<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">zabmedvestnik</journal-id><journal-title-group><journal-title xml:lang="ru">Забайкальский медицинский вестник</journal-title><trans-title-group xml:lang="en"><trans-title>Transbaikalian Medical Bulletin</trans-title></trans-title-group></journal-title-group><issn pub-type="epub">1998-6173</issn><publisher><publisher-name>Читинская государственная медицинская академия</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.52485/19986173_2021_3_93</article-id><article-id custom-type="elpub" pub-id-type="custom">zabmedvestnik-92</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>НАУЧНЫЕ ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>SCIENTIFIC REVIEWS</subject></subj-group></article-categories><title-group><article-title>KIR6.2 СУБЪЕДИНИЦА АТФ - ЧУВСТВИТЕЛЬНОГО КАЛИЕВОГО КАНАЛА: ФИЗИОЛОГИЧЕСКОЕ ЗНАЧЕНИЕ, ГЕНЕТИЧЕСКИЕ МУТАЦИИ</article-title><trans-title-group xml:lang="en"><trans-title>KIR6.2 SUBUNIT OF THE ATP-SENSITIVE POTASSIUM CHANNEL:  PHYSIOLOGICAL ROLE, GENETIC MUTATIONS</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Фёдорова</surname><given-names>А. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Fyodorova</surname><given-names>A. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>672000, г. Чита, ул. Горького, 39а</p></bio><bio xml:lang="en"><p>39a Gorky str., Chita, 672000</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Зайцев</surname><given-names>Д. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Zaytsev</surname><given-names>D.  N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>672000, г. Чита, ул. Горького, 39а</p></bio><bio xml:lang="en"><p>39a Gorky str., Chita, 672000</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Серебрякова</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Serebryakova</surname><given-names>O. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>672000, г. Чита, ул. Горького, 39а</p></bio><bio xml:lang="en"><p>39a Gorky str., Chita, 672000</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное образовательное учреждение высшего образования «Читинская государственная медицинская академия» Министерства&#13;
здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Chita State Medical Academy</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>01</day><month>08</month><year>2024</year></pub-date><volume>0</volume><issue>3</issue><fpage>93</fpage><lpage>100</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Фёдорова А.П., Зайцев Д.Н., Серебрякова О.В., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Фёдорова А.П., Зайцев Д.Н., Серебрякова О.В.</copyright-holder><copyright-holder xml:lang="en">Fyodorova A.P., Zaytsev D.N., Serebryakova O.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.zabmedvestnik.ru/jour/article/view/92">https://www.zabmedvestnik.ru/jour/article/view/92</self-uri><abstract><p>В обзоре приведены сведения о строении АТФ-чувствительных калиевых каналов, принципе их функционирования. Представлена современная информация о физиологической роли субъединицы Kir6.2 АТФ-чувствительных калиевых каналов в различных тканях. Приводится патология, связанная с мутациями в гене KCNJ11, регулирующем работу Kir6.2.</p></abstract><trans-abstract xml:lang="en"><p>This review contains information about the structure and principles of functioning of ATP-sensitive potassium channels. The article presents information about the physiological role of the Kir6.2 subunit of ATP-sensitive K + channels in various tissues, and the pathology associated with mutations in the KCNJ11 gene, which regulates the work of Kir6.2.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>АТФ-чувствительные калиевые каналы</kwd><kwd>Kir6.2</kwd><kwd>мутации KCNJ11</kwd></kwd-group><kwd-group xml:lang="en"><kwd>ATP-sensitive potassium channels</kwd><kwd>Kir6.2 subunit</kwd><kwd>mutations of the KCNJ11 gene</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование не имело финансовой поддержки.