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Fuchs, H. et al.: The German Mouse Clinic: A platform for systemic phenotype analysis of mouse models. Curr. Pharm. Biotechnol. 10, 236-243 (2009)
Rubio-Aliaga, I. et al.: Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processes. PLoS ONE 4:e6054 (2009)
Fröhlich Archangelo, L. et al.: The CALM and CALM/AF10 interactor CATS is a marker for proliferation. Mol. Oncol. 2, 356-367 (2008)
Lisse, T.S. et al.: ER stress-mediated apoptosis in a new mouse model of Osteogenesis imperfecta. PLoS Genet. 4:e7 (2008)
Rubio-Aliaga, I. et al.: A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse. Genetics 175, 1451-1463 (2007)
Rubio-Aliaga, I.* et al.: A genetic screen for modifiers of the delta1-dependent notch signalling function in the mouse. Vortrag: 19th Mouse Molecular Genetics Meeting, 5-9 September 2007, Hinxton/Cambridge, UK. (2007)
Tiedemann, H.B. et al.: Cell-based simulation of dynamic expression patterns in the presomitic mesoderm. J. Theor. Biol. 248, 120-129 (2007)
Beckers, J. ; Teppner, I.* ; Przemeck, G.K.H. ; Tiedemann, H.B.* & Hrabě de Angelis, M.: The Notch gene regulatory network during somitogenesis. Vortrag: Entwicklungsbiologischer Sino-German Workshop über Mesodermbildung und -differenzierung, 0.-03 September 2006, Beijing, China. (2006)
Beckers, J. ; Teppner, I.* ; Przemeck, G.K.H. ; Tiedemann, H.B. & Hrabě de Angelis, M.: The Notch gene regulatory network during somitogenesis. Vortrag: ICMSB, 2nd August 2006, München, Germany. (2006)
Hoefer, C.* ; Przemeck, G.K.H. & Hrabě de Angelis, M.: Towards the function of the PDZ-binding domain of Delta1. Vortrag: Mouse Molecular Genetics, 30th August 2006 - 3rd September 2006, Cold Spring Harbor, USA. (2006)
Zeiser, S. et al.: Number of active transcription factor binding sites is essential for the Hes7 oscillator. Theor. Biol. Med. Model. 3, 11:11 (2006)
Gailus-Durner, V. et al.: Introducing the German Mouse Clinic: Open access platform for standardized phenotyping. Nat. Methods 2, 403-404 (2005)
Jakupoglu, C. et al.: Cytoplasmic thioredoxin reductase is essential for embryogenesis but dispensable for cardiac development. Mol. Cell. Biol. 25, 1980-1988 (2005)
Willer, T.* et al.: Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality. Proc. Natl. Acad. Sci. U.S.A. 101, 14126-14131 (2004)
Pfister, S. et al.: Interaction of the MAGUK family member Acvrinp1 and the cytoplasmic domain of the notch ligand Delta1. J. Mol. Biol. 333, 229-235 (2003)
Przemeck, G.K.H. ; Heinzmann, U. ; Beckers, J. & Hrabě de Angelis, M.: Node and midline defects are associated with left-right development in Delta1 mutant embryos. Development 130, 3-13 (2003)
Brielmeier, M. ; Fuchs, H. ; Przemeck, G.K.H. ; Gailus-Durner, V. & Schmidt, J.: The GSF - Phenotype analysis center (German Mouse Clinic, GMC) : a sentinel-based health monitoring concept in a multi-user unit for standardized characterization of mouse mutants. In: Proceedings (8th FELASA Symposium). London: Laboratory Animals Ltd, 2002. 19-22
Berti, L. et al.: Isolation and Characterization of a Novel Gene from the DiGeorge Chromosomal Region That Encodes for a Mediator Subunit. Genomics 74, 320-332 (2001)