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1 UPF1, SMG1 kinase, SMG8, SMG9 and eukaryotic release factors).
2 retains its normal function as a translation release factor.
3 complex that may function as a peptidoglycan release factor.
4 12 N terminus functions to bind host vesicle release factors.
5 imited by truncation due to competition with release factors.
6  ensuring termination with either of the two release factors.
7 atically inhibit rates of peptide release by release factors.
8 induced by the stress hormone, corticotropin releasing factor.
9 alize with the stress hormone, corticotropin releasing factor.
10 were depolarised by exogenous corticotrophin releasing factor.
11 mone 44 (DH44), an ortholog of corticotropin-releasing factor.
12 ease factor complex that includes eukaryotic release factor 1 (eRF1) and eRF3.
13 he interaction between MoMLV RT and peptidyl release factor 1 (eRF1).
14  catalytic activity stimulated by eukaryotic release factor 1 (eRF1).
15 saturating and limiting levels of eukaryotic release factor 1 (eRF1).
16 ized by two similar class 1 release factors, release factor 1 (RF1) and release factor 2 (RF2).
17  recoded strains of Escherichia coli lacking Release Factor 1 (RF1) are becoming increasingly popular
18  3.1-A crystal structure of Escherichia coli release factor 1 (RF1) bound to the 70S ribosome in resp
19 acids (nnAAs) is limited by competition with release factor 1 (RF1).
20  UAA codons, which permitted the deletion of release factor 1 and reassignment of UAG translation fun
21                                  Deletion of release factor 1 in Escherichia coli enhances translatio
22 cherichia coli that lacks all TAG codons and release factor 1, endowing this organism with the orthog
23              It interacts with a translation-release factor 1-like protein Dom34/Pelota to direct dec
24                           Interestingly, the release factor 1-specific codon TAG maintains a more or
25 s any endogenous in-frame UAGN sequences and release factor 1.
26 hrough by silencing expression of eukaryotic release factors 1 and 3 (eRF1 and eRF3) or by introducin
27 de), D2R agonist (quinpirole), corticotropin-releasing factor 1 (CRF1) antagonist (antalarmin), and a
28 ne domains of the glucagon and corticotropin releasing factor 1 (CRF1) receptors to develop improved
29           Ablation of Ras-guanine nucleotide-releasing factor 1 (Ras-GRF1), a neuronal activator of R
30  examined the role of Ras Guanine Nucleotide Releasing Factor 1 (RasGRF1) and 2 (RasGRF2), upstream r
31 n of Ras protein-specific guanine nucleotide releasing factor 1 (RasGrf1), a Ras activator (5-fold, P
32 with Ras protein-specific guanine nucleotide-releasing factor 1 (RASGRF1), leading to impaired activa
33 s to palatable food results in corticotropin-releasing factor-1 (CRF1) receptor antagonist-reversible
34 don in the A site by specifically recruiting release factor 2 (RF2), initially in a compact preaccomm
35  release factors, release factor 1 (RF1) and release factor 2 (RF2).
36 26907 in the ras-specific guanine-nucleotide releasing factor 2 (RASGRF2) gene, encoding a protein th
37 e processes; Ras-specific guanine nucleotide releasing factor 2 (RasGRF2).
38 ene (Ras protein-specific guanine nucleotide-releasing factor 2) with all clinical events except stro
39                           Eukaryotic peptide release factor 3 (eRF3) is a conserved, essential gene i
40 o sterically occlude the binding of peptidyl release factor 3 (eRF3) to eRF1.
41    Normally, during termination, the class 2 release factor 3 (RF3), a GTPase, functions downstream o
42 nslation initiation factor 4G and eukaryotic release factor 3a (eRF3a).
43                        After considering the releasing factor (66.6%) from the swab, the final accura
44  parameters set based on the distribution of release factors across facilities.
