ライフサイエンスコーパス: lectin-like

1 tors include members of the NKRP1 and C-type lectin-like 2 (CLEC2) gene families, which constitute ge

2 planin and collagen/fibrin receptors, C-type-lectin-like-2 (CLEC-2) and glycoprotein VI (GPVI), respe

3 Here, we report on the role of LOX-1, a lectin-like 52-kDa receptor for oxidized low density lip

4 1-3 and human alpha-defensin 5; HD5) have a lectin-like ability to bind glycosylated proteins.

5 ty of Sepharose 4B or GM1 but did retain the lectin-like ability to bind to immobilized galactose on

6 stress-inducible ligand for NKG2D, a C-type lectin-like activating immunoreceptor.

7 a preferential expansion of licensed, C-type lectin-like activating receptor Ly49H+ NK cells with inc

8 Murine natural killer cells (NK) express lectin-like activation and inhibitory receptors, includi

9 ly, bacteria that lacked PRP-binding and the lectin-like activities detected by binding to MG2 failed

10 detella pertussis also express proteins with lectin-like activities.

11 These interactions depend largely on a lectin-like activity associated with the Actinomyces ori

12 VCC also exhibits prominent lectin-like activity in interacting with beta1-galactosy

13 ta-glucans but not by mannans, implicating a lectin-like activity in recognition but distinct in spec

14 However, whether the lectin-like activity of PTx is responsible for its abili

15 These findings uncover the importance of the lectin-like activity of the polymeric FimA shaft rather

16 er, by using Escherichia coli expressing the lectin-like adhesin FimH and guinea pig erythrocytes in

17 coaggregation of streptococci occurs when a lectin-like adhesin on one streptococcal species recogni

18 mensal S. oralis functions as a receptor for lectin-like adhesins on other members of the dental plaq

19 oralis and related species are recognized by lectin-like adhesins on other members of the oral biofil

20 L-selectin (CD62L), a lectin-like adhesion molecule, mediates lymphocyte homin

21 FimH protein is a lectin-like adhesive subunit of type 1, or mannose-sensi

22 nction of the LG module in calcium-dependent lectin-like alpha-DG binding.

23 roperties of alpha- and theta-defensins, the lectin-like behavior of defensins may contribute to many

24 The CTD forms a lectin-like beta-sandwich and contains four strictly con

25 d bind to phospholipid membranes via tandem, lectin-like C domains.

26 killer cell Ig-like receptors (KIRs) and the lectin-like CD94/NKG2A heterodimer.

27 lobulin-like receptors (KIRs) and the C-type lectin-like CD94:NKG2 receptors.

28 FcepsilonRI subunits, associates with the ER lectin-like chaperone calnexin, but not the structurally

29 The lectin-like chaperone calreticulin (CRT) and the thiol o

30 The lectin-like chaperone calreticulin associates with HC-be

31 o the 48 kDa glycoprotein tapasin and to the lectin-like chaperone calreticulin, in a multicomponent

32 Calnexin is a lectin-like chaperone that binds to class I MHC molecule

33 For example, calreticulin, a quality-control lectin-like chaperone, interacts with glucosylated manno

34 ribonuclease (RNase) as specific ligands of lectin-like chaperones calnexin (CNX) and calreticulin (

35 promoting subsequent reassociation with the lectin-like chaperones calreticulin and calnexin.

36 that reglucosylated proteins associate with lectin-like chaperones in vivo and provide evidence that

37 Theta-defensins are lectin-like, cyclic octadecapeptides found in the leukoc

38 CL forms a homodimer resembling other C-type lectin-like dimers, NKp65 is monomeric.

39 al amino acid residues located in the C-type lectin-like domain (CTLD) and the sperm-coating protein/

40 It possesses a C-type lectin-like domain (CTLD) followed by a poorly character

41 rystal structure of the extracellular C-type lectin-like domain (CTLD) of human CD69 at 2.27 A resolu

42 ent receptor 3 (CR3) (CD11b/CD18) contains a lectin-like domain (LLD) that can alter leukocyte functi

43 uble yeast beta-glucan, a ligand for the CR3 lectin-like domain (LLD), in the priming of CR3(+) HPC i

