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1 the transcription factor CREB (cAMP-response element binding protein).
2 e transcription factor CREB (cAMP-responsive element binding protein).
3 regulator CPEB3 (cytoplasmic polyadenylation element-binding protein).
4 f ERK1/2, pCREB [phospho-CREB (cAMP response element-binding protein)].
5 expression, as a SERT distal polyadenylation element binding protein.
6 ibosomal S6 kinase, c-Jun, and cAMP response element binding protein.
7 activation of Creb3l3/cyclic AMP-responsive element-binding protein.
8 athway involving Akt1/Akt2 and cAMP response element-binding protein.
9 on of the transcription factor cAMP response element-binding protein.
10 iption factors, especially sterol-regulatory element binding proteins.
11 inactivation of tristetraprolin, two AU-rich element-binding proteins.
12 pithelial cells, cytoplasmic polyadenylation element binding protein 1 (CPEB1) mediates the apical lo
13 ter through association with cAMP responsive element binding protein 1 (CREB)/CREB binding protein (C
14 AMP1-dependent activation of cAMP-responsive element binding protein 1 (CREB1) and SP7 (also known as
15 nteraction between Mesp1 and cAMP-responsive element binding protein 1 (Creb1) in vitro and in vivo.
16 lucocorticoid receptor (GR), cAMP responsive element binding protein 1 (CREB1), peroxisome proliferat
18 r the transcription factor sterol regulatory element binding protein 1 (SREBP-1) and its transcriptio
19 domain containing 1C), RREB1 (Ras responsive element binding protein 1), and SEC24C (SEC24 family mem
21 through the activation of sterol regulatory element binding protein 1, which is mediated by the indu
22 ls through interference with cAMP responsive element binding protein 1-mediated transcriptional regul
23 The transcription factor cyclic AMP-response element-binding protein 1 (CREB1) controls approximately
24 hms, we identified cyclin J and far upstream element-binding protein 1 (FUBP1) as novel miR-16 target
26 timulates lipogenesis in a sterol regulatory element-binding protein 1 (SREBP-1)-dependent manner.
27 eficiency inhibits hepatic sterol regulatory element-binding protein 1 (SREBP-1, ADD1) processing.
28 on 16 of the gene encoding sterol regulatory element-binding protein 1 (Srebp1), an activator of LC-P
30 n turn directly suppresses sterol regulatory element-binding protein 1 (SREBP1)-directed transcriptio
31 and activity and defined a sterol regulatory element-binding protein 1 (SREBP1)-mediated pathway thro
32 in cell number), increased sterol regulatory element-binding protein 1 expression (about 3-fold incre
33 synthetic promoters containing cAMP response element-binding protein 1(CREB1)-specific cAMP-responsiv
34 l factor CREB1 (cyclic AMP [cAMP]-responsive element-binding protein 1) had the strongest increase in
35 nd report the binding of FUBP1 (Far Upstream element-Binding Protein 1) to these elements and the rol
36 ch included higher nuclear sterol regulatory element-binding protein 1, higher Srepb2 messenger RNA (
37 nd duodenal homeobox 1 and sterol regulatory element-binding protein 1, together leading to poor proi
39 r-activated receptor gamma/sterol regulatory element-binding protein 1/CD36 in hepatocytes from high
40 f wild-type mice, SREBP-1 (sterol regulatory element binding protein-1) activates the same promoter i
42 nositide 3 kinase (PI3K)/Akt/sterol response element-binding protein-1 (SREBP-1) signaling pathway in
43 -bound precursor forms of sterol-regulatory, element-binding protein-1 and -2, transcription factors
44 ls increased expression of sterol regulatory element binding protein 1c (SREBP-1c) and its downstream
45 simulating the increase in sterol-regulatory element binding protein 1c (SREBP-1c) seen in NAFLD pati
49 n in hepatic expression of sterol regulatory element-binding protein 1c (SREBP-1c), acetyl-CoA carbox
50 egulates the expression of sterol regulatory element-binding protein 1c (SREBP-1c), leading to increa
51 with the LXR target genes, steroid receptor element-binding protein 1c and ATP binding cassette tran
53 ased in WT mice, including sterol regulatory element-binding protein 1c target gene fatty-acid syntha
54 nding protein) or SREBP1c (sterol regulatory element-binding protein 1c) regulation of Mstn expressio
55 se Acc1 phosphorylation, and sterol response element-binding protein 1c-dependent gene expression.
