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1  cancer and encodes a protein that acts as a steroid receptor coactivator.
2 interacts with LXXLL motifs (NR box) in p160 steroid receptor coactivators.
3 plicing in a manner differing from the other steroid receptor coactivators.
4        Overexpression of nuclear coactivator steroid receptor coactivator 1 (SRC-1) and aberrant acti
5 receptor beta (TRbeta) gene that cannot bind steroid receptor coactivator 1 (SRC-1) and Src-1(-/-) mi
6 gh inhibition of PR-dependent recruitment of steroid receptor coactivator 1 (SRC-1) and subsequent hi
7 e also demonstrate that UBCH7 interacts with steroid receptor coactivator 1 (SRC-1) and that UBCH7 co
8 cooperation of the coactivators CBP/p300 and steroid receptor coactivator 1 (SRC-1) and the p300/CBP-
9 nce analysis reveals that RAC3 is related to steroid receptor coactivator 1 (SRC-1) and transcription
10 xifen in the uterus requires a high level of steroid receptor coactivator 1 (SRC-1) expression.
11       Prominent in this diverse group is the steroid receptor coactivator 1 (SRC-1) family, which int
12 oic acid receptor, CREB-binding protein, and steroid receptor coactivator 1 (SRC-1) in cell transfect
13                              Coactivation by steroid receptor coactivator 1 (SRC-1) of mCAR did not d
14 y less ability than dexamethasone to trigger steroid receptor coactivator 1 (SRC-1) recruitment and h
15 risk HPV type 16 (HPV16) E7 oncoprotein with steroid receptor coactivator 1 (SRC-1), an essential com
16 nterestingly, this domain corresponds to the steroid receptor coactivator 1 (SRC-1)-interacting domai
17 n disrupts the direct interaction of GR with steroid receptor coactivator 1 (SRC-1).
18 dynamics of estrogen receptor alpha (ER) and steroid receptor coactivator 1 (SRC-1).
19 pathways, we examined the phosphorylation of steroid receptor coactivator 1 (SRC-1).
20 d receptor-interacting protein 1 (GRIP1) and steroid receptor coactivator 1 (SRC-1).
21 2 (TIF2) and is also partially homologous to steroid receptor coactivator 1 (SRC-1).
22 coactivators, CREB-binding protein (CBP) and steroid receptor coactivator 1 (SRC-1, a member of the p
23                        Coactivators, such as steroid receptor coactivator 1 (SRC-1A) and CREB (cAMP r
24 coid receptor interacting protein 1 (GRIP1), steroid receptor coactivator 1 (SRC-1a), and SRC-1e bind
25 eciphered a previously unappreciated role of Steroid receptor coactivator 1 (SRC1) in defining the li
26 tion, antibodies directed against the cloned steroid receptor coactivator 1 (SRC1) recognize ERAP160.
27 -dependent recruitment of a peptide from the steroid receptor coactivator 1 (SRC1) to the nuclear rec
28 iquitination greatly enhanced recruitment of steroid receptor coactivator 1 (SRC1), a coactivator cri
29 ement binding protein binding protein (CBP), steroid receptor coactivator 1 (SRC1), and protein argin
30 n and corresponds precisely with the minimal steroid receptor coactivator 1 (SRC1)-interacting domain
31 ion factor 1 and HNF3beta) all interact with steroid receptor coactivator 1 (SRC1).
32                Co-transfection with GRIP1 or steroid receptor coactivator 1 amplified both the positi
33 lular nuclear receptor coactivators, such as steroid receptor coactivator 1 and p300/CREB-binding pro
34  ARQ48 aggregates sequester mitochondria and steroid receptor coactivator 1 and stain positively for
35                  Its competitive reversal of steroid receptor coactivator 1 enhancement of ER activit
36 ation of VDR with the coactivators GRIP1 and steroid receptor coactivator 1 in vitro but had little o
37 ed the transcriptional coactivators p300 and steroid receptor coactivator 1 less efficiently than ros
38 TCO-mediated interaction between CAR and the steroid receptor coactivator 1 or the glucocorticoid rec
39 D bound to DAC and the fourth LXXLL motif of steroid receptor coactivator 1 reveals that the GR ligan
40 tryptophan-299 to activate hPXR; 5) recruits steroid receptor coactivator 1 to hPXR; 6) activates hPX
41 ated the recruitment of TTF-1, p65, CBP, and steroid receptor coactivator 1 to the TBE region of the
42                           Interestingly, the steroid receptor coactivator 1 together with ligand is a
43  by DAX-1, an SF-1 suppressor, and raised by steroid receptor coactivator 1, an SF-1 coactivator.
