Showing results (241-250 of 370) with videos related to
Sort By:
Pageof 37
Human Genomics|February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohortsAnna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.Journal of Neuromuscular Diseases|November 19, 2016
Adult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial DiseaseMaria Wesolowska, Grainne S Gorman, Charlotte L Alston, et al.Nature Genetics|October 9, 2012
Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmissionChristoph Freyer, Lynsey M Cree, Arnaud Mourier, et al.Annals of Neurology|August 9, 2007
Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's diseaseAn Goris, Caroline H Williams-Gray, Graeme R Clark, et al.Molecular Cell|August 31, 2022
The human mitochondrial genome contains a second light strand promoterBenedict G Tan, Christian D Mutti, Yonghong Shi, et al.Brain : a Journal of Neurology|December 11, 2007
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenanceGavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, et al.The Journal of Clinical Investigation|November 5, 2003
Mitochondrial DNA mutations in human colonic crypt stem cellsRobert W Taylor, Martin J Barron, Gillian M Borthwick, et al.Plos One|October 3, 2013
Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegiaCynthia Yu-Wai-Man, Fiona E Smith, Michael J Firbank, et al.Science Advances|December 8, 2021
Mitochondrial DNA heteroplasmy is modulated during oocyte development propagating mutation transmissionHaixin Zhang, Marco Esposito, Mikael G Pezet, et al.Neurology. Genetics|April 29, 2016
Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhoodDavid Lewis-Smith, Kimberli J Kamer, Helen Griffin, et al.Pageof 37