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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
6            Cotreatment with the prototypical pregnane X receptor activator, rifampicin, significantly
7 sults identify a novel mode of regulation of pregnane x receptor activity and highlight prominent fun
8  protein kinase-mediated repression of human pregnane x receptor activity.
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
17 ative binding sites for retinoid X receptor, pregnane X receptor, and estrogen receptor.
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
20 s: farnesoid X receptor, vitamin D receptor, pregnane X receptor, and TGR5.
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
24 h the ability of these compounds to activate pregnane X receptor-dependent pathways in vivo.
25  of the protein in vivo indicates that human pregnane x receptor exists as a phosphoprotein and that
26                            The human nuclear pregnane X receptor (hPXR) activates cytochrome P450-3A
27 rapeutic tool.The xenobiotic-activated human pregnane X receptor (hPXR) regulates drug metabolism.
28                                    The human pregnane X receptor (hPXR) regulates the expression of c
29        Many drugs bind to and activate human pregnane X receptor (hPXR) to upregulate drug-metabolizi
30 ed off-target activities, most notably human pregnane X receptor (hPXR) transactivation, and led to s
31                                        Human pregnane X receptor (hPXR), an orphan nuclear receptor k
32 bound to RNA polymerase (RNAP) and the human pregnane X receptor (hPXR), representative examples (2b-
33 role of the nuclear xenobiotic receptor PXR (pregnane X receptor) in this process.
34                                              Pregnane x receptor is a ligand-activated transcription
35                          We also report that pregnane X receptor is essential to maintain robust in v
36                                    The mouse pregnane X receptor is highly similar to the human ortho
37                    The nuclear receptor PXR (pregnane X receptor) is a broad-specificity sensor that
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
41                        Both constitutive and pregnane X receptor-mediated inducible activities were m
42                 Furthermore, IL-6 attenuated pregnane X receptor-mediated transcription of the CYP3A2
43                        The effect of IL-6 on pregnane X receptor-mediated transcription of the rat CY
44 n at 24 hrs, potentially via IL-6 effects on pregnane X receptor-mediated transcription.
45 tutive androstane receptor) (NR1I3) and PXR (pregnane X receptor) (NR1I2) was generated to study thei
46 f CYP3a13 by dexamethasone occurring only in pregnane X receptor null mice.
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
49          These data demonstrate an impact of pregnane X receptor polymorphisms on tacrolimus pharmaco
50                    The nuclear receptor PXR (pregnane X receptor) protects the body from hepatotoxici
51                       We show that the human pregnane x receptor protein can serve as an effective su
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
55        Ketoconazole binds to and antagonizes pregnane X receptor (PXR) activation.
56                      Upon treatment with the pregnane X receptor (PXR) activator rifampicin (RIF), hu
57                                          The pregnane X receptor (PXR) acts as a receptor to induce g
58 sm by which the nuclear xenobiotic receptors pregnane X receptor (PXR) and constitutive active/andros
59                 The orphan nuclear receptors pregnane X receptor (PXR) and constitutive androstane re
60                                  The nuclear pregnane X receptor (PXR) and constitutive androstane re
61 dicates that xenobiotic sensors, such as the pregnane X receptor (PXR) and constitutive androstane re
62                        The nuclear receptors pregnane X receptor (PXR) and constitutive androstane re
63                              Statins utilize pregnane X receptor (PXR) and serum/glucocorticoid regul
64 , a by-product of intestinal flora, activate pregnane X receptor (PXR) and subsequent CYP3A4 and CYP2
65                                          The pregnane X receptor (PXR) and the constitutive androstan
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
69                                          The pregnane X receptor (PXR) detects the presence of a wide
70 investigated whether the xenobiotic receptor pregnane X receptor (PXR) has a role in pathogenesis of
