ATP Synthase Diseases of Mitochondrial Genetic Origin-Reference-Cited by-同舟云学术

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ATP Synthase Diseases of Mitochondrial Genetic Origin

Published:2018-04-04 Issue: Volume:9 Page:
ISSN:1664-042X
Container-title:Frontiers in Physiology
language:
Short-container-title:Front. Physiol.

Author:

Dautant Alain,Meier Thomas,Hahn Alexander,Tribouillard-Tanvier Déborah,di Rago Jean-Paul,Kucharczyk Roza

Funder

Association Française contre les Myopathies

Agence Nationale de la Recherche

Wellcome Trust

Publisher

Frontiers Media SA

Subject

Physiology (medical),Physiology

Reference148 articles.

1. Structure at 2.8 Å resolution of F1-ATPase from bovine heart mitochondria;Abrahams;Nature,1994

2. Detection of mitochondrial respiratory dysfunction in circulating lymphocytes using resazurin;Abu-Amero;Arch. Pathol. Lab. Med.,2005

3. Mitochondrial abnormalities in patients with LHON-like optic neuropathies;Abu-Amero;Invest. Ophthalmol. Vis. Sci.,2006

4. Horizontal membrane-intrinsic α-helices in the stator a-subunit of an F-type ATP synthase;Allegretti;Nature,2015

5. Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations;Auré;Neurology,2013

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