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American Journal of Human Genetics|February 17, 2001
Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with ageJ L Elson, D C Samuels, D M Turnbull, et al.Nature Genetics|February 1, 1997
Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acidsR W Taylor, P F Chinnery, D M Turnbull, et al.Methods in Molecular Medicine|February 22, 2012
Analysis of mitochondrial DNA mutations : point mutationsR W Taylor, R M Andrews, P F Chinnery, et al.Eye (London, England)|March 9, 2000
Evaluation of bupivacaine-induced muscle regeneration in the treatment of ptosis in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndromeR M Andrews, P G Griffiths, P F Chinnery, et al.American Journal of Medical Genetics|February 13, 2001
Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?P F Chinnery, R M Andrews, D M Turnbull, et al.Human Reproduction (Oxford, England)|October 21, 2000
Transmission of the human mitochondrial genomeN Howell, P F Chinnery, S S Ghosh, et al.Neurology|October 27, 1997
CSF antigliadin antibodies and the Ramsay Hunt syndromeP F Chinnery, P J Reading, D Milne, et al.Neurology|October 27, 1997
A novel mitochondrial tRNA isoleucine gene mutation causing chronic progressive external ophthalmoplegiaP F Chinnery, M A Johnson, R W Taylor, et al.Annals of Neurology|March 1, 1997
A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysisP F Chinnery, M A Johnson, R W Taylor, et al.American Journal of Human Genetics|January 3, 2001
Random genetic drift determines the level of mutant mtDNA in human primary oocytesD T Brown, D C Samuels, E M Michael, et al.Pageof 27