PuSH - Publication Server of Helmholtz Zentrum München

63 Records found.
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1.
Vetrivel, S. et al.: Mutation in the mouse histone gene Hist2h3c1 leads to degeneration of the lens vesicle and severe microphthalmia. Exp. Eye Res., accepted (2019)
2.
André, V. et al.: Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data. PLoS Biol. 16:e2005019 (2018)
3.
Clemen, C.S.* et al.: The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice? Biochem. Biophys. Res. Commun. 503, 2770-2777 (2018)
4.
Comai, G.* et al.: Genetic and molecular insights into genotype-phenotype relationships in osteopathia striata with cranial sclerosis (OSCS) through the analysis of novel mouse Wtx mutant alleles. J. Bone Min. Res. 33, 875-887 (2018)
5.
Jensen, L.R.* et al.: A mouse model for intellectual disability caused by mutations in the X-linked 2′‑O‑methyltransferase Ftsj1 gene. Biochim. Biophys. Acta-Mol. Basis Dis., accepted (2018)
6.
Schmidt, M.O.* et al.: The role of Fibroblast growth factor binding protein 1 in skin carcinogenesis and inflammation. J. Invest. Dermatol. 138, 179-188 (2018)
7.
Garrett, L. et al.: Fgf9Y162C mutation alters information processing and social memory in mice. Mol. Neurobiol. 55, 4580–4595 (2017)
8.
Szibor, M.* et al.: Broad AOX expression in a genetically tractable mouse model does not disturb normal physiology. Dis. Model. Mech. 10, 163-171 (2017)
9.
Diener, S. et al.: Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia. Mamm. Genome 27, 111-121 (2016)
10.
Eden, M.* et al.: Myoscape controls cardiac calcium cycling and contractility via regulation of L-type calcium channel surface expression. Nat. Commun. 7:11317 (2016)
11.
Eden, M.* et al.: Erratum: Myoscape controls cardiac calcium cycling and contractility via regulation of L-type calcium channel surface expression. Nat. Commun. 7:11835 (2016)
12.
Fuchs, H. et al.: The first Scube3 mutant mouse line with pleiotropic phenotypic alterations. Genes Genomes Genetics G3 6, 4035-4046 (2016)
13.
Kumar, S.* et al.: Generation and standardized, systemic phenotypic analysis of Pou3f3L423P mutant mice. PLoS ONE 11:e0150472 (2016)
14.
Mulay, S.R.* et al.: Hyperoxaluria requires TNF receptors to initiate crystal adhesion and kidney stone disease. J. Am. Soc. Nephrol. 28, 761-768 (2016)
15.
Sabrautzki, S. et al.: Viable EdnraY129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation. Mamm. Genome 27, 587-598 (2016)
16.
Helmbrecht, M.S. et al.: Loss of Npn1 from motor neurons causes postnatal deficits independent from Sema3A signaling. Dev. Biol. 399, 2-14 (2015)
17.
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)
18.
Keeney, J.G.* et al.: Generation of mice lacking DUF1220 protein domains: Effects on fecundity and hyperactivity. Mamm. Genome 26, 33-42 (2015)
19.
Kessler, T.* et al.: ADAMTS-7 inhibits re-endothelialization of injured arteries and promotes vascular remodeling via cleavage of thrombospondin-1. Circulation 131, 1191-1201 (2015)
20.
Lagouge, M.* et al.: SLIRP regulates the rate of mitochondrial protein synthesis and protects LRPPRC from degradation. PLoS Genet. 11:e1005423 (2015)