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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 siological function of amylin binding to the calcitonin receptor.
4 s occurred at the concentration of the Kd of calcitonin receptor.
5 .9 nm) and was able to efficiently label the calcitonin receptor.
6 vasoactive intestinal polypeptide type 1 and calcitonin receptors.
7 um stability and specific affinity for human calcitonin receptors.
8 ant peptide sequence homology with the human calcitonin receptor, a member of the G-protein-coupled r
9 gest that the deltae13 variant of the rabbit calcitonin receptor acts to regulate the surface express
12 ssed mRNA for the noninserted isoform of the calcitonin receptor and excavated characteristic resorpt
14 ated from the gene for the G protein-coupled calcitonin receptor, and some of the splice variants sho
16 cells that stably express the cloned rabbit calcitonin receptor, as in many other cells that express
18 In addition, the activation of calcitonin-calcitonin receptor axis induced epithelial-mesenchymal
19 he first time identify actions of calcitonin-calcitonin receptor axis on prostate cancer cells that l
20 re potent stimulants of cAMP accumulation in calcitonin receptor-bearing human embryonic kidney 293 c
21 /or alanine replacement of the region of the calcitonin receptor between residues 150 and 153 resulte
22 lated all phases of angiogenesis through the calcitonin receptor, but its effect on tube morphogenesi
23 fail to multinucleate and do not up-regulate calcitonin receptor, but they express tartrate-resistant
26 ne that overexpresses the C1a isoform of the calcitonin receptor (C1a-HEK), calcitonin induces the ty
28 ession and that amylin functions through the calcitonin receptor (CalcR) and receptor activity modify
33 selectivity of the class B G protein-coupled calcitonin receptor (CTR) and the CTR-like receptor (CLR
34 The calcitonin-like receptor (CLR) and the calcitonin receptor (CTR) interact with receptor activit
37 how that the core component of the AmyR, the calcitonin receptor (CTR), is expressed on VTA dopamine
41 Although calcitonin was able to activate the calcitonin receptor fully with the first 58 residues abs
42 or activity-modifying protein-1 (RAMP-1) and calcitonin receptor gene (CT-R) expression in striatum [
44 affinities of these analogues for the human calcitonin receptor, hCTR(I1)(-), and for rat-brain memb
46 d sequencing of labeled wild type and mutant calcitonin receptors identified the sites of labeling fo
47 oclast marker genes NFATc1, cathepsin K, and calcitonin receptor in a RANKL-dependent manner, and con
50 cture of a full-length class B receptor, the calcitonin receptor, in complex with peptide ligand and
51 lls, that stably express a myc-tagged rabbit calcitonin receptor, induced the formation of complexes
52 dependent protein kinase plays a key role in calcitonin receptor-induced destabilization of cell-cell
55 consisting of 32 amino acid residues and the calcitonin receptor is a Class B G protein-coupled recep
60 at the deltae13 splice variant of the rabbit calcitonin receptor is expressed together with the more
63 enomedullin (AM) and its receptor complexes, calcitonin receptor-like receptor (Calcrl) and receptor
64 get CGRP receptor, produced in part from the calcitonin receptor-like receptor (Calcrl) gene, has bee
65 ator that transduces its effects through the calcitonin receptor-like receptor (calcrl) when the rece
68 Rs) is formed through the association of the calcitonin receptor-like receptor (CLR) and one of three
69 resence of CGRP and its receptor components, calcitonin receptor-like receptor (CLR) and receptor act
70 r is a heterodimer of two membrane proteins: calcitonin receptor-like receptor (CLR) and receptor act
71 pression and define cellular localization of calcitonin receptor-like receptor (CLR) and receptor act
76 ) with the G protein-coupled receptor (GPCR) calcitonin receptor-like receptor (CLR) enables selectiv
77 e contribution of endosomal signaling of the calcitonin receptor-like receptor (CLR) to pain transmis
78 ization of a G protein-coupled receptor, the calcitonin receptor-like receptor (CLR), and receptor ac
79 -related peptide (CGRP) co-internalizes with calcitonin receptor-like receptor (CLR), receptor activi
80 t identified through an interaction with the calcitonin receptor-like receptor (CLR), these single tr
83 eric CGRP receptor requires co-expression of calcitonin receptor-like receptor (CRLR) and an accessor
84 eatment of 293T cells expressing recombinant calcitonin receptor-like receptor (CRLR) and one of the
87 eteromer formation is the interaction of the calcitonin receptor-like receptor (CRLR) with different
88 ide (CGRP) receptor requires dimerization of calcitonin receptor-like receptor (CRLR) with receptor a
89 cently the G-protein coupled receptor (GPCR) calcitonin receptor-like receptor (CRLR), and receptor a
90 2 or RAMP3 (AM1R and AM2R, respectively) and calcitonin receptor-like receptor (CRLR), while a CRLR h
91 o act through the G protein-coupled receptor calcitonin receptor-like receptor (CRLR), with specifici
94 tonin gene-related peptide receptor subunits calcitonin receptor-like receptor and receptor activity
95 alcitonin gene-related peptide receptor, the calcitonin receptor-like receptor and the receptor activ
96 the CGRP-binding protein referred to as the calcitonin receptor-like receptor is highly concentrated
97 ion competing for RAMP3 association with the calcitonin receptor-like receptor to yield a functional
98 tance of the most likely candidate receptor, calcitonin receptor-like receptor, a gene-targeted knock
99 ented lysosomal trafficking and recycling of calcitonin receptor-like receptor, a non-ubiquitinated r
101 duce arterial differentiation in ECs via the calcitonin receptor-like receptor, thus revealing a surp
102 s and endothelial cells are known to express calcitonin receptor-like receptor, we examined the poten
103 ceptor with seven transmembrane domains, the calcitonin-receptor-like receptor (CRLR), can function a
107 13 accounting for less than 15% of the total calcitonin receptor mRNA in osteoclasts, kidney, and bra
108 action to estimate the relative abundance of calcitonin receptor mRNA, a 25-fold accumulation of the
111 n-polymerase chain reaction amplification of calcitonin receptor sequences from rabbit osteoclast RNA
112 eceptor, as in many other cells that express calcitonin receptors, shows little pertussis toxin sensi
113 e examined whether heterodimerization of the calcitonin receptor splice variants occurs and, if so, w
114 ated following stimulation of the rabbit C1a calcitonin receptor stably expressed in HEK-293 cells.
115 ta are two proximal signal effectors for the calcitonin receptor, the more distal signaling pathways
116 d sequencing of labeled wild-type and mutant calcitonin receptors, the site of attachment was identif
118 entrations of the G(s) protein-coupled human calcitonin receptor type 2 (hCTR2) cDNA produced suffici
122 Both probes specifically bound to the human calcitonin receptor with high affinity and were potent s
123 All compounds were full agonists at the calcitonin receptor with no activity at the secretin rec
124 thin the extracellular amino terminus of the calcitonin receptor, with the former adjacent to the fir
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