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The Journal of Cell Biology|December 17, 2009
Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP diseaseJeong-Sun Ju, Rodrigo A Fuentealba, Sara E Miller, et al.
The Journal of Biological Chemistry|June 18, 2010
Interaction with polyglutamine aggregates reveals a Q/N-rich domain in TDP-43Rodrigo A Fuentealba, Maria Udan, Shaughn Bell, et al.
Orphanet Journal of Rare Diseases|September 30, 2020
Phenotypic diversity in an international Cure VCP Disease registryChiseko Ikenaga, Andrew R Findlay, Michelle Seiffert, et al.
Neuromuscular Disorders : NMD|January 6, 2015
Autophagic vacuolar pathology in desminopathiesConrad C Weihl, Stanley Iyadurai, Robert H Baloh, et al.
Human Molecular Genetics|August 22, 2013
Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperonesMaria Udan-Johns, Rocio Bengoechea, Shaughn Bell, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 18, 2008
TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementiaC C Weihl, P Temiz, S E Miller, et al.
The Lancet. Neurology|August 16, 2025
Advances in the classification and management of idiopathic inflammatory myopathiesJoost Raaphorst, Anneke J van der Kooi, Christopher A Mecoli, et al.
Research Square|October 27, 2023
Defining Clinical Endpoints in Limb Girdle Muscular Dystrophy: A GRASP-LGMD studyAmy Doody, Lindsay Alfano, Jordi Diaz-Manera, et al.
Acta Neuropathologica|June 26, 2026
VMA21 deficiency leads to autophagic dysregulation and altered vesicle trafficking in X-linked myopathy with excessive autophagyChristian A Suarez, Sara K Pittman, Michio Inoue, et al.
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