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Molecular Medicine Peer-reviewed scientific journal

Found: 9

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 ↗
ОБЗОР2026 · pp. 93–99

Molecular and cellular characteristics of aortic aneurysm at different stages of its development

Introduction. An aortic aneurysm is defined as an irreversible progressive enlargement of the aorta with an increasing risk of rupture, often fatal. It is known that the imbalance of inhibitors and activators of cell matrix proteolysis and the death of smooth …

10.29296/24999490-2026-03-13Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 30–38

Serotonin, 5-HIAA, and membrane serotonin transporter in blood as biomarkers of familial hypercholesterolemia in immature low-density lipoprotein receptor-deficient mice

Introduction. Cardiovascular diseases are the main cause of death and disability in the world population. Serotonin plays a significant role in the development and progression of atherosclerotic processes due to its two classical functions – platelet aggregati…

10.29296/24999490-2025-04-05Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2025 · pp. 92–100

Morphological features of atherosclerotic plaque: modeling of atherosclerosis after stenting as a model of premature aging

Atherosclerosis and the installation of stents can be considered as a model of premature aging of the body. These processes are associated with chronic inflammation, oxidative stress, loss of cellular function, and impaired regeneration, which makes them a con…

10.29296/24999490-2025-03-12Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2023 · pp. 43–50

CLINICAL AND MICROSCOPIC ANALYSIS OF CELLULAR-MOLECULAR COMMUNICATIONS IN FOCAL CORTICAL DYSPLASIA IIIс

Cortical dyslamination with neuronal dysmorphism that occurs adjacent to an arteriovenous malformation (AVM) and is accompanied by epilepsy (E) is classified as FCD IIIc. Its etiology and pathogenesis have yet to be determined. Objective: to clarify the cellul…

10.29296/24999490-2023-03-06Details ↗
ОРИГИНАЛЬНОЕ ИССЛЕДОВАНИЕ2022 · pp. 44–49

POSSIBILITIES OF APPLICATION OF ALLOGENIC TISSUE ENGINEERING PRODUCTS IN THE EXPERIMENTAL URINARY BLADDER RECONSTRUCTION

The article describes the results of an experimental study of tissue-engineering constructions based on lactic acid – poly-L,L-lactide, containing allogeneic cells of various tissue origin. Aim: to show experimentally the possibility of using an allogeneic tis…

10.29296/24999490-2022-06-07Details ↗
ОБЗОР2022 · pp. 9–15

SASP OF ENDOTHELIUM AND VASCULAR SMOOTH MUSCLE CELLS: ROLE IN THE PATHOGENESIS AND THERAPY OF ATHEROSCLEROSIS

The senescence-associated secretory phenotype (SASP) is one of the causes of age-associated diseases, including atherosclerosis. The purpose of the review is to analyze data on the role of SASP cells of the cardiovascular system in the pathogenesis and pharmac…

10.29296/24999490-2022-04-02Details ↗
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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