Paternal inheritance of mitochondrial DNA

New England Journal of Medicine

Volumn 347, Issue 8, 2002, Pages 576-580

  Schwartz, Marianne ^a   Vissing, John ^a  

^a Rigshospitalet   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; CASE REPORT; DNA DETERMINATION; EXERCISE; GENE DELETION; GENE MUTATION; HUMAN; INHERITANCE; MALE; MITOCHONDRIAL MYOPATHY; MUSCLE BIOPSY; PRIORITY JOURNAL;

ADULT; DNA, MITOCHONDRIAL; EXERCISE TOLERANCE; EXTRACHROMOSOMAL INHERITANCE; FATHERS; FEMALE; FRAMESHIFT MUTATION; HAPLOTYPES; HUMANS; MALE; PEDIGREE; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION;

EID: 0037158599     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJMoa020350     Document Type: Article

References (26)

1. Uniparental inheritance of mitochondrial and chloroplast genes: Mechanisms and evolution
2. The inheritance of genes in mitochondria and chloroplasts: Laws, mechanisms, and models
3. Fate of microinjected sperm components in the mouse oocyte and embryo
4. Paternal inheritance of mitochondrial DNA in mice
5. Fate of microinjected spermatid mitochondria in the mouse oocyte and embryo
6. Maternal inheritance of mouse mtDNA in interspecific hybrids: Segregation of leaked paternal mtDNA followed by the prevention of subsequent paternal leakage
7. Selective and continuous elimination of mitochondria microinjected into mouse eggs from spermatids, but not from liver cells, occurs throughout embryogenesis
8. A forearm exercise screening test for mitochondrial myopathy
9. Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR
10. Sequence and organisation of the human mitochondrial genome
11. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
12. Quantitative analysis of human DNA sequences by PCR and solid-phase minisequencing
13. The emerging tree of West Eurasian mtDNAs: A synthesis of control-region sequences and RFLPs
14. Phylogenetic network for European mtDNA
15. Mitochondrial DNA variant 11719G is a marker for the mtDNA haplogroup duster HV
16. Mitochondrial encephalopathies
17. Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
18. MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts
19. Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy
20. Exercise intolerance due to a non-sense mutation in the mtDNA ND4 gene
21. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA
22. Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA
23. A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria
24. Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene
25. Failure of elimination of paternal mitochondrial DNA in abnormal embryos
26. Is paternal mitochondrial DNA transferred to the offspring following intracytoplasmic sperm injection?