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M A Sazonova

Showing results (1-10 of 13) with videos related to

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Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|August 1, 2015
[Association of mitochondrial genome mutations with lipofibrous plaques in human aortic intima]M A Sazonova
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|June 20, 2012
[Association of point mutations in human nuclear and mitochondrial genome with coronary artery disease]K Iu Mitrofanov, M A Sazonova
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|October 18, 2012
[Association of the mutations in the human mitochondrial genome with chronic non-inflammatory diseases: type 2 diabetes, hypertension and different types of cardiomyopathy]A V Zhelankin, M A Sazonova
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|October 18, 2012
[Human pathologies associated with mutations of mitochondrial genome]M M Ivanova, E N Borodachev, M A Sazonova
Genetika|January 31, 1998
[Molecular genetic analysis of TUB18 and TUB20 intragenic polymorphism and various mutations of the CFTR gene in the Moscow region]M A Sazonova, F A Amosenko, N I Kapranov, et al.
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|February 25, 2012
[A new method of quantitative estimation of mutant allele in mitochondrial genome]M A Sazonova, A Iu Postnov, A N Orekhov, et al.
Klinicheskaia Meditsina|October 11, 2018
[DESIALATED LOW DENSITY LIPOPROTEINS IN HUMAN BLOOD]A I Ryzhkova, V P Karagodin, V N Sukhorukov, et al.
Genetika|April 1, 1995
[Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region]F A Amosenko, M A Sazonova, N I Kapranov, et al.
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|August 1, 2015
[Analysis of mitochondrial haplogroups in persons with subclinical atherosclerosis based on high-throughput mtDNA sequencing]A V Zhelankin, M A Sazonova, Z B Khasanova, et al.
Genetika|February 1, 1997
[TUB9 polymorphism in the CFTR gene of cystic fibrosis patients, carriers, and healthy donors from the Moscow region. SSCP and restriction analyses]F A Amosenko, I S Trubnikova, V M Zakhar'ev, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|August 1, 2015
[Association of mitochondrial genome mutations with lipofibrous plaques in human aortic intima]M A Sazonova
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|June 20, 2012
[Association of point mutations in human nuclear and mitochondrial genome with coronary artery disease]K Iu Mitrofanov, M A Sazonova
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|October 18, 2012
[Association of the mutations in the human mitochondrial genome with chronic non-inflammatory diseases: type 2 diabetes, hypertension and different types of cardiomyopathy]A V Zhelankin, M A Sazonova
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|October 18, 2012
[Human pathologies associated with mutations of mitochondrial genome]M M Ivanova, E N Borodachev, M A Sazonova
Genetika|January 31, 1998
[Molecular genetic analysis of TUB18 and TUB20 intragenic polymorphism and various mutations of the CFTR gene in the Moscow region]M A Sazonova, F A Amosenko, N I Kapranov, et al.
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|February 25, 2012
[A new method of quantitative estimation of mutant allele in mitochondrial genome]M A Sazonova, A Iu Postnov, A N Orekhov, et al.
Klinicheskaia Meditsina|October 11, 2018
[DESIALATED LOW DENSITY LIPOPROTEINS IN HUMAN BLOOD]A I Ryzhkova, V P Karagodin, V N Sukhorukov, et al.
Genetika|April 1, 1995
[Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region]F A Amosenko, M A Sazonova, N I Kapranov, et al.
Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|August 1, 2015
[Analysis of mitochondrial haplogroups in persons with subclinical atherosclerosis based on high-throughput mtDNA sequencing]A V Zhelankin, M A Sazonova, Z B Khasanova, et al.
Genetika|February 1, 1997
[TUB9 polymorphism in the CFTR gene of cystic fibrosis patients, carriers, and healthy donors from the Moscow region. SSCP and restriction analyses]F A Amosenko, I S Trubnikova, V M Zakhar'ev, et al.
Pageof 2