(Q24300966)

mitochondrial ATP synthesis coupled electron transport

GOA release 2020-03-11

1 reference

Lysophosphatidylcholine acyltransferase YPR140W

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

1 reference

4

Ronald J A Wanders

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author name string

Lining Ma

1

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Frederic M Vaz

2

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Zhiming Gu

3

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Miriam L Greenberg

Journal of Biological Chemistry

5

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language of work or name

English

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publication date

22 October 2004

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published in

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volume

279

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issue

43

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page(s)

44394-9

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cites work

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Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

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Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

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X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts

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Peroxisomal beta-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndrome

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An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

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Analysis of polypeptide transit through yeast secretory pathway

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Gene disruption with PCR products in Saccharomyces cerevisiae

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2-Hydroxyphytanic acid oxidase activity in rat and human liver and its deficiency in the Zellweger syndrome

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The regulation of the matrix volume of mammalian mitochondria in vivo and in vitro and its role in the control of mitochondrial metabolism

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Dependence of yeast mitochondrial unselective channel activity on the respiratory chain

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The biosynthesis and functional role of cardiolipin

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X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)

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Lysocardiolipin formation and reacylation in isolated rat liver mitochondria

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Cardiolipin prevents rate-dependent uncoupling and provides osmotic stability in yeast mitochondria.

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Cardiolipin is not essential for the growth of Saccharomyces cerevisiae on fermentable or non-fermentable carbon sources

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Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome.

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Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolism

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Remodeling of cardiolipin by phospholipid transacylation.

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The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

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Linoleic acid supplementation of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatment

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Quantification of free sialic acid in urine by HPLC-electrospray tandem mass spectrometry: a tool for the diagnosis of sialic acid storage disease

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