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1 opressin, glucagon, parathyroid hormone, and calcitonin).
2 delta/notch-like EGF repeat containing; and calcitonin.
3 ure peptide as compared to undigested salmon calcitonin.
4 Alzheimer's amyloid-beta, human amylin, and calcitonin.
5 activation of the 1alpha(OH)ase promoter by calcitonin.
6 ction of small molecules relative to that of calcitonin.
8 eful work-up, including measurement of serum calcitonin and carcinoembryonic antigen (and their doubl
9 al based on such prognostic factors as serum calcitonin and carcinoembryonic antigen (CEA) doubling t
11 come of (18)F-FDG PET or (18)F-DOPA PET with calcitonin and CEA doubling times in 47 MTC patients.
13 separation, detection, and quantification of calcitonin and each of its precursors in human cancer ce
14 overy and characterization of O-glycosylated calcitonin and its analogous biosynthetic precursors.
15 he sequence from Asp(15) to Phe(19) of human calcitonin and reported as the minimal amyloidogenic mod
18 es and clinical observations (eg, oestrogen, calcitonin, and teriparatide) or opportunistic repurposi
19 The expression of Samd9L was upregulated by calcitonin, and this was preceded by a significant incre
20 ion of a subset of TRA, parathyroid hormone, calcitonin, and thyroglobulin, as part of an effort to b
21 or 4, heart-type fatty acid binding protein, calcitonin, and tumor necrosis factor-related apoptosis-
22 ses, and persistently elevated postoperative calcitonin; and argue for the aggressive management of e
24 ata strongly suggest antiparallel beta-sheet calcitonin assembly, whereas modeling studies on the sho
26 complex with a truncated analogue of salmon calcitonin ([BrPhe(22)]sCT(8-32)) has been determined to
27 re the first to address the dynamics between calcitonin, C/EBPbeta, and SWI/SNF in the regulation of
29 or (CTR) and the CTR-like receptor (CLR) for calcitonin (CT), amylin (Amy), calcitonin gene-related p
31 LDTg amylin receptors by the agonist salmon calcitonin dose-dependently reduces body weight, food in
33 amino-acid peptide hormone belonging to the calcitonin family, is an intrinsically disordered protei
35 or MTC in the United States with basal serum calcitonin for patients with thyroid nodules would cost
37 ion induced by the Katp agonists cromakalim, calcitonin gene related peptide (CGRP) and the Kca agoni
38 mediating sensory neuropeptides galanin and calcitonin gene related peptide (CGRP) in a model of neu
41 arch into the therapeutic potential of alpha-calcitonin gene-related peptide (alpha-CGRP) has been li
42 s, increased hippocampal expression of alpha calcitonin gene-related peptide (alphaCGRP) transcripts,
44 mouse bone induces a remarkable sprouting of calcitonin gene-related peptide (CGRP(+)) and neurofilam
46 ing site of the homologous receptors for the calcitonin gene-related peptide (CGRP) and adrenomedulin
47 nables selective recognition of the peptides calcitonin gene-related peptide (CGRP) and adrenomedulli
48 ed receptors involved in energy homeostasis: calcitonin gene-related peptide (CGRP) and amylin recept
49 s for the treatment of acute migraine target calcitonin gene-related peptide (CGRP) and serotonin (5-
50 and/or ARs lead to release of neuropeptides calcitonin gene-related peptide (CGRP) and substance P (
51 expression of the potent vasoactive agents' calcitonin gene-related peptide (CGRP) and vascular endo
53 However, the A11 does contain dopamine and calcitonin gene-related peptide (CGRP) and, by this comb
55 ntly suppressed basal neuronal expression of calcitonin gene-related peptide (CGRP) as well as stimul
58 CIM0216 elicited the release of the peptides calcitonin gene-related peptide (CGRP) from sensory nerv
59 usion of neural factors, norepinephrine, and calcitonin gene-related peptide (CGRP) in denervated kid
60 y of evidence supports an important role for calcitonin gene-related peptide (CGRP) in migraine patho
63 SIGNIFICANCE STATEMENT: The neuropeptide calcitonin gene-related peptide (CGRP) is a central play
72 ed immunoabsorbent assay was used to measure calcitonin gene-related peptide (CGRP) levels in blood.
