المؤلفون: E. N. Voropaeva, T. I. Pospelova, M. I. Churkina, A. A. Gurazheva, O. V. Berezina, V. N. Maksimov

المصدر: Успехи молекулярной онкологии, Vol 10, Iss 3, Pp 72-81 (2023)

مصطلحات موضوعية: tp53 gene, mutations, rs78378222, microrna, methylation, mir-34a, mir-34b, mir-34c, mir-129, mir-203, lymphoma, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://umo.abvpress.ru/jour/article/view/572; https://doaj.org/toc/2313-805X; https://doaj.org/toc/2413-3787

URL الوصول: https://doaj.org/article/2c5a0aec5d9a440d8da969f1b8d4b8a5

المؤلفون: V. N. Maksimov, O. M. Parkhomenko, N. G. Lozhkina, A. A. Gurazheva, S. V. Maksimova, A. A. Ivanova

المصدر: Атеросклероз, Vol 18, Iss 2, Pp 87-94 (2022)

مصطلحات موضوعية: progressive atherosclerosis, coronary artery disease, marker, rs3746444, gene, mir499a, rs6922269, Diseases of the blood and blood-forming organs, RC633-647.5, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://ateroskleroz.elpub.ru/jour/article/view/792/725; https://doaj.org/toc/2078-256X

URL الوصول: https://doaj.org/article/0c89cacef3d24c168f62e89f73cc215b

المؤلفون: E. N. Voropaeva, T. I. Pospelova, O. V. Berezina, M. I. Churkina, A. A. Gurazheva, V. N. Maksimov

المصدر: Сибирский онкологический журнал, Vol 21, Iss 2, Pp 130-142 (2022)

مصطلحات موضوعية: tp53, p53, mir-34a, mir34b/c, mir-145, mir-143, mir-203, hemoblastosis, expression, methylation, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://www.siboncoj.ru/jour/article/view/2098; https://doaj.org/toc/1814-4861; https://doaj.org/toc/2312-3168

URL الوصول: https://doaj.org/article/7824216a1a1d4d72bab5d8a936418337

المؤلفون: V. N. Maksimov, O. М. Parkhomenko, N. G. Lozhkina, A. A. Gurazheva, S. V. Maksimova, A. A. Ivanova

المصدر: Атеросклероз, Vol 18, Iss 1, Pp 6-13 (2022)

مصطلحات موضوعية: progressive atherosclerosis, cad, marker, i/d polymorphism, rs36232792, sod1 gene, casp8, rs3834129, Diseases of the blood and blood-forming organs, RC633-647.5, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://ateroskleroz.elpub.ru/jour/article/view/610/547; https://doaj.org/toc/2078-256X

URL الوصول: https://doaj.org/article/e91abc4d3da146eb98b15f07567bd39e

المؤلفون: I. N. Grigor’eva, O. V. Efimova, A. A. Gurazheva, V. N. Maksimov

المصدر: Сахарный диабет, Vol 24, Iss 6, Pp 511-520 (2022)

مصطلحات موضوعية: acute pancreatitis, chronic pancreatitis, pancreas cancer, fasting plasma glucose, tnf, tp53 polymorphism, Nutritional diseases. Deficiency diseases, RC620-627

وصف الملف: electronic resource

Relation: https://www.dia-endojournals.ru/jour/article/view/12439; https://doaj.org/toc/2072-0351; https://doaj.org/toc/2072-0378

URL الوصول: https://doaj.org/article/ad1d268b985f4e7281faeff250e02af4

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

المصدر: Рациональная фармакотерапия в кардиологии, Vol 17, Iss 4, Pp 564-569 (2021)

مصطلحات موضوعية: dilatation cardiomyopathy, genetic polymorphism, myocardial dilatation of ischemic origin, gene scn5a, rs1805124, heart failure, genetic predisposition, Therapeutics. Pharmacology, RM1-950, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://www.rpcardio.online/jour/article/view/2538; https://doaj.org/toc/1819-6446; https://doaj.org/toc/2225-3653

