ライフサイエンスコーパス: cell surface glycoprotein

1 rize Clr-a as a disulfide-linked homodimeric cell surface glycoprotein.

2 racellular domains of protocadherin-gamma, a cell surface glycoprotein.

3 ecies-specific binding of sperm is a 350-kDa cell surface glycoprotein.

4 phosphatidylinositol-anchored (GPI-anchored) cell surface glycoprotein.

5 the circulation or as a biologically active cell-surface glycoprotein.

6 that bound glycoprotein by ELISA recognized cell-surface glycoprotein.

7 uine, which interferes with the recycling of cell surface glycoproteins.

8 de is ubiquitously expressed on a variety of cell surface glycoproteins.

9 , increased expression of GAP-43 and certain cell surface glycoproteins.

10 yl-phosphatidylinositol anchor found on many cell surface glycoproteins.

11 ttached alpha2,3 or alpha2,6 sialic acids on cell surface glycoproteins.

12 rminal N-linked oligosaccharides on selected cell surface glycoproteins.

13 Here we report that CTB binds cell surface glycoproteins.

14 reatment time points as a method to identify cell surface glycoproteins.

15 with MS-based glycoproteomics for analyzing cell surface glycoproteins.

16 beta1,6GlcNAc-branched N-glycans attached to cell surface glycoproteins.

17 ne knot motif found in multisubunit external cell surface glycoproteins.

18 corporated into O-GlcNAcylated proteins over cell-surface glycoproteins.

19 The cell surface glycoprotein 2B4 (CD244) of the Ig superfam

20 ically active isoforms: a membrane-spanning, cell surface glycoprotein, a secreted glycoprotein, and

21 ke sequence) gene family encodes eight large cell-surface glycoproteins (Als1-Als7 and Als9) that hav

22 ion (cyclophilin C or rotamase) to the CD147 cell surface glycoprotein (also known as extracellular m

23 The cell surface glycoprotein and SLAM family member, CS1, e

24 ate many cellular processes by oligomerizing cell surface glycoproteins and glycolipids into higher-o

25 as well as a 75% reduction in sialylation of cell surface glycoproteins and glycosphingolipids.

26 zed aptamer conjugates against two different cell surface glycoproteins and show that these reagents

27 mechanism for regulation of the activity of cell-surface glycoproteins and likely contributes to mai

28 at galectin-1 binds to a restricted set of T cell surface glycoproteins, and that only CD45, CD43, an

29 e iridium-based photocatalysts on sialylated cell-surface glycoproteins as a means to profile local m

30 #3, and #10 antibodies can be used to detect cell surface glycoproteins bearing O-GlcNAc.

31 CD9 is a cell surface glycoprotein belonging to the transmembrane

32 These polymorphic cell-surface glycoproteins bind peptide antigens, formin

33 GPIHBP1, an endothelial cell-surface glycoprotein, binds LPL and is required for

34 We demonstrate that S1 is a cell surface glycoprotein capable of binding to host SLA

35 mphoid tissues express high levels of CD1, a cell surface glycoprotein capable of presenting lipids a

36 d MCT4 form heterodimeric complexes with the cell surface glycoprotein CD147 and exhibit tissue-speci

37 The cell surface glycoprotein CD163 is a member of the cyste

38 Genetic ablation of the B cell surface glycoprotein CD19 severely impairs the humo

39 henotype acute leukemia, we found that the T-cell surface glycoprotein CD3 delta chain may causally m

40 anscription factors Pax7, MyoD and Myf5, the cell-surface glycoprotein CD34, and the membrane lipid s

41 mily of proteins structurally related to the cell surface glycoprotein CD36.

42 ed from the N-terminal fragment STTAV of the cell surface glycoprotein CD43 have been investigated by

43 The cell surface glycoprotein CD44 is expressed primarily in

44 The cell surface glycoprotein CD44 plays an important role i

45 y upon MSC expression of the multifunctional cell surface glycoprotein CD44, a putative stem cell mar

46 Here we show that the cell surface glycoprotein CD44, which marks the acquisit

47 in cell communication revealed galectin-9 to cell-surface glycoprotein CD44 (LGALS9-CD44) as a critic

48 The cell-surface glycoprotein CD44 is expressed in chronic l

49 agglutinin appeared to bind primarily to the cell-surface glycoprotein CD45; since only the mature th

50 Galectin-1 binds to T cell-surface glycoproteins CD45, CD43, and CD7, although

51 Here, we investigated whether the cell surface glycoprotein CD47 was required for normal f

52 Recent data indicate that the cell surface glycoprotein CD5 functions as a negative re

53 Recently, IL-6 was found to also bind to the cell surface glycoprotein CD5, which would then engage g

54 terminants, specifically interact with the B cell-surface glycoprotein CD5.