45 re termination, including the stimulation of release factor activity and the dissociation and recycli
46 ated by PTRF (polymerase I transcription and release factor, also known as cavin-1), which has previo
47 trongly inhibits peptidyl-tRNA hydrolysis by release factors and, to a lesser extent, peptide bond fo
48 ess neurotransmitters, such as corticotropin-releasing factor and dynorphin, in the neurocircuitry of
49 ing by increased expression of corticotropin-releasing factor and its feedback regulation of TLR4 exp
50 stress and resilience, such as corticotropin-releasing factor and nociceptin, has been postulated to
51 ism in the brain to counteract corticotropin-releasing factor and/or stress.
52 cretin/orexin, norepinephrine, corticotropin-releasing factor, and cytokines.
53 ral stress response induced by corticotropin releasing factor, and promoting stress resilience.
54 PA axis-based interventions of corticotropin-releasing factor antagonists and the glucocorticoid rece
55                By sequestering the available release factors, Api promotes pervasive stop codon bypas
56 cal function in termination, both classes of release factor are also involved in a post peptidyl tran
57                           Furthermore, pause release factors are frequently dysregulated in MS brain
58 (especially neuropeptide Y and corticotropin-releasing factor) are modulated by alcohol drinking duri
59 ion because they have one of the alternative release factors, ArfA or ArfB.
60 nascent peptide exit tunnel and trapping the release factor associated with a terminating ribosome.
61 ent of Siglec-9, 'educated' myeloid cells to release factors associated with determination of the tum
62 ression of PTRF (polymerase I and transcript release factor) associated selectively with their glucos
63 RAD and suggest that positioning this client-release factor at the retrotranslocation site may afford
64                                Corticotropin releasing factor binding protein (CRF-BP) was originally
65                                Corticotropin-releasing factor binds with high affinity to CRF recepto
66 ed Crk SH3 domain-binding guanine-nucleotide releasing factor (C3G) binding to CrkII, whereas inhibit
67                     Infusion of hypothalamic-releasing factors can reactivate the thyroid axis in pat
68 nd asked whether SSc-injured epidermal cells release factors capable of promoting fibrosis.
69 ound that the availability of the functional release factor complex Sup45-Sup35 strongly influences t
70 c translational termination is mediated by a release factor complex that includes eukaryotic release
71 othalamus and primarily in non-corticotropin releasing factor-containing neurons of the bed nucleus o
72 os activation were observed in corticotropin releasing factor-containing neurons of the paraventricul
73 nical termination on stop codons, eukaryotic release factors contribute to cotranslational protein qu
74 BDNF signaling is mediated by corticotrophin-releasing factor (CRF) acting in the NAc.
75                 We report that corticotropin-releasing factor (CRF) acts in the ventral tegmental are
76 gh it has long been known that corticotropin-releasing factor (CRF) and CRF receptors are prominent i
77 ion between the stress hormone corticotropin releasing factor (CRF) and glutamate release onto dopami
78 d to partially colocalize with corticotropin-releasing factor (CRF) and growth hormone-releasing horm
79        The stress neuropeptide corticotropin releasing factor (CRF) and its receptors (CRF-R1, CRF-R2
80   Release of the neuropeptides corticotropin-releasing factor (CRF) and orexin-A in the ventral tegme
81                                Corticotropin-releasing factor (CRF) and the three related peptides ur
82                 To investigate corticotropin-releasing factor (CRF) contributions to fear memory in L
83                                Corticotropin releasing factor (CRF) coordinates the brains responses
84 elease the stress neuropeptide corticotropin-releasing factor (CRF) drive anxiety-like behaviors in r
85  the central extrahypothalamic corticotropin-releasing factor (CRF) expression is associated with str
86 enced by the highly conserved corticotrophin-releasing factor (CRF) family of peptides and receptors
87                            The corticotropin-releasing factor (CRF) family of peptides includes CRF a
88 tin 2 (Ucn2), a peptide of the corticotropin-releasing factor (CRF) family, binds with high affinity
89 n of the stress neuromediator, corticotropin-releasing factor (CRF) has been implicated in these diso
90 levant PI cells identified the corticotropin-releasing factor (CRF) homolog, DH44, as a circadian out
