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Molecular Medicine Peer-reviewed scientific journal

Found: 202

ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 30–40

A personalized approach to the treatment and prevention of diabetic foot: molecular mechanisms and the role of taxifolin

Aim. To substantiate the pathogenetic rationale for including aqueous solution of dihydroquercetin (taxifolin) in the comprehensive treatment of diabetic foot and to present the results of a case series on the application of this form in patients with trophic …

10.29296/24999490-2025-06-05Details ↗
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 ↗
ОБЗОР2025 · pp. 64–74

The Role of P2X7 Receptors in the Pathogenesis of Depression and Autism Spectrum Disorders

Introduction. Purinergic signaling pathways in brain cells can play an important role both in physiological conditions and in depression and autism spectrum disorders. The purpose of this literature review was a systematic analysis of information in the modern…

10.29296/24999490-2025-04-10Details ↗
ОБЗОР2025 · pp. 55–63

Neurotoxic complications of cancer chemotherapy

Introduction. Neurotoxicity is a common complication of chemotherapy that negatively affects the quality of life of cancer patients. Damage to the nervous system affects both the peripheral nerves (peripheral neuropathy) and the central nervous system (chemo b…

10.29296/24999490-2025-04-09Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 43–48

Prognostic significance of CD68+ macrophages in autoimmune inflammation in experimental study

Introduction. Autoimmune oophoritis is one of the causes of premature ovarian insufficiency in 3–40% of cases. Representative diagnosis is possible only through histological examination of ovarian biopsy material, which complicates the identification of early …

10.29296/24999490-2025-04-07Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 10–15

Single nucleotide variant of the epithelial sodium channel gene SCNN1A (RS11064153) as a predictor of the development of arterial hypertension

Relevance. Poor blood pressure control remains a leading cause of cardiovascular morbidity and mortality worldwide. Despite the fact that today information is actively accumulating about various genetic markers as predictors of many diseases, information about…

10.29296/24999490-2025-04-02Details ↗
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. 3–10

Pathogenetic aspects of steroid-resistant severe bronchial asthma

Purpose of the review. The purpose of this review was to summarize the available relevant data on pathogenetic mechanisms in the formation of steroid resistance in severe bronchial asthma. Material and methods. The analysis of domestic sources on the CyberLeni…

10.29296/24999490-2025-03-01Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 54–59

The effect of polymorphism of the NQO1 gene on the content of ubiquinone in blood plasma and the state of functional activity of mitochondria in patients with chronic heart failure

Introduction. Chronic heart failure is a multifactorial disease, an important role in the pathogenesis of which is played by disorders of the functions of mitochondria and energy metabolism in cardiomyocytes, as well as a significant contribution is made by ge…

10.29296/24999490-2025-02-07Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 56–64

COVID-19 IN THE CENTRAL NERVOUS SYSTEM: ROUTES OF ENTRY AND INFLUENCE ON GLIOMAGENESIS

Introduction. The pathogenesis of infection of the central nervous system (CNS) with SARS-CoV2 and nervourological complications are still poorly understood, as well as the link of viral infection with the risk and the course of gliomas. The aim. Evaluating of…

10.29296/24999490-2025-01-07Details ↗
ОБЗОР2024 · pp. 29–39

Innovative approaches to genome editing in the treatment of neurodegenerative diseases

The purpose of this review is to analyze current advances in the field of genome editing, their application for the modeling and treatment of neurodegenerative diseases, as well as to discuss current limitations and prospects for overcoming barriers in clinica…

10.29296/24999490-2024-06-04Details ↗
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 ↗
ОБЗОР2024 · pp. 14–20

Experimental models of lung sarcoidosis

Introduction. Sarcoidosis is a systemic granulomatous disease of unknown origin. The study of its features and the development of new diagnostic and treatment methods are limited by the absence of generally accepted experimental models. The purpose of the revi…

10.29296/24999490-2024-06-02Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2024 · pp. 53–56

PATHOGENETIC ROLE OF CHANGES SERUM LEVEL INTERLEUKIN-4 DURING THERAPY FOR ULCERATIVE COLITIS

Introduction. An important pathogenetic link in systemic inflammation in ulcerative colitis (UC) is dysregulation of the immune response. The aim of the study: to study pathogenetic changes in the serum level of interleukin (IL)-4 during UC therapy. Methods. 6…

10.29296/24999490-2024-04-08Details ↗
ОБЗОР2024 · pp. 3–11

FUNCTIONAL CHARACTERISTICS OF THE RAGE MOLECULE IN INTERCELLULAR INTERACTIONS IN NORMAL AND LUNG PATHOLOGY

Introduction. The receptor for advanced glycation end products (RAGE) is a pattern recognition receptor that is highly expressed in healthy lungs and performs homeostatic function there. However, the exact mechanisms of development of these diseases remain unk…

10.29296/24999490-2024-04-01Details ↗
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 ↗

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