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1 in receptor), 87.5% of which coexpressed the calcitonin receptor.
2 ielded cDNAs that encode two isoforms of the calcitonin receptor.
3 ronal expression of Calcr, which encodes the calcitonin receptor.
4 siological function of amylin binding to the calcitonin receptor.
5 s occurred at the concentration of the Kd of calcitonin receptor.
6 .9 nm) and was able to efficiently label the calcitonin receptor.
7 vasoactive intestinal polypeptide type 1 and calcitonin receptors.
8 um stability and specific affinity for human calcitonin receptors.
9 ant peptide sequence homology with the human calcitonin receptor, a member of the G-protein-coupled r
10 ls in the mPFC, supporting the idea that VTA calcitonin receptor activation decreases dopamine releas
11 To first establish that VTA amylin receptor (calcitonin receptor) activation can modulate mPFC activi
12 gest that the deltae13 variant of the rabbit calcitonin receptor acts to regulate the surface express
15 385, as well as nonselective dual amylin and calcitonin receptor agonists (DACRAs), with San45 being
18 ocalcitonin was shown to signal through both calcitonin receptor and calcitonin gene-related peptide
19 ssed mRNA for the noninserted isoform of the calcitonin receptor and excavated characteristic resorpt
21 te-resistant acid phosphatase), cathepsin K, calcitonin receptor, and RANK (receptor activator of nuc
22 ated from the gene for the G protein-coupled calcitonin receptor, and some of the splice variants sho
24 cells that stably express the cloned rabbit calcitonin receptor, as in many other cells that express
26 In addition, the activation of calcitonin-calcitonin receptor axis induced epithelial-mesenchymal
27 he first time identify actions of calcitonin-calcitonin receptor axis on prostate cancer cells that l
28 re potent stimulants of cAMP accumulation in calcitonin receptor-bearing human embryonic kidney 293 c
29 /or alanine replacement of the region of the calcitonin receptor between residues 150 and 153 resulte
30 lated all phases of angiogenesis through the calcitonin receptor, but its effect on tube morphogenesi
31 fail to multinucleate and do not up-regulate calcitonin receptor, but they express tartrate-resistant
34 ne that overexpresses the C1a isoform of the calcitonin receptor (C1a-HEK), calcitonin induces the ty
36 ession and that amylin functions through the calcitonin receptor (CalcR) and receptor activity modify
37 f DEX with D3 or PTH increased gene encoding calcitonin receptor (Calcr), acid phosphatase 5, tartrat
43 in receptors (AMY(1)R, AMY(2)R, AMY(3)R) and calcitonin receptor (CTR) and compare cagrilintide inter
44 mylin receptors (AMYRs), heterodimers of the calcitonin receptor (CTR) and one of three receptor acti
45 selectivity of the class B G protein-coupled calcitonin receptor (CTR) and the CTR-like receptor (CLR
47 The calcitonin-like receptor (CLR) and the calcitonin receptor (CTR) interact with receptor activit
48 he class B G protein-coupled receptor (GPCR) calcitonin receptor (CTR) is a drug target for osteoporo
49 e calcitonin receptor-like receptor (CLR) or calcitonin receptor (CTR) together with one of three acc
52 d AMY(3)R are heterodimers consisting of the calcitonin receptor (CTR), a G protein-coupled receptor,
53 ugh fusion of luciferase to either the human calcitonin receptor (CTR), human receptor activity-modif
54 how that the core component of the AmyR, the calcitonin receptor (CTR), is expressed on VTA dopamine
55 , the core component of the amylin receptor, calcitonin receptor (CTR), was depleted from POMC neuron
62 Although calcitonin was able to activate the calcitonin receptor fully with the first 58 residues abs
63 or activity-modifying protein-1 (RAMP-1) and calcitonin receptor gene (CT-R) expression in striatum [
65 affinities of these analogues for the human calcitonin receptor, hCTR(I1)(-), and for rat-brain memb
67 d sequencing of labeled wild type and mutant calcitonin receptors identified the sites of labeling fo
68 oclast marker genes NFATc1, cathepsin K, and calcitonin receptor in a RANKL-dependent manner, and con
72 cture of a full-length class B receptor, the calcitonin receptor, in complex with peptide ligand and
73 lls, that stably express a myc-tagged rabbit calcitonin receptor, induced the formation of complexes
74 dependent protein kinase plays a key role in calcitonin receptor-induced destabilization of cell-cell
77 consisting of 32 amino acid residues and the calcitonin receptor is a Class B G protein-coupled recep
82 at the deltae13 splice variant of the rabbit calcitonin receptor is expressed together with the more
