Therapeutic validation of MMR-associated genetic modifiers in a human ex vivo model of Huntington disease-Reference-Cited by-同舟云学术

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Therapeutic validation of MMR-associated genetic modifiers in a human ex vivo model of Huntington disease

Published:2024-06 Issue:6 Volume:111 Page:1165-1183
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ferguson Ross,Goold Robert,Coupland Lucy,Flower Michael,Tabrizi Sarah J.

Funder

CHDI Foundation

UK Dementia Research Institute

Alzheimer’s Research UK

Alzheimer's Society

Medical Research Council

Publisher

Elsevier BV

Reference115 articles.

1. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes;Ciosi;EBioMedicine,2019

2. CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset;Cell,2019

3. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes;Cell,1993

4. Somatic expansion of the Huntington’s disease CAG repeat in the brain is associated with an earlier age of disease onset;Swami;Hum. Mol. Genet.,2009

5. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington’s disease age of onset;Wexler;Proc. Natl. Acad. Sci. USA,2004

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