ライフサイエンスコーパス: cluster of differentiation

1 e include T cells that are restricted to the cluster of differentiation 1 (CD1) family members, known

2 that lipid antigen presentation mediated by cluster of differentiation 1 (CD1) proteins for T cell a

3 gnaling via Toll-like receptor 2 but not the cluster of differentiation 1 protein receptor, despite n

4 1d molecules consist of a transmembrane CD1 (cluster of differentiation 1) heavy chain in association

5 he presence of proliferating TILs expressing cluster of differentiation 103, programmed cell death pr

6 andomization evidence, we prioritized CD109 (cluster of differentiation 109) as a gene for which hete

7 CL17 is expressed in CCR2(+) macrophages and cluster of differentiation 11b(+) conventional dendritic

8 ukin 17A (IL-17A)-green fluorescent protein, cluster of differentiation 11c (CD11c)/diphtheria toxin

9 The membrane-anchored receptor cluster of differentiation 14 (CD14) and the transmembra

10 bind mycobacteria, only homodimers also bind cluster of differentiation 14 (CD14) and Toll-like recep

11 Recently, Zanoni et al. reported that cluster of differentiation 14 (CD14) is required for LPS

12 Elevated systemic levels of soluble cluster of differentiation 14 (sCD14) have been associat

13 Soluble cluster of differentiation 14 (sCD14), beta-D-glucan (BD

14 ceptors 1 and 2 (sTNFr1 and sTNFr2), soluble cluster of differentiation 14 (sCD14), C-reactive protei

15 osures-LPS-binding protein (LBP) and soluble cluster of differentiation 14 (sCD14)-in relation to inc

16 l DNA) and host response indicators (soluble cluster of differentiation 14 [sCD14] and lipopolysaccha

17 17-DMAG treatment decreased cluster of differentiation 14 mRNA and LPS-induced nucle

18 ) by innate immune system is mediated by the cluster of differentiation 14/Toll-like receptor 4/myelo

19 Prior to LPS-stimulation, the LPS-receptor cluster-of-differentiation 14 (CD14) and Toll-like recep

20 ctivation and proteoglycan secretion and CD (cluster of differentiation) 14 to be a mediator of Aldo-

21 Cluster of differentiation 147 (CD147) is a multifunctio

22 The ISR coordinately induced cluster of differentiation 155 (CD155) and PD-L1, enhanc

23 found accumulation of hemoglobin-scavenging cluster of differentiation 163 (CD163)(+) macrophages in

24 Circulating levels of SLPI, monocyte cluster of differentiation 163 (CD163), human leukocyte

25 In particular, soluble CD163 (cluster of differentiation 163) and CXCL12 (chemokine [C

26 umor necrosis factor receptor 2, and soluble cluster of differentiation-163 (borderline), were associ

27 essential role for splenic CD169(+)Tim4(+) (cluster of differentiation 169(+); T cell immunoglobulin

28 Using CD (cluster of differentiation) 169-DTR (diphtheria toxin re

29 unction in cancer pathogenesis, we found the cluster of differentiation 177 (CD177), a known neutroph

30 Cluster of differentiation 1c (CD1c)-dependent self-reac

31 ion domain of the human immune cell receptor cluster of differentiation 2 (hCD2ad) were studied syste

32 Cluster of differentiation 20 (CD20) is a B cell membran

33 ects against the B-lymphocyte antigen called cluster of differentiation 20 (CD20) on a B-cell chronic

34 receptor, programmed cell death 1 ligand 1, cluster of differentiation 20 and chimeric antigen recep

35 CD206 (cluster of differentiation 206)-positive/CD43(+) AMs and

36 Cluster of differentiation-22 (CD22) belongs to the sial

37 beta coefficient: 0.56; 95% CI: 0.41, 0.72), cluster of differentiation 244 (CD244, beta: 0.35; 95% C

