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Molecular Medicine Peer-reviewed scientific journal

Found: 73

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2026 · pp. 3–9

THE INVOLVEMENT OF GLUTAMATE AMPA RECEPTORS IN THE REGULATION OF T-CELL ADHESION IN MULTIPLE SCLEROSIS

Introduction. Glutamate receptors are involved in modulating key T-lymphocyte functions, including proliferation, chemotaxis, and others. In the context of the immunopathogenesis of multiple sclerosis (MS), studying the mechanisms underlying these effects is o…

10.29296/24999490-2026-02-01Details ↗
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. 58–69

Polypragmasy in elderly and senile patients with chronic kidney disease: START/STOP criteria in elderly and senile patients taking DOAC

Introduction. Thanks to the achievements of modern medicine, it was possible to significantly increase the life expectancy of the population. Molecular mechanisms of aging include telomere shortening, DNA damage accumulation, mitochondrial dysfunction, leading…

10.29296/24999490-2025-05-07Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 86–91

Characteristics of the gut microbiota of patients with dyspepsia

Introduction: Studying the relationship between functional dyspepsia and gut microbiota will provide insight into the role of individual microorganisms and their metabolic products in the development of this pathology. The aim of the study was to analyze the m…

10.29296/24999490-2025-03-11Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 56–61

Molecular genetic features of iron deficiency anemia phenotypes

Relevance. Iron deficiency anemia is a disease present all over the world and maintaining a high incidence rate of both general and primary morbidity despite various options for correction and prevention of this pathology. Molecular genotyping opens up new pos…

10.29296/24999490-2025-03-07Details ↗
ОБЗОР2025 · pp. 19–29

Molecular mechanisms and pharmacogenetic determinants of II–III generation antihistamines efficacy in allergic bronchial asthma: personalized therapy prospects

Introduction. Allergic bronchial asthma (BA) is accompanied by activation of histamine H1/H4 receptors and variable response to antihistamines. The aim of this review is to analyze the molecular mechanisms of action of second- and third-generation antihistamin…

10.29296/24999490-2025-03-03Details ↗
ОБЗОР2024 · pp. 21–28

Molecular aspects of pathogenesis of chronic lymphocytic leukemia

Introduction. Chronic lymphocytic leukemia (CLL) is the most common leukemia type in adults. CLL is characterized by significant changes in the patient's genome, including both various mutations and epigenetic changes. These changes currently play an important…

10.29296/24999490-2024-06-03Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2024 · pp. 57–64

The role of the AKT1 gene in the pathogenesis of type 2 diabetes mellitus and its complications

Introduction. Type 2 diabetes (T2D) is a chronic metabolic disorder. The number of diabetic people is increasing. AKT1 is a protein kinase and a participant in the PI3K/AKT/mTOR signaling pathway. The aim of the study was to analyze the association of polymorp…

10.29296/24999490-2024-03-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2024 · pp. 60–64

EVALUATION OF IMMUNOTROPIC PROPERTIES OF GLYPROLINE COMPOUNDS IN EXPERIMENTAL HYPERTHYROIDISM

Introduction. Thyroid disease is currently the most common among endocrine pathology. Hyperproduction of thyroid hormones is accompanied by stimulation of humoral reactions, contributing to the development of immune-mediated pathology under certain conditions,…

10.29296/24999490-2024-02-10Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2023 · pp. 27–32

Comparison of the sensitivity of restriction analysis and PCR with high-resolution melting curve analysis for the detection of the R882H mutation in the DNMT3A gene

Introduction. DNMT3A is one of the most frequently mutated genes in acute myeloid leukemia (AML), and the R882H (G>A) substitution is one of the most common mutations in this gene. Restriction analysis and high resolution melting (HRM) analysis are the most co…

10.29296/24999490-2023-06-04Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2023 · pp. 40–48

EXOSOMAL MIRNAS AS POSSIBLE PREDICTORS OF IMMUNE CHECKPOINT INHIBITORS THERAPY RESPONSE IN CLEAR CELL RENAL CELL CARCINOMA

Despite significant advance in clear cell renal cell carcinoma treatment, immune checkpoint inhibitors (ICIs) still have limited therapeutic efficacy. Taking into account the resistance to immunotherapy, observed in malignant neoplasms, the search for predicti…

10.29296/24999490-2023-04-06Details ↗
ОБЗОР2023 · pp. 25–33

MOLECULAR GENETIC BASIS OF CERVICAL CANCER

Introduction. Cervical cancer is one of the most common cancers of the female reproductive system, killing more than 250,000 women each year. The etiological agent that causes cervical cancer is well known. HPV infection with high oncogenic risk is the cause o…

10.29296/24999490-2023-04-04Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2022 · pp. 42–52

ASSOCIATION OF POLYMORPHIC VARIANTS OF NON-ALLELIC GENES ADIPOQ, MTHFR, PON1, KCNJ11, TCF7L2, ITLN1 AND PPARG WITH CLINICAL AND LABORATORY PARAMETERS AMONG OBESE PATIENTS FROM KYRGYZ REPUBLIC

Introduction. In Kyrgyzstan about 60% of the adult population suffers from lipid metabolism disorders of varying degrees. Early identification of persons at increased risk of developing obesity is of great importance, which can be achieved through the study of…

10.29296/24999490-2022-05-06Details ↗
ОБЗОР2021

HPgV INFECTION

Objective: to analyze the literature data on HPgV infection caused by the Human pegivirus-1 virus (formerly hepatitis G, HGV, GBV-C). Materials and methods: search, by keywords, publications in Scopus, PubMed and Elibrary databases for the period from 1995 to …

10.29296/24999490-2021-06-03Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

THE ASSOCIATION OF rs34643859 GENE KCNS1, rs12804550 GENE SCN4B, rs4514993 GENE SCN11A WITH THE SUDDEN CARDIAC DEATH

Introduction. Single nucleotide polymorphisms rs34643859 of the KCNS1 gene, rs12804550 of the SCN4B gene, and rs4514993 of the SCN11A gene were revealed in the analysis of the results of whole exome sequencing of a group of young man died by sudden cardiac dea…

10.29296/24999490-2021-05-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

Development of 3d structures for corneal fibroblasts

Introduction. Advances in biology and medicine in particular in the field of cell technologies allow us to test eye stem cells as an alternative to surgical treatment of corneal pathology. An option to increase the resistance of stem cells to adverse microenvi…

10.29296/24999490-2021-05-08Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2021

A comparison of the protein composition from coronary atherosclerotic plaque at different stages of development

Background: The aim of this study was to investigate individual changes of protein expression in atherosclerotic plaques of coronary arteries at different stages of development of coronary atherosclerosis. Methods: The research object was homogenates of athero…

10.29296/24999490-2021-05-09Details ↗

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