المؤلفون: A B Averyanov, I I Chercashina, S Yu Nikulina, V N Maksimov, V A Shestovitskiy

المصدر: Терапевтический архив, Vol 91, Iss 3, Pp 27-30 (2019)

مصطلحات موضوعية: socs5, bronchial asthma, allergy, polymorphism, allele, gene, Medicine

وصف الملف: electronic resource

Relation: https://ter-arkhiv.ru/0040-3660/article/viewFile/33008/pdf; https://doaj.org/toc/0040-3660; https://doaj.org/toc/2309-5342

URL الوصول: https://doaj.org/article/4c16ac88dfce46ff909b59de10a9b089

المؤلفون: T A Mulerova, E S Filimonov, S A Maksimov, V N Maksimov, M I Voevoda, M Yu Ogarkov

المصدر: Терапевтический архив, Vol 91, Iss 1, Pp 71-77 (2019)

مصطلحات موضوعية: albuminuria, polymorphism of candidate genes, factors of cardiovascular risk, ethnos, Medicine

وصف الملف: electronic resource

Relation: https://ter-arkhiv.ru/0040-3660/article/viewFile/32925/pdf; https://doaj.org/toc/0040-3660; https://doaj.org/toc/2309-5342

URL الوصول: https://doaj.org/article/8bd7d09429e449c8b611c0b6f922816f

المؤلفون: О L Barbarash, М I Voevoda, G V Artamonova, Т А Mulerova, Е N Voropaeva, V N Maksimov, М Yu Ogarkov

المصدر: Терапевтический архив, Vol 89, Iss 9, Pp 68-77 (2017)

مصطلحات موضوعية: ethnos, hypertension, candidate genes, associations, i/d polymorphism, endothelial synthase gene, Medicine

وصف الملف: electronic resource

Relation: https://ter-arkhiv.ru/0040-3660/article/viewFile/32308/pdf; https://doaj.org/toc/0040-3660; https://doaj.org/toc/2309-5342

URL الوصول: https://doaj.org/article/9b529f9ae3624889bc0e87a272492c57

المؤلفون: T A Mulerova, D P Tsygankova, E N Voropaeva, V N Maksimov, M Yu Ogarkov

المصدر: Системные гипертензии, Vol 13, Iss 3, Pp 48-57 (2016)

مصطلحات موضوعية: ethnicity, risk factors, candidate genes, association, i/d polymorphism, endothelial synthase gene, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://syst-hypertension.ru/2075-082X/article/viewFile/29150/pdf; https://doaj.org/toc/2075-082X; https://doaj.org/toc/2542-2189

URL الوصول: https://doaj.org/article/5d5ed33593474d8a852fe0db39e2e547

المؤلفون: T A Mulerova, A A Kuzmina, A N Chigisova, E N Voropaeva, V N Maksimov, M I Voevoda, M Yu Ogarkov

المصدر: Системные гипертензии, Vol 12, Iss 4, Pp 11-17 (2015)

مصطلحات موضوعية: candidate genes, hypertension, shor, left ventricular hypertrophy, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://syst-hypertension.ru/2075-082X/article/viewFile/29102/pdf; https://doaj.org/toc/2075-082X; https://doaj.org/toc/2542-2189

URL الوصول: https://doaj.org/article/f328f5e902854bff801ad3500ebbd9da

المؤلفون: T A Mulerova, E V Rubtsova, A A Kuz'mina, N P Tatarnikova, V N Maksimov, M I Voevoda, M Iu Ogarkov

المصدر: Системные гипертензии, Vol 12, Iss 2, Pp 38-42 (2015)

مصطلحات موضوعية: 4a/4b polymorphism of enos gene, a/g polymorphism of adrb1 gene, dyslipidemia, hypertension, ischemic heart disease, the native population, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://syst-hypertension.ru/2075-082X/article/viewFile/29072/pdf; https://doaj.org/toc/2075-082X; https://doaj.org/toc/2542-2189