91 e self-administration, reduced corticotropin-releasing factor (CRF) immunodensity in the paraventricu
92 k indicates a crucial role for corticotropin-releasing factor (CRF) in neurobiological responses asso
93 ole of the stress neurohormone corticotropin-releasing factor (CRF) in stress-induced binge eating in
94  work hypothesizing a role for corticotropin-releasing factor (CRF) in the IC during craving and rela
95 ed following overexpression of corticotropin-releasing factor (CRF) in the NAc of female and male rat
96 ggests that catecholamines and corticotropin-releasing factor (CRF) interact in a serial manner to ac
97                                Corticotropin-releasing factor (CRF) is an important link between stre
98        The stress neuropeptide corticotropin releasing factor (CRF) is anxiogenic and is produced by
99 emonstrate that, in the vBNST, corticotropin releasing factor (CRF) is expressed in neurons that inne
100                                Corticotropin-releasing factor (CRF) is expressed in the Ce, has a rol
101                                Corticotropin releasing factor (CRF) is the primary mediator of stress
102                                Corticotropin-releasing factor (CRF) mediates anxiogenic responses by
103 nous neuropeptide Y (NPY) and corticotrophin-releasing factor (CRF) modulate the responses of the bas
104                               Corticotrophin-releasing factor (CRF) modulates the influence of stress
105 alcohol exposure contains ~80% corticotropin-releasing factor (CRF) neurons and that the optogenetic
106 gh it has long-been known that corticotropin-releasing factor (CRF) neurons are prominent within the
107 on, potentially by activating corticotrophin releasing factor (CRF) neurons in the anterolateral cell
108 d activates a subpopulation of corticotropin-releasing factor (CRF) neurons in the bed nucleus of the
109 of an intravenous injection of corticotropin-releasing factor (CRF) on fructose malabsorption and the
110 nce of the stress neuropeptide corticotropin-releasing factor (CRF) on these responses.
111 ry but did not increase either corticotropin-releasing factor (CRF) or corticosterone.
112                                Corticotropin-releasing factor (CRF) orchestrates the stress response,
113                            The corticotropin-releasing factor (CRF) plays a key role in a variety of
114 derable evidence suggests that corticotropin-releasing factor (CRF) plays an important role in regula
115 stress-associated neuropeptide corticotropin releasing factor (CRF) produces a profound and reliable
116                            The corticotropin-releasing factor (CRF) receptor 1 (CRFR1) is a target fo
117 eta elevation are dependent on corticotropin-releasing factor (CRF) receptor 1 signaling and an intac
118 awal was mediated by increased corticotropin releasing factor (CRF) receptor-1 expression and signall
119                                Corticotropin-releasing factor (CRF) receptors are found in stress-rel
120                        Because corticotropin-releasing factor (CRF) receptors are implicated, we comp
121 emonstrated that activation of corticotropin-releasing factor (CRF) receptors in the caudal dorsomedi
122                                Corticotropin-releasing factor (CRF) receptors-which bind the hormone
123                                Corticotropin releasing factor (CRF) regulates physiological and behav
124 e stress-related neuropeptide, corticotropin-releasing factor (CRF) regulates the dorsal raphe nucleu
125                                Corticotropin releasing factor (CRF) signaling and CRF neurons in the
126                                Corticotropin-releasing factor (CRF) signaling at the CRF1 receptor (C
127                            The corticotropin releasing factor (CRF) system in the central amygdala (C
128                            The corticotropin releasing factor (CRF) system in the central amygdala (C
129 strated that activation of the corticotropin-releasing factor (CRF) system potentiates MC degranulati
130                            The corticotropin-releasing factor (CRF) system, which is involved in stre
131 gdala (Neo-A) lesions on brain corticotropin-releasing factor (CRF) systems and hypothalamic-pituitar
132                                Corticotropin-releasing factor (CRF) that is released from the paraven
133                            The corticotropin-releasing factor (CRF) type 1 receptor (CRF1R) for the 4
134           Systemic blockade of corticotropin-releasing factor (CRF) type 1 receptors (CRFR1s) reduces
135                                Corticotropin releasing factor (CRF) within the ventral tegmental area
136 ng peptide, PAC1 receptor, and corticotropin-releasing factor (CRF), (CRF1) receptor.
