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David A Stroud

Showing results (51-60 of 109) with videos related to

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NPJ Genomic Medicine|January 29, 2022
Oligonucleotide correction of an intronic TIMMDC1 variant in cells of patients with severe neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Nature Communications|December 20, 2023
Mtfp1 ablation enhances mitochondrial respiration and protects against hepatic steatosisCecilia Patitucci, Juan Diego Hernández-Camacho, Elodie Vimont, et al.
Nature|September 15, 2016
Accessory subunits are integral for assembly and function of human mitochondrial complex IDavid A Stroud, Elliot E Surgenor, Luke E Formosa, et al.
Journal of Lipid Research|November 14, 2025
HSD17β11 regulates PLIN5-ATGL mediated lipolysis, but not hepatic lipid metabolism in miceStacey N Keenan, Natasha D Suriani, Gio Fidelito, et al.
Molecular Biology of the Cell|January 21, 2021
The TIM22 complex mediates the import of sideroflexins and is required for efficient mitochondrial one-carbon metabolismThomas D Jackson, Daniella H Hock, Kenji M Fujihara, et al.
Journal of Molecular Biology|May 12, 2012
Role of MINOS in mitochondrial membrane architecture: cristae morphology and outer membrane interactions differentially depend on mitofilin domainsRalf M Zerbes, Maria Bohnert, David A Stroud, et al.
Human Molecular Genetics|July 11, 2015
COA6 is a mitochondrial complex IV assembly factor critical for biogenesis of mtDNA-encoded COX2David A Stroud, Megan J Maher, Caroline Lindau, et al.
Iscience|September 4, 2023
<i>LINC00116</i>-encoded microprotein mitoregulin regulates fatty acid metabolism at the mitochondrial outer membraneShan Zhang, Yabo Guo, Gio Fidelito, et al.
Clinical Genetics|July 10, 2026
Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome IntervalAngelo Condell, Elaine Zhang, Tim Sikora, et al.
Current Biology : CB|December 8, 2009
Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndromeNatalia Gebert, Amit S Joshi, Stephan Kutik, et al.
Pageof 11

Showing results (51-60 of 109) with videos related to

Sort By:
Pageof 11
NPJ Genomic Medicine|January 29, 2022
Oligonucleotide correction of an intronic TIMMDC1 variant in cells of patients with severe neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Nature Communications|December 20, 2023
Mtfp1 ablation enhances mitochondrial respiration and protects against hepatic steatosisCecilia Patitucci, Juan Diego Hernández-Camacho, Elodie Vimont, et al.
Nature|September 15, 2016
Accessory subunits are integral for assembly and function of human mitochondrial complex IDavid A Stroud, Elliot E Surgenor, Luke E Formosa, et al.
Journal of Lipid Research|November 14, 2025
HSD17β11 regulates PLIN5-ATGL mediated lipolysis, but not hepatic lipid metabolism in miceStacey N Keenan, Natasha D Suriani, Gio Fidelito, et al.
Molecular Biology of the Cell|January 21, 2021
The TIM22 complex mediates the import of sideroflexins and is required for efficient mitochondrial one-carbon metabolismThomas D Jackson, Daniella H Hock, Kenji M Fujihara, et al.
Journal of Molecular Biology|May 12, 2012
Role of MINOS in mitochondrial membrane architecture: cristae morphology and outer membrane interactions differentially depend on mitofilin domainsRalf M Zerbes, Maria Bohnert, David A Stroud, et al.
Human Molecular Genetics|July 11, 2015
COA6 is a mitochondrial complex IV assembly factor critical for biogenesis of mtDNA-encoded COX2David A Stroud, Megan J Maher, Caroline Lindau, et al.
Iscience|September 4, 2023
<i>LINC00116</i>-encoded microprotein mitoregulin regulates fatty acid metabolism at the mitochondrial outer membraneShan Zhang, Yabo Guo, Gio Fidelito, et al.
Clinical Genetics|July 10, 2026
Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome IntervalAngelo Condell, Elaine Zhang, Tim Sikora, et al.
Current Biology : CB|December 8, 2009
Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndromeNatalia Gebert, Amit S Joshi, Stephan Kutik, et al.
Pageof 11