Search Results - "V. A. Shul'man"

Association of rs3025058 polymorphism with the development of stroke in patients with cardiovascular pathology by Nikulina, S Y, Shulman, V A, Chernova, A A, Prokopenko, S V, Nikulin, D A, Platunova, I M, Tretyakova, S S, Semenchukov, A A, Marilovtseva, O V, Lebedeva, I I, Maksimov, V N, Gurazheva, A A

“…To study the association of single-nucleotide polymorphismrs3025058(5а/6а) with the development of stroke in patients of the East Siberian population with…”
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Genetic predictors of myocardial infarction in subjects of young age by Shesternia, P A, Nikulina, S Iu, Shul'man, V A, Martynova, E A, Demkina, A I, Orlov, P S, Maksimov, V N, Voevoda, M I

“…to investigate associations of single nucleotide polymorphisms (SNP) rs499818 (6p24.1), rs619203 of ROS1 gene (6q22), rs10757278 rs1333049 (9p21.3), rs2549513…”
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Infarction-like changes on electrocardiogram in acute disorder of cerebral circulation by Kuzhel', D A, Shul'man, V A, Matiushin, G V, Kaleĭchik, L V, Fedorova, T D

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Role of SNP markers on chromosome 10 in the pathogenesis of atrial fibrillation by Nikulina, S. Yu, Shishkova, K. Yu, Shulman, V. A., Chernova, A. A., Maximov, V. N.

“…Atrial fibrillation (AF) is one of the most common tachyarrhythmias, contributing to both environmental and genetic factors, a clear understanding of which can…”
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Genetics of atrial fibrillation by Nikulina, S Iu, Shul'man, V A, Kuznetsova, O O, Aksiutina, N V, Chernova, A A, Maksimov, V N, Kulikov, I V, Ustinov, S N, Kazarinova, Iu L, Romashchenko, A G, Voevoda, M I

“…We carried out examination of 103 probands with atrial fibrillation (AF) and 301 their 1st, 2nd, and 3rd degree relatives (main group). In addition we examined…”
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Apoptosis of leukocytes as a marker of neutrophil-endotheliocyte interaction in coronary heart disease by Salmina, A B, Shul'man, V A, Nikulina, S Yu, Trufanova, L V, Fursov, A A, But'yanov, P A, Kuskaev, A P, Bol'shakova, E V, Kotlovskii, M Yu

“…We studied the mechanism of interaction of peripheral blood neutrophils with endothelial cells (expression of cell adhesion molecules and production of NO) and…”
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Association of rs2230806 polymorphism with the development of acute cerebrovascular accident in patients with cardiovascular disease by Nikulina, S. Yu, Shulman, V. A., Chernova, A. A., Prokopenko, S. V., Nikulin, D. A., Platunova, I. M., Tretyakova, S. S., Semenchukov, A. A., Marilovtseva, O. V., Maksimov, V. N., Gurazheva, A. А.

“…Aim. To study the association of single nucleotide polymorphism (SNP) rs2230806 (C>T) with the development of acute cerebrovascular accident (CVA) in East…”
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GIANT CELL MYOCARDITIS IN HIV INFECTION: A FATAL TANDEM by Nikulina, S. Yu, Shesternya, P. A., Kirichenko, A. K., Chernova, A. A., Brusentsov, D. A., Shulman, V. A.

“…Giant cell myocarditis (GCM) is a rare autoimmune disease with the leading role of T-cell disorder in its pathogenesis. The associations are known of this…”
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Association of rs10507391 polymorphism with the development of acute cerebrovascular accident in patients with cardiovascular pathology by Nikulina, S. Yu, Shulman, V. A., Chernova, A. A., Prokopenko, S. V., Nikulin, D. A., Platunova, I. M., Tretyakova, S. S., Chernov, V. N., Marilovtseva, O. V., Kelemeneva, A. N., Maksimov, V. N., Gurazheva, A. A.

“…The aim of the study was to investigatey the association of single-nucleotide polymorphism (SNP) rs10507391 (A>T) with the acute cerebrovascular accident (CVA)…”
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PRIMENENIE EKSPRESS-TESTA «KARDIO-BSZhK» DLYa RANNEY DIAGNOSTIKI INFARKTA MIOKARDA by V. A. Shul'man, S. E. Golovenkin, E. K. Pilipetskaya, V. N. Simulin, V. V. Radionov

“…Инфаркт миокарда - тяжелое заболевание, нередко приводящее к летальному исходу. Ранняя постановка диагноза позволяет своевременно начать необходимые лечебные…”
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Association of rs556621 Polymorphism with Development of Stroke in Patients with Cardiovascular Pathology by Nikulina, S. Yu, Shulman, V. A., Chernova, A. A., Prokopenko, S. V., Nikulin, D. A., Platunova, I. M., Tretyakova, S. S., Maksimov, V. N., Gurazheva, A. A.

