Very Rare Complementation between Mitochondria Carrying Different Mitochondrial DNA Mutations Points to Intrinsic Genetic Autonomy of the Organelles in Cultured Human Cells
Open Access
- 1 April 2000
- journal article
- Published by Elsevier
- Vol. 275 (15) , 11207-11215
- https://doi.org/10.1074/jbc.275.15.11207
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- Aging-Dependent Large Accumulation of Point Mutations in the Human mtDNA Control Region for ReplicationScience, 1999
- Close Contacts with the Endoplasmic Reticulum as Determinants of Mitochondrial Ca 2+ ResponsesScience, 1998
- Human mitochondria: distinct organelles or dynamic network?Trends in Genetics, 1995
- Human mitochondria and mitochondrial genome function as a single dynamic cellular unit.The Journal of cell biology, 1994
- Nonviability of cells with oxidative defects in galactose medium: A screening test for affected patient fibroblastsBiochemical Medicine and Metabolic Biology, 1992
- Structural organization of surface domains of sperm mitochondriaMolecular Reproduction and Development, 1992
- Multiple mitochondrial DNA deletions in an elderly human individualFEBS Letters, 1992
- A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)Biochemical and Biophysical Research Communications, 1990
- Intermitochondrial contacts in myocardiocytesJournal of Molecular and Cellular Cardiology, 1983
- Mitochondrial profile of a mammalian lymphocyteJournal of Ultrastructure Research, 1975