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Characterization of the plasminogen activator inhibitor type 1 gene (PAI-1) and its role in the development of arterial thrombosis
Izmozherova N., Popov A., Antropova I., Kadnikov L., Polyanok A., Ispavsky V.
The prevalence of phakomatoses in Western Siberia
Maximova Y., Chupyrko N., Vasilyeva M., Garny V., Maximov V., Svechnikova E.
The role of collagen gene polymorphisms in the development of cardiovascular diseases
Izmozherova N., Popov A., Shambatov M., Tarasova E., Bakhtin V., Kadnikov L.
GSTT1 and GSTM1 deletion polymorphism as a predictor of response to hormonal therapy for breast cancer
Gulian I., Bystritskaya E., Otstavnykh N., Khudchenko E., Eliseeva E., Apanasevich V., Isaeva M.
Relationship of interleukin-1p gene -511c/t polymorphism with duodenal ulcer and erosive gastroduodenitis in children
Ikhsanov S., Shtepo M.
The role of rs12976445 polymorphism in the MIR125A gene in the clinical course of diffuse toxic goiter: a retrospective clinical study
Volkova A., Peykrishvili N., Dora S., Abramova I., Allamova G.
Genetic aspects of chronic lung diseases in children
Averina I., Sergienko D.
Genetic predictors of the pharmacological effects of dipeptidyl peptidase-4 inhibitors and sulfonylureas in patients with type 2 diabetes mellitus
Shorokhova P., Baranov V., Vorokhobina N., Shpilevaya O.
Analysis of congenital skin defects in newborns on the territory of the Novosibirsk region for 10 years
Vasilyeva M., Maximova Y., Barkovskaya O., Maximov V.
CLINICAL FEATURES OF THE ANTIOXIDANT SYSTEM AND SOME CANDIDATE GENES POLYMORPHISMS IN THE PATIENTS WITH NON-ALCOHOLIC FATTY LIVER DISEASE
Lapinsky I., Avalueva E., Bakulin I., Dadali V., Topanova A., Skazyvaeva E., Pushkina A.
Type 1 neurofibromatosis in Western Siberia, prevalence, features of clinical manifestations
Maximova Y., Dultseva D., Garny V., Reshetnikova E., Maximov V., Svechnikova E.
PROGNOSTIC SIGNIFICANSE OF THE POLYMORPHISM OF GENES ASSOCIATED WITH THE RISK OF TYPE 2 DIABETES MELLITUS AND OBESITY, FOR THE DEVELOPMENT OF LIVER FIBROSIS AND HEPATIC STEATHOSIS IN PATIENTS WITH NON-ALCOHOLIC FAT LIVER DISEASE
Sandler Y., Polukhina A., Vinnitskaya E., Bakulin I., Borunova Z., Keyyan V.
Clinical significance of genetic and inflammatory markers of bone metabolism in patients with chronic obstructive pulmonary disease and osteoporosis
Vasilyeva L., Bezzubtseva E., Evstratova E., Gosteva E., Zubkova I.
GENETIC ASPECTS OF PROGNOSIS OF EFFICIENCY AND SAFETY OF PHARMACOTHERAPY OF ATOPIC BRONCHIAL ASTHMA IN CHILDREN
Balabolkin I., Bulgakova V.
Clinical significance of genetic polymorphism of tamoxifen metabolic enzymes and transporters in breast cancer: results of a population-based cohort study
Golubenko E., Savelyeva M., Sozaeva Z., Poddubnaya I., Korennaya V.
Bronchopulmonary dysplasia in children in terms of genetic variability of the vitamin D receptor
Sergienko D., Khishtilova P.
ROL' ALLEL'NYKh VARIANTOV GENOV SVERTYVANIYa KROVI V SKOROSTI PROGRESSIROVANIYa FIBROZA PRI KhRONIChESKIKh ZABOLEVANIYaKh PEChENI
Starostina E., Fastovets S., Samokhodskaya L., Rozina T., Ignatova T., Krasnova T., Mukhin N.
Pharmacogenetic approaches to optimization of micronutrient support regimens in the period of pregravid preparation
Shikh E., Putintseva A.
The course of chronic lung diseases in children in terms of VDR gene FokI polymorphism
Averina I., Sergienko D.
Polimorfizm gena eNOS: rasprostranennost' i svyaz' s zabolevaniyami
Pozdnyakov N., Khokhlov A.
Effect of CYP2C9 gene polymorphism on losartan dosage regimen in patients with I-II degree arterial hypertension
Sinitsina I., Boyarko A., Temirbulatov I., Sychev D.
Effect of SFTPD gene rs721917 polymorphism on the course and outcomes of bronchopulmonary dysplasia in children
Khishtilova P., Sergienko D.
Personifitsirovannoe lechenie bol'nykh s sindromom slabosti sinusovogo uzla na osnove individual'nykh osobennostey genotipa
Chernova A., Nikulina S., Shul'man V., Tret'yakova S., Aksyutina N., Chernov V.
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