URL الوصول: https://doaj.org/article/8f303f3c559745b9bc68a2b773292cb4

المؤلفون: V V Gafarov, M I Voevoda, E A Gromova, V N Maksimov, I V Gagulin, N S Iudin, A V Gafarova, T M Mishakova

المصدر: Терапевтический архив, Vol 85, Iss 4, Pp 47-51 (2013)

مصطلحات موضوعية: trait anxiety, drd4 gene, dat gene, risk, cardiovascular diseases, Medicine

وصف الملف: electronic resource

Relation: https://ter-arkhiv.ru/0040-3660/article/view/31238; https://doaj.org/toc/0040-3660; https://doaj.org/toc/2309-5342

URL الوصول: https://doaj.org/article/bd5b72119f9d410d90975d51bace269c

المؤلفون: Valery Vasilyevich Gafarov, M I Voyevoda, E A Gromova, V N Maksimov, A V Gafarova, I V Gagulin, N S Yudin, T M Mishakova

المصدر: Неврология, нейропсихиатрия, психосоматика, Vol 4, Iss 1, Pp 57-63 (2012)

مصطلحات موضوعية: dat, vital exhaustion, drd4, dat genes, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://nnp.ima-press.net/nnp/article/view/333; https://doaj.org/toc/2074-2711; https://doaj.org/toc/2310-1342

URL الوصول: https://doaj.org/article/63071b7e3b55440aa86fa51682a3332d

المؤلفون: Alla Vladimirovna Shevchenko, Ol'ga Valer'evna Golovanova, Vladimir Iosifovich Konenkov, Ol'ga Mikhaylovna Tolkacheva, Vladimir Nikolaevich Maksimov, Mikhail Ivanovich Voevoda, Aida Gerasimovna Romashchenko, A V Shevchenko, O V Golovanova, V I Konenkov, O M Tolkacheva, V N Maksimov, M I Voyevoda, A G Romashchenko

المصدر: Терапевтический архив, Vol 0, Iss 1, Pp 31-34 (2010)

مصطلحات موضوعية: matrix metalloproteinase-2 (gelatinase a), matrix metalloproteinase-9 (gelatinase b), gene polymorphism in the promoter region, atherosclerosis, myocardial infarction, Medicine

وصف الملف: electronic resource

Relation: https://ter-arkhiv.ru/0040-3660/article/view/33382; https://doaj.org/toc/0040-3660; https://doaj.org/toc/2309-5342

URL الوصول: https://doaj.org/article/550b9229bbd94a5989e3c8be43f09135

المؤلفون: Irina Nikolaevna Grigor'eva, Tat'yana Mikhaylovna Nikitenko, Aleksandr Vilenovich Tikhonov, Tat'yana Ivanovna Romanova, V N Maksimov, Elena Vladimirovna Shakhtshneyder, Sof'ya Konstantinovna Malyutina, Mikhail Ivanovich Voevoda, I N Grigoryeva, T M Nikitenko, A V Tikhonov, T I Romanova, E V Shakhtshneider, S K Malyutina, M I Voyevoda

المصدر: Терапевтический архив, Vol 82, Iss 2, Pp 62-66 (2010)

مصطلحات موضوعية: psti/spink1, cftr, trpm8, polymorphisms of the prss1, apoe, trpm8 genes, pancreatitis, cholelithiasis, Medicine

وصف الملف: electronic resource

Relation: https://ter-arkhiv.ru/0040-3660/article/view/30563; https://doaj.org/toc/0040-3660; https://doaj.org/toc/2309-5342

URL الوصول: https://doaj.org/article/1ebbb75818684ea890273dcedb252023

المؤلفون: A. M. Gorbunova, O. N. Gerasimenko, I. S. Shpagin, M. S. Medvedkina, V. N. Maksimov, Yu. A. Nikolaev

المصدر: Сибирский научный медицинский журнал, Vol 44, Iss 3, Pp 151-160 (2024)

مصطلحات موضوعية: vibration disease, arterial hypertension, comorbidity, nutritional status, anthropometric indicators, mnsod gene, Medicine