56 ed up-regulated PGC-1beta, sterol regulatory element-binding proteins 1c and 2, acetyl-CoA carboxylas
57 X receptor (LXR)-mediated sterol regulatory element binding protein-1c (SREBP-1c) gene expression.
59 hich induced expression of sterol regulatory element binding protein-1c (SREBP-1c), resulting in indi
60 tor-gamma (PPAR-gamma) and sterol regulatory element binding protein-1c in WAT accounted for the phen
61 D-1 protein, activation of sterol regulatory element-binding protein-1c (SREBP-1), accumulation of ce
64 tial equation model of the sterol regulatory element binding protein 2 (SREBP-2) cholesterol genetic
66 hibiting the activation of sterol regulatory-element binding protein 2 and downregulating low-density
67 lational regulator cytosolic polyadenylation element-binding protein 2 (CPEB2) has two isoforms, CPEB
68 nds to the W-boxes of DEHYDRATION-RESPONSIVE ELEMENT-BINDING PROTEIN 2 (GhDREB2), which encodes a deh
69 e have previously identified iron-responsive element-binding protein 2 (IRP2) as an important COPD su
70 within the genes encoding sterol regulatory element-binding protein 2 (SREBP-2) and SREBP-1, respect
71 ynthesis by a reduction in sterol regulatory element-binding protein 2 (SREBP2)-regulated transcripti
73 n-vivo models suggest that sterol regulatory element-binding protein 2 is a key molecule in aggravati
75 take of cholesterol (human sterol-regulatory element-binding protein 2, human 3-hydroxy-3-methylgluta
77 neurotrophins activate the sterol regulatory element-binding protein-2 (SREBP2) that regulates genes
78 ER stress can activate the sterol regulatory element-binding protein-2 (SREBP2), an ER-localized tran
79 w a strong increase in the sterol-regulatory element-binding protein-2 yet are unable to maintain nor
80 ein partners, DREB2A (dehydration-responsive element-binding protein 2A), ANAC013, and ANAC046, consi
82 eolytic processing of CREB3L1 (cAMP response element-binding protein 3-like 1), a membrane-bound tran
84 show that the mRNA encoding cAMP responsive element-binding protein-3 like-1 (CREB3L1), a transcript
85 ic adenosine monophosphate (cAMP) responsive-element-binding protein, a crucial mediator in long-term
87 tes leptin transcription via cAMP-responsive element binding protein activation (CREB activation) and
91 n of cyclic adenosine monophosphate response element binding protein and activating transcription fac
92 ding to the phosphorylation of cAMP response element binding protein and, consequently, SMC rediffere
93 f the transcription factor cellular response element-binding protein and an increase in brain-derived
94 s C1q-activated phosphorylated cAMP-response element-binding protein and AP-1, two transcription fact
95 s mediated by hepatic cholesterol responsive element-binding protein and featured portal/lobular infl
97 g to cyclic adenosine monophosphate response element-binding protein and the induction of CD25, CD69,
98 by transcription factor CREB (cAMP-response element-binding protein) and silencing of CREB resulted
102 on via inhibition of carbohydrate-responsive element-binding protein-beta, pyruvate kinase L, SCD-1,
103 or 1alpha (PGC1alpha), cyclic AMP-responsive element binding protein binding protein (CBP), steroid r
105 Overexpression of the p300/cAMP-response element-binding protein-binding protein (CBP) potentiate
106 ment of the coregulators cyclic-AMP response element-binding protein-binding protein and nuclear core
107 inished, thereby enabling p300/cAMP response element-binding protein-binding protein to acetylate ERa
108 alpha, and HATs (p300 and p300/cAMP response element-binding protein-binding protein-associated facto
109 luding activator protein 1 and cAMP response element-binding protein, both of which were elevated ove
110 reduction in the activation of cAMP response element-binding protein, but not the activation of Ca(2+
111 n of cyclic adenosine monophosphate response element binding protein (CBP), p300, and Cbp/p300-intera
112 uced expression of the cyclic AMP-responsive element-binding protein (CBP), which as part of the p300
113 se-responsive factor Carbohydrate-Responsive Element Binding Protein (ChREBP) and GLP-1 secretion by
116 educes the activity of carbohydrate response element binding protein (ChREBP), a cellular hexose-phos
117 lleagues show that the carbohydrate response element-binding protein (ChREBP) coordinates an adaptive
118 egulated expression of carbohydrate response element-binding protein (ChREBP) in cells containing AR-
121 he expression of the carbohydrate-responsive element-binding protein (ChREBP) was decreased in adipos
122 we hypothesized that carbohydrate-responsive element-binding protein (ChREBP), a transcriptional acti
123 tor alpha (PPARalpha), carbohydrate response element-binding protein (ChREBP), and cAMP response elem
124 fficient to suppress carbohydrate-responsive-element-binding protein (ChREBP, a master lipogenic regu
125 tic glucose production through cAMP-response element-binding protein co-activators, we depleted these
127 n of VEGF by the cytoplasmic polyadenylation element-binding proteins CPEB1 and CPEB4 during developm
128 sed cAMP signaling and reduced cAMP-response-element binding protein (CREB) activation, a critical pa
131 activated PERK phosphorylates CAMP response element binding protein (CREB) and PSD95 directly at the
132 ected with a dominant-negative cAMP response element binding protein (CREB) and was eliminated by mut
133 how that the activity of the cAMP responsive element binding protein (CREB) family of transcription f
134 the transcriptional regulator cAMP response element binding protein (CREB) in both mouse and human B
136 rt, by activation of the cyclic AMP response element binding protein (Creb) in the aged hippocampus.
