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Annals of the New York Academy of Sciences|June 24, 2008
Recent structural and mechanistic insights into endplate acetylcholine receptorsSteven M Sine, Fan Gao, Won Yong Lee, et al.
Journal of the Neurological Sciences|January 20, 2012
A novel mutation in SCN4A causes severe myotonia and school-age-onset paralytic episodesHarumi Yoshinaga, Shunichi Sakoda, Jean-Marc Good, et al.
Annals of Neurology|December 17, 2008
Mutation in BAG3 causes severe dominant childhood muscular dystrophyDuygu Selcen, Francesco Muntoni, Barbara K Burton, et al.
Frontiers in Cell and Developmental Biology|February 4, 2022
Meclozine Attenuates the MARK Pathway in Mammalian Chondrocytes and Ameliorates FGF2-Induced Bone Hyperossification in Larval ZebrafishGenta Takemoto, Masaki Matsushita, Takaaki Okamoto, et al.
Parkinsonism & Related Disorders|December 26, 2021
Altered gut microbiota in Parkinson's disease patients with motor complicationsKai Takahashi, Hiroshi Nishiwaki, Mikako Ito, et al.
Applied Physiology, Nutrition, and Metabolism = Physiologie Appliquee, Nutrition Et Metabolisme|August 15, 2017
Interactions between genetic polymorphisms of glucose metabolizing genes and smoking and alcohol consumption in the risk of type 2 diabetes mellitusKaiping Gao, Yongcheng Ren, Jinjin Wang, et al.
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