<?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">kurskvest</journal-id><journal-title-group><journal-title xml:lang="ru">Человек и его здоровье</journal-title><trans-title-group xml:lang="en"><trans-title>Humans and their health</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1998-5746</issn><issn pub-type="epub">1998-5754</issn><publisher><publisher-name>Kursk State Medical University</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">kurskvest-17</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>МЕДИКО-БИОЛОГИЧЕСКИЕ НАУКИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>MEDICOBIOLOGICAL SCIENCES</subject></subj-group></article-categories><title-group><article-title>Исследование ассоциации полиморфизма R554K гена арил-гидрокарбонового рецептора (AHR) с риском развития врожденных дефектов межпредсердной и межжелудочковой перегородок сердца</article-title><trans-title-group xml:lang="en"><trans-title>Research of association of aryl-hydrocarbon receptor gene (AHR) R554K polymorphism with risk of developing congenital atrial and ventricular septal defects</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>Швецов</surname><given-names>Я. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Shvetsov</surname><given-names>Y. D.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лазарев</surname><given-names>К. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Lazarev</surname><given-names>K. Y.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Брайко</surname><given-names>О. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Brayko</surname><given-names>O. P.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бушуева</surname><given-names>О. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Bushueva</surname><given-names>O. Y.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Голубцов</surname><given-names>В. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Golubtsov</surname><given-names>V. I.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Полоников</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Polonikov</surname><given-names>A. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Курский государственный медицинский университет, Курск</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Kursk State Medical University, Kursk</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Кубанский государственный медицинский университет, Краснодар</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Kuban State Medical University, Krasnodar</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2015</year></pub-date><pub-date pub-type="epub"><day>15</day><month>12</month><year>2017</year></pub-date><volume>0</volume><issue>1</issue><fpage>99</fpage><lpage>103</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Швецов Я.Д., Лазарев К.Ю., Брайко О.П., Бушуева О.Ю., Голубцов В.И., Полоников А.В., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Швецов Я.Д., Лазарев К.Ю., Брайко О.П., Бушуева О.Ю., Голубцов В.И., Полоников А.В.</copyright-holder><copyright-holder xml:lang="en">Shvetsov Y.D., Lazarev K.Y., Brayko O.P., Bushueva O.Y., Golubtsov V.I., Polonikov A.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.kursk-vestnik.ru/jour/article/view/17">https://www.kursk-vestnik.ru/jour/article/view/17</self-uri><abstract><p>В рамках настоящего исследования была впервые изучена связь полиморфного варианта R554K гена AHR с развитием врожденных пороков межпредсердной и межжелудочковой перегородки сердца плода. Материалом для исследования послужили образцы ДНК 151 неродственных детей славянского происхождения (жители Краснодарского края) с врожденными пороками межпредсердной и межжелудочковой перегородки сердца, рожденных в родильных домах Краснодарского края и 219 здоровых детей. Генотипирование полиморфизма R554K гена AHR проводили методами полимеразной цепной реакции в режиме реального времени с использованием TaqMan-зондов. Сравнительный анализ частот аллелей и генотипов полиморфизма R554K гена AHR не выявил ассоциации с развитием врожденных пороков межпредсердной и межжелудочковой перегородки сердца плода. Тем не менее нельзя исключить возможность участия гена AHR в формировании наследственной предрасположенности к врожденным порокам сердца.