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1 on by targeting TNF alpha-induced protein 3 (TNFAIP3).
2 mor necrosis factor-alpha-induced protein 3 (TNFAIP3).
3 luding rs5029937, located in the intron 2 of TNFAIP3.
4 identified psoriasis variants near IL23R and TNFAIP3.
5 ed genetic association between psoriasis and TNFAIP3.
8 t least partially explained by repression of TNFAIP3, a negative regulator of NF-kappaB signaling.
9 ion of anti-inflammatory TNF targets such as TNFAIP3 (A20) and NFKBIA was selectively spared or augme
11 mor necrosis factor alpha-induced protein 3 (TNFAIP3, A20) gene, a negative regulator of NF-kappaB, w
12 reover, it provides novel targets related to TNFAIP3/A20 activity for superior therapeutic regimens i
15 evidence for an inverse relationship between TNFAIP3/A20 expression levels and IL-17A-producing T cel
17 s effect to the ability of miR-29b to target TNFAIP3/A20, a negative regulator of NF-kappaB signaling
18 onstrate that the ubiquitin-modifying enzyme TNFAIP3/A20, an upstream regulator of T cell receptor (T
23 tions in multiple genes, including negative (TNFAIP3, also called A20) and positive (CARD11, TRAF2, T
24 heless rapidly countered by the induction of TNFAIP3, an NF-kappaB inhibitor frequently inactivated i
25 factor alpha [TNF-alpha]-induced protein 3 [TNFAIP3]), an inhibitor of the NF-kappaB pathway and a n
26 After stratification by JIA subtype, the TNFAIP3 and C12orf30 variants were associated with oligo
28 protein 1 (TNIP1) gene, which interacts with TNFAIP3 and inhibits the TNF-alpha-induced nuclear facto
29 reover, the regulatory effects of miR-19a on TNFAIP3 and NF-kappaB signaling were confirmed using tum
30 6q23 (rs10499194, approximately 150 kb from TNFAIP3 and OLIG3) that was reproducibly associated with
34 ated genes (such as OAS1/2/3, TLR1/6/10, and TNFAIP3) and also encompass genes (including OCA2 and BN
35 G [P = 0.006], and rs2327832_G [P = 0.03] in TNFAIP3) and one with decreased risk (rs1004446_A in INS
37 pha and regulate NF-kappaB signaling (TNIP1, TNFAIP3) and two genes involved in the modulation of Th2
38 on to ZIKV, dengue, and GBS infection; ATF5, TNFAIP3, and BAMB1 were common to ZIKV, dengue, and WNF;
39 d arthritis (RA) susceptibility loci, TAGAP, TNFAIP3, and CCR6, in African American patients with RA.
41 of nonsynonymous coding polymorphisms within TNFAIP3, and found that the A125V coding-change variant
42 ariants, along with tagging polymorphisms in TNFAIP3, and identified a novel African-derived risk hap
43 c loci-HLA-C, IL12B, IL23R, IL23A, IL4/IL13, TNFAIP3, and TNIP1-and ongoing studies are revealing add
45 latory regions of TAGAP and an intronic SNP (TNFAIP3) are potential susceptibility loci in African Am
48 o two outcome groups (P = .037) and revealed TNFAIP3 as part of an optimized four-gene predictor asso
49 mor necrosis factor alpha-induced protein 3 (TNFAIP3) as a key endogenous suppressor of ASK1 activati
50 und evidence of two independent signals near TNFAIP3 associated with SLE, including one previously as
51 und evidence of two independent signals near TNFAIP3 associated with SLE, including one previously as
52 acts through chromatin looping not only with TNFAIP3, but also with IL20RA, located 680 kb upstream.
53 ced Tnfaip3 gene expression in DCs in either Tnfaip3(CD11c) or Tnfaip3(LysM) mice dose-dependently co
55 CXCL10), immune suppression (PD-L1, NFKB1B, TNFAIP3, CGB), apoptosis (CASP9, FAS, IL-24), and cell g
57 Hmgb1), assembling a NF-kappaB/Hmgb1/lincRNA-Tnfaip3 complex in macrophages after LPS stimulation.
58 These results establish that variants near TNFAIP3 contribute to differential risk of SLE and RA.
59 These results establish that variants near TNFAIP3 contribute to differential risk of SLE and RA.
61 ressor of ASK1 activation, and we found that TNFAIP3 directly interacts with and deubiquitinates ASK1
65 expression pattern of a regulator molecule, TNFAIP3, exhibited prominent variability between individ
66 Importantly, miR-125a/mir-125b effects on TNFAIP3 expression and NF-kappaB activity were confirmed
68 isms in the deubiquitinating (DUB) domain of TNFAIP3: F127C, which is in high-linkage disequilibrium
69 self-regulatory loop whereby termination of TNFAIP3 function by miR-125 could strengthen and prolong
70 R/NF-kappaB cooperation, suggesting that the TNFAIP3 GBS acts primarily as a docking site in this con
71 ese findings point to variability in the A20/TNFAIP3 gene as a modulator of CAD risk in type 2 diabet
72 ransgenic or adeno-associated virus-mediated TNFAIP3 gene delivery in the liver in both mouse and non
74 xposed mice with conditional deletion of the Tnfaip3 gene in either myeloid cells (by using the lysoz
76 cations in autoimmunity; A20, encoded by the TNFAIP3 gene, Lyp encoded by the PTPN22 gene, and the BC
77 mor necrosis factor-alpha-induced protein 3 (TNFAIP3) gene has been associated with psoriasis, rheuma
78 mor necrosis factor alpha-induced protein 3 (Tnfaip3) gene, is an early-primary response gene control
80 tudied germline and somatic abnormalities of TNFAIP3 in 574 patients with pSS, including 25 with lymp
81 rheumatoid arthritis susceptibility gene A20/Tnfaip3 in mice (A20(myel-KO) mice) triggers a spontaneo
82 is study we investigated the precise role of TNFAIP3 in myeloid cells for the development of TH2- and
84 back inhibitor mRNAs, such as Ier3, Dusp1 or Tnfaip3, in the absence of MK2-dependent TTP neutralizat
85 tiple single nucleotide polymorphisms in the TNFAIP3 interacting protein 1 (TNIP1) gene, which intera
87 s2233290) at position 151 (Pro-->Ala) in the TNFAIP3-interacting protein 1, TNIP1, confers even stron
88 overed that the negative NF-kappaB regulator TNFAIP3 is a direct target of miR-125a and miR-125b, whi
89 paB and extrinsic apoptosis, confirming that TNFAIP3 is a functionally relevant target of miR-29b.
