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1 sents the first successful purification of a chemoattractant receptor.
2 MP did inhibit the response to formylpeptide chemoattractant receptor.
3 s, we disrupted a gene that encodes a single chemoattractant receptor.
4 CL12 (SDF-1) but does not act as a classical chemoattractant receptor.
5 gand binding pocket of an eicosanoid-binding chemoattractant receptor.
6 otrimeric G protein that couples to the cAMP chemoattractant receptors.
7 to the lung is mediated by G alpha i-coupled chemoattractant receptors.
8 o the lung is an active process dependent on chemoattractant receptors.
9 expression of 'tissue-specific' adhesion and chemoattractant receptors.
10  in transcriptional regulation downstream of chemoattractant receptors.
11 r of seven-membrane span receptors including chemoattractant receptors.
12  of intracellular calcium, and exocytosis by chemoattractant receptors.
13 ory effect was specific for some but not all chemoattractant receptors.
14 yotic cells does not require polarization of chemoattractant receptors.
15 ed from murine eosinophils to identify novel chemoattractant receptors.
16 one of the most thoroughly studied leukocyte chemoattractant receptors.
17  gradient-induced asymmetric distribution of chemoattractant receptors.
18  the family of leukocyte, G protein-coupled, chemoattractant receptors.
19  human L-selectin along with human leukocyte chemoattractant receptors.
20 ty of G alpha(i2) protein that is coupled to chemoattractant receptors.
21 d fibrosarcoma cells downstream of activated chemoattractant receptors.
22 al RBL cells or cells transfected with other chemoattractant receptors.
23 seudopod region induced by G-protein coupled chemoattractant receptors.
24                              Human leukocyte chemoattractant receptors activate chemotactic and cytot
25                     As PAF and formylpeptide chemoattractant receptors activate PLC via different G p
26                               Signaling from chemoattractant receptors activates the cytoskeleton of
27                          We propose that for chemoattractant receptors agonist-induced phosphorylatio
28                                              Chemoattractant receptors also control leukocyte egress
29                                    Activated chemoattractant receptors also dock G protein-coupled re
30 odes a 130-kD cytosolic protein required for chemoattractant receptor and G protein-mediated activati
31 dification of the cells for their display of chemoattractant receptors and endothelial-cell-binding m
32                                              Chemoattractant receptors and G proteins are fairly even
33  involved in PLC beta2 activation by the two chemoattractant receptors and suggest that in COS-7 cell
34 an be phosphorylated following engagement of chemoattractant receptors and suggest that this may be a
35            A wide array of chemoattractants, chemoattractant receptors, and adhesion molecules expres
36  differences in mRNA for adhesion molecules, chemoattractant receptors, and cytokines compared with o
37 id and selective cross-inactivation of other chemoattractant receptors, and suggest that FPR1 is able
38 tivation and heterologous desensitization of chemoattractant receptors are involved in the inhibition
39 ts at the leading edge of a cell even though chemoattractant receptors are uniformly distributed on t
40 ation of cell surface adhesion molecules and chemoattractant receptors as the cells mature.
41 Thus neutrophils do not actively concentrate chemoattractant receptors at the leading edge during che
42 These observations elucidate a novel role of chemoattractant receptor, BLT-1, in promoting monocyte t
43  The G protein-coupled 7 transmembrane (STM) chemoattractant receptors can be inactivated by heterolo
44                                      Several chemoattractant receptors can support agonist-induced, i
45 lpha and beta chemokine as well as classical chemoattractant receptors can trigger robust adhesion as
46     Unlike most other cellular proteins, the chemoattractant receptor, cAR1, of Dictyostelium is resi
47                                     The cAMP chemoattractant receptor, cAR1, of Dictyostelium transdu
48 hat 6CK/SLC is an agonist for the lymphocyte chemoattractant receptor, CCR7 (EBI-1, BLR-2), previousl
49 urchin species-specific differences in sperm chemoattractant-receptor characteristics we show that re
50 ere enriched in their expression of specific chemoattractant receptors compared with peripheral blood
51 tor shares greatest sequence similarity with chemoattractant receptors compared with prostanoid recep
52                            Unlike Gi-coupled chemoattractant receptors, D2R activated NF-kappaB witho
53                               To visualize a chemoattractant receptor directly during chemotaxis, we
54                     The PAFR and the peptide chemoattractant receptors do not cross-regulate each oth
55 stribution of CD4(+) T cells directed by the chemoattractant receptor Ebi2.