140 e have demonstrated that cyclic AMP response element binding protein (CREB) is constitutively activat
141 ctor cyclic adenosine monophosphate response element binding protein (CREB) is overexpressed in many
142 , TDCA significantly increased cAMP response element binding protein (CREB) phosphorylation in FLO-1
144 ing to increased levels of the cAMP response element binding protein (CREB), a transcriptional factor
145 d protein kinase (p38 MAPK), cAMP-responsive element binding protein (CREB), and activating transcrip
146 e for the transcription factor cAMP response element binding protein (CREB), and we demonstrate that
147 iron-dependent activation of cAMP-responsive element binding protein (CREB), the transcription factor
148 racellular signaling molecule, cAMP-response element binding protein (CREB), which serves as a pivota
149 mutant S386/396E bound to the cAMP response element binding protein (CREB)-binding protein reveals t
150 arvation-inducible coactivator cAMP response element binding protein (CREB)-cAMP-regulated transcript
151 mic Ca(2+) elevation and cyclic AMP response element binding protein (CREB)-dependent transcription.
152 the cyclic adenosine monophosphate response element binding protein (CREB)-regulated transcription c
153 generates an unusual chimeric cAMP response element binding protein (CREB)-regulated transcriptional
154 w,Ind mice show changes on a cAMP-responsive element binding protein (CREB)-regulated transcriptional
158 of a persistent activation of cAMP-response element binding-protein (CREB) and C/EBPbeta expression.
159 d IL-10 resulted in epithelial cAMP response element-binding protein (CREB) activation and subsequent
160 by free fatty acid (FFA), and cAMP response element-binding protein (CREB) activation by glucagon, l
161 rk1/2 MAP-kinase signaling and cAMP response element-binding protein (CREB) activation in myeloid cel
163 negative regulation of cAMP/calcium response element-binding protein (CREB) and CREB-activated gene e
164 pressant action: activation of cAMP response element-binding protein (CREB) and induction of brain-de
165 hanceosome consisting of cyclic AMP response element-binding protein (CREB) and nuclear factor Y (NF-
166 through the phosphorylation of cAMP response element-binding protein (CREB) and the dephosphorylation
167 ith higher levels of the cyclic-AMP-response-element-binding protein (CREB) are more likely to be rec
168 KA subsequently phosphorylated cAMP response element-binding protein (CREB) at Ser-133 to activate it
169 the phosphorylation of cAMP/calcium response element-binding protein (CREB) at serine 133 and CREB-me
171 h the BRCA1 promoter and the cAMP-responsive element-binding protein (CREB) complex, a regulator of B
172 ting transcriptional activator cAMP response element-binding protein (CREB) coordinately regulate the
173 denosine 3',5'-monophosphate (cAMP) response element-binding protein (CREB) family transcription fact
175 nding protein (C/EBPbeta), and cAMP-response element-binding protein (CREB) have been involved in res
176 elays the dephosphorylation of cAMP response element-binding protein (CREB) in human neuroblastoma (S
177 ctor cyclic adenosine monophosphate response element-binding protein (CREB) in NSTEMI (p < 0.05 vs. c
178 ty of the transcription factor cAMP response element-binding protein (CREB) in young adult rodents fa
179 by the transcription factor cAMP-responsive element-binding protein (CREB) is essential for a wide r
180 tors, the phosphorylation of cAMP-responsive element-binding protein (CREB) is strongly decreased in
181 n under basal/nicotine-induced/cAMP-response element-binding protein (CREB) overexpressed conditions
183 olar PregS similarly activates cAMP response element-binding protein (CREB) phosphorylation (within 1
186 ccompanied by maintenance of cAMP responsive element-binding protein (CREB) signaling in neurons rath
188 genome sequencing) to identify cAMP response element-binding protein (CREB) targets following chronic
189 at HDAC2 is a direct target of cAMP response element-binding protein (CREB) that is activated by beta
190 dependent binding of FGFR1 and cAMP-response element-binding protein (CREB) to a conserved cAMP respo
191 kinase II (CaMKII) and Ca(2+)/cAMP response element-binding protein (CREB) transcription factor.
