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По вашему запросу найдено документов: 13

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IREB2, CHRNA5, CHRNA3, FAM13A & HEDGEHOG INTERACTING PROTEIN GENES POLYMORPHISMS & RISK OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE IN TATAR POPULATION FROM RUSSIA

Korytina, G.F., Akhmadishina, L.Z., Viktorova, E.V., Kochetova, O.V., Viktorova, T.V. (2016)

and hedgehog interacting protein (HHIP) genes in a Tatar population from Russia. Methods: Six single

ROLE OF ALLELIC GENES OF MATRIX METALLOPROTEINASES AND THEIR TISSUE INHIBITORS IN THE RISK OF PEPTIC ULCER DISEASE DEVELOPMENT

Shaymardanova, E.Kh., Nurgalieva, A.Kh., Khidiyatova, I.M., Gabbasova, L.V., Kuramshina, O.A., Kryukova, A.Ya., Sagitov, R.B., Munasipov, F.R., Khusnutdinova, E.Kh. (2016)

of the stomach and/or duodenum. Association analysis of common polymorphisms of matrix metalloproteinases genes

PADI4 GENE POLYMORPHISM AS A PREDICTOR OF RESPONSE TO METHOTREXATE IN PATIENTS WITH JUVENILE IDIOPATHIC ARTHRITIS

Nazarova, L.S., Danilko, K.V., Malievsky, V.A., Viktorova, T.V. (2016)

of the study was to assess whether the PADI4 rs2240336 gene polymorphism is a predictor of the disease severity

FORECASTING MODEL OF GENE ENZYME POLYMORPHISM DETOXIFICATION IN PATIENTS SUFFERED FROM HFRS

Hasanova, G.M. / Хасанова Г.М., Valishin, D.A. / Валишин Д.А, Tutel'jan, A.V. / Тутельян А.В., Hasanova, A.N. / Хасанова А.Н. (2016)

Aim: to study gene enzyme polymorphism of xenobiotic detoxification in patients suffered from HFRS

GENETIC DETERMINANTS OF ESSENTIAL HYPERTENSION IN THE POPULATION OF TATARS FROM RUSSIA

Timasheva, Y., Nasibullin, T., Imaeva, E., Mirsaeva, G., Mustafina, O. (2016)

and diastolic blood pressure level. We also showed that the rs213045 polymorphism in ECE1 gene was associated

INFLAMMATORY AND IMMUNE RESPONSE GENES POLYMORPHISMS ARE ASSOCIATED WITH SUSCEPTIBILITY TO CHRONIC OBSTRUCTIVE PULMONARY DISEASE IN TATARS POPULATION FROM RUSSIA

Korytina, G.F., Akhmadishina, L.Z., Kochetova, O.V., Aznabaeva, Y.G., Zagidullin, Sh.Z., Victorova, T.V. (2016)

as a case–control study aimed at investigating the association of COPD with polymorphisms

АНАЛИЗ АССОЦИАЦИЙ ПОЛИМОРФНОГО МАРКЕРА RS7903146 ГЕНА TCF7L2 С САХАРНЫМ ДИАБЕТОМ 2 ТИПА В ТАТАРСКОЙ ЭТНИЧЕСКОЙ ГРУППЕ, ПРОЖИВАЮЩЕЙ В БАШКОРТОСТАНЕ

THE ASSOCIATION OF TCF7L2 RS7903146 POLYMORPHISM WITH TYPE 2 DIABETES MELLITUS AMONG TATARS OF BASHKORTOSTAN

Авзалетдинова, Д.Ш., Шарипова, Л.Ф., Кочетова, О.В., Моругова, Т.В., Эрдман, В.В., Сомова, Р.Ш., Мустафина, О.Е., Avzaletdinova, D.S., Sharipova, L.F., Kochetova, O.V., Morugova, T.V., Erdman, V.V., Somova, R.S., Mustafina, O.E. (2016)

Aim. To perform the analysis of the association of transcription factor 7-like 2 (TCF7L2) gene rs

TWO NOVEL MUTATIONS IN GENE SPG4 IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA

Akhmetgaleyevaa, A.F., Khidiyatovaa, I.M., Saifullinac, E.V., Idrisovad, R.F., Magzhanov, R.V., Khusnutdinovaa, E.K. (2016)

in Europeans is HSP associated with mutations in the spastin gene (SPG4). Analysis of the gene SPG4 was carried

ASSOCIATION OF VARIABLE RS1801282 LOCUS OF PPARG2 GENE WITH DIABETIC NEPHROPATHY

Avzaletdinova, D.Sh., Sharipova, L.F., Kochetova, O.V., Morugova, T.V., Erdman, V.V., Mustafina, O.E. (2016)

The association of the variable rs1801282 locus of the PPARG2 gene (peroxisome proliferator

SPECTRUM AND FREQUENCY OF THE GJB2 GENE PATHOGENIC VARIANTS IN A LARGE COHORT OF PATIENTS WITH HEARING IMPAIRMENT LIVING IN A SUBARCTIC REGION OF RUSSIA (THE SAKHA REPUBLIC)

Pathogenic variants in the GJB2 gene, encoding connexin 26, are known to be a major cause

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