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1 (CXD2), as well as induction by rifampicin (pregnane X receptor).
2 involve the glucocorticoid receptor and the pregnane X receptor.
3 ling modulates the phosphorylation status of pregnane x receptor.
4 loss of the nuclear xenobiotic receptor PXR (pregnane X receptor), a regulator of enterohepatic drug
5 genes can be targeted for regulation by the pregnane X receptor activator pregnenolone-16alpha-carbo
7 sults identify a novel mode of regulation of pregnane x receptor activity and highlight prominent fun
9 y, is a potent ligand (K(i) = 27 nM) for the pregnane X receptor, an orphan nuclear receptor that reg
10 ation of the intestinal xenobiotic receptors pregnane X receptor and constitutive androstane receptor
11 ng pathway, which is a critical regulator of pregnane X receptor and hepatocyte nuclear factor 1alpha
12 ic AMP-dependent protein kinase signaling on pregnane x receptor and provide a molecular explanation
13 to determine whether the interaction between pregnane x receptor and these key biochemical pathways i
14 xenobiotic-activated nuclear receptors PXR (pregnane X receptor) and CAR (constitutive androstane re
15 ncoding P-glycoprotein), NR1I2 (encoding the pregnane X receptor), and PPIA (encoding cyclophilin).
16 the nuclear receptors farsenoid X receptor, pregnane X receptor, and constitutive androstane recepto
18 receptors constitutive androstane receptor, pregnane X receptor, and peroxisome proliferator-activat
19 including constitutive androstane receptor, pregnane X receptor, and retinoid X receptor (RXR), modu
21 as enhanced in mice lacking the SXR ortholog pregnane X receptor, and treatment of humans with the SX
22 ity is opposite to the sensitizing effect of pregnane X receptor, constitutive androstane receptor, a
23 ilirubinemia can be reduced by activation of pregnane X receptor, constitutive androstane receptor, o
25 of the protein in vivo indicates that human pregnane x receptor exists as a phosphoprotein and that
27 rapeutic tool.The xenobiotic-activated human pregnane X receptor (hPXR) regulates drug metabolism.
30 ed off-target activities, most notably human pregnane X receptor (hPXR) transactivation, and led to s
32 bound to RNA polymerase (RNAP) and the human pregnane X receptor (hPXR), representative examples (2b-
38 These findings suggest that treatment with pregnane X receptor ligands may be useful clinically in
39 ein kinase signaling pathway synergizes with pregnane x receptor-mediated gene activation in mouse he
40 inase signaling has a repressive effect upon pregnane x receptor-mediated gene activation in rat and
45 tutive androstane receptor) (NR1I3) and PXR (pregnane X receptor) (NR1I2) was generated to study thei
47 RDelta8 did not repress the nuclear receptor pregnane X receptor or estrogen receptor alpha but did r
48 HNSCC and focused on the role of the nuclear pregnane X receptor (or NR1I2) and epigenetic mechanisms
52 sistance 1 (MDR1 C3435T) P-glycoprotein, and pregnane X receptor (PXR C-25385T, C8055T, and A7635G).
