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Ann Saada

Showing results (71-80 of 144) with videos related to

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Plos One|June 12, 2018
Pathological presentation of cardiac mitochondria in a rat model for chronic kidney diseaseEinat Bigelman, Lena Cohen, Genya Aharon-Hananel, et al.
Journal of Medical Genetics|August 27, 2015
Hypomyelination and developmental delay associated with VPS11 mutation in Ashkenazi-Jewish patientsShimon Edvardson, Frank Gerhard, Chaim Jalas, et al.
European Journal of Human Genetics : EJHG|March 5, 2009
Mutated NDUFS6 is the cause of fatal neonatal lactic acidemia in Caucasus JewsRonen Spiegel, Avraham Shaag, Hanna Mandel, et al.
Endocrine-Related Cancer|June 27, 2015
Development of pheochromocytoma in ceramide synthase 2 null miceWoo-Jae Park, Ori Brenner, Aviram Kogot-Levin, et al.
European Journal of Human Genetics : EJHG|August 4, 2016
Mitochondrial hepato-encephalopathy due to deficiency of QIL1/MIC13 (C19orf70), a MICOS complex subunitAvraham Zeharia, Jonathan R Friedman, Ana Tobar, et al.
American Journal of Physiology. Endocrinology and Metabolism|March 21, 2013
Dietary copper supplementation restores β-cell function of Cohen diabetic rats: a link between mitochondrial function and glucose-stimulated insulin secretionSarah Weksler-Zangen, Anne Jörns, Limor Tarsi-Chen, et al.
American Journal of Human Genetics|May 7, 2005
Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletionOrly Elpeleg, Chaya Miller, Eli Hershkovitz, et al.
Journal of Cell Science|March 11, 2017
Oxidative stress elicited by modifying the ceramide acyl chain length reduces the rate of clathrin-mediated endocytosisGiora Volpert, Shifra Ben-Dor, Ohad Tarcic, et al.
Antioxidants (Basel, Switzerland)|February 27, 2026
Integrative Proteomic and Bioenergetic Profiling Reveals Diet- and Strain-Specific Mitochondrial Dysfunction in Cohen Diabetic Rat HeartsLauren Pavelich, Tasnim Arroum, Lucynda Pham, et al.
European Journal of Human Genetics : EJHG|June 17, 2010
Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenaseAviva Levitas, Emad Muhammad, Gali Harel, et al.
Pageof 15

Showing results (71-80 of 144) with videos related to

Sort By:
Pageof 15
Plos One|June 12, 2018
Pathological presentation of cardiac mitochondria in a rat model for chronic kidney diseaseEinat Bigelman, Lena Cohen, Genya Aharon-Hananel, et al.
Journal of Medical Genetics|August 27, 2015
Hypomyelination and developmental delay associated with VPS11 mutation in Ashkenazi-Jewish patientsShimon Edvardson, Frank Gerhard, Chaim Jalas, et al.
European Journal of Human Genetics : EJHG|March 5, 2009
Mutated NDUFS6 is the cause of fatal neonatal lactic acidemia in Caucasus JewsRonen Spiegel, Avraham Shaag, Hanna Mandel, et al.
Endocrine-Related Cancer|June 27, 2015
Development of pheochromocytoma in ceramide synthase 2 null miceWoo-Jae Park, Ori Brenner, Aviram Kogot-Levin, et al.
European Journal of Human Genetics : EJHG|August 4, 2016
Mitochondrial hepato-encephalopathy due to deficiency of QIL1/MIC13 (C19orf70), a MICOS complex subunitAvraham Zeharia, Jonathan R Friedman, Ana Tobar, et al.
American Journal of Physiology. Endocrinology and Metabolism|March 21, 2013
Dietary copper supplementation restores β-cell function of Cohen diabetic rats: a link between mitochondrial function and glucose-stimulated insulin secretionSarah Weksler-Zangen, Anne Jörns, Limor Tarsi-Chen, et al.
American Journal of Human Genetics|May 7, 2005
Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletionOrly Elpeleg, Chaya Miller, Eli Hershkovitz, et al.
Journal of Cell Science|March 11, 2017
Oxidative stress elicited by modifying the ceramide acyl chain length reduces the rate of clathrin-mediated endocytosisGiora Volpert, Shifra Ben-Dor, Ohad Tarcic, et al.
Antioxidants (Basel, Switzerland)|February 27, 2026
Integrative Proteomic and Bioenergetic Profiling Reveals Diet- and Strain-Specific Mitochondrial Dysfunction in Cohen Diabetic Rat HeartsLauren Pavelich, Tasnim Arroum, Lucynda Pham, et al.
European Journal of Human Genetics : EJHG|June 17, 2010
Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenaseAviva Levitas, Emad Muhammad, Gali Harel, et al.
Pageof 15