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Cell Reports|April 6, 2017
Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain UbiquitinationYouJin Lee, Tsui-Fen Chou, Sara K Pittman, et al.
Journal of Clinical Neuromuscular Disease|November 14, 2023
Patterns of Clinical Progression Among Patients With Autosomal Recessive Limb-Girdle Muscular Dystrophy: A Systematic ReviewAntoinette Cheung, Ivana F Audhya, Shelagh M Szabo, et al.
The Journal of Biological Chemistry|November 15, 2025
Mutations in Hsp40 co-chaperone change the canonical interdomain interactions stimulating LGMDD1 myopathyAnkan K Bhadra, Geetika Aggarwal, Anshuman Jaysingh, et al.
Biorxiv : the Preprint Server for Biology|July 14, 2025
Mutations in Hsp40 co-chaperone change the unique canonical inter-domain interactions stimulating LGMDD1 myopathyAnkan K Bhadra, Geetika Aggarwal, Anshuman Jaysingh, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 23, 1999
Mutant presenilin-1 induces apoptosis and downregulates Akt/PKBC C Weihl, G D Ghadge, S G Kennedy, et al.
Genes|June 24, 2022
Multisystem Proteinopathy Due to VCP Mutations: A Review of Clinical Heterogeneity and Genetic DiagnosisGerald Pfeffer, Grace Lee, Carly S Pontifex, et al.
Neuromuscular Disorders : NMD|December 7, 2010
Novel GNE mutations in two phenotypically distinct HIBM2 patientsConrad C Weihl, Sara E Miller, Craig M Zaidman, et al.
Muscle & Nerve|July 13, 2019
Limb-girdle muscular dystrophy: A perspective from adult patients on what matters mostMichael Hunter, Chad Heatwole, Matthew Wicklund, et al.
Human Molecular Genetics|December 20, 2012
mTOR dysfunction contributes to vacuolar pathology and weakness in valosin-containing protein associated inclusion body myopathyJames K Ching, Sarita V Elizabeth, Jeong-Sun Ju, et al.
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