Relation: https://sibmed.elpub.ru/jour/article/view/1562; https://doaj.org/toc/2410-2512; https://doaj.org/toc/2410-2520; https://doaj.org/article/75c4d82987fd4f808aac4cc293a15f67

الاتاحة: https://doi.org/10.18699/SSMJ20240317
https://doaj.org/article/75c4d82987fd4f808aac4cc293a15f67

المؤلفون: L. A. Shpagina, V. A. Kozik, V. N. Maksimov, I. S. Shpagin, L. A. Panacheva, S. A. Karmanovskaya, N. G. Lozhkina

المصدر: Российский кардиологический журнал, Vol 28, Iss 10 (2023)

مصطلحات موضوعية: acute coronary syndrome, covid-19, nucleotide sequence variant, angiotensin-converting enzyme, genetic markers, rs1799752, Diseases of the circulatory (Cardiovascular) system, RC666-701

Relation: https://russjcardiol.elpub.ru/jour/article/view/5503; https://doaj.org/toc/1560-4071; https://doaj.org/toc/2618-7620; https://doaj.org/article/9a0a97e3f97443b0bad500217098399f

الاتاحة: https://doi.org/10.15829/1560-4071-2023-5503
https://doaj.org/article/9a0a97e3f97443b0bad500217098399f

المؤلفون: N. M. Kryuchkova, S. Yu. Nikulina, A. A. Chernova, V. N. Maksimov

المصدر: Российский кардиологический журнал, Vol 28, Iss 10 (2023)

مصطلحات موضوعية: pulmonary embolism, polymorphism, genes, Diseases of the circulatory (Cardiovascular) system, RC666-701

Relation: https://russjcardiol.elpub.ru/jour/article/view/5507; https://doaj.org/toc/1560-4071; https://doaj.org/toc/2618-7620; https://doaj.org/article/948a54babd474a25b20ddce2ed9e4f11

الاتاحة: https://doi.org/10.15829/1560-4071-2023-5507
https://doaj.org/article/948a54babd474a25b20ddce2ed9e4f11

المؤلفون: O. O. Kuznetsova, S. Yu. Nikulina, G. V. Matyushin, A. A. Chernova, V. A. Sakovich, V. N. Maksimov

المصدر: Российский кардиологический журнал, Vol 28, Iss 10 (2023)

مصطلحات موضوعية: dilated cardiomyopathy, ischemic myocardial dilatation, heart failure, mmp3 gene polymorphism, Diseases of the circulatory (Cardiovascular) system, RC666-701

Relation: https://russjcardiol.elpub.ru/jour/article/view/5509; https://doaj.org/toc/1560-4071; https://doaj.org/toc/2618-7620; https://doaj.org/article/1411da27898442daa033220c976e77df

الاتاحة: https://doi.org/10.15829/1560-4071-2023-5509
https://doaj.org/article/1411da27898442daa033220c976e77df

المؤلفون: E. N. Voropaeva, T. I. Pospelova, A. M. Nesterets, V. N. Maksimov

المصدر: Сибирский онкологический журнал, Vol 22, Iss 3, Pp 134-143 (2023)

مصطلحات موضوعية: oncogenesis, microrna, mir-143, mir-145, expression, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

Relation: https://www.siboncoj.ru/jour/article/view/2586; https://doaj.org/toc/1814-4861; https://doaj.org/toc/2312-3168; https://doaj.org/article/00a681db88dd45c6b7e6921ceddb5f1a

الاتاحة: https://doi.org/10.21294/1814-4861-2023-22-3-134-143
https://doaj.org/article/00a681db88dd45c6b7e6921ceddb5f1a

المؤلفون: S. E. Golovenkin, S. Yu. Nikulina, M. G. Bubnova, V. N. Shulman, V. N. Maksimov

المصدر: Российский кардиологический журнал, Vol 28, Iss 10 (2023)

مصطلحات موضوعية: myocardial infarction, genetics, left ventricular systolic function, left ventricular diastolic function, heart failure, single nucleotide polymorphism, Diseases of the circulatory (Cardiovascular) system, RC666-701

