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Ophry Pines

Showing results (41-50 of 56) with videos related to

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Iscience|November 22, 2021
Fumarase affects the deoxyribonucleic acid damage response by protecting the mitochondrial desulfurase Nfs1p from modification and inactivationJoyce Yip, Suqing Wang, Jasper Tan, et al.
Annals of Neurology|October 3, 2009
SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosisRonen Spiegel, Avraham Shaag, Simon Edvardson, et al.
Cells|June 10, 2023
Systematic Approaches to Study Eclipsed Targeting of Proteins Uncover a New Family of Mitochondrial ProteinsMaayan Mark, Ofir Klein, Yu Zhang, et al.
Neurogenetics|January 7, 2017
Homozygous mutation, p.Pro304His, in IDH3A, encoding isocitrate dehydrogenase subunit is associated with severe encephalopathy in infancyAviva Fattal-Valevski, Hila Eliyahu, NItai D Fraenkel, et al.
Journal of Molecular Biology|October 15, 2020
Post-translational Modifications of Fumarase Regulate its Enzyme Activity and Function in Respiration and the DNA Damage ResponseSuqing Wang, Dharanidharan Ramamurthy, Jasper Tan, et al.
Journal of Molecular Medicine (Berlin, Germany)|September 19, 2019
A combination of two novel VARS2 variants causes a mitochondrial disorder associated with failure to thrive and pulmonary hypertensionHui-Lin Chin, Denise Li-Meng Goh, Furene Sijia Wang, et al.
American Journal of Human Genetics|March 13, 2012
Infantile cerebellar-retinal degeneration associated with a mutation in mitochondrial aconitase, ACO2Ronen Spiegel, Ophry Pines, Asaf Ta-Shma, et al.
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.
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|October 19, 2010
Infantile cerebral and cerebellar atrophy is associated with a mutation in the MED17 subunit of the transcription preinitiation mediator complexRami Kaufmann, Rachel Straussberg, Hanna Mandel, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Iscience|November 22, 2021
Fumarase affects the deoxyribonucleic acid damage response by protecting the mitochondrial desulfurase Nfs1p from modification and inactivationJoyce Yip, Suqing Wang, Jasper Tan, et al.
Annals of Neurology|October 3, 2009
SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosisRonen Spiegel, Avraham Shaag, Simon Edvardson, et al.
Cells|June 10, 2023
Systematic Approaches to Study Eclipsed Targeting of Proteins Uncover a New Family of Mitochondrial ProteinsMaayan Mark, Ofir Klein, Yu Zhang, et al.
Neurogenetics|January 7, 2017
Homozygous mutation, p.Pro304His, in IDH3A, encoding isocitrate dehydrogenase subunit is associated with severe encephalopathy in infancyAviva Fattal-Valevski, Hila Eliyahu, NItai D Fraenkel, et al.
Journal of Molecular Biology|October 15, 2020
Post-translational Modifications of Fumarase Regulate its Enzyme Activity and Function in Respiration and the DNA Damage ResponseSuqing Wang, Dharanidharan Ramamurthy, Jasper Tan, et al.
Journal of Molecular Medicine (Berlin, Germany)|September 19, 2019
A combination of two novel VARS2 variants causes a mitochondrial disorder associated with failure to thrive and pulmonary hypertensionHui-Lin Chin, Denise Li-Meng Goh, Furene Sijia Wang, et al.
American Journal of Human Genetics|March 13, 2012
Infantile cerebellar-retinal degeneration associated with a mutation in mitochondrial aconitase, ACO2Ronen Spiegel, Ophry Pines, Asaf Ta-Shma, et al.
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.
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|October 19, 2010
Infantile cerebral and cerebellar atrophy is associated with a mutation in the MED17 subunit of the transcription preinitiation mediator complexRami Kaufmann, Rachel Straussberg, Hanna Mandel, et al.
Pageof 6