44 e comprising the human tumor necrosis factor lectin-like domain (TIP domain) sequence, is currently b

45 fibronectin-like type II (FnII), and C-type lectin-like domain 1 (CTLD1) domains of PLA2R only under

46 Deletion of the N-terminal lectin-like domain and epidermal growth factor (EGF)-lik

47 Rather, the lectin-like domain appears to influence CD11b/CD18 bindi

48 reviously, we showed that the recombinant TM lectin-like domain binds to LPS and inhibits LPS-induced

49 remature termination codon in the C-terminal lectin-like domain found in most other ppGaNTase protein

50 xpression of a mutant form of TM lacking the lectin-like domain had no significant impact on metastas

51 A cavity in lectin-like domain III initiates docking through recogni

52 domain 1 (TMD1) to demonstrate the action of lectin-like domain in blocking Lewis Y antigen (LeY)-med

53 investigated the role of the thrombomodulin lectin-like domain in the host response to Gram-negative

54 me a detrimental role for the thrombomodulin lectin-like domain in the host response to sepsis caused

55 in can bind both Tir and Tir-M even when the lectin-like domain is disrupted.

56 2) The lectin-like domain is not sufficient for CD11b/CD18-C. a

57 we solved a crystal structure of the C-type lectin-like domain of a homologous protein, NKR-P1A, usi

58 inant C1qRp-Fc chimera containing the C-type lectin-like domain of C1qRp and found specific binding t

59 rystal structure of the extracellular C-type lectin-like domain of human Lox-1 reveals a heart-shaped

60 l-adhesion molecules, as interactors for the lectin-like domain of latrophilins.

61 terpret the solution structure of the C-type lectin-like domain of NKR-P1C using chemical cross-linki

62 Chemically induced shedding of the lectin-like domain of TBM resulted in significantly incr

63 n effect that appears to be dependent on the lectin-like domain of TBM.

64 LeY is a specific ligand of the recombinant lectin-like domain of thrombomodulin (TM).

65 not differ between groups, mice lacking the lectin-like domain of thrombomodulin displayed strongly

66 ue of Blood, Kuo et al have used recombinant lectin-like domain of thrombomodulin domain 1 (TMD1) to

67 The lectin-like domain of thrombomodulin has anti-inflammato

68 xposure to B. pseudomallei, mice lacking the lectin-like domain of thrombomodulin showed a survival a

69 Wild-type mice and mice lacking the lectin-like domain of thrombomodulin.

70 type mice (TM(wt/wt)) and mice that lack the lectin-like domain of TM (TM(LeD/LeD)), which is critica

71 Lack of lectin-like domain of TM resulted in a stronger inflamma

72 be formation and the role of the recombinant lectin-like domain of TM-TM domain 1 (rTMD1)-in antiangi

73 assessed the physiological relevance of the lectin-like domain of TNF in alveolar liquid clearance i

74 on and indicate a physiological role for the lectin-like domain of TNF in the resolution of alveolar

75 The TIP peptide, a mimic of the lectin-like domain of TNF, activates ENaC by binding to

76 channel, but not membrane expression, by the lectin-like domain of TNF.

77 nism by which the TIP peptide, mimicking the lectin-like domain of tumor necrosis factor (TNF), stimu

78 eins, with each subunit composed of a C-type lectin-like domain tethered to the membrane by a stalk r

79 ), is unique among integrins in containing a lectin-like domain that binds the fungal pathogen-associ

80 ombin-mediated proteolysis and an N-terminal lectin-like domain that controls inflammatory processes.

81 dditional antiparallel beta-sheet carrying a lectin-like domain that could be responsible for EPS bin

82 RCMV) encodes a 20-kDa protein with a C-type lectin-like domain that is expressed in the delayed-earl

83 nity and TM(LeD) mice lacking the N-terminal lectin-like domain.

84 or-like kinases with an extracellular legume lectin-like domain.

85 The structure revealed C-type lectin-like domains (CTLDs) that occur as dimers in A33

86 have named Sweet Tooth) contains four C-type lectin-like domains (CTLDs).

87 I domains were folded back to contact C-type lectin-like domains 1-6, and a "tail" comprising C-type

88 domains 1-6, and a "tail" comprising C-type lectin-like domains 7-8.

