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Human Molecular Genetics|November 5, 2011
An aggregation sensing reporter identifies leflunomide and teriflunomide as polyglutamine aggregate inhibitorsRodrigo A Fuentealba, Jayne Marasa, Marc I Diamond, et al.
The Journal of Biological Chemistry|June 13, 2014
Myopathy-causing mutations in an HSP40 chaperone disrupt processing of specific client conformersKevin C Stein, Rocio Bengoechea, Matthew B Harms, et al.
Experimental Eye Research|July 23, 2013
p62 expression and autophagy in αB-crystallin R120G mutant knock-in mouse model of hereditary cataractJonathan A Wignes, Joshua W Goldman, Conrad C Weihl, et al.
Data in Brief|July 21, 2017
Comparisons of ELISA and Western blot assays for detection of autophagy fluxSung-Hee Oh, Yong-Bok Choi, June-Hyun Kim, et al.
Neuromuscular Disorders : NMD|February 15, 2020
A cross-sectional study of hand function in inclusion body myositis: Implications for functional rating scaleAva Yun Lin, Maggie Clapp, Elizabeth Karanja, et al.
Archives of Neurology|August 12, 2009
Acute and bilateral blindness due to optic neuropathy associated with copper deficiencyRobert T Naismith, James B Shepherd, Conrad C Weihl, et al.
Annals of Clinical and Translational Neurology|November 25, 2022
LGMDD1 natural history and phenotypic spectrum: Implications for clinical trialsAndrew R Findlay, Sarah E Robinson, Stephanie Poelker, et al.
Journal of Neuromuscular Diseases|May 9, 2022
Progression to Loss of Ambulation Among Patients with Autosomal Recessive Limb-girdle Muscular Dystrophy: A Systematic ReviewIvana F Audhya, Antoinette Cheung, Shelagh M Szabo, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 3, 2019
Desmin forms toxic, seeding-competent amyloid aggregates that persist in muscle fibersNiraja Kedia, Khalid Arhzaouy, Sara K Pittman, et al.
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