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1 ships (metabotropic glutamate receptor 5 and calcium-sensing receptor).
2 cytes, which is identical to the parathyroid calcium-sensing receptor.
3 o utilize a unique signaling mechanism via a calcium-sensing receptor.
4 blast-like cells involves a G-protein-linked calcium-sensing receptor.
5 cellular calcium and mediated in part by the calcium-sensing receptor.
6 d magnesium and are tightly regulated by the calcium-sensing receptor.
7 ce, consistent with the existence of another calcium-sensing receptor.
8 eptor (CASR) is the prototypic extracellular calcium-sensing receptor.
9 channels; ions, protons and amino acids; the calcium-sensing receptor (a G protein-coupled receptor)
10 is due to loss-of-function mutations of the calcium-sensing receptor, a guanine nucleotide-binding p
12 calcimimetic compound NPS R-467, a selective calcium-sensing receptor activator, augmented the calciu
13 of studies have demonstrated a role for the calcium-sensing receptor along the entire gastrointestin
15 TC-1, and to evaluate the involvement of the calcium-sensing receptor and G-protein coupled receptor-
17 thways for pharmacological intervention, the calcium-sensing receptor and the receptor activator of n
18 ng its pathogenesis focus on the key role of calcium-sensing receptors and TRPV5 channels in the modu
21 V2 vasopressin receptor, ACTH receptor, and calcium-sensing receptor are responsible for retinitis p
23 t correlated in vivo with production of anti-calcium-sensing receptor autoantibodies, which are typic
25 n keratinocytes express both the full-length calcium sensing receptor (CaR) and an alternatively spli
26 ion(s) of the carboxyl terminus of the human calcium sensing receptor (CaR) by assessing extracellula
28 e have recently reported the presence of the calcium sensing receptor (CaR) in keratinocytes and sugg
30 been previously shown that the extracellular-calcium sensing receptor (CaR) is expressed in intact ra
32 The aminoglycoside antibiotics (AGAs) are calcium-sensing receptor (CaR) agonists that are toxic t
33 ocytes express the full-length extracellular calcium-sensing receptor (CaR) and an alternatively spli
34 rat striatum revealed that the extracellular calcium-sensing receptor (CaR) could be involved in sens
36 ed that the G protein-coupled, extracellular calcium-sensing receptor (CaR) forms disulfide-linked di
38 r Ca(2+) (Ca(2+)(o)) functioning through the calcium-sensing receptor (CaR) induces E-cadherin-mediat
48 functional significance of the extracellular calcium-sensing receptor (CaR) on human pancreatic beta-
49 , perhaps acting via the seven-transmembrane calcium-sensing receptor (CaR) on mature monocytes/macro
52 te in the coding region of the extracellular calcium-sensing receptor (CaR) that are associated with
53 ncreasing the sensitivity of the parathyroid calcium-sensing receptor (CaR) to extracellular calcium.
56 ored by the G-protein coupled, extracellular calcium-sensing receptor (CaR), but neither its ontogeny
57 aste receptors (T1Rs), and the extracellular calcium-sensing receptor (CaR), represent a distinct gro
58 express the G protein-coupled, extracellular calcium-sensing receptor (CaR), showed that activation o
60 ons through the seven-transmembrane-spanning calcium-sensing receptor (CaR), which we identified as b
63 g pathways in rat fibroblasts and implicates calcium-sensing receptors (CaR) as mediators of this res
67 ER, and CBS) expressed the human parathyroid calcium sensing receptor (CaSR) and that a function of e
70 cent studies show that the human parathyroid calcium sensing receptor (CaSR) is expressed in human co
73 reases in [Ca](o) activate the extracellular calcium sensing receptor (CaSR) which in turn inhibits n
75 ied the glycosylated extracellular domain of calcium-sensing receptor (CaSR) (ECD) (residues 20-612),
79 or (PAM) drugs enhance the activation of the calcium-sensing receptor (CaSR) and suppress parathyroid
82 ed normally to activation of the parathyroid calcium-sensing receptor (Casr) by both hypercalcemia an
83 activation and by another [Ca2+]o activates Calcium-sensing receptor (CaSR) closing the sodium-leak
89 ed in the coding region of the extracellular calcium-sensing receptor (CASR) gene and cause human aut
91 diabetes and to evaluate the association of calcium-sensing receptor (CaSR) gene single nucleotide p
92 deduced by the cloning of the extracellular calcium-sensing receptor (CaSR) in 1993 in the laborator
95 real-time internalization assay to show that calcium-sensing receptor (CaSR) internalization is beta-
102 ino acid and extracellular cations, of which calcium-sensing receptor (CASR) is the prototypic extrac