URL الوصول: https://doaj.org/article/3189415449d54fe1bd073029af34c07b

المؤلفون: A. A. Tolmacheva, N. G. Lozhkina, V. N. Maksimov, A. A. Gurazheva, Yu. I. Ragino

المصدر: Российский кардиологический журнал, Vol 27, Iss 2S (2022)

مصطلحات موضوعية: myocardial infarction, type 2 diabetes, cardiovascular diseases, molecular genetic markers, single nucleotide polymorphisms, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://russjcardiol.elpub.ru/jour/article/view/4605; https://doaj.org/toc/1560-4071; https://doaj.org/toc/2618-7620

URL الوصول: https://doaj.org/article/a28765e56578429682cb8067946ac68b

المؤلفون: A. A. Ivanova, A. A. Gurazheva, E. I. Akinshina, S. V. Maksimova, S. K. Malyutina, V. P. Novoselov, I. A. Rodina, O. V. Khamovich, V. N. Maksimov

المصدر: Бюллетень сибирской медицины, Vol 19, Iss 4, Pp 80-85 (2021)

مصطلحات موضوعية: внезапная сердечная смерть, метилирование, abca1, промотор, Medicine

وصف الملف: electronic resource

Relation: https://bulletin.ssmu.ru/jour/article/view/4153; https://doaj.org/toc/1682-0363; https://doaj.org/toc/1819-3684

URL الوصول: https://doaj.org/article/14fb2a2dee25450192d002c1ee67790c

المؤلفون: S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, S. V. Prokopenko, D. A. Nikulin, I. M. Platunova, S S. Tretyakova, A. A. Semenchukov, O. V. Marilovtseva, I. I. Lebedeva, V. N. Maksimov, A. A. Gurazheva

المصدر: Терапевтический архив, Vol 92, Iss 12, Pp 25-30 (2020)

مصطلحات موضوعية: stroke, supraventricular tachycardia, arterial hypertension, dyslipidemia, atherosclerosis, hemostasis, rs3025058, Medicine

وصف الملف: electronic resource

Relation: https://ter-arkhiv.ru/0040-3660/article/viewFile/60250/43412; https://doaj.org/toc/0040-3660; https://doaj.org/toc/2309-5342

URL الوصول: https://doaj.org/article/14f9e73ff8be4db8a2890b3e76e982bb

المؤلفون: S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, S. V. Prokopenko, D. A. Nikulin, I. M. Platunova, S. S. Tretyakova, V. N. Chernov, O. V. Marilovtseva, A. N. Kelemeneva, V. N. Maksimov, A. A. Gurazheva

المصدر: Бюллетень сибирской медицины, Vol 19, Iss 1, Pp 85-93 (2020)

مصطلحات موضوعية: онмк, наджелудочковая тахикардия, артериальная гипертензия, дислипидемия, атеросклероз, гемостаз, rs10507391., Medicine

وصف الملف: electronic resource

Relation: https://bulletin.ssmu.ru/jour/article/view/2685; https://doaj.org/toc/1682-0363; https://doaj.org/toc/1819-3684

URL الوصول: https://doaj.org/article/516078d0f85b41f7a63f529ca6a8d656

المؤلفون: S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, S. V. Prokopenko, D. A. Nikulin, I. M. Platunova, S. S. Tretyakova, V. N. Maksimov, A. A. Gurazheva

المصدر: Рациональная фармакотерапия в кардиологии, Vol 15, Iss 5, Pp 634-640 (2019)

مصطلحات موضوعية: stroke, supraventricular tachycardia, arterial hypertension, dyslipidemia, atherosclerosis, rs556621, Therapeutics. Pharmacology, RM1-950, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://www.rpcardio.online/jour/article/view/2032; https://doaj.org/toc/1819-6446; https://doaj.org/toc/2225-3653

URL الوصول: https://doaj.org/article/8c83998032c24eacb11def8a3113d8ff

المؤلفون: V. N. Maksimov, A. A. Gurazheva, P. S. Orlov, S. K. Malyutina, A. A. Ivanova, S. V. Maksimova, I. A. Rodina, O. V. Khamovich, V. P. Novosyolov