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Мельников К.Н., Вислобоков А.И., Колпакова М.Э., Борисова В.А., Игнатов Ю.Д. Калиевые ионные каналы клеточных мембран. Обзоры по клинической фармакологии и лекарственной терапии. 2009. 1. 3-27.</mixed-citation><mixed-citation xml:lang="en">Mel'nikov K.N., Vislobokov A.I., Kolpakova M.E., Borisova V.A., Ignatov Yu.D. Potassium of ionic channels of cellular membranes. Obzory po klinicheskoy farmakologii i lekarstvennoy terapii. 2009. 1. 3-27. in Russian.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Миронов Н.Ю., Голицын С.П. Калиевые каналы клеток проводящей системы сердца и рабочего миокарда: структурно-функциональные особенности, патофизиологическое и клиническое значение. Кардиология. 2013. 11. 66-73.</mixed-citation><mixed-citation xml:lang="en">Mironov N.Yu., Golitsyn S.P. Cardiac potassium channels: molecular structure, physiology, pathophysiology and therapeutic implications. Kardiologiya. 2013. 11. 66-73. in Russian.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Гризель А.В. Механизмы активации потенциалуправляемых калиевых каналов. Acta Naturae. 2014. 4 (23). 12-28.</mixed-citation><mixed-citation xml:lang="en">Grizel' A.V. Mechanisms of activation of voltage-gated potassium channels. Acta Naturae. 2014. 4 (23). 12-28. in Russian.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Зефиров А.Л., Ситдикова Г.Ф. Ионные каналы возбудимой клетки (структура, функция, патология). Казань. 2010. 270.</mixed-citation><mixed-citation xml:lang="en">Zefirov A.L., Sitdikova G.F. Ion channels of excitable cell (structure, function, pathology). Kazan'. 2010. 270. in Russian.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Hibino H., Inanobe A., Furutani K., Murakami S., Findlay I., Kurachi Y. Inwardly rectifying potassium channels: their structure, function, and physiological roles. Physiol Rev. 2010. 90 (1). 291-366. DOI 10.1152/physrev.00021.2009.</mixed-citation><mixed-citation xml:lang="en">Hibino H., Inanobe A., Furutani K., Murakami S., Findlay I., Kurachi Y. Inwardly rectifying potassium channels: their structure, function, and physiological roles. Physiol Rev. 2010. 90 (1). 291-366. DOI 10.1152/physrev.00021.2009.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Aziz Q., Li Y., Anderson N., Ojake L., Tsisanova E., Tinker A. Molecular and functional characterization of the endothelial ATP-sensitive potassium channel. J Biol Chem. 2017. 292 (43). 17587-17597. DOI 10.1074/jbc.M117.810325.</mixed-citation><mixed-citation xml:lang="en">Aziz Q., Li Y., Anderson N., Ojake L., Tsisanova E., Tinker A. Molecular and functional characterization of the endothelial ATP-sensitive potassium channel. J Biol Chem. 2017. 292 (43). 17587-17597. DOI 10.1074/jbc.M117.810325.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Huang Y., Hu D., Huang C., Nichols C.G. Genetic Discovery of ATP-Sensitive K+ Channels in Cardiovascular Diseases. Circ Arrhythm Electrophysiol. 2019. 12 (5). e007322. DOI 10.1161/CIRCEP.119.007322.</mixed-citation><mixed-citation xml:lang="en">Huang Y., Hu D., Huang C., Nichols C.G. Genetic Discovery of ATP-Sensitive K+ Channels in Cardiovascular Diseases. Circ Arrhythm Electrophysiol. 2019. 12 (5). e007322. DOI 10.1161/CIRCEP.119.007322.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Castro L., Noelia M., Vidal-Jorge M., Sánchez-Ortiz D., Gándara D., Martínez-Saez E., Cicuéndez M., Poca M.A., Simard J.M., Sahuquillo J. Kir6.2, the Pore-Forming Subunit of ATP-Sensitive K+ Channels, Is Overexpressed in Human Posttraumatic Brain Contusions. J Neurotrauma. 2019. 36 (1). 165-175. DOI 10.1089/neu.2017.5619.