85 enomedullin (AM) and its receptor complexes, calcitonin receptor-like receptor (Calcrl) and receptor
86 get CGRP receptor, produced in part from the calcitonin receptor-like receptor (Calcrl) gene, has bee
87 activity modifying protein 1 (RAMP1) and the calcitonin receptor-like receptor (CALCRL) to promote eg
88 activity modifying protein 1 (RAMP1) and the calcitonin receptor-like receptor (CALCRL) to promote eg
89 ator that transduces its effects through the calcitonin receptor-like receptor (calcrl) when the rece
92 Rs) is formed through the association of the calcitonin receptor-like receptor (CLR) and one of three
93 pression and define cellular localization of calcitonin receptor-like receptor (CLR) and receptor act
94 resence of CGRP and its receptor components, calcitonin receptor-like receptor (CLR) and receptor act
95 r is a heterodimer of two membrane proteins: calcitonin receptor-like receptor (CLR) and receptor act
100 ) with the G protein-coupled receptor (GPCR) calcitonin receptor-like receptor (CLR) enables selectiv
102 mers comprising two distinct components: the calcitonin receptor-like receptor (CLR) or calcitonin re
103 e contribution of endosomal signaling of the calcitonin receptor-like receptor (CLR) to pain transmis
104 ization of a G protein-coupled receptor, the calcitonin receptor-like receptor (CLR), and receptor ac
105 -related peptide (CGRP) co-internalizes with calcitonin receptor-like receptor (CLR), receptor activi
106 t identified through an interaction with the calcitonin receptor-like receptor (CLR), these single tr
109 eric CGRP receptor requires co-expression of calcitonin receptor-like receptor (CRLR) and an accessor
110 eatment of 293T cells expressing recombinant calcitonin receptor-like receptor (CRLR) and one of the
113 eteromer formation is the interaction of the calcitonin receptor-like receptor (CRLR) with different
114 ide (CGRP) receptor requires dimerization of calcitonin receptor-like receptor (CRLR) with receptor a
115 cently the G-protein coupled receptor (GPCR) calcitonin receptor-like receptor (CRLR), and receptor a
116 2 or RAMP3 (AM1R and AM2R, respectively) and calcitonin receptor-like receptor (CRLR), while a CRLR h
117 o act through the G protein-coupled receptor calcitonin receptor-like receptor (CRLR), with specifici
120 tonin gene-related peptide receptor subunits calcitonin receptor-like receptor and receptor activity
122 alcitonin gene-related peptide receptor, the calcitonin receptor-like receptor and the receptor activ
123 the CGRP-binding protein referred to as the calcitonin receptor-like receptor is highly concentrated
124 ion competing for RAMP3 association with the calcitonin receptor-like receptor to yield a functional
125 e encouraging the exploration of the AM-CLR (calcitonin receptor-like receptor) signaling pathway as
126 tance of the most likely candidate receptor, calcitonin receptor-like receptor, a gene-targeted knock
127 ented lysosomal trafficking and recycling of calcitonin receptor-like receptor, a non-ubiquitinated r
131 duce arterial differentiation in ECs via the calcitonin receptor-like receptor, thus revealing a surp
132 s and endothelial cells are known to express calcitonin receptor-like receptor, we examined the poten
134 gene-related peptide (CGRP) or its receptor (calcitonin receptor-like receptor/receptor activity modi
135 ceptor with seven transmembrane domains, the calcitonin-receptor-like receptor (CRLR), can function a
140 13 accounting for less than 15% of the total calcitonin receptor mRNA in osteoclasts, kidney, and bra
141 action to estimate the relative abundance of calcitonin receptor mRNA, a 25-fold accumulation of the
144 n-polymerase chain reaction amplification of calcitonin receptor sequences from rabbit osteoclast RNA
145 eceptor, as in many other cells that express calcitonin receptors, shows little pertussis toxin sensi
147 e examined whether heterodimerization of the calcitonin receptor splice variants occurs and, if so, w
148 ated following stimulation of the rabbit C1a calcitonin receptor stably expressed in HEK-293 cells.
149 ta are two proximal signal effectors for the calcitonin receptor, the more distal signaling pathways
150 d sequencing of labeled wild-type and mutant calcitonin receptors, the site of attachment was identif
152 entrations of the G(s) protein-coupled human calcitonin receptor type 2 (hCTR2) cDNA produced suffici
156 Both probes specifically bound to the human calcitonin receptor with high affinity and were potent s
157 All compounds were full agonists at the calcitonin receptor with no activity at the secretin rec
158 thin the extracellular amino terminus of the calcitonin receptor, with the former adjacent to the fir