55 with human complement by targeting the small cell-surface glycoprotein CD52, commonly called the CAMP

56 The T cell-surface glycoprotein CD6 is a modulator of cellular

57 The cell surface glycoprotein CD8 functions as a coreceptor

58 The dimeric cell-surface glycoprotein CD8 is crucial to the positive

59 The tetraspan cell surface glycoprotein, CD9, has been implicated in c

60 we found that CD26, in combination with the cell surface glycoprotein CD90, identifies a distinct su

61 We have identified the cell surface glycoprotein CDCP1 as a key regulator of EG

62 alterations coincide with persistent altered cell surface glycoprotein composition.

63 nding proteins (GBPs) that can interact with cell surface glycoprotein counterreceptors to regulate p

64 gically active isoforms: a membrane-spanning cell surface glycoprotein (csCSF-1), a secreted proteogl

65 the circulation or as a biologically active cell surface glycoprotein (csCSF-1).

66 ically active isoforms: a membrane-spanning, cell-surface glycoprotein (csCSF-1) and secreted glycopr

67 e developed the 6F10 mAb, which recognizes a cell surface glycoprotein designated lymphocyte endothel

68 ibody A33 (mAb A33) recognizes a M(r) 43,000 cell surface glycoprotein (designated A33) expressed in

69 The parasitic cell surface glycoprotein encoded by the SOWgp gene appe

70 CD26, a 110-kDa cell surface glycoprotein, exhibits dipeptidyl peptidase

71 rfamily protein basigin (EMMPRIN/CD147) is a cell surface glycoprotein expressed by tumor cells that

72 lt from conformational alteration of PrPC, a cell surface glycoprotein expressed in brain, spinal cor

73 henotype) that recognizes Ly5, a polymorphic cell surface glycoprotein expressed on hemopoietic cells

74 nal antibody (MAb) is highly reactive with a cell surface glycoprotein expressed on human breast canc

75 n of BAI1 (termed Vstat120) requires CD36, a cell surface glycoprotein expressed on microvascular end

76 CD2, a cell surface glycoprotein expressed on T cells and natur

77 activation molecule [SLAM]) is a self-ligand cell surface glycoprotein expressed on T cells, B cells,

78 ostate-specific membrane antigen (PSMA) is a cell surface glycoprotein expressed predominantly by pro

79 GspB is a large cell-surface glycoprotein expressed by Streptococcus gor

80 ated cell adhesion molecule-2 (CEACAM2) is a cell-surface glycoprotein expressed on blood, epithelial

81 ng biosynthesis of DG core protein or global cell surface glycoprotein expression.

82 that are similar to those of two nonspecific cell surface glycoproteins, FcgammaRIIb and FcgammaRIII,

83 hanges in GNE activity can alter affinity of cell-surface glycoproteins for the galectin lattice.

84 Glycoproteins were identified as cell surface glycoproteins from A498 cells when enzyme t

85 gest that DC-SIGN may not discriminate other cell surface glycoproteins from ICAM-3 binding.

86 The cell surface glycoprotein gamma-glutamyl transpeptidase

87 t is proteolytically cleaved to yield mature cell surface glycoproteins gp40 and gp15, which are impl

88 The Streptococcus gordonii cell surface glycoprotein GspB mediates high-affinity bi

89 strain M99 is mediated predominantly by the cell surface glycoprotein GspB.

90 aberrant expression of core 2 O-glycans on T cell surface glycoproteins has been associated with vari

91 Abnormal expression of TACSTD2 cell-surface glycoprotein has been reported in most epit

92 signal of Env, and the resulting increase in cell surface glycoprotein, has no effect on incorporatio

93 CD44, a cell-surface glycoprotein, has long been studied as a ca

94 GPI membrane anchors of cell surface glycoproteins have been shown to confer fun

95 Glypican-3 (GPC3) is a cell surface glycoprotein highly expressed on HCC.

96 The GA733-2 antigen is a cell surface glycoprotein highly expressed on most human

97 Mucin-4 (Muc4) is a large cell surface glycoprotein implicated in the protection a

98 unctions as growth factors, interacting with cell surface glycoproteins implicated in growth-promotin

99 nce) gene family of Candida albicans encodes cell-surface glycoproteins implicated in adhesion of the

100 ositol (GPI) structures are attached to many cell surface glycoproteins in lower and higher eukaryote

101 Galectin-3 binding to cell surface glycoproteins, including branched N-glycans

102 ant role in the cell biology of a variety of cell surface glycoproteins, including PrP protein.