56 l DC2 (cDC2), we discuss the contribution of chemoattractant receptors (EBI2 or GPR183, S1PR1, and CC
57  mediated by CC chemokine receptor (CCR)9, a chemoattractant receptor expressed at high levels by ess
58 myl peptide receptor (FPR) is a prototypical chemoattractant receptor expressed in neutrophils.
59 ide receptor 1 (FPR1) is a G protein-coupled chemoattractant receptor expressed mainly on leukocytes.
60 es calcium signaling of a discrete subset of chemoattractant receptors expressed by human leukocytes.
61 n atopic asthmatics to define the pattern of chemoattractant receptor expression on recruited T cells
62                                     The cAMP chemoattractant receptor family of Dictyostelium discoid
63 n of CMKLR1 (chemokine-like receptor 1), the chemoattractant receptor for chemerin, and was abrogated
64 s conclusively demonstrate that CB2 is not a chemoattractant receptor for murine macrophages.
65 ch requires that leukocytes display multiple chemoattractant receptors for successful homing and prov
66 n sites is partly driven by N-formyl peptide chemoattractant receptors (FPRs).
67 bits chemotaxis of neutrophils by preventing chemoattractant receptors from activating trimeric G pro
68 o IL-8 does not appear to be due to impaired chemoattractant receptor function, as the number of IL-8
69 ing the involvement of G protein subunits in chemoattractant receptor function.
70 y altered protrusive activity, bypassing the chemoattractant receptor/G-protein network.
71 ion, a phenomenon found in analysis of other chemoattractant receptor genes.
72                                   The orphan chemoattractant receptor GPR15 mediates regulatory T cel
73 ated with increased expression of the orphan chemoattractant receptor GPR15 on these cells.
74 stinal plasma cells sense oxysterols via the chemoattractant receptor GPR183 and couple their tissue
75                                          The chemoattractant receptor GPR35 is expressed by granulocy
76 eosinophils (both resting and activated) and chemoattractant receptor homolog expressed on Th2 cells
77 , D-type prostanoid (DP) and, in particular, chemoattractant receptor homologous molecule expressed o
78            The D-prostanoid receptor and the chemoattractant receptor homologous molecule expressed o
79                        Pathogenic responses--chemoattractant receptor homologous molecule expressed o
80 through 2 GPCRs, d-type prostanoid 1 and the chemoattractant receptor homologous molecule expressed o
81 ly mediated by the prostaglandin D2 receptor chemoattractant receptor homologous molecule on T(H)2 ce
82                  15dPGJ2 is a ligand for the Chemoattractant Receptor Homologous to the T helper 2 ce
83 ecules such as thymic stromal lymphopoietin, chemoattractant-receptor homologous molecule expressed o
84                                       CRTh2 (chemoattractant-receptor homologous molecule expressed o
85  established that interaction of PGD(2) with chemoattractant receptor- homologous molecule expressed
86 4 and IL-5) and chemotactic receptors (CCR4, chemoattractant receptor-homologous molecule expressed o
87            Dexamethasone inhibited (P = .04) chemoattractant receptor-homologous molecule expressed o
88 oid receptors (DPs) DP1 and DP2 (also called chemoattractant receptor-homologous molecule expressed o
89         AZD1981 is a selective antagonist of chemoattractant receptor-homologous molecule expressed o
90             peT(H)2 cells were identified as chemoattractant receptor-homologous molecule expressed o
91 hymic stromal lymphopoietin, as well as oral chemoattractant receptor-homologous molecule expressed o
92 of CD203c(bright), CD63(+), and CD107a(+) on chemoattractant receptor-homologous molecule expressed o
93 T2, the receptor for the cytokine IL-33, and chemoattractant receptor-homologous molecule expressed o
94  D prostanoid receptor 2 (DP2; also known as chemoattractant receptor-homologous molecule expressed o
95 as tested by using TM30089, an antagonist of chemoattractant receptor-homologous molecule expressed o
96                                              Chemoattractant receptor-homologous molecule expressed o
97                  The prostaglandin (PG) D(2)-chemoattractant receptor-homologous molecule expressed o
98  on 3 G protein-coupled receptors, including chemoattractant receptor-homologous molecule expressed o
99 ses through a high-affinity interaction with chemoattractant receptor-homologous molecule expressed o
100 mbrane-spanning/G protein-coupled receptors, chemoattractant receptor-homologous molecule expressed o
101                                          The chemoattractant receptor-homologous molecule expressed o
