Functional Characterization of Friedreich Ataxia iPS-Derived Neuronal Progenitors and Their Integration in the Adult Brain-Reference-Cited by-同舟云学术

Functional Characterization of Friedreich Ataxia iPS-Derived Neuronal Progenitors and Their Integration in the Adult Brain

Published:2014-07-07 Issue:7 Volume:9 Page:e101718
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Bird Matthew J.,Needham Karina,Frazier Ann E.,van Rooijen Jorien,Leung Jessie,Hough Shelley,Denham Mark,Thornton Matthew E.,Parish Clare L.,Nayagam Bryony A.,Pera Martin,Thorburn David R.,Thompson Lachlan H.,Dottori Mirella

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference39 articles.

1. Friedreich ataxia;M Pandolfo;Archives of Neurology,2008

2. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion;V Campuzano;Science,1996

3. Friedreich ataxia: the clinical picture;M Pandolfo;Journal of Neurology,2009

4. Histone deacetylase inhibitors reverse gene silencing in Friedreich's ataxia;D Herman;Nature Chemical Biology,2006

5. Repeat-induced epigenetic changes in intron 1 of the frataxin gene and its consequences in Friedreich ataxia;E Greene;Nucleic Acids Research,2007

Cited by 27 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. Human frataxin, the Friedreich ataxia deficient protein, interacts with mitochondrial respiratory chain;Cell Death & Disease;2023-12-08

2. Survival and process outgrowth of human iPSC-derived cells expressing Purkinje cell markers in a mouse model for spinocerebellar degenerative disease;Experimental Neurology;2023-11

3. Patient-derived iPSC models of Friedreich ataxia: a new frontier for understanding disease mechanisms and therapeutic application;Translational Neurodegeneration;2023-09-20

4. Replication dependent and independent mechanisms of GAA repeat instability;DNA Repair;2022-10

5. Analysis of Mitochondrial Dysfunction by Microplate Reader in hiPSC-Derived Neuronal Cell Models of Neurodegenerative Disorders;Methods in Molecular Biology;2022