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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)
Kaloff, C. et al.: Genome wide conditional mouse knockout resources. Drug Discov. Today, accepted (2017)
Karp, N.A.* et al.: Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat. Commun. 8:15475 (2017)
Hoppe, P.S. et al.: Early myeloid lineage choice is not initiated by random PU.1 to GATA1 protein ratios. Nature 535, 299-302 (2016)
Schick, J. et al.: CRISPR-Cas9 enables conditional mutagenesis of challenging loci. Sci. Rep. 6:32326 (2016)
Ramin, M.* et al.: Stability of cryopreserved samples of mutant mice. Biopreserv. Biobank. 12, 343-350 (2014)
Giesert, F.H.H. et al.: Expression analysis of lrrk1, lrrk2 and lrrk2 splice variants in mice. PLoS ONE 8:e63778 (2013)
Bradley, A.* et al.: The mammalian gene function resource: The International Knockout Mouse Consortium. Mamm. Genome 23, 580-586 (2012)