Monolysocardiolipin in cultured fibroblasts is a sensitive and specific marker for Barth Syndrome (Q24298288)

cardiolipin biosynthetic process

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

Michiel Adriaan van Werkhoven

1

0 references

David Ross Thorburn

2

0 references

Agi Kyra Gedeon

3

0 references

James Jonathon Pitt

Journal of Lipid Research

4

0 references

language of work or name

English

0 references

publication date

October 2006

0 references

published in

0 references

volume

47

0 references

issue

10

0 references

page(s)

2346-51

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Barth syndrome without 3-methylglutaconic aciduria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Phospholipid abnormalities in children with Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

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/10.1194%2FJLR.D600024-JLR200

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/10.1194%2FJLR.D600024-JLR200

Interactions between phospholipids and NADH:ubiquinone oxidoreductase (complex I) from bovine mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Photolabeling of cardiolipin binding subunits within bovine heart cytochrome c oxidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Cardiolipin metabolism and Barth Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Mitochondrial cardiolipin in diverse eukaryotes. Comparison of biosynthetic reactions and molecular acyl species.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Purification and characterization of monolysocardiolipin acyltransferase from pig liver mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Lysocardiolipin formation and reacylation in isolated rat liver mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Measurement of protein using bicinchoninic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

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/10.1194%2FJLR.D600024-JLR200

Molecular species of cardiolipin in relation to other mitochondrial phospholipids. Is there an acyl specificity of the interaction between cardiolipin and the ADP/ATP carrier?

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200

Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.D600024-JLR200