ライフサイエンスコーパス: CC chemokine receptor

1 dies indicate the potential involvement of a CC chemokine receptor.

2 gesting that MIP-3alpha acts through a novel CC chemokine receptor.

3 cture (CLP), blood PMN demonstrated mRNA for CC chemokine receptors.

4 is an orphan receptor with homology to other CC chemokine receptors.

5 ne receptor CXCR4 as well as to a variety of CC chemokine receptors.

6 n L1.2 cells tranfected with seven different CC chemokine receptors.

7 unusual among known CC chemokines and known CC chemokine receptors.

8 CC chemokine receptor 1 (CCR1) is expressed in neutrophi

9 CC chemokine receptor 1 (CCR1) is found on a variety of

10 nal down-modulation of the RANTES receptors, CC chemokine receptor 1 and CC chemokine receptor 5, dur

11 The total CC chemokine receptor 1 pool (surface and intracellular

12 ES was directly correlated with the level of CC chemokine receptor 1 surface expression.

13 cal laser scanning microscopy showed reduced CC chemokine receptor 1, but not CC chemokine receptor 5

14 inal tail), and 2) the N-terminal segment of CC chemokine receptor 1, which does not bind CXC chemoki

15 CC chemokine receptors 1 and 3 (CCR1 and CCR3) are expre

16 essing a hemagglutinin-tagged version of the CC-chemokine receptor 1 (CCR1), and using these reagents

17 dial smooth muscle cells, express functional CC chemokine receptor-1 (CCR1) and respond to RANTES by

18 The CC chemokine receptor-1 (CCR1) is a prime therapeutic ta

19 ession (IL-2, -4, -6, -10, and IFN-gamma and CC chemokine receptor-1 [CCR1]) was assayed in the lymph

20 uctures of PXR LBD with Adnectin-1 and CCR1 (CC chemokine receptor-1) antagonist Compound-1 were dete

21 CC chemokine receptor 10 and its ligand, CCL27, are impo

22 m of vitamin D3, signaled T cells to express CC chemokine receptor 10, which enabled them to migrate

23 Disruption of CC chemokine receptor 2 (CCR2) abolished both CNS inflam

24 CC Chemokine Receptor 2 (CCR2) and its endogenous ligand

25 ing restrictions to a linear aminobutyramide CC chemokine receptor 2 (CCR2) antagonist lead (2) led t

26 ocyte chemotactic protein-1 [MCP-1]) and its CC chemokine receptor 2 (CCR2) are critical regulators o

27 The CC chemokine ligand 2 (CCL2) and CC chemokine receptor 2 (CCR2) are expressed in the hear

28 Therefore, using CC chemokine receptor 2 (CCR2) as a GPCR model, we synth

29 Activation of CC chemokine receptor 2 (CCR2) by its cognate chemokine

30 Presently, we investigated the role of CC chemokine receptor 2 (CCR2) in acute EAE.

31 n the present study we addressed the role of CC chemokine receptor 2 (CCR2) in M. tuberculosis infect

32 CC chemokine receptor 2 (CCR2) is a part of the chemokin

33 CC chemokine receptor 2 (CCR2) is a prominent receptor f

34 CC chemokine receptor 2 (CCR2) is essential to acute ske

35 Here we report that CC chemokine receptor 2 (CCR2) is highly expressed on a

36 CC chemokine receptor 2 (CCR2) is one of 19 members of t

37 with relatively high numbers of parasites in CC chemokine receptor 2 (CCR2) KO mice, indicating that

38 dels that the expression of the inflammatory CC chemokine receptor 2 (CCR2) on donor-derived CD8+ T c

39 We show that inhibition of CC chemokine receptor 2 (CCR2) receptor signaling with p

40 n 1 (MCP-1) peptide amphiphile micelles bind CC chemokine receptor 2 (CCR2) that is upregulated in sy

41 huGFAP-CCL2hi tg+ mice lacking CC chemokine receptor 2 (CCR2) were normal, showing that

42 Signaling between the CC chemokine receptor 2 (CCR2) with its ligand, monocyte

43 Herein, we describe a soluble mimic of CC chemokine receptor 2 (CCR2), dubbed CROSS-N(2)E3(2),

44 CC chemokine ligand 2 (CCL2), a ligand of CC chemokine receptor 2 (CCR2), is essential to mount an

45 man brain microvessels, which suggested that CC chemokine receptor 2 (CCR2), the recognized receptor

46 CC chemokine receptor 2 (CCR2)-/-embryos display an iden

47 egeneration was examined in mice lacking the CC chemokine receptor 2 (CCR2).

