Research paper

From Pathogenesis to Therapeutics: A Review of 150 Years of Huntington's Disease Research

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Title
From Pathogenesis to Therapeutics: A Review of 150 Years of Huntington's Disease Research
Content partner
The University of Auckland Library
Collection
ResearchSpace@Auckland
Description

Huntington's disease (HD) is a debilitating neurodegenerative genetic disorder caused by an expanded polyglutamine-coding (CAG) trinucleotide repeat in the huntingtin (HTT) gene. HD behaves as a highly penetrant dominant disorder likely acting through a toxic gain of function by the mutant huntingtin protein. Widespread cellular degeneration of the medium spiny neurons of the caudate nucleus and putamen are responsible for the onset of symptomology that encompasses motor, cognitive, and behav...

Format
Research paper
Research format
Journal article
Date created
2023-08
Creator
Jiang, Andrew / Handley, Renee R / Lehnert, Klaus / Snell, Russell G
URL
https://hdl.handle.net/2292/66132
Related subjects
Caudate Nucleus / Humans / Huntington Disease / Heredodegenerative Disorders, Nervous System / Dopamine / Cytopathogenic Effect, Viral / Mutant Proteins / Huntington’s disease / pathogenesis / therapeutics / 31 Biological Sciences / 3105 Genetics / Orphan Drug / Neurodegenerative / Neurosciences / Rare Diseases / Genetics / Huntington's Disease / Brain Disorders / 2 Aetiology / 2.1 Biological and endogenous factors / Neurological / 0399 Other Chemical Sciences / 0604 Genetics / 0699 Other Biological Sciences / 3101 Biochemistry and cell biology / 3107 Microbiology / 3404 Medicinal and biomolecular chemistry

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