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13 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.
Muñoz-Fuentes, V.* et al.: The International Mouse Phenotyping Consortium (IMPC): A functional catalogue of the mammalian genome that informs conservation (vol 19, pg 995, 2018). Conservation genetics 20, 135-136 (2019)
3.
Moore, B.A.* et al.: Identification of genes required for eye development by high-throughput screening of mouse knockouts. Comm. Bio. 1:236 (2018)
4.
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)
5.
Dickinson, M.E.* et al.: Corrigendum: High-throughput discovery of novel developmental phenotypes. Nature 551, 398 (2017)
6.
Karp, N.A.* et al.: Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat. Commun. 8:15475 (2017)
7.
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)
8.
Dickinson, M.E.* et al.: High-throughput discovery of novel developmental phenotypes. Nature 537, 508-514 (2016)
9.
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)
10.
Karp, N.A.* et al.: Applying the ARRIVE guidelines to an in vivo database. PLoS Biol. 13:e1002151 (2015)
11.
Gates, H.* ; Mallon, A.M.* ; Brown, S.D.* & EUMODIC Consortium (Hölter, S.M. ; Glasl, S.): High-throughput mouse phenotyping. Methods 53, 394-404 (2011)
12.
Morgan, H.* et al.: EuroPhenome: A repository for high-throughput mouse phenotyping data. Nucleic Acids Res. 38, 1, D577-D585 (2010)
13.
Hancock, J.M. et al.: Integration of mouse phenome data resources. Mamm. Genome 18, 157-163 (2007)