137           We investigated how corticotrophin releasing factor (CRF), a critical stress response media
138            Here we report that corticotropin-releasing factor (CRF), a neuropeptide released in respo
139 e number of neurons expressing corticotropin releasing factor (CRF), a neuropeptide that has a promin
140 ited different sensitivity to corticotrophin-releasing factor (CRF), a stress hormone that has been i
141 this, the CEA highly expresses corticotropin-releasing factor (CRF), an important modulator of stress
142 opeptide related to vertebrate corticotropin-releasing factor (CRF), and its receptor, Dh44R1.
143  is thought to communicate via corticotropin-releasing factor (CRF), but studies have yet to examine
144              The neuropeptide, corticotropin-releasing factor (CRF), coordinates the physiological an
145 es indicate the involvement of corticotropin-releasing factor (CRF), noradrenaline, dopamine, glutama
146 s for the stress neuropeptide, corticotropin-releasing factor (CRF), that render the locus coeruleus
147                                Corticotropin-releasing factor (CRF), the major stress peptide in the
148 e focus is on the receptor for corticotropin-releasing factor (CRF), the orchestrator of the stress r
149                                Corticotropin-releasing factor (CRF), the stress-related neuropeptide,
150 ticotropes are stimulated with corticotropin releasing factor (CRF), whereupon SSTR2 exits the compar
151 g the stress-sensitive peptide corticotropin-releasing factor (CRF), which has been identified in cri
152 oradrenergic substrates [via a corticotropin-releasing factor (CRF)-dependent mechanism] that regulat
153 nd inhibitory transmission in corticotrophin-releasing factor (CRF)-expressing dorsal-medial (mpd) ne
154     Here, we demonstrate that corticotrophin-releasing factor (CRF)-expressing neurons in the central
155 en shown previously to cause a corticotropin-releasing factor (CRF)-mediated increase in tonic locus
156                                Corticotropin-releasing factor (CRF)-mediated mechanisms in the bed nu
157  in the brain that counteracts corticotropin-releasing factor (CRF)-mediated stress and anxiety sympt
158 D is functionally expressed on corticotropin-releasing factor (CRF)-positive BNST cells implicated in
159 uding neuropeptide Y (NPY) and corticotropin-releasing factor (CRF).
160  the stress-sensitive peptide, corticotropin releasing factor (CRF).
161 ocorticoid receptors (GRs) and corticotropin-releasing factor (CRF).
162 opaminergic neurons expressing corticotropin-releasing factor (CRF).
163 e prototypical stress hormone, corticotropin releasing factor (CRF).
164 e stress-related neuropeptide, corticotropin-releasing factor (CRF).
165 the anxiogenic neuromodulator, corticotropin releasing factor (CRF).
166 l antibody, CTRND05, targeting corticotropin-releasing factor (CRF).
167  that produce the neuropeptide corticotropin-releasing factor (CRF).
168 tested the hypothesis that the corticotropin-releasing factor (CRF1) antagonist GSK561679 differentia
169 T proteins function mechanistically as pause-release factors critical to expression of genes that are
170 sult in a tangible model disclosing how hPSC-released factors deflect CHIR99021-induced lineage commi
171 tment of brain stress systems (corticotropin-releasing factor, dynorphin, norepinephrine, hypocretin,
172 ly on an evolutionarily unrelated omnipotent release factor (eRF1) to recognize all three stop codons
173 the complex functional interplay between two release factors, eRF1 and eRF3, in which GTP hydrolysis
174                Downregulation of translation release factor eRF3 or eRF1 reduced SFL-mediated prematu
175 nal domain with eukaryotic polypeptide chain release factor, eRF3.
