Identification of inheritance modes of mitochondrial diseases by introduction of pure nuclei from mtDNA-less HeLa cells to patient-derived fibroblasts

Journal of Biological Chemistry

Volumn 272, Issue 19, 1997, Pages 12606-12610

  Isobe, Kotoyo ^a   Kishino, Satoshi ^a   Inoue, Kimiko ^a   Takai, Daisaku ^a   Hirawake, Hiroko ^b   Kita, Kiyoshi ^b   Miyabayashi, Shigeaki ^c   Hayashi, Jun Ichi ^a  

^a UNIVERSITY OF TSUKUBA   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL ENZYME;

ARTICLE; CELL NUCLEUS; DNA TRANSFER; ENZYME DEFICIENCY; FIBROBLAST; GENE MUTATION; HELA CELL; HUMAN; HUMAN CELL; INHERITANCE; MITOCHONDRION; PRIORITY JOURNAL;

ADENOSINE TRIPHOSPHATASES; CELL NUCLEUS; CYTOCHROME-C OXIDASE DEFICIENCY; DNA, MITOCHONDRIAL; ENZYME INHIBITORS; FIBROBLASTS; HELA CELLS; HUMANS; INFANT; MITOCHONDRIAL MYOPATHIES; OLIGOMYCINS; SUCCINATE DEHYDROGENASE;

EID: 0030918712     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.272.19.12606     Document Type: Article

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