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Olga Derbeneva

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Annals of the New York Academy of Sciences|December 17, 2008
A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's diseaseElza Khusnutdinova, Irina Gilyazova, Eduardo Ruiz-Pesini, et al.
Current Protocols in Bioinformatics|December 10, 2014
mtDNA Variation and Analysis Using Mitomap and MitomasterMarie T Lott, Jeremy N Leipzig, Olga Derbeneva, et al.
JAMA Psychiatry|August 24, 2017
Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum DisordersDimitra Chalkia, Larry N Singh, Jeremy Leipzig, et al.
Human Genetics|April 6, 2002
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup JMichael D Brown, Elena Starikovskaya, Olga Derbeneva, et al.
Pediatric Research|August 31, 2006
Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndromeJosé A Camacho, Rebecca Mardach, Natalia Rioseco-Camacho, et al.
Biochimica Et Biophysica Acta. Bioenergetics|July 13, 2018
Mitochondrial DNA associations with East Asian metabolic syndromeDimitra Chalkia, Yi-Cheng Chang, Olga Derbeneva, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
Mitochondrial energy deficiency leads to hyperproliferation of skeletal muscle mitochondria and enhanced insulin sensitivityRyan M Morrow, Martin Picard, Olga Derbeneva, et al.
Neurobiology of Aging|June 12, 2010
Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohortAnita Lakatos, Olga Derbeneva, Danny Younes, et al.
Journal of Endourology|September 29, 2025
Electromotive Drug Administration in the Porcine Ureter: First <i>In Vivo A</i>pplication for Ureteral DilationBruce M Gao, Yi Xi Wu, Seyed Hossein H Sharifi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 7, 2014
Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogrammingMartin Picard, Jiangwen Zhang, Saege Hancock, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Annals of the New York Academy of Sciences|December 17, 2008
A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's diseaseElza Khusnutdinova, Irina Gilyazova, Eduardo Ruiz-Pesini, et al.
Current Protocols in Bioinformatics|December 10, 2014
mtDNA Variation and Analysis Using Mitomap and MitomasterMarie T Lott, Jeremy N Leipzig, Olga Derbeneva, et al.
JAMA Psychiatry|August 24, 2017
Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum DisordersDimitra Chalkia, Larry N Singh, Jeremy Leipzig, et al.
Human Genetics|April 6, 2002
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup JMichael D Brown, Elena Starikovskaya, Olga Derbeneva, et al.
Pediatric Research|August 31, 2006
Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndromeJosé A Camacho, Rebecca Mardach, Natalia Rioseco-Camacho, et al.
Biochimica Et Biophysica Acta. Bioenergetics|July 13, 2018
Mitochondrial DNA associations with East Asian metabolic syndromeDimitra Chalkia, Yi-Cheng Chang, Olga Derbeneva, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
Mitochondrial energy deficiency leads to hyperproliferation of skeletal muscle mitochondria and enhanced insulin sensitivityRyan M Morrow, Martin Picard, Olga Derbeneva, et al.
Neurobiology of Aging|June 12, 2010
Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohortAnita Lakatos, Olga Derbeneva, Danny Younes, et al.
Journal of Endourology|September 29, 2025
Electromotive Drug Administration in the Porcine Ureter: First <i>In Vivo A</i>pplication for Ureteral DilationBruce M Gao, Yi Xi Wu, Seyed Hossein H Sharifi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 7, 2014
Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogrammingMartin Picard, Jiangwen Zhang, Saege Hancock, et al.
Pageof 2