A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement-Reference-Cited by-同舟云学术

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Published:2014-06-13 Issue:8 Volume:137 Page:2329-2345
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Bannwarth Sylvie,Ait-El-Mkadem Samira,Chaussenot Annabelle,Genin Emmanuelle C.,Lacas-Gervais Sandra,Fragaki Konstantina,Berg-Alonso Laetitia,Kageyama Yusuke,Serre Valérie,Moore David G.,Verschueren Annie,Rouzier Cécile,Le Ber Isabelle,Augé Gaëlle,Cochaud Charlotte,Lespinasse Françoise,N’Guyen Karine,de Septenville Anne,Brice Alexis,Yu-Wai-Man Patrick,Sesaki Hiromi,Pouget Jean,Paquis-Flucklinger Véronique

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Reference46 articles.

1. OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus' phenotype;Amati-Bonneau;Brain,2008

2. CHM1/CHCHD6, a novel mitochondrial protein linked to regulation of mitofilin and mitochondrial cristae morphology;An;J Biol Chem,2012

3. The coiled coil-helix coil-helix proteins may be redox proteins;Banci;FEBS Lett,2009

4. Structural characterization of CHCHD5 and CHCHD7: two atypical twin CX9C proteins;Banci;J Struct Biol,2012

5. The human MSH5 (MutS Homolog 5) gene localizes to mitochondria and protects the mitochondrial genome from oxidative damage;Bannwarth;Mitochondrion,2012

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