A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies-Reference-Cited by-同舟云学术

A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies

Published:2018-01-19 Issue:7 Volume:27 Page:1186-1195
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Bartsakoulia Marina¹,Pyle Angela¹,Troncoso-Chandía Diego²,Vial-Brizzi Josefa²,Paz-Fiblas Marysol V²,Duff Jennifer¹,Griffin Helen¹,Boczonadi Veronika¹,Lochmüller Hanns¹,Kleinle Stephanie³,Chinnery Patrick F⁴,Grünert Sarah⁵,Kirschner Janbernd⁶,Eisner Verónica²,Horvath Rita¹

Affiliation:

1. Wellcome Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK

2. Department of Cellular and Molecular Biology, School of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago, Chile

3. Medical Genetics Center, Munich, Germany

4. MRC Mitochondrial Biology Unit & Department of Clinical Neurosciences, University of Cambridge, Cambridge Biomedical Campus, Cambridge CB2 0QQ, UK

5. Department of General Pediatrics, Adolescent Medicine and Neonatology, Medical Center – University of Freiburg, Freiburg, Germany

6. Department of Neuropediatrics and Muscle Disorders, Faculty of Medicine, Medical Center – University of Freiburg, Freiburg, Germany

Funder

Wellcome Trust

Wellcome Centre for Mitochondrial Research

Medical Research Council

European Research Council

Wellcome Trust Pathfinder Scheme

Newton Fund

European Union Seventh Framework Programme

Wellcome Trust Senior Fellow in Clinical Science

NIHR

Medical Research Council Mitochondrial Biology Unit

National Institute for Health Research

Biomedical Research Centre

Cambridge University Hospitals NHS Foundation Trust

University of Cambridge

Centre for Translational Muscle Disease

FONDECYT

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/27/7/1186/24398878/ddy033.pdf

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3. Interactions between sarco-endoplasmic reticulum and mitochondria in cardiac and skeletal muscle - pivotal roles in Ca2+ and reactive oxygen species signaling;Eisner;J. Cell Sci,2013

4. Multi-system neurological disease is common in patients with OPA1 mutations;Yu-Wai-Man;Brain,2010

5. Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutations;Lodi;Arch. Neurol,2011

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