Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis

Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis

Barth syndrome (BTHS) is an X-linked recessive disorder that is biochemically characterized by low cellular levels of the mitochondrial phospholipid cardiolipin (CL). Previously, we discovered that the yeast disruptant of the TAZ ortholog in Saccharomyces cerevisiae not only displays CL deficiency b...

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Bibliographic Details
Main Authors: Fredoen Valianpour, Voula Mitsakos, Dimitri Schlemmer, Jeffrey A. Towbin, Juliet M. Taylor, Paul G. Ekert, David R. Thorburn, Arnold Munnich, Ronald J.A. Wanders, Peter G. Barth, Frédéric M. Vaz
Format: Article
Language:English
Published: Elsevier 2005-06-01
Series:Journal of Lipid Research
Subjects:
cardiolipin
tafazzin
lymphoblasts
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520330236

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http://www.sciencedirect.com/science/article/pii/S0022227520330236

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