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Genetic determinants of cardiovascular remodeling n Urbek patients with essential hypertension
Eliseeva M.R., Srozhidinova N.Z., Khamidullaeva G.A., Abdullaeva G.Z., Eliseeva M.R., Srozhidinova N.Z., Khamidullaeva G.A., Abdullaeva G.Z.
Association of thecomplex of polymorphic markers of ACE genes, aldosteronsynthetase and endothelial synthetase of nitric oxide withprogression of chronic glomerulonephritis
Kamyshova E.S., Kutyrina I.M., Nosikov V.V., Shvetsov M.Y., Gorashko N.M., Ignatyev I.V., Voronko О.Е., Shilo V.Y., Alyaev Y.G., Shilov E.M.
REMODELING OF CARDIOVASCULAR SYSTEM AND DEVELOPMENT OF CHRONIC KIDNEY DISEASE IN PATIENTS WITH METABOLIC SYNDROME AND OBESITY: ROLE OF GENES ENOS, SUBUNIT P22-PHOX OF NADPH-OXIDASE AND MTHFR
Saginova E.A., Gallyamov M.G., Balatsky A.V., Kolotvin A.V., Severova M.V., Samokhodskaya L.M., Fomin V.V., Krasnova T.N., Mukhin N.A.
Clinical value of TNF, IL-6, and IL-10 gene polymorphic markers in chronic glomerulonephritis
Kamyshova E.S., Shvetsov M.Y., Kutyrina I.M., Burdennyi A.M., Zheng A., Nosikov V.V., Bobkova I.N.
Possibility of diagnosis and treatment of thrombotic complications in primary mediastinal B-cell lymphoma
Dzhumabaeva В.Т., Kremenetskaya A.M., Vasilyev S.A., Shulutko E.M., Kravchenko S.K., Shevelev A.A., Sergeeva E.V., Sakhibov Y.D., Orel E.В., Romanova E.A., Frank G.A.
Investigation of the association between the HindIII polymorphism of the LPL gene and the Taq1b polymorphism of the CETP gene with the risk of atherothrombotic stroke in the dwellers of Central Russia
Bushueva O.Y., Stetskaya T.A., Korogodina T.V., Ivanov V.P., Polonikov A.V.
Genetic markers for trait anxiety as one of the risk factors for cardiovascular diseases (WHO-MONICA program, MONICA-Psychosocial subprogram)
Gafarov V.V., Voevoda M.I., Gromova E.A., Maksimov V.N., Gagulin I.V., Iudin N.S., Gafarova A.V., Mishakova T.M.
Progress in gene therapy
Glazkova D.V., Bogoslovskaya E.V., Shipulin G.A., Pokrovskiy V.I., Glazkova D.V., Bogoslovskaya E.V., Shipulin G.A., Pokrovsky V.I.
Study of the resistome of human microbial communities using a targeted panel of antibiotic resistance genes in COVID-19 patients
Yanushevich O.O., Maev I.V., Krikheli N.I., Levchenko O.V., Galeeva J.S., Starikova E.V., Andreev D.N., Sokolov P.S., Fomenko A.K., Devkota M.K., Andreev N.G., Zaborovsky A.V., Evdokimov V.V., Tsaregorodtsev S.V., Ilina E.N., Govorun V.M., Bely P.A., Sabelnikova E.A., Solodov A.A., Cheremushkin S.V., Shaburov R.I., Kebina A.L.
Analysis of the gene polymorphism of matrix metalloproteinase-2 and -9 in patients with coronary heart disease
Shevchenko A.V., Golovanova O.V., Konenkov V.I., Tolkacheva O.M., Maksimov V.N., Voevoda M.I., Romashchenko A.G., Shevchenko A.V., Golovanova O.V., Konenkov V.I., Tolkacheva O.M., Maksimov V.N., Voyevoda M.I., Romashchenko A.G.
Association of FOXP3 gene -3279 C>A polymorphism with the risk of pulmonary sarcoidosis
Malysheva I.E., Topchieva L.V., Tikhonovich E.L., Kurbatova I.V., Balan O.V.