المصدر: Атеросклероз, Vol 15, Iss 3, Pp 36-41 (2019)

مصطلحات موضوعية: mitochondrial dna (mtdna) copy number, risk factor, atherosclerosis, ihd, myocardial infarction, sudden cardiac death (scd), population, Diseases of the blood and blood-forming organs, RC633-647.5, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://ateroskleroz.elpub.ru/jour/article/view/108/97; https://doaj.org/toc/2078-256X

URL الوصول: https://doaj.org/article/9f9caa531d5a4a37a6ea99c65ed5d9b9

المؤلفون: V. N. Maksimov, A. A. Gurazheva, Yu. V. Maksimova

المصدر: Атеросклероз, Vol 14, Iss 3, Pp 64-69 (2018)

مصطلحات موضوعية: number of copies of mitochondrial dna (mtdna), risk factor, atherosclerosis, ihd, myocardial infarction, sudden cardiac death (scd), population, Diseases of the blood and blood-forming organs, RC633-647.5, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://ateroskleroz.elpub.ru/jour/article/view/84/84; https://doaj.org/toc/2078-256X

URL الوصول: https://doaj.org/article/b16a6b71fc5743eb90ee9d7c62113946

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

المؤلفون: Elena Voropaeva, Tatyana Pospelova, Maria Churkina, Olga Berezina, Anna Gurazheva, Vladimir Maximov

المصدر: HemaSphere, Vol 7, p e376587c (2023)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

Relation: http://journals.lww.com/10.1097/01.HS9.0000976228.37658.7c; https://doaj.org/toc/2572-9241; https://doaj.org/article/7ca76ffb9e0b4af89ff99461807b26bf

الاتاحة: https://doi.org/10.1097/01.HS9.0000976228.37658.7c
https://doaj.org/article/7ca76ffb9e0b4af89ff99461807b26bf

المؤلفون: Voropaeva, Elena, Pospelova, Tatyana, Churkina, Maria, Berezina, Olga, Gurazheva, Anna, Maximov, Vladimir

المصدر: HemaSphere ; volume 7, issue S3, page e376587c ; ISSN 2572-9241

الاتاحة: http://dx.doi.org/10.1097/01.hs9.0000976228.37658.7c
https://journals.lww.com/10.1097/01.HS9.0000976228.37658.7c

المؤلفون: Elena N. Voropaeva, Tatjana I. Pospelova, Yuriy L. Orlov, Maria I. Churkina, Olga V. Berezina, Anna A. Gurazheva, Tatjana A. Ageeva, Olga B. Seregina, Vladimir N. Maksimov

المصدر: Genes; Volume 13; Issue 8; Pages: 1401

مصطلحات موضوعية: microRNA, methylation, diffuse large B-cell lymphoma

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Molecular Genetics and Genomics; https://dx.doi.org/10.3390/genes13081401

الاتاحة: https://doi.org/10.3390/genes13081401

المؤلفون: V. V. Zorina, E. S. Melnikova, A. A. Ivanova, A. A. Gurazheva, V. N. Maksimov, В. В. Зорина, Е. С. Мельникова, А. А. Иванова, А. А. Гуражева, В. Н. Максимов

المصدر: Medical Genetics; Том 21, № 7 (2022); 52-55 ; Медицинская генетика; Том 21, № 7 (2022); 52-55 ; 2073-7998

