PuSH - Publication Server of Helmholtz Zentrum München

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1.
Schob, C.* et al.: Cognitive impairment and autistic-like behaviour in SAPAP4-deficient mice. Transl. Psychiatry 9:7 (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.
Hensel, T.* et al.: Combined targeting of the Ewing sarcoma transcriptional program by blocking epigenetic readers and transcription initiation via EWS-FLI1. Clin. Cancer Res. 24, 56-56 (2018)
5.
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)
6.
von Heyking, K.* et al.: The endochondral bone protein CHM1 sustains an undifferentiated, invasive phenotype promoting lung metastasis in Ewing sarcoma. Clin. Cancer Res. 24, 57-57 (2018)
7.
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)
8.
Egaña, I.* et al.: Female mice lacking Pald1 exhibit endothelial cell apoptosis and emphysema. Sci. Rep. 7:15453 (2017)
9.
Fuchs, H. et al.: Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse Clinic. Behav. Brain Res. 352, 187-196 (2017)
10.
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)
11.
Karp, N.A.* et al.: Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat. Commun. 8:15475 (2017)
12.
Kumar, S.* et al.: Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1I27N mutant mice. J. Biomed. Sci. 24:57 (2017)
13.
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)
14.
von Heyking, K.* et al.: The endochondral bone protein CHM1 sustains an undifferentiated, invasive phenotype, promoting lung metastasis in Ewing sarcoma. Mol. Oncol. 11, 1288-1301 (2017)
15.
Côme, C.* et al.: CIP2A promotes T-cell activation and immune response to Listeria monocytogenes infection. PLoS ONE 11:e0152996 (2016)
16.
Eden, M.* et al.: Myoscape controls cardiac calcium cycling and contractility via regulation of L-type calcium channel surface expression. Nat. Commun. 7:11317 (2016)
17.
Eden, M.* et al.: Erratum: Myoscape controls cardiac calcium cycling and contractility via regulation of L-type calcium channel surface expression. Nat. Commun. 7:11835 (2016)
18.
Fuchs, H. et al.: The first Scube3 mutant mouse line with pleiotropic phenotypic alterations. Genes Genomes Genetics G3 6, 4035-4046 (2016)
19.
Hensel, T.* et al.: Targeting the EWS-ETS transcriptional program by BET bromodomain inhibition in Ewing sarcoma. Oncotarget 7, 1451-1463 (2016)
20.
Hensel, T.* et al.: Combined targeting of the EWS/ETS Ttanscriptional program by BET bromodomain and PI3K pathway inhibition blocks tumorigenicity and increases apoptosis in ewing sarcoma. Pediatr. Blood Cancer 63, S20-S21 (2016)