News & Publications for:

Chris Weihl

Keap1/Cullin3 Modulates p62/SQSTM1 Activity via UBA Domain Ubiquitination

Posted on April 19, 2017

Lee, Y , Chou, T-F , Pittman, SK, Keith, AL , Razani, B , Weihl, CC: 2017 Cell Reports, 19 (1), pp 188-202 Read More

Posted in: HPAN, Neurodegeneration, Publications Faculty: ,

Autophagic vacuolar pathology in desminopathies

Posted on March 27, 2015

Weihl CC, Iyadurai S, Baloh RH, et al: 2015 Neuromuscular Disorders, 25(3), pp199-206 Read More

Posted in: HPAN, Neurodegeneration, Neurogenetics, Publications Faculty: , , ,

Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis

Posted on February 23, 2015

Conrad C. Weihl, Robert H. Baloh, Youjin Lee, Tsui-Fen Chou, Sara K. Pittman, Glenn Lopate, Peggy Allred, Jennifer Jockel-Balsarotti, and others; Neuromuscular Disorders Published online: January 6, 2015 Read More

Posted in: HPAN, Neurodegeneration, Publications Faculty:

Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis

Posted on February 12, 2015

Conrad C. Weihl, Robert H. Baloh, Youjin Lee, Tsui-Fen Chou, Sara K. Pittman, Glenn Lopate, Peggy Allred, Jennifer Jockel-Balsarotti, and others; 2015, Neuromuscular Disorders Read More

Posted in: HPAN, Neurodegeneration, Neurogenetics, Publications Faculty: , ,

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

Posted on October 20, 2014

Meyer H, Weihl CC; Journal of Cell Science, Volume 127(18), 2014, p3877-3883 Read More

Posted in: HPAN, Neurodegeneration, Publications Faculty: