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Human Molecular Genetics|September 27, 2006
C-terminal truncation and Parkinson's disease-associated mutations down-regulate the protein serine/threonine kinase activity of PTEN-induced kinase-1Chou Hung Sim, Daisy Sio Seng Lio, Su San Mok, et al.Human Molecular Genetics|September 27, 2006
FGF19 is a target for FOXC1 regulation in ciliary body-derived cellsYahya Tamimi, Jonathan M Skarie, Tim Footz, et al.Human Molecular Genetics|September 30, 2006
A novel PtdIns3P and PtdIns(3,5)P2 phosphatase with an inactivating variant in centronuclear myopathyValérie Tosch, Holger M Rohde, Hélène Tronchère, et al.Human Molecular Genetics|September 30, 2006
Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behaviorIchiko Nishijima, Takanori Yamagata, Corinne M Spencer, et al.Human Molecular Genetics|April 29, 2006
Atm-deficient mice: an osteoporosis model with defective osteoblast differentiation and increased osteoclastogenesisNaslin Rasheed, Xueying Wang, Qing-Tian Niu, et al.Human Molecular Genetics|April 29, 2006
The role of PI3K/AKT, MAPK/ERK and NFkappabeta signalling in the maintenance of human embryonic stem cell pluripotency and viability highlighted by transcriptional profiling and functional analysisLyle Armstrong, Owen Hughes, Sun Yung, et al.Human Molecular Genetics|April 29, 2006
Pharmacologic and genetic inhibition of hsp90-dependent trafficking reduces aggregation and promotes degradation of the expanded glutamine androgen receptor without stress protein inductionMonzy Thomas, Jennifer M Harrell, Yoshihiro Morishima, et al.Human Molecular Genetics|August 4, 2006
Evolutionary insights into the high worldwide prevalence of MBL2 deficiency allelesPaul Verdu, Luis B Barreiro, Etienne Patin, et al.Human Molecular Genetics|April 8, 2006
Early development of aberrant synaptic plasticity in a mouse model of Huntington's diseaseAusten J Milnerwood, Damian M Cummings, Glenn M Dallérac, et al.Human Molecular Genetics|April 8, 2006
Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5Xinhua Shu, Brian Tulloch, Alan Lennon, et al.Pageof 1,196