(Q36594262)

15 August 2017

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title

Barth syndrome, a human disorder of cardiolipin metabolism (English)

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15 August 2017

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1

Michael Schlame

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15 August 2017

Mindong Ren

2

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PubMed ID

16973164

15 August 2017

language of work or name

English

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publication date

17 July 2006

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15 August 2017

6

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based on heuristic

inferred from page(s)

published in

FEBS Letters

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15 August 2017

580

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15 August 2017

23

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15 August 2017

5450-5455

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

15 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Genetic analysis of the G4.5 gene in families with suspected Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Preliminary evidence for a cognitive phenotype in Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Transcriptional organization of a 450-kb region of the human X chromosome in Xq28

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Mutation characterization and genotype-phenotype correlation in Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Barth syndrome: TAZ gene mutations, mRNAs, and evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Barth syndrome may be due to an acyltransferase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

The biosynthesis and functional role of cardiolipin

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Phospholipid abnormalities in children with Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Characterization of lymphoblast mitochondria from patients with Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Remodeling of cardiolipin by phospholipid transacylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Molecular symmetry in mitochondrial cardiolipins

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Evidence of a tetradocosahexaenoic cardiolipin in some marine bivalves

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

The nonequivalence of the phosphorus atoms in cardiolipin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Purification and characterization of monolysocardiolipin acyltransferase from pig liver mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

A novel cardiolipin-remodeling pathway revealed by a gene encoding an endoplasmic reticulum-associated acyl-CoA:lysocardiolipin acyltransferase (ALCAT1) in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Specific roles of protein-phospholipid interactions in the yeast cytochrome bc1 complex structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Structure of mitochondrial ADP/ATP carrier in complex with carboxyatractyloside

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Gluing the respiratory chain together. Cardiolipin is required for supercomplex formation in the inner mitochondrial membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Cardiolipin stabilizes respiratory chain supercomplexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

Mitochondrial regular arrangement in muscle cells: a "crystal-like" pattern

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.07.022

10.1016/J.FEBSLET.2006.07.022

21 January 2018

Identifiers

DOI

1 reference

15 August 2017

1 reference

PubMed ID

16973164