News & Publications for:

Chris Weihl

A knock-in mouse model for the R120G mutation of AlphaB-crystallin recapitulates human hereditary myopathy and cataracts

Posted on October 24, 2011

Andley UP, Hamilton PD, Ravi N, Weihl CC (2011). PLoS One, 6(3):e17671
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Posted in: HPAN, Neurodegeneration, Publications Faculty:

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

Posted on October 14, 2011

Ritz D, Vuk M, Kirchner P, Bug M, Schütz S, Hayer A, Bremer S, Lusk C, Baloh RH, Lee H, Glatter T, Gstaiger M, Aebersold R, Weihl CC, Meyer H (2011). Nat Cell Biol, 13(9):1116-23
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Posted in: HPAN, Neurodegeneration, Publications Faculty: ,

Mitochondrial pathology in immune and inflammatory myopathies

Posted on October 24, 2010

Varadhachary AS, Weihl CC, Pestronk A (2010). Curr Opin Rheumatol, 22(6):651-7
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Posted in: HPAN, Neurodegeneration, Publications Faculty: ,

Interaction with polyglutamine aggregates reveals a Q/N-rich domain in TDP-43

Posted on October 13, 2010

Fuentealba RA, Udan M, Bell S, Wegorzewska I, Shao J, Diamond MI, Weihl CC, Baloh RH (2010). J Biol Chem, 285(34):26304-14
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Posted in: HPAN, Neurodegeneration, Neurogenetics, Publications, Therapeutics & Diagnostics Faculty: , ,