Objective - The aim of the study was to investigate the relationship of the
alleles and genotypes
Zagidullin, N.,
Plechev, V.,
Badykova, E.,
Badykov, M.,
Akhmadishina, L.,
Korytina, G.,
Sagitov, I. (2019) ion channel gens involved in the pathogenesis of
non-familial SSS.
Methods
In the case-control study
Роль полиморфного локуса VNTR гена аггрекана
в развитии остеоартроза у женщинShapovalova, D.A.,
Tyurin, A.V.,
Litvinov, S.S.,
Kchusnutdinova, E.K.,
Khusainova, R.I.,
Д.А. Шаповалова,
А.В.Тюрин,
С.С. Литвинов,
Э.К. Хуснутдинова,
Р.И. Хусаинова (2018) of the localization of the pathological process, as well as with the presence of uCTO signs. Twelve
allelic variants
URAKOV, A.L.,
MUSTAFIN, I.G.,
NABIULLINA, R.M.,
BASHIROVA, L.I.,
MOCHALOV, K.S.,
SAMORODOV, A.V.,
KHALIULLIN, F.A.,
LIPATOV, D.O.,
KORUNAS, V.I.,
KHALIMOV, A.R. (2020) male donors (n = 20); 0.2 М CaCl2,
recombinant TF, and thrombin were used as TEG activators. General