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Journal of Molecular Biology|June 1, 2014
Specific inhibition of p97/VCP ATPase and kinetic analysis demonstrate interaction between D1 and D2 ATPase domainsTsui-Fen Chou, Stacie L Bulfer, Conrad C Weihl, et al.
Clinical Genetics|October 16, 2007
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementiaG D J Watts, D Thomasova, S K Ramdeen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 21, 2019
Estimating prevalence for limb-girdle muscular dystrophy based on public sequencing databasesWei Liu, Sander Pajusalu, Nicole J Lake, et al.
Brain : a Journal of Neurology|August 16, 2014
A novel mutation in VCP causes Charcot-Marie-Tooth Type 2 diseaseMichael A Gonzalez, Shawna M Feely, Fiorella Speziani, et al.
Autophagy Reports|May 21, 2025
Gentiacaulein inhibits glucose transport to induce PRKAA1-mediated autophagy to clear amyloid beta and associated inflammation in primary astrocytesAnkita Sharma, Sukhleen Kaur, Abubakar Wani, et al.
Nature Cell Biology|August 9, 2011
Endolysosomal sorting of ubiquitylated caveolin-1 is regulated by VCP and UBXD1 and impaired by VCP disease mutationsDanilo Ritz, Maja Vuk, Philipp Kirchner, et al.
Acta Neuropathologica Communications|December 5, 2019
A metastable subproteome underlies inclusion formation in muscle proteinopathiesPrajwal Ciryam, Matthew Antalek, Fernando Cid, et al.
Molecular Therapy. Nucleic Acids|June 22, 2023
DNAJB6 isoform specific knockdown: Therapeutic potential for limb girdle muscular dystrophy D1Andrew R Findlay, May M Paing, Jil A Daw, et al.
Science Translational Medicine|November 27, 2024
Seeding-competent TDP-43 persists in human patient and mouse muscleEileen M Lynch, Sara Pittman, Jil Daw, et al.
Biorxiv : the Preprint Server for Biology|April 15, 2024
Seeding competent TDP-43 persists in human patient and mouse muscleEileen M Lynch, Sara Pittman, Jil Daw, et al.
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