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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.
3                       Infection enhanced AHR/AHR nuclear translocator and AHR/RELB DNA binding and st
4           The AHR and heterodimeric partners AHR nuclear translocator and RELB are robustly expressed
5                                 However, the AHR nuclear translocator and transcriptional heterodimer
6                 Basal expression of AhR, the AhR nuclear translocator, and the CYP1 family members do
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
9      The aryl hydrocarbon receptor (AHR) and AHR nuclear translocator (ARNT) are DNA binding transcri
10              Limited digestion of [(35)S]AhR/AhR nuclear translocator (Arnt) by trypsin produced a pe
11  B (LMB) resulted in increased levels of AHR-AHR nuclear translocator (ARNT) complex in the nucleus a
12 nd binds the aryl hydrocarbon receptor (AhR)-AhR nuclear translocator (Arnt) complex.
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
15                                          The AhR nuclear translocator (ARNT) protein was highly expre
16   In all treatments the concentration of the AHR nuclear translocator (ARNT) protein was unchanged an
17                  Since dimerization with the AhR Nuclear Translocator (ARNT) protein, occurring throu
18 anslocation and DNA binding, the AhR and the AhR nuclear translocator (Arnt) protein, whose combined
19 ion with the heterodimerization partner, the AhR nuclear translocator (Arnt) protein.
20 drocarbon receptor (AhR) level and defective AhR nuclear translocator (ARNT) protein.
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
28 sponse element (XRE) in partnership with the AhR nuclear translocator (Arnt).
29 a8, but not AHRR(715), formed a complex with AHR nuclear translocator (ARNT).
30  aromatic hydrocarbon receptor (AhR) and the AhR nuclear translocator (Arnt).
31 quire heterodimerization between AhR and the AhR nuclear translocator (Arnt).
32 AhR) and its heterodimerization partner, the AhR nuclear translocator (Arnt).
33 ription factor that heterodimerizes with the AhR nuclear translocator (ARNT/HIF-1beta) to form an AhR
34          Transactivation domains of VP16 and AhR nuclear translocator, but not Sp1, can substitute fo
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
38 nfirmed that induction of CYP1A1 was AhR and AhR nuclear translocator-dependent.
39 e human AhR or its dimerization partner, the AhR nuclear translocator, interacts with pRb as a basis
40                                          The AhR nuclear translocator is not affected by this treatme
41                           Down-regulation of AhR nuclear translocator levels using short interfering
42 e of events following the binding of the AhR/AhR nuclear translocator protein (ARNT) heterodimer to d
43 /hsp90 complex prior to association with the AhR nuclear translocator protein (ARNT).
44 ds DNA in the form of a heterodimer with the AHR nuclear translocator protein (ARNT).
45 ent AhR translocation to the nucleus, or AhR-AhR nuclear translocator protein interactions.
46 transcription factor that dimerizes with the AHR nuclear translocator protein to mediate gene regulat
47 tween either AhR-hsp90, AhR-XAP2, and/or AhR-AhR nuclear translocator protein.
48 eraction between pRb and the AhR but not the AhR nuclear translocator protein.
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
51  member of the basic helix-loop-helix/period AhR nuclear translocator single minded family.
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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