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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Association of SOCS5 gene polymorphism with allergic bronchial asthma
Averyanov A.B., Chercashina I.I., Nikulina S.Y., Maksimov V.N., Shestovitskiy V.A.
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.
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.
Crohn's disease: Genetic aspects
Loranskaya I.D., Stepanova E.V., Loranskaya I.D., Stepanova E.V.
Family hyperaldosteronism type I: a clinical case and review of literature
Chikladze N.M., Favorova O.O., Chazova I.E.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
1 - 32 of 32 Items

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