Tryptophan metabolism and oxidative stress in patients with Huntington's disease-Reference-Cited by-同舟云学术

Tryptophan metabolism and oxidative stress in patients with Huntington's disease

Published:2005-04-04 Issue:3 Volume:93 Page:611-623
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:Journal of Neurochemistry

Author:

Stoy N.¹,Mackay G. M.¹,Forrest C. M.¹,Christofides J.¹,Egerton M.¹,Stone T. W.¹,Darlington L. G.¹

Affiliation:

1. *Royal Hospital for Neuro‐Disability, Putney, London, UK   †Institute of Biomedical & Life Sciences, University of Glasgow, Glasgow, UK   ‡West Park Biochemistry Laboratories and §Department of Rheumatology, Epsom General Hospital, Epsom, Surrey, UK

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1471-4159.2005.03070.x

Reference71 articles.

1. Huntingtin aggregation and toxicity in Huntington's disease

2. Does impairment of energy metabolism result in excitotoxic neuronal death in neurodegenerative illnesses?

3. Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid

4. Kynurenine Pathway Measurements in Huntington's Disease Striatum: Evidence for Reduced Formation of Kynurenic Acid

5. Chronic quinolinic acid lesions in rats closely resemble Huntington's disease

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