Heteroplasmy of the Human mtDNA Control Region Remains Constant during Life

This publication has 14 references indexed in Scilit:

• A Sensitive Denaturing Gradient-Gel Electrophoresis Assay Reveals a High Frequency of Heteroplasmy in Hypervariable Region 1 of the Human mtDNA Control Region**Disclaimer: The opinions and assertions expressed herein are solely those of the authors and are not to be construed as official or the views of the United States Department of Defense, the United States Department of the Army, or the United States Department of Commerce. This paper is a contribution of the United States National Institute of Standards and Technology (NIST) and the United States Department of Defense and is not subject to copyright. Certain commercial equipment, instruments, or companies are identified in this paper to specify the experimental procedure. Such identification does not imply recommendation or endorsement by the government, nor does it imply that the materials or equipment identified are the best available for this purpose.
  American Journal of Human Genetics, 2000
• Persistent Heteroplasmy of a Mutation in the Human mtDNA Control Region: Hypermutation as an Apparent Consequence of Simple-Repeat Expansion/Contraction
  American Journal of Human Genetics, 2000
• The Frequency of Heteroplasmy in the HVII Region of mtDNA Differs across Tissue Types and Increases with Age
  American Journal of Human Genetics, 2000
• Aging-Dependent Large Accumulation of Point Mutations in the Human mtDNA Control Region for Replication
  Science, 1999
• A high observed substitution rate in the human mitochondrial DNA control region
  Nature Genetics, 1997
• Human brain contains high levels of heteroplasmy in the noncoding regions of mitochondrial DNA.
  Proceedings of the National Academy of Sciences, 1996
• Mitochondrial DNA sequence heteroplasmy in the Grand Duke of Russia Georgij Romanov establishes the authenticity of the remains of Tsar Nicholas II
  Nature Genetics, 1996
• Heteroplasmy in the control region of human mitochondrial DNA.
  Genome Research, 1995
• Quantification of point mutations associated with Leber hereditary optic neuroretinopathy by solid-phase minisequencing
  Human Genetics, 1994
• Quantification of tRNA₃₂₄₃^Leu point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription
  Human Molecular Genetics, 1993