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32 Records found.
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21.
Ryan, D.P.* et al.: A paternal methyl donor-rich diet altered cognitive and neural functions in offspring mice. Mol. Psychiatry 23, 1345-1355 (2017)
22.
Salminen, A.V. et al.: Meis1 effects on motor phenotypes and the sensorimotor system in mice. Dis. Model. Mech. 10, 981-991 (2017)
23.
Schludi, M.H.* et al.: Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron loss. Acta Neuropathol. 134, 241–254 (2017)
24.
Schriever, S.C. et al.: Alterations in neuronal control of body weight and anxiety behavior by glutathione peroxidase 4 deficiency. Neuroscience 357, 241-254 (2017)
25.
Xie, K.* et al.: Every-other-day feeding extends lifespan but fails to delay many symptoms of aging in mice. Nat. Commun. 8:155 (2017)
26.
Zimprich, A. et al.: Analysis of locomotor behavior in the German Mouse Clinic. J. Neurosci. Methods, accepted (2017)
27.
Kumar, S.* et al.: Generation and standardized, systemic phenotypic analysis of Pou3f3L423P mutant mice. PLoS ONE 11:e0150472 (2016)
28.
Sabrautzki, S. et al.: Viable EdnraY129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation. Mamm. Genome 27, 587-598 (2016)
29.
Hochrath, K.* et al.: Cholestatic ABCB4-deficient mice reveal depression/anxiety-like behavior. In:. 2013. K283 (Z. Gastroenterol. ; 51)
30.
Grzmil, P.* et al.: Targeted disruption of the mouse Npal3 gene leads to deficits in behavior, increased IgE levels, and impaired lung function. Cytogenet. Genome Res. 125, 186-200 (2009)
31.
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)
32.
Poët, M.* et al.: Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6. Proc. Natl. Acad. Sci. U.S.A. 103, 13854-13859 (2006)