PuSH - Publication Server of Helmholtz Zentrum München

97 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
1.
Einer, C. et al.: A high calorie diet aggravates mitochondrial dysfunction and triggers severe liver damage in Wilson disease rats. Cell. Mol. Gast. Hept. 7, 571-596 (2019)
2.
Segal, J.* et al.: Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase (TPI) deficiency. J. Inherit. Metab. Dis., accepted (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.
André, V. et al.: Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data. PLoS Biol. 16:e2005019 (2018)
5.
Clemen, C.S.* et al.: The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice? Biochem. Biophys. Res. Commun. 503, 2770-2777 (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.
Fischer, I.P. et al.: A history of obesity leaves an inflammatory fingerprint in liver and adipose tissue. Int. J. Obes. 42, 507-517 (2018)
8.
Frankó, A. et al.: Epigallocatechin gallate (EGCG) reduces the intensity of pancreatic amyloid fibrils in human islet amyloid polypeptide (hIAPP) transgenic mice. Sci. Rep. 8:1116 (2018)
9.
Molatore, S. et al.: Characterization of neuroendocrine tumors in heterozygous mutant MENX rats: A novel model of invasive medullary thyroid carcinoma. Endocr. Relat. Cancer 25, 145-162 (2018)
10.
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)
11.
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)
12.
Treise, I. et al.: Defective immuno- and thymoproteasome assembly causes severe immunodeficiency. Sci. Rep. 8:5975 (2018)
13.
Xie, K.* et al.: Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice. Proc. Natl. Acad. Sci. U.S.A. 115, E2348-E2357 (2018)
14.
Altamura, S.* et al.: Lack of the ferroptosis inhibitor GPX4 in erythroid cells causes a block in reticulocyte maturation and a hypoxic signature with impaired hepcidin regulation. Haematologica 102, 333-333 (2017)
15.
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)
16.
Egaña, I.* et al.: Female mice lacking Pald1 exhibit endothelial cell apoptosis and emphysema. Sci. Rep. 7:15453 (2017)
17.
Frankó, A. et al.: Bezafibrate ameliorates diabetes via reduced steatosis and improved hepatic insulin sensitivity in diabetic TallyHo mice. Mol. Metab. 6, 256-266 (2017)
18.
Jall, S. et al.: Monomeric GLP-1/GIP/glucagon triagonism corrects obesity, hepatosteatosis, and dyslipidemia in female mice. Mol. Metab. 6, 440-446 (2017)
19.
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)
20.
Keipert, S. et al.: Long-term cold adaptation does not require FGF21 or UCP1. Cell Metab. 26, 437-446.e5 (2017)