44          While all three coactivators ARA70, steroid receptor coactivator 1, and RAC3/ACTR can enhanc
45 ta in vitro and supported the recruitment of steroid receptor coactivator 1.
46 the ER interaction domain of the coactivator steroid receptor coactivator 1.
47 nd GW409544 and a coactivator motif from the steroid receptor coactivator 1.
48 s, transcriptional intermediary factor 2 and steroid receptor coactivator 1.
49 ch contains the nuclear receptor coactivator steroid receptor coactivator 1.
50 teraction of FXR with a peptide derived from steroid receptor coactivator 1.
51 CI, Gao and colleagues present evidence that steroid receptor coactivators 1 and 2 (SRC-1 and SRC-2)
52       Here, we evaluated the contribution of steroid receptor coactivators 1 and 2 (SRC-1 and SRC-2),
53 r, cotransfection of SNURF with prototypical steroid receptor coactivators 1, 2, and 3 that contain L
54     Also, coactivator binding studies with a steroid receptor coactivator-1 (receptor interaction dom
55                                              Steroid receptor coactivator-1 (SRC-1 or NCOA1) is overe
56 that includes the histone acetyltransferases steroid receptor coactivator-1 (SRC-1) and CREB binding
57        We previously isolated and identified steroid receptor coactivator-1 (SRC-1) and peroxisome pr
58                                              Steroid receptor coactivator-1 (SRC-1) and PPAR-binding
59 to interact with two other coactivators, the steroid receptor coactivator-1 (SRC-1) and the peroxisom
60 activated receptor binding protein (PBP) and steroid receptor coactivator-1 (SRC-1) are required for
61 mouse liver cDNA library and have identified steroid receptor coactivator-1 (SRC-1) as a PPAR transcr
62      These subclasses include members of the steroid receptor coactivator-1 (SRC-1) coactivator famil
63  25 amino acid residue fragment of the human steroid receptor coactivator-1 (SRC-1) containing one LX
64                            In breast cancer, steroid receptor coactivator-1 (SRC-1) expression positi
65                                              Steroid receptor coactivator-1 (SRC-1) family members in
66  coactivators CREB-binding protein (CBP) and steroid receptor coactivator-1 (SRC-1) for maximal activ
67 tigated further the coactivator functions of steroid receptor coactivator-1 (SRC-1) in terms of its f
68 yzed roles of CREB-binding protein (CBP) and steroid receptor coactivator-1 (SRC-1) in TTF-1 regulati
69                           Here, we show that Steroid Receptor Coactivator-1 (SRC-1) interacts with a
70                                              Steroid receptor coactivator-1 (SRC-1) is a coactivator
71                                              Steroid receptor coactivator-1 (SRC-1) is a member of a
72 o part of the active receptor complex is the steroid receptor coactivator-1 (SRC-1) which interacts w
73                                              Steroid receptor coactivator-1 (SRC-1), a coregulatory p
74      Members of the p160 coactivator family (steroid receptor coactivator-1 (SRC-1), glucocorticoid r
75 hat interacts only with coactivators such as steroid receptor coactivator-1 (SRC-1), RU486-bound PR b
76     During the decade since the discovery of steroid receptor coactivator-1 (SRC-1), the first authen
77 lpha), which requires co-activators, such as steroid receptor coactivator-1 (SRC-1), to facilitate th
78 ude p300 and CREB-binding protein (CBP), the steroid receptor coactivator-1 (SRC-1)-related family of
79 ncluding CREB-binding protein (CBP/p300) and steroid receptor coactivator-1 (SRC-1).
80 n and can be partially overcome by exogenous steroid receptor coactivator-1 (SRC-1).
81 ires the involvement of coactivators such as steroid receptor coactivator-1 (SRC-1).
82  recently identified coactivators, including steroid receptor coactivator-1 (SRC-1).
83 entified in a number of coactivators such as steroid receptor coactivator-1 (SRC-1).
84 timulate receptor-dependent transcription is steroid receptor coactivator-1 (SRC-1).
85 rs recruit coactivator proteins, such as the steroid receptor coactivator-1 (SRC1).
86 corticosterone and the fourth LXXLL motif of steroid receptor coactivator-1 (SRC1-4).
