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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)
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)
Kaklamanos, A.* et al.: Extensive phenotypic characterization of a new transgenic mouse reveals pleiotropic perturbations in physiology due to mesenchymal hGH minigene expression. Sci. Rep. 7:2397 (2017)
Kumar, S.* et al.: Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1I27N mutant mice. J. Biomed. Sci. 24:57 (2017)
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)
Côme, C.* et al.: CIP2A promotes T-cell activation and immune response to Listeria monocytogenes infection. PLoS ONE 11:e0152996 (2016)
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)
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)
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)
Eisenberg, T.* et al.: Cardioprotection and lifespan extension by the natural polyamine spermidine. Nat. Med. 22, 1428-1438 (2016)
Fuchs, H. et al.: The first Scube3 mutant mouse line with pleiotropic phenotypic alterations. Genes Genomes Genetics G3 6, 4035-4046 (2016)
Korner, G.* et al.: Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in mice. J. Inherit. Metab. Dis. 39, 309-319 (2016)
Kumar, S.* et al.: Generation and standardized, systemic phenotypic analysis of Pou3f3L423P mutant mice. PLoS ONE 11:e0150472 (2016)
Wittmann, A. et al.: Sphingomyelin synthase 1 is essential for male fertility in mice. PLoS ONE 11:e0164298 (2016)
Deng, T.* et al.: Functional compensation among HMGN variants modulates the DNase I hypersensitive sites at enhancers. Genome Res. 25, 1295-1308 (2015)
Halama, A. et al.: Metabolic switch during adipogenesis: From branched chain amino acid catabolism to lipid synthesis. Arch. Biochem. Biophys. 589, 93-107 (2015)
Horsch, M. et al.: Cox4i2, Ifit2, and Prdm11 mutant mice: Effective selection of genes predisposing to an altered airway inflammatory response from a large compendium of mutant mouse lines. PLoS ONE 10:e0134503 (2015)
Keeney, J.G.* et al.: Generation of mice lacking DUF1220 protein domains: Effects on fecundity and hyperactivity. Mamm. Genome 26, 33-42 (2015)
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)
Lagouge, M.* et al.: SLIRP regulates the rate of mitochondrial protein synthesis and protects LRPPRC from degradation. PLoS Genet. 11:e1005423 (2015)