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

David R Thorburn

Showing results (21-30 of 173) with videos related to

Pageof 18
Sort By:
IUBMB Life|July 19, 2011
The molecular basis of human complex I deficiencyElena J Tucker, Alison G Compton, Sarah E Calvo, et al.
Helicobacter|February 10, 2017
No evidence of a role for mitochondrial complex I in Helicobacter pylori pathogenesisGarrett Z Ng, Bi-Xia Ke, Adrienne Laskowski, et al.
European Journal of Human Genetics : EJHG|June 8, 2021
Genomic sequencing for the diagnosis of childhood mitochondrial disorders: a health economic evaluationYou Wu, Shanti Balasubramaniam, Rocio Rius, et al.
The FEBS Journal|October 22, 2009
Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondriaMichael Lazarou, Stacey M Smith, David R Thorburn, et al.
Open Biology|December 7, 2022
Mitochondrial biology and dysfunction in secondary mitochondrial diseaseMegan J Baker, Jordan J Crameri, David R Thorburn, et al.
Stem Cell Research|January 7, 2026
Generation of a pluripotent human AGK knockout embryonic stem cell model (WAe009-A-3C) of Sengers syndromeYau Chung Low, Cameron L McKnight, Diana Stojanovski, et al.
JIMD Reports|April 11, 2014
Thiamine-Responsive and Non-responsive Patients with PDHC-E1 Deficiency: A Retrospective AssessmentSanne van Dongen, Ruth M Brown, Garry K Brown, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2019
Biparental inheritance of mitochondrial DNA in humans is not a common phenomenonRocio Rius, Mark J Cowley, Lisa Riley, et al.
NPJ Genomic Medicine|March 31, 2025
Review: Utility of mass spectrometry in rare disease research and diagnosisTeresa Zhao, Daniella H Hock, James Pitt, et al.
Stem Cell Research|March 13, 2026
Generation of a pluripotent embryonic stem cell TAFAZZIN hESC model (WAe009-A-3H) of Barth syndromeYau Chung Low, Cameron L McKnight, David A Elliott, et al.
Pageof 18

Showing results (21-30 of 173) with videos related to

Sort By:
Pageof 18
IUBMB Life|July 19, 2011
The molecular basis of human complex I deficiencyElena J Tucker, Alison G Compton, Sarah E Calvo, et al.
Helicobacter|February 10, 2017
No evidence of a role for mitochondrial complex I in Helicobacter pylori pathogenesisGarrett Z Ng, Bi-Xia Ke, Adrienne Laskowski, et al.
European Journal of Human Genetics : EJHG|June 8, 2021
Genomic sequencing for the diagnosis of childhood mitochondrial disorders: a health economic evaluationYou Wu, Shanti Balasubramaniam, Rocio Rius, et al.
The FEBS Journal|October 22, 2009
Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondriaMichael Lazarou, Stacey M Smith, David R Thorburn, et al.
Open Biology|December 7, 2022
Mitochondrial biology and dysfunction in secondary mitochondrial diseaseMegan J Baker, Jordan J Crameri, David R Thorburn, et al.
Stem Cell Research|January 7, 2026
Generation of a pluripotent human AGK knockout embryonic stem cell model (WAe009-A-3C) of Sengers syndromeYau Chung Low, Cameron L McKnight, Diana Stojanovski, et al.
JIMD Reports|April 11, 2014
Thiamine-Responsive and Non-responsive Patients with PDHC-E1 Deficiency: A Retrospective AssessmentSanne van Dongen, Ruth M Brown, Garry K Brown, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2019
Biparental inheritance of mitochondrial DNA in humans is not a common phenomenonRocio Rius, Mark J Cowley, Lisa Riley, et al.
NPJ Genomic Medicine|March 31, 2025
Review: Utility of mass spectrometry in rare disease research and diagnosisTeresa Zhao, Daniella H Hock, James Pitt, et al.
Stem Cell Research|March 13, 2026
Generation of a pluripotent embryonic stem cell TAFAZZIN hESC model (WAe009-A-3H) of Barth syndromeYau Chung Low, Cameron L McKnight, David A Elliott, et al.
Pageof 18