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1 ta in vitro and supported the recruitment of steroid receptor coactivator 1.
2 the ER interaction domain of the coactivator steroid receptor coactivator 1.
3 nd GW409544 and a coactivator motif from the steroid receptor coactivator 1.
4 s, transcriptional intermediary factor 2 and steroid receptor coactivator 1.
5 ch contains the nuclear receptor coactivator steroid receptor coactivator 1.
6 teraction of FXR with a peptide derived from steroid receptor coactivator 1.
7 r, cotransfection of SNURF with prototypical steroid receptor coactivators 1, 2, and 3 that contain L
8 r activator RNA 1 (SRA1) that is part of the steroid receptor coactivator-1 acetyltransferase complex
9 , nuclear receptor coactivators p300/CBP and steroid receptor coactivator-1 act individually as well
12 lular nuclear receptor coactivators, such as steroid receptor coactivator 1 and p300/CREB-binding pro
13 ARQ48 aggregates sequester mitochondria and steroid receptor coactivator 1 and stain positively for
14 e interactions of hCAR with the coactivators steroid receptor coactivator-1 and glucocorticoid recept
16 rinsic activity of p160 coactivators such as steroid receptor coactivator-1 and promoted the interact
17 y between PBP and other coactivators such as steroid receptor coactivator-1 and that PBP plays a crit
18 ently identified to be highly related to the steroid receptor coactivator-1 and transcriptional inter
19 CI, Gao and colleagues present evidence that steroid receptor coactivators 1 and 2 (SRC-1 and SRC-2)
22 ion of the complex between ERR gamma and the steroid receptor coactivator-1, and led to an inhibition
24 d to spironolactone, finerenone inhibits MR, steroid receptor coactivator-1, and RNA polymerase II bi
25 , transcriptional intermediate factor 2, and steroid receptor coactivator-1 are expressed in specific
26 e nuclear receptor interacting domain of the steroid receptor coactivator-1 as a model for exploring
27 ion of the retinoid X receptor decreases the steroid receptor coactivator-1-dependent thyroid hormone
28 glucose increased PPARalpha interaction with steroid receptor coactivator-1, DNA binding, and transac
30 functional synergy of the p160 coactivators [steroid receptor coactivator-1, glucocorticoid receptor
31 ation of VDR with the coactivators GRIP1 and steroid receptor coactivator 1 in vitro but had little o
32 and promoted the interaction between PR and steroid receptor coactivator-1 in a mammalian two-hybrid
33 to bind the IL-4 promoter in the presence of steroid receptor coactivator-1, indicating that PPARalph
35 ed the transcriptional coactivators p300 and steroid receptor coactivator 1 less efficiently than ros
36 TCO-mediated interaction between CAR and the steroid receptor coactivator 1 or the glucocorticoid rec
37 element-binding protein-binding protein and steroid receptor coactivator-1, participate in both the
39 Also, coactivator binding studies with a steroid receptor coactivator-1 (receptor interaction dom
40 ene and also remarkably reduces basal MR and steroid receptor coactivator-1 recruitment, unraveling a
41 D bound to DAC and the fourth LXXLL motif of steroid receptor coactivator 1 reveals that the GR ligan
42 receptor beta (TRbeta) gene that cannot bind steroid receptor coactivator 1 (SRC-1) and Src-1(-/-) mi
43 gh inhibition of PR-dependent recruitment of steroid receptor coactivator 1 (SRC-1) and subsequent hi
44 e also demonstrate that UBCH7 interacts with steroid receptor coactivator 1 (SRC-1) and that UBCH7 co
45 cooperation of the coactivators CBP/p300 and steroid receptor coactivator 1 (SRC-1) and the p300/CBP-
46 nce analysis reveals that RAC3 is related to steroid receptor coactivator 1 (SRC-1) and transcription
49 oic acid receptor, CREB-binding protein, and steroid receptor coactivator 1 (SRC-1) in cell transfect
51 y less ability than dexamethasone to trigger steroid receptor coactivator 1 (SRC-1) recruitment and h
52 risk HPV type 16 (HPV16) E7 oncoprotein with steroid receptor coactivator 1 (SRC-1), an essential com
53 nterestingly, this domain corresponds to the steroid receptor coactivator 1 (SRC-1)-interacting domai
59 coactivators, CREB-binding protein (CBP) and steroid receptor coactivator 1 (SRC-1, a member of the p
61 coid receptor interacting protein 1 (GRIP1), steroid receptor coactivator 1 (SRC-1a), and SRC-1e bind
63 that includes the histone acetyltransferases steroid receptor coactivator-1 (SRC-1) and CREB binding
66 to interact with two other coactivators, the steroid receptor coactivator-1 (SRC-1) and the peroxisom
67 activated receptor binding protein (PBP) and steroid receptor coactivator-1 (SRC-1) are required for
68 mouse liver cDNA library and have identified steroid receptor coactivator-1 (SRC-1) as a PPAR transcr
70 25 amino acid residue fragment of the human steroid receptor coactivator-1 (SRC-1) containing one LX
73 coactivators CREB-binding protein (CBP) and steroid receptor coactivator-1 (SRC-1) for maximal activ
74 tigated further the coactivator functions of steroid receptor coactivator-1 (SRC-1) in terms of its f
75 yzed roles of CREB-binding protein (CBP) and steroid receptor coactivator-1 (SRC-1) in TTF-1 regulati
78 o part of the active receptor complex is the steroid receptor coactivator-1 (SRC-1) which interacts w
81 hat interacts only with coactivators such as steroid receptor coactivator-1 (SRC-1), RU486-bound PR b
82 During the decade since the discovery of steroid receptor coactivator-1 (SRC-1), the first authen
83 lpha), which requires co-activators, such as steroid receptor coactivator-1 (SRC-1), to facilitate th
84 ude p300 and CREB-binding protein (CBP), the steroid receptor coactivator-1 (SRC-1)-related family of
91 icoid-receptor-interactive protein-1(GRIP-1)/steroid-receptors coactivator-1 (SRC-1)) without breakin
92 eciphered a previously unappreciated role of Steroid receptor coactivator 1 (SRC1) in defining the li
93 tion, antibodies directed against the cloned steroid receptor coactivator 1 (SRC1) recognize ERAP160.
94 -dependent recruitment of a peptide from the steroid receptor coactivator 1 (SRC1) to the nuclear rec
95 iquitination greatly enhanced recruitment of steroid receptor coactivator 1 (SRC1), a coactivator cri
96 ement binding protein binding protein (CBP), steroid receptor coactivator 1 (SRC1), and protein argin
97 n and corresponds precisely with the minimal steroid receptor coactivator 1 (SRC1)-interacting domain
101 BD interacted with the C-terminal portion of steroid receptor coactivator-1, they did not enhance the
102 ated the recruitment of TTF-1, p65, CBP, and steroid receptor coactivator 1 to the TBE region of the
104 t insulin facilitated the recruitment of the steroid receptor coactivator-1 to the SREBP-1c promoter.
106 interaction with fatty acid metabolites and steroid receptor coactivator-1 while increasing PPARalph
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