87 r activator RNA 1 (SRA1) that is part of the steroid receptor coactivator-1 acetyltransferase complex
88 , nuclear receptor coactivators p300/CBP and steroid receptor coactivator-1 act individually as well
89        ACTR and related p160 family members (steroid receptor coactivator-1 and glucocorticoid recept
90 e interactions of hCAR with the coactivators steroid receptor coactivator-1 and glucocorticoid recept
91 eases the functional interaction between the steroid receptor coactivator-1 and hPXR but not mouse PX
92 rinsic activity of p160 coactivators such as steroid receptor coactivator-1 and promoted the interact
93 y between PBP and other coactivators such as steroid receptor coactivator-1 and that PBP plays a crit
94 ently identified to be highly related to the steroid receptor coactivator-1 and transcriptional inter
95 , transcriptional intermediate factor 2, and steroid receptor coactivator-1 are expressed in specific
96 e nuclear receptor interacting domain of the steroid receptor coactivator-1 as a model for exploring
97  and promoted the interaction between PR and steroid receptor coactivator-1 in a mammalian two-hybrid
98           BEL attenuated the agonist-induced steroid receptor coactivator-1 interaction with hPXR, an
99                 Furthermore, coexpression of steroid receptor coactivator-1 is required for ligand-de
100 ypeptides in mammalian cells, along with the steroid receptor coactivator-1 protein (SRC-1).
101 ene and also remarkably reduces basal MR and steroid receptor coactivator-1 recruitment, unraveling a
102                         GSK3987 recruits the steroid receptor coactivator-1 to human LXRalpha and LXR
103 t insulin facilitated the recruitment of the steroid receptor coactivator-1 to the SREBP-1c promoter.
104  interaction with fatty acid metabolites and steroid receptor coactivator-1 while increasing PPARalph
105 ion of the complex between ERR gamma and the steroid receptor coactivator-1, and led to an inhibition
106       Multiple coactivators, including p300, steroid receptor coactivator-1, and p300/cAMP-response e
107 d to spironolactone, finerenone inhibits MR, steroid receptor coactivator-1, and RNA polymerase II bi
108 glucose increased PPARalpha interaction with steroid receptor coactivator-1, DNA binding, and transac
109 functional synergy of the p160 coactivators [steroid receptor coactivator-1, glucocorticoid receptor
110 to bind the IL-4 promoter in the presence of steroid receptor coactivator-1, indicating that PPARalph
111  element-binding protein-binding protein and steroid receptor coactivator-1, participate in both the
112 BD interacted with the C-terminal portion of steroid receptor coactivator-1, they did not enhance the
113 ion of the retinoid X receptor decreases the steroid receptor coactivator-1-dependent thyroid hormone
114 icoid-receptor-interactive protein-1(GRIP-1)/steroid-receptors coactivator-1 (SRC-1)) without breakin
115 ly of nuclear receptor coactivators, such as steroid receptor coactivator 1a and glucocorticoid recep
116 gate binding and dissociation of full-length steroid receptor coactivator-1a (SRC1a) from full-length
117                  Herein, we demonstrate that Steroid Receptor Coactivator 2 (SRC-2) orchestrates a hi
118 of the oncogenic transcriptional coregulator steroid receptor coactivator 2 (SRC-2), also known as NC
119 rs that block the association of TRbeta with steroid receptor coactivator 2 (SRC2), we identified a n
120 ding between VDR and a fluorescently labeled steroid receptor coactivator 2 peptide was applied to di
121 corporated them into a sequence derived from steroid receptor coactivator 2, which interacts with est
122 ion between the vitamin D receptor (VDR) and steroid receptor coactivator 2.
