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Molecular Medicine Peer-reviewed scientific journal

Found: 27

ОБЗОР2026 · pp. 107–116

Genetic architecture and molecular mechanisms of cerebrovascular diseases: ischemic stroke, cerebral small vessel disease and intracranial aneurysms in the context of personalized medicine

Introduction. Cerebrovascular diseases are a heterogeneous group of conditions shaped by the interaction of polygenic susceptibility, rare monogenic variants, vascular remodeling, neuroinflammation, dysregulated hemostasis, and epigenetic reprogramming. Recent…

10.29296/24999490-2026-03-15Details ↗
ОБЗОР2025 · pp. 89–96

The Impact of Genetic Polymorphisms in Toll-like Receptor Genes on Interaction with Helicobacter pylori

The aim of the study. To describe the interaction between Helicobacter pylori and Toll-like receptors, and to outline the role of TLRs gene polymorphisms in the pathogenesis of this infection. Material and methods. An analysis of publications from 2000 to 2025…

10.29296/24999490-2025-05-10Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 79–88

Glutathione: a key molecule of redox homeostasis and its potential for nutritional and metabolic regulation. a review of the literature

Introduction. Glutathione (GSH) is a key intracellular antioxidant involved in maintaining redox homeostasis, detoxifying xenobiotics, regulating immune and neurotransmitter systems, and supporting protein folding and degradation. Depletion of GSH is associate…

10.29296/24999490-2025-05-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 39–47

Ways to increase freedom from DOAC-dependent complications in elderly patients with polypharmacy and chronic kidney disease: molecular and genetic aspects

Introduction. Thanks to advances in modern medicine, it has been possible to significantly increase life expectancy. With the high effectiveness of methods for diagnosing and treating many chronic pathologies, a sharp increase in the number of elderly patients…

10.29296/24999490-2025-03-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2024 · pp. 48–53

Genetic predictors of the risk of developing complications in the immediate postoperative period following combat trauma

Introduction. Paratraumatic eczema (PTE), being a type of microbial eczema, occurs after surgical interventions, chronic wound healing, accompanied by pronounced inflammatory changes with hyperemia, edema, exudation, soreness and itching. Genetic polymorphisms…

10.29296/24999490-2024-02-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2022

THE ROLE OF SOME GENETIC POLYMORPHISMS OF IL-10 IN THE DEVELOPMENT OF VARICELLA IN MILITARY PERSONNEL

Introduction. Currently, scientists are paying increasing attention to the genetic condition of various pathologies. According to recent studies, cytokines play an essential role in the immune response in various pathological processes. The detection of geneti…

10.29296/24999490-2022-01-10Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2019

ANALYSIS OF POLYMORPHISM OF GENES OF THE HEMOSTASIS SYSTEM IN PREGNANT WOMEN SUFFERING A MIGRAINE

Introduction. The study of the genetic mechanisms of migraines is based on the investigation of genes of possible susceptibility and analysis of the influence of gene polymorphism in combination with environmental factors that form the pathogenetic chain of th…

10.29296/24999490-2019-03-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

GENETIC POLYMORPHISM OF F2, F5 AND VKORC1 IN POPULATIONS OF BURYATS, TELEUTS AND RUSSIANS OF THE EASTERN SIBERIA

Introduction. The study of the prevalence of genetic risk factors for thrombosis-associated diseases in the indigenous population of Siberia is an important issue in current medicine. The aim of the study. The aim of this work is to study the allele frequencie…

10.29296/24999490-2018-03-06Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2018

«RISKY» COMBINATIONS OF CANDIDATE GENES FOR HYPERPLASTIC PROCESSES OF THE ENDOMETRIUM

Introduction. Endometrial hyperplasia represents a chronic progressive disease characterized by high prevalence among women in older age groups. The aim of the study. To study the involvement of combinations of candidate genes in the formation of hyperplastic …

10.29296/24999490-2018-02-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2017

TOLL-LIKE RECEPTOR-4 GENETIC POLYMORPHISM IN ERYSIPELAS PATIENTS

Introduction. Erysipelas is characterized by consistently high morbidity rate, pronounced tendency to recur, the frequent change of lymph circulation, formation of secondary elephantiasis and others symptoms. The prediction of the course of erysipelas is unres…

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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

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

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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ОБЗОР2016

STEROID SENSITIVITY IN BRONCHIAL ASTHMA

The main purpose of the treatment of bronchial asthma is achievement and maintenance of the control over the symptoms of disease at optimal level. For this purpose in terms of basic therapy there is used inhalation of as glucocorticosteroids as well systemic g…

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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

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

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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ОБЗОР2015

THE PHARMACOGENETIC MECHANISMS OF DEVELOPMENT OF METABOLIC DISORDERS ASSOCIATED WITH THE SECOND-GENERATION ANTIPSYCHOTICS

Antipsychotics are the main medication for schizophrenia treatment. Recently the wideused group of them became second-generation antipsychotics (SGA). Due to that, problem of metabolic disturbances as side effect of SGA is more actually. The development of pha…

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