Khidiyatova, I.M.,
Saifullina, E.V.,
Karunas, A.S.,
Akhmetgaleyeva, A.F.,
Kutlubaeva, R.F.,
Smakova, L.A.,
Lobov, S.L.,
Polyakov, A.V.,
Shchagina, O.A.,
Kadnikova, V.A.,
Ryzhkova, O.P.,
Magzhanov, R.V. (2022) in the ATL1
gene, is one of the most common forms of HSP in European populations. Analysis of the ATL1
geneMingazheva, E.T.,
Prokofyeva, D.S.,
Valova, Ya.V.,
Andreeva, E.A.,
Nurgalieva, A.Kh.,
Valiev, R.R.,
Ekomasova, N.V.,
Faishanova, R.R.,
Romanova, A.R.,
Khusnutdinova, E.K. (2022) The high risk of ovarian cancer is primarily associated with mutations in BRCA1 and BRCA
2 genesYanchao, L.,
Sibin, Z.,
Gareev, I.,
Huan, X.,
Junfei, Z.,
Chunyang, L.,
Beylerli, O.,
Sufianov, A.,
Chao, Y.,
Yuyan, G.,
Xun, X.,
Ahmad, A. (2022) patients, to clarify the common
genes of both, and to identify common pathways and potential drugs
Ivanova, E.,
Asadullina, D.,
Rakhimov, R.,
Izmailov, A.,
Izmailov, Al.,
Gilyazova, G.,
Galimov, Sh.,
Pavlov, V.,
Khusnutdinova, E.,
Gilyazova, I. (2022) expression level in ccRCC patients with CTCAE grade 3–4 (M±SEM 1.71 ± 0.13) compared to CTCAE grade 0–
2 group
ASSOCIATIONS OF THE NRF2/KEAP1 PATHWAY AND ANTIOXIDANT DEFENSE GENE POLYMORPHISMS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASEKorytina, G.F.,
Akhmadishina, L.Z.,
Aznabaeva, Y.G.,
Kochetova, O.V.,
Zagidullin, N.S.,
Kzhyshkowska, J.G.,
Zagidullin, S.Z.,
Viktorova, T.V. (2019) parenchyma. This work was designed as a case-control study aimed at investigating the association of the NRF
2 Zaplakhova, O. V.,
Nasibullin, T. R.,
Tuktarova, I. A.,
Timasheva, Y. R.,
Erdman, V. V.,
Bakhtiyarova, K. Z.,
Mustafina, O. E. (2018) 3129934 (C6orf10), rs1109670 (DDEF
2/MBOAT
2 gene), rs9523762 (GPC5
gene), rs28362491 (NFKB1
gene), rs
FACHAL, L.,
KAR, S.,
TYRER, J.P.,
GHOUSSAINI, M.,
HARRINGTON, P.A.,
HEALEY, C.S.,
MAYES, R.,
SHAH, M.,
PHAROAH, P.D.P.,
EASTON, D.F.,
DUNNING, A.M.,
ASCHARD, H.,
JIANG, X.,
TAMIMI, R.M.,
KHUSNUTDINOVA, E.,
BIAŁKOWSKA, K.,
и др. соавторы (2020) significantly over-represented in active
gene regulatory regions and transcription factor binding sites. We
ВЛИЯНИЕ ПОЛИМОРФИЗМА ГЕНА G1082AIL-10 НА ТЕЧЕНИЕ ОСТРЫХ КИШЕЧНЫХ ИНФЕКЦИЙ is played by the polymorphism of
genes responsible for the induction of the synthesis of inflammatory
Ассоциация Gasdermin B Gene GSDMB полиморфизма с риском аллергических заболеванийКарунас, А.С.,
Федорова, Ю.Ю.,
Гималова, Г. Ф.,
Эткина, Э.И.,
Хуснутдинова, Э.К.,
Karunas, A.S.,
Fedorova, Y.Y.,
Gimalova, G.F.,
Etkina, E.I.,
Khusnutdinova, E.K. (2021) семейства IKAROS), ZPBP
2 (подобный белку , связывающий пеллюцидную зону ), GSDMB (газдермин B), ORMDL3