103 The addition of sialic acid to T cell surface glycoproteins influences essential T cell f

104 y affect expression and functions of CD44, a cell-surface glycoprotein influencing immunologic, infla

105 ntercellular adhesion molecule-1 (ICAM-1), a cell surface glycoprotein involved in extravasation into

106 Flo11p, a member of a large family of fungal cell surface glycoproteins involved in adherence.

107 activation molecule (SLAM), a T/B/dendritic cell surface glycoprotein, is a costimulatory receptor i

108 e stem cell antigen (PSCA), a 123-amino acid cell surface glycoprotein, is highly expressed in both l

109 sphatidylinositol anchor 1 (MDGA1), a unique cell surface glycoprotein, is similar to Ig-containing c

110 itopes and polylactosamine glycan containing cell surface glycoproteins, is the major nonintegrin cel

111 unization with autologous megalin, a 600-kDa cell surface glycoprotein isolated from crude renal extr

112 recognition by T lymphocytes is mediated by cell-surface glycoproteins known as T-cell antigen recep

113 contrast, attachment of the lectin to a host cell surface glycoprotein leads to lectin-induced host c

114 The propinquity of CD22 and cell-surface glycoprotein ligands has led to the conclus

115 evels, suggesting that increased exposure of cell surface glycoproteins mediated the effect, whereas

116 The cell-surface glycoprotein MUC1 is a particularly appeali

117 Cell surface glycoprotein MUC18 (alias CD146 or melanoma

118 quent homophilic interaction mediated by the cell surface glycoprotein MUC18 (also known as melanoma

119 ing and characterization of rat CDO, a novel cell surface glycoprotein of the Ig superfamily that con

120 Emmprin (CD147; basigin) is a cell surface glycoprotein of the immunoglobulin superfam

121 The OX-40 receptor (OX-40R) is a cell surface glycoprotein of the tumor necrosis factor r

122 against a recombinant PIR protein identified cell surface glycoproteins of approximately 85 and appro

123 MCAM/MUC18 is a cell-surface glycoprotein of 113 kDa, originally identif

124 Thy-1 is a major cell-surface glycoprotein of mature neurons and certain

125 Drosophila basigin is a cell-surface glycoprotein of the Ig superfamily and a me

126 tracellular glycoproteins or glycolipids and cell surface glycoproteins or glycolipids on their own a

127 d affect energy utilization and synthesis of cell-surface glycoproteins or glycolipids involved in ce

128 tin that binds to oligosaccharide ligands on cell surface glycoproteins, or to oligosaccharide ligand

129 Folate (FA) receptor is a cell surface glycoprotein overexpressed on many cancer c

130 ) epitope on O-glycans linked to a leukocyte cell-surface glycoprotein, P-selectin Glycoprotein Ligan

131 Cell surface glycoproteins participate in various cellul

132 CD47, a cell surface glycoprotein, plays an important role in mo

133 The PKD1 gene codes for a large cell-surface glycoprotein, polycystin-1, of unknown func

134 was stimulated by direct Gal-1 engagement to cell surface glycoproteins, principally CD45, on activat

135 ers that result from conversion of a normal, cell surface glycoprotein (PrP(C)) into a conformational

136 om conformational transformation of a normal cell surface glycoprotein, PrP(C), into a pathogenic iso

137 sttranslational structural alteration in the cell surface glycoprotein PrPc (cellular isoform of the

138 gen is part of the extracellular domain of a cell surface glycoprotein receptor called gp330 or megal

139 lial cell adhesion molecule-1 (PECAM-1) is a cell surface glycoprotein receptor expressed on a range

140 a (CLL) cells express high levels of CD44, a cell-surface glycoprotein receptor for hyaluronic acid.

141 Galectin-3 binds to a complement of T cell surface glycoprotein receptors distinct from that r

142 or advanced glycation end-products and other cell surface glycoprotein receptors on MDSC, signal thro

143 However, the T cell surface glycoprotein receptors responsible for deli

144 Cell-surface glycoprotein receptors have varying numbers

145 Cell surface glycoproteins recognized by CTD110.6 antibo

146 The MHC-encoded butyrophilin, BTN2A1, is a cell surface glycoprotein related to the extended family

147 that overexpression of core 2 O-glycans on T cell surface glycoproteins renders T cell-B cell interac

148 ates transcription of FLO11, which encodes a cell surface glycoprotein required for invasive growth.

