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Chris Weihl

Chris Weihl‘s Faculty Page

VCP maintains lysosomal homeostasis and TFEB activity in differentiated skeletal muscle

Posted on February 12, 2019

Khalid Arhzaouy, Chrisovalantis Papadopoulos, Nina Schulze, Sara K. Pittman, Hemmo Meyer & Conrad C. Weihl. Autophagy 2019 Read More

Posted in: HPAN, Neurodegeneration, Publications Faculty:

Loss of lipin 1-mediated phosphatidic acid phosphohydrolase activity in muscle leads to skeletal myopathy in mice

Posted on January 8, 2019

George G. Schweitzer, Sara L. Collier, Zhouji Chen, Kyle S. McCommis, Sara K. Pittman, Jun Yoshino, Scot J. Matkovich, Fong-Fu Hsu, Roman Chrast, James M. Eaton, Thurl E. Harris, Conrad C. Weihl, and Brian N. Finck. FASEB Journal, Volume 33, Issue 1, January 2019, Pages 652-667 Read More

Posted in: HPAN, Neurodegeneration, Publications Faculty:

Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks

Posted on January 2, 2019

Melanie Meister-Broekema, Rebecca Freilich, Chandhuru Jagadeesan, Jennifer N. Rauch, Rocio Bengoechea, William W. Motley, E. F. Elsiena Kuiper, Melania Minoia, Gabriel V. Furtado, Maria A. W. H. van Waarde, Shawn J. Bird, Adriana Rebelo, Stephan Zuchner, Peter Pytel, Steven S. Scherer, Federica F. Morelli, Serena Carra, Conrad C. Weihl, Steven Bergink, Jason E. Gestwicki & Harm H. Kampinga. Nature Communications, Volume 9, Issue 1, 1 December 2018, Article number 5342 Read More

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234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8–10 December 2017

Posted on November 20, 2018

Conrad C. Weihl, Bjarne Udd, Michael Hanna on behalf of the ENMC workshop study group. Neuromuscular Disorders 2018 Read More

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TIA1 variant drives myodegeneration in multisystem proteinopathy with SQSTM1 mutations.

Posted on March 13, 2018

YueJin Lee, […], Conrad C. Weihl, and Bjarne Udd. J Clin Invest. 2018 Mar 1;128(3):1164-1177. doi: 10.1172/JCI97103. Epub 2018 Feb 19. Read More

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