123 t-binding protein (CREB)-binding protein and steroid receptor coactivators 2 and 3 was decreased in f
124 reviously demonstrated the potential role of steroid receptor coactivator-2 (SRC-2) as a co-regulator
125 sly shown that the transcriptional regulator steroid receptor coactivator-2 (SRC-2) controls activati
126 y androgen receptor (AR) and its coregulator steroid receptor coactivator-2 (SRC-2) enhances mitochon
127                                      Loss of steroid receptor coactivator-2 (SRC-2) results in a reve
128                  Although we have shown that steroid receptor coactivator-2 (SRC-2), a member of the
129 es and in HepG2 cells reduced recruitment of steroid receptor coactivator-2 by RORalpha at an endogen
130                                              Steroid receptor coactivator 3 (SRC-3) coactivator phosp
131                                              Steroid receptor coactivator 3 (SRC-3) is a critical med
132                                              Steroid receptor coactivator 3 (SRC-3) is an oncogenic n
133                                              Steroid receptor coactivator 3 (SRC-3) is most strongly
134                                          The steroid receptor coactivator 3 (SRC-3) is overexpressed
135 that ERK3 interacted with and phosphorylated steroid receptor coactivator 3 (SRC-3), an oncogenic pro
136 rect interaction of the liganded TRbeta with steroid receptor coactivator 3 (SRC-3), which recruits p
137 E3 ligases, such as C-MYC, beta-catenin, and steroid receptor coactivator 3 (SRC-3).
138                                              Steroid receptor coactivator 3 (SRC-3/AIB1) interacts wi
139                                              Steroid receptor coactivator 3 (SRC-3/AIB1/ACTR/NCoA-3)
140 e of an active complex of DNA-bound ERalpha, steroid receptor coactivator 3 (SRC-3/NCOA3), and a seco
141                                              Steroid receptor coactivator 3 (SRC-3/p/CIP/AIB1/ACTR/RA
142  proteins, including androgen receptor (AR), steroid receptor coactivator 3 (SRC3) and BRD4, for degr
143  of purified full-length PR and intact CoRs, steroid receptor coactivator 3 (SRC3) and p300, as compl
144 as a model, we have investigated the role of steroid receptor coactivator 3 (SRC3) in gene activation
145      Here, we report that the ER coactivator steroid receptor coactivator 3 (SRC3) is also a coactiva
146                We have previously shown that steroid receptor coactivator 3 (SRC3) is expressed and u
147 enced by histone acetylation and require the steroid receptor coactivator 3 (SRC3), which mediates in
148 ctivation of gene expression was enhanced by steroid receptor coactivator 3 coactivator, and required
149                                          The steroid receptor coactivator 3 gene (SRC-3) (AIB1/ACTR/p
150 ied in breast cancer 1 (AIB1), also known as steroid receptor coactivator 3 or NCOA3, is a transcript
151 parate assays, both the recruitment of SRC3 (steroid receptor coactivator 3, a transcriptional coacti
152 gh-throughput screening to identify SMIs for steroid receptor coactivator-3 (SRC-3 or AIB1), a large
153      In the present study, we find that high steroid receptor coactivator-3 (SRC-3) expression is cor
154       Here we demonstrate that reprogramming steroid receptor coactivator-3 (SRC-3) function by chang
155  Molecular Cell, Yu et al. reported that the steroid receptor coactivator-3 (SRC-3) has a novel cytop
156 ctivator amplified in breast cancer 1 (AIB1)/steroid receptor coactivator-3 (SRC-3) have been shown t
157 ent study aimed to elucidate the role of the steroid receptor coactivator-3 (SRC-3) in thyroid carcin
158 oncogene amplified in breast cancer 1 (AIB1)/steroid receptor coactivator-3 (SRC-3) induces mammary t
159                                              Steroid receptor coactivator-3 (SRC-3) is a coactivator
160             Here, we show that the oncogenic steroid receptor coactivator-3 (SRC-3) is a critical reg
161                                              Steroid receptor coactivator-3 (SRC-3) is a histone acet
162                                              Steroid receptor coactivator-3 (SRC-3) is a transcriptio
163          Phosphorylation and activity of the Steroid Receptor Coactivator-3 (SRC-3) is reduced upon H
164              Estrogen receptor (ER) recruits steroid receptor coactivator-3 (SRC-3) primary coactivat
165       We report here the characterization of steroid receptor coactivator-3 (SRC-3), a coactivator of
166 y also caused a failure in downregulation of steroid receptor coactivator-3 (SRC-3), a potent ERalpha
167                                              Steroid receptor coactivator-3 (SRC-3)/AIB1 is a member
168                                          The steroid receptor coactivator-3 (SRC-3, also known as pCI
169                                              Steroid receptor coactivator-3 (SRC-3, p/CIP, AIB1, ACTR
170                                              Steroid receptor coactivator-3 (SRC-3/AIB1) is a coactiv
171                                              Steroid receptor coactivator-3 (SRC-3/AIB1) is an oncoge
172 sphorylated alternate-spliced isoform of the steroid receptor coactivator-3 (SRC-3Delta4) bridges EGF
173 d crystallographic studies, we identify that steroid receptor coactivator-3 (SRC3) (also named as amp
174 exes did not readily recruit the coactivator steroid receptor coactivator-3 (SRC3) or ER to the PS2 p
175 er region for recruiting nuclear coactivator steroid receptor coactivator-3 and p300 for histone epig
176 ociated with the displacement of ERalpha and steroid receptor coactivator-3 from the target EBRs lead
177 shown that TR recruits the coactivator SRC3 (steroid receptor coactivator-3) and that coactivator rec
178 ceptor-associated coactivator 3 (RAC3)/AIB-1/steroid receptor coactivator-3, a nuclear coregulator an
179          Amplified in breast cancer 1 (AIB1; steroid receptor coactivator-3, p/CIP, RAC3, ACTR, TRAM-
180                   Overexpression of the p160 steroid receptor coactivator ACTR is associated with bre
181 or CBP and the activation domain of the p160 steroid receptor coactivator ACTR.