مصطلحات موضوعية: rs1799883, BMI, FTO, rs9939609, TCF7L2, rs7903146, FABP2, ИМТ

وصف الملف: application/pdf

Relation: https://www.medgen-journal.ru/jour/article/view/2113/1580; Статистическая информация [Электронный ресурс]. - https://www.rosminzdrav.ru/documents/6686-statisticheskaya-informatsiya; Ершова E.В., Трошина Е.А., Федорова О.С. и др. Морбидное ожирение - возможности консервативной терапии. Ожирение и метаболизм. 2010;7(4):40-43.; Yang W., Tanika K., He J. Genetic epidemiology of obesity. Epidem Rev. 2007(29):49-61. doi:10.1093/epirev/mxm004.; Salim S., Kartawidjajaputra F., Suwanto A. Association of FTO rs9939609 and CD36 rs1761667 with Visceral Obesity. J Nutr Sci Vitaminol (Tokyo). 2020;66:329-335. doi:10.3177/jnsv.66.S329.; Bride L., Naslavsky M., Lopes Yamamoto G. et al. TCF7L2 rs7903146 polymorphism association with diabetes and obesity in an elderly cohort from Brazil. PeerJ. 2021 May 9:e11349. doi:10.7717/peerj.11349.; Wang H., Dong S., Xu H. et al. Genetic variants in FTO associated with metabolic syndrome: a meta- and gene-based analysis. Mol Biol Rep. 2012 May;39(5):5691-8. doi:10.1007/s11033-011-1377-y.; Liu Y., Wu G., Han L. et al. Association of the FABP2 Ala54Thr polymorphism with type 2 diabetes, obesity, and metabolic syndrome: a population-based case-control study and a systematic meta-analysis. Genet Mol Res. 2015 Feb 6;14(1):1155-68. doi:10.4238/2015.; Амельянович М.Д., Морозик П.М., Гончар А.Л. и др. Генетические факторы риска развития метаболического синдрома. Молекулярная и прикладная генетика. 2013(16):24-31.; Гречухина Е.И., Гречухина М.И., Кывыржик Д.С. и др. Ген FTO как генетический фактор. Universum: медицина и фармакология. 2019;2(57):4-6.; Zhou Y., Hambly B.D., McLachlan C.S. FTO associations with obesity and telomere length. J Biomed Sci. 2017 Sep 24(1):65. doi:10.1186/s12929-017-0372-6.; Rivera M., Locke A.E., Corre T. et al.Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals. Br J Psychiatry. 2017 Aug 211(2):70-76. doi:10.1192/bjp. bp.116.183475.; Garcés Da Silva M.F., Guarin Y.A., Carrero Y. et al. Postprandial Hypertriglyceridemia Is Associated with the Variant 54 Threonine FABP2 Gene. J Cardiovasc Dev Dis. 2018 Sep 13;5(3):47. doi:10.3390/jcdd5030047.; Мельникова Е.С., Рымар О.Д., Иванова А.А. и др. Ассоциация полиморфизмов генов TCF7L2, FABP2, KCNQ1, ADIPOQ с прогнозом развития сахарного диабета 2-го типа. Терапевтический архив. 2020;92(10):40-47.; Aboelkhair N.T., El-Edel R.H., Kasem H.E. et al. TCF7L2 gene polymorphism as a risk for type 2 diabetes mellitus and diabetic microvascular complications. Mol Biol Rep. 2021 Jun 48(6):5283-5290. doi:10.1007/s11033-021-06537-0.; https://www.medgen-journal.ru/jour/article/view/2113

الاتاحة: https://www.medgen-journal.ru/jour/article/view/2113
https://doi.org/10.25557/2073-7998.2022.07.52-55

المؤلفون: A. M. Nesterets, A. A. Kuznetsov, A. A. Ivanova, A. A. Gurazheva, S. K. Maliutina, D. V. Denisova, V. N. Maksimov, А. М. Нестерец, А. А. Кузнецов, А. А. Иванова, А. А. Гуражева, С. К. Малютина, Д. В. Денисова, В. Н. Максимов

المساهمون: Работа поддержана грантом РФФИ № 17-29-06026, бюджетными проектами № АААА-А17-117112850280-2, № AAAA-A19-119100990053-4.

المصدر: Complex Issues of Cardiovascular Diseases; Том 11, № 2 (2022); 18-26 ; Комплексные проблемы сердечно-сосудистых заболеваний; Том 11, № 2 (2022); 18-26 ; 2587-9537 ; 2306-1278

مصطلحات موضوعية: внезапная сердечная смерть, NOS1AP, rs12143842, rs4657139, QT interval, Long QT syndrome, Sudden cardiac death, интервал QT, синдром удлиненного интервала QT

