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Segal, J.* et al.: Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase (TPI) deficiency. J. Inherit. Metab. Dis., accepted (2019)
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)
André, V. et al.: Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data. PLoS Biol. 16:e2005019 (2018)
Clemen, C.S.* et al.: The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice? Biochem. Biophys. Res. Commun. 503, 2770-2777 (2018)
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)
Hertel, J.* et al.: Dilution correction for dynamically influenced urinary analyte data. Anal. Chim. Acta 1032, 18-31 (2018)
Hinrichs, A.* et al.: Growth hormone receptor-deficient pigs resemble the pathophysiology of human Laron syndrome and reveal altered activation of signaling cascades in the liver. Mol. Metab. 11, 113-128 (2018)
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)
Komnig, D.* et al.: Faim2 contributes to neuroprotection by erythropoietin in transient brain ischemia. J. Neurochem. 145, 258-270 (2018)
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)
Renner, S.* et al.: Metabolic syndrome and extensive adipose tissue inflammation in morbidly obese Göttingen minipigs. Mol. Metab., accepted (2018)
Rotter, M. et al.: Night shift work affects urine metabolite profiles of nurses with early chronotype. Metabolites 8:45 (2018)
Rozman, J. et al.: Identification of genetic elements in metabolism by high-throughput mouse phenotyping.   Nat. Commun. 9:288 (2018)
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)
Treise, I. et al.: Defective immuno- and thymoproteasome assembly causes severe immunodeficiency. Sci. Rep. 8:5975 (2018)
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)
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)
Blutke, A.* et al.: The Munich MIDY Pig Biobank - A unique resource for studying organ crosstalk in diabetes. Mol. Metab. 6, 931-940 (2017)
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)
Egaña, I.* et al.: Female mice lacking Pald1 exhibit endothelial cell apoptosis and emphysema. Sci. Rep. 7:15453 (2017)