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

Ann Saada

Showing results (111-120 of 144) with videos related to

Pageof 15
Sort By:
EMBO Reports|March 17, 2023
Mitochondrial-derived vesicles retain membrane potential and contain a functional ATP synthaseReut Hazan Ben-Menachem, Dvora Lintzer, Tamar Ziv, et al.
Orphanet Journal of Rare Diseases|April 24, 2025
Using chanarin-dorfman syndrome patient fibroblasts to explore disease mechanisms and new treatment avenuesMor Angel, Yuval Kleinberg, Tanmoy Newaz, et al.
European Journal of Human Genetics : EJHG|January 16, 2014
Delineation of C12orf65-related phenotypes: a genotype-phenotype relationshipRonen Spiegel, Hanna Mandel, Ann Saada, et al.
Neurochemical Research|April 11, 2019
Primary Coenzyme Q deficiency Due to Novel ADCK3 Variants, Studies in Fibroblasts and Review of LiteratureAdel Shalata, Michael Edery, Clair Habib, et al.
Brain : a Journal of Neurology|November 17, 2021
Infantile SOD1 deficiency syndrome caused by a homozygous SOD1 variant with absence of enzyme activityShlomit Ezer, Muhannad Daana, Julien H Park, et al.
American Journal of Human Genetics|September 27, 2008
Mutations in LPIN1 cause recurrent acute myoglobinuria in childhoodAvraham Zeharia, Avraham Shaag, Riekelt H Houtkooper, et al.
American Journal of Human Genetics|September 8, 2009
Acute infantile liver failure due to mutations in the TRMU geneAvraham Zeharia, Avraham Shaag, Orit Pappo, et al.
Cells|April 13, 2023
The Beneficial Effect of Mitochondrial Transfer Therapy in 5XFAD Mice via Liver-Serum-Brain ResponseSahar Sweetat, Keren Nitzan, Nir Suissa, et al.
Cells|February 15, 2022
Multifaceted Analyses of Isolated Mitochondria Establish the Anticancer Drug 2-Hydroxyoleic Acid as an Inhibitor of Substrate Oxidation and an Activator of Complex IV-Dependent State 3 RespirationKumudesh Mishra, Mária Péter, Anna Maria Nardiello, et al.
Antioxidants (Basel, Switzerland)|January 28, 2026
Bioenergetic Signatures of DLD Deficiency: Dissecting PDHc- and α-KGDHc-Linked DefectsYarden Haham Zarbib, Shira Huri Ohev-Shalom, Shani Kassia Lyskov, et al.
Pageof 15

Showing results (111-120 of 144) with videos related to

Sort By:
Pageof 15
EMBO Reports|March 17, 2023
Mitochondrial-derived vesicles retain membrane potential and contain a functional ATP synthaseReut Hazan Ben-Menachem, Dvora Lintzer, Tamar Ziv, et al.
Orphanet Journal of Rare Diseases|April 24, 2025
Using chanarin-dorfman syndrome patient fibroblasts to explore disease mechanisms and new treatment avenuesMor Angel, Yuval Kleinberg, Tanmoy Newaz, et al.
European Journal of Human Genetics : EJHG|January 16, 2014
Delineation of C12orf65-related phenotypes: a genotype-phenotype relationshipRonen Spiegel, Hanna Mandel, Ann Saada, et al.
Neurochemical Research|April 11, 2019
Primary Coenzyme Q deficiency Due to Novel ADCK3 Variants, Studies in Fibroblasts and Review of LiteratureAdel Shalata, Michael Edery, Clair Habib, et al.
Brain : a Journal of Neurology|November 17, 2021
Infantile SOD1 deficiency syndrome caused by a homozygous SOD1 variant with absence of enzyme activityShlomit Ezer, Muhannad Daana, Julien H Park, et al.
American Journal of Human Genetics|September 27, 2008
Mutations in LPIN1 cause recurrent acute myoglobinuria in childhoodAvraham Zeharia, Avraham Shaag, Riekelt H Houtkooper, et al.
American Journal of Human Genetics|September 8, 2009
Acute infantile liver failure due to mutations in the TRMU geneAvraham Zeharia, Avraham Shaag, Orit Pappo, et al.
Cells|April 13, 2023
The Beneficial Effect of Mitochondrial Transfer Therapy in 5XFAD Mice via Liver-Serum-Brain ResponseSahar Sweetat, Keren Nitzan, Nir Suissa, et al.
Cells|February 15, 2022
Multifaceted Analyses of Isolated Mitochondria Establish the Anticancer Drug 2-Hydroxyoleic Acid as an Inhibitor of Substrate Oxidation and an Activator of Complex IV-Dependent State 3 RespirationKumudesh Mishra, Mária Péter, Anna Maria Nardiello, et al.
Antioxidants (Basel, Switzerland)|January 28, 2026
Bioenergetic Signatures of DLD Deficiency: Dissecting PDHc- and α-KGDHc-Linked DefectsYarden Haham Zarbib, Shira Huri Ohev-Shalom, Shani Kassia Lyskov, et al.
Pageof 15