Comparison of Huntington’s disease CAG Repeat Length Stability in Human Motor Cortex and Cingulate Gyrus-Reference-Cited by-同舟云学术

Comparison of Huntington’s disease CAG Repeat Length Stability in Human Motor Cortex and Cingulate Gyrus

Published:2016-10-01 Issue:3 Volume:5 Page:297-301
ISSN:1879-6397
Container-title:Journal of Huntington's Disease
language:
Short-container-title:JHD

Author:

Geraerts Fiona C.A.¹,Snell Russell G.¹,Faull Richard L.M.²,Williams Liam¹,Jacobsen Jessie C.¹,Reid Suzanne J.¹

Affiliation:

1. School of Biological Sciences, Centre for Brain Research, Faculty of Science, The University of Auckland, Auckland, New Zealand

2. Department of Anatomy and Medical Imaging, Centre for Brain Research, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand

Publisher

IOS Press

Subject

Cellular and Molecular Neuroscience,Neurology (clinical)

Reference18 articles.

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2. Characterization of a large group of individuals with huntington disease and their relatives enrolled in the COHORT study;Dorsey;PLoS One,2012

3. Normal and expanded Huntington’s disease gene alleles produce distinguishable proteins due to translation across the CAG repeat;Persichetti;Mol Med,1995

4. Cortical interneuron loss and symptom heterogeneity in Huntington disease;Kim;Ann Neurol,2014

5. Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain;Shelbourne;Hum Mol Genet,2007

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3. Modifiers of CAG/CTG Repeat Instability: Insights from Mammalian Models;Journal of Huntington's Disease;2021-02-09

4. Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice;eLife;2020-09-29

5. Patterns of CAG repeat instability in the central nervous system and periphery in Huntington’s disease and in spinocerebellar ataxia type 1;Human Molecular Genetics;2020-07-07