Mitochondria and Huntington's Disease Pathogenesis
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
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3. 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
4. The hunt for huntingtin function: interaction partners tell many different stories;Harjes;Trends Biochem. Sci.,2003
5. Huntingtin-HAP40 complex is a novel Rab5 effector that regulates early endosome motility and is up-regulated in Huntington's disease;Pal;J. Cell Biol.,2006
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1. Preserved VPS13A distribution and expression in Huntington’s disease: divergent mechanisms of action for similar movement disorders?;Frontiers in Neuroscience;2024-06-05
2. BDNF and TRiC-inspired reagent rescue cortical synaptic deficits in a mouse model of Huntington's disease;Neurobiology of Disease;2024-06
3. Ribosome Profiling and Mass Spectrometry Reveal Widespread Mitochondrial Translation Defects in a Striatal Cell Model of Huntington Disease;Molecular & Cellular Proteomics;2024-04
4. Modeling Huntington’s disease: An insight on in-vitro and in-vivo models;Behavioural Brain Research;2024-02
5. Bypassing mitochondrial defects rescues Huntington's phenotypes in Drosophila;Neurobiology of Disease;2023-09
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