</mixed-citation><mixed-citation xml:lang="en">Castro L., Noelia M., Vidal-Jorge M., Sánchez-Ortiz D., Gándara D., Martínez-Saez E., Cicuéndez M., Poca M.A., Simard J.M., Sahuquillo J. Kir6.2, the Pore-Forming Subunit of ATP-Sensitive K+ Channels, Is Overexpressed in Human Posttraumatic Brain Contusions. J Neurotrauma. 2019. 36 (1). 165-175. DOI 10.1089/neu.2017.5619.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Shi W.W., Yang Y., Shi Y., Jiang C. K(ATP) channel action in vascular tone regulation: from genetics to diseases. Sheng Li Xue Bao. 2012. 64 (1). 1-13.</mixed-citation><mixed-citation xml:lang="en">Shi W.W., Yang Y., Shi Y., Jiang C. K(ATP) channel action in vascular tone regulation: from genetics to diseases. Sheng Li Xue Bao. 2012. 64 (1). 1-13.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Yoshida H., Feig J.E., Morrissey A., Ghiu I.A., Artman M., Coetzee W.A. K ATP channels of primary human coronary artery endothelial cells consist of a heteromultimeric complex of Kir6.1, Kir6.2, and SUR2B subunits. J Mol Cell Cardiol. 2004. 37 (4). 857-69. DOI 10.1016/j.yjmcc.2004.05.022.</mixed-citation><mixed-citation xml:lang="en">Yoshida H., Feig J.E., Morrissey A., Ghiu I.A., Artman M., Coetzee W.A. K ATP channels of primary human coronary artery endothelial cells consist of a heteromultimeric complex of Kir6.1, Kir6.2, and SUR2B subunits. J Mol Cell Cardiol. 2004. 37 (4). 857-69. DOI 10.1016/j.yjmcc.2004.05.022.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Wu J.X., Ding D., Wang M., Kang Y., Zeng X., Chen L. Ligand binding and conformational changes of SUR1 subunit in pancreatic ATP-sensitive potassium channels. Protein Cell. 2018. 9 (6). 553-567. DOI 10.1007/s13238-018-0530-y.</mixed-citation><mixed-citation xml:lang="en">Wu J.X., Ding D., Wang M., Kang Y., Zeng X., Chen L. Ligand binding and conformational changes of SUR1 subunit in pancreatic ATP-sensitive potassium channels. Protein Cell. 2018. 9 (6). 553-567. DOI 10.1007/s13238-018-0530-y.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Walczewska-Szewc K., Nowak W. Structural Determinants of Insulin Release: Disordered NTerminal Tail of Kir6.2 Affects Potassium Channel Dynamics through Interactions with Sulfonylurea Binding Region in a SUR1 Partner. J Phys Chem B. 2020. 124 (29). 6198-6211. DOI 10.1021/acs.jpcb.0c02720.</mixed-citation><mixed-citation xml:lang="en">Walczewska-Szewc K., Nowak W. Structural Determinants of Insulin Release: Disordered NTerminal Tail of Kir6.2 Affects Potassium Channel Dynamics through Interactions with Sulfonylurea Binding Region in a SUR1 Partner. J Phys Chem B. 2020. 124 (29). 6198-6211. DOI 10.1021/acs.jpcb.0c02720.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Du Q., Jovanović S., Sukhodub A., Ngoi Y.S., Lal A., Zheleva M., Jovanović A. Insulin downregulates cardioprotective SUR2A in the heart-derived H9c2 cells: A possible explanation for some adverse effects of insulin therapy. Biochem Biophys Rep. 2018. 16. 12-18. DOI 10.1016/j.bbrep.2018.08.005</mixed-citation><mixed-citation xml:lang="en">Du Q., Jovanović S., Sukhodub A., Ngoi Y.S., Lal A., Zheleva M., Jovanović A. Insulin downregulates cardioprotective SUR2A in the heart-derived H9c2 cells: A possible explanation for some adverse effects of insulin therapy. Biochem Biophys Rep. 2018. 16. 12-18. DOI 10.1016/j.bbrep.2018.08.005.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Циркин В. И., Трухина В. И., Трухин А. Н. Нейрофизиология: основы нейрофизиологии. Учебник для вузов. Москва. Юрайт. 2020. 504.</mixed-citation><mixed-citation xml:lang="en">Tsirkin V. I., Trukhina V. I., Trukhin A. N. Neurophysiology: fundamentals of neurophysiology. University textbook. Moskva. Yurayt. 2020. 504. in Russian.