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Conrad C Weihl

Showing results (11-20 of 127) with videos related to

Pageof 13
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Autophagy|January 20, 2010
p97/VCP at the intersection of the autophagy and the ubiquitin proteasome systemJeong-Sun Ju, Conrad C Weihl
Autophagy|February 27, 2013
Rapamycin-induced autophagy aggravates pathology and weakness in a mouse model of VCP-associated myopathyJames K Ching, Conrad C Weihl
Continuum (Minneapolis, Minn.)|December 20, 2022
Genetic-Based Treatment Strategies for Muscular Dystrophy and Congenital MyopathiesAndrew R Findlay, Conrad C Weihl
Neurology. Genetics|March 31, 2017
Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathiesAhmed K Bamaga, Conrad C Weihl
Journal of the Neurological Sciences|December 23, 2008
Inflammatory myopathies with mitochondrial pathology and protein aggregatesPeyker Temiz, Conrad C Weihl, Alan Pestronk
Genes|February 25, 2022
Current and Future Approaches to Classify VUSs in LGMD-Related GenesChengcheng Li, Gabe Haller, Conrad C Weihl
Neuromuscular Disorders : NMD|November 15, 2018
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8-10 December 2017Conrad C Weihl, Bjarne Udd, Michael Hanna, et al.
Neurology|June 16, 2006
Valproate may improve strength and function in patients with type III/IV spinal muscle atrophyConrad C Weihl, Anne M Connolly, Alan Pestronk
Current Opinion in Rheumatology|September 10, 2010
Mitochondrial pathology in immune and inflammatory myopathiesArun S Varadhachary, Conrad C Weihl, Alan Pestronk
Neuromuscular Disorders : NMD|April 22, 2009
Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementiaConrad C Weihl, Alan Pestronk, Virginia E Kimonis
Pageof 13

Showing results (11-20 of 127) with videos related to

Sort By:
Pageof 13
Autophagy|January 20, 2010
p97/VCP at the intersection of the autophagy and the ubiquitin proteasome systemJeong-Sun Ju, Conrad C Weihl
Autophagy|February 27, 2013
Rapamycin-induced autophagy aggravates pathology and weakness in a mouse model of VCP-associated myopathyJames K Ching, Conrad C Weihl
Continuum (Minneapolis, Minn.)|December 20, 2022
Genetic-Based Treatment Strategies for Muscular Dystrophy and Congenital MyopathiesAndrew R Findlay, Conrad C Weihl
Neurology. Genetics|March 31, 2017
Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathiesAhmed K Bamaga, Conrad C Weihl
Journal of the Neurological Sciences|December 23, 2008
Inflammatory myopathies with mitochondrial pathology and protein aggregatesPeyker Temiz, Conrad C Weihl, Alan Pestronk
Genes|February 25, 2022
Current and Future Approaches to Classify VUSs in LGMD-Related GenesChengcheng Li, Gabe Haller, Conrad C Weihl
Neuromuscular Disorders : NMD|November 15, 2018
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8-10 December 2017Conrad C Weihl, Bjarne Udd, Michael Hanna, et al.
Neurology|June 16, 2006
Valproate may improve strength and function in patients with type III/IV spinal muscle atrophyConrad C Weihl, Anne M Connolly, Alan Pestronk
Current Opinion in Rheumatology|September 10, 2010
Mitochondrial pathology in immune and inflammatory myopathiesArun S Varadhachary, Conrad C Weihl, Alan Pestronk
Neuromuscular Disorders : NMD|April 22, 2009
Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementiaConrad C Weihl, Alan Pestronk, Virginia E Kimonis
Pageof 13