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Neurology. Genetics|September 16, 2024
Elevated VCP ATPase Activity Correlates With Disease Onset in Multisystem Proteinopathy-1Sarah E Robinson, Andrew R Findlay, Shan Li, et al.
Annals of Neurology|February 16, 2012
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathyMatthew B Harms, R Brian Sommerville, Peggy Allred, et al.
Nature Communications|February 6, 2023
The p97-UBXD8 complex regulates ER-Mitochondria contact sites by altering membrane lipid saturation and compositionRakesh Ganji, Joao A Paulo, Yuecheng Xi, et al.
Iscience|June 5, 2023
Genetic deletion of skeletal muscle iPLASung Ho Moon, Beverly Gibson Dilthey, Shaoping Guan, et al.
BMC Neurology|March 16, 2024
Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD studyAmy Doody, Lindsay Alfano, Jordi Diaz-Manera, et al.
Neuromuscular Disorders : NMD|January 25, 2015
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositisConrad C Weihl, Robert H Baloh, Youjin Lee, et al.
Neurology|July 26, 2015
SQSTM1 splice site mutation in distal myopathy with rimmed vacuolesRobert C Bucelli, Khalid Arhzaouy, Alan Pestronk, et al.
Case Reports in Genetics|April 17, 2015
Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP MutationNivedita U Jerath, Cameron D Crockett, Steven A Moore, et al.
The Journal of Clinical Investigation|May 20, 2020
Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophyRocio Bengoechea, Andrew R Findlay, Ankan K Bhadra, et al.
The EMBO Journal|November 1, 2016
VCP/p97 cooperates with YOD1, UBXD1 and PLAA to drive clearance of ruptured lysosomes by autophagyChrisovalantis Papadopoulos, Philipp Kirchner, Monika Bug, et al.
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