وصف الملف: application/pdf

Relation: https://www.nii-kpssz.com/jour/article/view/1067/667; Markwerth P., Bajanowski T., Tzimas I., Dettmeyer R. Sudden cardiac death-update. Int J Legal Med. 2021;135(2):483- 495. doi:10.1007/s00414-020-02481-z; Wong C.X, Brown A., Lau D.H., Chugh S.S., Albert C.M., Kalman J.M., Sanders P. Epidemiology of Sudden Cardiac Death: Global and Regional Perspectives. Heart Lung. Circ. 2019; 28 (1): 6-14. doi:10.1016/j.hlc.2018.08.026; Пиголкин Ю.И., Шилова М.А., Захаров С.Н., Середа А.П., Жолинский А.В., Круглова И.В., Шигеев С.В. Внезапная смерть лиц молодого возраста при различных видах физической нагрузки. Судебно-медицинская экспертиза. 2019; 62(1): 50-55. doi:10.17116/sudmed20196201150; Линчак Р.М., Недбайкин А.М., Семенцова Е.В., Юсова И.А., Струкова В.В. Частота и структура внезапной сердечной смертности трудоспособного населения Брянской области. Данные регистра ГЕРМИНА (регистр внезапной сердечной смертности трудоспособного населения Брянской области). Рациональная фармакотерапия в кардиологии. 2016; 12 (1): 45–50.; Зайцев Д.Н., Василенко П.В., Говорин А.В., Василенко Е.А., Муха Н.В., Филёв А.П., Брижко А.Н., Петрова Н.Г., Сазонова Е.А. Результаты регистра внезапной сердечной смертности населения Забайкальского края (ЗОДИАК) 2017-2019гг. Российский кардиологический журнал. 2020; 25 (11): 3997. doi:10.15829/1560-4071-2020-3997; Scrocco C., Bezzina C.R., Ackerman M.J., Behr E.R. Genetics and genomics of arrhythmic risk: current and future strategies to prevent sudden cardiac death. Nature Reviews Cardiology. Nat Rev Cardiol. 2021; 18 (11): 774-784. doi:10.1038/s41569-021-00555-y; Priori S.G., Blomström-Lundqvist C., Mazzanti A., Blom N., Borggrefe M., Camm J., Elliott P.M., Fitzsimons D., Hatala R., Hindricks G., Kirchhof P., Kjeldsen K., Kuck K.H., HernandezMadrid A., Nikolaou N., Norekvål T.M., Spaulding C., Van Veldhuisen D.J., Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC). 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC). Eur. Heart J. 2015; 36 (41): 2793-2867. doi:10.1093/eurheartj/ehv316; Crotti L., Monti M.C., Insolia R., Peljto A., Goosen A., Brink P.A., Greenberg D.A., Schwartz P.J., George A.L. Jr. NOS1AP is a genetic modifier of the long-QT syndrome. Circulation. 2009; 120 (17): 1657-1663. doi:10.1161/CIRCULATIONAHA.109.879643; Winbo A., Stattin E.L., Westin I.M., Norberg A., Persson J., Jensen S.M., Rydberg A. Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis. BMC Med Genet. 2017; 18 (1): 74. doi:10.1186/s12881-017-0435-2; Ronchi C., Bernardi J., Mura M., Stefanello M., Badone B., Rocchetti M., Crotti L., Brink P., Schwartz P.J., Gnecchi M., Zaza A. NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis. Cardiovasc Res. 2021; 117 (2): 472–483. doi:10.1093/cvr/cvaa036; Tomás M., Napolitano C., De Giuli L., Bloise R., Subirana I., Malovini A., Bellazzi R., Arking D.E., Marban E., Chakravarti A., Spooner P.M., Priori S.G. Polymorphisms in the NOS1AP Gene Modulate QT Interval Duration and Risk of Arrhythmias in the Long QT Syndrome. J Am Coll Cardiol. 2010; 55 (24): 2745–2752. doi:10.1016/j.jacc.2009.12.065; Jamshidi Y., Nolte I.M., Dalageorgou С., Zheng D., Johnson T., Bastiaenen R., Ruddy S., Talbott D., Norris K.P., Snieder H., George A.L., Marshall V., Shakir S., Kannankeril P.J., Munroe P.B., Camm A.J., Jeffery S., Roden D.M., Behr E.R. Common variation in the NOS1AP gene is associated with druginduced QT prolongation and ventricular arrhythmia. J Am Coll Cardiol. 