192 gets of protein kinase A (PKA)-cAMP response element-binding protein (CREB), a pathway activated by f
193 NA for a transcription factor, cAMP response element-binding protein (CREB), and by an inhibitor of i
194 horylation of a CaN substrate, cAMP response element-binding protein (CREB), in the brains of Rcan1 k
195 ownstream substrate of PKAc, cAMP-responsive element-binding protein (CREB), is inhibited in cells ex
197 However, phosphorylation of cAMP-response element-binding protein (CREB), the cAMP-regulated trans
198 scriptional coactivators cyclic-AMP response element-binding protein (CREB)-binding protein (CBP) and
199 show that high glucose induced cAMP response element-binding protein (CREB)-binding protein (CBP)-med
200 normal ryanodine receptor and cAMP response element-binding protein (CREB)-dependent gene expression
201 gon via a cAMP-dependent and cAMP-responsive element-binding protein (CREB)-dependent mechanism in pr
202 712 on memory formation and on cAMP response element-binding protein (CREB)-regulated genes in aged m
207 ivation and subsequent cyclic AMP-responsive element-binding protein (CREB)/CREB-regulated transcript
208 ted the transcription factor cAMP-responsive element binding protein (Creb1) and its transcriptional
209 let alpha cells by GS/cAMP/PKA/cAMP-response element-binding protein-dependent activation of PC1.
210 : p38-dependent growth arrest, cAMP response element-binding protein-dependent cell survival, and ERK
212 s and subsequent increase in cAMP responsive element binding protein DNA-binding activity and inducti
213 2, ribosomal S6 kinase 1, or cAMP responsive element binding protein DNA-binding activity prevented t
214 1 interacts with the adenylateuridylate-rich element-binding protein embryonic lethal abnormal vision
217 Transcription factors of the far-upstream element-binding protein (FBP) family represent cellular
218 R) protein that transports sterol regulatory element-binding proteins from the ER to Golgi, where the
220 d transcription factor cyclic-AMP-responsive-element-binding protein H (CREBH) but not by peroxisome
221 Here we reported that cyclic AMP-responsive element-binding protein H (CREBH) positively regulates m
223 ike) gene encoding the carbohydrate response element binding protein has been associated with lower t
224 riched transcription factor, cAMP-responsive element-binding protein hepatic-specific (CREBH), modula
226 -binding protein (ChREBP), and cAMP response element-binding protein, hepatocyte specific (CREBH).