176 cy of competition for the stop codon between release factors (eRFs) and near-cognate tRNAs is largely
177 teral amygdala (BLA) away from corticotropin releasing factor-expressing (CRF(+)) centrolateral amygd
178  neuropeptides vasopressin and corticotropin-releasing factor facilitate, while serotonin inhibits, a
179 rs, which bind peptides of the corticotropin releasing factor family and are key mediators in the str
180                                              Release factor homolog C12orf65 (mtRF-R) and RNA binding
181  al. provide a causal link between histamine-releasing factor (HRF) interactions with IgE and food al
182 lacks a secreted factor related to histamine-releasing factor (HRF).
183                                    Histamine-releasing factor (HRF; also known as translationally con
184 ther suggest that an activated corticotropin-releasing factor/hypothalamic-pituitary-adrenal axis sys
185 discovered that UPF3B (i) interacts with the release factors, (ii) delays translation termination and
186 thropin-releasing hormone, and corticotropin-releasing factor immunoreactive cells in the paraventric
187 ned in vitro system, we explored the role of release factors in canonical termination and post PT QC.
188 l axis, including signaling by corticotropin-releasing factor, in the pathophysiology of PTSD.
189  A1 and aromatase enhanced local bone marrow-releasing factors, including androgen receptor, estrogen
190                                Corticotropin-releasing factor infusions into LA impair the consolidat
191                                Corticotropin-releasing factor infusions into the central nucleus of t
192 suggests muscle contractions during exercise release factors into the blood which cross into the brai
193                In preeclampsia, the placenta releases factors into the maternal circulation that caus
194       The variability of refinery subprocess release factors is characterized using log-normal distri
195                         While corticotrophin releasing factor is the prototypic member of this class,
196 p codons, suggesting a general mechanism for release-factor-mediated translational termination in whi
197 cting to vasopressinergic and corticotrophin releasing factor neurons in the paraventricular nucleus,
198 acts with the neuromodulators, corticotropin-releasing factor, norepinephrine, dopamine, and serotoni
199 e cell, thereby establishing its function as release factor of mislocalized palmitoylated proteins in
200 l impact of treatment with such hypothalamic releasing factors on recovery from critical illness as w
201 ess of the way PoTC was prepared with either release factors or puromycin.
202 ss of Upf (up-frameshift) factors, defective release factors, or the presence of the aminoglycoside g
203 ior hypothalamus that may gate corticotropin-releasing factor output from the amygdala to the anterio
204 d (i.e., serotonin, dynorphin, corticotropin-releasing factor, oxytocin).
205 pluripotency genes by dissociating the pause release factor P-TEFb from an inactive complex containin
206   Active transcription starts when the pause release factor P-TEFb is recruited to initiate productiv
207 leading to recruitment of BRD4 and the pause release factor P-TEFb, followed by productive elongation
208       Cohesin dynamics are controlled by the releasing factors Pds5 and Wapl and the cohesin stabiliz
209 ed competition between ternary complexes and release factors perturbs the UGA readthrough level.
210 appetite regulation, including corticotropin releasing factor, pro-opiomelanocortin B, and glucose tr
211                               The eukaryotic release factor protein family has also been dramatically
212           Similarly, polymerase I transcript release factor (PTRF) deficiency resulted in decreased i
213          Cavin-1/polymerase I and transcript release factor (PTRF) is a requisite component of caveol
214 logical consequence of central corticotropin-releasing factor receptor (CRF-R) activation.
215 ed differential involvement of corticotropin-releasing factor receptor (CRFR) 1 and 2 in acute stress
216 haracterize the effects of the corticotropin-releasing factor receptor 1 (CRF-R1) antagonist, GW87600
217  (NE) receptors (alpha1) via a corticotropin-releasing factor receptor 1 (CRF-R1)-dependent mechanism
218 g the efficacy of GSK561679, a corticotropin-releasing factor receptor 1 (CRF1 receptor) antagonist i
219                    Blockade of corticotropin-releasing factor receptor 1 (CRF1) suppresses stress-ind
220  member of a class B GPCR, the corticotropin releasing factor receptor 1 (CRF1R).
