PuSH - Publication Server of Helmholtz Zentrum München

12 Records found.
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1.
Bowl, M.R.* et al.: A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Nat. Commun. 8:886 (2017)
2.
Dickinson, M.E.* et al.: Corrigendum: High-throughput discovery of novel developmental phenotypes. Nature 551, 398 (2017)
3.
Kaloff, C. et al.: Genome wide conditional mouse knockout resources. Drug Discov. Today, accepted (2017)
4.
Meehan, T.F.* et al.: Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat. Genet. 49, 1231-1238 (2017)
5.
Dickinson, M.E.* et al.: High-throughput discovery of novel developmental phenotypes. Nature 537, 508-514 (2016)
6.
Schick, J. et al.: CRISPR-Cas9 enables conditional mutagenesis of challenging loci. Sci. Rep. 6:32326 (2016)
7.
Ayadi, A.* et al.: Mouse large-scale phenotyping initiatives: Overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute mouse genetics project. Mamm. Genome 23, 600-610 (2012)
8.
Bradley, A.* et al.: The mammalian gene function resource: The International Knockout Mouse Consortium. Mamm. Genome 23, 580-586 (2012)
9.
Ringwald, M.* et al.: The IKMC web portal: A central point of entry to data and resources from the International Knockout Mouse Consortium. Nucleic Acids Res. 39, 1, D849-D855 (2011)
10.
Nord, A.S.* et al.: The International Gene Trap Consortium website: A portal to all publicly available gene trap cell lines in mouse. Nucleic Acids Res. 34, D642-D648 (2006)
11.
Skarnes, W.C.* et al.: A public gene trap resource for mouse functional genomics. Nat. Genet. 36, 543-544 (2004)
12.
Nadeau, J.H.* et al.: Sequence interpretation. Functional annotation of mouse genome sequences. Science 291, 1251-1255 (2001)