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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.
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.
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.
Obesity and diabetes – are they always together?
Shestakova M.V., Shestakova E.A., Sklyanik I.A., Stafeev I.S.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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