38 on of IFNG, TNF (tumor necrosis factor), and Cluster of Differentiation 247 (CD247) among Th cell gen

39 Cluster of differentiation 25-positive (CD25(+) ) forkhe

40 ated with increased levels of sCD27 (soluble cluster of differentiation 27) and BAFF (B-cell activati

41 ormation of a BsAb with two target antigens, cluster of differentiation 3 (CD3) and B-cell maturation

42 cell receptor (TCR) together with accessory cluster of differentiation 3 (CD3) molecules (TCR-CD3 co

43 with picomolar affinity fused to a humanized cluster of differentiation 3 (CD3)-specific single-chain

44 esion molecule (EpCAM) on tumor cells with a cluster of differentiation 3 epsilon (CD3epsilon) on T c

45 erentiation 68)-positive macrophage and CD3 (clusters of differentiation 3)-positive T-cell counts, r

46 othelial hyaluronan receptor 1 (LYVE-1), and cluster of differentiation 31 (CD31) by immunohistochemi

47 phorylated histone 3(+)/vimentin(+)/CD31(-) (cluster of differentiation 31) fibroblasts were higher i

48 In multivariable analysis, a 50% decrease in cluster of differentiation 34 (CD34+) or CD34+/vascular

49 The cluster of differentiation 34+ cell population was a pre

50 tic BM showed an inverse correlation between cluster of differentiation 34+HSCs and Model of End-Stag

51 r endothelial growth factor (VEGF), insulin, cluster of differentiation-34, and pancreatic duodenal h

52 approaches, we discovered that the membrane cluster of differentiation 36 (CD36) binds to and facili

53 We sequenced coding regions of the cluster of differentiation 36 (CD36) gene in 184 French

54 e secretagogue receptor 1a (GHS-R1a) and the cluster of differentiation 36 (CD36) receptor.

55 iled a mechanism by which scavenger receptor cluster of differentiation 36 (CD36) suppresses TAM infl

56 Consistent with this premise, cluster of differentiation 36 (CD36)(-/-) mice exhibited

57 G protein-coupled receptor 120 (GPR120) and cluster of differentiation 36 (CD36), in a spatiotempora

58 tical role for Trem-1 in the upregulation of cluster of differentiation 36 (CD36), thereby promoting

59 assette subfamily G member 5/8 (Abcg5/8) and cluster of differentiation 36 (Cd36), was lower in arsen

60 latory Element-Binding Proteins (SREBPs) and cluster of differentiation 36 (CD36).

61 shown unprecedented binding affinity to the cluster of differentiation 36 receptor (CD36) and abilit

62 n potent cyclic azapeptide modulators of the cluster of differentiation 36 receptor (CD36) identified

63 , selectivity, and modulator activity on the cluster of differentiation 36 receptor (CD36).

64 he conformational requirements of opioid and cluster of differentiation 36 receptor peptide ligands.

65 r fatty acid and glucose transporters, CD36 (cluster of differentiation 36) and GLUT4 (glucose transp

66 n of the fatty acid-handling molecules CD36 (cluster of differentiation 36) and LIPG (endothelial typ

67 CD36 (cluster of differentiation 36) is a scavenger receptor t

68 y acid (FA) transporter CD36 (FA translocase/cluster of differentiation 36) is the gatekeeper of card

69 av-1 is required for the expression of CD36 (cluster of differentiation 36) scavenger receptor.

