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Conrad C Weihl

Showing results (1-10 of 127) with videos related to

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Continuum (Minneapolis, Minn.)|December 4, 2019
Sporadic Inclusion Body Myositis and Other Rimmed Vacuolar MyopathiesConrad C Weihl
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|February 15, 2013
Monitoring autophagy in the treatment of protein aggregate diseases: steps toward identifying autophagic biomarkersConrad C Weihl
The Journal of Clinical Investigation|November 23, 2011
Another VCP interactor: NF is enoughConrad C Weihl
Autophagy|August 17, 2017
Regulation of SQSTM1/p62 via UBA domain ubiquitination and its role in diseaseYouJin Lee, Conrad C Weihl
Autophagy|October 11, 2021
Loss-of-function mutation in VCP mimics the characteristic pathology as in FTLD-TARDBPAbubakar Wani, Conrad C Weihl
Muscle & Nerve|August 25, 2006
Motor neuron disease associated with copper deficiencyConrad C Weihl, Glenn Lopate
Current Opinion in Neurology|June 9, 2025
Myofibrillar myopathy: towards a mechanism-based definition as a Z-disk-opathyMichio Inoue, Conrad C Weihl
Current Opinion in Neurology|July 29, 2010
Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkersConrad C Weihl, Alan Pestronk
Journal of Cell Science|August 23, 2014
The VCP/p97 system at a glance: connecting cellular function to disease pathogenesisHemmo Meyer, Conrad C Weihl
Human Molecular Genetics|April 23, 2010
Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagyJeong-Sun Ju, Conrad C Weihl
Pageof 13

Showing results (1-10 of 127) with videos related to

Sort By:
Pageof 13
Continuum (Minneapolis, Minn.)|December 4, 2019
Sporadic Inclusion Body Myositis and Other Rimmed Vacuolar MyopathiesConrad C Weihl
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|February 15, 2013
Monitoring autophagy in the treatment of protein aggregate diseases: steps toward identifying autophagic biomarkersConrad C Weihl
The Journal of Clinical Investigation|November 23, 2011
Another VCP interactor: NF is enoughConrad C Weihl
Autophagy|August 17, 2017
Regulation of SQSTM1/p62 via UBA domain ubiquitination and its role in diseaseYouJin Lee, Conrad C Weihl
Autophagy|October 11, 2021
Loss-of-function mutation in VCP mimics the characteristic pathology as in FTLD-TARDBPAbubakar Wani, Conrad C Weihl
Muscle & Nerve|August 25, 2006
Motor neuron disease associated with copper deficiencyConrad C Weihl, Glenn Lopate
Current Opinion in Neurology|June 9, 2025
Myofibrillar myopathy: towards a mechanism-based definition as a Z-disk-opathyMichio Inoue, Conrad C Weihl
Current Opinion in Neurology|July 29, 2010
Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkersConrad C Weihl, Alan Pestronk
Journal of Cell Science|August 23, 2014
The VCP/p97 system at a glance: connecting cellular function to disease pathogenesisHemmo Meyer, Conrad C Weihl
Human Molecular Genetics|April 23, 2010
Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagyJeong-Sun Ju, Conrad C Weihl
Pageof 13