182 R function by selectively competing with the steroid receptor coactivator AIB1 but not GRIP1 or SRC1
183         Overexpression and activation of the steroid receptor coactivator amplified in breast cancer
184                                          The steroid receptor coactivator amplified in breast cancer
185 eroid receptors, it has been identified as a steroid receptor coactivator, and was thought not to be
186 s reactivation of mutant p53, stimulation of steroid receptor coactivators, and induction of protein
187 enotypes indicate that these two families of steroid receptor coactivators are not functionally equiv
188 sferase (HAT) domain, EIA-binding domain and steroid-receptor coactivator binding domains of CBP.
189             We show here that AIB1 and other steroid receptor coactivators can enhance the functional
190 xes, DRIP (VDR-interacting protein) and SRC (steroid receptor coactivator), during keratinocyte diffe
191 or complex disassembly by methylation of the steroid receptor coactivator family coactivators and p30
192  human breast tumors and belongs to the p160 steroid receptor coactivator family.
193  Both SRC-1 and TIF2 are members of the p160 steroid receptor coactivator family.
194  coactivators such as PBP and members of the steroid receptor coactivator family.
195 d coactivator 3 (RAC3), which belongs to the steroid receptor coactivator family.
196 ominent among these coactivators is the SRC (steroid receptor coactivator) family, which consists of
197 refore, SRC-3, a third member of a family of steroid receptor coactivators, has a distinct tissue dis
198                                   Currently, steroid receptor coactivators have been proposed to medi
199  a novel function of Cdc25B that serves as a steroid receptor coactivator in addition to its role as
200                To explore a possible role of steroid receptor coactivators in transcriptional synergi
201       In this study we explore the impact of steroid receptor coactivator inhibitor, other targeted a
202  the most active members inhibit the ERalpha/steroid receptor coactivator interaction with K i's in t
203 ty and the C-terminal region (containing the steroid receptor coactivator/p160-binding region and the
204 s induced by GR signaling, and the important steroid receptor coactivator PELP1 was also found to be
205 (Pol II), estrogen receptor alpha (ERalpha), steroid receptor coactivator proteins (SRC), and acetyla
206 een the AR N and C termini or recruitment of steroid receptor coactivator proteins (SRC-1 or -2), alt
207                             In contrast, the steroid receptor coactivator SRC-1 increases transcripti
208 stant patients showed high expression of the steroid receptor coactivator SRC-1.
209 ctivator REGgamma directs degradation of the steroid receptor coactivator SRC-3 by the 20S proteasome
210 ctivator REGgamma directs degradation of the steroid receptor coactivator SRC-3 by the 20S proteasome
211 rence (RNAi) depletions of CYC, MET, and the steroid receptor coactivator SRC/FISC.
212  in the recruitment of RNA polymerase II and steroid receptor coactivators SRC-2 and SRC-3, and chang
213                                          The steroid-receptor coactivator SRC-1 is a coactivator for
214 ne (JH) receptor, Methoprene-tolerant (Met), steroid receptor coactivator (SRC) and GATAa but not ecd
215 tivators, VDR-interacting protein (DRIP) and steroid receptor coactivator (SRC) at different stages o
216 mains of transcription factors, those of the steroid receptor coactivator (SRC) family are poorly cha
217 invasion, and metastasis, including the p160 steroid receptor coactivator (SRC) family composed of SR
218                      The recently identified steroid receptor coactivator (SRC) family contains three
219 ne receptor (TR) include members of the p160/steroid receptor coactivator (SRC) family of proteins, p
220       SRC3, a highly conserved member of the steroid receptor coactivator (SRC) family, is recruited
221 ied of these coactivators are members of the steroid receptor coactivator (SRC) family, SRC-1, TIF2/G
222  other VDR coactivators such as those in the steroid receptor coactivator (SRC) family.
