Barth syndrome: Cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation-Reference-Cited by-同舟云学术

Barth syndrome: Cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation

Published:2013-08 Issue:8 Volume:1832 Page:1194-1206
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Gonzalvez François,D'Aurelio Marilena,Boutant Marie,Moustapha Aoula,Puech Jean-Philippe,Landes Thomas,Arnauné-Pelloquin Laeticia,Vial Guillaume,Taleux Nellie,Slomianny Christian,Wanders Ronald J.,Houtkooper Riekelt H.,Bellenguer Pascale,Møller Ian Max,Gottlieb Eyal,Vaz Frederic M.,Manfredi Giovanni,Petit Patrice X.

Funder

Centre National de la Recherche Scientifique (CNRS)

Association Française contre les Myopathies (AFM) Grants

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference59 articles.

1. Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis;Kuijpers;Blood,2004

2. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update;Barth;Am. J. Med. Genet. A,2004

3. Barth syndrome, a human disorder of cardiolipin metabolism;Schlame;FEBS Lett.,2006

4. A novel X-linked gene, G4.5. is responsible for Barth syndrome;Bione;Nat. Genet.,1996

5. Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome;Vreken;Biochem. Biophys. Res. Commun.,2000

Cited by 146 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. The subtherapeutic dose of valproic acid induces the activity of cardiolipin-dependent proteins;Biochimica et Biophysica Acta (BBA) - Bioenergetics;2024-11

2. Interorganelle phospholipid communication, a house not so divided;Trends in Endocrinology & Metabolism;2024-07

3. Reduced protein kinase C delta in a high molecular weight complex in mitochondria and elevated creatine uptake into Barth syndrome B lymphoblasts;Journal of Translational Genetics and Genomics;2024-05-30

4. Stem cell models of TAFAZZIN deficiency reveal novel tissue-specific pathologies in Barth Syndrome;2024-04-29

5. Curvature sensing lipid dynamics in a mitochondrial inner membrane model;Communications Biology;2024-01-05