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196 Records found.
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1.
Graw, J.: Mouse models for microphthalmia, anophthalmia and cataracts. Hum. Genet., accepted (2019)
2.
Graw, J. ; Vetrivel, S. ; Fuchs, H. ; Sabrautzki, S. & Tiso, N.*: Mutation in the mouse histone gene Hist2h3c1 leads to degeneration of the lens vesicle and severe microphthalmia. Vortrag: EVER-Meeting 2019, 17-19 October 2019, Nizza. (2019)
3.
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)
4.
Amarie, O.V. ; Fuchs, H. ; Gailus-Durner, V. ; Hrabě de Angelis, M. & Graw, J.: Animal case. Acta Ophthalmol. 96, 4-4 (2018)
5.
André, V. et al.: Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data. PLoS Biol. 16:e2005019 (2018)
6.
Dalke, C. et al.: Lifetime study in mice after acute low-dose ionizing radiation: A multifactorial study with special focus on cataract risk. Radiat. Environ. Biophys. 57, 99-113 (2018)
7.
Heermann, T. et al.: Crybb2 mutations consistently affect schizophrenia endophenotypes in mice. Mol. Neurobiol., accepted (2018)
8.
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)
9.
Nikolakopoulou, P.* et al.: Streptozotocin-induced beta-cell damage, high fat diet, and metformin administration regulate Hes3 expression in the adult mouse brain. Sci. Rep. 8:11335 (2018)
10.
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)
11.
Shi, R.* et al.: Peroxidasin contributes to lung host defense by direct binding and killing of gram-negative bacteria. PLoS Pathog. 14:e1007026 (2018)
12.
Sun, M.* ; Ahmad, N.* ; Zhang, R.* & Graw, J.: Crybb2 associates with Tmsb4X and is crucial for dendrite morphogenesis. Biochem. Biophys. Res. Commun. 503, 123-130 (2018)
13.
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)
14.
Egaña, I.* et al.: Female mice lacking Pald1 exhibit endothelial cell apoptosis and emphysema. Sci. Rep. 7:15453 (2017)
15.
Garrett, L. et al.: Fgf9Y162C mutation alters information processing and social memory in mice. Mol. Neurobiol. 55, 4580–4595 (2017)
16.
Graw, J.: From eyeless to neurological diseases. Exp. Eye Res. 156, 5-9 (2017)
17.
Karp, N.A.* et al.: Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat. Commun. 8:15475 (2017)
18.
Neu, E.* et al.: On importance of pathophysiology for an integrative toxicology. Toxicol. Lett. 280, S305-S305 (2017)
19.
Reitmeir, P. et al.: Common eye diseases in older adults of Southern Germany: Results from the KORA-Age Study. Age Ageing 46, 481-486 (2017)
20.
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)