassier, L. (Laurent), Moulaert, D. (David), Muller, S. (Stéphanie), Naton, B. (B), Neff, F. (F), Nolan, P. (P) M. (M), Nutter, L. (L) M. (M), Ollert, M. (M), Pavlovic, G. (Guillaume), Pellegata, N. (N) S. (S), Peter, E. (E), Petit-Demouliere, B. (Benoît), Pickard, A. (A), Podrini, C. (C), Potter, P. (P), Pouilly, L. (Laurent), Puk, O. (O), Richardson, D. (D), Rousseau, S. (Stéphane), Quintanilla-Fend, L. (L), Quwailid, M. (M) M. (M), Racz, I. (I), Rathkolb, B. (B), Riet, F. (Fabrice), Rossant, J. (J), Roux, M. (Michel), Rozman, J. (J), Ryder, E. (E), Salisbury, J. (J), Santos, L. (L), Schable, K. (K) H. (H), Schiller, E. (E), Schrewe, A. (A), Schulz, H. (H), Steinkamp, R. (R), Simon, M. (M), Stewart, M. (M), Stoger, C. (C), Stoger, T. (T), Sun, M. (M), Sunter, D. (D), Teboul, L. (L), Tilly, I. (I), Tocchini-Valentini, G. (G) P. (P), Tost, M. (M), Treise, I. (I), Vasseur, L. (Laurent), Velot, E. (E), Vogt-Weisenhorn, D. (D), Wagner, C. (Christel), Walling, A. (A), Wattenhofer-Donze, M. (Marie), Weber, B. (Bruno), Wendling, O. (Olivia), Westerberg, H. (H), Willershauser, M. (M), Wolf, E. (E), Wolter, A. (A), Wood, J. (J), Wurst, W. (W), Yildirim, A. (A) O. (O), Zeh, R. (R), Zimmer, A. (A), Zimprich, A. (A), Consortium, E. (Eumodic), Holmes, C. (C), Steel, K. (K) P. (P), Herault, Y. (Yann), Gailus-Durner, V. (V), Mallon, A. (A) M. (M), Brown, S. (S) D. (D)

Publikováno v: de Angelis, M H, Nicholson, G, Selloum, M, White, J K, Morgan, H, Ramirez-Solis, R, Sorg, T, Wells, S, Fuchs, H, Fray, M, Adams, D J, Adams, N C, Adler, T, Aguilar-Pimentel, A, Ali-Hadji, D, Amann, G, André, P, Atkins, S, Auburtin, A, Ayadi, A, Becker, J, Becker, L, Bedu, E, Bekeredjian, R, Birling, M-C, Blake, A, Bottomley, J, Bowl, M R, Brault, V, Busch, D H, Bussell, J N, Calzada-Wack, J, Cater, H, Champy, M-F, Charles, P, Chevalier, C, Chiani, F, Codner, G F, Combe, R, Cox, R, Dalloneau, E, Dierich, A, Di Fenza, A, Doe, B, Duchon, A, Eickelberg, O, Esapa, C T, Fertak, L E, Feigel, T, Ollert, M & EUMODIC Consortium 2015, ' Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics ', Nature Genetics, vol. 47, no. 9, pp. 969–978 . https://doi.org/10.1038/ng.3360
Nature genetics 47(9), 969-978 (2015). doi:10.1038/ng.3360
Europe PubMed Central

The function of the majority of genes in the mouse and human genomes remains unknown. The mouse embryonic stem cell knockout resource provides a basis for the characterization of relationships between genes and phenotypes. The EUMODIC consortium deve

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https://portal.findresearcher.sdu.dk/da/publications/23c76d69-b52b-4f1e-b534-60544aef3c78

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Mutant p53 tumor suppressor alleles release ras-induced cell cycle growth arrest

Autor: Hicks, G G, Egan, S E, Greenberg, A H, Mowat, M

Publikováno v: Molecular and Cellular Biology; March 1991, Vol. 11 Issue: 3 p1344-1352, 9p

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Genome Wide Conditional Mouse Knockout Resources.

