Showing results (51-60 of 136) with videos related to
Sort By:
Pageof 14
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.Neuromuscular Disorders : NMD|March 24, 2024
272nd ENMC international workshop: 10 Years of progress - revision of the ENMC 2013 diagnostic criteria for inclusion body myositis and clinical trial readiness. 16-18 June 2023, Hoofddorp, The NetherlandsJames B Lilleker, Elie Naddaf, Christiaan G J Saris, 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.Pageof 14