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Brain : a Journal of Neurology|October 4, 2017
Monitoring clinical progression with mitochondrial disease biomarkersHannah E Steele, Rita Horvath, Jon J Lyon, 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.Trends in Genetics : TIG|September 13, 2005
mtDNA mutations and common neurodegenerative disordersNeil Howell, Joanna L Elson, Patrick F Chinnery, et al.Methods in Molecular Biology (Clifton, N.J.)|January 30, 2015
Deep resequencing of mitochondrial DNABrendan A I Payne, Kristian Gardner, Jonathan Coxhead, et al.Proceedings of the National Academy of Sciences of the United States of America|June 11, 2010
Dissociation of duration-based and beat-based auditory timing in cerebellar degenerationManon Grube, Freya E Cooper, Patrick F Chinnery, et al.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.Plos Genetics|May 24, 2014
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseasesGavin Hudson, Aurora Gomez-Duran, Ian J Wilson, et al.European Journal of Human Genetics : EJHG|June 5, 2014
Use of stereotypical mutational motifs to define resolution limits for the ultra-deep resequencing of mitochondrial DNAKristian Gardner, Brendan A I Payne, Rita Horvath, et al.Toxicologic Pathology|September 27, 2013
HIV treatment and associated mitochondrial pathology: review of 25 years of in vitro, animal, and human studiesKristian Gardner, Peter A Hall, Patrick F Chinnery, et al.Journal of Neuromuscular Diseases|November 19, 2016
Adult-onset Mendelian PEO Associated with Mitochondrial DiseaseEwen W Sommerville, Patrick F Chinnery, Gráinne S Gorman, et al.Pageof 43