102 n eosinophil/mast cell densities, density of chemoattractant receptor-homologous molecule expressed o
103 ndin D2 (PGD2) acting at the CRTH2 receptor (chemoattractant receptor-homologous molecule expressed o
104                                          The chemoattractant receptor-homologous molecule expressed o
105                                          The chemoattractant receptor-homologous molecule expressed o
106                                              Chemoattractant receptor-homologous molecule on Th2 cell
107 SCR1 bound to and physically interacted with chemoattractant receptor-homologous molecule(CRTH2), whi
108 bitors that suppress inflammation (targeting chemoattractant receptor-homologous molecules expressed
109 roperties of a series of clinically relevant chemoattractant receptor-homologous molecules expressed
110      However, the ability of CB2 to act as a chemoattractant receptor in macrophages remains largely
111 To study the biology of individual leukocyte chemoattractant receptors in a defined lymphoid environm
112  tissue, we performed expression analyses of chemoattractant receptors in a related family that inclu
113 ctions resulting from Galpha(16) coupling of chemoattractant receptors in a transfected cell model sy
114 view recent advances in our understanding of chemoattractant receptors in disease pathogenesis, with
115 G-protein-coupled receptors that function as chemoattractant receptors in innate immune responses.
116 s, LPS selectively modulates the function of chemoattractant receptors in microglia and may promote h
117 e receptor-mediated desensitization of bound chemoattractant receptors in neutrophils.
118 mphocyte trafficking, but the involvement of chemoattractant receptors in the physiologic recruitment
119 or CCR6 and CXCR3, in conjunction with other chemoattractant receptors, in the recruitment of inflamm
120 eutrophils infiltrate the joint via multiple chemoattractant receptors, including the leukotriene B(4
121                     These data indicate that chemoattractant receptors induce chemokine production in
122 inhibitor, staurosporine, completely blocked chemoattractant receptor-induced phosphorylation of L-se
123 is study, we have investigated whether human chemoattractant receptors internalize via clathrin-coate
124 cking, we integrate a number of nonchemokine chemoattractant receptors into our discussion.
125 tion of siRNA to silence a G protein-coupled chemoattractant receptor involved in inflammation and su
126                            Signaling through chemoattractant receptors involves a standard G-protein-
127                A family of G-protein-coupled chemoattractant receptors is known to mediate the transp
128                 Leukocyte activation through chemoattractant receptors leads to Pak activation and tr
129 eraction with D prostanoid receptor (DP) and chemoattractant receptor-like molecule expressed on Th2
130 or receptors, D prostanoid receptor (DP) and chemoattractant receptor-like molecule on the Th2 cell.
131  phosphorylation in cross-desensitization of chemoattractant receptors, M2CXCR1 was coexpressed with
132 is that interaction between autoantigens and chemoattractant receptors may be an important step in th
133                                     However, chemoattractant receptors may couple to more than one ty
134 zed that signaling through G protein-coupled chemoattractant receptors may stimulate cytokine product
135 ver, the regulatory role of TRPC channels in chemoattractant receptor-mediated signaling has not yet
136 ymmetric macromolecular complex formation of chemoattractant receptors mediates gradient sensing and
137 ress this issue, we purified cAR1, the major chemoattractant receptor of Dictyostelium discoideum by
138 ere that elimination of phosphorylation of a chemoattractant receptor of Dictyostelium, either by sit
139 ormyl peptide receptor 2 (FPR2), a classical chemoattractant receptor of G-protein-coupled receptors,
140                                              Chemoattractant receptors of the serpentine, heterotrime
141 g with HIV-1 fusion cofactors, downregulates chemoattractant receptors on monocytes by a CD4-dependen
142                    While the localization of chemoattractant receptors on randomly oriented cells has
143 20, implying the contribution of alternative chemoattractant receptors other than spingosine 1-phosph
144 he apparent functional redundancy with other chemoattractant-receptor pairs in vitro, LTB(4) and BLTR
145  mediated through additional Galphai-coupled chemoattractant receptor pathways, including CCR5.