221 what has been observed for the corticotropin-releasing factor receptor 1 (CRFR1), SAP97 expression is
222 r-activated receptor gamma and corticotropin-releasing factor receptor 1 were notable exceptions.
223 ed significant upregulation of corticotropin releasing factor receptor 2 (CrfR2) in the amygdala of m
224 constitutive activation of the corticotropin-releasing factor receptor family homologue SEB-3.
225 d psychological stress through corticotropin-releasing factor receptor subtype 1 (CRF(1)) expressed o
226 dy we investigated the role of corticotropin-releasing factor receptor subtype 2 (CRF(2)) as a modula
227 ent study examines the role of corticotropin releasing factor receptor subtypes 1 and 2 (CRFR1, CRFR2
228  CRF(2(a))R and the homologous corticotropin-releasing factor receptor type 1 (CRF(1)R) possessing a
229 vestigated whether blockade of corticotropin-releasing factor receptor type 1 (CRF-R1) could prevent
230 ctions in anandamide driven by corticotropin-releasing factor receptor type 1 (CRF1) potentiation of
231 re the interaction between the corticotropin releasing factor receptor type 1 (CRF1R) and its native
232 ed interactions of the class B corticotropin-releasing factor receptor type 1 (CRF1R) with two peptid
233                                Corticotropin-releasing factor receptor type 1 (CRFR1) is involved in
234 compartments, we show that the corticotropin-releasing factor receptor type 1 has a specific monomer/
235 nsmembrane domain of the human corticotropin-releasing factor receptor type 1 in complex with the sma
236                            The corticotropin-releasing factor receptor type 1 is a class B receptor w
237 librium is established for the corticotropin-releasing factor receptor type 1.
238                                Corticotropin-releasing factor receptor type 2 (CRFR2) has been implic
239 central stress response, while corticotropin-releasing factor receptor type 2 (CRFR2) has been sugges
240 bserved abnormal expression of corticotropin-releasing factor receptor type 2 (CRFR2) to be associate
241                            The corticotropin-releasing factor receptor type 2a (CRF(2(a))R) possesses
242 is unaffected by alpha1-AR and corticotropin-releasing factor receptor-1 (CRFR(1)) antagonists, but i
243 tention were attenuated by the corticotropin-releasing factor receptor-1 antagonist antalarmin but no
244                                Corticotropin-Releasing Factor Receptors (CRFRs) are class B1 G-protei
245                                Corticotropin-releasing factor receptors (CRFRs), class B G protein-co
246                             Codon selection, releasing factor recognition sequence and specific intro
247                                              Release factors recognize stop codons in the ribosomal A
248 uential ATPase and GTPase activities license release factors Rei1 and Yvh1 to trigger Arx1 and Mrt4 r
249  it has been shown to increase corticotropin-releasing factor release in extrahypothalamic brain regi
250 codons are recognized by two similar class 1 release factors, release factor 1 (RF1) and release fact
251 osome encounters a stop codon, it recruits a release factor (RF) to hydrolyze the ester bond between
252  steady state amount of mRNA and protein for release factors RF1 and RF2 during exponential growth.
