Protein oxidation in Huntington disease-Reference-Cited by-同舟云学术

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Protein oxidation in Huntington disease

Published:2012-03-31 Issue:3 Volume:38 Page:173-185
ISSN:0951-6433
Container-title:BioFactors
language:en
Short-container-title:BioFactors

Author:

Sorolla M. Alba,Rodríguez-Colman María José,Vall-llaura Núria,Tamarit Jordi,Ros Joaquim,Cabiscol Elisa

Publisher

Wiley

Subject

Clinical Biochemistry,Molecular Medicine,General Medicine,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/biof.1013/fullpdf

Reference121 articles.

1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes;The Huntington's Disease Collaborative Research Group;Cell,1993

2. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease;Andrew;Nat. Genet.,1993

3. Onset and rate of striatal atrophy in preclinical Huntington disease;Aylward;Neurology.,2004

4. Glial fibrillary acidic protein: GFAP-thirty-one years (1969-2000);Eng;Neurochem. Res.,2000

5. Is the ubiquitin-proteasome system impaired in Huntington's disease?;Ortega;Cell Mol. Life Sci.,2007

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