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Sarah E Calvo

Showing results (11-20 of 47) with videos related to

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Archives of Neurology|September 12, 2012
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsCaterina Garone, Juan Carlos Rubio, Sarah E Calvo, et al.
Cell|April 8, 2020
Genetic Screen for Cell Fitness in High or Low Oxygen Highlights Mitochondrial and Lipid MetabolismIsha H Jain, Sarah E Calvo, Andrew L Markhard, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 2025
Mitochondrial genome copy number variation across tissues in mice and humansSneha P Rath, Rahul Gupta, Ellen Todres, et al.
BMC Medical Genetics|March 8, 2014
Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiencyDaniel S Lieber, Steven G Hershman, Nancy G Slate, et al.
Cell Metabolism|September 27, 2016
A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative PhosphorylationJason D Arroyo, Alexis A Jourdain, Sarah E Calvo, et al.
BMC Medical Genetics|January 10, 2012
Atypical case of Wolfram syndrome revealed through targeted exome sequencing in a patient with suspected mitochondrial diseaseDaniel S Lieber, Scott B Vafai, Laura C Horton, et al.
Nature Communications|May 5, 2022
Combinatorial GxGxE CRISPR screen identifies SLC25A39 in mitochondrial glutathione transport linking iron homeostasis to OXPHOSXiaojian Shi, Bryn Reinstadler, Hardik Shah, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Nuclear genetic control of mtDNA copy number and heteroplasmy in humansRahul Gupta, Masahiro Kanai, Timothy J Durham, et al.
Neurogenetics|September 7, 2014
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathySenda Ajroud-Driss, Faisal Fecto, Kaouther Ajroud, et al.
Molecular Cell|April 14, 2021
Loss of LUC7L2 and U1 snRNP subunits shifts energy metabolism from glycolysis to OXPHOSAlexis A Jourdain, Bridget E Begg, Eran Mick, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Archives of Neurology|September 12, 2012
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsCaterina Garone, Juan Carlos Rubio, Sarah E Calvo, et al.
Cell|April 8, 2020
Genetic Screen for Cell Fitness in High or Low Oxygen Highlights Mitochondrial and Lipid MetabolismIsha H Jain, Sarah E Calvo, Andrew L Markhard, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 2025
Mitochondrial genome copy number variation across tissues in mice and humansSneha P Rath, Rahul Gupta, Ellen Todres, et al.
BMC Medical Genetics|March 8, 2014
Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiencyDaniel S Lieber, Steven G Hershman, Nancy G Slate, et al.
Cell Metabolism|September 27, 2016
A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative PhosphorylationJason D Arroyo, Alexis A Jourdain, Sarah E Calvo, et al.
BMC Medical Genetics|January 10, 2012
Atypical case of Wolfram syndrome revealed through targeted exome sequencing in a patient with suspected mitochondrial diseaseDaniel S Lieber, Scott B Vafai, Laura C Horton, et al.
Nature Communications|May 5, 2022
Combinatorial GxGxE CRISPR screen identifies SLC25A39 in mitochondrial glutathione transport linking iron homeostasis to OXPHOSXiaojian Shi, Bryn Reinstadler, Hardik Shah, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Nuclear genetic control of mtDNA copy number and heteroplasmy in humansRahul Gupta, Masahiro Kanai, Timothy J Durham, et al.
Neurogenetics|September 7, 2014
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathySenda Ajroud-Driss, Faisal Fecto, Kaouther Ajroud, et al.
Molecular Cell|April 14, 2021
Loss of LUC7L2 and U1 snRNP subunits shifts energy metabolism from glycolysis to OXPHOSAlexis A Jourdain, Bridget E Begg, Eran Mick, et al.
Pageof 5