Barth Syndrome: From Mitochondrial Dysfunctions Associated with Aberrant Production of Reactive Oxygen Species to Pluripotent Stem Cell Studies (Q26772690)

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English	Barth Syndrome: From Mitochondrial Dysfunctions Associated with Aberrant Production of Reactive Oxygen Species to Pluripotent Stem Cell Studies	scientific article

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scholarly article

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6 March 2020

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Barth Syndrome: From Mitochondrial Dysfunctions Associated with Aberrant Production of Reactive Oxygen Species to Pluripotent Stem Cell Studies (English)

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6 March 2020

reactive oxygen species

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based on heuristic

inferred from title

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based on heuristic

inferred from title

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based on heuristic

inferred from title

2

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6 March 2020

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Ana Saric

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6 March 2020

Anne-Sophie Armand

3

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Ian M Møller

4

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6 March 2020

Patrice X Petit

5

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1 January 2015

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6 March 2020

Frontiers in Genetics

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359

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6 March 2020

A mitochondrial pathway for biosynthesis of lipid mediators

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LC3 binds externalized cardiolipin on injured mitochondria to signal mitophagy in neurons: implications for Parkinson disease

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Characterization of cardiolipins and their oxidation products by LC-MS analysis

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20 March 2017

Cardiolipin asymmetry, oxidation and signaling

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Cas9 as a versatile tool for engineering biology

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Cardiolipin externalization to the outer mitochondrial membrane acts as an elimination signal for mitophagy in neuronal cells

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Human trifunctional protein alpha links cardiolipin remodeling to beta-oxidation

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Lipidomics identifies cardiolipin oxidation as a mitochondrial target for redox therapy of brain injury

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Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth

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Characterization of tafazzin splice variants from humans and fruit flies

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Formation of molecular species of mitochondrial cardiolipin. 1. A novel transacylation mechanism to shuttle fatty acids between sn-1 and sn-2 positions of multiple phospholipid species

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Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography

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Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients

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

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20 March 2017

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

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20 March 2017

LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing

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Mitochondria-targeted agents: Future perspectives of mitochondrial pharmaceutics in cardiovascular diseases

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20 March 2017

Cardiolipin and its different properties in mitophagy and apoptosis

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Modeling inherited cardiac disorders

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After the banquet: mitochondrial biogenesis, mitophagy, and cell survival

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Barth syndrome.

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Structural and functional analysis of PTPMT1, a phosphatase required for cardiolipin synthesis

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Deacylation on the matrix side of the mitochondrial inner membrane regulates cardiolipin remodeling

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Tam41 is a CDP-diacylglycerol synthase required for cardiolipin biosynthesis in mitochondria

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The translocator maintenance protein Tam41 is required for mitochondrial cardiolipin biosynthesis

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20 March 2017

Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins

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

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

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The CDS1 gene encoding CDP-diacylglycerol synthase in Saccharomyces cerevisiae is essential for cell growth

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20 March 2017

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20 March 2017

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20 March 2017

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

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20 March 2017

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20 March 2017

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

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20 March 2017

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

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20 March 2017

Mitochondrial phosphatase PTPMT1 is essential for cardiolipin biosynthesis

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20 March 2017

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20 March 2017

Patient-specific induced pluripotent stem-cell models for long-QT syndrome

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7 April 2017

Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons

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7 April 2017

AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1alpha

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7 April 2017

The biosynthesis and functional role of cardiolipin

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7 April 2017

Structural and functional analyses of Barth syndrome-causing mutations and alternative splicing in the tafazzin acyltransferase domain.

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28 September 2017

Tafazzins from Drosophila and mammalian cells assemble in large protein complexes with a short half-life.

