A Drosophila model of Barth syndrome (Q34984428)

5 August 2017

A Drosophila model of Barth syndrome (English)

1 reference

5 August 2017

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1 reference

GOA release 2020-03-11

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7

Michael Schlame

1 reference

5 August 2017

Yang Xu

1

1 reference

5 August 2017

Morgan Condell

2

1 reference

5 August 2017

Heide Plesken

3

1 reference

5 August 2017

Irit Edelman-Novemsky

4

1 reference

5 August 2017

Jinping Ma

5

1 reference

5 August 2017

Mindong Ren

6

1 reference

5 August 2017

language of work or name

English

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publication date

19 July 2006

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Proceedings of the National Academy of Sciences of the United States of America

5 August 2017

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5 August 2017

103

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5 August 2017

31

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5 August 2017

11584-11588

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BEHAVIORAL MUTANTS OF Drosophila ISOLATED BY COUNTERCURRENT DISTRIBUTION

5 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

FlyBase: anatomical data, images and queries

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Characterization of lymphoblast mitochondria from patients with Barth syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Barth syndrome: TAZ gene mutations, mRNAs, and evolution

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

The mitochondrial inner membrane protein mitofilin controls cristae morphology

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Mitochondrial "swirls" induced by oxygen stress and in the Drosophila mutant hyperswirl

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Protein measurement with the Folin phenol reagent

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Phospholipid abnormalities in children with Barth syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

The ATP synthase is involved in generating mitochondrial cristae morphology

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

The biosynthesis and functional role of cardiolipin

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

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

8 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

8 July 2018

https://api.crossref.org/works/10.1073%2FPNAS.0603242103

Barth syndrome may be due to an acyltransferase deficiency

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Aging Changes in Insect Flight Muscle

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Remodeling of cardiolipin by phospholipid transacylation.

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0603242103

Molecular symmetry in mitochondrial cardiolipins

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0603242103

Screening assays for heart function mutants in Drosophila.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1544213

Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16855048

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

2 Separation of methyl esters of fatty acids by gas chromatography on capillary columns, including the separation of deuterated from nondeuterated fatty acids

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16855048

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Microanalysis of cardiolipin in small biopsies including skeletal muscle from patients with mitochondrial disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16855048

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0603242103

1 reference

5 August 2017

0 references

1 reference

5 August 2017

1 reference