(Q37340280)

19 August 2017

Evidence for nuclear modifier gene in mitochondrial cardiomyopathy (English)

1 reference

19 August 2017

1 reference

Claudia Nesti

4

0 references

author name string

Mercy M Davidson

series ordinal

1

1 reference

19 August 2017

Winsome F Walker

series ordinal

2

1 reference

19 August 2017

Evelyn Hernandez-Rosa

series ordinal

3

1 reference

19 August 2017

21 February 2009

1 reference

Journal of Molecular and Cellular Cardiology

19 August 2017

1 reference

19 August 2017

46

1 reference

19 August 2017

6

1 reference

19 August 2017

936-942

1 reference

Mitochondrial DNA and disease

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Mitochondrial dysfunction as a cause of optic neuropathies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Modifier genes for hypertrophic cardiomyopathy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Copper supplementation restores cytochrome c oxidase activity in cultured cells from patients with SCO2 mutations

6 September 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

6 September 2017

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2009.02.011

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

7 January 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Novel cell lines derived from adult human ventricular cardiomyocytes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Differences in nuclear gene expression between cells containing monomer and dimer mitochondrial genomes

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Long-term analysis of differentiation in human myoblasts repopulated with mitochondria harboring mtDNA mutations.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

An evaluation of the measurement of the activities of complexes I-IV in the respiratory chain of human skeletal muscle mitochondria.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing loss.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Maternally inherited cardiomyopathy: clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

Evidence for a Novel X-Linked Modifier Locus for Leber Hereditary Optic Neuropathy

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2741011

3 December 2018

Mitochondrial diseases

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2009.02.011

A Novel mtDNA Point Mutation in Maternally Inherited Cardiomyopathy

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2009.02.011

Deletion of the MTO2 gene related to tRNA modification causes a failure in mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2009.02.011

10.1016/J.YJMCC.2009.02.011

7 January 2021

Identifiers

DOI

1 reference

release_avlr63tdg5f6jhaj6l5wjyk2zu

19 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/avlr63tdg5f6jhaj6l5wjyk2zu

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

19 August 2017

PubMed publication ID

19233192

1 reference