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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)
Garrett, L. et al.: Fgf9Y162C mutation alters information processing and social memory in mice. Mol. Neurobiol. 55, 4580–4595 (2017)
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)
Fuchs, H. et al.: The first Scube3 mutant mouse line with pleiotropic phenotypic alterations. Genes Genomes Genetics G3 6, 4035-4046 (2016)
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)
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)
Knier, B.* et al.: Neutralizing IL-17 protects the optic nerve from autoimmune pathology and prevents retinal nerve fiber layer atrophy during experimental autoimmune encephalomyelitis. J. Autoimmun. 56, 34-44 (2015)
Kunze, S. et al.: New mutation in the mouse Xpd/Ercc2 gene leads to recessive cataracts. PLoS ONE 10:e0125304 (2015)
Lagouge, M.* et al.: SLIRP regulates the rate of mitochondrial protein synthesis and protects LRPPRC from degradation. PLoS Genet. 11:e1005423 (2015)
Marcos, S.* et al.: Meis1 coordinates a network of genes implicated in eye development and microphthalmia. Development 142, 3009-3020 (2015)
Kraus, P.* et al.: Pleiotropic functions for transcription factor Zscan10. PLoS ONE 9:e104568 (2014)
Neff, F. et al.: Rapamycin extends murine lifespan but has limited effects on aging. J. Clin. Invest. 123, 3272-3291 (2013)
Puk, O. et al.: Novel small-eye allele in paired box gene 6 (Pax6) is caused by a point mutation in intron 7 and creates a new exon. Mol. Vis. 19, 877-884 (2013)
Puk, O. ; Hrabě de Angelis, M. & Graw, J.: Longitudinal fundus and retinal studies with SD-OCT: A comparison of five mouse inbred strains. Mamm. Genome 24, 198-205 (2013)
Puk, O. ; Hrabě de Angelis, M. & Graw, J.: Lens density tracking in mice by Scheimpflug imaging. Mamm. Genome 24, 295-302 (2013)
Puk, O. ; Fuchs, H. ; Gailus-Durner, V. ; Hrabě de Angelis, M. & Graw, J.: The eye screen of the German Mouse Clinic (GMC) - new genetic insights into eye development and ocular disorders. Acta Ophthalmol. 91 (2013)
Renner, S.* et al.: Permanent neonatal diabetes in INSC94Y transgenic pigs. Diabetes 62, 1505-1511 (2013)
Simon, M.M.* et al.: A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome Biol. 14:R82 (2013)