Relation: https://russjcardiol.elpub.ru/jour/article/view/5536; https://doaj.org/toc/1560-4071; https://doaj.org/toc/2618-7620; https://doaj.org/article/5a0621a2d6a0441199eae440d58e4857

الاتاحة: https://doi.org/10.15829/1560-4071-2023-5536
https://doaj.org/article/5a0621a2d6a0441199eae440d58e4857

المؤلفون: E. N. Voropaeva, T. I. Pospelova, M. I. Churkina, A. A. Gurazheva, O. V. Berezina, V. N. Maksimov, Е. Н. Воропаева, Т. И. Поспелова, М. И. Чуркина, А. А. Гуражева, О. В. Березина, В. Н. Максимов

المساهمون: The research was supported by the Russian Science Found (grant No. 22-25-00222)., Исследование выполнено при финансовой поддержке Российского научного фонда (грант № 22-25-00222).

المصدر: Advances in Molecular Oncology; Том 10, № 3 (2023); 72-81 ; Успехи молекулярной онкологии; Том 10, № 3 (2023); 72-81 ; 2413-3787 ; 2313-805X ; 10.17650/2313-805X-2023-10-3

مصطلحات موضوعية: лимфома, mutations, rs78378222, microRNA, methylation, miR-34a, miR-34b, miR-34c, miR-129, miR-203, lymphoma, мутации, микроРНк, метилирование

وصف الملف: application/pdf

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الاتاحة: https://umo.abvpress.ru/jour/article/view/572
https://doi.org/10.17650/2313-805X-2023-10-3-72-81

المؤلفون: V. V. Gafarov, E. A. Gromova, I. V. Gagulin, D. O. Panov, V. N. Maksimov, А. V. Gafarova, В. В. Гафаров, Е. А. Громова, И. В. Гагулин, Д. О. Панов, В. Н. Максимов, А. В. Гафарова

المصدر: Neurology, Neuropsychiatry, Psychosomatics; Vol 15, No 3 (2023); 16-21 ; Неврология, нейропсихиатрия, психосоматика; Vol 15, No 3 (2023); 16-21 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2023-3

مصطلحات موضوعية: популяция, gene ARNTL/BMAL1, population, ген ARNTL/BMAL1

وصف الملف: application/pdf

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Proc Natl Acad Sci USA. 1998;95:5474-9. doi:10.1073/pnas.95.10.5474; Bunger MK, Wilsbacher LD, Moran SM, et al. Mop3 is an essential component of the master circadian pacemaker in mammals. Cell. 2000;103:1009-17. doi:10.1016/s00928674(00)00205-1; Partonen T, Treutlein J, Alpman A, et al. Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression. Ann Med. 2007;39:229-38. doi:10.1080/07853890701278795; Гафаров ВВ, Гагулин ИВ, Громова ЕА и др. Ассоциация полиморфизма rs2278749 гена ARNTL c некоторыми компонентами аффективных расстройств и нарушениями сна в мужской Новосибирской популяции 25–44 лет. Мир науки, культуры, образования. 2016;6(61):315-9.; https://nnp.ima-press.net/nnp/article/view/2024

الاتاحة: https://nnp.ima-press.net/nnp/article/view/2024
https://doi.org/10.14412/2074-2711-2023-3-16-21

المؤلفون: V. V. Gafarov, E. A. Gromova, I. V. Gagulin, D. O. Panov, V. N. Maksimov, M. A. Gubina, A. V. Gafarova, В. В. Гафаров, Е. А. Громова, И. В. Гагулин, Д. О. Панов, В. Н. Максимов, М. А. Губина, А. В. Гафарова

المساهمون: The investigation has been conducted within government funded scientific topic No. 122031700094-5., Исследование выполнено в рамках бюджетной темы рег. № 122031700094-5.