Analysis of an association of TNF –308G>A polymorphism with a risk for pulmonary sarcoidosis in the Russian population of the Republic of Karelia
Malysheva I.E., Topchieva L.V., Tikhonovich E.L., Barysheva O.Y.
Association of adiponectin gene G276T polymorphism with the development of metabolic syndrome in ethnic Kyrgyz patients
Isakova J.T., Lunegova O.S., Talaibekova E.T., Asambaeva D.A., Kerimkulova A.S., Aldashev A.A.
Analysis of genotypes combinations at the polymorphic points of the promoter regions of the genes of three matrix metalloproteinases and the gene of vascular endothelial growth factor (VEGF) in patients with prior acute myocardial infarction
Shevchenko A.V., Konenkov V.I., Prokof'ev V.F., Pokushalov E.A.
Pharmacogenetic features of the effect of metformin in patients with coronary heart disease in the presence of metabolic syndrome and type 2 diabetes mellitus in terms of PPAR-γ2 gene polymorphism
Lavrenko A.V., Shlykova O.A., Kutsenko L.A., Mamontova T.V., Kaĭdashev I.P.
Population association features of interleukine gene polymorphism in khakases with gastroduodenal diseases
Ageeva E.S., Shtygasheva O.V., Ryazantseva N.V., Ageeva E.S., Shtygasheva O.V., Ryazantseva N.V.
A rare variant in the TTR gene (p.E112K) is associated with systemic amyloidosis and a new symptom – skin hyperemia in response to ethanol intake: family segregation analysis, literature review, and a clinical case. Case report
Chumakova O.S., Nasonova S.N., Frolova Y.V., Stepanova E.A., Mershina E.A., Sinitsyn V.E., Zateyshchikov D.A., Zhirov I.V.
Association of SOCS5 gene polymorphism with allergic bronchial asthma
Averyanov A.B., Chercashina I.I., Nikulina S.Y., Maksimov V.N., Shestovitskiy V.A.
Genetic determinants of hypertension in two national cohorts of Mountain Shoria
Barbarash О.L., Voevoda М.I., Artamonova G.V., Mulerova Т.А., Voropaeva Е.N., Maksimov V.N., Ogarkov М.Y.
The influence of STAT4 rs7574865 (G/T) polymorphism on the risk of clinical and immunological phenotypes of systemic sclerosis in a Russian patient population: Results of a pilot study
Krylov M.Y., Ananyeva L.P., Koneva О.А., Starovoytova M.N., Desinova O.V., Ovsyannikova O.B., Aleksandrova E.N., Novikov A.A., Guseva I.A., Konovalova N.V., Varlamov D.A.
Association of CTLA4 and TNF gene polymorphisms with endocrine ophthalmopathy in ethnic Russian patients with Graves’ disease
Martirosian N.S., Burdennyi A.M., Trukhina L.V., Panteleeva O.G., Saakyan S.V., Petunina N.A., Nosikov V.V.
Gene expression of vascular endothelial growth factors and their receptors in different variants of the course of multiple myeloma
Golenkov A.K., Buravtsova I.V., Dudina G.A., Lutskaia T.D., Mitina T.A., Kataeva E.V., Karamysheva A.F., Kakpakova E.S., Sablina I.A., Stavrovskaia A.A.
Cytokine gene polymorphism in type 2 diabetes mellitus in the Europeoid women of Russia
Konenkov V.I., Korolev M.A., Shevchenko A.V., Lapsina S.A., Koroleva E.A., Zonova E.V., Prokof'ev V.F.
Effect of TT genotype of the vitamin D receptor gene on bone mineral density in dialysis patients
Shishkin A.N., Mazurenko S.O., Aseyev M.V.
The course and clinical manifestations of Peutz–Jeghers syndrome in the Russian population
Savelyeva Т.A., Ponomarenko А.A., Shelygin Y.A., Kuzminov А.M., Vyshegorodtsev D.V., Loginova А.N., Pikunov D.Y., Goncharova Е.P., Likutov А.A., Mainovskaya О.A., Tsukanov А.S.
Family hyperaldosteronism type I: a clinical case and review of literature
Chikladze N.M., Favorova O.O., Chazova I.E.