92 mor necrosis factor (TNF)-induced protein 3 (TNFAIP3) is a negative regulator of nuclear factor-kappa
94 We report here that the lincRNA gene lincRNA-Tnfaip3, located at mouse chromosome 10 proximal to the
97 wide association studies have implicated the TNFAIP3 locus in susceptibility to autoimmune disorders
98 ci including rs10499194 and rs6920220 in the TNFAIP3 locus, rs6679677 in the RSBN1 locus, rs17696736
99 xpression in DCs in either Tnfaip3(CD11c) or Tnfaip3(LysM) mice dose-dependently controlled developme
100 to depict how the A125V amino acid change in TNFAIP3 may affect the three-dimensional structure of th
102 as rescue assays and genetic modulation of a TNFAIP3-null model defined the essential role of the TNF
103 Ablation of TNF-alpha-induced protein 3 (TNFAIP3), one of the crucial negative regulators of nucl
106 ting either A20's deubiquitinating activity (Tnfaip3(OTU) mice) or A20's ZF4 (Tnfaip3(ZF4) mice).
110 on (ARID1A and MEF2B), NF-kappaB (CARD11 and TNFAIP3), PI3 kinase (PIK3CD, PIK3R1, and MTOR), B-cell
111 s the first report of an association between TNFAIP3 polymorphisms and autoimmunity in African-Americ
112 d methylation of cytosine nucleotides in the TNFAIP3 promoter was found to be correlated with this va
113 with variants in 29 other regions, including TNFAIP3, PTTG1, PRDM1, DGKQ, FCGR2A, IRAK1BP1, ITSN2 and
114 We show that three independent SNPs in the TNFAIP3 region (rs13192841, rs2230926 and rs6922466) are
115 We show that three independent SNPs in the TNFAIP3 region (rs13192841, rs2230926 and rs6922466) are
118 pression of an miR-29b-refractory isoform of TNFAIP3 restored NF-kappaB and extrinsic apoptosis, conf
119 erse populations, we fully characterized the TNFAIP3 risk haplotype and identified a TT>A polymorphic
121 an association between SLE and a variant in TNFAIP3 (rs5029939, meta-analysis P = 2.89 x 10(-12), OR
122 an association between SLE and a variant in TNFAIP3 (rs5029939, meta-analysis P = 2.89 x 10(-12), OR
123 27 SNPs (CCR6 rs3093023, TAGAP rs394581, and TNFAIP3 rs6920220) demonstrated ORs in the opposite dire
124 s were significantly associated with RA: the TNFAIP3 rs719149 A allele (OR 1.22 [95% confidence inter
125 0 patients with paired germline and lymphoma TNFAIP3 sequence data had functional abnormalities of A2
126 sponse of psoriasis to TNF blockers with two TNFAIP3 single-nucleotide polymorphisms (rs2230926 in ex
128 associations between JIA and variants in the TNFAIP3, STAT4, and C12orf30 regions that have previousl
129 ude and direction of the association between TNFAIP3, STAT4, and PTPN22 variants and childhood-onset
130 tor A (VEGFA) pathway directly, and elevated TNFAIP3 suppressed SOCS3 (suppressor of cytokine signali
131 null model defined the essential role of the TNFAIP3 targeting on miR-125a/miR-125b-mediated lymphoma
132 n CD loci (ICOSLG and TNFSF15) and T1D loci (TNFAIP3) that confer UC risk, known UC loci (HERC2 and I
134 A new study identifies somatic mutations in TNFAIP3, the gene encoding the NF-kappaB inhibitor A20,
135 Along with other associations near TRAF1 and TNFAIP3, this implies a central role for the CD40 signal
138 regulatory role of NF-kappaB-induced lincRNA-Tnfaip3 to act as a coactivator of NF-kappaB for the tra
139 ve generated mice bearing a floxed allele of Tnfaip3 to interrogate A20's roles in regulating B cell
141 fully identified several MRs including SOX3, TNFAIP3, TRAFD1, POU3F3, STAT2, and PML that govern the
142 n A20 closely mirrored the expression of the TNFAIP3 transcript, and was inversely related to NF-kapp
143 uced inflammatory responses through inducing Tnfaip3 transcription and controlling the metabolic repr
144 ptor (TLR)-induced inflammation by promoting Tnfaip3 transcription and fine-tuning of metabolic repro
147 ith JIA risk or protection were observed for TNFAIP3 variants rs10499194 (OR 0.74 [95% CI 0.61-0.91],
148 mor necrosis factor-alpha-induced protein 3 (TNFAIP3) was identified as a new regulatory component of
151 enetrance heterozygous germline mutations in TNFAIP3, which encodes the NF-kappaB regulatory protein
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