</p></abstract><trans-abstract xml:lang="en"><p>The present research for the first time investigates the connection of polymorphic variant R554K of AHR gene with the development of congenital atrial and ventricular septal defects of fetus. The material for study was DNA samples of 151 unrelated children of Slavic origin (residents of the Krasnodar region) with congenital atrial and ventricular septal defects, born in maternity hospitals of Krasnodar region and 219 healthy children. Genetic typing of AHR gene R554K polymorphisms was performed by polymerase chain reaction in real time using TaqMan-probes. A comparative analysis of allele frequencies and genotypes of AHR gene R554K polymorphism showed no association with the development of congenital atrial and ventricular septal defects in fetus. However, we cannot exclude the possibility of AHR gene involvement in the development of inherited predisposition to congenital heart defects.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>врожденные пороки межпредсердной и межжелудочковой перегородок сердца плода</kwd><kwd>ДНК-полиморфизм</kwd><kwd>арил-гидрокарбоновый рецептор</kwd><kwd>congenital atrial and ventricular septal defects in fetus</kwd><kwd>DNA polymorphism</kwd><kwd>aryl-hydrocarbon receptor</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Брайко О.П., Лазарев К.Ю., Щвецов Я.Д., Голубцов В.И., Полоников А.В. Анализ ассоциаций полиморфизмов g590a гена NAT2 и с3435т гена ABCB1 у детей с изолированным дефектом межжелудочковой перегородки в Краснодарском крае // Курск. научн.-практ. вестн. «Человек и его здоровье». - 2013. - № 4. - C. 15-20.</mixed-citation><mixed-citation xml:lang="en">Брайко О.П., Лазарев К.Ю., Щвецов Я.Д., Голубцов В.И., Полоников А.В. Анализ ассоциаций полиморфизмов g590a гена NAT2 и с3435т гена ABCB1 у детей с изолированным дефектом межжелудочковой перегородки в Краснодарском крае // Курск. научн.-практ. вестн. «Человек и его здоровье». - 2013. - № 4. - C. 15-20.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Вейр Б. Анализ генетических данных. Дискретные генетические признаки. - М. : Мир, 1995. - С. 85-104.</mixed-citation><mixed-citation xml:lang="en">Вейр Б. Анализ генетических данных. Дискретные генетические признаки. - М. : Мир, 1995. - С. 85-104.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Маниатис Т., Фрич Э., Сэмбрук Д. Методы генетической инженерии // В кн. Молекулярное клонирование. - М. : Мир, 1984. - 480 c.</mixed-citation><mixed-citation xml:lang="en">Маниатис Т., Фрич Э., Сэмбрук Д. Методы генетической инженерии // В кн. Молекулярное клонирование. - М. : Мир, 1984. - 480 c.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Birnbaum L.S., Harris M.W., Stocking L.M., Clark A.M., Morrissey R.E. Retinoic acid and 2,3,7,8-tetrachlorodibenzo-p-dioxin selectively enhance teratogenesis in C57BL/6N mice // Toxicol. Appl. Pharmacol. - 1989. - Vol. 98. - P. 487-500.</mixed-citation><mixed-citation xml:lang="en">Birnbaum L.S., Harris M.W., Stocking L.M., Clark A.M., Morrissey R.E. Retinoic acid and 2,3,7,8-tetrachlorodibenzo-p-dioxin selectively enhance teratogenesis in C57BL/6N mice // Toxicol. Appl. Pharmacol. - 1989. - Vol. 98. - P. 487-500.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Denison M.S., Nagy S.R. Activation of the aryl hydrocarbon receptor by structurally diverse exogenous and endogenous chemicals // Pharmacol. Toxicol. - 2003. - Vol. 43. - P. 309-334.</mixed-citation><mixed-citation xml:lang="en">Denison M.S., Nagy S.R. Activation of the aryl hydrocarbon receptor by structurally diverse exogenous and endogenous chemicals // Pharmacol. Toxicol. - 2003. - Vol. 43. - P. 309-334.