73 inase and estrogen receptor (CreER) into the calcitonin gene-related peptide (CGRP) locus that encode
74 very migraine patient.SIGNIFICANCE STATEMENT Calcitonin gene-related peptide (CGRP) monoclonal antibo
75 the contribution to cancer anorexia made by calcitonin gene-related peptide (CGRP) neurons in the pa
81 X: an ultrapotent analog of capsaicin) and a calcitonin gene-related peptide (CGRP) receptor blocker
83 eover NO increased neuronal excitability and calcitonin gene-related peptide (CGRP) release and these
84 PA1-selective agonist, mustard oil (MO), for calcitonin gene-related peptide (CGRP) release from rat
85 idine (CLON) or their combination to inhibit calcitonin gene-related peptide (CGRP) release from spin
86 rmacologic inhibition of substance P (SP) or calcitonin gene-related peptide (CGRP) signaling in Vglu
87 pharmacological inhibition of substance P or calcitonin gene-related peptide (CGRP) signaling in Vglu
88 had no effect on acanthosis; restoration of calcitonin gene-related peptide (CGRP) signaling reverse
89 DCN A and C fibers and their relationship to calcitonin gene-related peptide (CGRP) staining in the d
91 s depend, in part, on its ability to release calcitonin gene-related peptide (CGRP) through an uniden
93 sal root ganglia (DRG), some neurons express calcitonin gene-related peptide (CGRP) without substance
94 y trigeminal nerve fibers immunoreactive for calcitonin gene-related peptide (CGRP), a marker for pol
95 that reacted with a labeled antibody against calcitonin gene-related peptide (CGRP), a marker of noci
96 tor (CLR) for calcitonin (CT), amylin (Amy), calcitonin gene-related peptide (CGRP), and adrenomedull
97 rves induced production of the neuropeptide, calcitonin gene-related peptide (CGRP), and CGRP treatme
98 ron somata, especially those also expressing calcitonin gene-related peptide (CGRP), and in central p
99 The relative numbers of neurons containing calcitonin gene-related peptide (CGRP), cocaine- and amp
100 ed transcript (cart), cholecystokinin (cck), calcitonin gene-related peptide (cgrp), galanin, hypocre
101 b, a humanized monoclonal antibody targeting calcitonin gene-related peptide (CGRP), is being investi
102 reactive (IR) for neurofilament 200 (N52) or calcitonin gene-related peptide (CGRP), or labeled by is
103 characterized by using six neuronal markers: calcitonin gene-related peptide (CGRP), substance P (SP)
104 ytochemical studies combined CTb with either calcitonin gene-related peptide (CGRP), substance P (SP)
105 did not colocalize with the C-fiber markers calcitonin gene-related peptide (CGRP), substance P, and
107 n exists between migraine and release of the calcitonin gene-related peptide (CGRP), the possibility
108 the PBel neurons that respond to CO2 express calcitonin gene-related peptide (CGRP), we hypothesized
109 ological states, we injected the vasodilator calcitonin gene-related peptide (CGRP), which induces he
110 nerve fibers innervating taste buds contain calcitonin gene-related peptide (CGRP), which may be as
114 afferent neurons are almost exclusively non-calcitonin gene-related peptide (CGRP)-immunoreactive (-
119 and a population of cisplatin-activated lPBN calcitonin gene-related peptide (CGRP, a marker for glut
121 hinly myelinated and unmyelinated fibers) or calcitonin gene-related peptide (CGRP; a marker more typ
122 ochemistry analysis using antibodies against calcitonin gene-related peptide (CGRP; sensory nerve fib
124 related peptide and the receptor antagonists calcitonin gene-related peptide 8-37 and olcegepant on t
125 d and thin myelinated afferents labeled with calcitonin gene-related peptide and isolectin B4, and in
127 pression of mu opioid receptor and increased calcitonin gene-related peptide and substance P immunore
128 peptidergic nociceptive fibers (positive for calcitonin gene-related peptide and substance P) and mye
129 ther tested the effect of microiontophoresed calcitonin gene-related peptide and the receptor antagon
130 subset of sensory neurons that colabel with calcitonin gene-related peptide and TRPV1 suggestive of
131 assess the safety and efficacy of monoclonal calcitonin gene-related peptide antibodies for the preve
133 ADA reduces blood levels of the neuropeptide calcitonin gene-related peptide but increases the neurop
134 AMP-dependent secretion of IL-1beta and beta-calcitonin gene-related peptide by dendritic cells.
135 een confirmed, and the subsequent release of calcitonin gene-related peptide from a mouse heart has b
137 ated release of the neuropeptide transmitter calcitonin gene-related peptide in mouse DRG neurons.
138 evention and provide support for the role of calcitonin gene-related peptide in the pathogenesis of m
139 vascular activation, including expression of calcitonin gene-related peptide in the trigeminal gangli
141 E11.5, followed by neurofilament-M neurons, calcitonin gene-related peptide neurons (peak cell cycle
142 Regenerated unmyelinated axons expressing calcitonin gene-related peptide project only to superfic
143 ibers were predominant (tyrosine hydroxylase/calcitonin gene-related peptide ratio 25.1 +/- 33.4; p <
144 ric synthesis of the major metabolite of the calcitonin gene-related peptide recepotor antagonist BMS
145 nputs and tested the effect of olcegepant, a calcitonin gene-related peptide receptor antagonist (1 m
148 This is the first report on the efficacy of calcitonin gene-related peptide receptor antagonists at
149 pathway, showing that the central effects of calcitonin gene-related peptide receptor antagonists ext
150 uture non-vasoconstrictor approaches include calcitonin gene-related peptide receptor antagonists.
