Characterization of a transgenic short hairpin RNA-induced murine model of Tafazzin deficiency (Q24604918)

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16 January 2020

title

Characterization of a transgenic short hairpin RNA-induced murine model of Tafazzin deficiency (English)

1 reference

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16 January 2020

1 reference

6

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16 January 2020

5

Michael Schlame

1 reference

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16 January 2020

author name string

Meghan S Soustek

1

1 reference

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16 January 2020

Darin J Falk

2

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16 January 2020

Cathryn S Mah

3

1 reference

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16 January 2020

Matthew J Toth

4

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16 January 2020

Barry J Byrne

7

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16 January 2020

language of work or name

English

0 references

publication date

19 May 2011

1 reference

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16 January 2020

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16 January 2020

volume

22

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16 January 2020

issue

7

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16 January 2020

page(s)

865-871

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describes a project that uses

16 January 2020

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3166794/fullTextXML

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cites work

Role of calcium-independent phospholipase A2 in the pathogenesis of Barth syndrome

1 reference

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

7 April 2017

1 reference

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Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

7 April 2017

1 reference

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A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

7 April 2017

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

7 April 2017

1 reference

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Barth syndrome may be due to an acyltransferase deficiency

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

The enzymatic function of tafazzin

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

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

7 April 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

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

7 April 2017

1 reference

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

7 April 2017

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

The biosynthesis and functional role of cardiolipin

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

Cardiolipin remodeling in the heart

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

Matrix-assisted laser desorption/ionization time-of-flight mass spectrometric analysis of cellular glycerophospholipids enabled by multiplexed solvent dependent analyte-matrix interactions

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

A Drosophila model of Barth syndrome

27 September 2017

1 reference

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Cardiac and clinical phenotype in Barth syndrome

27 September 2017

1 reference

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Pathophysiology of cardiac dysfunction in congestive heart failure.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

Doxycycline therapy for abdominal aneurysm: Improved proteolytic balance through reduced neutrophil content

27 September 2017

1 reference

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A zebrafish model of human Barth syndrome reveals the essential role of tafazzin in cardiac development and function

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

Molecular symmetry in mitochondrial cardiolipins

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166794

Altered phospholipid metabolism in pressure-overload hypertrophied hearts

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21091282

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21091282

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1089/HUM.2010.199

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21091282%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

2 references

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16 January 2020

2 references