АССОЦИАЦИЯ АЛЛЕЛЬНЫХ ВАРИАНТОВ ГЕНОВ IL2, IL2RA И IL7R С РАССЕЯННЫМ СКЛЕРОЗОМTIMASHEVA, Y.R.,
ZAPLAKHOVA, O.V.,
NASIBULLIN, T.R.,
TUKTAROVA, I.A.,
ERDMAN, V.V.,
MUSTAFINA, O.E.,
BAKHTIIAROVA, K.Z.,
ТИМАШЕВА Я.Р.,
ЗАПЛАХОВА О.В.,
НАСИБУЛЛИН Т.Р.,
ТУКТАРОВА И.А.,
ЭРДМАН В.В.,
БАХТИЯРОВА К.,
МУСТАФИНА О.Е. (2019) and neurodegenerative processes. We performed the
analysis of association between multiple sclerosis and polymorphic
% CI 1.46–2.22), p = 0.0001] were significantly associated with type 2 diabetes. Regression
analysisPSHENNIKOVA, V.G.,
BARASHKOV, N.A.,
ROMANOV, G.P.,
TERYUTIN, F.M.,
SOLOV'EV, A.V.,
GOTOVTSEV, N.N.,
NIKANOROVA, A.A.,
FEDOROVA, S.A.,
NAKHODKIN, S.S.,
SAZONOV, N.N.,
MOROZOV, I.V.,
BONDAR, A.A.,
POSUKH, O.L,
DZHEMILEVA, L.U.,
KHUSNUTDINOVA, E.K. (2019) .833). The results of this study may be applicable for
analysis of novel missense variants of the GJB2 (Cx26), GJB6
Zagidullin, N.,
Plechev, V.,
Badykova, E.,
Badykov, M.,
Akhmadishina, L.,
Korytina, G.,
Sagitov, I. (2019) in the control group (36.2%) compared with SSS patients (28.9%) Padj=0.052.
Analysis, depending on the type
Bogliolo, M.,
Catucci, I.,
Caleca, L.,
Lasheras, S.V.,
Pujol, R.,
Kiiski, J.I.,
Muranen, T.A.,
Barnes, D.R.,
Dennis, J.,
Michailidou, K.,
Bolla, M.K.,
Leslie, G.,
Figlioli, G. (2019) .44, P = 0.034 and OR = 3.79; P = 0.009, respectively). In a country-restricted
analysis, we confirmed