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Dolwick K.M., Swanson H.I., Bradfield C.A. In vitro analysis of Ah receptor domains involved in ligand-activated DNA recognition // Proc. Natl. Acad. Sci. - 1993. - Vol. 90. - P. 8566-8570.</mixed-citation><mixed-citation xml:lang="en">Dolwick K.M., Swanson H.I., Bradfield C.A. In vitro analysis of Ah receptor domains involved in ligand-activated DNA recognition // Proc. Natl. Acad. Sci. - 1993. - Vol. 90. - P. 8566-8570.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Ferencz C., Rubin J.D., Loffredo C.A., Magee C.M. The epidemiology of congenital heart disease, The Baltimore-Washington Infant Study (1981-1989). Perspectives in Pediatric Cardiology. - Mount Kisco, NY, 1993. - Vol. 4.</mixed-citation><mixed-citation xml:lang="en">Ferencz C., Rubin J.D., Loffredo C.A., Magee C.M. The epidemiology of congenital heart disease, The Baltimore-Washington Infant Study (1981-1989). Perspectives in Pediatric Cardiology. - Mount Kisco, NY, 1993. - Vol. 4.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Fernandez-Salguero P., Pineau T., Hilbert D.M., McPhail T., Lee S.S., Kimura S., Nebert D.W., Rudikoff S., Ward J.M., and Gonzalez F.J. Immune system impairment and hepatic fibrosis in mice lacking the dioxin-binding Ah receptor // Science. - 1995. - Vol. 268. - P. 722-726.</mixed-citation><mixed-citation xml:lang="en">Fernandez-Salguero P., Pineau T., Hilbert D.M., McPhail T., Lee S.S., Kimura S., Nebert D.W., Rudikoff S., Ward J.M., and Gonzalez F.J. Immune system impairment and hepatic fibrosis in mice lacking the dioxin-binding Ah receptor // Science. - 1995. - Vol. 268. - P. 722-726.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Fyler D.C. Ventricular septal defect // Nadas’ Pediatric Cardiology. - Philadelphia, Pa: Hanley &amp; Delfus, Inc., 1992. - P. 435-457.</mixed-citation><mixed-citation xml:lang="en">Fyler D.C. Ventricular septal defect // Nadas’ Pediatric Cardiology. - Philadelphia, Pa: Hanley &amp; Delfus, Inc., 1992. - P. 435-457.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Hinton R.B. Jr., Yutzey K.E., Benson D.W. Congenital heart disease: Genetic causes and developmental insights // Progress in Pediatric Cardiology. - 2005. - Vol. 20. - P. 101-111.</mixed-citation><mixed-citation xml:lang="en">Hinton R.B. Jr., Yutzey K.E., Benson D.W. Congenital heart disease: Genetic causes and developmental insights // Progress in Pediatric Cardiology. - 2005. - Vol. 20. - P. 101-111.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Hoffman J., Kaplan S. The incidence of congenital heart disease // J. Am.Coll. Cardiol. - 2002. - Vol. 39. - P. 1890-1900.</mixed-citation><mixed-citation xml:lang="en">Hoffman J., Kaplan S. The incidence of congenital heart disease // J. Am.Coll. Cardiol. - 2002. - Vol. 39. - P. 1890-1900.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Hoffman J.I. Incidence of congenital heart disease: I. Postnatal incidence // Pediatr. Cardiol. - 1995. - Vol. 16. - P. 103-113.</mixed-citation><mixed-citation xml:lang="en">Hoffman J.I. Incidence of congenital heart disease: I. Postnatal incidence // Pediatr. Cardiol. - 1995. - Vol. 16. - P. 103-113.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Kaname K., Junko W., Hidetaka E., Kei N., Chikako K., Shinichi H. Polymorphisms of human Ah receptor gene are not involved in lung cancer // Pharmacogen. and genom. - 1995 - Vol. 5 - P. 151-158.</mixed-citation><mixed-citation xml:lang="en">Kaname K., Junko W., Hidetaka E., Kei N., Chikako K., Shinichi H. Polymorphisms of human Ah receptor gene are not involved in lung cancer // Pharmacogen. and genom. - 1995 - Vol. 5 - P. 151-158.