89 se findings for the ligand binding in C-type lectin-like domains are discussed.

90 C-type lectin-like domains are very common components of extrac

91 A comparison with homologous lectin-like domains from the immunoreceptor family revea

92 Also, role(s) of these lectin-like domains in the mode of action of VCC remain

93 s the possibility that a protein with C-type lectin-like domains regulated development in the last co

94 ns within the receptor, the inserted (I) and lectin-like domains within the CD11b subunit, and the CD

95 tein with predicted transmembrane and C-type lectin-like domains, regulates UNC-40-mediated axon outg

96 rane-spanning receptors containing eight-ten lectin-like domains, which appear to play a key role in

97 ich lies between the aggretin alpha and beta lectin-like domains.

98 t from the cytolysin domain, VCC harbors two lectin-like domains: the beta-Trefoil and the beta-Prism

99 lization of AICL is determined by its C-type lectin-like ectodomain.

100 ated surface-exposed cell wall proteins, the lectin-like epithelial adhesins (Epas).

101 bin-independent, constitutive manner via its lectin-like extracellular domain; and inhibits the infla

102 cRLKs) are members of RLK family composed of lectin-like extracellular recognition domain, transmembr

103 uperfamily (KIRs and LIRs) and of the C-type lectin-like family (Ly49, NKG2D, and CD94/NKG2).

104 structure reveals conservation of the C-type lectin-like fold, including preservation of the two alph

105 Our study shows that most EpaA domains exert lectin-like functions and together recognize a wide vari

106 onstrated that the core promoter of the RCMV lectin-like gene contains a GATA rather than a TATA box.

107 Some plant lectins like Griffonia simplicifolia lectin I and wheat

108 termined the crystal structures of the human lectin-like head domain of CD23 in its Ca(2+)-free and C

109 solved the crystal structure of the soluble lectin-like "head" domain of CD23 (derCD23) bound to a s

110 Two lectin-like "head" domains of CD23 bind to IgE-Fc with a

111 The NKG2x/CD94 family of C-type lectin-like immunoreceptors (x = A, B, C, E, and H) medi

112 NKG2A, which is encoded by Klrc1, is a lectin-like inhibitory receptor that is expressed as a h

113 h in beta-glucans, which are recognized by a lectin-like innate immune receptor, Dectin-1.

114 this association does not require the known lectin-like interaction between L-selectin and PSGL-1, t

115 Sugar inhibition assays indicated that lectin-like interactions were involved in the attachment

116 1, NKRP1A, NKp80, NKp65) instead bind C-type lectin-like ligands to which they are genetically linked

117 I to including related NK cell receptors for lectin-like ligands, and reflect genetic strategies for

118 lanking the N and C termini of the consensus lectin-like Link module, bridged by a third conserved di

119 e DCAL-1 locus is within a cluster of C-type lectin-like loci on human chromosome 12p12-13 just 3' to

120 The lectin-like low-density lipoprotein 1 receptor, encoded

121 inhibitory receptors belonging to the C-type lectin-like (Ly-49, CD94/NKG2) and Ig superfamily-relate

122 Lectins like mannan-binding protein are part of the inna

123 in interacts not only with Tir but also in a lectin-like manner with a host cell intimin receptor.

124 included EGF3, the rest of the wire, and the lectin-like module and in the presence of calcium.

125 el whereby at low calcium concentrations the lectin-like module drops away from EGF3 concomitant with

126 PEC to induce A/E lesions requires an intact lectin-like module residing at the carboxy-terminus of t

127 odule with 13 calcium-binding repeats, and a lectin-like module) binds 30 calcium ions and forms exte

128 the context of EGF1, EGF3, the wire, and the lectin-like module.

129 e modules, EGF2 and EGF3, and the C-terminal lectin-like module.

130 e modules, 13 calcium-binding repeats, and a lectin-like module.

131 upport the idea that the EGF-like, wire, and lectin-like modules constitute a dynamic and interactive

132 plasia when found in the homologous wire and lectin-like modules of thrombospondin-5 (THBS-5).

