High-throughput discovery of novel developmental phenotypes.International Mouse Phenotyping ConsortiumDickinson M.E., Flenniken A.M., Ji X., Teboul L., Wong M.D., White J.K., Meehan T.F., Weninger W.J., Westerberg H.[...], Murakami A.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 2154278PubMedEurope PMCNature 537:508-514 (2016)Mapped to99+
A conditional knockout resource for the genome-wide study of mouse gene function.Skarnes W.C., Rosen B., West A.P., Koutsourakis M., Bushell W., Iyer V., Mujica A.O., Thomas M., Harrow J.[...], Bradley A.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2154278PubMedEurope PMCNature 474:337-342 (2011)Mapped to99+
EUCOMM--the European conditional mouse mutagenesis program.Friedel R.H., Seisenberger C., Kaloff C., Wurst W.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2154278PubMedEurope PMCBrief Funct Genomic Proteomic 6:180-185 (2007)Mapped to99+
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.Zambrowicz B.P., Abuin A., Ramirez-Solis R., Richter L.J., Piggott J., BeltrandelRio H., Buxton E.C., Edwards J., Finch R.A.[...], Sands A.T.View abstractCategoryPhenotypes & VariantsSourceMGI: 2154278PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 100:14109-14114 (2003)Cited in1Mapped to99+