48 ssion (CC chemokine ligand [CCL]5, CCL2, and CC chemokine receptor 2 [CCR2]) remained unchanged.

49 ice was reduced by 67%, but was unaltered in CC chemokine receptor 2(-/-) (CCR2(-/-)), CCR3(-/-), or

50 ory chemokine/receptor and cytokines (MCP-1, CC chemokine receptor 2, and interleukins 1beta and 6),

51 CC chemokine receptors 2 (CCR2) and 5 (CCR5) are involve

52 are rapidly mobilized upon inflammation in a CC-chemokine receptor 2-dependent manner, and the noncla

53 6- and 2.4-fold increases in Ly6-C(high) and CC-chemokine receptor 2-positive cells in lesions of apo

54 Here, we find inflammatory-related CC-chemokine-receptor 2 (Ccr2) expression in non-hematop

55 To understand the regulation of CC chemokine receptor 3 (CCR3) expression, its gene stru

56 The CC chemokine receptor 3 (CCR3) is expressed by eosinophi

57 The CC chemokine receptor 3 (CCR3) plays an important role i

58 axin induces chemotaxis mediated through the CC chemokine receptor 3 (CCR3) present on basophils as w

59 y activity is demonstrated to be mediated by CC chemokine receptor 3 (CCR3).

60 CC chemokine receptor-3 (CCR-3) is a major receptor invo

61 g with our previously described(20) class of CC chemokine receptor-3 (CCR3) antagonist, we improved t

62 Eotaxin and other CC chemokines acting via CC chemokine receptor-3 (CCR3) are believed to play an i

63 actic and activating peptides acting through CC chemokine receptor-3 (CCR3).

64 Mogamulizumab is a humanized anti-CC chemokine receptor 4 (CCR4) antibody approved for the

65 This study demonstrates that expression of CC chemokine receptor 4 (CCR4) by DCs is required for EA

66 The role of CC chemokine receptor 4 (CCR4) during the development an

67 ive of this study was to examine the role of CC chemokine receptor 4 (CCR4) in macrophage polarizatio

68 CC chemokine receptor 4 (CCR4) is expressed by Th2 and r

69 One candidate, CC chemokine receptor 4 (CCR4), is expressed by innate a

70 ve also examined the interaction of MDC with CC chemokine receptor 4 (CCR4), recently shown to be a r

71 amulizumab, a defucosylated, humanized, anti-CC chemokine receptor 4 monoclonal antibody, in 41 pretr

72 However, this is not related to CC chemokine receptor 4, cutaneous lymphocyte-associated

73 ecurrent somatic mutations in CCR4, encoding CC chemokine receptor 4.

74 e in the airways of allergic mice upregulate CC-chemokine receptor 4 (CCR4) expression.

75 ssion of coreceptors, cytokine regulation of CC chemokine receptor 5 (CCR5) and CD4 expression on mon

76 The differential use of CC chemokine receptor 5 (CCR5) and CXC chemokine recepto

77 In particular, immature DC express CC chemokine receptor 5 (CCR5) and migrate in response t

78 matory proteins 1alpha and 1beta to activate CC chemokine receptor 5 (CCR5) and the ability to inhibi

79 T-cell expression levels of CC chemokine receptor 5 (CCR5) are a critical determinan

80 independent of the presence of a mutation in CC chemokine receptor 5 (CCR5) associated with resistanc

81 iency virus-HIV chimera (SHIV) that uses the CC chemokine receptor 5 (CCR5) co-receptor.

82 In the current study, we characterized CC chemokine receptor 5 (CCR5) expression and function o

83 CC chemokine receptor 5 (CCR5) functions physiologically

84 of a 32 bp deletion (Delta32) allele of the CC chemokine receptor 5 (CCR5) gene are reported to be m

85 CC chemokine receptor 5 (CCR5) has recently been identif

86 n the present study, we explored the role of CC chemokine receptor 5 (CCR5) in a murine model of chro

