Aberrant molecular properties shared by familial Parkinson’s disease-associated mutant UCH-L1 and carbonyl-modified UCH-L1-Reference-Cited by-同舟云学术

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Aberrant molecular properties shared by familial Parkinson’s disease-associated mutant UCH-L1 and carbonyl-modified UCH-L1

Published:2008-02-04 Issue:10 Volume:17 Page:1482-1496
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Kabuta Tomohiro,Setsuie Rieko,Mitsui Takeshi,Kinugawa Aiko,Sakurai Mikako,Aoki Shunsuke,Uchida Kenko,Wada Keiji

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/17/10/1482/17244951/ddn037.pdf

Reference55 articles.

1. The ubiquitin pathway in Parkinson’s disease;Leroy;Nature,1998

2. Dopaminergic neuronal loss in transgenic mice expressing the Parkinson’s disease-associated UCH-L1 I93M mutant;Setsuie;Neurochem. Int,2007

3. UCHL1 is a Parkinson’s disease susceptibility gene;Maraganore;Ann. Neurol,2004

4. UCHL-1 is not a Parkinson’s disease susceptibility gene;Healy;Ann. Neurol,2006

5. The neuron-specific protein PGP 9.5 is a ubiquitin carboxyl-terminal hydrolase;Wilkinson;Science,1989

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