المؤلفون: I. I. Krott

المصدر: Омский научный вестник: Серия "Общество. История. Современность", Vol 4, Iss 4, Pp 45-50 (2019)

مصطلحات موضوعية: social conflict, conflict of consciousness, kyrgyz population, kazakhs, rural entrepreneurs, revolution, civil war, land seizures, History (General) and history of Europe, Economics as a science, HB71-74, Newspapers, AN

وصف الملف: electronic resource

العلاقة: https://www.omgtu.ru/general_information/media_omgtu/journal_of_omsk_research_journal/files/arhiv/2019/%D0%A2.%204,%20%E2%84%96%204%20Test(%D0%9E%D0%98%D0%A1)/45-50%20%D0%9A%D1%80%D0%BE%D1%82%D1%82%20%D0%98.%20%D0%98..pdf; https://doaj.org/toc/2542-0488Test; https://doaj.org/toc/2541-7983Test

الوصول الحر: https://doaj.org/article/7d8a3b3016144bbbbe875d92eff00280Test

المؤلفون: Zh. Isakova T., V. Kipen N., K. Akynbek SAMARA, K. Aitbaev A., N. Aldasheva M., E. Talaibekova T., S. Mukeeva B., K. Osmonkul MEERIM, S. Beishenalieva T., E. Mirrakhimov M., Ж. Исакова Т., В. Кипень Н., Кызы Акынбек Самара, К. Айтбаев А., Н. Алдашева М., Э. Талайбекова Т., С. Мукеева Б., Кызы Осмонкул Мээрим, С. Бейшеналиева Т., Э. Миррахимов М.

المصدر: Medical Genetics; Том 20, № 1 (2021); 44-56 ; Медицинская генетика; Том 20, № 1 (2021); 44-56 ; 2073-7998

مصطلحات موضوعية: obesity, gene, association, ADIPOQ, MTHFR, PON1, KCNJ11, TCF7L2, ITLN1, PPARG, Kyrgyz population, ожирение, ген, ассоциация, кыргызская популяция

