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1 induced by the stress hormone, corticotropin releasing factor.
2 alize with the stress hormone, corticotropin releasing factor.
3 were depolarised by exogenous corticotrophin releasing factor.
4 mone 44 (DH44), an ortholog of corticotropin-releasing factor.
5 y active clinical candidate of corticotropin-releasing factor 1 (CRF 1) antagonist 1 showed a signifi
7 de), D2R agonist (quinpirole), corticotropin-releasing factor 1 (CRF1) antagonist (antalarmin), and a
8 ne domains of the glucagon and corticotropin releasing factor 1 (CRF1) receptors to develop improved
10 examined the role of Ras Guanine Nucleotide Releasing Factor 1 (RasGRF1) and 2 (RasGRF2), upstream r
11 n of Ras protein-specific guanine nucleotide releasing factor 1 (RasGrf1), a Ras activator (5-fold, P
12 with Ras protein-specific guanine nucleotide-releasing factor 1 (RASGRF1), leading to impaired activa
13 armacologic inhibition (with a corticotropin-releasing factor 1 receptor antagonist) of pain-related
14 earlier lead pyrazinone-based corticotropin-releasing factor-1 (CRF(1)) receptor antagonist, reveale
15 al-like state characterized by corticotropin-releasing factor-1 (CRF(1)) receptor antagonist-reversib
18 s to palatable food results in corticotropin-releasing factor-1 (CRF1) receptor antagonist-reversible
19 26907 in the ras-specific guanine-nucleotide releasing factor 2 (RASGRF2) gene, encoding a protein th
21 ene (Ras protein-specific guanine nucleotide-releasing factor 2) with all clinical events except stro
25 ess neurotransmitters, such as corticotropin-releasing factor and dynorphin, in the neurocircuitry of
26 ing by increased expression of corticotropin-releasing factor and its feedback regulation of TLR4 exp
27 and Hcrt systems in which the corticotropin-releasing factor and N/OFQ systems coordinately modulate
28 stress and resilience, such as corticotropin-releasing factor and nociceptin, has been postulated to
33 PA axis-based interventions of corticotropin-releasing factor antagonists and the glucocorticoid rece
34 (especially neuropeptide Y and corticotropin-releasing factor) are modulated by alcohol drinking duri
38 ed Crk SH3 domain-binding guanine-nucleotide releasing factor (C3G) binding to CrkII, whereas inhibit
40 othalamus and primarily in non-corticotropin releasing factor-containing neurons of the bed nucleus o
41 os activation were observed in corticotropin releasing factor-containing neurons of the paraventricul
42 at baseline and in response to corticotropin-releasing factor (CRF) (0.5 microg kg(1)) plus arginine
44 s, including a coordination of corticotropin-releasing factor (CRF) actions at both of its receptors,
46 also posit a central role for corticotrophin-releasing factor (CRF) and an interaction between CRF an
47 tine SA on the coexpression of corticotropin-releasing factor (CRF) and arginine vasopressin (AVP) mR
48 gh it has long been known that corticotropin-releasing factor (CRF) and CRF receptors are prominent i
49 esent review is on the role of corticotropin-releasing factor (CRF) and CRF-related peptides in the d
50 ng-term alterations in central corticotropin-releasing factor (CRF) and glucocorticoid receptor (GR)
51 ion between the stress hormone corticotropin releasing factor (CRF) and glutamate release onto dopami
52 d to partially colocalize with corticotropin-releasing factor (CRF) and growth hormone-releasing horm
53 xtrahypothalamic expression of corticotropin-releasing factor (CRF) and its G-protein-coupled CRF1 an
56 europharmacological actions of corticotropin-releasing factor (CRF) and norepinephrine in extrahypoth
57 Release of the neuropeptides corticotropin-releasing factor (CRF) and orexin-A in the ventral tegme
61 e report the identification of corticotropin-releasing factor (CRF) as a critical component of the ca
63 ne arm of the stress response, corticotropin-releasing factor (CRF) can act in the brain to modulate
64 ase of neuromodulators such as corticotropin-releasing factor (CRF) can drive drug-dependent behavior
67 e stress-related neuropeptide, corticotropin-releasing factor (CRF) directs this by a bimodal regulat
68 elease the stress neuropeptide corticotropin-releasing factor (CRF) drive anxiety-like behaviors in r
69 the central extrahypothalamic corticotropin-releasing factor (CRF) expression is associated with str
71 enced by the highly conserved corticotrophin-releasing factor (CRF) family of peptides and receptors
73 tin 2 (Ucn2), a peptide of the corticotropin-releasing factor (CRF) family, binds with high affinity
74 n of the stress neuromediator, corticotropin-releasing factor (CRF) has been implicated in these diso
75 levant PI cells identified the corticotropin-releasing factor (CRF) homolog, DH44, as a circadian out
76 e self-administration, reduced corticotropin-releasing factor (CRF) immunodensity in the paraventricu
77 ence of somatostatin (SS) and corticotrophin-releasing factor (CRF) in forebrain neurons that project
78 lation of cytosolic calcium by corticotropin-releasing factor (CRF) in midbrain dopamine neurons.