70 -1 bonds are ten times lower than iRBC-CD36 (cluster of differentiation 36), a receptor that shows no

71 3TSR binding to its receptor, CD36 (cluster of differentiation 36), increased binding of CD3

72 n through the innate immunity receptor CD36 (cluster of differentiation 36), which, in turn, activate

73 olving exogenous PCSK9, as well as levels of cluster of differentiation 36, a fatty acid transporter,

74 TP citrate lyase, stearoyl-CoA desaturase 1, cluster of differentiation 36, carnitine palmitoyltransf

75 peptide 6 (GHRP-6) demonstrated a promising cluster of differentiation-36 receptor (CD36) binding af

76 the safety and efficacy of ORBCEL-C (CD362 [cluster of differentiation 362]-enriched, umbilical cord

77 ells, and B cells expressed higher levels of cluster of differentiation 38 (CD38) and CD69 but low le

78 uman leukocyte antigen (HLA) DR isotope, and cluster of differentiation 38 (CD38) expression by cervi

79 Cluster of differentiation 38 (CD38) is a type II transm

80 s of NAD+ catabolites produced by ectoenzyme cluster of differentiation 38 (CD38) that have been impl

81 jectives: To determine the role of AEC CD38 (cluster of differentiation 38) in promoting cellular agi

82 However, cluster of differentiation 38-positive (CD38(+) ) human

83 human immunodeficiency virus (HIV) receptor cluster of differentiation 4 (CD4) and coreceptors chemo

84 t through the downregulation of cell surface cluster of differentiation 4 (CD4) and major histocompat

85 proteins of potential therapeutic interest, cluster of differentiation 4 (CD4) and sortilin.

86 the patients had advanced HIV with a median cluster of differentiation 4 (CD4) count of 58 cells/L (

87 Cluster of differentiation 4 (CD4) is an important glyco

88 tween HIV-1 surface glycoprotein (gp120) and cluster of differentiation 4 (CD4) receptor extends beyo

89 How pathogenic cluster of differentiation 4 (CD4) T cells in rheumatoid

90 tructured questions focusing on HIV testing, cluster of differentiation 4 (CD4) testing, HIV viral lo

91 range, alone or in combination with soluble cluster of differentiation 4 (CD4)), enhanced spontaneou

92 and the density of inflammatory infiltrate, cluster of differentiation 4 (CD4)-positive and CD8(+) T

93 ) are sharply induced upon the activation of cluster of differentiation 4 (CD4)-positive and cluster

94 HCV/HIV-coinfected donors had median cluster of differentiation 4 count 210 cells/mm(3), and

95 le HIV RNA at time of transplant with median cluster of differentiation 4 count 499 cells/mm(3).

96 an immunodeficiency virus interacts with the cluster of differentiation 4 receptors and one of the tw

97 and S100A9 homodimers enhanced activation of cluster of differentiation 4(+) and 8(+) T cells, which

98 marily infects immune cells, such as CD(4+) (cluster of differentiation 4(+)) T lymphocytes (T cells)

99 or temsavir prevents the viral receptor CD4 (cluster of differentiation 4) from interacting with the

100 erived gene pathways and proteins in CD4(+) (cluster of differentiation 4) T cells (and specifically

101 significantly lowered the numbers of CD4(+) (cluster of differentiation 4) T cells (P=0.025), inflamm

102 type 2 inflammation, with roles for CD4(+) (cluster of differentiation 4) T-helper cell type 1 cells

103 Both single-pass (cluster of differentiation 4, CD4) and multiple-pass (G

104 mechano-regulators of the stability of human cluster of differentiation 4, receptor of HIV-1.

105 2-inducible T-cell kinase (Itk) signaling in cluster of differentiation 4-positive (CD4(+)) T cells p

106 expression from the HIV-1 LTR in coinfected cluster of differentiation 4-positive (CD4(+)) T lymphoc

107 tokine secreting frequencies of Mtb-specific cluster of differentiation 4-positive (CD4+) T cells wit

108 ytokines secreted from primary mouse CD4(+) (cluster of differentiation 4-positive) T cells, to disco

109 nority children with asthma.Methods: CD4(+) (cluster of differentiation 4-positive) Th cells from 59

110 attenuated blood-brain barrier damage, fewer cluster of differentiation 4-positive, IL-17A-positive T

111 ype I membrane protein constructs, including cluster of differentiation 4.

