Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease-Reference-Cited by-同舟云学术

Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease

Published:2009-10-04 Issue:11 Volume:11 Page:1370-1375
ISSN:1465-7392
Container-title:Nature Cell Biology
language:en
Short-container-title:Nat Cell Biol

Author:

da Costa Cristine Alves,Sunyach Claire,Giaime Emilie,West Andrew,Corti Olga,Brice Alexis,Safe Stephen,Abou-Sleiman Patrick M.,Wood Nicholas W.,Takahashi Hitoshi,Goldberg Mathew S.,Shen Jie,Checler Frédéric

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology

Link

http://www.nature.com/articles/ncb1981.pdf

Reference31 articles.

1. Kitada, T. et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392, 605–608 (1998).

2. Shimura, H. et al. Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase. Nature Genet. 25, 302–305 (2000).

3. Jiang, H., Ren, Y., Zhao, J. & Feng, J. Parkin protects human dopaminergic neuroblastoma cells against dopamine-induced apoptosis. Hum. Mol. Genet. 13, 1745–1754 (2004).

4. Pesah, Y. et al. Drosophila parkin mutants have decreased mass and cell size and increased sensitivity to oxygen radical stress. Development 131, 2183–2194 (2004).

5. Cookson, M. R. et al. RING finger 1 mutations in Parkin produce altered localization of the protein. Hum. Mol. Genet. 12, 2957–2965 (2003).

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