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43 Records found.
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21.
Kemter, E.* et al.: Standardized, systemic phenotypic analysis of Slc12a1 I299F mutant mice. J. Biomed. Sci. 21:68 (2014)
22.
Pradier, B.* et al.: Smad-interacting protein 1 affects acute and tonic, but not chronic pain. Eur. J. Pain 18, 249-257 (2014)
23.
Thor, T.* et al.: MiR-34a deficiency accelerates medulloblastoma formation in vivo. Int. J. Cancer 136, 2293-2303 (2014)
24.
Zumbrennen-Bullough, K.B.* et al.: Abnormal brain iron metabolism in Irp2 deficient mice is associated with mild neurological and behavioral impairments. PLoS ONE 9:e98072 (2014)
25.
Ju, L.* et al.: SMC6 is an essential gene in mice, but a hypomorphic mutant in the ATPase domain has a mild phenotype with a range of subtle abnormalities. DNA Repair 12, 356-366 (2013)
26.
Kugler, J.E.* et al.: High mobility group N proteins modulate the fidelity of the cellular transcriptional profile in a tissue- and variant-specific manner. J. Biol. Chem. 288, 16690-16703 (2013)
27.
Neff, F. et al.: Rapamycin extends murine lifespan but has limited effects on aging. J. Clin. Invest. 123, 3272-3291 (2013)
28.
Fuchs, H. et al.: Mouse genetics and metabolic mouse phenotyping. In: Suhre, K.* [Eds.]: Genetics Meets Metabolomics: from Experiment to Systems Biology. Springer, 2012. 85-106
29.
Fuchs, H. et al.: Innovations in phenotyping of mouse models in the German Mouse Clinic. Mamm. Genome 23, 611-622 (2012)
30.
Staropoli, J.F.* et al.: Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous system. PLoS ONE 7:e38310 (2012)
31.
Fuchs, H. et al.: Mouse phenotyping. Methods 53, 120-135 (2011)
32.
Horsch, M. et al.: Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice. J. Biol. Chem. 286, 18614-18622 (2011)
33.
Jeub, M.* et al.: The transcription factor Smad-interacting protein 1 controls pain sensitivity via modulation of DRG neuron excitability. Pain 152, 2384-2398 (2011)
34.
Morgan, H.* et al.: EuroPhenome: A repository for high-throughput mouse phenotyping data. Nucleic Acids Res. 38, 1, D577-D585 (2010)
35.
Rosemann, M. et al.: Microphthalmia, parkinsonism, and enhanced nociception in Pitx3(416insG ) mice. Mamm. Genome 21, 13-27 (2010)
36.
Enard, W.* et al.: A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell 137, 961-971 (2009)
37.
Fuchs, H. et al.: The German Mouse Clinic: A platform for systemic phenotype analysis of mouse models. Curr. Pharm. Biotechnol. 10, 236-243 (2009)
38.
Wirth, E.K.* et al.: Neuronal 3',3,5-triiodothyronine (T₃) uptake and behavioral phenotype of mice deficient in Mct8, the neuronal T₃ transporter mutated in Allan-Herndon-Dudley syndrome. J. Neurosci. 29, 9439-9449 (2009)
39.
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)
40.
Fuchs, H. et al.: Systemic analysis of mouse mutants at the German Mouse Clinic. Vortrag: NGFN-Projektleiter-Treffen, 10-11 November 2007, Heidelberg, Germany. (2007)