PuSH - Publication Server of Helmholtz Zentrum München

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1.
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)
2.
Russkamp, D. et al.: IL-4 receptor α blockade prevents sensitization and alters acute and long-lasting effects of allergen-specific immunotherapy of murine allergic asthma. Allergy, accepted (2019)
3.
Schob, C.* et al.: Cognitive impairment and autistic-like behaviour in SAPAP4-deficient mice. Transl. Psychiatry 9:7 (2019)
4.
Segal, J.* et al.: Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase (TPI) deficiency. J. Inherit. Metab. Dis., accepted (2019)
5.
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)
6.
Amarie, O.V. ; Fuchs, H. ; Gailus-Durner, V. ; Hrabě de Angelis, M. & Graw, J.: Animal case. Acta Ophthalmol. 96, 4-4 (2018)
7.
André, V. et al.: Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data. PLoS Biol. 16:e2005019 (2018)
8.
Bartsch, K.* et al.: RNase H2 loss in murine astrocytes results in cellular defects reminiscent of nucleic acid-mediated autoinflammation. Front. Immunol. 9:587 (2018)
9.
Clemen, C.S.* et al.: The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice? Biochem. Biophys. Res. Commun. 503, 2770-2777 (2018)
10.
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)
11.
Heermann, T. et al.: Crybb2 mutations consistently affect schizophrenia endophenotypes in mice. Mol. Neurobiol., accepted (2018)
12.
Jain, M.* et al.: RNA editing of Filamin A pre-mRNA regulates vascular contraction and diastolic blood pressure. EMBO J.:e94813 (2018)
13.
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)
14.
Massner, C. et al.: Genetically controlled lysosomal entrapment of superparamagnetic ferritin for multimodal and multiscale imaging and actuation with low tissue attenuation. Adv. Func. Mat. 28:1706793 (2018)
15.
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)
16.
Rajendran, J.* et al.: Alternative oxidase-mediated respiration prevents lethal mitochondrial cardiomyopathy. EMBO Mol. Med. 10:e9456 (2018)
17.
Rozman, J. et al.: Identification of genetic elements in metabolism by high-throughput mouse phenotyping.   Nat. Commun. 9:288 (2018)
18.
Russkamp, D.* et al.: A thermosensitive hydrogel as delivery system for immunomodulatory substances and allergens during allergen-specific immunotherapy. Allergy 73, 233-233 (2018)
19.
Russkamp, D.* et al.: Sustained inhibition of the IL4/IL13 receptor complex during allergen specific immunotherapy. Allergy 73, 232-232 (2018)
20.
Sakkou, M.* et al.: Mesenchymal TNFR2 promotes the development of polyarthritis and comorbid heart valve stenosis. JCI insight 3:98864 (2018)