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">De Franco E., Saint-Martin C., Brusgaard K., Knight Johnson A.E., Aguilar-Bryan L., Bowman P., Arnoux J.B., Larsen A.R., Sanyoura M., Greeley S., Calzada-León R., Harman B., Houghton J., Nishimura-Meguro E., Laver T.W., Ellard S., Del Gaudio D., Christesen H.T., BellannéChantelot C., Flanagan S.E. Update of variants identified in the pancreatic β-cell KATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes. Hum Mutat. 2020. 41 (5). 884-905. DOI 10.1002/humu.23995.</mixed-citation><mixed-citation xml:lang="en">De Franco E., Saint-Martin C., Brusgaard K., Knight Johnson A.E., Aguilar-Bryan L., Bowman P., Arnoux J.B., Larsen A.R., Sanyoura M., Greeley S., Calzada-León R., Harman B., Houghton J., Nishimura-Meguro E., Laver T.W., Ellard S., Del Gaudio D., Christesen H.T., BellannéChantelot C., Flanagan S.E. Update of variants identified in the pancreatic β-cell KATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes. Hum Mutat. 2020. 41 (5). 884-905. DOI 10.1002/humu.23995.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Barrett T.G. Differential diagnosis of type 1 diabetes: which genetic syndromes need to be considered? Pediatr Diabetes. 2007. 6. 15-23. DOI 10.1111/j.1399-5448.2007.00278.x.</mixed-citation><mixed-citation xml:lang="en">Barrett T.G. Differential diagnosis of type 1 diabetes: which genetic syndromes need to be considered? Pediatr Diabetes. 2007. 6. 15-23. DOI 10.1111/j.1399-5448.2007.00278.x.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Ashcroft F.M., Puljung M.C., Vedovato N. Neonatal Diabetes and the KATP Channel: From Mutation to Therapy. Trends Endocrinol Metab. 2017. 28 (5). 377-387. DOI 10.1016/j.tem.2017.02.003.</mixed-citation><mixed-citation xml:lang="en">Ashcroft F.M., Puljung M.C., Vedovato N. Neonatal Diabetes and the KATP Channel: From Mutation to Therapy. Trends Endocrinol Metab. 2017. 28 (5). 377-387. DOI 10.1016/j.tem.2017.02.003.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Hashimoto Y., Dateki S., Hirose M., Satomura K., Sawada H., Mizuno H., Sugihara S., Maruyama K., Urakami T., Sugawara H., Shirai K., Yorifuji T. Molecular and clinical features of KATP - channel neonatal diabetes mellitus in Japan. Pediatr Diabetes. 2017. 18 (7). 532-539. DOI 10.1111/pedi.12447.</mixed-citation><mixed-citation xml:lang="en">Hashimoto Y., Dateki S., Hirose M., Satomura K., Sawada H., Mizuno H., Sugihara S., Maruyama K., Urakami T., Sugawara H., Shirai K., Yorifuji T. Molecular and clinical features of KATP - channel neonatal diabetes mellitus in Japan. Pediatr Diabetes. 2017. 18 (7). 532-539. DOI 10.1111/pedi.12447.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Demirbilek H., Rahman S.A., Buyukyilmaz G.G., Khalid H. Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology. Int J Pediatr Endocrinol. 2017. 9. DOI 10.1186/s13633-017-0048-8.</mixed-citation><mixed-citation xml:lang="en">Demirbilek H., Rahman S.A., Buyukyilmaz G.G., Khalid H. Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology. Int J Pediatr Endocrinol. 2017. 9. DOI 10.1186/s13633-017-0048-8.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Koo B.K., Cho Y.M., Park B.L., Cheong H.S., Shin H.D., Jang H.C., Kim S.Y., Lee H.K., Park K.S. Polymorphisms of KCNJ11 (Kir6.2 gene) are associated with Type 2 diabetes and hypertension in the Korean population. Diabet Med. 2007. 24 (2). 178-86. DOI 10.1111/j.1464-5491.2006.02050.x.</mixed-citation><mixed-citation xml:lang="en">Koo B.K., Cho Y.M., Park B.L., Cheong H.S., Shin H.D., Jang H.C., Kim S.Y., Lee H.K., Park K.S. Polymorphisms of KCNJ11 (Kir6.2 gene) are associated with Type 2 diabetes and hypertension in the Korean population. Diabet Med. 2007. 24 (2). 178-86. DOI 10.1111/j.1464-5491.2006.02050.x.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Haghvirdizadeh P., Mohamed Z., Abdullah N.A., Haghvirdizadeh P., Haerian M.S., Haerian B.S. KCNJ11: Genetic Polymorphisms and Risk of Diabetes Mellitus. J Diabetes Res. 2015. 