The in vivo mitochondrial two-step maturation of human frataxin-Reference-Cited by-同舟云学术

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The in vivo mitochondrial two-step maturation of human frataxin

Published:2008-08-25 Issue:22 Volume:17 Page:3521-3531
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Schmucker Stéphane,Argentini Manuela,Carelle-Calmels Nadège,Martelli Alain,Puccio Hélène

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/17/22/3521/13939426/ddn244.pdf

Reference49 articles.

1. Friedreich’s ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features;Harding;Brain,1981

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

3. Sticky DNA, a self-associated complex formed at long GAA*TTC repeats in intron 1 of the frataxin gene, inhibits transcription;Sakamoto;J. Biol. Chem.,2001

4. Histone deacetylase inhibitors reverse gene silencing in Friedreich’s ataxia;Herman;Nat. Chem. Biol.,2006

5. Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia;Rotig;Nat. Genet.,1997

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3. An In Silico Analysis of Genetic Variants and Structural Modeling of the Human Frataxin Protein in Friedreich’s Ataxia;International Journal of Molecular Sciences;2024-05-26

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