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Molecular cardiology: from decoding the genetic nature and mechanisms of the diseases development to the introduction into the clinic
Zateyshchikov D., Favorova O., Chumakova O.
Various phenotypes of postpartum atypical hemolytic uremic syndrome: the role of genetic testing in determining prognosis. Case report
Kirsanova T., Balakireva A., Fedorova T., Pyregov A., Rogachevskiy O.
Irritable bowel syndrome phenotypes: leading factors of genetics and epigenetics, mechanisms of formation
Gaus O., Livzan M.
TNFRSF13B gene mutation in adult patient with common variable immunodeficiency. Case report
Sviridov P., Bodunova N., Danishevich A., Litvinova M.
General and particular issues of etiopathogenesis of peptic ulcer and gastric cancer: current status of the problem
Osadchuk A., Davydkin I., Gricenko T., Osadchuk M.
Cryoglobulinemic vasculitis in chronic hepatitis C: Genetic aspects
Artemova M., Abdurakhmanov D.
The development of functional gastrointestinal diseases: Genetic aspects
Akhmedov V.
Polymorphism of ethanol metabolism genes in alcoholic chronic pancreatitis
Gubergrits N., Kishenia M., Golubova O.
Clopidogrel resistance in patients with acute coronary syndrome
Frolova N., Shakhnovich R., Sirotkina O., Dobrovolsky A., Ruda M.
Left ventricular non - compaction: contemporary view of genetic background, clinical course, diagnostic and treatment
Streltsova A., Gudkova A., Kostareva A.
The 2015-2016 epidemic season in Russia and the world: Circulation of influenza viruses, trends in incidence, clinical aspects, and treatment algorithm
Lvov D., Kolobukhina L., Burtseva E., Kruzhkova I., Malyshev N., Fedyakina I., Kirillova E., Trushakova S., Feodoritova E., Merkulova L., Krasnoslobodtsev K., Mukasheva Е., Garina E., Vartanyan R., Kisteneva L., Prilipov A., Bazarova M., Devyatkin A., Sutochnikova O.
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., Stetskaya T., Korogodina T., Ivanov V., Polonikov A.
Aspirin resistance candidate genes and their association with the risk of fatal cardiovascular events
Grinshteĭn I., Kosinova A., Grinshteĭn I.
HCV genome variability in acute and chronic viral hepatitis C
Yushchuk N., Klimova E., Znoyko O., Gadzhikulieva M., Il'ina E., Yashina T., Malyshev N., Tsyganova E., Yuschuk N., Klimova E., Znoiko O., Gadzhikulieva M., Ilyina E., Yashina T., Malyshev N., Tsyganova E.
Molecular markers as risk factors for thyroid cancer
Rogova M., Novosad S., Martirosian N., Trukhina L., Petunina N.
Genetic diversity of human immunodeficiency viruses and antiretroviral therapy
Bobkova M.
Composite lymphoma: Simultaneous development of three different lymphomas in a single patient: A clinical case
Chernova N., Sidorova Y., Sinitsina M., Sudarikov A., Kovrigina A., Zvonkov E.
Impact of angiotensionogen and angiotensin II receptor type 1 gene polymorphisms on the development and course of chronic heart failure
Tepliakov A., Shilov S., Berezikova E., Efremov A., Safronov I., Pustovetova M., Maianskaia S., Torim I., Karpov R.
Polymorphism -930A > G of the cytochrome b gene is a novel genetic marker of predisposition to bronchial asthma
Polonikov A., Ivanov V., Solodilova M., Kozhukhov M., Panfilov V., Bulgakova I., Polonikov A., Ivanov V., Solodilova M., Kozhukhov M., Panfilov V., Bulgakova I.
Efficacy of H. pylori eradication depending on genetic polymorphism of CYP2C19, MDR1 and IL-1β
Bakulina N., Maev I., Savilova I., Bakulin I., Il'chishina T., Zagorodnikova K., Murzina A., Andreev D.
Association of the -844G>A polymorphism in the catalase gene with the increased risk of essential hypertension in smokers
Bushueva O., Ivanov V., Ryzhaeva V., Ponomarenko I., Churnosov M., Polonikov A.
Assessment of the role of matrix metalloproteinase-2 gene polymorphism in the development of chronic heart failure
Teplyakov A., Berezikova E., Shilov S., Grakova E., Torim Y., Efremov A., Safronov I., Pustovetova M., Karpov R.
A GENETIC ANALYSIS OF A H1N1 PANDEMIC INFLUENZA VIRUS IN THE COURSE OF THE EPIDEMIC
Kostryukova E., Zakharzhevskaya N., Kostin P., Ilyina E., Larin A., Gribanov O., Selezneva O., Prikhodko E., Akopian T., Generozov E., Lazarev V., Levitsky S., Kondratov I., Alekseev D., Bazaleev N., Klimova E., Esaulova M., Yuschuk N., Govorun V., Sergienko V.
Allele polymorphism of alkaline, acid soluble phosphatase genes and vitamin D-binding protein in postmenopausal osteoporosis
Krylov M., Korotkova T., Myakotkin V., Benevolenskaya L.