Risk of type 2 diabetes mellitus in the Kyrgyz population in the presence of ADIPOQ (G276T), KCNJ11 (Glu23Lys), TCF7L2 (IVS3C>T) gene polymorphisms
Isakova Z.T., Talaibekova E.T., Asambaeva D.A., Kerimkulova A.S., Lunegova O.S., Aldasheva N.M., Aldashev A.A.
Association of the polymorphic marker Glu23Lys in the KCNJ11 gene with hypertension in Kyrgyz patients
Isakova Z.T., Talaibekova E.T., Asambaeva D.A., Kerimkulova A.S., Lunegova O.S., Aldashev A.A.
Characterization of the genotypes of patients with Gaucher disease type 1 in the Russian Federation
Lukina K.A., Fevraleva I.S., Sysoeva E.P., Mamonov V.E., Sudarikov A.B., Lukina E.A.
Determinants for iron overload in patients with acute leukemias and aplastic anemia
Makeshova A.B., Levina A.A., Mamukova Y.I., Tsibulskaya M.M., Makarova P.M., Romanova E.A., Fevraleva I.S., Sudarikov A.B., Golovkina L.L., Stremoukhova A.G., Parovichnikova E.N., Savchenko V.G.
Current methods of immune and gene diagnosis in clinical practice
Suchkov S.V., Moskalets О.V., Cherepakhina N.E., Burdakova Y.A., Suntsova I.G., Shumsky V.I., Shaikhaev G.O., Elbeik Т., Beringer S., Petrauskene O.
Obesity and diabetes – are they always together?
Shestakova M.V., Shestakova E.A., Sklyanik I.A., Stafeev I.S.
Gene therapy of type 2 diabetes mellitus: state of art
Stafeev Y.S., Menshikov M.Y., Parfyonova Y.V.
Molecular epidemiological analysis of HIV-1 variants circulating in Russia in 1987—2015
Lapovok I.A., Lopatukhin A.E., Kireev D.E., Kazennova E.V., Lebedev A.V., Bobkova M.R., Kolomeets A.N., Turbina G.I., Shipulin G.A., Ladnaya N.N., Pokrovsky V.V.
Role of polymorphic markers for the genes of hemostasis and platelet receptors in liver fibrosis progression in patients with chronic hepatitis C
Starostina E.E., Samokhodskaya L.M., Rozina T.P., Krasnova T.N., Yarovaya E.B., Mukhin N.A.
SOCS1 gene mutations in patients with diffuse large B-cell lymphoma
Gavrilina O.A., Zvonkov E.E., Biderman B.V., Severina N.A., Parovichnikova E.N.
Perspectives of molecular visualization in cardiology
Sergienko V.B., Samoylenko L.E., Sergienko V.B., Samoilenko L.E.
Crohn's disease: Genetic aspects
Loranskaya I.D., Stepanova E.V., Loranskaya I.D., Stepanova E.V.
Role of polymorphism of angiotensinconverting enzyme gene in development of metabolic syndrome
Roitberg G.E., Tikhonravov A.V., Dorosh Z.V.
Features of genetic manifestations in patients with abdominal obesity during atrial fibrillation in combination with arterial hypertension
Hidirova L.D., Yakhontov D.A., Maksimov V.N.
Prediction of features of the course of chronic hepatitis C using Bayesian networks
Samokhodskaya L.M., Starostina E.E., Sulimov A.V., Krasnova T.N., Rosina T.P., Avdeev V.G., Savkin I.A., Sulimov V.B., Mukhin N.A., Tkachuk V.A., Sadovnichii V.A.
Hepatitis C can be cured: will hepatitis B become next?
Chulanov V.P., Zueva A.P., Kostyushev D.S., Brezgin S.A., Volchkova E.V., Maleyev V.V.
A rare case of myeloproliferative disease with t(8;13)(p11;q12) associated with eosinophilia and lymphadenopathy
Tsyba N.N., Turkina A.G., Chelysheva E.Y., Nemchenko I.S., Kovrigina A.M., Obukhova T.N., Urnova E.S., Kuzmina L.A., Savchenko V.G.
