The Cardiomyopathy and Lens Cataract Mutation in αB-crystallin Alters Its Protein Structure, Chaperone Activity, and Interaction with Intermediate Filaments in Vitro
Open Access
- 1 November 1999
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 274 (47) , 33235-33243
- https://doi.org/10.1074/jbc.274.47.33235
Abstract
No abstract availableKeywords
This publication has 59 references indexed in Scilit:
- Fatal attraction: When chaperone turns harlotNature Medicine, 1999
- A dysfunctional desmin mutation in a patient with severe generalized myopathyProceedings of the National Academy of Sciences, 1998
- A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathyNature Genetics, 1998
- Missense mutations in desmin associated with familial cardiac and skeletal myopathyNature Genetics, 1998
- Lessons from Keratin 18 Knockout Mice: Formation of Novel Keratin Filaments, Secondary Loss of Keratin 7 and Accumulation of Liver-specific Keratin 8-Positive AggregatesThe Journal of cell biology, 1998
- Desmin pathology in neuromuscular diseasesVirchows Archiv B Cell Pathology Including Molecular Pathology, 1993
- The C-terminal region of α-crystallin: involvement in protection against heat-induced denaturationBiochemical Journal, 1993
- Alpha-crystallin can function as a molecular chaperone.Proceedings of the National Academy of Sciences, 1992
- αB crystallin expression in nonlenticular tissues and selective presence in ubiquitinated inclusion bodies in human diseaseThe Journal of Pathology, 1992
- αB-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brainCell, 1989