151 ore used to migraine, such as naproxen and a calcitonin gene-related peptide receptor inhibitor, olce
152 nucleus by specifically co-staining for the calcitonin gene-related peptide receptor subunits calcit
153 human monoclonal antibody that inhibits the calcitonin gene-related peptide receptor, for the preven
154 e presence of the components of a functional calcitonin gene-related peptide receptor, the calcitonin
155 ain G-protein-coupled receptors, such as the calcitonin gene-related peptide receptor, to the plasma
156 ng to demonstrate the presence of functional calcitonin gene-related peptide receptors in the ventrop
157 icin-evoked nocifensive responses, increased calcitonin gene-related peptide release from hindpaw ski
159 ch, in return, allowed endoneurally released calcitonin gene-related peptide to pass through the nerv
160 As for sensory axons (immunostained for calcitonin gene-related peptide) in the urinary bladders
161 ng factor, thyrotropin-releasing hormone and calcitonin gene-related peptide) involved in the mediati
162 axons (peripherin-positive axons containing calcitonin gene-related peptide), without changes in sym
164 omatostatin, gastric inhibitory polypeptide, calcitonin gene-related peptide, and adrenomedullin.
165 apsaicin measured by (Ca(2+))(i), release of calcitonin gene-related peptide, and inward currents.
166 e fly homolog of the vertebrate neuropeptide calcitonin gene-related peptide, as a circadian wake-pro
167 42, a fully humanised monoclonal antibody to calcitonin gene-related peptide, for migraine prevention
168 nt differences were observed in substance P, calcitonin gene-related peptide, or neuropeptide Y prote
170 modicum of investment, new targets, such as calcitonin gene-related peptide-based mechanisms, and en
171 born dopaminergic, GABAergic, nitrergic, and calcitonin gene-related peptide-expressing neurons and a
173 dult mice, MET was restricted to a subset of calcitonin gene-related peptide-immunoreactive (IR) myen
175 y, accompanied by increased axonal growth of calcitonin gene-related peptide-labeled fibers in the do
176 ased the density of PGP9.5-positive, but not calcitonin gene-related peptide-positive, free nerve end
182 staltic transmitters 5-hydroxytryptamine and calcitonin gene-related peptide; antagonists of these tr
183 mpanied by substantial increases of neuronal calcitonin gene-related polypeptide-alpha (CGRP) in both
184 l circuit for appetite suppression involving calcitonin gene-related protein (CGRP)-expressing PBN (C
187 the lateral parabrachial nucleus (lPBN) and calcitonin-gene related peptide (CGRP) projections from
188 des vasoactive intestinal polypeptide (VIP), calcitonin-gene related peptide (CGRP), substance P (SP)
189 knowledge, between the internal dynamics of calcitonin-gene-related peptide (CGRP) and amylin (islet
191 and cOv are characterized with expression of calcitonin-gene-related peptide and cholecystokinin.
192 vation by icilin blocked capsaicin-triggered calcitonin-gene-related peptide release from colon tissu
193 onic levels of the inflammatory neuropeptide calcitonin-gene-related peptide, although inflammatory i
194 f rat spinal sensory afferents identified by Calcitonin-Gene-Related-Peptide (CGRP) for peptidergic t
196 etrogradely labeled neurons from the DP were calcitonin-gene-related-peptide-positive (peptide-expres
199 rosis and Paget's disease for decades, human calcitonin (hCT) forms fibrils in aqueous solution that
200 o degradative release of encapsulated salmon calcitonin in gastric conditions while yielding rapid an
201 cription factor C/EBPbeta is up-regulated by calcitonin in kidney cells and results in a significant
202 igin of thyroid C cells, the major source of calcitonin in mammals and ancestors to neuroendocrine th
205 ining of rat kidney slices demonstrated that calcitonin induced a significant redistribution of AQP2
208 and results in a significant enhancement of calcitonin induction of 1alpha(OH)ase transcription and
216 e relationship between the incremental serum calcitonin level before reoperation and the number of ly
218 artment, and for an MTC with increased basal calcitonin level of 20-200 pg/ml (ipsilateral dissection
219 means of 5.3 vs 17.6 years) and having lower calcitonin levels (means of 115 vs 25,519 pg/mL), smalle
220 ary thyroid cancer (MTC) stratified by basal calcitonin levels before reoperation and the number of l
222 ective CND based on preoperative basal serum calcitonin levels is an effective and safe alternative t
223 olvement, and in MTC with preoperative basal calcitonin levels more than 200 pg/ml (normal limit <10
230 ate crosslinker, a small polypeptide (salmon calcitonin) loads and releases up to 45 mug/mg hydrogel
