Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Patrick F Chinnery

Showing results (251-260 of 473) with videos related to

Pageof 48
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 2012
Adult-onset spinocerebellar ataxia syndromes due to MTATP6 mutationsGerald Pfeffer, Emma L Blakely, Charlotte L Alston, et al.
Nature Genetics|June 28, 2011
Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutationsBrendan A I Payne, Ian J Wilson, Charlotte A Hateley, et al.
Nature Reviews. Disease Primers|October 25, 2016
Mitochondrial diseasesGráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, et al.
Journal of Neuromuscular Diseases|May 17, 2024
Increased Diagnostic Yield by Reanalysis of Whole Exome Sequencing Data in Mitochondrial DiseaseCatarina Olimpio, Ida Paramonov, Leslie Matalonga, et al.
Human Molecular Genetics|May 21, 2010
OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA moleculesPatrick Yu-Wai-Man, Kamil S Sitarz, David C Samuels, et al.
Journal of Neurogenetics|November 5, 2013
Late-onset sacsinopathy diagnosed by exome sequencing and comparative genomic hybridizationAngela Pyle, Helen Griffin, Jennifer Duff, et al.
Hearing, Balance and Communication|June 4, 2016
The frequency of the m.1555A>G (<i>MTRNR1</i>) variant in UK patients with suspected mitochondrial deafnessPeter Kullar, Charlotte L Alston, Sarah Ball, et al.
Annals of Neurology|May 21, 2014
Molecular pathogenesis of polymerase γ-related neurodegenerationCharalampos Tzoulis, Gia Tuong Tran, Jonathan Coxhead, et al.
Brain : a Journal of Neurology|April 12, 2012
MFN2 mutations cause compensatory mitochondrial DNA proliferationKamil S Sitarz, Patrick Yu-Wai-Man, Angela Pyle, et al.
Lancet (London, England)|December 20, 2005
Mitochondrial DNA and survival after sepsis: a prospective studySimon V Baudouin, David Saunders, Watcharee Tiangyou, et al.
Pageof 48

Showing results (251-260 of 473) with videos related to

Sort By:
Pageof 48
Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 2012
Adult-onset spinocerebellar ataxia syndromes due to MTATP6 mutationsGerald Pfeffer, Emma L Blakely, Charlotte L Alston, et al.
Nature Genetics|June 28, 2011
Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutationsBrendan A I Payne, Ian J Wilson, Charlotte A Hateley, et al.
Nature Reviews. Disease Primers|October 25, 2016
Mitochondrial diseasesGráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, et al.
Journal of Neuromuscular Diseases|May 17, 2024
Increased Diagnostic Yield by Reanalysis of Whole Exome Sequencing Data in Mitochondrial DiseaseCatarina Olimpio, Ida Paramonov, Leslie Matalonga, et al.
Human Molecular Genetics|May 21, 2010
OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA moleculesPatrick Yu-Wai-Man, Kamil S Sitarz, David C Samuels, et al.
Journal of Neurogenetics|November 5, 2013
Late-onset sacsinopathy diagnosed by exome sequencing and comparative genomic hybridizationAngela Pyle, Helen Griffin, Jennifer Duff, et al.
Hearing, Balance and Communication|June 4, 2016
The frequency of the m.1555A>G (<i>MTRNR1</i>) variant in UK patients with suspected mitochondrial deafnessPeter Kullar, Charlotte L Alston, Sarah Ball, et al.
Annals of Neurology|May 21, 2014
Molecular pathogenesis of polymerase γ-related neurodegenerationCharalampos Tzoulis, Gia Tuong Tran, Jonathan Coxhead, et al.
Brain : a Journal of Neurology|April 12, 2012
MFN2 mutations cause compensatory mitochondrial DNA proliferationKamil S Sitarz, Patrick Yu-Wai-Man, Angela Pyle, et al.
Lancet (London, England)|December 20, 2005
Mitochondrial DNA and survival after sepsis: a prospective studySimon V Baudouin, David Saunders, Watcharee Tiangyou, et al.
Pageof 48