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81.
Gailus-Durner, V. et al.: Systemic first-line phenotyping. Methods Mol. Biol. 530, 463-509 (2009)
82.
Gailus-Durner, V. et al.: Systemic first-line phenotyping. Methods Mol. Biol. 530, 463-509 (2009)
83.
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)
84.
Klonisch, T.* et al.: The C-terminal cytoplasmic domain of human proEGF is a negative modulator of body and organ weights in transgenic mice. FEBS Lett. 583, 1349-1357 (2009)
85.
Noyes, H.A.* et al.: Mechanisms controlling anaemia in Trypanosoma congolense infected mice. PLoS ONE 4:e5170 (2009)
86.
Puk, O. et al.: A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: A novel model for dry-eye disease? Invest. Ophthalmol. Vis. Sci. 50, 4311-4318 (2009)
87.
Rathkolb, B. et al.: Clinical chemistry of congenic mice with quantitative trait loci for predicted responses to Trypanosoma congolense infection. Infect. Immun. 77, 3948-3957 (2009)
88.
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)
89.
Aigner, B.* et al.: Diabetes models by screen for hyperglycemia in phenotype-driven ENU mouse mutagenesis projects. Am. J. Physiol. Endocrinol. Metab. 294, 232-240 (2008)
90.
Lisse, T.S. et al.: ER stress-mediated apoptosis in a new mouse model of Osteogenesis imperfecta. PLoS Genet. 4:e7 (2008)
91.
Puk, O. et al.: Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype. Invest. Ophthalmol. Vis. Sci. 49, 1525-1532 (2008)
92.
Schneider, M.R.* ; Wolf, E.* ; Braun, J.* ; Kolb, H.-J. & Adler, H.: Canine embryo-derived stem cells and models for human diseases. Hum. Mol. Genet. 17, R42-R47 (2008)
93.
Söker, T. et al.: Pleiotropic effects in Eya3 knockout mice. BMC Dev. Biol. 8:118 (2008)
94.
Aigner, B.* et al.: Generation of ENU-induced mouse mutants with hypocholesterolemia: Novel tools for dissecting plasma lipoprotein homeostasis. Lipids 42, 731-737 (2007)
95.
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)
96.
Enard, W.* et al.: A mouse model for human-specific changes in FOXP2, a gene important for speech and language. Vortrag: Neuroscience Conference, 3-07 November 2007, San Diego, USA. (2007)
97.
Herbach, N.* et al.: Dominant-Negative Effects of a Novel Mutated Ins2 Allele Causes Early-Onset Diabetes and Severe ß-Cell Loss in Munich Ins2C95S Mutant Mice. Diabetes 56, 1268-1276 (2007)
98.
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)
99.
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)
100.
Schneider, M.R.* et al.: Canine embryo-derived stem cells — toward clinically relevant animal models for evaluating efficacy and safety of cell therapies. Stem Cells 25, 1850-1851 (2007)