223                                          The steroid receptor coactivator (SRC) proteins are coactiva
224  the bHLH transcription factors studied, the steroid receptor coactivator (SRC) showed the most sever
225 cetyltransferase complexes, such as p300/CBP-steroid receptor coactivator (SRC), as well as the multi
226 rene-tolerant transcription factor (Met) and steroid receptor coactivator (SRC), would be expressed c
227                    Genetic disruption of the steroid receptor coactivator (SRC)-1 and transcriptional
228                                          The steroid receptor coactivator (SRC)-1 enhances the activi
229 lencing mediator for retinoid and thyroid or steroid receptor coactivator (SRC)-1 with RARalpha versu
230 OOH-terminal interaction and are enhanced by steroid receptor coactivator (SRC)-1, whereas the bicalu
231 gamma) regulate bone metabolism, and because steroid receptor coactivator (SRC)-2 (TIF-2) enhances ER
232                                              Steroid receptor coactivator (SRC)-3, also called amplif
233  phosphorylation signaling pathway involving steroid receptor coactivator (Src)-mitogen-activated pro
234 eraction domains of p300/CBP, as well as the steroid receptor coactivator (SRC).
235 ne receptors involves the recruitment of the steroid receptor coactivator (SRC)/p160 coactivator LXXL
236 R FXXLF motif binding and the recruitment of steroid receptor coactivator (SRC)/p160 coactivator LXXL
237  further dissect the roles of members of the steroid receptor coactivator (SRC)/p160 family in PR-med
238 eam target of progesterone receptor (PR) and steroid receptor coactivator (SRC-1) action in the uteru
239                             Both PXR and the steroid receptor coactivator (SRC-1) were found to bind
240          Our previous research revealed that steroid receptor coactivators (Src)-1 and -2 serve a cri
241  growth pathways on which cancer cells rely, steroid receptor coactivators (SRC-1, SRC-2, and SRC-3)
242      The three members of the p160 family of steroid receptor coactivators (SRC-1, SRC-2, and SRC-3)
243  interplay and demonstrated that it requires steroid receptor coactivators (SRC-2, SRC-3) and the med
244 rect interactions with full-length ER or the steroid receptor coactivator, SRC-1.
245 man (Tai) protein is homologous to the human steroid-receptor coactivators SRC1-3 and activates trans
246 ray by immunofluorescence were two different steroid receptor coactivators (SRC1 and CBP) with acetyl
247 B-613, a potent small molecule stimulator of steroid receptor coactivators (SRCs) attenuates patholog
248 gate functional relationships between PR and steroid receptor coactivators (SRCs) in distinct cell ty
249             Thus far, a mechanistic role for steroid receptor coactivators (SRCs) in the progression
250  of nuclear receptors and suggested that the steroid receptor coactivators (SRCs) play an important r
251                                              Steroid receptor coactivators (SRCs) regulate nuclear re
252                                     The p160 steroid receptor coactivators (SRCs) SRC-1, SRC-2 [nucle
253               Most nuclear receptors recruit steroid receptor coactivators (SRCs) to their ligand bin
254 cription factors, and their association with steroid receptor coactivators (SRCs) upon binding to DNA
255 ase 1 (CARM1/PRMT4) binds the p160 family of steroid receptor coactivators (SRCs).
256 rmone-dependent interaction with a family of steroid receptor coactivators (SRCs).
257                                   AR and its steroid receptor coactivators (SRCs; SRC-1, -2 and -3) w
258                                  The role of steroid receptor coactivators such as AIB1 in breast can
259 ranscription that is a member of a family of steroid receptor coactivators that includes SRC-1 and tr
260 ry gland development observed previously for steroid receptor coactivator type 1 (SRC-1) and SRC-3 fe
261         The in vivo biological function of a steroid receptor coactivator was assessed in mice in whi
262                              SRC-3/AIB1 is a steroid receptor coactivator with potent growth-promotin
263 ruitment of yellow fluorescent protein (YFP)-steroid receptor coactivators (YFP-SRC-1 and YFP-CREB bi

 
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