وصف الملف: application/pdf

العلاقة: https://www.medgen-journal.ru/jour/article/view/1841/1470Test; ВОЗ. Здоровье-2020: основы европейской политики и стратегия для XXI века. https://www.euro.who.int/__data/assets/pdf_file/0017/215432/Health2020-Long-Rus.pdfTest; Derek J. Chadwick. Gail Cardew, et al., Genetics of Obesity in Humans: Current Issues. 28 September 2007.; Stunkard A.J., Sorensen T.I.A. Obesity and socioeconomic status-a complex relation. N Engl J Med. 1993; 329:1036-1037. doi:10.1007/s13679-015-0185-4; Speliotes E.K., Willer C.J., Berndt S.I., et al. Association analyses of 249796 individuals reveal 18 new loci associated with body mass index. Nat Genet. 2010; 42 (11): 937-948. doi:10.1038/ng.686.; Teasdale T.W., Sørensen T.I., Stunkard A.J., et al. Genetic and early environmental components in sociodemographic influences on adult body fatness. BMJ. 1990;300(6740):1615-8. DOI:10.1136/bmj.300.6740.1615; Teasdale T.W., Sørensen T.I., Stunkard A.J., et al. Intelligence and educational level in relation to body mass index of adult males. Human Biology. 1992; 64(1):99-106. DOI:10.1371/journal.pone.0016290; Gu H.F., Abulaiti A., Ostenson C.G., et al. Single nucleotide polymorphisms in the proximal promoter region of the adiponectin (APM1) gene are associated with type 2 diabetes in Swedish caucasians. Diabetes. 2004; 1:S31-5. DOI:10.2337/diabetes.53.2007.s31; Hara K., Boutin P., Mori Y., et al. Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the Japanese population. Diabetes. 2002; 51(2):536-40. DOI:10.2337/diabetes.51.2.536; Rosenblatt D.S. Methylenetetrahydrofolate reductase. Clinical and Investigative medicine. Medecine Clinique et Experimentale. 2001; 24(1):56-59; Schwanstecher C., Schwanstecher M. et al. (IR)6.2 polymorphism predisposes to type 2 diabetes by inducing overactivity of pancreatic beta-cell ATP-sensitive K(+) channels. Diabetes. 2002;51(3):875-9. DOI:10.2337/diabetes.51.3.875; Loder M.K., da Silva Xavier G., McDonald A., et al., TCF7L2 controls insulin gene expression and insulin secretion in mature pancreatic beta-cells. Biochem Soc Trans. 2008;36(Pt 3):357-9. doi:10.1042/BST0360357.; Cauchi S., El Achhab Y., Choquet H. et al. TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis. J Mol Med. 2007; 85, 777-782. https://doi.org/10.1007/s00109-007-0203-4Test; Schäffler A., Zeitoun M., Wobser H., et al. Herfarth H.Frequency and significance of the novel single nucleotide missense polymorphism Val109Asp in the human gene encoding omentin in Caucasian patients with type 2 diabetes mellitus or chronic inflammatory bowel diseases. Cardiovasc Diabetol. 2007; 13;6:3. DOI:10.1186/1475-2840-6-3; Pan H.Y., Guo L., Li Q., et al. Changes of serum omentin-1 levels in normal subjects and in patients with impaired glucose regulation and with newly diagnosed and untreated type 2 diabetes. Diabetes Res Clin Pract. 2010;88(1):29-33. doi:10.1016/j.diabres.2010.01.013.; Vaccaro O., Lapice E., Monticelli A., et al. Pro12Ala polymorphism of the PPARgamma2 locus modulates the relationship between energy intake and body weight in type 2 diabetic patients. Diabetes Care. 2007; 30(5):1156-61. https://doi.org/10.2337/dc06-1153Test.; Zayani N., Omezzine A., Boumaiza I., et al. Association of ADIPOQ, leptin, LEPR, and resistin polymorphisms with obesity parameters in Hammam Sousse Sahloul Heart Study. J Clin Lab Anal. 2017;31:e22148. doi:10.1002/jcla.22148.; Yin R.X., Wu D.F., Miao L., et al. Several genetic polymorphisms interact with overweight/obesity to influence serum lipid levels. Cardiovascular Diabetology. 2012, 11:123. https://doi.org/10.1186/1475-2840-11-123Test; Wrzosek M., Sawicka A., Wrzosek M., et al. Age at onset of obesity, transcription factor 7-like 2 (TCF7L2) rs7903146 polymorphism, adiponectin levels and the risk of type 2 diabetes in obese patients. Arch Med Sci. 2019; 15, 2: 321-329. DOI: https://doi.org/10.5114/aoms.2017.69638Test.; Kassim N.B., Huri H.Z., Vethakkan S.R., et al. Genetic polymorphisms associated with overweight and obesity in uncontrolled Type 2 diabetes mellitus. Biomarkers in Medice. 2016;10(4):403-15. doi:10.2217/bmm-2015-0037.; Fu M., Chen H., Li X., et al. Association of Pro12Ala variant in peroxisome proliferator-activated receptor-gamma2 gene with type 2 diabetes mellitus. