PuSH - Publication Server of Helmholtz Zentrum München

7 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.
Dickinson, M.E.* et al.: High-throughput discovery of novel developmental phenotypes. Nature 537, 508-514 (2016)
5.
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)
6.
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)
7.
Bradley, A.* et al.: The mammalian gene function resource: The International Knockout Mouse Consortium. Mamm. Genome 23, 580-586 (2012)