المصدر: Neurology, Neuropsychiatry, Psychosomatics; Vol 15, No 1 (2023); 43-49 ; Неврология, нейропсихиатрия, психосоматика; Vol 15, No 1 (2023); 43-49 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2023-1

مصطلحات موضوعية: ген 5-HTTLPR SNP rs25531 A>G, sleep duration, population, 5-HTTLPR SNP rs25531 A>G gene, продолжительность сна, популяция

وصف الملف: application/pdf

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الاتاحة: https://nnp.ima-press.net/nnp/article/view/1952
https://doi.org/10.14412/2074-2711-2023-1-43-49

المؤلفون: A. A. Ivanova, A. A. Gurazheva, E. S. Mel’nikova, V. N. Maksimov, E. G. Nemcova, А. А. Иванова, А. А. Гуражева, Е. С. Мельникова, В. Н. Максимов, Е. Г. Немцова

المساهمون: The study was carried out with the financial support of the Government of the Novosibirsk region within the framework of the State Budget No. 122031700094-5 of Research Institutе of Internal and Preventive Medicine – Branch of the Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences., Исследование выполнено при финансовой поддержке Правительства Новосибирской области в рамках ГЗ № 122031700094-5.

المصدر: Bulletin of Siberian Medicine; Том 22, № 2 (2023); 39-45 ; Бюллетень сибирской медицины; Том 22, № 2 (2023); 39-45 ; 1819-3684 ; 1682-0363 ; 10.20538/1682-0363-2023-22-2

مصطلحات موضوعية: неконъюгированная гипербилирубинемия, rs3064744, rs34993780, rs56059937, rs4148323, rs4124874, UGT1A1 gene, unconjugated hyperbilirubinemia, ген UGT1А1

وصف الملف: application/pdf

Relation: https://bulletin.ssmu.ru/jour/article/view/5218/3391; https://bulletin.ssmu.ru/jour/article/view/5218/3414; King D., Armstrong M.J. Overview of Gilbert’s syndrome. Drug Ther. Bull. 2019;57(2):27–31. DOI:10.1136/dtb.2018.000028. PMID: 30709860.; Kringen M.K., Piehler A.P., Grimholt R.M., Opdal M.S., Haug K.B., Urdal P. Serum bilirubin concentration in healthy adult North-Europeans is strictly controlled by the UGT1A1 TA-repeat variants. PLoS One. 2014;9(2):e90248. DOI:10.1371/journal.pone.0090248.; Maruo Y., D’Addario C., Mori A., Iwai M., Takahashi H., Sato H. et al. Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome. Hum. Genet. 2004;115(6):525–526. DOI:10.1007/s00439-004-1183-x.; Steventon G. Uridine diphosphate glucuronosyltransferase 1A1. Xenobiotica. 2020;50(1):64–76. DOI:10.1080/00498254.2019.1617910.; Gazzin S., Masutti F., Vitek L., Tiribelli C. The molecular basis of jaundice: An old symptom revisited. Liver Int. 2017;37(8):1094–1102. DOI:10.1111/liv.13351.; Udomuksorn W., Elliot D.J., Lewis B.C., Mackenzie P.I., Yoovathaworn K., Miners J.O. Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates. Pharmacogenet Genomics. 2007;17(12):1017–1029. DOI:10.1097/FPC.0b013e328256b1b6.; Zhou J., Yang C., Zhu W., Chen S., Zeng Y., Wang J. et al. Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study. Biomed. Res. Int. 2018;2018:7803175. DOI:10.1155/2018/7803175.; Bale G., Avanthi U.S., Padaki N.R., Sharma M., Duvvur N.R., Vishnubhotla V.R.K. Incidence and risk of gallstone disease in Gilbert’s syndrome patients in indian population. J. Clin. Exp. Hepatol. 2018;8(4):362–366. DOI:10.1016/j.jceh.2017.12.006.; Sugatani J., Yamakawa K., Yoshinari K., Machida T., Takagi H., Mori M. et al. Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia. Biochem. Biophys. Res. Commun. 2002;292(2):492– 497. DOI:10.1006/bbrc.2002.6683.; https://bulletin.ssmu.ru/jour/article/view/5218

الاتاحة: https://bulletin.ssmu.ru/jour/article/view/5218
https://doi.org/10.20538/1682-0363-2023-2-39-45