Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees (Q33965082)

30 July 2017

title

Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees (English)

1 reference

Leber hereditary optic neuropathy

30 July 2017

1 reference

1 reference

N. Howell

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

27 June 2024

I. Kubacka

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

27 June 2024

S. Halvorson

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

27 June 2024

B. Howell

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

27 June 2024

D. A. McCullough

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

27 June 2024

D. Mackey

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

27 June 2024

language of work or name

English

0 references

publication date

1 May 1995

1 reference

30 July 2017

number of pages

18

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full work available at URL

inferred from page(s)

https://academic.oup.com/genetics/article-pdf/140/1/285/34665482/genetics0285.pdf

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7635294/?tool=EBI

27 June 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

http://intl.genetics.org/cgi/content/abstract/140/1/285

27 June 2024

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7635294/pdf/?tool=EBI

27 June 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

https://europepmc.org/articles/PMC1206556

27 June 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

https://europepmc.org/articles/PMC1206556?pdf=render

27 June 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:7635294

http://academic.oup.com/genetics/article-pdf/140/1/285/34665482/genetics0285.pdf

27 June 2024

1 reference

10.1093/GENETICS/140.1.285

https://api.crossref.org/works/10.1093/GENETICS/140.1.285

27 June 2024

1 reference

30 July 2017

volume

140

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30 July 2017

issue

1

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30 July 2017

page(s)

285-302

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LEBER'S DISEASE IN THE NETHERLANDS.

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Mitochondrial DNA "clock" for the Amerinds and its implications for timing their entry into North America

28 July 2018

1 reference

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Application and accuracy of molecular phylogenies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Mitochondrial gene mutations and human diseases: a prolegomenon

28 July 2018

1 reference

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Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs

28 July 2018

1 reference

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Maternal inheritance of human mitochondrial DNA

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Mutational analysis of the mouse mitochondrial cytochrome b gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Intraspecific nucleotide sequence differences in the major noncoding region of human mitochondrial DNA.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence-specific oligonucleotide probes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Extensive mitochondrial diversity within a single Amerindian tribe

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Estimating substitution rates from molecular data using the coalescent

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

The sequence of human mtDNA: the question of errors versus polymorphisms

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

Leber hereditary optic neuropathy in Australia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1206556

New approaches to dating suggest a recent age for the human mtDNA ancestor

28 July 2018

1 reference

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Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees

28 July 2018

1 reference

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Cytochrome b mutations in Leber hereditary optic neuropathy

29 October 2018

1 reference

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Blindness in offspring of women blinded by Leber's hereditary optic neuropathy

29 October 2018

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12 December 2020

Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation

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12 December 2020

Leber's hereditary optic neuropathy. Clinical manifestations of the 15257 mutation

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12 December 2020

The application of mitochondrial DNA typing to the study of white Caucasian genetic identification

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12 December 2020

The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy

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12 December 2020

Heteroplasmy in Leber's hereditary optic neuropathy

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12 December 2020

Cytochrome c oxidase mutations in Leber hereditary optic neuropathy

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12 December 2020

Lines of descent in the diffusion approximation of neutral Wright-Fisher models

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12 December 2020

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease

1 reference

12 December 2020

10.1093/GENETICS/140.1.285

Identifiers

DOI

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7635294

27 June 2024

1 reference

30 July 2017

1 reference