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1 ns, the aryl hydrocarbon receptor (AhR), and AhR nuclear translocator.
2 and that does not contain either the AhR or AhR nuclear translocator.
7 ed AHR but not its dimerization partner, the AHR nuclear translocator, and the repressive effects of
8 g competition with AHR for dimerization with AHR nuclear translocator (ARNT) and binding to AHR-respo
11 B (LMB) resulted in increased levels of AHR-AHR nuclear translocator (ARNT) complex in the nucleus a
13 rthologs of AHR and its dimerization partner AHR nuclear translocator (ARNT) in the nematode Caenorha
14 for the aryl hydrocarbon receptor (AhR) and AhR nuclear translocator (ARNT) mRNAs in MCF-7 breast ca
16 In all treatments the concentration of the AHR nuclear translocator (ARNT) protein was unchanged an
18 anslocation and DNA binding, the AhR and the AhR nuclear translocator (Arnt) protein, whose combined
21 ydrocarbon receptor (AHR) dimerizes with the AHR nuclear translocator (ARNT) to form a functional com
22 eterodimeric aryl hydrocarbon receptor (AhR)/AhR nuclear translocator (ARNT) transcription factor com
23 odimerizes with its DNA binding partner, the AhR nuclear translocator (ARNT), and activates specific
24 dibenzo-p-dioxin (TCDD), associates with the AHR nuclear translocator (ARNT), and the dimer so formed
25 eptor (AHR) and its DNA binding partner, the AHR nuclear translocator (ARNT), are basic helix-loop-he
26 ription factor that, in conjunction with the AhR nuclear translocator (Arnt), binds to dioxin respons
27 t the AHR and its heterodimeric partner, the AHR nuclear translocator (ARNT), play a role in the deve
33 ription factor that heterodimerizes with the AhR nuclear translocator (ARNT/HIF-1beta) to form an AhR
35 eptor rapidly suppresses activity of the AhR/AhR nuclear translocator complex in the CYP1B1 enhancer
36 s in an increase in the concentration of AHR.AHR nuclear translocator complexes associated with DNA a
37 failed to induce CYP1A1 in AhR-deficient and AhR nuclear translocator-deficient murine hepatoma cell
39 e human AhR or its dimerization partner, the AhR nuclear translocator, interacts with pRb as a basis
42 e of events following the binding of the AhR/AhR nuclear translocator protein (ARNT) heterodimer to d
46 transcription factor that dimerizes with the AHR nuclear translocator protein to mediate gene regulat
49 gs to the basic helix-loop-helix/periodicity/AhR nuclear translocator/simple-minded (Per-Arnt-Sim) fa
50 minus of the AHR "Per-ARNT-Sim" (periodicity/AHR nuclear translocator/simple-minded) domain and the B
52 wo forms of the AhR (97 and 104 kDa) and the AhR nuclear translocator were detected in BMS2 cells.
53 ncreased NK cell AHR levels, and the AHR and AHR nuclear translocator were required for optimal produ
54 nscriptionally active heterodimer with ARNT (AHR nuclear translocator), which recognizes the dioxin r
55 he AHR, relevant chaperone proteins, and the AHR nuclear translocator, which heterodimerizes with the
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