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СОВРЕМЕННЫЙ ВЗГЛЯД НА НЕЙРОБИОЛОГИЧЕСКИЕ ГИПОТЕЗЫ ШИЗОФРЕНИИ
HYPOTHESIS OF SCHIZOPHRENIA
ГАРЕЕВА, А.Э., Gareeva A.E. (2019)
РОЛЬ ГЛУТАМАТА В ПАТОГЕНЕЗЕ РАССЕЯННОГО СКЛЕРОЗА
THE ROLE OF GLUTAMATE IN THE PATHOGENESIS OF MULTIPLE SCLEROSIS
КУЗЬМИНА, У.Ш., ЗАЙНУЛЛИНА, Л.Ф., ВАХИТОВ, В.А., БАХТИЯРОВА, К.З., ВАХИТОВА, Ю.В., Kuzmina U.Sh., Zainullina L.F., Vakhitov V.A., Bakhtiyarova K.Z., Vakhitova Yu.V. (2019)
IDENTIFICATION OF HUB GENES AND SMALL-MOLECULE COMPOUNDS RELATED TO INTRACEREBRAL HEMORRHAGE WITH BIOINFORMATICS ANALYSIS
LIU, Z., ZHANG, R., CHEN, X., YAO, P., YAN, T., LIU, W., YAO, J., ZHAO, S., SOKHATSKII, A., GAREEV, I. (2019)
of intracerebral hemorrhage (ICH). We aimed to identify the hub genes associated with intracerebral hemorrhage
CHEMOKINE GENE POLYMORPHISMS ASSOCIATION WITH INCREASED RISK OF TYPE 2 DIABETES MELLITUS IN TATAR ETHNIC GROUP, RUSSIA
KOCHETOVA, O.V., MUSTAFINA, O.E., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2019)
revealed that some SNPs in chemokine genes are associated with obesity, insulin resistance, type 2 diabetes
ASSOCIATION BETWEEN ALLELIC VARIANTS OF THE GENES INVOLVED IN GLUCOCORTICOIDS METABOLISM AND ASTHMA
FEDOROVA, Y.Y., KARUNAS, A.S., GIMALOVA, G.F., KHUSNUTDINOVA, E.K., SAVELIEVA, O.N, MURZINA, R.R., GATIYATULLIN, R.F., ETKINA, E.I. (2019)
polymorphic variants of four genes involved in the metabolism of glucocorticosteroids in patients with asthma
IL1RN MEDIATES THE SUPPRESSIVE EFFECT OF METHIONINE DEPRIVATION ON GLIOMA PROLIFERATION
WANG, K., LIU, H., LIU, J., WANG, X., TENG, L., ZHANG, J., CHEN, X., WANG, N., ZHONG, Y., HOU, X., JIANG, H., ZHANG, X., ZHAO, S., LIU, Y., YAO, Y., WANG, J., QU, Y., PENG, F., BEYLERLI, O., LIAO, X. (2019)
confirmed that IL1RN is a tumor associated gene and its expression is negatively correlated
ASSOCIATIONS OF THE NRF2/KEAP1 PATHWAY AND ANTIOXIDANT DEFENSE GENE POLYMORPHISMS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE
KORYTINA, G.F., AKHMADISHINA, L.Z., KOCHETOVA, O.V., VIKTOROVA, T.V., AZNABAEVA, Y.G., ZAGIDULLIN, N.SH., ZAGIDULLIN, SH.Z., KZHYSHKOWSKA, J.G (2019)
/KEAP1 signaling system, and antioxidant defense gene polymorphisms with COPD in population from Russia
PATHOPHYSIOLOGY OF CALCIUM MEDIATED VENTRICULAR ARRHYTHMIAS AND NOVEL THERAPEUTIC OPTIONS WITH FOCUS ON GENE THERAPY
Paar, V., Jirak, P., Larbig, R., Zagidullin, N.S., Brandt, M.C., Lichtenauer, M., Hoppe, U.C., Motloch, L.J. (2019)
. We highlight the therapeutic potential of gene therapy as a novel and innovative approach for future
ASSOCIATIONS OF THE NRF2/KEAP1 PATHWAY AND ANTIOXIDANT DEFENSE GENE POLYMORPHISMS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE
Korytina, G.F., Akhmadishina, L.Z., Aznabaeva, Y.G., Kochetova, O.V., Zagidullin, N.S., Kzhyshkowska, J.G., Zagidullin, S.Z., Viktorova, T.V. (2019)
/KEAP1 signaling system, and antioxidant defense gene polymorphisms with COPD in population from Russia
МАЖОРНАЯ МУТАЦИЯ В ГЕНЕ SPAST У ПАЦИЕНТОВ С АУТОСОМНО-ДОМИНАНТНОЙ СПАСТИЧЕСКОЙ ПАРАПЛЕГИЕЙ ИЗ РЕСПУБЛИКИ БАШКОРТОСТАН
MAJOR MUTATION IN THE SPAST GENE IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA FROM THE REPUBLIC OF BASHKORTOSTAN
KHIDIYATOVA, I.M., AKHMETGALEYEVA, A.F., YANKINA, M.A., KHUSNUTDINOVA, E.K., SHAVALIEVA, V.V., SAIFULLINA, E.V., MAGZHANOV, R.V., IDRISOVA, R.F., ХИДИЯТОВА И.М., АХМЕТГАЛЕЕВА А.Ф., САЙФУЛЛИНА Е.В., ИДРИСОВА Р.Ф., ЯНКИНА М.А., ШАВАЛИЕВА В.В., МАГЖАНОВ Р.В., ХУСНУТДИНОВА Э.К. (2019)
in more than 70 genetic loci. The main causes of HSP development are mutations in the SPAST gene

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