253 ion-like protein (RepA-WH1) into the E. coli releasing factor RF1 promotes its aggregation and enable
254        Stop codons are recognized by class I release factors (RF1 and RF2 in Escherichia coli), which
255 ecognizes stalled ribosomes and recruits the release factor RF2, which catalyses the termination of p
256 mes stalled on truncated mRNAs by recruiting release factor RF2, which normally binds stop codons to
257 tion in Bacteria and Archaea is initiated by release factors (RFs) 1 or 2 recognizing a stop codon in
258                                              Release factors (RFs) decode the stop codon, hydrolyze p
259  of the specificity of the bacterial class I release factors (RFs) in decoding stop codons has evolve
260         Alterations in central corticotropin-releasing factor signaling pathways have been implicated
261                   In addition to this strain release factor, steric and inductive effects contribute
262  forces and an inflammatory microenvironment release factors such as a disintegrin and metalloprotein
263 n-gamma (IFN-gamma) and induce cytolysis via releasing factors such as perforin, which permeabilizes
264  Moreover, Tia1/Pub1 acts cooperatively with release factor Sup35/eRF3 to establish a two-protein sel
265          Here, we examined how the canonical release factors Sup45-Sup35 (eRF1-eRF3) and their paralo
266 s), (4) the (gastrointestinal) corticotropin-releasing factor system, and (5) the intestinal response
267 s probed using a dexamethasone/corticotropin-releasing factor test.
268 de the kinase domain constitute a nucleotide release factor that likely interacts with the small lobe
269             For example, apoptotic cells can release factors that influence the proliferation and sur
270 jor differentially activate keratinocytes to release factors that limit infection in monocytes.
271  fibroblasts overexpress matrix proteins and release factors that promote further recruitment of acti
272 w that mast cells sense colder temperatures, release factors that promote UCP1 expression, and are an
273      p53-expressing senescent stellate cells release factors that skew macrophage polarization toward
274                  The TNFalpha-activated PAEC released factors that induce huTreg chemotaxis, partiall
275 ontrol of the pathogen, but B. dendrobatidis releases factors that inhibit in vitro and in vivo lymph
276 spected of initiating childhood leukaemia by releasing factors that cause DNA damage in cord blood an
277 strocytes play a key role in this process by releasing factors that promote the formation of excitato
278  role in maintaining vascular homeostasis by releasing factors that regulate local blood flow, system
279 counteracting the functions of corticotropin-releasing factor, the primary stress-mediating neuropept
280 lin, nesfatin-1, somatostatin, corticotropin-releasing factor, thyrotropin-releasing hormone and calc
281  During normal translation, the binding of a release factor to one of the three stop codons (UGA, UAA
282 buting ions, removing neurotransmitters, and releasing factors to influence blood flow and neuronal a
283                                Corticotropin releasing factor type 1 (CRF1) is a key component in the
284                  Activation of corticotropin-releasing factor type 1 (CRF1) receptors in the CeA play
285 ve effect is mediated via the corticotrophin-releasing factor type 1 receptor (CRF1R, also known as C
286 peated social stress decreased corticotropin-releasing factor type 1 receptor and increased mu-opioid
287                  We found that corticotropin-releasing factor type 1 receptor within the paraventricu
288 LTCC-based mechanism; instead, corticotropin-releasing factor type 1 receptors (CRF1s) mediate alcoho
289 LTCC-based mechanism; instead, corticotropin-releasing factor type 1 receptors (CRF1s) mediate alcoho
290                            The corticotropin-releasing factor type 2 receptor (CRFR2) is suggested to
291 hat the mechanism involved the corticotropin-releasing factor type 2 receptor, cAMP elevation, and ac
292     We identify an FxxP motif in the cohesin release factor WAPL and show that this regulates WAPL ph
293              Here we report that the cohesin release factor WAPL creates a pool of free cohesin, in a
294                      Conversely, the cohesin-release factor Wapl(13,14) restricts loop extension(10,1
295 ified cohesin ligands, including the cohesin release factor WAPL(2,3).
296 hesin with chromatin depends on WAPL cohesin release factor (WAPL) and on PDS5 cohesin-associated fac
297 ion of diverse microbial moieties, including released factors, which modulate host immune responses t
298 ombined administration of those hypothalamic releasing factors, which have been identified as suppres
299 complexes on DNA by antagonizing the cohesin release factor Wings-apart like protein (Wapl).
300 cteria decode stop codons using two separate release factors with differing specificities for the sec

 
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