79 k indicates a crucial role for corticotropin-releasing factor (CRF) in neurobiological responses asso
80 ole of the stress neurohormone corticotropin-releasing factor (CRF) in stress-induced binge eating in
81 work hypothesizing a role for corticotropin-releasing factor (CRF) in the IC during craving and rela
82 tionship between dynorphin and corticotropin-releasing factor (CRF) in the induction of dysphoria, th
86 ed following overexpression of corticotropin-releasing factor (CRF) in the NAc of female and male rat
88 d that the stress neurohormone corticotropin-releasing factor (CRF) inhibits 5-HT neurons in the dors
89 ggests that catecholamines and corticotropin-releasing factor (CRF) interact in a serial manner to ac
90 ces the release of the peptide corticotropin-releasing factor (CRF) into the ventral tegmental area (
94 emonstrate that, in the vBNST, corticotropin releasing factor (CRF) is expressed in neurons that inne
99 nous neuropeptide Y (NPY) and corticotrophin-releasing factor (CRF) modulate the responses of the bas
100 t experiments examined whether corticotropin-releasing factor (CRF) modulates memory consolidation vi
103 alcohol exposure contains ~80% corticotropin-releasing factor (CRF) neurons and that the optogenetic
104 gh it has long-been known that corticotropin-releasing factor (CRF) neurons are prominent within the
105 on, potentially by activating corticotrophin releasing factor (CRF) neurons in the anterolateral cell
106 d activates a subpopulation of corticotropin-releasing factor (CRF) neurons in the bed nucleus of the
107 pecifically recruited GABA and corticotropin-releasing factor (CRF) neurons in the mPFC and produced
108 hip between corticosterone and corticotropin-releasing factor (CRF) on both beta-amyloid (Abeta) and
109 of an intravenous injection of corticotropin-releasing factor (CRF) on fructose malabsorption and the
111 was to examine the ability of corticotropin releasing factor (CRF) or antibody to insulin growth fac
113 , arginine-vasopressin (AVP), corticotrophin-releasing factor (CRF) or tyrosine hydroxylase (TH).
119 derable evidence suggests that corticotropin-releasing factor (CRF) plays an important role in regula
120 stress-associated neuropeptide corticotropin releasing factor (CRF) produces a profound and reliable
122 eta elevation are dependent on corticotropin-releasing factor (CRF) receptor 1 signaling and an intac
124 awal was mediated by increased corticotropin releasing factor (CRF) receptor-1 expression and signall
127 emonstrated that activation of corticotropin-releasing factor (CRF) receptors in the caudal dorsomedi
128 lation increases the levels of corticotropin-releasing factor (CRF) receptors in the serotonergic dor
131 e stress-related neuropeptide, corticotropin-releasing factor (CRF) regulates the dorsal raphe nucleu
132 e through alterations in brain corticotropin-releasing factor (CRF) regulation of neurocircuitry invo
