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1.
Treise, I. et al.: Defective immuno- and thymoproteasome assembly causes severe immunodeficiency. Sci. Rep. 8:5975 (2018)
2.
Kunze, S. et al.: New mutation in the mouse Xpd/Ercc2 gene leads to recessive cataracts. PLoS ONE 10:e0125304 (2015)
3.
Rathkolb, B. et al.: Screen for alterations of iron related parameters in N-ethyl-N-nitrosurea-treated mice identified mutant lines with increased plasma ferritin levels. Biometals 28, 293-306 (2015)
4.
Fuchs, H. et al.: Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines. Eur. J. Oral Sci. 120, 269-277 (2012)
5.
Sabrautzki, S. et al.: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis. Mamm. Genome 23, 416-430 (2012)
6.
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)
7.
Aigner, B.* et al.: Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in hematological parameters. Mamm. Genome 22, 495-505 (2011)
8.
Graw, J. et al.: Optic nerve phenotypes. Vortrag: EUMODIC-Abschluss-Meeting, 21-22 November 2011, Genf. (2011)
9.
Hoeschen, C. et al.: Autostereoscopic display. Schutzrecht WO 2011/057681 A8 (2011)
10.
Graw, J. et al.: Mutation in the Bmpr1b gene affects optic nerve development. Vortrag: EVER-Meeting (Eurpean Vision and Eye Researchers), 6.-9. Oktober 2010, Kreta. (2010)
11.
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)
12.
Schegerer, A.A. et al.: Development and quality characterization of a novel CT system. Proc. SPIE 7622:762230 (2010)
13.
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)
14.
Abe, K. et al.: Genome-wide search for genes that modulate inflammatory arthritis caused by Ali18 mutation in mice. Mamm. Genome 20, 152-161 (2009)
15.
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)
16.
Hoeschen, C. ; Hrabě de Angelis, M. ; Klaften, M.* & Tischenko, O.: Scanner device and method for computed tomography imaging. Schutzrecht WO 2009/146937 A1 (2009)
17.
Kemter, E.* et al.: Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism. Am. J. Physiol.-Renal Physiol. 297, F1391-F1398 (2009)
18.
Puk, O. et al.: Reduced corneal thickness and enlarged anterior chamber in a novel ColVIIIa2(G257D) mutant mouse. Invest. Ophthalmol. Vis. Sci. 50, 5653-5661 (2009)
19.
Soewarto, D.* ; Klaften, M. & Rubio-Aliaga, I.*: Features and strategies of ENU mouse mutagenesis. Curr. Pharm. Biotechnol. 10, 198-213 (2009)
20.
Aigner, B.* et al.: Screening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease models. Am. J. Physiol.-Renal Physiol. 292, 1560-1567 (2007)