71 Ralpha) as well as its heterodimeric partner pregnane X receptor (PXR) in mice.
72 CYP3A4, hepatocyte nuclear factor-4alpha, or pregnane X receptor (PXR) in PHHs.
73                        Here we show that the pregnane X receptor (PXR) interacts more strongly with S
74                                          The pregnane X receptor (PXR) is a key regulator of xenobiot
75                                              Pregnane X receptor (PXR) is a ligand-dependent transcri
76                                          The pregnane X receptor (PXR) is a master regulator of xenob
77                                          The pregnane X receptor (PXR) is a master regulator of xenob
78                                              Pregnane X receptor (PXR) is a nuclear receptor consider
79                                          The pregnane X receptor (PXR) is a nuclear receptor signific
80                                    The human pregnane X receptor (PXR) is a promiscuous nuclear recep
81                                              Pregnane X receptor (PXR) is a xenobiotic receptor that
82                         The nuclear receptor pregnane X receptor (PXR) is activated by a range of xen
83                                          The pregnane X receptor (PXR) is an important transcriptiona
84                                          The pregnane X receptor (PXR) is an orphan nuclear receptor
85                                              Pregnane X receptor (PXR) is known to function as a xeno
86              The nuclear xenobiotic receptor pregnane X receptor (PXR) is promiscuously activated by
87                                          The pregnane X receptor (PXR) is the molecular target for ca
88                                              Pregnane X receptor (PXR) mediates xenobiotic and endobi
89 GSTA2 and expression plasmids for either GR, pregnane X receptor (PXR) or a combination of both.
90                                  The nuclear pregnane X receptor (PXR) plays a central role in regula
91                               In mammals the pregnane X receptor (PXR) plays a key role in the regula
92                                              Pregnane X receptor (PXR) plays an important role in det
93                                          The pregnane X receptor (PXR) plays an important role in the
94  constitutive androstane receptor (CAR), and pregnane X receptor (PXR) regulate and alter the metabol
95                                    The human pregnane X receptor (PXR) regulates genes involved in dr
96            Upon drug activation, the nuclear pregnane X receptor (PXR) regulates not only hepatic dru
97                                          The pregnane X receptor (PXR) regulates the metabolism and e
98                               By employing a pregnane X receptor (PXR) reporter gene assay to priorit
99                   The human nuclear receptor pregnane X receptor (PXR) responds to a wide variety of
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
102 nduced by the farnesoid X receptor (FXR) and pregnane X receptor (PXR) through the same IR0.
103                                          The pregnane X receptor (PXR) was isolated as a xenosensor r
104                                              Pregnane X receptor (PXR) was originally characterized a
105 ells had reduced nuclear localization of the pregnane X receptor (PXR), a key transcriptional regulat
106                                              Pregnane X receptor (PXR), a member of the NR1I nuclear
107        In contrast, expression levels of the pregnane X receptor (PXR), a nuclear receptor most simil
108 cluding BPA, have been shown to activate the pregnane X receptor (PXR), a nuclear receptor that funct
109                                              Pregnane X receptor (PXR), a previously known "xenobioti
110                  Recent reports suggest that pregnane X receptor (PXR), a xenobiotic nuclear receptor
111 in was transcriptionally up-regulated by the pregnane X receptor (PXR), a xenobiotic-activated nuclea
112                                              Pregnane X receptor (PXR), acting as a xenobiotic-activa
113 ydrocarbon receptor (AhR), activation of the pregnane X receptor (PXR), activation of the estrogen re
114                                          The pregnane X receptor (PXR), along with its sister recepto
115                                    The human pregnane X receptor (PXR), also known as steroid and xen
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
123 s constitutive androstane receptor (CAR) and pregnane X receptor (PXR), respectively.
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
132                                Here, using a pregnane X receptor (PXR)-humanized mouse model, we foun
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
136 multiple mechanisms, including activation of pregnane X receptor (PXR).
137 hift assays showed that CAR-RE binds CAR and pregnane X receptor (PXR).
138 s regulated by nuclear receptors such as the pregnane X receptor (PXR).
139 e constitutive androstane receptor (CAR) and pregnane X receptor (PXR).
140 rier function through the xenobiotic sensor, pregnane X receptor (PXR).
141 ted during confluence in a process involving pregnane X receptor (PXR).
142 n of constitutive androstane receptor and/or pregnane X receptor (PXR).
143 tagonists have been identified for the human pregnane X receptor (PXR).
144 vated the human nuclear xenobiotic receptor, pregnane X receptor (PXR).
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
147                                          The pregnane X receptor (PXR, NR1I2) is a xenobiotic-sensing
148            Ligand-mediated activation of the pregnane X receptor (PXR, NR1I2) is postulated to affect
149                                              Pregnane X receptor (PXR, NR1I2), a member of the superf
150                                Recently, the pregnane X receptor (PXR, NR1I2), initially characterize
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
154 itutive androstane receptor (CAR; NR1I3) and pregnane X receptor (PXR; NR1I2), respectively.
155 ted with rifampicin in order to identify new pregnane-X receptor (PXR) target genes.
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
161                          Expression of other pregnane X receptor target enzymes and transporter genes
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
164 signaling also modulates the interactions of pregnane x receptor with protein cofactors.

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