(Q37594930)

English

X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation

scientific article published on September 1991

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Statements

scholarly article

1 reference

Europe PubMed Central

21 August 2017

X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation (English)

1 reference

Europe PubMed Central

21 August 2017

1 reference

based on heuristic

inferred from title

Leber hereditary optic neuropathy

1 reference

based on heuristic

inferred from title

author name string

X D Bu

1

1 reference

Europe PubMed Central

21 August 2017

J I Rotter

2

1 reference

Europe PubMed Central

21 August 2017

language of work or name

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publication date

1 September 1991

1 reference

Europe PubMed Central

21 August 2017

number of pages

5

1 reference

based on heuristic

inferred from page(s)

Proceedings of the National Academy of Sciences of the United States of America

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Europe PubMed Central

21 August 2017

88

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Europe PubMed Central

21 August 2017

8198-8202

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Europe PubMed Central

21 August 2017

18

1 reference

Europe PubMed Central

21 August 2017

A test for segregation ratios in family data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

23 August 2017

A unified model for complex segregation analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

23 August 2017

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

23 August 2017

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

23 August 2017

Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

23 August 2017

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

23 August 2017

Evidence for preferential X-chromosome inactivation in a family with Fabry disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

23 August 2017

Biogenesis of mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

6 September 2017

Maternal genes: mitochondrial diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

14 September 2017

Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

28 September 2017

Regressive logistic models for familial disease and other binary traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

25 June 2018

Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

25 June 2018

The molecular basis of severe hemophilia B in a girl

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

25 June 2018

Complete replacement of mitochondrial DNA in Drosophila

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

25 June 2018

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

25 June 2018

Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

25 June 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=52474

25 June 2018

Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

25 June 2018

The early phase in Leber hereditary optic atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

25 June 2018

Christmas Disease in a Girl

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

1 September 2018

Female haemophilia A in a family with seeming extreme bidirectional lyonization tendency: abnormal premature X-chromosome inactivation?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=52474

1 September 2018

Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The inheritance of Leber's disease. A genealogical follow-up study

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Charcot-Marie-Tooth disease with Leber optic atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leber's optic neuropathy: a clinical and visual evoked potential study of affected and asymptomatic members of a six generation family

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leber's disease. V

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leber's disease. IV

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leber's disease. 3

1 reference

https://pubmed.ncbi.nlm.nih.gov/1896469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.88.18.8198

1 reference

Europe PubMed Central

21 August 2017

1991PNAS...88.8198B

0 references

1 reference

Europe PubMed Central

21 August 2017

1 reference

Europe PubMed Central

21 August 2017

ResearchGate publication ID

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