87 CC chemokine receptor 5 (CCR5) is a coreceptor for cellu

88 CC chemokine receptor 5 (CCR5) is a receptor for chemoki

89 CC Chemokine Receptor 5 (CCR5) is an important mediator

90 CC chemokine receptor 5 (CCR5) is expressed preferential

91 CC chemokine receptor 5 (CCR5) is prominently expressed

92 CC chemokine receptor 5 (CCR5) is the major HIV-1 corece

93 CC chemokine receptor 5 (CCR5) is the receptor for sever

94 The CC chemokine receptor 5 (CCR5) is used by the human immu

95 us 24-bp deletion (Delta24) was found in the CC chemokine receptor 5 (CCR5) of 11 out of 15 red-cappe

96 f the viral envelope glycoprotein gp120 with CC chemokine receptor 5 (CCR5) or CXC chemokine receptor

97 eptor, CD4, and through a coreceptor, either CC chemokine receptor 5 (CCR5) or CXC chemokine receptor

98 glycoproteins, CD4 and a coreceptor, usually CC chemokine receptor 5 (CCR5) or CXC receptor 4 (CXCR4)

99 We demonstrate that signaling through the CC chemokine receptor 5 (CCR5) prevents uncontrolled pos

100 laria-infected women contain 3 times as much CC chemokine receptor 5 (CCR5) RNA as placentas of women

101 s of HIV-1 require the cell-surface receptor CC chemokine receptor 5 (CCR5) to infect specific leukoc

102 globulin (Ig) G4 monoclonal antibody against CC chemokine receptor 5 (CCR5) with robust in vitro acti

103 estigated this issue in living cells for the CC chemokine receptor 5 (CCR5), a major receptor in infl

104 a32, a complete loss-of-function mutation in CC chemokine receptor 5 (CCR5), has been previously asso

105 of both CXC chemokine receptor 4 (CXCR4) and CC chemokine receptor 5 (CCR5), major coreceptors for T

106 Human CC chemokine receptor 5 (CCR5), mediates the activation

107 Expression of CC chemokine receptor 5 (CCR5), the major coreceptor for

108 Polymorphisms in CC chemokine receptor 5 (CCR5), the major coreceptor of

109 Genetic variation in CC chemokine receptor 5 (CCR5), the major HIV-1 corecept

110 8-coated beads are resistant to infection by CC chemokine receptor 5 (CCR5)-dependent HIV-1 isolates.

111 -SIGN1 is expressed on endothelial cells and CC chemokine receptor 5 (CCR5)-positive macrophage-like

112 CD25, CXC chemokine receptor 4 (CXCR4), and CC chemokine receptor 5 (CCR5).

113 lines by blocking interaction of gp120 with CC chemokine receptor 5 (CCR5).

114 deficiency virus type-1 (HIV-1) co-receptor, CC chemokine receptor 5 (CCR5).

115 These cells expressed high levels of CC chemokine receptor 5 and were commonly double negativ

116 CC chemokine receptor 5 antagonists are a new class of a

117 normal CD45 splicing and the presence of the CC chemokine receptor 5 deletion 32 (CCR5del32) allele,

118 SIV hosts from AIDS and the discovery of low CC chemokine receptor 5 expression on CD4+ T cells as a

119 The human gene for CC chemokine receptor 5, a coreceptor for human immunode

120 ANTES receptors, CC chemokine receptor 1 and CC chemokine receptor 5, during culture.

121 wed reduced CC chemokine receptor 1, but not CC chemokine receptor 5, expression by HaCaT cells at lo

122 viral burden and further implicate roles for CC chemokine receptor 5, macrophages, and Vpr in the lif

123 ll expressed and secreted), a ligand for the CC chemokine receptor 5, potently inhibits HIV-1 replica

124 macaques with CXC chemokine receptor 4- and CC chemokine receptor 5-specific simian/human immunodefi

125 ng genetic variants of their major receptor, CC chemokine receptor 5.

126 iruses were found to play important roles in CC-chemokine receptor 5 (CCR5) coreceptor utilization, a

127 To investigate nonhuman primate CC-chemokine receptor 5 (CCR5) homologue structure and f

128 The CC-chemokine receptor 5 (CCR5) is the major coreceptor f

129 t on macrophagetropic viruses that enter via CC-chemokine receptor 5 (CCR5), despite binding to the s

130 nce assay (HTRF) to quantify properly folded CC-chemokine receptor 5 (CCR5).

131 chemokine receptor 4 (CXCR4), but not of the CC-chemokine receptor 5 in purified populations of prima

132 detected for galactosyl ceramide but not for CC-chemokine receptor 5, CXC-chemokine receptor 4, or CD

133 vated by typical chemokine receptors such as CC-chemokine receptor-5 (CCR5).