112 roinflammation caused by IFN-gamma-producing clusters of differentiation 4-positive (CD4(+)) T cells.

113 e (apolipoprotein E)-deficient mice with CD (cluster of differentiation) 4(+) or CD8(+) T cell-specif

114 CD (cluster of differentiation) 4(+) T-cell responses to APO

115 The CD (cluster of differentiation) 4:CD8 T-cell ratios were bet

116 ivation of the immune costimulatory molecule cluster of differentiation 40 (CD40) in Muller glia has

117 dy, targeting a c-Myc tag on CAR T cells and cluster of differentiation 40 (CD40), could also enhance

118 57.4 [43.4-87.2] pg/mL, P < 0.0001), soluble cluster of differentiation 40 ligand (7.0 +/- 2.2 versus

119 c risk factors, serum levels of LPS, soluble cluster of differentiation 40 ligand and p-selectin (two

120 biomarkers (soluble TNF receptor 1, soluble cluster of differentiation 40, and urinary collagen type

121 r large artery atherosclerosis included ABO, cluster of differentiation 40, apolipoprotein(a), and ma

122 algesia by HMWH is mediated by its action at cluster of differentiation 44 (CD44) and activation of i

123 inducers and basal-enriched molecules, while cluster of differentiation 44 (CD44) behaved in an oppos

124 3K/pAkt/NFkappaB)-signaling pathway, whereas cluster of differentiation 44 (CD44) binding and mammali

125 e 1 (TIMP1)/Matrix metallopeptidase 9 (MMP9)/Cluster of differentiation 44 (CD44) ternary complex, in

126 ti-hyperalgesia is mediated by its action at cluster of differentiation 44 (CD44), the cognate hyalur

127 algesia, an effect mediated by its action at cluster of differentiation 44 (CD44), the cognate hyalur

128 oxynucleotide antisense (AS-ODN) to mRNA for cluster of differentiation 44 (CD44), the cognate hyalur

129 Here, we show that homodimerization of a cluster-of-differentiation-44 or of pro-neuregulin-1 mon

130 tailed t-test) elevated signals representing cluster of differentiation 45 (80%; 95% confidence inter

131 ered aggregates of infiltrating inflammatory cluster of differentiation 45 (CD45)-positive cells.

132 noreactivity in the dorsal horn and Iba1 and cluster of differentiation 45 expression in the sciatic

133 Single-cell mRNA sequencing of CD45 (cluster of differentiation 45)(+) cells 3 and 7 days aft

134 (enhanced green fluorescent protein), CD45 (cluster of differentiation 45), CD31, CD34, podocin, and

135 matory protein 1, interleukin-1, P-selectin, cluster of differentiation 45-positive cells); and oxida

136 ons inversely correlating with the number of cluster of differentiation 45-positive inflammatory lesi

137 helial complement inhibitory proteins (CIPs) cluster of differentiation 46 and 55 (CD46 and CD55) reg

138 resence of anti-phagocytotic signals such as cluster of differentiation 47 (CD47) on the surface of t

139 Cluster of differentiation 47 (CD47) plays an important

140 The exact value of cluster of differentiation 47 (CD47), known as the "don'

141 Cluster of differentiation 47 blockade by magrolimab pro

142 l surface: the innate immune regulator CD47 (cluster of differentiation 47) and the adaptive immune c

143 rolimab is a monoclonal antibody that blocks cluster of differentiation 47, a don't-eat-me signal ove

144 -class humanized monoclonal antibody against cluster of differentiation 47, an antiphagocytic signal

145 sus-host disease (GVHD) and removal of CD52 (cluster of differentiation 52) for a survival advantage

146 te-associated protein 4, interleukin-10, and cluster of differentiation 59 compared to controls.

147 hese Trx1-overexpressing T cells exhibited a cluster of differentiation 62L(hi) (CD62L(hi)) central m

148 The subcellular localization of the cluster of differentiation 63 (CD63) tetraspanin and its

149 nic antigen-related cell adhesion molecule 6/cluster of differentiation 66c (C6).

