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Data on association of mitochondrial heteroplasmy and cardiovascular risk factors: Comparison of samples from Russian and Mexican populations.

Data in brief

Kirichenko TV, Sobenin IA, Khasanova ZB, Orekhova VA, Melnichenko AA, Demakova NA, Grechko AV, Orekhov AN, Ble Castillo JL, Shkurat TP.
PMID: 29896485
Data Brief. 2018 Mar 12;18:16-21. doi: 10.1016/j.dib.2018.02.068. eCollection 2018 Jun.

Despite the fact that the role of mitochondrial genome mutations in a number of human diseases is widely studied, the effect of mitochondrial heteroplasmy in the development of cardiovascular disease has not been adequately investigated. In this study, we...

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Kirichenko TV, Sobenin IA, Khasanova ZB, et al. Data on association of mitochondrial heteroplasmy and cardiovascular risk factors: Comparison of samples from Russian and Mexican populations. Data Brief. 2018;18:16-21doi: 10.1016/j.dib.2018.02.068.
Kirichenko, T. V., Sobenin, I. A., Khasanova, Z. B., Orekhova, V. A., Melnichenko, A. A., Demakova, N. A., Grechko, A. V., Orekhov, A. N., Ble Castillo, J. L., & Shkurat, T. P. (2018). Data on association of mitochondrial heteroplasmy and cardiovascular risk factors: Comparison of samples from Russian and Mexican populations. Data in brief, 1816-21. https://doi.org/10.1016/j.dib.2018.02.068
Kirichenko, Tatiana V, et al. "Data on association of mitochondrial heteroplasmy and cardiovascular risk factors: Comparison of samples from Russian and Mexican populations." Data in brief vol. 18 (2018): 16-21. doi: https://doi.org/10.1016/j.dib.2018.02.068
Kirichenko TV, Sobenin IA, Khasanova ZB, Orekhova VA, Melnichenko AA, Demakova NA, Grechko AV, Orekhov AN, Ble Castillo JL, Shkurat TP. Data on association of mitochondrial heteroplasmy and cardiovascular risk factors: Comparison of samples from Russian and Mexican populations. Data Brief. 2018 Mar 12;18:16-21. doi: 10.1016/j.dib.2018.02.068. eCollection 2018 Jun. PMID: 29896485; PMCID: PMC5995799.
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Association of SNPs in Lipid Metabolism Gene Single Nucleotide Polymorphism with the Risk of Obesity in Children.

Genetic testing and molecular biomarkers

Kulaeva ED, Volchik VV, Bocharova OV, Teplakova ED, Shkurat MA, Derevyanchuk EG, Mashkina EV.
PMID: 34152846
Genet Test Mol Biomarkers. 2021 Jun;25(6):419-425. doi: 10.1089/gtmb.2020.0343.

No abstract available.

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Kulaeva ED, Volchik VV, Bocharova OV, et al. Association of SNPs in Lipid Metabolism Gene Single Nucleotide Polymorphism with the Risk of Obesity in Children. Genet Test Mol Biomarkers. 2021;25(6):419-425doi: 10.1089/gtmb.2020.0343.
Kulaeva, E. D., Volchik, V. V., Bocharova, O. V., Teplakova, E. D., Shkurat, M. A., Derevyanchuk, E. G., & Mashkina, E. V. (2021). Association of SNPs in Lipid Metabolism Gene Single Nucleotide Polymorphism with the Risk of Obesity in Children. Genetic testing and molecular biomarkers, 25(6), 419-425. https://doi.org/10.1089/gtmb.2020.0343
Kulaeva, Elizaveta D, et al. "Association of SNPs in Lipid Metabolism Gene Single Nucleotide Polymorphism with the Risk of Obesity in Children." Genetic testing and molecular biomarkers vol. 25,6 (2021): 419-425. doi: https://doi.org/10.1089/gtmb.2020.0343
Kulaeva ED, Volchik VV, Bocharova OV, Teplakova ED, Shkurat MA, Derevyanchuk EG, Mashkina EV. Association of SNPs in Lipid Metabolism Gene Single Nucleotide Polymorphism with the Risk of Obesity in Children. Genet Test Mol Biomarkers. 2021 Jun;25(6):419-425. doi: 10.1089/gtmb.2020.0343. PMID: 34152846.
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Mitochondrial diseases caused by mtDNA mutations: a mini-review.

Therapeutics and clinical risk management

Ryzhkova AI, Sazonova MA, Sinyov VV, Galitsyna EV, Chicheva MM, Melnichenko AA, Grechko AV, Postnov AY, Orekhov AN, Shkurat TP.
PMID: 30349272
Ther Clin Risk Manag. 2018 Oct 09;14:1933-1942. doi: 10.2147/TCRM.S154863. eCollection 2018.

There are several types of mitochondrial cytopathies, which cause a set of disorders, arise as a result of mitochondria's failure. Mitochondria's functional disruption leads to development of physical, growing and cognitive disabilities and includes multiple organ pathologies, essentially disturbing...

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Ryzhkova AI, Sazonova MA, Sinyov VV, et al. Mitochondrial diseases caused by mtDNA mutations: a mini-review. Ther Clin Risk Manag. 2018;14:1933-1942doi: 10.2147/TCRM.S154863.
Ryzhkova, A. I., Sazonova, M. A., Sinyov, V. V., Galitsyna, E. V., Chicheva, M. M., Melnichenko, A. A., Grechko, A. V., Postnov, A. Y., Orekhov, A. N., & Shkurat, T. P. (2018). Mitochondrial diseases caused by mtDNA mutations: a mini-review. Therapeutics and clinical risk management, 141933-1942. https://doi.org/10.2147/TCRM.S154863
Ryzhkova, Anastasia I, et al. "Mitochondrial diseases caused by mtDNA mutations: a mini-review." Therapeutics and clinical risk management vol. 14 (2018): 1933-1942. doi: https://doi.org/10.2147/TCRM.S154863
Ryzhkova AI, Sazonova MA, Sinyov VV, Galitsyna EV, Chicheva MM, Melnichenko AA, Grechko AV, Postnov AY, Orekhov AN, Shkurat TP. Mitochondrial diseases caused by mtDNA mutations: a mini-review. Ther Clin Risk Manag. 2018 Oct 09;14:1933-1942. doi: 10.2147/TCRM.S154863. eCollection 2018. PMID: 30349272; PMCID: PMC6186303.
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