231 mic conditions, previous studies showed that calcitonin, not PTH, has an important role in the mainte
232 impact on DT (>/=100% increase of pre-pRAIT calcitonin or CEA DT or prolonged decrease of the biomar
233 nitiation of treatment with bisphosphonates, calcitonin, or raloxifene were treated as competing risk
237 ession and that amylin functions through the calcitonin receptor (CalcR) and receptor activity modify
238 The CAL-RAMP1 selectively activates the calcitonin receptor (CR), whereas, the CGRP-RAMP1 activa
239 selectivity of the class B G protein-coupled calcitonin receptor (CTR) and the CTR-like receptor (CLR
240 how that the core component of the AmyR, the calcitonin receptor (CTR), is expressed on VTA dopamine
242 /or alanine replacement of the region of the calcitonin receptor between residues 150 and 153 resulte
245 Although calcitonin was able to activate the calcitonin receptor fully with the first 58 residues abs
246 or activity-modifying protein-1 (RAMP-1) and calcitonin receptor gene (CT-R) expression in striatum [
247 oclast marker genes NFATc1, cathepsin K, and calcitonin receptor in a RANKL-dependent manner, and con
248 consisting of 32 amino acid residues and the calcitonin receptor is a Class B G protein-coupled recep
250 All compounds were full agonists at the calcitonin receptor with no activity at the secretin rec
252 cture of a full-length class B receptor, the calcitonin receptor, in complex with peptide ligand and
254 enomedullin (AM) and its receptor complexes, calcitonin receptor-like receptor (Calcrl) and receptor
255 get CGRP receptor, produced in part from the calcitonin receptor-like receptor (Calcrl) gene, has bee
257 Rs) is formed through the association of the calcitonin receptor-like receptor (CLR) and one of three
258 resence of CGRP and its receptor components, calcitonin receptor-like receptor (CLR) and receptor act
259 r is a heterodimer of two membrane proteins: calcitonin receptor-like receptor (CLR) and receptor act
260 pression and define cellular localization of calcitonin receptor-like receptor (CLR) and receptor act
263 ) with the G protein-coupled receptor (GPCR) calcitonin receptor-like receptor (CLR) enables selectiv
264 e contribution of endosomal signaling of the calcitonin receptor-like receptor (CLR) to pain transmis
265 ization of a G protein-coupled receptor, the calcitonin receptor-like receptor (CLR), and receptor ac
267 tonin gene-related peptide receptor subunits calcitonin receptor-like receptor and receptor activity
268 alcitonin gene-related peptide receptor, the calcitonin receptor-like receptor and the receptor activ
269 duce arterial differentiation in ECs via the calcitonin receptor-like receptor, thus revealing a surp
271 tin immunoprecipitation analysis showed that calcitonin recruits C/EBPbeta to the 1alpha(OH)ase promo
273 ndary visceral nucleus, which also expressed calcitonin-related polypeptide alpha (calca), a marker o
274 II afferents of two genes found in C-fibers: calcitonin-related polypeptide alpha (Calca/Cgrpalpha),
275 rs for fast motor neurons (Chondrolectin and calcitonin-related polypeptide alpha [Calca]), we analyz
276 that substantially change the proportions of calcitonin-related species released into the culture med
277 insertion into the disulfide bond of salmon calcitonin (sCT) demonstrates the utility for fluorescen
280 onjugation to the therapeutic peptide salmon calcitonin (sCT) via bridging of the Cys(1)-Cys(7) disul
281 sidues of both leucine enkephalin and salmon calcitonin (sCT) were targeted using appropriate diazoni
283 ion of acylation of octreotide (Oct), salmon calcitonin (sCT), and human parathyroid hormone (hPTH) w
288 a neuroendocrine cancer that originates from calcitonin-secreting parafollicular cells, or C cells.
290 a broad localization within the brain, while calcitonin, SIFamide, vasotocin, RGWamide, DLamide, FLam
291 ork, we first predict the structure of human calcitonin through two complementary molecular dynamics
293 e tested in vitro with model proteins salmon calcitonin, urokinase, and rituximab to determine the ef
295 int disruption afforded by dexamethasone and calcitonin was established in comparison to the melanoco
297 P responses to four non-peptidyl ligands and calcitonin were studied in COS-1 cells expressing wild-t
298 ype II turn is the preferred conformation of calcitonin, whereas a type I turn is the preferred confo
299 al performance for the small peptide, salmon calcitonin, whereas lower crosslinking density of 1 mol%
300 ly investigated with a small protein, salmon calcitonin, which could be analyzed both without and wit
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