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1 niche(3,4,6), CGRP acts directly on HSCs via receptor activity modifying protein 1 (RAMP1) and the ca
2 niche(3,4,6), CGRP acts directly on HSCs via receptor activity modifying protein 1 (RAMP1) and the ca
3 Calcitonin receptor-like receptor (CLR) and receptor activity modifying protein 1 (RAMP1) comprise a
6 that 5-HTR1E can regulate the expression of Receptor activity modifying protein 1 (RAMP1), Nuclear r
8 lacking functional CGRP receptors on ECs (EC receptor activity modifying protein 1 [RAMP1] knockout m
9 on together with its two accessory proteins, receptor activity modifying protein 1 and CGRP-receptor
10 he calcitonin receptor-like receptor and the receptor activity modifying protein 1, within the area o
14 the calcitonin receptor (CTR) interact with receptor activity-modifying protein 1 (RAMP1) at the cel
15 citonin receptor-like receptor (CLR) and the receptor activity-modifying protein 1 (RAMP1) comprise a
16 calcitonin receptor-like receptor (CLR) and receptor activity-modifying protein 1 (RAMP1), and the d
17 ith calcitonin receptor-like receptor (CLR), receptor activity-modifying protein 1 (RAMP1), beta-arre
18 Our findings demonstrate that a single gene, receptor activity-modifying protein 1 (RAMP1), can be a
19 calcitonin receptor-like receptor (CLR) and receptor activity-modifying protein 1 (RAMP1), respectiv
21 receptor (calcitonin receptor-like receptor/receptor activity modifying protein-1, CLR/RAMP1) implic
22 in vitro and in vivo by expression of human receptor activity-modifying protein-1 (hRAMP1), an oblig
23 evealed marked anatomical gradients for both receptor activity-modifying protein-1 (RAMP-1) and calci
24 lcitonin receptor-like receptor (Calcrl) and receptor activity modifying protein 2/3, are highly expr
25 citonin receptor-like receptor (CLR) and the receptor activity-modifying protein 2 (RAMP2) comprise a
26 hrough calcitonin receptor-like receptor and receptor activity-modifying protein 2 and modulates lung
27 ADM, calcitonin receptor-like receptor, and receptor activity-modifying protein 2 in vitro decreased
28 calcitonin receptor-like receptor (CLR), and receptor activity-modifying proteins 2 and 3 (RAMP2 and
29 iation with the receptor-interacting protein receptor activity-modifying protein-2 (RAMP2), and the r
30 through the calcitonin receptor (CalcR) and receptor activity modifying protein 3 (RAMP3) to inhibit
31 e calcitonin receptor (CTR) and one of three receptor activity-modifying proteins, are promising obes
33 ptor, calcitonin receptor-like receptor, and receptor activity-modifying proteins in human microvesse
34 mbrane-domain proteins, which we have called receptor-activity-modifying proteins or RAMPs, are expre
36 eceptor (CRLR) with different members of the receptor activity modifying protein (RAMP) family, which
38 CR) which requires coexpression of different receptor activity modifying proteins (RAMP) to become a
40 r the human calcitonin receptor (CTR), human receptor activity-modifying protein (RAMP)-1, RAMP1 (AMY
41 A library, we isolated a cDNA clone encoding receptor activity-modifying protein (RAMP)-like triterpe
43 ptor (CLR), which heterodimerizes with three receptor activity-modifying proteins (RAMP1-3) that dete
46 alcitonin receptor-like receptor (CRLR), and receptor activity modifying proteins (RAMPs) have become
55 or-like receptor (CRLR) and one of the three receptor activity-modifying proteins (RAMPs) showed that
56 ified an interaction of CXCR4 and ACKR3 with receptor activity-modifying proteins (RAMPs), and RAMP3
57 er of GPCRs have been shown to interact with receptor activity-modifying proteins (RAMPs), which can