Positive effect of low-activity thromboxane A synthase 1 gene on prognosis in coronary heart disease
Kopylov F.Y., Mesitskaya D.F., Nikitina Y.M., Aksenova M.G., Dobrovolsky A.V., Lomakin O.V., Chernyi O.V.
TNF-α, IL-10, and еNOS gene polymorphisms in patients with influenza A/H1N1 complicated by pneumonia
Romanova E.N., Govorin A.V.
Familial hypercholesterolemia in Russia: genetic and phenotypic characteristics
Meshkov A.N., Malyshev P.P., Kukharchuk V.V., Meshkov A.N., Malyshev P.P., Kukharchuk V.V.
Genetic determinants of hereditary thrombophilia in pathogenesis of venous thrombosis
Kapustin S.I., Blinov M.N., Kargin V.D., Filanovskaya L.I., Saltykova N.В., Belyazo O.E., Golovina O.G., Shmeleva V.M., Panshina A.M., Papayan L.P.
Diagnosis of thrombotic thrombocytopenic purpura
Galstyan G.M., Klebanova E.E.
Literature review and clinical observation of acquired idiopathic hemophilia with a new missense mutation in the factor VIII gene (His2026Arg)
ERSHOV V.I., GADAEV I.Y., BUDANOVA D.A., PERINA F.G., SURIN V.L., SALOMASHKINA V.V., PSHENICHNIKOVA O.S., ZOZULYA N.I.
Analysis of VEGF-A/VEGFR1/VEGFR2 gene expression in patients with myelodysplastic syndrome
Kalitin N.N., Dudina G.A., Semochkin S.V., Karamysheva A.F.
Catalase gene rs1001179 polymorphism and oxidative stress in patients with chronic hepatitis C and ulcerative colitis
Bulatova I.A., Tret'iakova I.I., Shchekotov V.V., Shchekotova A.P., Ulitina P.V., Krivtsov A.V., Nenasheva O.I.
Plasminogen activator inhibitor type 1 gene polymorphism and thromboses in patients with antiphospholipid syndrome
Reshetniak T.M., Ostriakova E.V., Patrusheva2 N.L., Patrushev L.I., Aleksandrova E.N., Seredavkina N.V., Volkov A.V., Nasonov E.L.
Extremely high concentration of mexotrexate in blood serum leading to development of acute renal failure in a patient with acute lymphoblastic leukemia after high-dose consolidation
Pimenova M.A., Sokolov A.N., Biryukova L.S., Ustinova E.N., Shaforostova I.I., Donskova I.A., Bogdanov R.F., Parovichnikova E.N., Savchenko V.G., Pimenova M.A., Sokolov A.N., Biryukova L.S., Ustinova E.N., Shaforostova I.I., Donskova I.A., Bogdanov R.F., Parovichnikova E.N., Savchenko V.G.
Rituximab treatment of rheumatoid arthritis: new evidence
Nasonov E.L., Nasonov E.L.
MicroRNA-499a in heart diseases: prospects for use in diagnostics. A review
Pisklova M.V., Baulina N.M., Kiselev I.S., Favorova O.O.
Clinical case of combined genetic pathology in a patient
Losik E.A., Yakushina I.I., Skhirtladze M.R., Balahonova N.P., Kerchev V.V., Garanina I.A.
Genetic determinants of the development and course of membranous nephropathy
Kamyshova E.S., Bobkova I.N., Gorelova I.A., Kakhsurueva P.A., Filatova E.E.
Association of ITGB3, P2RY12, and CYP2C19 gene polymorphisms with platelet functional activity in patients with coronary heart disease during dual antiplatelet therapy
Muslimova E.F., Afanasiev S.A., Rebrova T.Y., Sergienko T.N., Repin A.N.
Irritable bowel syndrome in the light of Rome consensus III (2006): 10 years later
Parfenov A.I., Albulova E.A., Ruchkina I.N.
Association of Т174М polymorphism of the angiotensinogen gene with the higher risk of cerebral stroke in women
Stetskaia T.A., Bushueva O.I., Bulgakova I.V., Vialykh E.K., Shuteeva T.V., Biriukov A.E., Ivanov V.P., Polonikov A.V.
