KAZANTSEVA, A.V.,
DAVYDOVA, YU.D.,
ENIKEEVA, R.F.,
LOBASKOVA, M.M.,
MUSTAFIN, R.N.,
MALYKH, S.B.,
TAKHIROVA, Z.R.,
KHUSNUTDINOVA, E.K. (2020) of
genetic variants in a moderately large sample, was used. Conclusions: Our preliminary findings indicate
and hypofibrinolysis (PAI-1) as molecular
genetic markers of avascular necrosis of the femoral head (AVNFH). Material
Nurgalieva, A.Kh.,
Bashkatov, S.A.,
Volkova, E.V.,
Petrova, S.G.,
Takhirova, Z.R.,
Mustafin, R.N.,
Fedorova, Y.Y.,
Prokofyeva, D.S.,
Khusnutdinova, E.K. (2023) of future endeavors. There has been conducted a molecular
genetic study of the frequency distribution
ЭПИГЕНЕТИКА АГРЕССИВНОГО ПОВЕДЕНИЯMUSTAFIN, R.N.,
KHUSNUTDINOVA, E.K.,
KAZANTSEVA, A.V.,
ENIKEEVA, R.F.,
DAVYDOVA, Y.D.,
KARUNAS, A.S.,
MALYKH, S.B.,
МУСТАФИН Р. Н.,
КАЗАНЦЕВА А.В.,
ЕНИКЕЕВА Р.Ф.,
ДАВЫДОВА Ю.Д.,
КАРУНАС А.С.,
МАЛЫХ С.Б.,
ХУСНУТДИНОВА Э.К. (2019) owing to the impaired interaction with noncoding RNAs, which results in modified functioning of
genetic in the programmed activation of mobile
genetic elements, which is reflected in changes in the body’s epigenetic
of
Genetics, 2024, Vol. 60, No. 10, pp. 1295–1310. Pleiades Publishing, Inc., 2024.