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28 September 2017

Genome editing in human stem cells

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28 September 2017

Mitochondria-targeted antioxidant prevents cardiac dysfunction induced by tafazzin gene knockdown in cardiac myocytes

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28 September 2017

Directed differentiation of patient-specific induced pluripotent stem cells identifies the transcriptional repression and epigenetic modification of NKX2-5, HAND1, and NOTCH1 in hypoplastic left heart syndrome

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28 September 2017

Transplanted terminally differentiated induced pluripotent stem cells are accepted by immune mechanisms similar to self-tolerance

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28 September 2017

DNAJC19, a mitochondrial cochaperone associated with cardiomyopathy, forms a complex with prohibitins to regulate cardiolipin remodeling

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28 September 2017

Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies

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28 September 2017

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28 September 2017

Metabolism and function of mitochondrial cardiolipin

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28 September 2017

The functions of cardiolipin in cellular metabolism-potential modifiers of the Barth syndrome phenotype

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28 September 2017

Patient-specific stem cells and cardiovascular drug discovery

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28 September 2017

Mammalian cardiolipin biosynthesis

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28 September 2017

The Taz1p transacylase is imported and sorted into the outer mitochondrial membrane via a membrane anchor domain.

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28 September 2017

Lipids of mitochondria

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28 September 2017

Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs

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28 September 2017

Fetal reprogramming and senescence in hypoplastic left heart syndrome and in human pluripotent stem cells during cardiac differentiation

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28 September 2017

Recapitulating maladaptive, multiscale remodeling of failing myocardium on a chip

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28 September 2017

Stem cell therapy for pediatric dilated cardiomyopathy

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28 September 2017

Barth syndrome: cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation

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28 September 2017

Allele-specific RNA interference rescues the long-QT syndrome phenotype in human-induced pluripotency stem cell cardiomyocytes

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28 September 2017

The role of mitochondria in aging

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28 September 2017

Oxidative stress and sarcomeric proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cardiolipin remodeling and the function of tafazzin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Loss of cardiolipin leads to perturbation of mitochondrial and cellular iron homeostasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Tafazzin knockdown in mice leads to a developmental cardiomyopathy with early diastolic dysfunction preceding myocardial noncompaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Seven functional classes of Barth syndrome mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Tafazzin senses curvature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Ablation of ALCAT1 mitigates hypertrophic cardiomyopathy through effects on oxidative stress and mitophagy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

The physical state of lipid substrates provides transacylation specificity for tafazzin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Modeling of catecholaminergic polymorphic ventricular tachycardia with patient-specific human-induced pluripotent stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Muscle on a chip: in vitro contractility assays for smooth and striated muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Lysocardiolipin acyltransferase 1 (ALCAT1) controls mitochondrial DNA fidelity and biogenesis through modulation of MFN2 expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Comparison of cardiolipins from Drosophila strains with mutations in putative remodeling enzymes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Barth syndrome in a female patient

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Advances in nuclear cardiac instrumentation with a view towards reduced radiation exposure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Skeletogenic phenotype of human Marfan embryonic stem cells faithfully phenocopied by patient-specific induced-pluripotent stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Dantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Ensembles of engineered cardiac tissues for physiological and pharmacological study: heart on a chip

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

The permeability transition pore controls cardiac mitochondrial maturation and myocyte differentiation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Protein carbonylation and metal-catalyzed protein oxidation in a cellular perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Barth syndrome mutations that cause tafazzin complex lability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

The sites and topology of mitochondrial superoxide production

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Coassembly of Mgm1 isoforms requires cardiolipin and mediates mitochondrial inner membrane fusion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Function and biogenesis of iron-sulphur proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

The role of cardiolipin in the structural organization of mitochondrial membranes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Phenotypic and functional characterization of human mammary stem/progenitor cells in long term culture.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

PINK1-associated Parkinson's disease is caused by neuronal vulnerability to calcium-induced cell death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

AMPK and the biochemistry of exercise: implications for human health and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Mitochondrial defects lie at the basis of neutropenia in Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cardiolipin biosynthesis and remodeling enzymes are altered during development of heart failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cardiolipin provides an essential activating platform for caspase-8 on mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

AMPK: a key regulator of energy balance in the single cell and the whole organism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cardiolipin, the heart of mitochondrial metabolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Acute metabolic decompensation and sudden death in Barth syndrome: report of a family and a literature review.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Mitochondrial oxidative metabolism is required for the cardiac differentiation of stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Barth syndrome, a human disorder of cardiolipin metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Role of cardiolipin alterations in mitochondrial dysfunction and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cardiac and clinical phenotype in Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