150 Key markers of the UPR and cluster of differentiation 68 (CD68) as surrogate of inf

151 ed between microglial/macrophage activation (cluster of differentiation 68 immunostaining) and (11)C-

152 IL-8, intercellular adhesion molecule 1, and cluster of differentiation 68 was induced in alcohol-fed

153 n=26/27) and 31% (n=9/29) had elevated CD68 (clusters of differentiation 68)-positive macrophage and

154 Cluster of Differentiation 69 (CD69) is an endogenous ne

155 Recent studies identified cluster of differentiation 70 (CD70) as a promising targ

156 Cluster of differentiation 73 (CD73) converts adenosine

157 Blockade of MIF receptor cluster of differentiation 74 (CD74) but not of CXCR2 or

158 We hypothesized that cluster of differentiation 74 (CD74) downregulation on p

159 including the binding and activation of the cluster of differentiation 74 (CD74) receptor to mediate

160 activity in vitro and the activation of the cluster of differentiation 74 receptor in vivo, highligh

161 Cluster of differentiation 8 (CD8) is a cell surface gly

162 Highly phenotypically exhausted cluster of differentiation 8 (CD8) T cells expand in fre

163 performed a comprehensive mRNA profiling of cluster of differentiation 8 (CD8) T cells in a murine m

164 ster of differentiation 4 (CD4)-positive and cluster of differentiation 8 (CD8)-positive T cells and

165 Cluster of differentiation 8 knockout (CD8(-/-) ) and CD

166 decrease in the number of tumor-infiltrating cluster of differentiation 8(+) (CD8(+)) T cells in the

167 Depletion of cluster of differentiation 8(+) T cells and additional t

168 ted macrophages, and enhanced trafficking of cluster of differentiation 8(+) T cells, which exhibit d

169 7-color multiplex staining to evaluate CD8 (cluster of differentiation 8), CD68, PD-L1 (programmed d

170 re disease had increased proportions of CD8 (cluster of differentiation 8)-positive T cells expressin

171 d IMMULITE assay on blood natural killer and cluster of differentiation 8-positive (CD8(+) ) lymphocy

172 gue-Dawley rats, resulting in high levels of cluster of differentiation 8-positive (CD8(+) ) T-cell r

173 sulted in increased priming of OT-I T cells [cluster of differentiation 8-positive (CD8(+))] but decr

174 ller cells, innate lymphoid cells-2, and CD (cluster of differentiation)-8 T cells form prominent and

175 Programmed death ligand-1 (PD-L1) and cluster of differentiation 80/86 (CD80/86) interact with

176 Cluster of differentiation 81 (CD81) is a widely express

177 ata suggest that upon exposure to low pH and Cluster of Differentiation 81 (CD81), the amino terminus

178 ition, in a dose-dependent manner, either by cluster of differentiation 81 or envelope protein 2-spec

179 mpatibility complex I), and viral infection (cluster of differentiation 81).

180 We aimed to determine the role of CD (cluster of differentiation)-84 in acute ischemic stroke

181 ression of the immune response-related genes cluster of differentiation 8a (Cd8a), Cd14, and intercel

182 ha subunit or Tac, transferrin receptor, and cluster of differentiation 8a, unexpectedly displayed su

183 anoparticle tracking analysis), and markers (clusters of differentiation 9, 63, and 81 by immunoblot)

184 Homeobox 5 (NKX2-5)+ cardiomyocytes and 25% Cluster of Differentiation 90 OR (CD90)+ nonmyocytes opt

185 ncluding CD105 (or endoglin), Thy1 [or CD90 (cluster of differentiation 90)], and 6C3 [ENPEP glutamyl

186 -containing G protein-coupled receptor], CD [clusters of differentiation] 90, EpCAM [epithelial cell