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002;19(3):234-8.; Fu L., Zhang M., Hu Y.Q., et al. Gene-gene interactions and associations of six hypertension related single nucleotide polymorphisms with obesity risk in a Chinese children population. Gene. 2018;679:320-327. doi:10.1016/j.gene.2018.09.019.; Goni L., Cuervo M., Milagro F.I., et al. A genetic risk tool for obesity predisposition assessment and personalized nutrition implementation based on macronutrient intake. Genes Nutr. 2015;10(1):445. doi:10.1007/s12263-014-0445-z.; Cauchi S., Nead K.T., Choquet H., et al. The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies. BMC Med Genet. 2008;9:45. doi:10.1186/1471-2350-9-45.; Morgan A.R., Thompson J.M., Murphy R., et al. Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study. BMC Med Genet. 2010;11:125. doi:10.1186/1471-2350-11-125; DeVos L., Chanson A., Liu Z., et al. Associations between single nucleotide polymorphisms in folate uptake and metabolizing genes with blood folate, homocysteine, and DNA uracil concentrations. Am J Clin Nutr. 2008;88(4):1149-58. doi:10.1093/ajcn/88.4.1149; Wu L.L., Wu J.T. Hyperhomocysteinemia is a risk factor for cancer and a new potential tumor marker. Clin Chim Acta. 2002;322(1-2):21-8. doi:10.1016/s0009-8981(02)00174-2; Kos B.J.P., Leemagz S.Y., McCormack C.D., et al. The association of parental methylenetetrahydrofolate reductase polymorphisms (MTHFR 677C > T and 1298A > C) and fetal loss: a case-control study in South Australia. J Matern Fetal Neonatal Med. 2020;33(5):752-757. doi:10.1080/14767058.2018.1500546; Jiajin L., Shuyan C., Ying W., et al. Genetic polymorphisms in folate metabolism as risk for Down syndrome in the southern China. J Matern Fetal Neonatal Med. 2019;32(12):2030-2035. doi:10.1080/14767058.2018.1424818.; Pérez-Ramírez C., Cañadas-Garre M., Alnatsha A., et al. Pharmacogenetics of platinum-based chemotherapy: impact of DNA repair and folate metabolism gene polymorphisms on prognosis of non-small cell lung cancer patients. Pharmacogenomics J. 2019;19(2):164-177. doi:10.1038/s41397-018-0014-8.; Ma L., Jiang Y., Kong X., Liu Q., et al. Interaction of MTHFR C677T polymorphism with smoking in susceptibility to diabetic nephropathy in Chinese men with type 2 diabetes. Journal of Human Genetics. 2018; 64(1):23-28 doi:10.1038/s10038-018-0531-y; Lewis S.J., Lawlor D.A., Nordestgaard B.G., et al. The methylenetetrahydrofolate reductase C677T genotype and the risk of obesity in three large population-based cohorts. Eur J Endocrinol. 2008; doi:10.1530/EJE-08-0056; Borai I.H., Soliman A.F., Hendawey M.H., et al.Association of MTHFR C677T and ABCA1 G656A polymorphisms with obesity among Egyptian children. Gene Reports. 2018; Volume 11, P. 143-149. DOI:10.1016/j.genrep.2018.03.011; Mansur R.B., Brietzke E., McIntyre R.S. et al. Is there a “metabolic-mood syndrome”? A review of the relationship between obesity and mood disorders. Neurosci Biobehav Rev. 2015;52:89-104. doi:10.1016/j.neubiorev.2014.12.017.; Amare A.T., Schubert K.O., Klingler-Hoffmann M., et al. The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies. Transl Psychiatry. 2017;7(1):e1007. doi:10.1038/tp.2016.261.; Мазо Г.Э., Кибитов А.О. Механизмы формирования коморбидности депрессии и ожирения. Обозрение психиатрии и медицинской психологии имени В.М. Бухтерева. 2018; 1: 65-78.; Zhou D., Zhang D., Liu Y., et al. The E23K variation in the KCNJ11 gene is associated with type 2 diabetes in Chinese and East Asian population. J Hum Genet. 2009;54(7):433-5. doi:10.1038/jhg.2009.54.; Sakamoto Y., Inoue H., Keshavarz P., et al. SNPs in the KCNJ11-ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population. J Hum Genet. 2007; 52(10):781-793. doi:10.1007/s10038-007-0190-x.; Koo B.K., Cho Y.M., Park B.L., et al. Polymorphisms of KCNJ11 (Kir6.2 gene) are associated with Type 2 diabetes and hypertension in the Korean population. Diabet Med. 2007; 24:178-186 doi:10.1111/j/1464-5491.2006.02050.x; Gloyn A.L., Weedon M.N., Owen K.R., et al. Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes. Diabetes. 2003;52:568-572. doi:10.2337/diabetes.52.2.568.; Исакова Ж.Т., Кипень В.Н., Талайбекова Э.Т., и др. Роль и взаимодействие полиморфных вариантов аллельных генов KCNJ11, ADIPOQ, ITLN1, LEP, TCF7L2 и PPARG в увлечении риска развития сахарного диабета типа 2 в Кыргызской Республике. Молекулярная медицина. 2019; 4: 34-45.; https://www.medgen-journal.ru/jour/article/view/1841Test

