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CNS Neuroscience & Therapeutics|July 19, 2016
The Potential of Indole/Indolylquinoline Compounds in Tau Misfolding Reduction by Enhancement of HSPB1Kuo-Hsuan Chang, Chih-Hsin Lin, Hsuan-Chiang Chen, et al.Journal of Biomedical Science|May 27, 2017
Improving the regenerative potential of olfactory ensheathing cells by overexpressing prostacyclin synthetase and its application in spinal cord repairMay-Jywan Tsai, Chi-Ting Huang, Yong-San Huang, et al.Annals of Neurology|April 17, 2008
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's diseaseOwen A Ross, Yih-Ru Wu, Mei-Ching Lee, et al.Cell|September 13, 2011
Acetylation of yeast AMPK controls intrinsic aging independently of caloric restrictionJin-Ying Lu, Yu-Yi Lin, Jin-Chuan Sheu, et al.Human Molecular Genetics|July 23, 2003
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) geneMing-Jen Lee, Dennis A Stephenson, Michael J Groves, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 17, 2008
PPP2R2B CAG repeat length in the Han Chinese in Taiwan: Association analyses in neurological and psychiatric disorders and potential functional implicationsChiung-Mei Chen, Yi-Ting Hou, Ju-Yun Liu, et al.Neurobiology of Disease|March 1, 2015
Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during developmentMing-Shian Tsai, Meng-Larn Lee, Chun-Yun Chang, et al.Plos One|November 20, 2009
Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalusMing-Jen Lee, Ching-Pang Chang, Yi-Hsin Lee, et al.Journal of Medicinal Chemistry|October 13, 2006
Structural basis for the structure-activity relationships of peroxisome proliferator-activated receptor agonistsNeeraj Mahindroo, Yi-Hui Peng, Chia-Hui Lin, et al.Plos One|December 17, 2013
Genetic variants ofLRRK2 in Taiwanese Parkinson's diseaseYih-Ru Wu, Kuo-Hsuan Chang, Wen-Teng Chang, et al.Pageof 93