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Sze Chern Lim

Showing results (1-10 of 17) with videos related to

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American Journal of Cancer Research|May 15, 2015
Anti-cancer analogues ME-143 and ME-344 exert toxicity by directly inhibiting mitochondrial NADH: ubiquinone oxidoreductase (Complex I)Sze Chern Lim, Kirstyn T Carey, Matthew McKenzie
Journal of Molecular Biology|November 22, 2021
MicroRNA-101-3p Modulates Mitochondrial Metabolism via the Regulation of Complex II AssemblyMark Ziemann, Sze Chern Lim, Yilin Kang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 2, 2016
Loss of mitochondrial DNA-encoded protein ND1 results in disruption of complex I biogenesis during early stages of assemblySze Chern Lim, Jana Hroudová, Nicole J Van Bergen, et al.
Scientific Reports|January 11, 2018
Loss of the Mitochondrial Fatty Acid β-Oxidation Protein Medium-Chain Acyl-Coenzyme A Dehydrogenase Disrupts Oxidative Phosphorylation Protein Complex Stability and FunctionSze Chern Lim, Makiko Tajika, Masaru Shimura, et al.
European Journal of Human Genetics : EJHG|February 26, 2026
Mainstreaming genomic testing for mitochondrial disease in AustraliaMegan Ball, Naomi Baker, Sze Chern Lim, et al.
American Journal of Human Genetics|July 6, 2010
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndromeLisa G Riley, Sandra Cooper, Peter Hickey, et al.
Neurogenetics|January 5, 2019
Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndromeNurun Nahar Borna, Yoshihito Kishita, Masakazu Kohda, et al.
Human Mutation|September 16, 2014
Capture of somatic mtDNA point mutations with severe effects on oxidative phosphorylation in synaptosome cybrid clones from human brainMatthew McKenzie, Maria Chiotis, Jana Hroudová, et al.
Molecular Genetics and Metabolism Reports|September 5, 2022
Severe spinal cord hypoplasia due to a novel <i>ATAD3A</i> compound heterozygous deletionTomohiro Ebihara, Taro Nagatomo, Yohei Sugiyama, et al.
Human Molecular Genetics|July 2, 2013
Mutations in LYRM4, encoding iron-sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexesSze Chern Lim, Martin Friemel, Justine E Marum, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
American Journal of Cancer Research|May 15, 2015
Anti-cancer analogues ME-143 and ME-344 exert toxicity by directly inhibiting mitochondrial NADH: ubiquinone oxidoreductase (Complex I)Sze Chern Lim, Kirstyn T Carey, Matthew McKenzie
Journal of Molecular Biology|November 22, 2021
MicroRNA-101-3p Modulates Mitochondrial Metabolism via the Regulation of Complex II AssemblyMark Ziemann, Sze Chern Lim, Yilin Kang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 2, 2016
Loss of mitochondrial DNA-encoded protein ND1 results in disruption of complex I biogenesis during early stages of assemblySze Chern Lim, Jana Hroudová, Nicole J Van Bergen, et al.
Scientific Reports|January 11, 2018
Loss of the Mitochondrial Fatty Acid β-Oxidation Protein Medium-Chain Acyl-Coenzyme A Dehydrogenase Disrupts Oxidative Phosphorylation Protein Complex Stability and FunctionSze Chern Lim, Makiko Tajika, Masaru Shimura, et al.
European Journal of Human Genetics : EJHG|February 26, 2026
Mainstreaming genomic testing for mitochondrial disease in AustraliaMegan Ball, Naomi Baker, Sze Chern Lim, et al.
American Journal of Human Genetics|July 6, 2010
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndromeLisa G Riley, Sandra Cooper, Peter Hickey, et al.
Neurogenetics|January 5, 2019
Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndromeNurun Nahar Borna, Yoshihito Kishita, Masakazu Kohda, et al.
Human Mutation|September 16, 2014
Capture of somatic mtDNA point mutations with severe effects on oxidative phosphorylation in synaptosome cybrid clones from human brainMatthew McKenzie, Maria Chiotis, Jana Hroudová, et al.
Molecular Genetics and Metabolism Reports|September 5, 2022
Severe spinal cord hypoplasia due to a novel <i>ATAD3A</i> compound heterozygous deletionTomohiro Ebihara, Taro Nagatomo, Yohei Sugiyama, et al.
Human Molecular Genetics|July 2, 2013
Mutations in LYRM4, encoding iron-sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexesSze Chern Lim, Martin Friemel, Justine E Marum, et al.
Pageof 2