134 Because CC chemokine receptor 6 (CCR6) deficiency affects the ge

135 The CC chemokine receptor 6 (CCR6) is a potential target for

136 as that of memory markers such as CD45RO and CC chemokine receptor 6 (CCR6).

137 r gut homing, as indicated by high levels of CC chemokine receptor 6 and integrin beta7 expression.

138 C-type chemokine that binds to and activates CC chemokine receptor-6 (CCR6).

139 A subset of CC chemokine receptor-6(+) (CCR6(+)), gammadelta-low (GD

140 CC chemokine receptor 7 (CCR-7) is expressed on mature d

141 In this study we identify residues on CC chemokine receptor 7 (CCR-7) that are involved in ago

142 that, even when LN retention signals such as CC chemokine receptor 7 (CCR7) are down-regulated, T cel

143 CC chemokine receptor 7 (CCR7) is expressed in IIP biops

144 s T helper 1 (Th1) effector memory cells and CC chemokine receptor 7 (CCR7)(+) cells resembling centr

145 Desensitization of the TCA-4 receptor, CC chemokine receptor 7 (CCR7), blocked T(GFP) cell adhe

146 ndary lymphoid chemokine (SLC), a ligand for CC chemokine receptor 7 (CCR7), has been demonstrated to

147 by functional deletion (desensitization) of CC chemokine receptor 7 (CCR7), the receptor for SLC and

148 xis of lymphocytes and DCs via its receptor, CC chemokine receptor 7 (CCR7).

149 ELC stimulated cells transfected with EBI-1/CC chemokine receptor 7 (CCR7).

150 CD27Lo CD28Lo CD45RA- CD62 ligand- (CD62L-) CC chemokine receptor 7- (CCR7-) interleukin-7 receptor

151 that migration to lymph nodes occurred in a CC chemokine receptor 7-independent manner but, overall,

152 Although the CC chemokine receptor 7-positive (CCR7+) population of b

153 mentation of LXA(4) identified modulation of CC-chemokine receptor 7 (CCR7) and sphingosine 1- phosph

154 CC-chemokine receptor 7 (CCR7) is expressed on the surfa

155 otaxis assay system, we demonstrate that the CC chemokine receptor-7 (CCR7) ligands 6Ckine and macrop

156 The CC-chemokine receptor-7 (CCR7) ligand CCL21 is required

157 CC chemokine receptor 8 (CCR8) has been detected in vitr

158 The CC chemokine receptor 8 (CCR8) is expressed on monocytes

159 The CC chemokine receptor 8 (CCR8) is expressed on monocytes

160 chemokine ligand 18 (CCL18), acting through CC chemokine receptor 8 (CCR8) on mononuclear cells, was

161 been increasing evidence indicating that the CC chemokine receptor 8 (CCR8) plays an important role i

162 svirus (KSHV) that selectively activates the CC chemokine receptor 8 (CCR8), for which the endogenous

163 sm depended on alpha(4) beta(7) integrin and CC chemokine receptor 9 (CCR9) expression by LSEC-primed

164 CC chemokine receptor 9 (CCR9) is a specific receptor fo

165 Here we report that GPR-9-6, now called CC chemokine receptor 9 (CCR9), is a receptor for thymus

166 CC chemokine receptor 9 (CCR9), which is a unique recept

167 Hence, GPR-9-6 has been designated as CC chemokine receptor 9 (CCR9).

168 re a gut-homing phenotype (alpha 4 beta 7(+) CC chemokine receptor 9(+)) and the capacity to home to

169 signaling by CC chemokine ligand 25 through CC chemokine receptor 9, and binding of the integrins al

170 r appears to be present in a large number of CC chemokine receptors and thereby could play a more gen

171 0), IL-1 binding proteins, G protein-coupled CC chemokine receptor, and epidermal growth factor-like

172 ors cyclo-oxygenase-2 and 5-lipoxygenase and CC chemokine receptor antagonist Met-RANTES.

173 uitment upon exposure to DEPs and that these CC chemokine receptors are important in the DEP-induced

174 CC chemokine receptors are important modulators of infla

175 in human T cells selectively through CCR8, a CC chemokine receptor associated with Th2 lymphocytes.

