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Molecular Medicine Peer-reviewed scientific journal

Found: 45

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

ASSOTIATION OF GENES POLYMORPHISMS OF XENOBIOTICS-METABOLIZING ENZYMES WITH RECURRENT MISCARRIAGE

Introduction. Recurrent miscarriage (RM) – a prevalent pathology in women. However, the mechanisms of its occurrence are studied insufficiently. A genetic factor may be one of the causes of RM in women. The aim of the study was to investigate the association o…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

ASSOCIATION OF ADRENERGIC RECEPTORS GENES POLYMORPHISMS (ADRA2A, ADRB3) WITH OBESITY IN TATARS WOMEN

Association of adrenergic receptors gene polymorphisms in overweight persons has been shown by Gagnon J. et al. in 1996. For the locus Trp64Arg (rs4994) β3-adrenoceptor gene was shown to be associated with the risk of obesity, confirmed by the works of a numbe…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

PROTEOMIC AND METABOLOMIC MANIFESTATIONS OF DIFFERENT VARIANTS OF APOLIPOPROTEIN E GENES POLYMORPHISM IN OBESE PATIENTS

Introduction. Currently questions on the role of genes polymorphism that regulate metabolism and implicated in metabolic disorders are disputed. Objective. The study of proteomic and metabolomic manifestations of different variants of apolipoprotein E genes po…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

ASSOCIATION OF INFECTIVE ENDOCARDITIS WITH GENE POLYMORPHISMS OF THE PHASE II XENOBIOTIC DETOXICATION SYSTEM ENZYMES

Introduction. Pathogenesis of infective endocarditis (IE) is not quite clear till now. In last years research of variants of the genes connected with pathogenesis of IE was performed. The aim. The investigation of IE association with gene single-nucleotide pol…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

POLYMORPHISM OF UGT1A1 GENE IN PATIENTS WITH COLORECTAL CANCER OF THE SOUTH OF RUSSIA: RESULTS OF PILOT RESEARCH

Introduction. Irinotekan is widely used in the treatment of oncological diseases and allows to achieve the objective answer in 35–70% of cases depending on the applied schedule of the treatment. Individual toxicity of a preparation for patients is determined b…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

G276T ADIPONECTIN GENE POLYMORPHISM IN DEVELOPMENT OF OBESITY AND OBESITY-RELATED DISEASES IN KYRGYZ POPULATION

The aim of this work was to study the relationship between adiponectin gene polymorphisms G276T with obesity and obesity-related diseases in the Kyrgyz population. Material and methods. We genotyped 288 Kyrgyz subjects (143 women and 145 men; age range: 30–75 …

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

ASSOCIATIONS OF CANDIDATE GENES IN THE FORMATION OF UTERINE FIBROIDS

Introduction. Uterine fibroids – a benign tumor, growing from immature muscle cells of the vascular wall of the uterus. It ranked first among the benign tumors of the genital organs, with one in ten suffers from gynecological patients with uterine myoma. The a…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2016

GENETIC AND MORPHOLOGICAL MARKERS OF NON-DEVELEPING PREGNANCY

Introduction. High rate of non-developing pregnancy in the structure of reproductive loss dictates the need to identify the etiological factors of this disease at different levels of organization of alive matter. The aim of the study. The search for associatio…

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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

TNF GENE POLYMORPHISMS AFFECT THE PROGRESSION OF THE DISEASE IN BREAST CANCER PATIENTS

Introduction. Tumor necrosis factor (TNF) plays a central role in the development of inflammatory and neoplastic processes. In the TNF gene promoter region there are -308(g/a) and -238(G/A) polymorphisms with different influence on the level of expression of T…

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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 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

PREVALENCE OF CYP2C19 GENETIC POLYMORPHISMS IN RUSSIAN PATIENTS WITH PEPTIC ULCERS TREATED WITH PROTON PUMP INHIBITORS

Introduction. Cytochrome P-450 2C19 is the main isoenzyme responsible for the metabolism of proton pump inhibitors, the main group of drugs for treating stomach and duodenal ulcer. There are genetic differences that affect the activity of this enzyme: there ar…

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

CONCENTRATION OF INTERLEUKINES IN BLOOD PLASMA IN PATIENTS WITH CHRONIC CEREBRAL ISCHEMIA – CARRIERS OF ANTI-INFLAMMATORY CYTOKINES GENES POLYMORPHISMS

Introduction. There were examined 195 patients with chronic сerebrovasсular pathology and 149 healthy residents of the Zabaykalsky region. The aim of the study. Detection of genetic polymorphism in cytokines IL4-589С>T, IL10-1082G>A, IL10-819C>T, IL10-592C>A, …

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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

ANALYSIS OF GENES POLYMORPHISM: TNFΑ (-308G/A), IL6 (-174G/C), TGFΒ1 (-509 C/T), IL10 (-1082 G/A) AND PTPN22 (RS 2476601) (G/A) AT ATHEROSCLEROSIS

Introduction. According to inflammatory theory of atherosclerosis the immune damage of arteries with an autoimmune component – is the main link of its pathogenesis. The imbalance of cytokines production influences on course and prognosis of atherosclerosis. As…

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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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ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2015

APPLICATION OF PHARMACOGENETICS TESTING IN PATIENTS WITH CARDIAC VALVE REPLACEMENT

Introduction. Pharmacogenetic testing allows of increasing efficacy of anticoagulation therapy, reducing time required for adjusting therapeutic dose, and considerably reducing number of complications. The aim of the study. To investigate the dependence of the…

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Research article2014

IL1β GENE POLYMORPHISM IN CHRONIC VIRAL HEPATITIS B AND C IN CHILDREN

Introduction. One of the important tasks of hepatology is the prognosis of viral hepatitides. The prognosis is based on the analysis of genetic determination of the functioning of antiviral immunity, particularly, of the cytokine system. The aim of the study w…

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