Three Huntington’s Disease Specific Mutation-Carrying Human Embryonic Stem Cell Lines Have Stable Number of CAG Repeats upon In Vitro Differentiation into Cardiomyocytes-Reference-Cited by-同舟云学术

Three Huntington’s Disease Specific Mutation-Carrying Human Embryonic Stem Cell Lines Have Stable Number of CAG Repeats upon In Vitro Differentiation into Cardiomyocytes

Published:2015-05-20 Issue:5 Volume:10 Page:e0126860
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Jacquet Laureen,Neueder Andreas,Földes Gabor,Karagiannis Panagiotis,Hobbs Carl,Jolinon Nelly,Mioulane Maxime,Sakai Takao,Harding Sian E.,Ilic Dusko

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference58 articles.

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

2. Huntington's disease gene (IT15) is widely expressed in human and rat tissues;SH Li;Neuron,1993

3. Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues;TV Strong;Nat Genet,1993

4. Widespread expression of Huntington's disease gene (IT15) protein product;AH Sharp;Neuron,1995

5. Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset;Y Trottier;J Med Genet,1994

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cell Reprogramming to Model Huntington’s Disease: A Comprehensive Review;Cells;2021-06-22

2. CAG repeat instability in embryonic stem cells and derivative spermatogenic cells of transgenic Huntington’s disease monkey;Journal of Assisted Reproduction and Genetics;2021-02-20

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

4. Mitochondrial and Redox Modifications in Huntington Disease Induced Pluripotent Stem Cells Rescued by CRISPR/Cas9 CAGs Targeting;Frontiers in Cell and Developmental Biology;2020-09-22

5. Human cellular models of medium spiny neuron development and Huntington disease;Life Sciences;2018-09