Autor: Kaloff C; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Anastassiadis K; Biotechnology Center (BIOTEC) of the Technische Universität Dresden, 01307 Dresden, Germany., Ayadi A; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris (ICS), CNRS, INSERM, University of Strasbourg, 1 rue Laurent Fries, F-67404 Illkirch-Graffenstaden, France., Baldock R; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, College of Medicine and Veterinary Medicine, Edinburgh, Scotland EH4 2XU, UK., Beig J; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Birling MC; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris (ICS), CNRS, INSERM, University of Strasbourg, 1 rue Laurent Fries, F-67404 Illkirch-Graffenstaden, France., Bradley A; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Brown S; Mammalian Genetics Unit, MRC Harwell, Harwell Science and Innovation Campus, Oxfordshire, OX110RD, UK., Bürger A; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Bushell W; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Chiani F; Istituto di Biologia Cellulare, Consiglio Nazionale delle Ricerche (CNR), Monterotondo-Scalo, I-00015 Rome, Italy., Collins FS; Office of the Director, National Institutes of Health, Bethesda, Maryland, 20892, USA., Doe B; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Eppig JT; The Jackson Laboratory, Bar Harbor, ME 04609, USA., Finnel RH; The Texas A&M Institute for Genomic Medicine, College Station, Texas, 77843-4485 USA; University of Texas at Austin, Austin, Texas, 78712, USA., Fletcher C; National Institutes of Health, Bethesda, Maryland, 20205, USA., Flicek P; European Bioinformatics Institute (EBI), Hinxton, Cambridge, CB101ST, UK., Fray M; Mammalian Genetics Unit, MRC Harwell, Harwell Science and Innovation Campus, Oxfordshire, OX110RD, UK., Friedel RH; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Gambadoro A; Istituto di Biologia Cellulare, Consiglio Nazionale delle Ricerche (CNR), Monterotondo-Scalo, I-00015 Rome, Italy., Gates H; Mammalian Genetics Unit, MRC Harwell, Harwell Science and Innovation Campus, Oxfordshire, OX110RD, UK., Hansen J; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Herault Y; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, 1 rue Laurent Fries, 67404 Illkirch, France.; Centre National de la Recherche Scientifique, UMR7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, France.; Université de Strasbourg, 1 rue Laurent Fries, 67404 Illkirch, France., Hicks GG; University of Manitoba, Manitoba Institute of Cell Biology, Winnipeg, MB, R3EOV9, Canada., Hörlein A; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Hrabé de Angelis M; Institute of Experimental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Iyer V; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., de Jong PJ; Children's Hospital Oakland Research Institute, CHORI, Oakland, CA, 94609, USA., Koscielny G; European Bioinformatics Institute (EBI), Hinxton, Cambridge, CB101ST, UK., Kühn R; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Liu P; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Lloyd KC; Mouse Biology Program, School of Veterinary Medicine, University of California, Davis, California 95616, USA., Lopez RG; Instituto de Neurociencias (UMH-CSIC), San Juan de Alicante., Marschall S; Institute of Experimental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Martínez S; Instituto de Neurociencias (UMH-CSIC), San Juan de Alicante., McKerlie C; The Centre for Phenogenomics and Translation Medicine, The Hospital for Sick Children, Toronto, CANADA., Meehan T; European Bioinformatics Institute (EBI), Hinxton, Cambridge, CB101ST, UK., von Melchner H; Department of Molecular Haematology, University of Frankfurt Medical School, 60590 Frankfurt am Main, Germany., Moore M; IMPC, San Anselmo, California, US., Murray SA; The Jackson Laboratory, Bar Harbor, ME 04609, USA., Nagy A; Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Joseph and Wolf Lebovic Health Complex, Toronto, ON, M5G1X5, Canada., Nutter L; The Centre for Phenogenomics and Translation Medicine, The Hospital for Sick Children, Toronto, CANADA., Pavlovic G; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris (ICS), CNRS, INSERM, University of Strasbourg, 1 rue Laurent Fries, F-67404 Illkirch-Graffenstaden, France., Pombero A; Instituto de Neurociencias (UMH-CSIC), San Juan de Alicante., Prosser H; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Ramirez-Solis R; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Ringwald M; The Jackson Laboratory, Bar Harbor, ME 04609, USA., Rosen B; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Rosenthal N; The Jackson Laboratory, Bar Harbor, ME 04609, USA., Rossant J; Research Institute, The Hospital for Sick Children, SickKids Foundation, Toronto, ON, M5G2L3, Canada., Ruiz Noppinger P; Department of Vertebrate Genomics, Charité, 10115 Berlin, Germany., Ryder E; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Skarnes WC; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Schick J; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Schnütgen F; Department of Molecular Haematology, University of Frankfurt Medical School, 60590 Frankfurt am Main, Germany., Schofield P; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, CB23EG, UK., Seisenberger C; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany., Selloum M; CELPHEDIA, PHENOMIN, Institut Clinique de la Souris (ICS), CNRS, INSERM, University of Strasbourg, 1 rue Laurent Fries, F-67404 Illkirch-Graffenstaden, France., Smedley D; European Bioinformatics Institute (EBI), Hinxton, Cambridge, CB101ST, UK.; Clinical Pharmacology, Queen Mary, University of London, Gower Street, London WC1E 6BT, UK., Simpson EM; Centre for Molecular Medicine and Therapeutics at the BC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.; Department of Psychiatry, University of British Columbia, Vancouver, British Columbia, Canada., Stewart AF; Biotechnology Center (BIOTEC) of the Technische Universität Dresden, 01307 Dresden, Germany., Teboul L; Mammalian Genetics Unit, MRC Harwell, Harwell Science and Innovation Campus, Oxfordshire, OX110RD, UK., Tocchini Valentini GP; Istituto di Biologia Cellulare, Consiglio Nazionale delle Ricerche (CNR), Monterotondo-Scalo, I-00015 Rome, Italy., Valenzuela D; Velocigene Division, Regeneron Pharmaceuticals Inc., Tarrytown, New York, 10591, USA., West A; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB101HH, UK., Wurst W; Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany.; Deutsches Zentrum für Neurodegenerative Erkrankungen e. V. (DZNE), Standort München - Feodor-Lynen-Str. 17, 81377 München Germany.; Munich Cluster for Systems Neurology (SyNergy), Feodor-Lynen-Str. 17, 81377 Munich, Germany.; Technische Universität München-Weihenstephan, Lehrstuhl für Entwicklungsgenetik, c/o Helmholtz Zentrum München, Ingolstädter Landstr. 1, 85764 Neuherberg, Germany.

Publikováno v: Drug discovery today. Disease models [Drug Discov Today Dis Models] 2016 Summer; Vol. 20, pp. 3-12. Date of Electronic Publication: 2017 Sep 12.