Another VCP interactor: NF is enough

by Weihl, Conrad C.
Published 2011

Valosin containing protein mutations in fronto-temporal lobar degeneration: Clinical presentation, pathology and pathogenesis

by Weihl, Conrad C.
Published 2011

Monitoring Autophagy in the Treatment of Protein Aggregate Diseases: Steps Toward Identifying Autophagic Biomarkers

by Weihl, Conrad C.
Published 2013

Sporadic Inclusion Body Myositis: Possible pathogenesis inferred from biomarkers

by Weihl, Conrad C., Pestronk, Alan
Published 2010

The VCP/p97 system at a glance: connecting cellular function to disease pathogenesis

by Meyer, Hemmo, Weihl, Conrad C.
Published 2014

Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy

by Ju, Jeong-Sun, Weihl, Conrad C.
Published 2010

p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system

by Ju, Jeong-Sun, Weihl, Conrad C.
Published 2010

Rapamycin-induced autophagy aggravates pathology and weakness in a mouse model of VCP-associated myopathy

by Ching, James K., Weihl, Conrad C.
Published 2013

Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathies

by Bamaga, Ahmed K., Weihl, Conrad C.
Published in Neurol Genet (2017)

Regulation of SQSTM1/p62 via UBA domain ubiquitination and its role in disease

by Lee, YouJin, Weihl, Conrad C.
Published in Autophagy (2017)

234(th) ENMC International Workshop: Chaperone dysfunction in muscle disease December 8-10th 2017, Naarden, Netherlands

by Weihl, Conrad C., Udd, Bjarne, Hanna, Michael
Published in Neuromuscul Disord (2018)

Alternative Translation Initiation of Theiler’s Murine Encephalomyelitis Virus

by Yamasaki, Kenji, Weihl, Conrad C., Roos, Raymond P.
Published 1999

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

by Weihl, Conrad C., Pestronk, Alan, Kimonis, Virginia E.
Published 2009

215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13–15 November 2015, Heemskerk, The Netherlands

by Evangelista, Teresinha, Weihl, Conrad C., Kimonis, Virginia, Lochmüller, Hanns
Published in Neuromuscul Disord (2016)

Client processing is altered by novel myopathy-causing mutations in the HSP40 J domain

by Pullen, Melanie Y., Weihl, Conrad C., True, Heather L.
Published in PLoS One (2020)

A Knock-In Mouse Model for the R120G Mutation of αB-Crystallin Recapitulates Human Hereditary Myopathy and Cataracts

by Andley, Usha P., Hamilton, Paul D., Ravi, Nathan, Weihl, Conrad C.
Published 2011

Quantitation of “autophagic flux” in mature skeletal muscle

by Ju, Jeong-Sun, Varadhachary, Arun S, Miller, Sara E, Weihl, Conrad C
Published 2010

Homozygous Recessive MYH2 Mutation Mimicking Dominant MYH2 Associated Myopathy

by Findlay, Andrew R., Harms, Matthew B., Pestronk, Alan, Weihl, Conrad C.
Published in Neuromuscul Disord (2018)

Impaired Protein Aggregate Handling and Clearance Underlie the Pathogenesis of p97/VCP-associated Disease

by Ju, Jeong-Sun, Miller, Sara E., Hanson, Phyllis I., Weihl, Conrad C.
Published 2008

Acute and Bilateral Blindness Due to Optic Neuropathy Associated With Copper Deficiency

by Naismith, Robert T., Shepherd, James B., Weihl, Conrad C., Tutlam, Nhial T., Cross, Anne H.
Published 2009