Mitochondrial DNA variation in human evolution and disease (Q28138400)

Sequence and organization of the human mitochondrial genome

Europe PubMed Central

title

Mitochondrial DNA variation in human evolution and disease (English)

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D C Wallace

1

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M D Brown

series ordinal

2

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M T Lott

series ordinal

3

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language of work or name

English

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publication date

30 September 1999

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published in

Gene

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volume

238

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issue

1

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page(s)

211-30

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cites work

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy

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7 January 2021

A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies

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7 January 2021

Molecular basis of mitochondrial DNA disease

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7 January 2021

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

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7 January 2021

Expression of genes from the human active and inactive X chromosomes

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7 January 2021

mtDNA haplogroup X: An ancient link between Europe/Western Asia and North America?

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7 January 2021

Polymorphism in mitochondrial DNA of humans as revealed by restriction endonuclease analysis

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7 January 2021

Rapid evolution of animal mitochondrial DNA

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7 January 2021

Mitochondrial DNA and human evolution

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7 January 2021

Maternal inheritance of mitochondrial DNA polymorphisms in cultured human fibroblasts

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA

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7 January 2021

Branching pattern in the evolutionary tree for human mitochondrial DNA.

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7 January 2021

Association of the 11778 mitochondrial DNA mutation and demyelinating disease

1 reference

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7 January 2021

Cerebellar ataxia in patients with Leber's hereditary optic neuropathy

1 reference

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7 January 2021

Maternal inheritance of human mitochondrial DNA

1 reference

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7 January 2021

The Settlement of the Americas: A Comparison of the Linguistic, Dental, and Genetic Evidence [and Comments and Reply]

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7 January 2021

Paternal inheritance of mitochondrial DNA in mice

1 reference

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7 January 2021

Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Human origins and analysis of mitochondrial DNA sequences

1 reference

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7 January 2021

Death to sperm mitochondria

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7 January 2021

Mitochondrial DNA polymorphism in Japanese. II. Analysis with restriction enzymes of four or five base pair recognition

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7 January 2021

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

1 reference

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7 January 2021

Leber hereditary optic neuropathy: how do mitochondrial DNA mutations cause degeneration of the optic nerve?

1 reference

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7 January 2021

Leber hereditary optic neuropathy: respiratory chain dysfunction and degeneration of the optic nerve

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Cytochrome b mutations in Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Elimination of paternal mitochondrial DNA in intraspecific crosses during early mouse embryogenesis

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Leber's hereditary optic neuropathy and complex I deficiency in muscle

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

The structure of human mitochondrial DNA variation.

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Mitochondrial DNA copy number in bovine oocytes and somatic cells

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Leber's disease and dystonia: a mitochondrial disease

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Different genetic components in the Ethiopian population, identified by mtDNA and Y-chromosome polymorphisms

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Mitochondrial DNA variation in Koryaks and Itel'men: population replacement in the Okhotsk Sea-Bering Sea region during the Neolithic

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

mtDNA diversity in Chukchi and Siberian Eskimos: implications for the genetic history of Ancient Beringia and the peopling of the New World

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Ancient DNA from a pre-Columbian Amerindian population.

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Accuracy of estimated phylogenetic trees from molecular data. I. Distantly related species

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Human origins and analysis of mitochondrial DNA sequences

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Mitochondrial DNA analysis in Tibet: implications for the origin of the Tibetan population and its adaptation to high altitude

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Late Pleistocene and Holocene population history of East Asia based on dental variation

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

African Populations and the Evolution of Human Mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Mitotic segregation of mitochondrial DNAs in human cell hybrids and expression of chloramphenicol resistance.

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Dramatic founder effects in Amerindian mitochondrial DNAs

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Mitochondrial DNA mutations in epilepsy and neurological disease

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Extensive mitochondrial diversity within a single Amerindian tribe

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Genetic and linguistic differentiation in the Americas

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021

Length mutations in human mitochondrial DNA: direct sequencing of enzymatically amplified DNA

1 reference

https://api.crossref.org/works/10.1016/S0378-1119(99)00295-4

7 January 2021