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Ann Saada

Showing results (91-100 of 144) with videos related to

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Antioxidants (Basel, Switzerland)|January 26, 2024
High Sucrose Diet-Induced Subunit I Tyrosine 304 Phosphorylation of Cytochrome <i>c</i> Oxidase Leads to Liver Mitochondrial Respiratory Dysfunction in the Cohen Diabetic Rat ModelTasnim Arroum, Lucynda Pham, Taryn E Raisanen, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2014
Mitochondrial STAT3 plays a major role in IgE-antigen-mediated mast cell exocytosisTal Hadad Erlich, Zohar Yagil, Gillian Kay, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathyRonen Spiegel, Ann Saada, Jonatan Halvardson, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1Ofer Sarig, Dorit Goldsher, Janna Nousbeck, et al.
Molecular Genetics and Metabolism|October 25, 2011
Early prenatal ventriculomegaly due to an AIFM1 mutation identified by linkage analysis and whole exome sequencingItai Berger, Ziva Ben-Neriah, Talia Dor-Wolman, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Allele-specific antisense oligonucleotide treatment rescues <i>atad3-</i> associated phenotype in zebrafishShlomit Ezer, Shira Yanovsky-Dagan, Amit Granit, et al.
Journal of Alzheimer'S Disease : JAD|October 24, 2019
Mitochondrial Transfer Ameliorates Cognitive Deficits, Neuronal Loss, and Gliosis in Alzheimer's Disease MiceKeren Nitzan, Sandrine Benhamron, Michael Valitsky, et al.
The Journal of Biological Chemistry|January 4, 2013
Ablation of ceramide synthase 2 causes chronic oxidative stress due to disruption of the mitochondrial respiratory chainHila Zigdon, Aviram Kogot-Levin, Joo-Won Park, et al.
Journal of Medical Genetics|December 15, 2010
TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndromeRonen Spiegel, Morad Khayat, Stavit A Shalev, et al.
Bioorganic & Medicinal Chemistry|February 28, 2007
Novel selective human mitochondrial kinase inhibitors: design, synthesis and enzymatic activityNunzia Ciliberti, Stefano Manfredini, Angela Angusti, et al.
Pageof 15

Showing results (91-100 of 144) with videos related to

Sort By:
Pageof 15
Antioxidants (Basel, Switzerland)|January 26, 2024
High Sucrose Diet-Induced Subunit I Tyrosine 304 Phosphorylation of Cytochrome <i>c</i> Oxidase Leads to Liver Mitochondrial Respiratory Dysfunction in the Cohen Diabetic Rat ModelTasnim Arroum, Lucynda Pham, Taryn E Raisanen, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2014
Mitochondrial STAT3 plays a major role in IgE-antigen-mediated mast cell exocytosisTal Hadad Erlich, Zohar Yagil, Gillian Kay, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathyRonen Spiegel, Ann Saada, Jonatan Halvardson, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1Ofer Sarig, Dorit Goldsher, Janna Nousbeck, et al.
Molecular Genetics and Metabolism|October 25, 2011
Early prenatal ventriculomegaly due to an AIFM1 mutation identified by linkage analysis and whole exome sequencingItai Berger, Ziva Ben-Neriah, Talia Dor-Wolman, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Allele-specific antisense oligonucleotide treatment rescues <i>atad3-</i> associated phenotype in zebrafishShlomit Ezer, Shira Yanovsky-Dagan, Amit Granit, et al.
Journal of Alzheimer'S Disease : JAD|October 24, 2019
Mitochondrial Transfer Ameliorates Cognitive Deficits, Neuronal Loss, and Gliosis in Alzheimer's Disease MiceKeren Nitzan, Sandrine Benhamron, Michael Valitsky, et al.
The Journal of Biological Chemistry|January 4, 2013
Ablation of ceramide synthase 2 causes chronic oxidative stress due to disruption of the mitochondrial respiratory chainHila Zigdon, Aviram Kogot-Levin, Joo-Won Park, et al.
Journal of Medical Genetics|December 15, 2010
TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndromeRonen Spiegel, Morad Khayat, Stavit A Shalev, et al.
Bioorganic & Medicinal Chemistry|February 28, 2007
Novel selective human mitochondrial kinase inhibitors: design, synthesis and enzymatic activityNunzia Ciliberti, Stefano Manfredini, Angela Angusti, et al.
Pageof 15