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Kern P.A., Fishman R.B., Song W., Brown A.D., Fonseca V. The effect of 2,3,7,8-tetachlorodibenzo-p-dioxin (TCDD) on oxidative enzymes in adipocytes and liver // Toxicology. - 2002. - Vol. 171. - P. 117-125.</mixed-citation><mixed-citation xml:lang="en">Kern P.A., Fishman R.B., Song W., Brown A.D., Fonseca V. The effect of 2,3,7,8-tetachlorodibenzo-p-dioxin (TCDD) on oxidative enzymes in adipocytes and liver // Toxicology. - 2002. - Vol. 171. - P. 117-125.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Koyano S., Saito Y., Fukushima-Uesaka H., Ishida S., Ozawa S., Kamatani N., Minami H., Ohtsu A., Hamaguchi T. Functional analysis of six human aryl hydrocarbon receptor variantsIn a japanese population // Am. Soc. for Pharm. and Exp. Therap. - 2005. - Vol. 33. - P. 1254-1260.</mixed-citation><mixed-citation xml:lang="en">Koyano S., Saito Y., Fukushima-Uesaka H., Ishida S., Ozawa S., Kamatani N., Minami H., Ohtsu A., Hamaguchi T. Functional analysis of six human aryl hydrocarbon receptor variantsIn a japanese population // Am. Soc. for Pharm. and Exp. Therap. - 2005. - Vol. 33. - P. 1254-1260.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Lahvis G.P., Pyzalski R.W., Glover E., Pitot H.C., McElwee M.K., and Bradfield C. The aryl hydrocarbon receptor is required for developmental closure of the ductus venosus in the neonatal mouse // Mol. Pharmacol. - 2005. - Vol. 67. - P. 714-720.</mixed-citation><mixed-citation xml:lang="en">Lahvis G.P., Pyzalski R.W., Glover E., Pitot H.C., McElwee M.K., and Bradfield C. The aryl hydrocarbon receptor is required for developmental closure of the ductus venosus in the neonatal mouse // Mol. Pharmacol. - 2005. - Vol. 67. - P. 714-720.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Lund A.K., Peterson S.L., Timmins G.S., and Walker M.K. Endothelin-1-mediated increase in reactive oxygen species and NADPH Oxidase activity in hearts of aryl hydrocarbon receptor (AhR) null mice // Toxicol. Sci. - 2005. - Vol. 88. - P. 265-273.</mixed-citation><mixed-citation xml:lang="en">Lund A.K., Peterson S.L., Timmins G.S., and Walker M.K. Endothelin-1-mediated increase in reactive oxygen species and NADPH Oxidase activity in hearts of aryl hydrocarbon receptor (AhR) null mice // Toxicol. Sci. - 2005. - Vol. 88. - P. 265-273.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Lund A.K., Goens M.B., Kanagy N.L., and Walker M.K. Cardiac hypertrophy in aryl hydrocarbon receptor null mice is correlated with elevated angiotensin II, endothelin-1, and mean arterial blood pressure // Toxicol. Appl. Pharmacol. - 2003. - Vol. 193. - P. 177-187.</mixed-citation><mixed-citation xml:lang="en">Lund A.K., Goens M.B., Kanagy N.L., and Walker M.K. Cardiac hypertrophy in aryl hydrocarbon receptor null mice is correlated with elevated angiotensin II, endothelin-1, and mean arterial blood pressure // Toxicol. Appl. Pharmacol. - 2003. - Vol. 193. - P. 177-187.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Lund A.K., Goens M.B., Nunez B.A., and Walker M.K. Characterizing the role of endothelin-1 in the progression of cardiac hypertrophy in aryl hydrocarbon receptor (AhR) null mice // Toxicol. Appl. Pharmacol. - 2006. - Vol. 212. - P. 127-135.</mixed-citation><mixed-citation xml:lang="en">Lund A.K., Goens M.B., Nunez B.A., and Walker M.K. Characterizing the role of endothelin-1 in the progression of cardiac hypertrophy in aryl hydrocarbon receptor (AhR) null mice // Toxicol. Appl. Pharmacol. - 2006. - Vol. 212. - P. 127-135.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Moller J.H., Moodie D.S., Blees M., Norton J.B., Nouri S. Symptomatic heart disease in infants: comparison of three studies performed during 1969-1987 // Pediatr. Cardiol. - 1995. - Vol. 16. - P. 216-222.</mixed-citation><mixed-citation xml:lang="en">Moller J.H., Moodie D.S., Blees M., Norton J.B., Nouri S. Symptomatic heart disease in infants: comparison of three studies performed during 1969-1987 // Pediatr. Cardiol. - 1995. - Vol. 16. - P. 216-222.