PuSH - Publication Server of Helmholtz Zentrum München

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1.
Abe, K.* et al.: Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humans. Proc. Natl. Acad. Sci. U.S.A. 116, 11872-11877 (2019)
2.
Altamura, S.* et al.: Glutathione peroxidase 4 and vitamin E control reticulocyte maturation, stress erythropoiesis and iron homeostasis. Haematologica, accepted (2019)
3.
Backman, M.* et al.: Multi-omics insights into functional alterations of the liver in insulin-deficient diabetes mellitus. Mol. Metab., accepted (2019)
4.
Casas, A.I.* et al.: Calcium-dependent blood-brain barrier breakdown by NOX5 limits postreperfusion benefit in stroke. J. Clin. Invest. 129, 1772-1778 (2019)
5.
Häring, H.-U. ; Hrabě de Angelis, M. ; Roden, M.* ; Schürmann, A.* & Solimena, M.: Vom Labor zum Patienten - Translationale Diabetesforschung. Diabetes akt. 17, 96 (2019)
6.
Heermann, T. et al.: Crybb2 mutations consistently affect Schizophrenia endophenotypes in mice. Mol. Neurobiol. 56, 4215-4230 (2019)
7.
Kempe-Teufel, D. et al.: A polygenic risk score of lipolysis-increasing alleles determines visceral fat mass and proinsulin conversion. J. Clin. Endocrinol. Metab. 104, 1090-1098 (2019)
8.
Keuper, M. et al.: Preadipocytes of obese humans display gender-specific bioenergetic responses to glucose and insulin. Mol. Metab. 20, 28-37 (2019)
9.
Moore, B.A.* et al.: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts. Comm. Bio. 2:97 (2019)
10.
Muñoz-Fuentes, V.* et al.: The International Mouse Phenotyping Consortium (IMPC): A functional catalogue of the mammalian genome that informs conservation (vol 19, pg 995, 2018). Conservation genetics 20, 135-136 (2019)
11.
Nezhad, F.Y.* et al.: Genes whose gain or loss-of-function increases endurance performance in Mice: A systematic literature review. Front. Physiol. 10:262 (2019)
12.
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)
13.
Schob, C.* et al.: Cognitive impairment and autistic-like behaviour in SAPAP4-deficient mice. Transl. Psychiatry 9:7 (2019)
14.
Segal, J.* et al.: Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency. J. Inherit. Metab. Dis., accepted (2019)
15.
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)
16.
Amarie, O.V. ; Fuchs, H. ; Gailus-Durner, V. ; Hrabě de Angelis, M. & Graw, J.: Animal case. Acta Ophthalmol. 96, 4-4 (2018)
17.
André, V. et al.: Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data. PLoS Biol. 16:e2005019 (2018)
18.
Babbar, R.* et al.: Prediction of glucose tolerance without an oral glucose tolerance test. Front. Endocrin. 9:82 (2018)
19.
Barbone, G.E.* et al.: Micro-imaging of brain cancer radiotherapy using phase-contrast computed tomography. Int. J. Radiat. Oncol. Biol. Phys. 101, 965-984 (2018)
20.
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)