Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing (Q35881405)

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scientific article published in February 1996

Language	Label	Description	Also known as
English	Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing	scientific article published in February 1996

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8571959 AND SRC:MED&resulttype=core&format=json

14 October 2019

Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8571959 AND SRC:MED&resulttype=core&format=json

14 October 2019

1 reference

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inferred from title

Leber hereditary optic neuropathy

1 reference

based on heuristic

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author name string

S S Ghosh

1

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14 October 2019

E Fahy

2

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14 October 2019

I Bodis-Wollner

3

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14 October 2019

J Sherman

4

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14 October 2019

N Howell

5

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14 October 2019

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1 February 1996

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14 October 2019

American Journal of Human Genetics

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14 October 2019

58

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14 October 2019

2

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14 October 2019

325-334

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14 October 2019

Leber's hereditary optic neuropathy. New genetic considerations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914528

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A heteroplasmic LHON family: tissue distribution and transmission of the 11778 mutation.

1 reference

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Intracellular heteroplasmy for disease-associated point mutations in mtDNA: implications for disease expression and evidence for mitotic segregation of heteroplasmic units of mtDNA

1 reference

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

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Sequence and organization of the human mitochondrial genome

1 reference

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Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows

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Mitochondrial DNA transmission genetics in crickets

1 reference

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11 July 2018

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

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Rapid segregation of heteroplasmic bovine mitochondria

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11 July 2018

Variable genotype of Leber's hereditary optic neuropathy patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914528

11 July 2018

Segregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathy

1 reference

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11 July 2018

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

1 reference

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11 July 2018

Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy

1 reference

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Organization of multiple nucleoids and DNA molecules in mitochondria of a human cell

1 reference

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Replacement of bovine mitochondrial DNA by a sequence variant within one generation

1 reference

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11 July 2018

Leber hereditary optic neuropathy in Australia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914528

11 July 2018

Mitochondrial gene segregation in mammals: is the bottleneck always narrow?

1 reference

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Purification of all forms of HeLa cell mitochondrial DNA and assessment of damage to it caused by hydrogen peroxide treatment of mitochondria or cells.

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24 September 2018

Noninvasive diagnosis of the MELAS syndrome from blood DNA

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heteroplasmy in Leber's hereditary optic neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8571959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantification of point mutations associated with Leber hereditary optic neuroretinopathy by solid-phase minisequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/8571959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8571959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8571959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/8571959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA. I. Intramitochondrial distribution and structural relations of single- and double-length circular DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8571959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutation and heteroplasmy in type I Leber hereditary optic neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8571959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8571959 AND SRC:MED&resulttype=core&format=json

14 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8571959 AND SRC:MED&resulttype=core&format=json

14 October 2019

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