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Trends in Genetics : TIG|August 18, 2004
Two direct repeats cause most human mtDNA deletionsDavid C Samuels, Eric A Schon, Patrick F Chinnery
American Journal of Human Genetics|November 4, 2008
The distribution of mitochondrial DNA heteroplasmy due to random genetic driftPassorn Wonnapinij, Patrick F Chinnery, David C Samuels
Human Reproduction (Oxford, England)|January 9, 2013
Preventing the transmission of pathogenic mitochondrial DNA mutations: Can we achieve long-term benefits from germ-line gene transfer?David C Samuels, Passorn Wonnapinij, Patrick F Chinnery
American Journal of Human Genetics|February 7, 2008
Selection against pathogenic mtDNA mutations in a stem cell population leads to the loss of the 3243A-->G mutation in bloodHarsha Karur Rajasimha, Patrick F Chinnery, David C Samuels
Journal of Theoretical Biology|April 26, 2003
A model of the nuclear control of mitochondrial DNA replicationGraham J Capps, David C Samuels, Patrick F Chinnery
Lancet (London, England)|November 5, 2002
Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?Patrick F Chinnery, David C Samuels, Joanna Elson, et al.
American Journal of Human Genetics|March 15, 2006
The power to detect disease associations with mitochondrial DNA haplogroupsDavid C Samuels, Andrew D Carothers, Robin Horton, et al.
Nucleic Acids Research|October 8, 2003
A compositional segmentation of the human mitochondrial genome is related to heterogeneities in the guanine mutation rateDavid C Samuels, Richard J Boys, Daniel A Henderson, et al.
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