Changes in the human mitochondrial genome after treatment of malignant disease
- 7 January 2003
- journal article
- Published by Elsevier in Mutation Research
- Vol. 525 (1-2), 19-27
- https://doi.org/10.1016/s0027-5107(02)00313-5
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- High frequency of mitochondrial DNA mutations in glioblastoma multiforme identified by direct sequence comparison to blood samplesInternational Journal of Cancer, 2001
- Random Intracellular Drift Explains the Clonal Expansion of Mitochondrial DNA Mutations with AgeAmerican Journal of Human Genetics, 2001
- Decrease of 3243 A→G mtDNA Mutation from Blood in MELAS Syndrome: A Longitudinal StudyAmerican Journal of Human Genetics, 2001
- Thymidine Phosphorylase Gene Mutations in MNGIE, a Human Mitochondrial DisorderScience, 1999
- Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscleAnnals of Neurology, 1998
- Mitochondrial DNA Deletion Analysis: A Comparison of PCR Quantitative MethodsBiochemical and Biophysical Research Communications, 1995
- Cytochrome c oxidase activity in single muscle fibers: Assay techniques and diagnostic applicationsAnnals of Neurology, 1993
- Multiple short direct repeats associated with single mtDNA deletionsBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1992
- Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non‐invasive diagnosis of mitochondrial myopathyClinical Genetics, 1991
- Sequence and organization of the human mitochondrial genomeNature, 1981