Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny (Q34514996)

2 August 2017

Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny (English)

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2 August 2017

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Eloisa Arbustini

4

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author name string

Michael V Zaragoza

1

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2 August 2017

Martin C Brandon

2

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2 August 2017

Marta Diegoli

3

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2 August 2017

Douglas C Wallace

5

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2 August 2017

27 October 2010

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European Journal of Human Genetics

2 August 2017

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2 August 2017

19

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2 August 2017

2

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2 August 2017

200-207

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describes a project that uses

2 August 2017

1 reference

https://scigraph.springernature.com/pub.10.1038/ejhg.2010.169

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cites work

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The diversity present in 5140 human mitochondrial genomes

7 July 2018

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Estimating the number of unseen variants in the human genome

7 July 2018

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Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

7 July 2018

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MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequences

7 July 2018

1 reference

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Mitochondrial DNA mutations in oxyphilic and chief cell parathyroid adenomas

7 July 2018

1 reference

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An enhanced MITOMAP with a global mtDNA mutational phylogeny

7 July 2018

1 reference

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Somatic mitochondrial DNA mutations in prostate cancer and normal appearing adjacent glands in comparison to age-matched prostate samples without malignant histology

7 July 2018

1 reference

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A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

7 July 2018

1 reference

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Effects of purifying and adaptive selection on regional variation in human mtDNA.

7 July 2018

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Natural selection shaped regional mtDNA variation in humans

7 July 2018

1 reference

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Progressive cardiomyopathy as manifestation of mitochondrial disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Mitochondrial DNA variation in human evolution and disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

The mitochondrial A3243G mutation presenting as severe cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Cardiomyopathy and abnormal mitochondrial function

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Mitochondrial DNA variation in human populations and implications for detection of mitochondrial DNA mutations of pathological significance

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Sequence and organization of the human mitochondrial genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

The structure of human mitochondrial DNA variation.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3025796

Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.169

Mitochondrial DNA analysis by multiplex denaturing high-performance liquid chromatography and selective sequencing in pediatric patients with cardiomyopathy.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.169

mtDNA tree Build 17 (18 Feb 2016)

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.169

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

21 January 2018

1 reference

12 December 2020

Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy

1 reference

12 December 2020

Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations

1 reference

12 December 2020

Sequence analysis of the entire mitochondrial genome in Parkinson's disease

1 reference

12 December 2020

Identifiers

DOI

10.1038/EJHG.2010.169

1 reference

2 August 2017

1 reference

2 August 2017

1 reference