908152. DOI 10.1155/2015/908152.</mixed-citation><mixed-citation xml:lang="en">Haghvirdizadeh P., Mohamed Z., Abdullah N.A., Haghvirdizadeh P., Haerian M.S., Haerian B.S. KCNJ11: Genetic Polymorphisms and Risk of Diabetes Mellitus. J Diabetes Res. 2015. 2015. 908152. DOI 10.1155/2015/908152.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Zhuang L., Zhao Y., Zhao W., Li M., Yu M., Lu M., Zhang R., Ge X., Zheng T., Li C., Yin J., Yin J., Bao Y., Liu L., Jia W., Liu Y. The E23K and A190A variations of the KCNJ11 gene are associated with early-onset type 2 diabetes and blood pressure in the Chinese population. Mol Cell Biochem. 2015. 404 (1-2). 133-41. DOI 10.1007/s11010-015-2373-7.</mixed-citation><mixed-citation xml:lang="en">Zhuang L., Zhao Y., Zhao W., Li M., Yu M., Lu M., Zhang R., Ge X., Zheng T., Li C, Yin J., Yin J., Bao Y., Liu L., Jia W., Liu Y. The E23K and A190A variations of the KCNJ11 gene are associated with early-onset type 2 diabetes and blood pressure in the Chinese population. Mol Cell Biochem. 2015. 404 (1-2). 133-41. DOI 10.1007/s11010-015-2373-7.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Fedele F., Mancone M., Chilian W.M., Severino P., Canali E., Logan S., De Marchis M.L., Volterrani M., Palmirotta R., Guadagni F. Role of genetic polymorphisms of ion channels in the pathophysiology of coronary microvascular dysfunction and ischemic heart disease. Basic Res Cardiol. 2013. 108 (6). 387. DOI 10.1007/s00395-013-0387-4.</mixed-citation><mixed-citation xml:lang="en">Fedele F., Mancone M., Chilian W.M., Severino P., Canali E., Logan S., De Marchis M.L., Volterrani M., Palmirotta R., Guadagni F. Role of genetic polymorphisms of ion channels in the pathophysiology of coronary microvascular dysfunction and ischemic heart disease. Basic Res Cardiol. 2013. 108 (6). 387. DOI 10.1007/s00395-013-0387-4.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Severino P., D'Amato A., Netti L., Pucci M., Mariani M.V., Cimino S., Birtolo L.I., Infusino F., De Orchi P., Palmirotta R., Lovero D., Silvestris F., Caputo V., Pizzuti A., Miraldi F., Maestrini V., Mancone M., Fedele F. Susceptibility to ischaemic heart disease: Focusing on genetic variants for ATP-sensitive potassium channel beyond traditional risk factors. Eur J Prev Cardiol. 2020. 2. 2047487320926780. DOI 10.1177/2047487320926780.</mixed-citation><mixed-citation xml:lang="en">Severino P., D'Amato A., Netti L., Pucci M., Mariani M.V., Cimino S., Birtolo L.I., Infusino F., De Orchi P., Palmirotta R., Lovero D., Silvestris F., Caputo V., Pizzuti A., Miraldi F., Maestrini V., Mancone M., Fedele F. Susceptibility to ischaemic heart disease: Focusing on genetic variants for ATP-sensitive potassium channel beyond traditional risk factors. Eur J Prev Cardiol. 2020. 2. 2047487320926780. DOI 10.1177/2047487320926780.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">URL: https://www.ncbi.nlm.nih.gov/clinvar/variation/8678/ (дата обращения: 07.05.2021)</mixed-citation><mixed-citation xml:lang="en">URL: https://www.ncbi.nlm.nih.gov/clinvar/variation/8678/ (дата обращения: 07.05.2021)</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Xi H.L., Liu J.F., Li L., Wan J. Relationship between dilated cardiomyopathy and the E23K and I337V polymorphisms in the Kir6.2 subunit of the KATP channel. Genet Mol Res. 2013. 12 (4). 4383-92. DOI 10.4238/2013.October.10.4.</mixed-citation><mixed-citation xml:lang="en">Xi H.L., Liu J.F., Li L., Wan J. Relationship between dilated cardiomyopathy and the E23K and I337V polymorphisms in the Kir6.2 subunit of the KATP channel. Genet Mol Res. 2013. 12(4). 4383-92. DOI 10.4238/2013.October.10.4.