227 cy reduced the activation of cAMP-responsive element binding protein-hepatocyte specific and peroxiso
230 but not its paralog carbohydrate-responsive element-binding protein, is the predominant glucose-resp
231 eby impeding activation of sterol regulatory element-binding proteins (key regulators of lipid metabo
232 ng reduction in phosphorylated cAMP-response element binding protein levels in the NAcSh that could a
233 nflammatory cytokines, carbohydrate response element binding protein-mediated transcription, and micr
234 anscription factors CREB/CREM (cAMP response element-binding protein/modulator) is linked to atrial f
235 critical for ChREBP (carbohydrate-responsive element-binding protein) or SREBP1c (sterol regulatory e
236 s of their respective targets, cAMP response element-binding protein, p38, and extracellular signal-r
237 e cyclase --> cAMP --> PKA --> cAMP response element-binding protein pathway mediating cell survival
239 ogram, including Ras and cyclic AMP response element-binding protein pathways and other Gata factors,
240 ced levels of phosphorylated cAMP-responsive element binding protein (pCREB) in the CA1s of a-FMHis-t
241 lower levels of phosphorylated cAMP response element-binding protein (pCREB), an activity-dependent t
242 s protein kinase A-dependent cAMP-responsive element-binding protein phosphorylation, the effect of c
244 creases in PKA activity, CREB (cAMP-response element-binding protein) phosphorylation, induction of p
245 fatostatin A, which blocks sterol regulatory element-binding protein proteolytic cleavage and activat
246 olipoprotien C3 (Apoc3), CREB (cAMP Response Element Binding Protein) Regulated Transcription Coactiv
247 ates the transcription factor, cAMP response element-binding protein, regulating miR-212, which targe
248 elevated STMN Ser-63 and CREB (cAMP-response element-binding protein) Ser-133 phosphorylation that wa
249 B (cyclic adenosine monophosphate-responsive element-binding protein) shut-off and nuclear accumulati
252 first evidence that enhancing cAMP response element binding protein signaling can alleviate RTT phen
253 eviously unappreciated role of cAMP response element binding protein signaling in RTT pathogenesis, a
254 Consequently, the cAMP-->PKA-->cAMP response element-binding protein signaling axis is inhibited, the
255 -terminal Kinase (JNK) and Sterol Regulatory Element Binding Protein (SREBP) activity in neurons lead
257 to be an inhibitor of the sterol regulatory element binding protein (SREBP), a key regulator of chol
258 elate with the activity of sterol regulatory element binding protein (SREBP), the master regulator of
259 a and serum deprivation on sterol regulatory element-binding protein (SREBP) activity and the express
260 djusts gene expression and sterol regulatory element-binding protein (SREBP) activity in enterocytes
262 romotes N-glycosylation of sterol regulatory element-binding protein (SREBP) cleavage-activating prot
263 e-specific inactivation of sterol regulatory element-binding protein (SREBP) cleavage-activating prot
265 25-HC acts by antagonizing sterol response element-binding protein (SREBP) processing to reduce Il1
266 lized complex required for sterol regulatory element-binding protein (SREBP) transcription factor act
267 tightly controlled by the sterol regulatory element-binding protein (SREBP) transcription factor tha
271 c growth of fungi requires sterol regulatory element-binding protein (SREBP) transcription factors, a
272 analogous to the mammalian sterol regulatory element-binding protein (SREBP)-1 and SREBP-2 transcript
273 and overactivation of the sterol regulatory element-binding protein (SREBP)-1-mediated lipogenic pro
274 located in introns of the sterol regulatory element-binding protein (SREBP)-encoding genes and contr
275 ipose metabolism including sterol regulatory element-binding protein (SREBP-1), insulin receptor (IR)
278 leads to activation of the sterol regulatory element-binding proteins (SREBP1 and SREBP2) that are re
279 entified a pivotal role of sterol-regulatory element binding proteins (SREBPs), in the HCV-mediated s
280 liver X receptors (LXRs), sterol regulatory element-binding proteins (SREBPs) and the G protein-coup
281 have learned how it binds sterol regulatory element-binding proteins (SREBPs) and transports them fr
283 omeostasis by transporting sterol regulatory element-binding proteins (SREBPs) from the ER to the Gol
285 TORC1 is known to activate sterol regulatory element-binding proteins (SREBPs) including SREBP-2, a m
286 fatty acid synthase (FAS), sterol regulatory element-binding proteins (SREBPs) play a pivotal role in
287 formed a complex with the sterol regulatory element-binding proteins (SREBPs) through their C-termin
288 hibiting the processing of sterol regulatory element-binding proteins (SREBPs), transcription factors
292 lex interact with the STOREKEEPER RELATED1/G-Element Binding Protein (STKR1) inside the plant cell nu
293 E FACTOR of the APETALA2/ethylene responsive element binding protein superfamily, as a DELLA interact
294 t signaling by hepatic carbohydrate response element binding protein that improves glucose tolerance
295 pressor forms, and activates cAMP-responsive element binding protein that in turn represses gli1 tran
296 membranes that transports sterol regulatory element-binding proteins to the Golgi complex for proteo
297 essed binding of phospho-CREB (cAMP response element binding protein) to Bdnf promoters in VTA, which
300 s via phosphorylation of cyclic-AMP response element binding protein, which requires activation of es
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