176 used CCR3 as an entry cofactor, despite this CC chemokine receptor being expressed on the cell surfac

177 ix (ECM) organization, mast cell activation, CC-chemokine receptor binding, circulating immunoglobuli

178 addition, we demonstrate that IL-15 induces CC chemokine receptors, but not CXC chemokine receptors,

179 or cells resulted in decreased expression of CC chemokine receptor (CCR) 1 and increased CCR7 express

180 icular, the content of T lymphocytes bearing CC chemokine receptor (CCR) 1, CCR3, and CCR5 receptors

181 Also, CXCR4 forms heteromers with CC chemokine receptor (CCR) 2, CCR5, the Na(+)/H(+) exch

182 nophil signaling molecules [eg, eotaxins and CC chemokine receptor (CCR) 3] in IL-13-mediated airway

183 CC chemokine receptor (CCR) 4 was dispensable for donor

184 CCR5Delta32, a 32-base pair deletion of the CC chemokine receptor (CCR) 5 gene, is associated with s

185 CC chemokine receptor (CCR) 5 plays a crucial role in th

186 CC chemokine receptor (CCR) 5 promotes inflammatory resp

187 The chemokine receptors CC chemokine receptor (CCR) 7 and CXC chemokine receptor

188 The authors compared CC chemokine receptor (CCR) expression by mouse liver my

189 Cytokine and CC chemokine receptor (CCR) gene expression was analyzed

190 ne receptor messenger RNA (mRNA) expression, CC chemokine receptor (CCR) protein activation during th

191 points to cross-talk between FcepsilonRI and CC chemokine receptor (CCR)-mediated signaling pathways

192 Human melanoma cells frequently express CC chemokine receptor (CCR)10, a receptor whose ligand (

193 We tested the hypothesis that the CC chemokine receptor (CCR)2 and CCR5 and the chemokine

194 Mice deficient for the major MCP-1 receptor, CC chemokine receptor (CCR)2, did not develop EAE after

195 Here we report that deficiency in CC chemokine receptor (CCR)2, the receptor for MCP-1, co

196 CD4 cells from allergic individuals express CC chemokine receptor (CCR)3 and CCR4 after expansion in

197 s, which uniformly express the TARC receptor CC chemokine receptor (CCR)4.

198 sted naloxone-induced down-regulation of the CC chemokine receptor (CCR)5 in NY1DD mice but not in co

199 HisRS selectively activated CC chemokine receptor (CCR)5-transfected HEK-293 cells,

200 xpression of CC chemokine ligand (CCL) 20, a CC chemokine receptor (CCR)6 ligand, in human keratinocy

201 led altered expression of the CCL20 receptor CC chemokine receptor (CCR)6, suggesting that Fpr2/3 reg

202 resses LC markers: E-Cadherin, Langerin, and CC chemokine receptor (CCR)6.

203 The mechanisms by which CC chemokine receptor (CCR)7 ligands are selectively pre

204 Responses to the CC chemokine receptor (CCR)7 ligands secondary lymphoid

205 L-selectin and required chemokines that bind CC chemokine receptor (CCR)7.

206 Recently, it has been shown that CC chemokine receptor (CCR)8 is selectively expressed by

207 re that vMIP-I is a specific agonist for the CC chemokine receptor (CCR)8 that is preferentially expr

208 This attraction is mediated by CC chemokine receptor (CCR)9, a chemoattractant receptor

209 CC-chemokine receptor (CCR) 6 is the only known receptor

210 erized PMN priming and maturation factor, on CC-chemokine receptor (CCR) expression in PMN was invest

211 This study investigates whether cytokine and CC-chemokine receptor (CCR) production by DCs stimulated

212 Mice with genetic deficiency of CC-chemokine receptor (CCR) type 5, the common receptor

213 n-1beta, monocyte chemoattractant protein-1, CC-chemokine receptor (CCR)-1, CCR2, CCR5, and F4/80) th

214 A genetic defect in a CC-chemokine receptor (CCR)-5, the principal coreceptor

215 CC-chemokine/CC-chemokine receptors (CCR), including CCR2/ MCP-1 (mon

216 e biology, we investigated the expression of CC chemokine receptors CCR1, CCR2, CCR3, CCR5, CXCR3, an

217 The receptor cavity shares six residues with CC-chemokine receptors CCR1 through CCR4, while seven re

218 When EGFP-NPs from CC chemokine receptor CCR2 knock-out mice were transplan

219 1, MCP-2, RANTES, MIG, IP-10, I-TAC, and two CC chemokine receptors CCR2 and CCR5 were highly express

220 We hypothesized that CC chemokine receptors CCR2, CCR5, and CCR6 critically m

221 blood vessels in the lungs by acting on the CC chemokine receptor CCR3, which is located on the leuk

222 ng assays, we determined that r129 binds rat CC chemokine receptors CCR3, CCR4, CCR5, and CCR7.