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Reyes S., Terzic A., Mahoney D.W., Redfield M.M., Rodeheffer R.J., Olson T.M. K(ATP) channel polymorphism is associated with left ventricular size in hypertensive individuals: a large-scale community-based study. Hum Genet. 2008. 123 (6). 665-7. DOI 10.1007/s00439-008-0519-3.</mixed-citation><mixed-citation xml:lang="en">Reyes S., Terzic A., Mahoney D.W., Redfield M.M., Rodeheffer R.J., Olson T.M. K(ATP) channel polymorphism is associated with left ventricular size in hypertensive individuals: a large-scale community-based study. Hum Genet. 2008. 123 (6). 665-7. DOI 10.1007/s00439-008-0519-3.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Han Y.Y., Wang L.J., Zhang L., Ma K.T., Li L., Si J.Q. Association between potassium channel SNPs and essential hypertension in Xinjiang Kazak Chinese patients. Exp Ther Med. 2017. 14 (3). 1999-2006. DOI 10.3892/etm.2017.4734</mixed-citation><mixed-citation xml:lang="en">Han Y.Y., Wang L.J., Zhang L., Ma K.T., Li L., Si J.Q. Association between potassium channel SNPs and essential hypertension in Xinjiang Kazak Chinese patients. Exp Ther Med. 2017. 14 (3). 1999-2006. DOI 10.3892/etm.2017.4734.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Железнякова А.В., Викулова О.К., Савельева С.А., Носиков В.В., Шестакова М.В. Полиморфный маркер rs5219 гена KCNJ11 показал достоверную ассоциацию со скоростью клубочковой фильтрации при хронической болезни почек у пациентов с сахарным диабетом 2 типа. Проблемы Эндокринологии. 2016. 62 (5). 11-12. DOI 10.14341/probl201662511-12.</mixed-citation><mixed-citation xml:lang="en">Zheleznyakova A.V., Vikulova O.K., Savelyeva S.A., Nosikov V.V., Shestakova M.V. An analysis of the association between a polymorphism rs5219 of KCNJ11 and GFR in CKD development in patients with type 2 diabetes in Russian population. Problems of Endocrinology. 2016. 62 (5). 11-12. in Russian. DOI 10.14341/probl201662511-12.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Reyes S., Park S., Johnson B.D., Terzic A., Olson T.M. KATP channel Kir6.2 E23K variant overrepresented in human heart failure is associated with impaired exercise stress response. Hum Genet. 2009. 126 (6). 779-789. DOI 10.1007/s00439-009-0731-9.</mixed-citation><mixed-citation xml:lang="en">Reyes S., Park S., Johnson B.D., Terzic A., Olson T.M. KATP channel Kir6.2 E23K variant overrepresented in human heart failure is associated with impaired exercise stress response. Hum Genet. 2009. 126 (6). 779-789. DOI 10.1007/s00439-009-0731-9.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Поздняков Н.О., Каграманян И.Н., Мирошников А.Е., Емельянов Е.С., Груздева А.А., Сироткина А.М., Духанина И.А., Милкина А.А., Хохлов А.А., Поздняков С.О. Фармакогенетические аспекты в терапии сахарного диабета 2-го типа. Acta Biomedica Scientifica. 2020. 5 (3). 13-23. DOI 10.29413/ABS.2020-5.3.2</mixed-citation><mixed-citation xml:lang="en">Pozdnyakov N.O., Kagarmanyan I.N., Miroshnikov A.E., Emelyanov E.S., Gruzdeva A.A., Sirotkina A.M., Dukhanina I.A., Milkina A.A., Khokhlov A.A., Pozdnyakov S.O. Pharmacogenetic Aspects of Type 2 Diabetes Treatment. Acta Biomedica Scientifica. 2020. 5 (3). 13-23. in Russian. DOI 10.29413/ABS.2020-5.3.2.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Шорохова П.Б., Загородникова К.А., Баранов В.Л., Ворохобина Н.В. Значение полиморфизма в генах KCNJ11, ABCC8 и TCF7L2 для ответа на терапию основными группами пероральных сахароснижающих препаратов. Фармакогенетика и Фармакогеномика. 2018. 1. 9-14. DOI 10.24411/2588-0527-2018-10002.</mixed-citation><mixed-citation xml:lang="en">Shorokhova P.B., Zagorodnikova K.A., Baranov V.L., Vorokhobina N.V. The value polymorphism in gen KCNJ11, ABCC8 and TCF7L2 for response to therapy of the main oral hypoglycemic drugs. Pharmacogenetics and Pharmacogenomics. 2018. 1. 9-14. in Russian. DOI 10.24411/2588-0527-2018-10002.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