146                                    Leukocyte chemoattractant receptors play key roles in the pathogen
147                                              Chemoattractant receptors regulate leukocyte accumulatio
148                            Since many of the chemoattractant receptors regulated by cADPR bind to lig
149       To define the molecular basis of human chemoattractant receptor regulation, rat basophilic leuk
150                                        While chemoattractant receptors rely upon canonical G-protein
151                  Therefore, we conclude that chemoattractant receptors require Galphai subunits only
152                  These findings suggest that chemoattractant receptors require PANX1 to trigger excit
153                                High-affinity chemoattractant receptors responsible for PMN chemotaxis
154                            G-protein-coupled chemoattractant receptors signal transiently upon ligand
155 ould explain the inhibition of formylpeptide chemoattractant receptor signaling by cAMP.
156 rophil migration requires B(2) integrins and chemoattractant receptor signaling for motility and dire
157 pear to be critical downstream components of chemoattractant receptor signaling in human neutrophils,
158              Here we show how LN anatomy and chemoattractant receptor signaling organize B lymphocyte
159 sensitivity to background signals, prolonged chemoattractant receptor signaling, and inappropriate CX
160 ein kinase A (PKA) activation, which blocked chemoattractant receptor signaling.
161 nits remain GTP bound, RGS proteins modulate chemoattractant receptor signaling.
162 or chemotaxis and phagocytosis indicate that chemoattractant receptor-signaling is not essential for
163               These data suggest that of the chemoattractant receptors studied, G-protein usage varie
164 esponding to fMLF, a peptide agonist for two chemoattractant receptor subtypes, formyl peptide recept
165 egulation of Th1/2 effector tissue-targeting chemoattractant receptors such as CCR4, CCR5, CXCR6, and
166 ollowing the activation of G-protein coupled chemoattractant receptors such as CXCR2 whose signaling
167                              Galphai-coupled chemoattractant receptors, such as the 5-oxo-6E,8Z,11Z,1
168 B4, did not inhibit the responses of peptide chemoattractant receptors, suggesting distinct signaling
169          The selectin adhesion molecules and chemoattractant receptors synergistically regulate leuko
170 Thus, the 5-HIAA-GPR35 axis is an eosinophil chemoattractant receptor system that modulates the clear
171 lls that differentially express adhesion and chemoattractant receptors targeting them to the correspo
172 rect T cell expression of these adhesion and chemoattractant receptors, targeting the resulting effec
173        Formyl peptide receptor 2 (FPR2) is a chemoattractant receptor that recognizes proinflammatory
174                                 GPR15 is the chemoattractant receptor that regulates T-cell migration
175 he innate immune system express adhesion and chemoattractant receptors that allow them to migrate dir
176                                  To identify chemoattractant receptors that control this homing patte
177 uishable by their expression of adhesion and chemoattractant receptors that directed their homing to
178 cking programs (combinations of adhesion and chemoattractant receptors) that target their migration t
179 geted disruption of two abundantly expressed chemoattractant receptors, the receptors for C3a and C5a
180  the expression and function of a variety of chemoattractant receptors through a process of heterolog
181 CAM-1, suggesting common mechanisms coupling chemoattractant receptors to activation of distinct inte
182                            Redistribution of chemoattractant receptors to the anterior pole of a pola
183             The signaling pathways that link chemoattractant receptors to the cytoskeleton and cellul
184 aling pathway leading from G protein-coupled chemoattractant receptors to the generation of oxidants
185 gest that Rho participates in signaling from chemoattractant receptors to trigger rapid adhesion in l
186                               Ligand-engaged chemoattractant receptors trigger Galpha(i) subunit nucl
187              Activation of G-protein-coupled chemoattractant receptors triggers dissociation of Galph
188  of the overall structure of other chemokine/chemoattractant receptors, underscoring an important evo
189 ally expressed in neutrophils, and acts as a chemoattractant receptor via an Akt-dependent pathway.
190 vation takes place through G protein-coupled chemoattractant receptors via a pathway that requires ho
191 , following segmental allergen challenge, no chemoattractant receptor was specifically increased.
192          Interactions between L-selectin and chemoattractant receptors were therefore examined using

 
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