Khusnutdinova, E.K.,
Dzhemileva, L.U.,
Lobov, S.L.,
Kuznetzov, D.U.,
Nazirova, A.G.,
Nurgalina, E.M.,
Barashkov, N.A.,
Fedorova, S.A. (2017) carrier frequency of c.35delG,
c.167delT and c.235delC mutations of the
GJB2 gene in 17 populations
Solovyev, A.V.,
Dzhemileva, L.U.,
Posukh, O.L.,
Barashkov, N.A.,
Bady-Khoo, M.S.,
Lobov, S.L.,
Popova, N.Y.,
Romanov, G.P.,
Sazonov, N.N.,
Bondar, A.A.,
Morozov, I.V.,
Tomsky, M.I.,
Fedorova, S.A.,
Khusnutdinova, E.K. (2017) children
with HI due to mutations in the
GJB2 gene and 91 questionnaires
about the presumed causes
-sensory neuropathies caused by mutations in the
GJB1
gene (gap junction B1 type). The authors have established earlier
revealed that some SNPs in chemokine
genes are associated with obesity, insulin resistance, type
2 diabetes
LIU, Z.,
ZHANG, R.,
CHEN, X.,
YAO, P.,
YAN, T.,
LIU, W.,
YAO, J.,
ZHAO, S.,
SOKHATSKII, A.,
GAREEV, I. (2019) for differentially expressed
genes (DEGs) in ICH, with a fold change (FC) value of (|log
2FC|) >
2 and a P-value of <0