137 VN) have been shown to inhibit corticotropin releasing factor (CRF) synthesis via GABA(A) receptors.
138 H secretion by activating the corticotrophin-releasing factor (CRF) system and sympathoadrenal pathwa
143 strated that activation of the corticotropin-releasing factor (CRF) system potentiates MC degranulati
144 ncluding the extrahypothalamic corticotropin-releasing factor (CRF) system, following long-term drug
146 gdala (Neo-A) lesions on brain corticotropin-releasing factor (CRF) systems and hypothalamic-pituitar
150 gdala (CeA), ethanol acts via corticotrophin-releasing factor (CRF) type 1 receptors to enhance GABA
155 e number of neurons expressing corticotropin releasing factor (CRF), a neuropeptide that has a promin
156 imolecular interaction between corticotropin-releasing factor (CRF), a neuropeptide, and its type 1 r
157 ited different sensitivity to corticotrophin-releasing factor (CRF), a stress hormone that has been i
158 this, the CEA highly expresses corticotropin-releasing factor (CRF), an important modulator of stress
159 excitatory amino acids (EAAs), corticotropin-releasing factor (CRF), and endogenous opioids acting at
161 r modulation by dopamine (DA), corticotropin-releasing factor (CRF), and their combination (DA plus C
162 The neuroactive substances corticotropin-releasing factor (CRF), arginine-vasopressin (AVP), hist
163 is thought to communicate via corticotropin-releasing factor (CRF), but studies have yet to examine
166 ed receptor B1 family includes corticotropin-releasing factor (CRF), growth hormone-releasing hormone
167 axis-activating neuropeptide, corticotropin-releasing factor (CRF), may be the keystone in drug-indu
168 es indicate the involvement of corticotropin-releasing factor (CRF), noradrenaline, dopamine, glutama
170 s for the stress neuropeptide, corticotropin-releasing factor (CRF), that render the locus coeruleus
172 e focus is on the receptor for corticotropin-releasing factor (CRF), the orchestrator of the stress r
174 ticotropes are stimulated with corticotropin releasing factor (CRF), whereupon SSTR2 exits the compar
175 g the stress-sensitive peptide corticotropin-releasing factor (CRF), which has been identified in cri
176 oradrenergic substrates [via a corticotropin-releasing factor (CRF)-dependent mechanism] that regulat
177 nd inhibitory transmission in corticotrophin-releasing factor (CRF)-expressing dorsal-medial (mpd) ne
178 Here, we demonstrate that corticotrophin-releasing factor (CRF)-expressing neurons in the central
179 en shown previously to cause a corticotropin-releasing factor (CRF)-mediated increase in tonic locus
181 in the brain that counteracts corticotropin-releasing factor (CRF)-mediated stress and anxiety sympt
182 D is functionally expressed on corticotropin-releasing factor (CRF)-positive BNST cells implicated in
195 nal aggression) is impaired by corticotropin-releasing factor-(CRF) related peptides, but where these
196 tested the hypothesis that the corticotropin-releasing factor (CRF1) antagonist GSK561679 differentia
197 tment of brain stress systems (corticotropin-releasing factor, dynorphin, norepinephrine, hypocretin,
198 teral amygdala (BLA) away from corticotropin releasing factor-expressing (CRF(+)) centrolateral amygd
200 region-specific alterations of corticotropin-releasing factor expression and promoter methylation, ch
201 neuropeptides vasopressin and corticotropin-releasing factor facilitate, while serotonin inhibits, a
202 rs, which bind peptides of the corticotropin releasing factor family and are key mediators in the str
206 al. provide a causal link between histamine-releasing factor (HRF) interactions with IgE and food al
209 ther suggest that an activated corticotropin-releasing factor/hypothalamic-pituitary-adrenal axis sys
210 thropin-releasing hormone, and corticotropin-releasing factor immunoreactive cells in the paraventric
211 s the physiological actions of corticotropin-releasing factor in the anterior pituitary gland and the
213 A1 and aromatase enhanced local bone marrow-releasing factors, including androgen receptor, estrogen
218 s in restraint-induced Fos and corticotropin-releasing factor mRNA expression in the neurosecretory r
219 cting to vasopressinergic and corticotrophin releasing factor neurons in the paraventricular nucleus,
220 acts with the neuromodulators, corticotropin-releasing factor, norepinephrine, dopamine, and serotoni
221 role of brain stress systems (corticotropin-releasing factor, norepinephrine, orexin [hypocretin], v
222 l impact of treatment with such hypothalamic releasing factors on recovery from critical illness as w
223 lockade of the stress hormone corticotrophin-releasing factor or of peripheral GC action, as well as
224 ior hypothalamus that may gate corticotropin-releasing factor output from the amygdala to the anterio
225 n of the brain stress system's corticotropin-releasing factor outside of the hypothalamus in the exte
228 this region of receptors for corticotrophin-releasing factor, pituitary adenylate cyclase-activating
229 appetite regulation, including corticotropin releasing factor, pro-opiomelanocortin B, and glucose tr
231 ed differential involvement of corticotropin-releasing factor receptor (CRFR) 1 and 2 in acute stress
233 dministration of the selective corticotropin-releasing factor receptor 1 (CRF(1)) antagonist R121919
234 n, we examined the role of the corticotropin-releasing factor receptor 1 (CRF(1)) in this behavior as
235 haracterize the effects of the corticotropin-releasing factor receptor 1 (CRF-R1) antagonist, GW87600
236 (NE) receptors (alpha1) via a corticotropin-releasing factor receptor 1 (CRF-R1)-dependent mechanism
237 g the efficacy of GSK561679, a corticotropin-releasing factor receptor 1 (CRF1 receptor) antagonist i
242 what has been observed for the corticotropin-releasing factor receptor 1 (CRFR1), SAP97 expression is
243 r-activated receptor gamma and corticotropin-releasing factor receptor 1 were notable exceptions.