“…Aim . To study the association of single nucleotide polymorphism rs556621 (G> T) with development of stroke in patients of the East Siberian population with…”
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Role of Single Nucleotide Polymorphism of СУР17А Gene in the Development of Stroke by Nikulina, S. Yu, Shulman, V. A., Chernova, A. A., Nikulin, D. A., Semenchukov, A. A., Marilovceva, O. V., Tret'jakova, S. S., Lebedeva, I. I., Maksimov, V. N.

“…Background.  The search for genetic predictors of stroke development is actively studied in all developed countries due to the need to address the primary…”
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Polymorphisms of α-2-β-adrenergic receptor and endothelial NO-synthase genes in patients with atrial fibrillation by Shul'man, V A, Nikulina, S Iu, Dudkina, K V, Voevoda, M I, Maksimov, V N, Aksiutina, N V, Chernova, A A, Zlodeev, K V, Allakhverdian, A A

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Differences in the Incidence of Major Risk Factors in Patients with Ischemic or Hemorrhagic Stroke in the Siberian Population by Nikulina, S. Yu, Chernova, A. A., Nikulin, D. A., Shulman, V. A., Prokopenko, S. V., Platunova, I. M., Marilovceva, O. V., Lebedeva, I. I., Semenchukov, A. A., Yakovleva, D. A., Maksimov, V. N., Kuskaeva, A. V.

“…Background.  The study of the incidence of risk factors (RF) of stroke for primary and secondary prevention of this disease remains relevant. There are…”
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FIRST RUSSIA-BASED STUDY OF POLYMORPHISM rs2200733 CHROMOSOME 4q25 ASSOCIATION WITH DEVELOPMENT OF THE LONE ATRIAL FIBRILLATION by Shulman, V. A., Nikulina, S. Yu, Aksyutina N, N. V., Poplavskaya, E. E., Nazarov, B. V., Maksimov, V. N.

“…Atrial fibrillation (AF) is one of the most prevalent tachiarrhythmias, with at date non fully understood etiology. Recently, the attention is paid to genetic…”
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Association of polymorphisms of chromosome 4q25 in patients with atrial fibrillation by Shulman, V. A, Nikulina, S. Yu, Poplavskaya, E. E, Maksimov, V. N, Aksyutina, N. V, Nazarov, B. V

“…The article deals with the issue of genetic determination of atrial fibrillation. In particular, it is shown that a rare polymorphism rs2200733 T allele on…”
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THE ROLE OF ROS1 GENE IN DEVELOPMENT OF STROKE by Nikulin, D. A., Nikulina, D. A., Chernova, A. A., Shulman, V. A., Tretyakova, S. S.

“…Aim. To study the relation of mononucleotide polymorphism G?C (rs619203) of ROS1 gene with the risk of ischemic and hemorrhagic stroke development.Material and…”
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FORECASTING OF CCD IN FAMILIES BY MEANS OF A METHOD OF LOGISTIC REGRESSION IN KRASNOYARSK by Nikulina, S. Yu, Chernova, A. A., Shulman, V. A., Vereshchagina, T. D., Chernov, V. N.

“…Aim. Forecasting of emergence of cardiac conduction defects (CCD) by means of a method of multiple logistic regression for implementation of early diagnostics,…”
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THE POLYMORPHISM OF Α2B-ADRENERGIC RECEPTOR GENE — A NEW GENETIC MARKER OF THE HEREDITARY SICK SINUS SYNDROME by Nikulina, S. Iu, Shulman, V. A., Chernova, A. A., Nikulin, D. A., Voevoda, M. I., Maksimov, V. N.

“…Aim. To study the association of the hereditary sick sinus syndrome (SSS) with gene α2B-adrenergic receptor (ADRA2B) polymorphism.Material and methods. 29…”
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The Role of Transcriptional Factor Gene TBX5 in Development of Disorders of Cadiac Conduction by Nikulina, S Yu, Shulman, V A, Chernova, A A, Tretiyakova, S S, Bazarova, A S, Maximov, V N, Voevoda, M I

“…In order to study relationship between development of idiopathic atrioventricular (AV) and intraventricular disorders of cardiac conduction (DCC) with single…”
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