133 ability of interactions between the wire and lectin-like modules, stabilities of the EGF-like and wir

134 pidermal growth factor (EGF)-like, wire, and lectin-like modules.

135 ed by epidermal growth factor (EGF)-like and lectin-like modules.

136 Of these, the lectin-like molecule CD44 has been particularly implicat

137 first characterization of the orphan C-type lectin-like molecule Clr-a encoded by the Clec2e gene in

138 The chB1 lectin-like molecule may thus modulate intrabursal B cel

139 CLEC-2 is a C-type lectin-like molecule that has recently been identified a

140 Human C-type lectin-like molecule-1 (CLL1) is a recently identified m

141 dant function of these highly related C-type lectin-like molecules in the context of intestinal immun

142 nvolves NK gene complex (NKC)-encoded C-type lectin-like molecules such as NKG2D and Nkrp1 receptors.

143 Ly49A, an inhibitory C-type lectin-like mouse natural killer cell receptor, function

144 by structural studies to bind to the C type-lectin-like natural killer receptor, providing insight i

145 Interactions between C-type lectin-like NK cell receptors and their protein ligands

146 iller (NK) gene complex (NKC) encodes orphan lectin-like NK cell receptors that may explain uncharact

147 interacting with H-2D(d) through its C-type-lectin-like NK receptor domain.

148 dopts a fold similar to that of other C-type lectin-like NK receptors, including Ly49A, NKG2D and CD6

149 As with other lectin-like NK receptors, NKp80 is encoded in the natura

150 tory of the NKC, we characterized the C-type lectin-like NKC genes and their organization from four m

151 The stimulatory lectin-like NKG2D receptor is expressed by NK cells, act

152 scavenger receptor class A, types I and II, lectin-like ox-LDL receptor-1, macrophage receptor with

153 perties of cardiomyocytes in relation to the lectin-like oxidized LDL receptor (LOX-1).

154 The lectin-like oxidized LDL receptor LOX-1 mediates endothe

155 hown to activate platelets via its receptor, lectin-like oxidized LDL receptor-1 (LOX-1), and alphabe

156 ed the association of 3 polymorphisms in the lectin-like oxidized LDL receptor-1 (LOX1 or OLR1) gene

157 ough platelet-activating factor receptor and lectin-like oxidized LDL receptor-1 to attenuate Akt act

158 receptors, including TLR9, pentraxin-3, and lectin-like oxidized LDL receptor-1, was regulated, in p

159 cted when the entire intracellular domain of lectin-like oxidized low density lipoprotein receptor 1

160 ndicate that three members of the SR family (lectin-like oxidized low density lipoprotein receptor 1;

161 The lectin-like oxidized low density lipoprotein receptor-1

162 Lectin-like oxidized low-density lipoprotein (LOX-1), th

163 CD68, scavenger receptor (SR)-A, SR-BII, and lectin-like oxidized low-density lipoprotein receptor (L

164 acrophage scavenger receptor type AI/AII and lectin-like oxidized low-density lipoprotein receptor-1

165 The gene expression of CD36, SR-BII, and lectin-like oxidized low-density lipoprotein receptor-1

166 Lectin-like oxidized low-density lipoprotein receptor-1

167 Lectin-like oxidized low-density lipoprotein receptor-1

168 LOX-1 (lectin-like oxidized low-density lipoprotein receptor-1)

169 he MSR genes CD36 and CD68, SR-A and SR-BII, lectin-like oxidized low-density lipoprotein receptor-1,

170 l of this study was to determine the role of lectin-like oxidized low-density lipoprotein receptors (

171 Lectin-like oxidized low-density lipoprotein receptors a

172 antigens to human DCs via DC-ASGPR, but not lectin-like oxidized-LDL receptor, Dectin-1, or DC-speci

173 ive stress via interaction with the receptor lectin-like oxLDL receptor (LOX)-1 and subsequent NAD(P)

174 Rho kinase inhibition and the absence of the lectin-like OxLDL receptor-1 in knockout mice also ablat

175 ors of mitochondrial processing peptidase or lectin-like OxLDL receptor-1 knockout attenuated OxLDL-m

176 t the 14-kDa protein of B. abortus possesses lectin-like properties and is essential for the virulenc

177 l, cysteine-rich antimicrobial peptides with lectin-like properties exist in plants, theta-defensins

178 Despite its lectin-like properties, HNP-1 could bind to Env, CD4, an

179 s that appeared to be based on the protein's lectin-like properties.