187 G-protein-coupled receptors (AGPCRs)-namely cluster-of-differentiation 97 (CD97) and epidermal-growt

188 dilution and characterized in terms of their cluster of differentiation and T cell receptor V beta ph

189 cells were inhibited by an antibody against cluster of differentiation antigen 14 (CD14), an adhesio

190 chinery, resulting in the down-regulation of cluster of differentiation antigen 4 (CD4) and major his

191 elated apoptosis-inducing ligand (TRAIL) and cluster of differentiation (CD) 107a expression, which r

192 derived dendritic cells (DCs), lung-resident cluster of differentiation (CD) 11b(+) conventional DCs

193 T-lymphocyte-associated protein 4 (CTLA-4), cluster of differentiation (CD) 160, and CD244 was measu

194 n set), the key components haptoglobin (HP), cluster of differentiation (CD) 163, heme oxygenase-1 (H

195 IV showed greater activation, as measured by cluster of differentiation (CD) 38/human leukocyte antig

196 k the expression of ATP degrading ectoenzyme cluster of differentiation (CD) 39.

197 yclin-dependent kinase 1a (Cdkn1a or p21) in cluster of differentiation (CD) 4(+) T cells using murin

198 Antigen-primed cluster of differentiation (CD) 4+ T follicular helper (

199 stituted by thymocyte negative selection and cluster of differentiation (CD) 4+ thymic regulatory T (

200 Most intrahepatic cluster of differentiation (CD) 8-positive (CD8(+)) T ce

201 Cluster of differentiation (CD) antigens are expressed o

202 review will cover molecules included in the cluster of differentiation (CD) from CD1 to CD166 and ly

203 While flow cytometry and cluster of differentiation (CD) markers have revolutioni

204 In this study, we used a cluster of differentiation (CD) microarray to predict th

205 for cell classification rather than a single cluster of differentiation (CD) protein normally used in

206 arative lipidomics analysis shows that human cluster of differentiation (CD) proteins CD1a, CD1b, CD1

207 to the quantification of four cell-specific cluster of differentiation (CD) proteins used to count c

208 echnology, and almost the entire spectrum of cluster of differentiation (CD) surface markers has been

209 ith immunohistochemistry showing substantial cluster of differentiation (CD)-11b(+) macrophages and C

210 Cluster of differentiation (CD)-40 is a cell surface rec

211 Cluster of differentiation (CD)10(pos) and CD10(neg) neu

212 carried out to isolate single cell-derived, cluster of differentiation (CD)105-positive PDL clones a

213 Using WBM and matched cluster of differentiation (CD)138-selected tumor gene e

214 Cluster of differentiation (CD)14(+)/45(+) and CD31(+) c

215 mistry was performed for Factor XIIIa(+) and cluster of differentiation (CD)1a(+) immature DCs and CD

216 on and cytokine production in the absence of cluster of differentiation (CD)28-mediated costimulation

217 EpCAM(+) CD49f(hi) cells expressed cluster of differentiation (CD)29, CD133, and stem cell

218 alysis revealed that lymphomatous cells were cluster of differentiation (CD)3(+), gammadelta T-cell r

219 in cardiovascular diseases, we found reduced cluster of differentiation (CD)36 expression with reduce

220 -2 expression was suppressed by blocking the cluster of differentiation (CD)36 fatty acid translocase

221 The scavenger receptor cluster of differentiation (CD)36 protein was detected o

222 side triphosphate diphosphohydrolase [ENTPD; cluster of differentiation (CD)39] and ecto-5'-nucleotid

223 tology, in splenocyte fractions positive for cluster of differentiation (CD)3epsilon, CD4, CD8, CD62L

224 Spike-specific cluster of differentiation (CD)4 T cells and plasmablast

225 ditional end points included gluten-specific cluster of differentiation (CD)4 T-cell analysis with HL

