Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolism (Q24317315)

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7 November 2019

title

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

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7 November 2019

1 reference

GOA release 2020-03-11

1-acylglycerophosphocholine O-acyltransferase activity

1 reference

GOA release 2020-03-11

author

Riekelt H Houtkooper

2

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7 November 2019

5

Ronald J A Wanders

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7 November 2019

author name string

Frédéric M Vaz

1

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7 November 2019

Fredoen Valianpour

3

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7 November 2019

Peter G Barth

4

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7 November 2019

language of work or name

English

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publication date

20 August 2003

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Journal of Biological Chemistry

7 November 2019

published in

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7 November 2019

volume

278

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7 November 2019

page(s)

43089-43094

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7 November 2019

issue

44

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

7 November 2019

cites work

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X chromosome inactivation in carriers of Barth syndrome

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Mutation characterization and genotype-phenotype correlation in Barth syndrome

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

21 January 2018

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Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

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Functional binding of cardiolipin to cytochrome c oxidase

21 January 2018

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PCR-synthesis of marker cassettes with long flanking homology regions for gene disruptions in S. cerevisiae

21 January 2018

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SHY1, the yeast homolog of the mammalian SURF-1 gene, encodes a mitochondrial protein required for respiration

21 January 2018

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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Molecular and Biochemical Characterization of Rat epsilon -N-Trimethyllysine Hydroxylase, the First Enzyme of Carnitine Biosynthesis

21 January 2018

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

21 January 2018

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

21 January 2018

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Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

21 January 2018

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A novel mutation in the G4.5 (TAZ) gene in a kindred with Barth syndrome.

21 January 2018

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A novel intronic mutation of the TAZ ( G4.5) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exon

21 January 2018

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The mitochondrial phosphate carrier has an essential requirement for cardiolipin

21 January 2018

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7 January 2021

High-efficiency transformation of yeast by electroporation

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7 January 2021

Analysis of polypeptide transit through yeast secretory pathway

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7 January 2021

Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction

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7 January 2021

An essential requirement of cardiolipin for mitochondrial carnitine acylcarnitine translocase activity. Lipid requirement of carnitine acylcarnitine translocase

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7 January 2021