الإتاحة: https://doi.org/10.25557/2073-7998.2021.01.44-56Test
https://doi.org/10.1007/s13679-015-0185-4Test
https://doi.org/10.1038/ng.686Test
https://doi.org/10.1136/bmj.300.6740.1615Test
https://doi.org/10.1371/journal.pone.0016290Test
https://doi.org/10.2337/diabetes.53.2007.s31Test
https://doi.org/10.2337/diabetes.51.2.536Test
https://doi.org/10.2337/diabetes.51.3.875Test
https://doi.org/10.1042/BST0360357Test
https://doi.org/10.1007/s00109-007-0203-4Test

المؤلفون: N. Aldasheva M., E. Mambetsadykova M., E. Talaibekova T., S. Bokonbaeva Zh., Ch. Sushanlo M., Zh. Isakova T., Н. Алдашева М., Э. Мамбетсадыкова М., Э. Талайбекова Т., С. Боконбаева Дж., Х. Сушанло М., Ж. Исакова Т.

المصدر: Medical Genetics; Том 18, № 9 (2019); 3-8 ; Медицинская генетика; Том 18, № 9 (2019); 3-8 ; 2073-7998

مصطلحات موضوعية: ген MTHFR, С677Т, А1298С, ассоциация, дефект нервной трубки, киргизская популяция, MTHFR gene, association, neural tube defects, Kyrgyz population

وصف الملف: application/pdf

العلاقة: https://www.medgen-journal.ru/jour/article/view/717/442Test; https://www.medgen-journal.ru/jour/article/view/717Test

الإتاحة: https://doi.org/10.25557/2073-7998.2019.09.3-8Test
https://www.medgen-journal.ru/jour/article/view/717Test

المؤلفون: Jainagul Isakova, Elnura Talaibekova, Denis Vinnikov, Nazira Aldasheva, Erkin Mirrakhimov, Almaz Aldashev

المصدر: BMC Endocrine Disorders, Vol 18, Iss 1, Pp 1-6 (2018)

مصطلحات موضوعية: Intelectin 1 gene, Val109Asp polymorphism, Abdominal obesity, Kyrgyz population, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s12902-018-0242-6Test; https://doaj.org/toc/1472-6823Test

الوصول الحر: https://doaj.org/article/c909528cb1294db0881ab009afb66a3dTest

المؤلفون: Jainagul Isakova, Elnura Talaibekova, Nazira Aldasheva, Denis Vinnikov, Almaz Aldashev

المصدر: BMC Cancer, Vol 17, Iss 1, Pp 1-7 (2017)

مصطلحات موضوعية: Breast cancer, XRCC1, TP53, MDM2, Kyrgyz population, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s12885-017-3762-yTest; https://doaj.org/toc/1471-2407Test

الوصول الحر: https://doaj.org/article/fe92b1f9c05c4cb197ebabab33f7e625Test

المؤلفون: Zh T Isakova, E T Talaibekova, D A Asambaeva, A S Kerimkulova, O S Lunegova, N M Aldasheva, A A Aldashev

المصدر: Терапевтический архив, Vol 89, Iss 10, Pp 40-47 (2017)

مصطلحات موضوعية: polymorphism, gene, adipoq, kcnj11, tcf7l2, type 2 diabetes mellitus, kyrgyz population, Medicine

