Mitochondrial DNA in sickness and in health.

American journal of human genetics ·Vol. 46 ·No. 3 ·1990-03-00 ·Pages 415-7

Grossman LI

Abstract

暂无摘要

MeSH Terms

DNA, Mitochondrial/genetics Genetics, Medical Humans Mutation

Chemicals

DNA, Mitochondrial

Authors & Affiliations

1 authors, click to expand affiliations / ORCID

Grossman L I

Department of Molecular Biology and Genetics, Wayne State University School of Medicine, Detroit, MI 48201.

References (22)

22 references, click to expand

Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis.
Am J Hum Genet. 1990 Mar;46(3):418-27 PMID: 1689952
Mitochondrial DNA: Advances, Problems, and Goals.
Science. 1969 Jul 4;165(3888):25-35 PMID: 17840675
Sequence and organization of the human mitochondrial genome.
Nature. 1981 Apr 9;290(5806):457-65 PMID: 7219534
Deletion of blood mitochondrial DNA in pancytopenia.
Lancet. 1988 Sep 3;2(8610):567-8 PMID: 2900946
Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
Proc Natl Acad Sci U S A. 1989 Dec;86(23):9509-13 PMID: 2556715
Leber's optic atrophy, a possible example of maternal inheritance.
Am J Hum Genet. 1972 May;24(3):348-9 PMID: 5063796
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
Science. 1988 Dec 9;242(4884):1427-30 PMID: 3201231
A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.
Am J Hum Genet. 1990 Mar;46(3):428-33 PMID: 2137962
Replication of animal mitochondrial DNA.
Cell. 1982 Apr;28(4):693-705 PMID: 6178513
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
N Engl J Med. 1989 May 18;320(20):1293-9 PMID: 2541333
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.
Nature. 1988 Feb 25;331(6158):717-9 PMID: 2830540
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.
J Med Genet. 1989 Dec;26(12):739-43 PMID: 2575667
Deletions of mitochondrial DNA in Kearns-Sayre syndrome.
Neurology. 1988 Sep;38(9):1339-46 PMID: 3412580
Mitotic segregation of mitochondrial DNAs in human cell hybrids and expression of chloramphenicol resistance.
Somat Cell Mol Genet. 1986 Jan;12(1):41-9 PMID: 3003930
Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy.
Biochem Biophys Res Commun. 1988 Aug 15;154(3):1240-7 PMID: 2841928
Kearns-Sayre syndrome with muscle mitochondrial DNA deletion.
Lancet. 1988 Apr 16;1(8590):885 PMID: 2895391
Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study.
Am J Pathol. 1989 May;134(5):1167-73 PMID: 2541614
A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy.
N Engl J Med. 1989 May 18;320(20):1300-5 PMID: 2566116
Rapid segregation of heteroplasmic bovine mitochondria.
Nucleic Acids Res. 1989 Sep 25;17(18):7325-31 PMID: 2798094
Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.
Nucleic Acids Res. 1989 Oct 25;17(20):8117-24 PMID: 2813058
Deletions of muscle mitochondrial DNA.
Lancet. 1988 Jun 25;1(8600):1462 PMID: 2898614
Duplications of mitochondrial DNA in mitochondrial myopathy.
Lancet. 1989 Feb 4;1(8632):236-40 PMID: 2563411

Article Info

Journal

American journal of human genetics

Abbr.

Am J Hum Genet

ISSN

0002-9297

Published

1990-03-00

Pages

415-7

Language

English

Region

United States

NLM ID

0370475

PMCID

PMC1683610

Subset

External Links

PubMed source PMC Full Text View journal details

Analysis Services

Mitochondrial DNA in sickness and in health.

Contact

WeChat Official Account