Ribosome Profiling and Mass Spectrometry Reveal Widespread Mitochondrial Translation Defects in a Striatal Cell Model of Huntington Disease-Reference-Cited by-同舟云学术

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Ribosome Profiling and Mass Spectrometry Reveal Widespread Mitochondrial Translation Defects in a Striatal Cell Model of Huntington Disease

Published:2024-04 Issue:4 Volume:23 Page:100746
ISSN:1535-9476
Container-title:Molecular & Cellular Proteomics
language:en
Short-container-title:Molecular & Cellular Proteomics

Author:

Dagar Sunayana^ORCID,Sharma Manish,Tsaprailis George^ORCID,Tapia Catherina Scharager,Crynen Gogce^ORCID,Joshi Preksha Sandipkumar^ORCID,Shahani Neelam^ORCID,Subramaniam Srinivasa

Funder

NINDS

Publisher

Elsevier BV

Reference83 articles.

1. Decreased pyruvate dehydrogenase complex activity in Huntington and Alzheimer brain;Sorbi;Ann. Neurol.,1983

2. Evidence for a defect in NADH: ubiquinone oxidoreductase (complex I) in Huntington's disease;Parker;Neurology,1990

3. Mitochondrial defect in Huntington's disease caudate nucleus;Gu;Ann. Neurol.,1996

4. Complex I defect in muscle from patients with Huntington's disease;Arenas;Ann. Neurol.,1998

5. Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model;Aidt;PLoS Curr.,2013

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