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Nature Genetics|December 29, 2009
Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4Han-Xiang Deng, Christopher J Klein, Jianhua Yan, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 26, 2006
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondriaHan-Xiang Deng, Yong Shi, Yoshiaki Furukawa, et al.
Journal of Agricultural and Food Chemistry|November 29, 2024
Existing Forms of Notoginsenoside R1 in Rats and Their Potential BioactivitiesMeng-Ge Feng, Lin-Han Xiang, Yang Li, et al.
Archives of Neurology|November 16, 2011
SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosisFaisal Fecto, Jianhua Yan, S Pavan Vemula, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 24, 2014
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2George H Gorrie, Faisal Fecto, Daniel Radzicki, et al.
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