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Fuchs, H. et al.: Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse Clinic. Behav. Brain Res. 352, 187-196 (2017)
Garrett, L. et al.: Fgf9Y162C mutation alters information processing and social memory in mice. Mol. Neurobiol. 55, 4580–4595 (2017)
Giesert, F.H.H. et al.: The pathogenic LRRK2 R1441C mutation induces specific deficits modeling the prodromal phase of Parkinson's disease in the mouse. Neurobiol. Dis. 105, 179-193 (2017)
Graveline, R.* et al.: The chromatin associated Phf12 protein maintains nucleolar integrity and prevents premature cellular senescence. Mol. Cell. Biol. 37:e00522-16 (2017)
Kaloff, C. et al.: Genome wide conditional mouse knockout resources. Drug Discov. Today, accepted (2017)
Karp, N.A.* et al.: Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat. Commun. 8:15475 (2017)
Kleinberger, G.* et al.: The FTD-like syndrome causing TREM2 T66M mutation impairs microglia function, brain perfusion, and glucose metabolism. EMBO J., accepted (2017)
Mazaheri, F.* et al.: TREM2 deficiency impairs chemotaxis and microglial responses to neuronal injury. EMBO Rep. 18, 1186-1198 (2017)
Meehan, T.F.* et al.: Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat. Genet. 49, 1231-1238 (2017)
Metzger, M.W.* et al.: Genetically dissecting P2rx7 expression within the central nervous system using conditional humanized mice. Purinergic Signal. 13, 153–170 (2017)
Metzger, M.W.* et al.: Heterozygosity for the mood disorder-associated variant Gln460Arg alters P2X7 receptor function and sleep quality. J. Neurosci. 37, 11688-11700 (2017)
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)
Salminen, A.V. et al.: Meis1 effects on motor phenotypes and the sensorimotor system in mice. Dis. Model. Mech. 10, 981-991 (2017)
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)
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)
Symvoulidis, P. et al.: NeuBtracker-imaging neurobehavioral dynamics in freely behaving fish. Nat. Methods 14, 1079-1082 (2017)
Szibor, M.* et al.: Broad AOX expression in a genetically tractable mouse model does not disturb normal physiology. Dis. Model. Mech. 10, 163-171 (2017)
Trümbach, D. et al.: ENCoRE: An efficient software for CRISPR screens identifies new players in extrinsic apoptosis. BMC Genomics 18:905 (2017)
Vartholomaiou, E.* et al.: Cytosolic Hsp90a and its mitochondrial isoform Trap1 are differentially required in a breast cancer model. Oncotarget 8, 17428-17442 (2017)
Wefers, B. ; Bashir, S.* ; Rossius, J.* ; Wurst, W. & Kühn, R.*: Gene editing in mouse zygotes using the CRISPR/Cas9 system. Methods 121-122, 55-67 (2017)