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 A Stroud

Showing results (71-80 of 109) with videos related to

Pageof 11
Sort By:
American Journal of Human Genetics|January 28, 2014
A founder mutation in PET100 causes isolated complex IV deficiency in Lebanese individuals with Leigh syndromeSze Chern Lim, Katherine R Smith, David A Stroud, et al.
Proteomics|April 30, 2015
FunRich: An open access standalone functional enrichment and interaction network analysis toolMohashin Pathan, Shivakumar Keerthikumar, Ching-Seng Ang, et al.
Elife|June 18, 2021
Cavin3 released from caveolae interacts with BRCA1 to regulate the cellular stress responseKerrie-Ann McMahon, David A Stroud, Yann Gambin, et al.
Molecular Biology of the Cell|August 25, 2012
Role of mitochondrial inner membrane organizing system in protein biogenesis of the mitochondrial outer membraneMaria Bohnert, Lena-Sophie Wenz, Ralf M Zerbes, et al.
Cell Metabolism|October 5, 2022
Two independent respiratory chains adapt OXPHOS performance to glycolytic switchErika Fernández-Vizarra, Sandra López-Calcerrada, Ana Sierra-Magro, et al.
Molecular Cell|December 14, 2011
Dual function of Sdh3 in the respiratory chain and TIM22 protein translocase of the mitochondrial inner membraneNatalia Gebert, Michael Gebert, Silke Oeljeklaus, et al.
Human Molecular Genetics|May 3, 2023
Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial diseaseSumudu S C Amarasekera, Daniella H Hock, Nicole J Lake, et al.
Molecular Cell|June 27, 2025
Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translationJiemin Nah, Sreya Mahendran, Baptiste Kerouanton, et al.
International Journal of Molecular Sciences|February 25, 2023
Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head TraumaNicole J Van Bergen, Karen Gunanayagam, Adam M Bournazos, et al.
Nature Communications|March 3, 2025
Proximity proteomics reveals a mechanism of fatty acid transfer at lipid droplet-mitochondria- endoplasmic reticulum contact sitesAyenachew Bezawork-Geleta, Camille J Devereux, Stacey N Keenan, et al.
Pageof 11

Showing results (71-80 of 109) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|January 28, 2014
A founder mutation in PET100 causes isolated complex IV deficiency in Lebanese individuals with Leigh syndromeSze Chern Lim, Katherine R Smith, David A Stroud, et al.
Proteomics|April 30, 2015
FunRich: An open access standalone functional enrichment and interaction network analysis toolMohashin Pathan, Shivakumar Keerthikumar, Ching-Seng Ang, et al.
Elife|June 18, 2021
Cavin3 released from caveolae interacts with BRCA1 to regulate the cellular stress responseKerrie-Ann McMahon, David A Stroud, Yann Gambin, et al.
Molecular Biology of the Cell|August 25, 2012
Role of mitochondrial inner membrane organizing system in protein biogenesis of the mitochondrial outer membraneMaria Bohnert, Lena-Sophie Wenz, Ralf M Zerbes, et al.
Cell Metabolism|October 5, 2022
Two independent respiratory chains adapt OXPHOS performance to glycolytic switchErika Fernández-Vizarra, Sandra López-Calcerrada, Ana Sierra-Magro, et al.
Molecular Cell|December 14, 2011
Dual function of Sdh3 in the respiratory chain and TIM22 protein translocase of the mitochondrial inner membraneNatalia Gebert, Michael Gebert, Silke Oeljeklaus, et al.
Human Molecular Genetics|May 3, 2023
Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial diseaseSumudu S C Amarasekera, Daniella H Hock, Nicole J Lake, et al.
Molecular Cell|June 27, 2025
Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translationJiemin Nah, Sreya Mahendran, Baptiste Kerouanton, et al.
International Journal of Molecular Sciences|February 25, 2023
Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head TraumaNicole J Van Bergen, Karen Gunanayagam, Adam M Bournazos, et al.
Nature Communications|March 3, 2025
Proximity proteomics reveals a mechanism of fatty acid transfer at lipid droplet-mitochondria- endoplasmic reticulum contact sitesAyenachew Bezawork-Geleta, Camille J Devereux, Stacey N Keenan, et al.
Pageof 11