226 -E2) involving autoantibody and autoreactive cluster of differentiation (CD)4(+) and CD8(+) T-cell re

227 pha-, IFNgamma-, and IL-17- and -4-producing cluster of differentiation (CD)4(+) cells as well as IL-

228 women exhibit a Th1 bias, we isolated naive cluster of differentiation (CD)4(+) T cells from periphe

229 ligand (CCL)8 results in the recruitment of cluster of differentiation (CD)4(+) T cells to supernata

230 l therapy (HAART) and their association with cluster of differentiation (CD)4+ and CD4+ nadir T-cell

231 is fungoides (MF) is a low-grade lymphoma of cluster of differentiation (CD)4+, CD45RO+, cutaneous le

232 Isolated B cells were stimulated with anti-cluster of differentiation (CD)40 antibodies and Toll-li

233 B) cells, and maintenance therapy based on a cluster of differentiation (CD)40/CD154 co-stimulation p

234 The cross-talk of cluster of differentiation (CD)40/CD40 ligand (CD40L) pl

235 flammatory T cell differentiation, including cluster of differentiation (CD)44 and CD80.

236 Y (sex-determining region Y) box (Sox)9(low) cluster of differentiation (CD)44(low)CD140(low) prechon

237 ge M1M2 phenotype [the ratio of inflammatory cluster of differentiation (CD)54+CD80 and proresolution

238 oleus, ccl2, interleukin (il)6, il1beta, and cluster of differentiation (cd)68 mRNA levels increased

239 F signals through 1 or more of its receptors cluster of differentiation (CD)74, CXC-motif chemokine r

240 recruitment of other immune cells, including cluster of differentiation (CD)8(+) and CD4(+) T cells,

241 Activation of naive cluster of differentiation (CD)8(+) cytotoxic T lymphocy

242 Cluster of differentiation (CD)8(+) T cells exist as nai

243 e checkpoint inhibitors (ICIs) indicate that cluster of differentiation (CD)8(+) T cells, by means of

244 odominant, HLA-B27-restricted, HCV-specific, cluster of differentiation (CD)8(+) T-cell epitope, nons

245 A*01(+) rhesus monkeys was only found in the cluster of differentiation (CD)8alpha/beta+ T lymphocyte

246 The T helper (Th)17 subset of cluster-of-differentiation (CD)4 T cells, which is ident

247 n markers (programmed death [PD]-1, 2B4, and cluster of differentiation [CD] 160) on T cells, the num

248 th-1 (PD-1)+ peripheral blood T cells (PD-1+ cluster of differentiation [CD]4+; 95% CI, 2.68-6.63; P

249 chemokine receptor 3 high-expressing) CD8+ (cluster of differentiation) effector T lymphocytes in th

250 a and RIalpha-P overexpression upregulated a cluster of differentiation genes, while downregulating t

251 an increase of the inflammatory CD14++CD16+ (cluster of differentiation) intermediate monocyte subset

252 h proteomic dataset allowed us to define the cluster of differentiation marker profiles of the ILC su

253 n a high-throughput screen of neutrophil CD (cluster of differentiation) marker expression and a thor

254 sion of chemokines, chemokine receptors, and clusters of differentiation markers by RNAase protection

255 and their hypothalamic microglia showed more cluster of differentiation molecule 11b (Cd11b) activati

256 al(-/-)) systemically increased expansion of cluster of differentiation molecule 11b (CD11b), lymphoc

257 hesion molecule-1, and the macrophage marker cluster of differentiation molecule 11b.

258 This motif was sufficient to target CD4 (cluster of differentiation molecule 4) molecules to inhi

259 Immunohistochemistry revealed positivity for cluster of differentiation (or CD) markers, which have b

260 In particular, intratumor human cluster of differentiation-positive (hCD14(+) ) cells co

261 holine acetyltransferase deletion in CD4(+) (cluster of differentiation) T cells.