(Q28272001)

Journal of Biological Chemistry

GOA release 2020-03-11

4

Michael Schlame

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author name string

Yang Xu

series ordinal

1

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Ashim Malhotra

series ordinal

2

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Mindong Ren

series ordinal

3

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language of work or name

English

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publication date

22 December 2006

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published in

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volume

281

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issue

51

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page(s)

39217-24

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cites work

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1 reference

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

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Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

21 January 2018

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Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

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Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblasts

21 January 2018

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Phospholipid abnormalities in children with Barth syndrome

21 January 2018

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

21 January 2018

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

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A Drosophila model of Barth syndrome

21 January 2018

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

21 January 2018

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The human TAZ gene complements mitochondrial dysfunction in the yeast taz1Delta mutant. Implications for Barth syndrome

21 January 2018

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Ypr140wp, 'the yeast tafazzin', displays a mitochondrial lysophosphatidylcholine (lyso-PC) acyltransferase activity related to triacylglycerol and mitochondrial lipid synthesis

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Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome

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Remodeling of cardiolipin by phospholipid transacylation.

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Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines

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A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

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Molecular symmetry in mitochondrial cardiolipins

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Acyltransferases and transacylases involved in fatty acid remodeling of phospholipids and metabolism of bioactive lipids in mammalian cells

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N-Acylation of ethanolamine phospholipids in canine myocardium

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Transacylase and phospholipases in the synthesis of bis(monoacylglycero)phosphate

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Characterization of lymphoblast mitochondria from patients with Barth syndrome

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Barth syndrome: TAZ gene mutations, mRNAs, and evolution

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Complex expression pattern of the Barth syndrome gene product tafazzin in human cell lines and murine tissues

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Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins

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