Role of methyltetrahydrofolate reductase (MTHFR) gene polymorphism in the development of ischemic stroke in the dwellers of the Kyrgyz Republic
Kudaĭbergenova N.T., Moldotashev I.K., Aldashev A.A., Mukhanova A.K.
A protective effect of Gly272Ser polymorphism of GNB3 gene in development of essential hypertension and its relations with environmental hypertension risk factors
Polonikov A.V., Solodilova M.A., Ivanov V.P., Shestakov A.M., Ushachev D.V., Vyalykh E.K., Vasil'eva O.V., Polyakova N.V., Antsupov V.V., Kabanina V.A., Kupriyanova Y.S., Bulgakova I.V., Kozhukhov M.A., Tevs D.S., Polonikov A.V., Solodilova M.A., Ivanov V.P., Shestakov A.M., Ushachev D.V., Vyalykh E.K., Vasilyeva O.V., Polyakova N.V., Antsupov V.V., Kabanina V.A., Kupriyanova Y.S., Bulgakova I.V., Kozhukhov M.A., Tevs D.S.
The study of parameters of mesenchymal stromal cells differentiation in donors and patients with aplastic anemia
Svinareva D.A., Petrova T.V., Shipunova (Nifontova) I.N., Momotyuk K.S., Mikhaylova E.A., Drize N.I., Svinareva D.A., Petrova T.V., Shipunova (Nifontova) I.N., Momotyuk K.S., Mikhailova E.A., Drize N.I.
Polymorphism of RAAS genes in patients with COVID-19: comparison with frequency in population and relationship with severity of course
Bragina A.E., Rodionova Y.N., Ogibenina E.S., Fomin A.S., Podzolkov V.I.
The role of the mLDL-induced activation of the complement system classical pathway and C3 expression stimulation in atherosclerosis
Drapkina O.M., Gegenava B.B., Fomin V.V.
Polymorphism in the regulatory regions –С2578A and +C936T of the vascular endothelial growth factor (VEGF-A) gene in Russian women with rheumatoid arthritis
Shevchenko A.V., Prokofyev V.F., Korolev M.A., Banshchikova N.E., Konenkov V.I.
FIP1L1-PDGFRА-positive myeloproliferative disease with eosinophilia: A rare case with multiple organ dysfunction and a response to tyrosine kinase inhibitor therapy
Nemchenko I.S., Turkina A.G., Chelysheva E.Y., Galstyan G.M., Kovrigina A.M., Khuazheva N.K., Savchenko V.G.
Effect of original and generic clopidogrel on prognosis in relation to different gene polymorphisms
Mesitskaia D.F., Nikitina I.M., Lomakin O.V., Shchekochikhin D.I., Kopylov F.I.
Immunogenetic predictors of a rapid virologic response to antiviral therapy in patients with chronic hepatitis C
Iushchuk N.D., Znoĭko O.O., Balmasova I.P., Fedoseeva N.V., Shmeleva E.V., Dudina K.R., Klimova E.A., Petrova T.V., Trofimov D.I., Belyĭ P.A., Safiullina N.K., Pypkina E.V.
Association of gene TP53 polymorphic marker Pro72Arg with clinical characteristics of chronic glomerulonephritis
Kamyshova E.S., Shvetsov M.Y., Shestakov A.E., Kutyrina I.M., Nosikov V.V., Kamyshova E.S., Shvetsov M.Y., Shestakov A.E., Kutyrina I.M., Nosikov V.V.
Dasatinib treatment of imatinib-resistant and imatinib-intolerant patients with chronic myeloid leukemia in a chronic phase
Vinogradova O.Y., Turkina A.G., Vorontsova A.V., Chelysheva E.Y., Gusarova G.A., Kuznetsov S.V., Goryacheva S.R., Sokolova M.A., Abakumov E.M., Stakhina O.V., Domracheva E.V., Misyurin A.V., Khoroshko N.D., Vinogradova O.Y., Turkina A.G., Vorontsova A.V., Chelysheva E.Y., Gusarova G.A., Kuznetsov S.V., Goryacheva S.R., Sokolova M.A., Abakumov E.M., Stakhina O.V., Domracheva E.V., Misyurin A.V., Khoroshko N.D.
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