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61.
* et al.: A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease. Am. J. Hum. Genet. 89, 168-175 (2011)
62.
Abe, K. et al.: A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model. Arthritis Rheum. 63, 1301-1311 (2011)
63.
Aigner, B.* et al.: Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in hematological parameters. Mamm. Genome 22, 495-505 (2011)
64.
Fuchs, H. et al.: Mouse phenotyping. Methods 53, 120-135 (2011)
65.
Horsch, M. et al.: Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice. J. Biol. Chem. 286, 18614-18622 (2011)
66.
Raab, M.* et al.: Toxicity modelling of Plk1-targeted therapies in genetically engineered mice and cultured primary mammalian cells. Nat. Commun. 2:395 (2011)
67.
Saarikangas, J.* et al.: Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia. J. Cell Sci. 124, 1245-1255 (2011)
68.
Spyroglou, A.* et al.: Utilization of a mutagenesis screen to generate mouse models of hyperaldosteronism. Endocrinology 152, 326-331 (2011)
69.
Kemter, E.* et al.: Mutation of the Na⁺-K⁺-2Cl‾ cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia. Am. J. Physiol.-Renal Physiol. 298, F1405-F1415 (2010)
70.
Morgan, H.* et al.: EuroPhenome: A repository for high-throughput mouse phenotyping data. Nucleic Acids Res. 38, 1, D577-D585 (2010)
71.
Rosemann, M. et al.: Microphthalmia, parkinsonism, and enhanced nociception in Pitx3(416insG ) mice. Mamm. Genome 21, 13-27 (2010)
72.
Schneider, M.R.* et al.: EGFR ligands exert diverging effects on male reproductive organs. Exp. Mol. Pathol. 88, 216-218 (2010)
73.
Schneider, M.R.* ; Wolf, E.* ; Braun, J.* ; Kolb, H.-J. & Adler, H.: Canine embryonic stem cells: State of the art. Theriogenology 74, 492-497 (2010)
74.
Tocchetti, A.* et al.: Loss of the actin remodeler Eps8 causes intestinal defects and improved metabolic status in mice. PLoS ONE 5:e9468 (2010)
75.
van Bürck, L.* et al.: Phenotypic and pathomorphological characteristics of a novel mutant mouse model for maturity-onset diabetes of the young type 2 (MODY 2). Am. J. Physiol. Endocrinol. Metab. 298, E512-E523 (2010)
76.
Aigner, B.* et al.: N-ethyl-N-nitrosourea mutagenesis produced a small number of mice with altered plasma electrolyte levels. J. Biomed. Sci. 16:53 (2009)
77.
Aigner, B.* et al.: Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models. Exp. Physiol. 94, 412-421 (2009)
78.
Diehl, D.* et al.: IGFBP-2 overexpression reduces the appearance of dysplastic aberrant crypt foci and inhibits growth of adenomas in chemically induced colorectal carcinogenesis. Int. J. Cancer 124, 2220-2225 (2009)
79.
Enard, W.* et al.: A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell 137, 961-971 (2009)
80.
Fuchs, H. et al.: The German Mouse Clinic: A platform for systemic phenotype analysis of mouse models. Curr. Pharm. Biotechnol. 10, 236-243 (2009)