223 rmore that DARC hetero-oligomerizes with the CC chemokine receptor CCR5.

224 CC chemokine receptors CCR5 and CCR2 are both expressed

225 Multiple extracellular domains of the CC-chemokine receptor CCR5 are important for its functio

226 The CC-chemokine receptor CCR5 has been shown to be the majo

227 The CC-chemokine receptor CCR5 is required for the efficient

228 The CC-chemokine receptor CCR5 mediates fusion and entry of

229 reted), which are the natural ligands of the CC-chemokine receptor CCR5, inhibit replication of MT-2-

230 Here we demonstrate that, like the CC-chemokine receptors CCR5 and CCR2b, CXCR4 is posttran

231 Genetic variations in the CC chemokine receptor (CCR5) leading to reduced or absen

232 Among 11 surveyed chemokine receptors, only CC chemokine receptor (CCR5), CXC chemokine receptor (CX

233 e fluorescent ligand Mz437 (4) targeting the CC chemokine receptor CCR7 at an intracellular allosteri

234 zin-1-yl]ethoxy}ethanol (ZK 756326), for the CC chemokine receptor CCR8.

235 Here, we analyzed the role of the CC-chemokine receptor CCR8 for the biological functions

236 A subset of CC chemokines, acting through CC chemokine receptors (CCRs) 1 to 5, is instrumental in

237 cells in the joint, mediated in part by such CC chemokine receptors (CCRs) as CCR2 and CCR5, respecti

238 iral protein competes with the host cellular CC-chemokine receptors (CCRs), reducing inflammation and

239 , interleukin 1 receptor (IL-1R), and type 8 CC-chemokine receptors; cytokine binding proteins (BP),

240 Here we show that a promiscuous CC chemokine receptor, D6, can function as a coreceptor

241 The CC chemokine receptor encoded by the human cytomegalovir

242 ls transfected with human and murine CCR2, a CC chemokine receptor expressed on monocytes.

243 did translational studies to examine CXC and CC chemokine receptor expression by flow cytometry on ne

244 Thus, CCR2B is the first member of the CC chemokine receptor family shown to be a glycoprotein

245 hemotaxis does not occur at the level of the CC chemokine receptor for MCP-1, CCR2, since MIF does no

246 description of functional promoters for any CC chemokine receptor gene, and we speculate that the co

247 chromosome 3q22, which is distinct from most CC chemokine receptor genes at 3p21.

248 In an effort to map the closely linked CC chemokine receptor genes, we identified a novel chemo

249 Although CC chemokine receptors have been found predominantly on

250 EC is significant, more so as it and several CC chemokine receptors have been shown to serve as fusio

251 used to reveal expression of various CXC and CC chemokine receptors in human umbilical vein EC.

252 ration was associated with downregulation of CC chemokine receptors in renal macrophages.

253 rotein-coupled receptors that includes other CC chemokine receptors, INCB3344 is at least 100-fold se

254 r, PAF did not provide sufficient signal for CC chemokine receptor ligand 2 (CCL2) production in cell

255 putative seven transmembrane receptor, CCRL1-CC chemokine receptor like 1.

256 nines and tyrosines in the N-termini of many CC chemokine receptors suggests that these posttranslati

257 emonstrate that pUL21.5 protein is a soluble CC chemokine receptor that functions as a decoy to modul

258 ceptor US28 but do not express mRNA of other CC chemokine receptors that bind RANTES (CCR1, CCR4, CCR

259 In a DMD mouse model, mdx(5cv) mice, CC chemokine receptor type 2 (CCR2) deficiency diminishe

260 etic ablation or pharmacologic inhibition of CC chemokine receptor type 2 (CCR2) reduced macrophage (

261 in rectal tissue (both P < .001), and plasma CC chemokine receptor type 5 (CCR5) ligand (macrophage-i

262 reted), the ligands for HIV entry coreceptor CC chemokine receptor type 5.

263 CC chemokine receptor type 9 (CCR9) activation by CCL25

264 fected cells express mRNA of the CMV-encoded CC chemokine receptor US28 but do not express mRNA of ot

265 Thus, through expression of the CC chemokine receptor US28, CMV may utilize resident G p