A crucial role of mitochondrial Hsp40 in preventing dilated cardiomyopathy-Reference-Cited by-同舟云学术

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A crucial role of mitochondrial Hsp40 in preventing dilated cardiomyopathy

Published:2005-12-04 Issue:1 Volume:12 Page:128-132
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Hayashi Masaaki,Imanaka-Yoshida Kyoko,Yoshida Toshimichi,Wood Malcolm,Fearns Colleen,Tatake Revati J,Lee Jiing-Dwan

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm1327.pdf

Reference31 articles.

1. Young, J.C., Agashe, V.R., Siegers, K. & Hartl, F.U. Pathways of chaperone-mediated protein folding in the cytosol. Nat. Rev. Mol. Cell Biol. 5, 781–791 (2004).

2. Barral, J.M., Broadley, S.A., Schaffar, G. & Hartl, F.U. Roles of molecular chaperones in protein misfolding diseases. Semin. Cell Dev. Biol. 15, 17–29 (2004).

3. Frey, N. & Olson, E.N. Cardiac hypertrophy: the good, the bad, and the ugly. Annu. Rev. Physiol. 65, 45–79 (2003).

4. Seidman, J.G. & Seidman, C. The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms. Cell 104, 557–567 (2001).

5. Chien, K.R. Genomic circuits and the integrative biology of cardiac diseases. Nature 407, 227–232 (2000).

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