2012; 60 (9): 841–850. doi:10.1016/j.jacc.2012.03.031; Peasey A., Bobak M., Kubinova R., Malyutina S., Pajak A., Tamosiunas A., Pikhart H., Nicholson A., Marmot M. Determinants of cardiovascular disease and other noncommunicable diseases in Central and Eastern Europe: Rationale and design of the HAPIEE study. BMC Public Health. 2006; 6: 255. doi:10.1186/1471-2458-6-255.; Ragino Yu.I., Kuzminykh N.A., Shcherbakova L.V., Denisova D.V., Shramko V.S., Voevoda M.I. Prevalence of coronary heart disease (by epidemiological criteria) and its association with lipid and non-lipid risk factors in the Novosibirsk population of 25-45 years. Russian Journal of Cardiology. 2019; (6): 78-84. doi:10.15829/1560-4071-2019-6-78-84.; Aarnoudse A.J., Newton-Cheh C., de Bakker P.I., Straus S.M., Kors J.A., Hofman A., Uitterlinden A.G., Witteman J.C., Stricker B.H. Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study. Circulation. 2007; 116 (1): 10-16. doi:10.1161/CIRCULATIONAHA.106.676783; Lahrouchi N., Tadros R., Crotti L., Mizusawa Y., Postema P.G., Beekman L., Walsh R., Hasegawa K., Barc J., Ernsting M. et al. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Circulation. 2020; 142 (4): 324-338. doi:10.1161/CIRCULATIONAHA.120.045956; Arking D.E., Pulit S.L., Crotti L., van der Harst P., Munroe P.B., Koopmann T.T., Sotoodehnia N., Rossin E.J., Morley M. et al. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat Genet. 2014; 46 (8): 826–836. doi:10.1038/ng.3014; Mitchell R.N., Ashar F.N., Jarvelin M.R., Froguel P., Sotoodehnia N., Brody J.A., Sebert S., Huikuri H., Rioux J., Goyette P., Newcomb C.E., Junttila M.J., Arking D.E. Effect of Sex and Underlying Disease on the Genetic Association of QT Interval and Sudden Cardiac Death. J Am Heart Assoc. 2019; 8 (23): e013751. doi:10.1161/JAHA.119.013751; Орлов П.С., Иванощук Д.Е., Иванова А.А., Малютина С.К., Новоселов В.П., Воевода М.И., Максимов В.Н. Исследование ассоциаций полиморфизмов генов KCNN2 и NOS1AP с внезапной сердечной смертью. Российский кардиологический журнал. 2018; (10): 59-63. doi:10.15829/1560-4071-2018-10-59-63; Porthan K., Marjamaa A., Viitasalo M., Väänänen H., Jula A., Toivonen L., Nieminen M.S., Newton-Cheh C., Salomaa V., Kontula K., Oikarinen L. Relationship of common candidate gene variants to electrocardiographic T-wave peak to T-wave end interval and T-wave morphology parameters. Heart Rhythm. 2010; 7 (7): 898-903. doi:10.1016/j.hrthm.2010.03.002; https://www.nii-kpssz.com/jour/article/view/1067

الاتاحة: https://www.nii-kpssz.com/jour/article/view/1067
https://doi.org/10.17802/2306-1278-2022-11-2-18-26

المؤلفون: E. Voropaeva, T. Pospelova, M. Churkina, O. Berezina, A. Gurazheva, V. Maximov

المصدر: HemaSphere, Vol 6, Pp 2039-2040 (2022)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

Relation: http://journals.lww.com/10.1097/01.HS9.0000851504.32738.42; https://doaj.org/toc/2572-9241; https://doaj.org/article/9a8cb94fdab44177a0348b70b3ec761c

الاتاحة: https://doi.org/10.1097/01.HS9.0000851504.32738.42
https://doaj.org/article/9a8cb94fdab44177a0348b70b3ec761c