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1 ated with the RA susceptibility haplotype of PADI4.
4 hat the expression and enzymatic activity of Padi4 are also induced under conditions of ground-state
5 sults provide support for PTPN22, CTLA4, and PADI4 as RA susceptibility genes and demonstrate novel a
8 4_92*G/C, and padi4_104*T/C), mapping to the PADI4 gene and defining a haplotype previously reported
12 pe of the peptidylarginine deiminase 4 gene (PADI4) has recently been identified as a gene conferring
13 driver analysis identifies six genes (LTB4R, PADI4, IL1R2, PPP1R3D, KLHL2, and ECHDC3) predicted to c
14 ptidylarginine deiminase 4 (PAD4, encoded by Padi4 in mice), an enzyme important in chromatin deconde
15 ullination by peptidyl arginine deiminase-4 (PADI4) in contact to particulate agents to extrude decon
18 ne deiminase family member PAD4 (also called PADI4) is markedly overexpressed in a majority of human
21 of CTLA4 (CT60 allele, OR 1.23; P=.001) and PADI4 (PADI4_94, OR 1.24; P=.001) with the development o
22 rotein modification; suggestively, Padi2 and Padi4 RNA expression was correlated with arthritis sever
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