180 nes, a newly identified four-exon gene for a lectin-like protein (in rat cytomegalovirus), and 10 pro

181 Convulxin (CVX) is a C-type lectin-like protein from the venom of the South American

182 e show that a complex encompassing the yeast lectin-like protein Htm1 and the oxidoreductase Pdi1 con

183 A lectin-like protein with a high match to lectins in othe

184 teomic analyses of mucus have identified the lectin-like protein ZG16 (zymogen granulae protein 16) a

185 r histocompatibility complex class I, C-type lectin-like protein, and transforming growth factor beta

186 family and is classified as a group 7 C-type lectin-like protein.

187 -1), a novel, type II, transmembrane, C-type lectin-like protein.

188 d aspartyl protease, and another AED, LEGUME LECTIN-LIKE PROTEIN1 (LLP1), were induced locally and sy

189 MHC molecules, by heterodimers of the C-type lectin-like proteins CD94 and NKG2.

190 pled receptors glycoprotein (GP)VI or C-type lectin-like receptor (CLEC)-2 is associated with only a

191 or platelet-specific deletion of the C-type-lectin-like receptor (CLEC-2) exhibit hemorrhaging in th

192 NKp65 is an activating human C-type lectin-like receptor (CTLR) triggering cellular cytotoxi

193 The C-type lectin-like receptor 2 (CLEC-2) activates platelets thro

194 C-type lectin-like receptor 2 (CLEC-2) is a platelet receptor t

195 C-type lectin-like receptor 2 (CLEC-2) is an essential platelet

196 Platelet C-type lectin-like receptor 2 (CLEC-2) is known to maintain the

197 e development, binding of Pdpn to the C-type lectin-like receptor 2 (CLEC-2) on platelets is critical

198 h lymphatic endothelial cells through C-type lectin-like receptor 2 (CLEC-2) receptors.

199 ein VI (GPVI)-FcR gamma-chain and the C-type lectin-like receptor 2 (CLEC-2), respectively, support c

200 lycoprotein (GP)VI-FcRgamma chain and C-type lectin-like receptor 2 (CLEC-2)-mediated platelet activa

201 latelet formation by interaction with C-type lectin-like receptor 2 (CLEC-2).

202 receptor glycoprotein (GP) VI and the C-type lectin-like receptor 2 (CLEC-2).

203 as an activating ligand for platelet C-type lectin-like receptor 2 (CLEC-2, also known as CLEC1B).

204 ein VI (GPVI) and podoplanin receptor C-type lectin-like receptor 2 (CLEC2) are receptors implicated

205 nt for the platelet-specific receptor C-type lectin-like receptor 2 (CLEC2) as blood backfills the ly

206 Glycoprotein VI and C-type lectin-like receptor 2 are essential platelet activating

207 pletely inhibited glycoprotein VI and C-type lectin-like receptor 2 signaling.

208 specifically inhibited collagen- and C-type lectin-like receptor 2-induced human platelet aggregatio

209 e and essential role in collagen- and C-type lectin-like receptor 2-mediated platelet activation and

210 gh the collagen receptor GPVI and the C-type lectin-like receptor 2.

211 agen receptor glycoprotein VI and the C-type lectin-like receptor 2.

212 CD141(+) DC in humanized mice express C-type lectin-like receptor 9A, XCR1, CADM1, and TLR3 but lack

213 ction of Abs against human DEC-205 or C-type lectin-like receptor 9A.

214 NKp80 is a C-type lectin-like receptor broadly expressed on human natural

215 The C-type lectin-like receptor CD161, which has recently been desc

216 cal MHC-I-peptide (pMHC-I) complexes and the lectin-like receptor CD94-NKG2A by nonclassical pMHC-I c

217 The C-type lectin-like receptor CLEC-2 mediates platelet activation

218 increased expression of SIGLEC-1 (CD169), a lectin-like receptor expressed on CD14(+) monocytes.

