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Conrad C Weihl

Showing results (21-30 of 127) with videos related to

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Plos One|June 5, 2020
Client processing is altered by novel myopathy-causing mutations in the HSP40 J domainMelanie Y Pullen, Conrad C Weihl, Heather L True
Nature Reviews. Molecular Cell Biology|July 14, 2021
Molecular and cellular basis of genetically inherited skeletal muscle disordersJames J Dowling, Conrad C Weihl, Melissa J Spencer
Neuromuscular Disorders : NMD|July 14, 2023
Exploring hand and upper limb function in patients with inclusion body myositis (IBM)Stephanie Hunn, Lindsay Alfano, Michelle Seiffert, et al.
Neuromuscular Disorders : NMD|June 18, 2016
215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13-15 November 2015, Heemskerk, The NetherlandsTeresinha Evangelista, Conrad C Weihl, Virginia Kimonis, et al.
Human Molecular Genetics|December 3, 2005
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradationConrad C Weihl, Seema Dalal, Alan Pestronk, et al.
Plos One|March 30, 2011
A knock-in mouse model for the R120G mutation of αB-crystallin recapitulates human hereditary myopathy and cataractsUsha P Andley, Paul D Hamilton, Nathan Ravi, et al.
Neuromuscular Disorders : NMD|June 24, 2018
Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathyAndrew R Findlay, Matthew B Harms, Alan Pestronk, et al.
Human Molecular Genetics|March 3, 2007
Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in miceConrad C Weihl, Sara E Miller, Phyllis I Hanson, et al.
Inflammation|April 2, 2024
VCP Inhibition Augments NLRP3 Inflammasome ActivationAnkita Sharma, Dhruva D Dhavale, Paul T Kotzbauer, et al.
The Journal of Biological Chemistry|August 22, 2008
Impaired protein aggregate handling and clearance underlie the pathogenesis of p97/VCP-associated diseaseJeong-Sun Ju, Sara E Miller, Phyllis I Hanson, et al.
Pageof 13

Showing results (21-30 of 127) with videos related to

Sort By:
Pageof 13
Plos One|June 5, 2020
Client processing is altered by novel myopathy-causing mutations in the HSP40 J domainMelanie Y Pullen, Conrad C Weihl, Heather L True
Nature Reviews. Molecular Cell Biology|July 14, 2021
Molecular and cellular basis of genetically inherited skeletal muscle disordersJames J Dowling, Conrad C Weihl, Melissa J Spencer
Neuromuscular Disorders : NMD|July 14, 2023
Exploring hand and upper limb function in patients with inclusion body myositis (IBM)Stephanie Hunn, Lindsay Alfano, Michelle Seiffert, et al.
Neuromuscular Disorders : NMD|June 18, 2016
215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13-15 November 2015, Heemskerk, The NetherlandsTeresinha Evangelista, Conrad C Weihl, Virginia Kimonis, et al.
Human Molecular Genetics|December 3, 2005
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradationConrad C Weihl, Seema Dalal, Alan Pestronk, et al.
Plos One|March 30, 2011
A knock-in mouse model for the R120G mutation of αB-crystallin recapitulates human hereditary myopathy and cataractsUsha P Andley, Paul D Hamilton, Nathan Ravi, et al.
Neuromuscular Disorders : NMD|June 24, 2018
Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathyAndrew R Findlay, Matthew B Harms, Alan Pestronk, et al.
Human Molecular Genetics|March 3, 2007
Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in miceConrad C Weihl, Sara E Miller, Phyllis I Hanson, et al.
Inflammation|April 2, 2024
VCP Inhibition Augments NLRP3 Inflammasome ActivationAnkita Sharma, Dhruva D Dhavale, Paul T Kotzbauer, et al.
The Journal of Biological Chemistry|August 22, 2008
Impaired protein aggregate handling and clearance underlie the pathogenesis of p97/VCP-associated diseaseJeong-Sun Ju, Sara E Miller, Phyllis I Hanson, et al.
Pageof 13