111 amino acid-containing peptide agonist of the calcium-sensing receptor (CaSR) that is being evaluated
112 lopment of the resistance of the parathyroid calcium-sensing receptor (CaSR) to circulating calcium t
113 otein alpha-11 (Galpha11), which couples the calcium-sensing receptor (CaSR) to intracellular calcium
115 y cytokines by up-regulating the parathyroid calcium-sensing receptor (CaSR) with consequent developm
116 sis patients, subjects with GG at rs7627468 (calcium-sensing receptor (CASR)) have lower pH level in
119 rafficking of membrane proteins, such as the calcium-sensing receptor (CaSR), a G-protein coupled rec
121 en embryos of both sexes, our data show that calcium-sensing receptor (CaSR), a G-protein-coupled rec
122 was associated with higher expression of the calcium-sensing receptor (CaSR), a heterotrimeric G-prot
123 dium phosphate co-transporter (SLC34A1), the calcium-sensing receptor (CASR), and fibroblast growth f
124 oduce parathyroid hormone (PTH), express the calcium-sensing receptor (CASR), and mobilize intracellu
125 ride channel CLCNKB, barttin (BSND), and the calcium-sensing receptor (CASR), each of which is import
133 id hormone receptor (PTH1R; type B), and the calcium-sensing receptor (CaSR; type C) using fluorescen
134 GLUT2, could act as a glucose sensor and the calcium-sensing receptor, CasR, could detect amino acids
135 his hypercalcaemia acts on the extracellular calcium-sensing receptor, CaSR, to promote fluid-driven
136 eport a central role in this process for the calcium-sensing receptor, CaSR, which enables cellular r
137 report of ER Ca(2+) oscillations mediated by calcium sensing receptors (CaSRs), and revealed ER Ca(2+
139 ctivity were attributable to the activity of calcium-sensing receptors (CaSRs), which appear to be fu
140 disulfide bond-mediated dimerization of the calcium-sensing receptor contributes to stabilization of
142 ial role for the G protein-coupled receptor, calcium-sensing receptor (CSR), in the regulation of Ca(
144 sphate response of cloned human keratinocyte calcium-sensing receptor expressed in human embryonic ki
145 hese results support the hypothesis that the calcium-sensing receptor expressed in keratinocytes medi
146 tide receptor, P2Y2 purinergic receptor, and calcium-sensing receptor) expressed in murine dendritic
148 in of function, like the mutations effecting calcium-sensing receptor gain of function that cause aut
149 ty of a parathyroid-specific enhancer of the Calcium Sensing Receptor gene, which contains a risk all
153 found that cells expressing wild-type human calcium-sensing receptor (hCaSR-wt) and its gain of func
155 vious studies demonstrated the presence of a calcium-sensing receptor in human keratinocytes, which i
156 ctly inhibit PTH secretion by activating the calcium-sensing receptor in the parathyroid glands, but
157 pport a role for the luminal and basolateral calcium-sensing receptors in mediating some of the effec
159 asts to extracellular calcium and imply that calcium-sensing receptors may play a role in regulating
161 um calcium is mediated by G-protein coupled, calcium-sensing receptors on parathyroid cells, whereas
162 stry of calcium equilibrium results from the calcium-sensing receptors on the parathyroid glands, whi
165 rotein, the phosphate cotransporter Pit-1, a calcium-sensing receptor related factor, osteoprotegerin
166 g gastric acid secretion through the stomach calcium-sensing receptor (SCAR) located on the basolater
167 mutations on Galpha11 protein structure and calcium-sensing receptor signaling in human embryonic ki
168 s of function, since Galpha11 is involved in calcium-sensing receptor signaling, and its gene (GNA11)
169 All studies were carried out on the human calcium-sensing receptor tagged at the carboxyl terminus
170 The calcimimetic cinacalcet HCl acts on the calcium-sensing receptor to increase its sensitivity to
171 ecreased the sensitivity of cells expressing calcium-sensing receptors to changes in extracellular ca
172 n D additionally regulates the expression of calcium-sensing receptors to indirectly alter PTH secret
174 s, the vasopressin V2 receptor (V2R) and the calcium sensing receptor, using the novel V2R antagonist
175 the amount of biotinylated UT-A1 but not the calcium-sensing receptor was increased by forskolin.
176 racellular Ca(2+)-mediated activation of the calcium-sensing receptor was reduced by polyamines.
177 Candidate genes encoding the VDR and the calcium-sensing receptor were localized to regions on ra
178 ent of drugs targeting receptors such as the calcium-sensing receptor, which binds at least five calc
179 calcimimetics, allosteric modulators of the calcium-sensing receptor, would reduce cyst growth by in