The role of AMP-activated protein kinase in mitochondrial biogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cloning and characterization of a cDNA encoding human cardiolipin synthase (hCLS1).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Ventricular arrhythmia in the X-linked cardiomyopathy Barth syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cardiolipin is essential for organization of complexes III and IV into a supercomplex in intact yeast mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Characterization of lymphoblast mitochondria from patients with Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Regulation of mitochondrial proliferation in the heart: power-plant failure contributes to cardiac failure in hypertrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cell biology of cardiac mitochondrial phospholipids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Purification and characterization of monolysocardiolipin acyltransferase from pig liver mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Cardiolipin: a proton trap for oxidative phosphorylation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Selective targeting of a redox-active ubiquinone to mitochondria within cells: antioxidant and antiapoptotic properties

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

X chromosome inactivation in carriers of Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Mutation characterization and genotype-phenotype correlation in Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Lipids of mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

28 September 2017

Tafazzin splice variants and mutations in Barth syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Cardiolipin deficiency affects respiratory chain function and organization in an induced pluripotent stem cell model of Barth syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Identification of cardiolipin binding sites on cytochrome c oxidase at the entrance of proton channels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Generation of HIV-1 resistant and functional macrophages from hematopoietic stem cell-derived induced pluripotent stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Tafazzin knockdown causes hypertrophy of neonatal ventricular myocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Loss of tafazzin in yeast leads to increased oxidative stress during respiratory growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

The role of docosahexaenoic acid in mediating mitochondrial membrane lipid oxidation and apoptosis in colonocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Structural remodeling and mechanical dysfunction of cardiac myocytes in heart failure.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Biosynthesis of cardiolipin in liver mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

3-Hydroxy-3-methylglutaric aciduria: deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4719219

31 May 2018

Mitochondria-targeted plastoquinone derivatives as tools to interrupt execution of the aging program. 1. Cationic plastoquinone derivatives: synthesis and in vitro studies.

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Cardiac energetics correlates to myocardial hypertrophy in Friedreich's ataxia.

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Identification and functional characterization of hCLS1, a human cardiolipin synthase localized in mitochondria

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Cardiolipin deficiency releases cytochrome c from the inner mitochondrial membrane and accelerates stimuli-elicited apoptosis

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Tafazzin knockdown interrupts cell cycle progression in cultured neonatal ventricular fibroblasts.

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Control of mitochondrial biogenesis, ROS level, and cytosolic Ca2+ concentration during the cell cycle and the onset of differentiation in L6E9 myoblasts

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

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

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Oxidative phosphorylation in cardiolipin-lacking yeast mitochondria

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Barth syndrome associated with compound hemizygosity and heterozygosity of the TAZ and LDB3 genes.

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Cardiomyopathy, mitochondria and Barth syndrome: iPSCs reveal a connection.

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Molecular symmetry in mitochondrial cardiolipins

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Comparative studies of oxidative stress and mitochondrial function in aging

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Unveiling the last missing link of the cardiolipin synthetic pathway in mitochondria

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

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

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Mechanisms and effects of curcumin on spatial learning and memory improvement in APPswe/PS1dE9 mice

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Remodeling of cardiolipin by phospholipid transacylation.

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Absence of cardiolipin results in temperature sensitivity, respiratory defects, and mitochondrial DNA instability independent of pet56.

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Your heart on a chip: iPSC-based modeling of Barth-syndrome-associated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Improved methods to isolate and subfractionate rat liver mitochondria. Lipid composition of the inner and outer membrane

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Phospholipid asymmetry of the outer membrane of rat liver mitochondria

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

The role of contact sites between inner and outer mitochondrial membrane in energy transfer

1 reference

https://api.crossref.org/works/10.3389%2FFGENE.2015.00359

21 January 2018

Mitochondrial contact sites. Lipid composition and dynamics

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Barth Syndrome Registry: Distinguishing disease characteristics and growth data from a longitudinal study

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrophoretic analysis of the mitochondrial outer membrane rupture induced by permeability transition

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An X-linked recessive cardiomyopathy with abnormal mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Left ventricular noncompaction cardiomyopathy in Barth syndrome: an example of an undulating cardiac phenotype necessitating mechanical circulatory support as a bridge to transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human embryonic stem cells commonly display large mitochondrial DNA deletions

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of Barth syndrome using a novel LC-MS/MS method for leukocyte cardiolipin analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/26834781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3389/FGENE.2015.00359

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26834781%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26834781%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26834781%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

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