219 Recently, a novel lectin-like receptor for ox-LDL (LOX-1) has been identif

220 We have recently demonstrated a lectin-like receptor for oxidized (ox)-LDL (LOX-1) in hu

221 rance of short-lived (CD127(low) killer cell lectin-like receptor G 1-high) and memory-precursor (CD1

222 nd memory-precursor (CD127(high) killer cell lectin-like receptor G 1-low) effector cells.

223 ells proliferate and up-regulate killer cell lectin-like receptor G-1 expression.

224 iferation coupled with decreased killer cell lectin-like receptor G-1 up-regulation on responding CD8

225 fied by reciprocal expression of killer cell lectin-like receptor G1 (KLRG1) and CD127, have differen

226 cells coexpress the NK receptors killer cell lectin-like receptor G1 (KLRG1) and NKG2A.

227 rogrammed death-1 (PD-1) and the killer cell lectin-like receptor G1 (KLRG1) delineated subpopulation

228 he T cell differentiation marker killer cell lectin-like receptor G1 (KLRG1) during M. tuberculosis i

229 had decreased CD27 and increased killer cell lectin-like receptor G1 (KLRG1) expression.

230 We determined the structure of killer cell lectin-like receptor G1 (KLRG1) in complex with E-cadher

231 igh expression of the inhibitory killer cell lectin-like receptor G1 (KLRG1) in individuals >70 y.

232 Killer cell lectin-like receptor G1 (KLRG1) is one of several inhibi

233 The killer cell lectin-like receptor G1 (KLRG1) is the mouse homologue o

234 robust terminally differentiated killer cell lectin-like receptor G1 (KLRG1)(hi) effector population,

235 ha expression did not rescue the killer cell lectin-like receptor G1 (KLRG1)(hi) short-lived effector

236 ng CD8 T cell subsets expressing killer cell lectin-like receptor G1 (KLRG1)(high) or KLRG1(low) had

237 s virus infection, we found most killer cell lectin-like receptor G1 (KLRG1)(lo)IL-7R(hi) effector an

238 several inhibitory molecules such as killer lectin-like receptor G1 (KLRG1).

239 h fewer old cells expressing the killer cell lectin-like receptor G1 (KLRG1).

240 ace activation markers CD62L and killer cell lectin-like receptor G1 (KLRG1).

241 d death-1 (PD1) receptor and the killer cell lectin-like receptor G1 (KLRG1).

242 cells expressing high levels of killer cell lectin-like receptor G1 (KLRG1).

243 kin-7 receptor and low levels of killer cell lectin-like receptor G1 [IL-7Rhi KLRG1lo]) and had highe

244 ers of terminal differentiation, killer cell lectin-like receptor G1 and CD57, were expressed at lowe

245 Using killer cell lectin-like receptor G1 as a marker to distinguish these

246 This led to generation of CD8(+)/killer cell lectin-like receptor G1 high (KLRG1(hi))/IL-7R(lo) short

247 educed numbers of ADAP-deficient killer cell lectin-like receptor G1(-) CD8 resident memory T (TRM) c

248 tus, including CXCR3, CD127, and killer cell lectin-like receptor G1, and are superior to CD62L in pr

249 R-alpha, decreased expression of killer cell lectin-like receptor G1, and enhanced persistence of the

250 n of a population that expresses killer cell lectin-like receptor G1, and the majority of the resulti

251 Analysis of transcripts for killer cell lectin-like receptor G1, IL-7R, and CD57 implied that lu

252 HIVAN4 candidate genes include killer lectin-like receptor genes as well as A2m and Ptpro, who

253 The dectin-1 lectin-like receptor has shown to recognize fungal beta

254 The determinant is dependent on the putative lectin-like receptor Htm1/Mnl1p.

255 ived effector cells (SLECs) that express the lectin-like receptor KLRG-1, but how it operates remains

256 tically significant reduction in killer cell lectin-like receptor mRNA expression between cultures wi

257 ession cloning of two murine ligands for the lectin-like receptor NKG2D.

258 Among these is the C-type lectin-like receptor NKp80 which is encoded in the human

259 The mouse C-type lectin-like receptor Nkrp1g was previously shown to form

260 beta1,4-galactosyltransferase I (GalT I), a lectin-like receptor on the sperm surface.