The prevalence of components of metabolic syndrome in the patients with diabetes melitus type 2 and mody diabetes in young people of Novosibirsk
Mustafina S., Ovsyannikova A., Voevoda M., Denisova D., Sherbakova L., Rymar O.
Diabetes mellitus and chronic kidney disease: Possibilities of prediction, early diagnosis, and nephroprotection in the 21st century
Shestakova M.
Association of Т174М polymorphism of the angiotensinogen gene with the higher risk of cerebral stroke in women
Stetskaia T., Bushueva O., Bulgakova I., Vialykh E., Shuteeva T., Biriukov A., Ivanov V., Polonikov 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., Solodilova M., Ivanov V., Shestakov A., Ushachev D., Vyalykh E., Vasil'eva O., Polyakova N., Antsupov V., Kabanina V., Kupriyanova Y., Bulgakova I., Kozhukhov M., Tevs D., Polonikov A., Solodilova M., Ivanov V., Shestakov A., Ushachev D., Vyalykh E., Vasilyeva O., Polyakova N., Antsupov V., Kabanina V., Kupriyanova Y., Bulgakova I., Kozhukhov M., Tevs D.
Multiple molecular-genetic defects in a female with mixed hyperlipoproteinemia and earlyischemic heart disease
Malyshev P., Stambolsky D., Meshkov A., Davydova Y., Kukharchuk V.
Association between polymorphic markers in candidate genes and the risk of manifestationof endocrine ophthalmopathy in patients with Graves’ disease
Petunina N., Martirosian N., Trukhina L., Saakyan S., Panteleeva O., Burdennyy A., Nosikov V.
Molecular genetics of maturity-onset diabetes of the young
Voevoda M., Ivanova A., Shakhtshneider E., Ovsyannikova A., Mikhailova S., Astrakova K., Voevoda S., Rymar O.
The problem of rare (orphan) diseases in the Russian Federation: Medical and normative legal aspects of its solution
Novikov P.
Genetic polymorphisms coding hemostasis protein synthesis and venous thromboembolic complications in Moscow population
Vorob'eva N., Khasanova Z., Konovalova N., Postnov A., Kirienko A., Panchenko E., Vorobieva N., Khasanova Z., Konovalova N., Postnov A., Kirienko A., Panchenko E.
Polymorphism of FcyRIIIA-l58F/V and promotion region of IL-10 genes in systemic lupus erythematosus in Kazakhs
Guseva I., Omarbekova Z., Myakotkin V.
Production and genetic risk factors for cardiovascular diseases among petrochemical industry workers
Gimaeva Z., Bakirov A., Karimova L., Gimranova G., Mukhammadiyeva G., Karimov D.
Promising markers for the risk and prognosis of gestational diabetes mellitus
Prokhorenko T., Saprina T., Budeeva S.
The 2013-2014 epidemic season. Hospital monitoring and antiviral therapy for influenza
Kolobukhina L., Burtseva E., Shchelkanov M., Al'khovskiĭ S., Prilipov A., Merkulova L., Kisteneva L., Vartanian R., Kruzhkova I., Trushakova S., Krasnoslobovtsev K., Avdeev S., Sutochnikova O., Bazarova M., Kelli E., Ambrosi O., Malyshev N., L'vov D., Chuchalin A.
Impact of Gly389Arg 1-adrenoceptor polymorphism on the risk of chronic heart failure, the nature of its course, and on the efficiency of its treatment with carvedilol
Teplyakov A., Shilov S., Berezikova E., Torim Y., Efremov A., Safronov I., Mayanskaya S., Popova A., Voronina E., Karpov R., Teplyakov A., Shilov S., Berezikova E., Torim Y., Efremov A., Safronov I., Mayanskaya S., Popova A., Voronina E., Karpov R.
Chronic pancreatitis and underlying causes
Zhukov N., Akhmedov V., Shirinskaya N., Zhukova Е.
Clinical case of combined genetic pathology in a patient
Losik E., Yakushina I., Skhirtladze M., Balahonova N., Kerchev V., Garanina I.
Giant cell arteritis: Genetic and epigenetic aspects
Guliaev S., Strizhakov L., Novikov P., Mukhin N., Fomin V.
The possibility of selecting optimal antiplatelet therapy in patients with coronary heart disease in terms of CYP2C19 polymorphism
Bockeria O., Kudzoeva Z., Shvarts V., Koasari A., Donakanyan S.
Endothelial dysfunction gene polymorphisms and the rate of liver fibrosis in chronic hepatitis C
Taratina O., Krasnova T., Samokhodskaia L., Lopatkina T., Tkachuk V., Mukhin N.
Influence of genetic factors on the development of target organ lesions in relation to age at diagnosis of arterial hypertension
Kuznetsova T., Gavrilov D., Samokhodskaya L., Postnov A., Boytsov S., Kuznetsova T., Gavrilov D., Samokhodskaya L., Postnov A., Boitsov S.
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