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Tal Yardeni

Showing results (21-30 of 27) with videos related to

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The American Journal of Pathology|February 11, 2012
The Gne M712T mouse as a model for human glomerulopathySravan Kakani, Tal Yardeni, Justin Poling, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2022
Combination of common mtDNA variants results in mitochondrial dysfunction and a connective tissue dysregulationPatrick M Schaefer, Leonardo Scherer Alves, Maria Lvova, et al.
Human Gene Therapy|April 27, 2011
Hereditary inclusion body myopathy: single patient response to intravenous dosing of GNE gene lipoplexGregory Nemunaitis, Chris M Jay, Phillip B Maples, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 3, 2025
Mitochondrial DNA lineages determine tumor progression through T cell reactive oxygen signalingTal Yardeni, Arnold Z Olali, Hsiao-Wen Chen, et al.
Human Mutation|October 19, 2017
A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiencyMay Christine V Malicdan, Thierry Vilboux, Bruria Ben-Zeev, et al.
Brain : a Journal of Neurology|April 2, 2017
Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathyOrtal Barel, May Christine V Malicdan, Bruria Ben-Zeev, et al.
Cell|December 16, 2025
HLA export by melanoma cells decoys cytotoxic T cells to promote immune evasionYoav Chemla, Orit Itzhaki, Stav Melamed, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
The American Journal of Pathology|February 11, 2012
The Gne M712T mouse as a model for human glomerulopathySravan Kakani, Tal Yardeni, Justin Poling, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2022
Combination of common mtDNA variants results in mitochondrial dysfunction and a connective tissue dysregulationPatrick M Schaefer, Leonardo Scherer Alves, Maria Lvova, et al.
Human Gene Therapy|April 27, 2011
Hereditary inclusion body myopathy: single patient response to intravenous dosing of GNE gene lipoplexGregory Nemunaitis, Chris M Jay, Phillip B Maples, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 3, 2025
Mitochondrial DNA lineages determine tumor progression through T cell reactive oxygen signalingTal Yardeni, Arnold Z Olali, Hsiao-Wen Chen, et al.
Human Mutation|October 19, 2017
A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiencyMay Christine V Malicdan, Thierry Vilboux, Bruria Ben-Zeev, et al.
Brain : a Journal of Neurology|April 2, 2017
Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathyOrtal Barel, May Christine V Malicdan, Bruria Ben-Zeev, et al.
Cell|December 16, 2025
HLA export by melanoma cells decoys cytotoxic T cells to promote immune evasionYoav Chemla, Orit Itzhaki, Stav Melamed, et al.
Pageof 3