244 ivated by either neurokinin I, corticotropin-releasing factor receptor 1, or dopamine D(1) receptors.
246 ed significant upregulation of corticotropin releasing factor receptor 2 (CrfR2) in the amygdala of m
248 d psychological stress through corticotropin-releasing factor receptor subtype 1 (CRF(1)) expressed o
249 dy we investigated the role of corticotropin-releasing factor receptor subtype 2 (CRF(2)) as a modula
250 ent study examines the role of corticotropin releasing factor receptor subtypes 1 and 2 (CRFR1, CRFR2
251 CRF(2(a))R and the homologous corticotropin-releasing factor receptor type 1 (CRF(1)R) possessing a
252 vestigated whether blockade of corticotropin-releasing factor receptor type 1 (CRF-R1) could prevent
253 ctions in anandamide driven by corticotropin-releasing factor receptor type 1 (CRF1) potentiation of
254 re the interaction between the corticotropin releasing factor receptor type 1 (CRF1R) and its native
255 ed interactions of the class B corticotropin-releasing factor receptor type 1 (CRF1R) with two peptid
257 compartments, we show that the corticotropin-releasing factor receptor type 1 has a specific monomer/
258 nsmembrane domain of the human corticotropin-releasing factor receptor type 1 in complex with the sma
262 central stress response, while corticotropin-releasing factor receptor type 2 (CRFR2) has been sugges
263 bserved abnormal expression of corticotropin-releasing factor receptor type 2 (CRFR2) to be associate
266 pyrazolo[1,5-a]-1,3,5-triazine corticotropin releasing factor receptor-1 (CRF(1)) receptor antagonist
267 pyrazolo[1,5-a]-1,3,5-triazine corticotropin releasing factor receptor-1 (CRF(1)) receptor antagonist
268 is unaffected by alpha1-AR and corticotropin-releasing factor receptor-1 (CRFR(1)) antagonists, but i
269 tention were attenuated by the corticotropin-releasing factor receptor-1 antagonist antalarmin but no
274 Urocortin 3 (Ucn 3) is a corticotrophin-releasing factor related neuropeptide highly expressed i
275 it has been shown to increase corticotropin-releasing factor release in extrahypothalamic brain regi
276 ion-like protein (RepA-WH1) into the E. coli releasing factor RF1 promotes its aggregation and enable
278 n-gamma (IFN-gamma) and induce cytolysis via releasing factors such as perforin, which permeabilizes
279 s), (4) the (gastrointestinal) corticotropin-releasing factor system, and (5) the intestinal response
282 spected of initiating childhood leukaemia by releasing factors that cause DNA damage in cord blood an
283 strocytes play a key role in this process by releasing factors that promote the formation of excitato
284 role in maintaining vascular homeostasis by releasing factors that regulate local blood flow, system
285 counteracting the functions of corticotropin-releasing factor, the primary stress-mediating neuropept
286 lin, nesfatin-1, somatostatin, corticotropin-releasing factor, thyrotropin-releasing hormone and calc
287 buting ions, removing neurotransmitters, and releasing factors to influence blood flow and neuronal a
288 ation between histamine release to histamine releasing factor/translationally controlled tumor protei
289 hesis was investigated for the corticotropin-releasing factor type 1 (CRF(1)) receptor using a novel
292 ve effect is mediated via the corticotrophin-releasing factor type 1 receptor (CRF1R, also known as C
293 peated social stress decreased corticotropin-releasing factor type 1 receptor and increased mu-opioid
295 LTCC-based mechanism; instead, corticotropin-releasing factor type 1 receptors (CRF1s) mediate alcoho
296 LTCC-based mechanism; instead, corticotropin-releasing factor type 1 receptors (CRF1s) mediate alcoho
298 hat the mechanism involved the corticotropin-releasing factor type 2 receptor, cAMP elevation, and ac
300 ombined administration of those hypothalamic releasing factors, which have been identified as suppres