وصف الملف: electronic resource

العلاقة: https://ter-arkhiv.ru/0040-3660/article/viewFile/32306/pdfTest; https://doaj.org/toc/0040-3660Test; https://doaj.org/toc/2309-5342Test

الوصول الحر: https://doaj.org/article/0fee45493b7e439dadc71b2db27b90e9Test

المؤلفون: Zh T Isakova, E T Talaibekova, D A Asambaeva, A S Kerimkulova, O S Lunegova, A A Aldashev

المصدر: Терапевтический архив, Vol 89, Iss 1, Pp 14-17 (2017)

مصطلحات موضوعية: kir62, kcnj11 gene, glu23lys polymorphism, association, hypertension, kyrgyz population, Medicine

وصف الملف: electronic resource

العلاقة: https://ter-arkhiv.ru/0040-3660/article/viewFile/32145/pdfTest; https://doaj.org/toc/0040-3660Test; https://doaj.org/toc/2309-5342Test

الوصول الحر: https://doaj.org/article/a63f3e0c186a41e0817eb5db72428b94Test

المؤلفون: Солод, Юлия Александровна, Давыдов, Роман Вячеславович

المصدر: Arkheologiia Evraziiskikh Stepei (Archaeology of the Eurasian Steppes); No. 5 (2019); 187-195 ; Археология Евразийских степей; № 5 (2019); 187-195 ; 2618-9488 ; 2587-6112

مصطلحات موضوعية: археология, Южная Сибирь, средневековье, енисейские кыргызы, кремация, окалина, торевтика, серебряная инкрустация, консервация, реставрация, archaeology, Southern Siberia, Middle Ages, Yenisei Kyrgyz population, cremation, oxidation, toreutics, silver inlays, conservation, restoration

وصف الملف: application/pdf

العلاقة: https://www.evrazstep.ru/index.php/aes/article/view/527/569Test; https://www.evrazstep.ru/index.php/aes/article/view/527Test

الإتاحة: https://www.evrazstep.ru/index.php/aes/article/view/527Test

المؤلفون: Zh. Isakova T., V. Kipen N., N. Bykyev M., E. Talaibekova T., K. Aitbaev A., N. Aldasheva M., E. Tilekov A., B. Shaimbetov O., B. Sultangazieva B., Ж. Исакова Т., В. Кипень Н., Н. Букуев М., Э. Талайбекова Т., К. Айтбаев А., Н. Алдашева М., Э. Тилеков А., Б. Шаимбетов О., Б. Султангазиева Б.

المصدر: Medical Genetics; Том 18, № 7 (2019); 26-33 ; Медицинская генетика; Том 18, № 7 (2019); 26-33 ; 2073-7998

مصطلحات موضوعية: ТР53, киргизская популяция, gene, ТP53, XRCC1, polymorphism, tumor markers, CEA, SCC, cervical cancer, Kyrgyz population, полиморфизм, онкомаркеры, РЭА, рак шейки матки, ген

وصف الملف: application/pdf

العلاقة: https://www.medgen-journal.ru/jour/article/view/698/433Test; https://www.medgen-journal.ru/jour/article/view/698Test

الإتاحة: https://doi.org/10.25557/2073-7998.2019.07.26-33Test
https://www.medgen-journal.ru/jour/article/view/698Test

المؤلفون: J T Isakova, O S Lunegova, E T Talaibekova, D A Asambaeva, A S Kerimkulova, A A Aldashev

المصدر: Терапевтический архив, Vol 87, Iss 10, Pp 85-90 (2015)

مصطلحات موضوعية: g276t polymorphism in the adiponectin (adipoq) gene, metabolic syndrome, leptin, kyrgyz population, Medicine

وصف الملف: electronic resource

العلاقة: https://ter-arkhiv.ru/0040-3660/article/view/31845Test; https://doaj.org/toc/0040-3660Test; https://doaj.org/toc/2309-5342Test

الوصول الحر: https://doaj.org/article/153c27786cb44f48a2c59edd191aa8c2Test