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Molecular Medicine Peer-reviewed scientific journal

Found: 137

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

POLYMORPHISM ANALYSIS OF THE ACTA2 GENE BY PYROSEQUENCING IN PATIENTS WITH NON-FAMILIAL THORACIC AORTIC ANEURYSMS

Introduction. The ACTA2 gene encodes α-actin in aortic smooth muscle cells, and its mutations may cause thoracic aortic aneurysms. Analysis of ACTA2 polymorphism can be used in a complex risk assessment of non-familial thoracic aortic aneurysms. The aim of the…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

ASSOCIATION BETWEEN XRCC1 ARG399GLN AND P53 ARG72PRO POLYMORPHIC MARKERS AND THE RISK OF BREAST CANCER RISK IN KYRGYZ WOMEN

Aim. To investigate the possible association between XRCC1 Arg399Gln and p53 Arg72Pro polymorphism and the risk of breast cancer (BC) risk in Kyrgyz women. Methods. The XRCC1 Arg399Gln and p53 Arg72Pro genotypes were determined with the use of the polymerase c…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

GENE SLCO1B1 ASSOCIATED WITH STATIN-INDUCED MYOPATHY IN RUSSIAN AND SAKHA (YAKUTIA) STATIN INTAKE PATIENTS SUFFERED FROM HYPERLIPIDEMIA

Introduction. SLCO1B1 encodes the organic anion-transporting polypeptide which has been shown to regulate the hepatic uptake of statins. SLCO1B1*5 genetic variant is associated with the high risk for statin-induced myopathy in patients with statins therapy. Ai…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

TO THE MECHANISM OF MYOCARDIAL REMODELING IN THE ACUTEST PHASE OF EXPERIMENTAL MYOCARDIAL INFARCTION

The purpose of research. The study of the features of the left ventricle remodeling in the acutest stage of experimental myocardial infarction and the possibility of the correction of detected injuries. Methods. Experimental myocardial infarction in rats was i…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

MOLECULAR-GENETIC CHARACTERISTICS OF EARLY RHEUMATOID ARTHRITIS

Objective. To study the distribution of PTPN22, TNFAIP3, CTLA4, TNFA, IL-6, IL-6R, IL-10, MCP-1, ICAM1 alleles and genotypes in early rheumatoid arthritis (eRA) patients and controls, and assess their value as potential molecular-genetic markers of predisposit…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

CAV1 GENE POLYMORPHISM IN PATIENTS WITH PRIMARY OPEN-ANGLE GLAUCOMA

Introduction. Glaucoma is associated with a progressive decrease of visual functions, leading to blindness. One of the important factors is the outflow of the ocular fluid. А genetic association study has identified a sequence variant at the chromosome 7q31 (r…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

INFLAMMATORY MARKERS OF CORONARY ATHEROSCLEROSIS

Introduction. Currently in the world there are conducted numerous studies on the search for biomarkers associated with increased risk of coronary heart disease (CHD). The aim of the study. The study of the levels of such inflammatory biomarkers as the tumor ne…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

ASSOCIATION ANALYSIS OF POLYMORPHISM IN MODIFYING GENES FOR BLOOD PRESSURE AND GENES FOR IMMUNE RESPONSE REGULATION WITH ISCHEMIC HEART DISEASE

Introduction. Genetic predispose to ischemic heart disease (CHD) are the priority directions in the study of etiological factors this condition. The aim of the study. Association analysis of polymorphism in modifying genes for blood pressure and genes for immu…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

ABOUT POSSIBILITY OF THE USE OF AFOBAZOL FOR TREATMENT OF ALCOHOLIC CARDIOMYOPATHY AND PREVENTION OF ITS CONCOMITANT COMPLICATIONS

The aim of the study. The proof of afobazole efficacy for treatment and prevention of alcoholic cardiomyopathy and attendant complications using the previously developed translational model. Materials and methods. Alcoholic cardiomyopathy was produced by conti…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

GE-ASSOSIATED ASPECTS OF THE EXPRESSION OF HUMAN ENDOTHELIAL SIGNAING MOLECULES AND THEIR ROLE IN THE DEVELOPMENT OF CARDIO-VASCULAR PATHOLOGY

Introduction. Age-assosiated endothelial changes are one of the reasons of the development of cardio-vascular pathology. Moreover, molecular mechanisms of human endothelium aging are investigated only slightly. Thus, the problem of pathogenesis of cardio-vascu…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

ANALYSIS OF ASSOCIATION BETWEEN THE CHEMOKINE AND CHEMOKINE RECEPTOR GENES AND ESSENTIAL HYPERTENSION

Introduction. Chemokines are a group of proteins that plays an active role in the regulation of the vascular wall inflammation during the development of essential hypertension. The aim of the study was to investigate an association between essential hypertensi…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

TRANSLATION MODEL OF ALCOHOLIC CARDIOMYOPATHY

The aim of the study – the development of translational models of the alcoholic cardiomyopathy in rats to search and study the action mechanism of new original drugs for the treatment of this pathology. Methods. The complex of echocardiographic, electrophysiol…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

SOMATIC AND GERMLINE MUTATIONS IN GASTRIC CANCER

Introduction. Most cases of gastric cancer (GC) occur sporadically. Until recently, diffuse hereditary gastric cancer associated with the CDH1 gene mutations was considered the only hereditary form (about 1–3% of all tumors of the stomach). However, a signific…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

ACTUAL ASPECTS OF MOLECULAR-BIOLOGY CLASSIFICATION OF BREAST CANCER

There is represented immunohistochemical and molecular biological characteristic of some histological types of breast cancer. The assessment of molecular biomarkers in breast cancer has two practical results: identification of risk groups, requiring additional…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

CLINICAL AND MOLECULAR ASPECTS OF GASTRIC CANCEROGENESIS

Gastric cancer (GC) arises through a multistep process characterized by the progressive accumulation of molecular alterations of tumor cells that is involving genetic and epigenetic mechanisms. GC is a very complex and heterogeneous disease, and although much …

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

PREDICTION THE RISK OF ISCHEMIC STROKE ON THE BASE ON GENETIC [APOE (Ε2, Ε3, Ε4), ACE (I / D), MTHFR (677S> T)] AND NON-GENETIC FACTORS WITH THE USE OF MODERN METHODS OF THE THEORY OF RECOGNITION BY PRECEDENTS

Introduction. Ischemic stroke (IS) is a multifactorial disease, resulting from a complex interaction of genetic and environmental factors. Individual cause of the disease, multiple factors and symptoms require advanced mathematical methods of predicting IS ris…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

ASSOCIATION OF MOLECULAR GENETIC VARIANTS OF VITAMIN D RECEPTOR WITH THE GRADE OF INFLAMMATORY CHANGES

Introduction. Although the interrelationship between disorders of the skeletal system with chronic gastroduodenitis (HGD) and infection with Helicobacter pylori (HP) currently has been well-studied in the literature practically there are no data reflecting the…

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