Weihl, Conrad C.

Endolysosomal sorting of ubiquitylated caveolin-1 is regulated by VCP and UBXD1 and impaired by VCP disease mutations

Ritz, D., Vuk, M., Kirchner, P., Bug, M., Schütz, S., Hayer, A., Bremer, S., Lusk, C., Baloh, R. H., Lee, H., et al. (2011) · Nature Cell Biology

Ubiquitin and proteasome pathwaysCaveolin-1 and cellular processes

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SQSTM1 splice site mutation in distal myopathy with rimmed vacuoles

Bucelli, R. C., Arhzaouy, K., Pestronk, A., Pittman, S. K., Rojas, L., Sue, C. M., Evilä, A., Hackman, P., Udd, B., Harms, M. B., et al. (2015) · Neurology

Muscle Physiology and DisordersAmyotrophic Lateral Sclerosis Research

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

Naismith, R. T., Shepherd, J. B., Weihl, C. C., Tutlam, N. T., & Cross, A. H. (2009) · Archives of Neurology

Trace Elements in HealthAlcoholism and Thiamine Deficiency

Cited by 90

Rapamycin nanoparticles target defective autophagy in muscular dystrophy to enhance both strength and cardiac function

Bibee, K. P., Cheng, Y., Ching, J. K., Marsh, J. N., Li, A. J., Keeling, R. M., Connolly, A. M., Golumbek, P. T., Myerson, J. W., Hu, G., et al. (2014) · The FASEB Journal

Muscle Physiology and DisordersAutophagy in Disease and Therapy

Cited by 83

Motor neuron disease associated with copper deficiency

Weihl, C. C., & Lopate, G. (2006) · Muscle & Nerve

Trace Elements in HealthHereditary Neurological Disorders

Cited by 79

Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkers.

Weihl, C. C., & Pestronk, A. (2010) · Current Opinion in Neurology

Inflammatory Myopathies and DermatomyositisMuscle Physiology and Disorders

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