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22 Records found.
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1.
Moore, B.A.* et al.: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts. Comm. Bio. 2:97 (2019)
2.
Moore, B.A.* et al.: Identification of genes required for eye development by high-throughput screening of mouse knockouts. Comm. Bio. 1:236 (2018)
3.
Rozman, J. et al.: Identification of genetic elements in metabolism by high-throughput mouse phenotyping.   Nat. Commun. 9:288 (2018)
4.
Wierling, C.* et al.: CanPathPro-development of a platform for predictive pathway modelling using genetically engineered mouse models. Cancer Res. 78 (2018)
5.
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)
6.
Dickinson, M.E.* et al.: Corrigendum: High-throughput discovery of novel developmental phenotypes. Nature 551, 398 (2017)
7.
Kaloff, C. et al.: Genome wide conditional mouse knockout resources. Drug Discov. Today, accepted (2017)
8.
Karp, N.A.* et al.: Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat. Commun. 8:15475 (2017)
9.
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)
10.
del Hierro, M.J.* et al.: EMMA: The European Mouse Mutant Archive. Transgenic Res. 25, 228 (2016)
11.
Dickinson, M.E.* et al.: High-throughput discovery of novel developmental phenotypes. Nature 537, 508-514 (2016)
12.
Hrabě de Angelis, M. et al.: Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nat. Genet. 47, 969-978 (2015)
13.
Karp, N.A.* et al.: Applying the ARRIVE guidelines to an in vivo database. PLoS Biol. 13:e1002151 (2015)
14.
Fernández, J.* et al.: The INFRAFRONTIER research infrastructure and EMMA: The European mouse mutant archive. Transgenic Res. 23, 851 (2014)
15.
Karp, N.A.* et al.: Impact of temporal variation on design and analysis of mouse knockout phenotyping studies. PLoS ONE 9:e111239 (2014)
16.
Simon, M.M.* et al.: A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome Biol. 14:R82 (2013)
17.
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)
18.
Bradley, A.* et al.: The mammalian gene function resource: The International Knockout Mouse Consortium. Mamm. Genome 23, 580-586 (2012)
19.
Wilkinson, P.* et al.: EMMA - mouse mutant resources for the international scientific community. Nucleic Acids Res. 38, D570-D576 (2010)
20.
Magnol, L.* et al.: KIT is required for hepatic function during mouse post-natal development. BMC Dev. Biol. 7:81 (2007)