scholarly article | Q13442814 |
P50 | author | Carsten Carlberg | Q18977815 |
P2093 | author name string | Christian Frank | |
Thomas W Dunlop | |||
Carita Oinonen | |||
Manuel Macias Gonzalez | |||
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Reciprocal activation of xenobiotic response genes by nuclear receptors SXR/PXR and CAR | Q24290621 | ||
The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions | Q24310512 | ||
Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor | Q24311650 | ||
A new orphan member of the nuclear hormone receptor superfamily that interacts with a subset of retinoic acid response elements | Q24324246 | ||
DNA deformability as a recognition feature in the reverb response element | Q27635498 | ||
Structural determinants of nuclear receptor assembly on DNA direct repeats | Q27730227 | ||
Structural elements of an orphan nuclear receptor-DNA complex | Q27760617 | ||
The nuclear receptor superfamily: the second decade | Q27860725 | ||
The repressed nuclear receptor CAR responds to phenobarbital in activating the human CYP2B6 gene | Q28137778 | ||
A unified nomenclature system for the nuclear receptor superfamily | Q28142509 | ||
Identification of a novel human constitutive androstane receptor (CAR) agonist and its use in the identification of CAR target genes | Q28213013 | ||
Nuclear receptor that identifies a novel retinoic acid response pathway | Q28238002 | ||
Differential transactivation by two isoforms of the orphan nuclear hormone receptor CAR | Q28248788 | ||
Activation by diverse xenochemicals of the 51-base pair phenobarbital-responsive enhancer module in the CYP2B10 gene | Q28267971 | ||
The c-erb-A protein is a high-affinity receptor for thyroid hormone | Q28282719 | ||
Single thyroid hormone receptor monomers are competent for co-activator-mediated transactivation | Q28364607 | ||
Orphan nuclear receptors constitutive androstane receptor and pregnane X receptor share xenobiotic and steroid ligands | Q28375193 | ||
Nuclear receptors and lipid physiology: opening the X-files | Q29619362 | ||
Mechanisms of nuclear signalling by vitamin D3. Interplay with retinoid and thyroid hormone signalling | Q33366885 | ||
The nuclear orphan receptor CAR-retinoid X receptor heterodimer activates the phenobarbital-responsive enhancer module of the CYP2B gene | Q33779787 | ||
Lipid soluble vitamins in gene regulation. | Q33803263 | ||
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Identification of the DNA binding site for NGFI-B by genetic selection in yeast | Q34955524 | ||
Natural vitamin D3 response elements formed by inverted palindromes: polarity-directed ligand sensitivity of vitamin D3 receptor-retinoid X receptor heterodimer-mediated transactivation. | Q36549658 | ||
Modular structure of a chicken lysozyme silencer: involvement of an unusual thyroid hormone receptor binding site | Q38340913 | ||
A novel role for helix 12 of retinoid X receptor in regulating repression | Q39447809 | ||
Thyroid hormone and retinoic acid receptors form heterodimers with retinoid X receptors on direct repeats, palindromes, and inverted palindromes | Q41477912 | ||
Differential nuclear receptor signalling from DR4-type response elements | Q42525591 | ||
The phenobarbital response enhancer module in the human bilirubin UDP-glucuronosyltransferase UGT1A1 gene and regulation by the nuclear receptor CAR. | Q43601213 | ||
Orphan nuclear receptors--new ligands and new possibilities. | Q46247763 | ||
A tissue-specific enhancer confers Pit-1-dependent morphogen inducibility and autoregulation on the pit-1 gene. | Q46870965 | ||
RZRs, a new family of retinoid-related orphan receptors that function as both monomers and homodimers | Q55950888 | ||
How to finger DNA | Q59087958 | ||
VDR-Alien: a novel, DNA-selective vitamin D(3) receptor-corepressor partnership | Q73947559 | ||
P433 | issue | 44 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 43299-43310 | |
P577 | publication date | 2003-08-01 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Characterization of DNA complexes formed by the nuclear receptor constitutive androstane receptor | |
P478 | volume | 278 |
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Q44902256 | Agonist-dependent and agonist-independent transactivations of the human constitutive androstane receptor are modulated by specific amino acid pairs |
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Q36020962 | Cross-talk between xenobiotic detoxication and other signalling pathways: clinical and toxicological consequences |
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Q92886852 | Emerging roles of bile acids in mucosal immunity and inflammation |
Q36440873 | Evolution and function of the NR1I nuclear hormone receptor subfamily (VDR, PXR, and CAR) with respect to metabolism of xenobiotics and endogenous compounds |
Q37774291 | Hepatocyte differentiation. |
Q58794880 | In vivo genome-wide binding interactions of mouse and human constitutive androstane receptors reveal novel gene targets |
Q37865512 | Mechanisms of induction of cytosolic and microsomal glutathione transferase (GST) genes by xenobiotics and pro-inflammatory agents |
Q37553490 | Metformin represses drug-induced expression of CYP2B6 by modulating the constitutive androstane receptor signaling |
Q35231096 | Multi-species analyses of direct activators of the constitutive androstane receptor |
Q28285494 | Nrf2-Keap1 signaling pathway regulates human UGT1A1 expression in vitro and in transgenic UGT1 mice |
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Q24796058 | Regulation of the human cyclin C gene via multiple vitamin D3-responsive regions in its promoter |
Q33781766 | Retinoid X receptor-alpha-dependent transactivation by a naturally occurring structural variant of human constitutive androstane receptor (NR1I3). |
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