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<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">jsms</journal-id><journal-title-group><journal-title xml:lang="ru">Journal of Siberian Medical Sciences</journal-title><trans-title-group xml:lang="en"><trans-title>Journal of Siberian Medical Sciences</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2542-1174</issn><publisher><publisher-name>Federal state budgetary educational institution of higher education "Novosibirsk state medical university" of  Ministry of Health of the Russian Federation (FSBEI HE NSMU MOH Russia)</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">jsms-36</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>14.00.00 МЕДИЦИНСКИЕ НАУКИ</subject></subj-group></article-categories><title-group><article-title>ПОЛИМОРФИЗМ ГЕНОВ ЭНДОТЕЛИАЛЬНОЙ ДИСФУНКЦИИ И СИСТЕМНОГО ГЕМОСТАЗА У БОЛЬНЫХ ВИБРАЦИОННОЙ БОЛЕЗНЬЮ В СОЧЕТАНИИ С АРТЕРИАЛЬНОЙ ГИПЕРТЕНЗИЕЙ</article-title><trans-title-group xml:lang="en"><trans-title>GENETICAL POLYMORPHISM OF ENDOTHELIAL DYSFUNCTION AND SYSTEMIC HEMOSTASIS AT PATIENTS WITH VIBRATION DISEASE COMBINED WITH ARTERIAL HYPERTENSION</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>Шпагина</surname><given-names>Л. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Shpagina</surname><given-names>L. A.</given-names></name></name-alternatives><email xlink:type="simple">adm@muzgkb2.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>Герасименко</surname><given-names>О. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Gerasimenko</surname><given-names>O. N.</given-names></name></name-alternatives><email xlink:type="simple">ger@muzgkb2.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>Дробышев</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Chachibaya</surname><given-names>Z. K.</given-names></name></name-alternatives><email xlink:type="simple">zaza@muzgkb2.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>Чачибая</surname><given-names>З. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Drobyshev</surname><given-names>V. A.</given-names></name></name-alternatives><email xlink:type="simple">Doctorvik@yandex.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ГБОУ ВПО «Новосибирский государственный медицинский университет» Минздрава России; ГБУЗ НСО «Городская клиническая больница № 2»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>SBEI HPE «Novosibirsk State Medical University of Ministry of Health»; SBHE NR «City clinical hospital № 2»</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ГБОУ ВПО «Новосибирский государственный медицинский университет» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>SBEI HPE «Novosibirsk State Medical University of Ministry of Health»</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2015</year></pub-date><pub-date pub-type="epub"><day>04</day><month>06</month><year>2018</year></pub-date><volume>0</volume><issue>1</issue><fpage>35</fpage><lpage>35</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Шпагина Л.А., Герасименко О.Н., Дробышев В.А., Чачибая З.К., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Шпагина Л.А., Герасименко О.Н., Дробышев В.А., Чачибая З.К.</copyright-holder><copyright-holder xml:lang="en">Shpagina L.A., Gerasimenko O.N., Chachibaya Z.K., Drobyshev V.A.</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://jsms.elpub.ru/jour/article/view/36">https://jsms.elpub.ru/jour/article/view/36</self-uri><abstract><p>В статье представлена характеристика полиморфизма генов EDN1 эндотелина-1, NOS3(e) эндотелиальной NO-синтазы, PAI1 активатора плазминогена типа 1, GP1ba тромбоцитарного гликопротеина-1в и гена TGF-b, как ранних предикторов поражения эндотелия и нарушений системного гемостаза при сочетании вибрационной болезни и артериальной гипертензии. Показано, что у больных с сочетанными формами патологии с высокой частотой выявляются патологические полиморфные варианты генов, отвечающих за состояние эндотелиальных и гемостазиологических процессов.</p></abstract><trans-abstract xml:lang="en"><p>The characteristic of genetical polymorphism of endothelin-1 EDN1, NOS3(e) endothelial NO synthase, PAI1 activator of plasminogen of type 1, GP1ba of thrombocytic glycoprotein-1в and TGF-b gene, as early predictors of endothelium lesion and disease illness and arterial hypertension. It is shown that at patients with combined forms of pathobiology the genetical pathological polymorphic options which are responsible for state endothelial and hemostasiological processes with high frequency are revealed.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>полиморфизм генов</kwd><kwd>эндотелиальная дисфункция</kwd><kwd>аллели</kwd><kwd>вибрационная болезнь</kwd><kwd>артериальная гипертензия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>genetic polymorphism</kwd><kwd>endothelial dysfunction</kwd><kwd>alleles</kwd><kwd>vibration diseases</kwd><kwd>arterial hypertension</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">Кузник Б. И. Клеточные и молекулярные механизмы регуляции системы гемостаза в норме и патологии / Б. И. Кузник. - Чита : Экспресс-издательство, 2010. - 240 с.</mixed-citation><mixed-citation xml:lang="en">Кузник Б. И. 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