53 mes and drug export pumps, but only one, the pregnane X receptor (PXR in rodents, SXR in humans), reg
54 ehyde-O-(3,4-dichlorobenz yl)oxime (CITCO)], pregnane X receptor (PXR) [rifampicin], and peroxisome p
58 sm by which the nuclear xenobiotic receptors pregnane X receptor (PXR) and constitutive active/andros
61 dicates that xenobiotic sensors, such as the pregnane X receptor (PXR) and constitutive androstane re
64 , a by-product of intestinal flora, activate pregnane X receptor (PXR) and subsequent CYP3A4 and CYP2
66 s constitutive androstane receptor (CAR) and pregnane X receptor (PXR) are involved in the transcript
67 Constitutive androstane receptor (CAR) and pregnane X receptor (PXR) are xenobiotic sensors that en
68 The steroid and xenobiotic-responsive human pregnane X receptor (PXR) binds a broad range of structu
70 investigated whether the xenobiotic receptor pregnane X receptor (PXR) has a role in pathogenesis of
94 constitutive androstane receptor (CAR), and pregnane X receptor (PXR) regulate and alter the metabol
100 man hepatocytes, but does not activate human pregnane X receptor (PXR) significantly in cell-based tr
101 iosgenin increased the expression of several pregnane X receptor (PXR) target genes and the cholereti
105 ells had reduced nuclear localization of the pregnane X receptor (PXR), a key transcriptional regulat
108 cluding BPA, have been shown to activate the pregnane X receptor (PXR), a nuclear receptor that funct
111 in was transcriptionally up-regulated by the pregnane X receptor (PXR), a xenobiotic-activated nuclea
113 ydrocarbon receptor (AhR), activation of the pregnane X receptor (PXR), activation of the estrogen re
116 eptors including farnesoid X receptor (FXR), pregnane X receptor (PXR), and constitutive active/andro
117 tream promoter-transcription factor COUP-TF, pregnane X receptor (PXR), and hepatocyte nuclear factor
118 ar receptors, farnesoid X receptor (FXR) and pregnane X receptor (PXR), are important in maintaining
119 cells and hepatoma cells overexpressing the pregnane X receptor (PXR), but not in hepatoma cells in
120 al regulation by nuclear factors such as the pregnane X receptor (PXR), constitutive androstane recep
121 f CYP2B6 and CYP3A4, targets of hCAR and the pregnane X receptor (PXR), in HPH, HepaRG, and PXR-knock
122 e investigated the role of nuclear receptor, pregnane X receptor (PXR), in M. tuberculosis infection
124 -carbonitrile (PCN), a ligand for the rodent pregnane X receptor (PXR), significantly enhances the ra
125 uman (h) orphan nuclear receptor, termed the pregnane X receptor (PXR), that binds to a response elem
126 a novel orphan nuclear receptor, termed the pregnane X receptor (PXR), that is activated by naturall
127 y increased in mice lacking the SXR ortholog pregnane X receptor (PXR), thereby demonstrating a direc
128 promoter element has been shown to bind the pregnane X receptor (PXR), this receptor does not mediat
129 to the hCAR: PK1195 strongly activated human pregnane X receptor (PXR), whereas it did not alter the
130 mplicated in activating the nuclear receptor pregnane X receptor (PXR), which acts as a xenobiotic se
131 expression is transcriptionally regulated by pregnane X receptor (PXR), which is a ligand-dependent t
133 id, antimineralocorticoid, progestogenic and pregnane X receptor (PXR)-like activities (mug standard-
134 olished in hepatocyte cultures prepared from pregnane X receptor (PXR)-null mice, and cotransfection
135 n CYP3A4-null animals, suggesting that other pregnane X receptor (PXR)-regulated pathways may contrib
145 nuclear receptors, including the xenobiotic pregnane X receptor (PXR); (c) the ability to induce hum
146 own that MRP2 expression is regulated by the pregnane X receptor (PXR, NR1I2) and constitutive andros
151 that the ligand-activated nuclear receptors pregnane X receptor (PXR; NR1I2) and constitutive andros
152 ers of the nuclear receptor superfamily, the pregnane X receptor (PXR; NR1I2) and constitutive andros
153 ptor (CAR; NR1I3) and to a lesser extent the pregnane X receptor (PXR; NR1I2) are responsible for med
156 Genes encoding CYP3A6, in addition to the pregnane-X-receptor (PXR) and P-glycoprotein (P-gp) were
157 arbonitrile to activate the nuclear receptor pregnane X receptor restores P-glycoprotein expression a
158 pathways and biological functions, including pregnane X receptor/retinoic acid receptor activation as
159 biotic receptor) and its rodent homolog PXR (pregnane X receptor) serve as functional bile acid recep
160 e acids as CYP3A4 inducers and activators of pregnane X receptor/steroid and xenobiotic receptor (PXR
162 that topotecan and etoposide are ligands of pregnane X receptor that induce CYP3A4 transcription.
163 ptors, constitutive androstane receptor, and pregnane X receptor, these results suggest that decrease
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