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Mиnzel P.A., Schmohl S., Heel H., Kälberer K., Bock-Hennig B.S., Bock K.W. Induction of Human UDP Glucuronosyltransferases (UGT1A6, UGT1A9, and UGT2B7) by t-Butylhydroquinone and 2,3,7,8-Tetrachlorodibenzo-p-Dioxin in Caco-2 Cells // Drug Metab. Dispos. - 1999. - Vol. 27. - P. 569-573.</mixed-citation><mixed-citation xml:lang="en">Mиnzel P.A., Schmohl S., Heel H., Kälberer K., Bock-Hennig B.S., Bock K.W. Induction of Human UDP Glucuronosyltransferases (UGT1A6, UGT1A9, and UGT2B7) by t-Butylhydroquinone and 2,3,7,8-Tetrachlorodibenzo-p-Dioxin in Caco-2 Cells // Drug Metab. Dispos. - 1999. - Vol. 27. - P. 569-573.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Quattrochi L.C., Vu T., Tukey R.H. The human CYP1A2 gene and induction by 3-ethylcholanthrene // J. Biol. Chem. - 1994. - Vol. 269. - P. 6949-6954.</mixed-citation><mixed-citation xml:lang="en">Quattrochi L.C., Vu T., Tukey R.H. The human CYP1A2 gene and induction by 3-ethylcholanthrene // J. Biol. Chem. - 1994. - Vol. 269. - P. 6949-6954.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Sugatani J., Nishitani S., Yamakawa K., Yoshinari K., Sueyoshi T., Negishi M. Transcriptional Regulation of Human UGT1A1 Gene Expression: Activated Glucocorticoid Receptor Enhances constitutive Androstane Receptor/Pregnane X Receptor-Mediated UDP-Glucuronosyltransferase 1A1 Regulation with Glucocorticoid Receptor-Interacting Protein 1 // Mol. Pharm. - 2005. - Vol. 67. - P. 845-855.</mixed-citation><mixed-citation xml:lang="en">Sugatani J., Nishitani S., Yamakawa K., Yoshinari K., Sueyoshi T., Negishi M. Transcriptional Regulation of Human UGT1A1 Gene Expression: Activated Glucocorticoid Receptor Enhances constitutive Androstane Receptor/Pregnane X Receptor-Mediated UDP-Glucuronosyltransferase 1A1 Regulation with Glucocorticoid Receptor-Interacting Protein 1 // Mol. Pharm. - 2005. - Vol. 67. - P. 845-855.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Takahata S., Sogawa K., Kobayashi A., Ema M., Mimura J., Ozaki N. Transcriptionally Active Heterodimer Formation of an Arnt-like PAS Protein, Arnt3, with HIF-1a, HLF, and Clock // Bioch. bioph. res. Commun. - 1998. - Vol. 248. - P. 789-794.</mixed-citation><mixed-citation xml:lang="en">Takahata S., Sogawa K., Kobayashi A., Ema M., Mimura J., Ozaki N. Transcriptionally Active Heterodimer Formation of an Arnt-like PAS Protein, Arnt3, with HIF-1a, HLF, and Clock // Bioch. bioph. res. Commun. - 1998. - Vol. 248. - P. 789-794.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Whitlock J.P. Induction of cytochrome P4501A1 // Annu. Rev. Toxicol. - 1999. - Vol. 39. - P. 103-125.</mixed-citation><mixed-citation xml:lang="en">Whitlock J.P. Induction of cytochrome P4501A1 // Annu. Rev. Toxicol. - 1999. - Vol. 39. - P. 103-125.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Yueh M., Huang Y., Chen S., Nguyen N., Tukey R. Involvement of the xenobiotic response element (XRE) in Ah receptor-mediated induction of human UDP-glucuronosyltransfer-ase 1A1 // J. Biol. Chem. - 2003. - Vol. 278. - P. 15001-15006.</mixed-citation><mixed-citation xml:lang="en">Yueh M., Huang Y., Chen S., Nguyen N., Tukey R. Involvement of the xenobiotic response element (XRE) in Ah receptor-mediated induction of human UDP-glucuronosyltransfer-ase 1A1 // J. Biol. Chem. - 2003. - Vol. 278. - P. 15001-15006.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang R., Zuckerman J.H., Giller C.A., Levine B.D. Transfer function analysis of dynamic cerebral autoregulation in humans // Am. J. Physiol. - 1998. - Vol. 274. - P. 233-241.</mixed-citation><mixed-citation xml:lang="en">Zhang R., Zuckerman J.H., Giller C.A., Levine B.D. Transfer function analysis of dynamic cerebral autoregulation in humans // Am. J. Physiol. - 1998. - Vol. 274. - P. 233-241.</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>