261 Ly49Q, a C-type lectin-like receptor specific for MHC-I, possesses a cyt

262 this study, we demonstrate that killer cell lectin-like receptor subfamily G member 1 (KLRG1), a tra

263 ction of an inhibitory receptor, killer cell lectin-like receptor subfamily G member 1 (KLRG1), in th

264 expression of NKG2D (CD314) and killer cell lectin-like receptor subfamily G member 1 (KLRG1).

265 tiation including an increase in killer cell lectin-like receptor subfamily G member 1 and shorter te

266 cells expressing high levels of killer cell lectin-like receptor subfamily G, member 1 (KLRG1), and

267 Using CD161, a lectin-like receptor that is a marker of human Th17, we

268 NKG2D, a homodimeric lectin-like receptor, is a unique stimulatory molecule t

269 usly described the cloning of a novel C-type lectin-like receptor, KLRH1, encoded in the NK complex a

270 accumulation of ox-LDL and expression of its lectin-like receptor, LOX-1, have been shown in atherosc

271 xidatively modified LDL (ox-LDL) activates a lectin-like receptor, LOX-1, which results in the expres

272 L-selectin, a lectin-like receptor, mediates rolling of lymphocytes on

273 mbosis within vessels via ligation of C-type lectin-like receptor-2 (CLEC-2) on platelets by podoplan

274 owing receptors: glycoprotein (GP)VI, C-type lectin-like receptor-2 (CLEC-2)>GPIb>alpha6beta1, alphaI

275 Rhodocytin, an agonist of the C-type lectin-like receptor-2 (CLEC-2), elicits powerful platel

276 ergic beta-2 receptor (ADRB2), oxidized LDL (lectin-like) receptor 1 (OLR1), and IL-8 receptor-alpha

277 Because some C-type lectin-like receptors (e.g. dectin-1 and DCSIGN) were sh

278 in-like receptors (KIRs) and the killer cell lectin-like receptors (KLRs), and attempt to trace their

279 Ly49 lectin-like receptors and killer cell Ig-like receptors

280 The NKR-P1 family of C-type lectin-like receptors are expressed on natural killer (N

281 G1) is one of several inhibitory killer cell lectin-like receptors expressed by NK cells and T lympho

282 gene complex-encoded immunomodulatory C-type lectin-like receptors include members of the NKRP1 and C

283 x and the corresponding repertoire of C-type lectin-like receptors on murine NK cells.

284 cells in mice detect cells in distress using lectin-like receptors that bind to self-MHC class I mole

285 ) gene complex (NKC) encodes numerous C-type lectin-like receptors that govern the activity of NK cel

286 The asialoglycoprotein receptor or other lectin-like receptors were not detected on the apical su

287 Natural killer (NK) cells express C-type lectin-like receptors, encoded in the NK gene complex, t

288 s in vitro was not affected by inhibitors of lectin-like receptors, phosphatidylserine receptors, the

289 ogen recognition receptors, including C-type lectin-like receptors, TLRs, and nucleotide oligomerizat

290 mplex (NKC) encodes a large number of C-type lectin-like receptors, which are expressed on NK and oth

291 domain III of Cry1Ac and therefore support a lectin-like role for this domain.

292 he Sam n1 allergen fit best with a monomeric lectin like SELlm (Mr 34.2 kDa) found in shoots of dwarf

293 lergen could be a sequence-related monomeric lectin like SELlm present in shoots of Sambucus ebulus r

294 it belongs to the C-type (calcium-dependent) lectin-like superfamily.

295 l streptococci function as receptors for the lectin-like surface adhesins on other members of the ora

296 udy was to reveal a possible role of NKR-P1A/lectin-like transcript 1 (LLT1) interaction in NK cell-m

297 The innate lectin-like transcript 1 (LLT1) is known to be expressed

298 LLT1 (lectin-like transcript 1), the ligand for CD161a, was ov

299 Lectin-like transcript-1 (LLT1) (also named osteoclast i

300 In this study, we demonstrate that the lectin-like transcript-1 (LLT1) is a physiologic ligand