149 Neural cell adhesion molecule L1 is a cell surface glycoprotein required for the correct devel

150 Tissue factor (TF) is a cell-surface glycoprotein responsible for initiating the

151 ith the mucinlike domains of these mammalian cell surface glycoproteins result not only in adhesion b

152 alectins and the glycan ligands presented on cell surface glycoproteins results in high-avidity bindi

153 aberrant expression of core 2 O-glycans on T cell surface glycoproteins results in impaired humoral i

154 es against axonal guidance cues, such as the cell surface glycoproteins Semaphorin 1a (Sema 1a) and F

155 lent display of carbohydrate groups found on cell surface glycoprotein structures may contribute to t

156 triggers the galectin-driven endocytosis of cell-surface glycoproteins, such as integrins, that are

157 t the glycosyl phosphatidylinositol-anchored cell surface glycoprotein T-cadherin (encoded by Cdh13)

158 (and factor XII) bind to HUVECs via a 33-kDa cell surface glycoprotein that appears to be identical t

159 Glypican-3 is a cell surface glycoprotein that associates with Wnt in li

160 class B, type I (SR-BI), is a homooligomeric cell surface glycoprotein that controls HDL structure an

161 the sialomucin CD34, a highly O-glycosylated cell surface glycoprotein that has also been shown to be

162 CD200 (OX-2) is a cell surface glycoprotein that imparts immune privileges

163 In this report, we have identified a cell surface glycoprotein that is a likely candidate for

164 on of the LIM-domain factors with axonin1, a cell surface glycoprotein that is a member of the immuno

165 CD24 is a cell surface glycoprotein that is expressed on both immu

166 CD34 is a cell surface glycoprotein that is selectively expressed

167 CD2 is a T cell surface glycoprotein that mediates both cell-cell a

168 As a cell surface glycoprotein that mediates filamentation an

169 enger receptor, class B, type I (SR-BI) is a cell surface glycoprotein that mediates selective uptake

170 CD6 is a T cell surface glycoprotein that plays an important role i

171 actor (TF) (CD142) is a 47 kDa transmembrane cell surface glycoprotein that triggers the extrinsic co

172 e prion protein PrP(C) is a Cu(2)(+)-binding cell surface glycoprotein that, when misfolded, is respo

173 ss II genes encode a series of heterodimeric cell surface glycoproteins that bind peptide antigen.

174 e receptors (KIR) are structurally unrelated cell surface glycoproteins that evolved independently to

175 adhesion molecules-A, -B, and -C (Jams) are cell surface glycoproteins that have been shown to play

176 ith MHC and related class I H chains to form cell surface glycoproteins that mediate a variety of fun

177 MHC class II (MHCII) molecules are cell surface glycoproteins that play an important role t

178 tocompatibility (MHC) class II molecules are cell surface glycoproteins that present extracellular an

179 Alpha-dystroglycan (alpha-DG) is a cell-surface glycoprotein that acts as a receptor for bo

180 20, recognizes a rapidly internalized 180-kd cell-surface glycoprotein that is abundantly expressed o

181 Glypican-3 (GPC3) is a cell-surface glycoprotein that is frequently overexpress

182 ation of human mannose receptor 1 (hMRC1), a cell-surface glycoprotein that is involved in the host i

183 L-selectin is a leukocyte cell-surface glycoprotein that mediates adhesive interac

184 enger receptor, class B, type I (SR-BI) is a cell-surface glycoprotein that mediates selective uptake

185 ene family of Candida albicans encodes large cell-surface glycoproteins that are implicated in the pr

186 ous transcripts of trypomastigote-associated cell-surface glycoproteins that are preferentially expre

187 alpha, FRbeta and FRgamma) are cysteine-rich cell-surface glycoproteins that bind folate with high af

188 L1 (programmed death ligand 1) and PD-L2 are cell-surface glycoproteins that interact with programmed

189 rate major histocompatibility complex encode cell-surface glycoproteins that present peptides to T ce

190 The Ig superfamily cell surface glycoprotein Thy-1 expressed on immune cell

191 We identified the cell surface glycoprotein Thy-1 on the endothelium of ne

192 ctins bind to branched N-glycans attached to cell surface glycoproteins to control the distribution,

193 f cytoskeleton-associated proteins that link cell surface glycoproteins to the actin cytoskeleton.

194 group of the Protein 4.1 family, which links cell surface glycoproteins to the actin cytoskeleton.

195 The cell surface glycoprotein Trask/CDCP1 is phosphorylated

196 antibody that binds carbonic anhydrase IX, a cell surface glycoprotein ubiquitously expressed in clea

197 Several decades ago, cell surface glycoproteins were found to have an importa

198 Six candidate cell surface glycoproteins were identified.

199 Cluster of differentiation 8 (CD8) is a cell surface glycoprotein, which is expressed as 2 forms

200 MICA encodes a cell surface glycoprotein, which is not associated with

201 from the CBD of TS1 affinity label a 52-kDa cell surface glycoprotein, which we show is integrin-ass

202 mediated by structurally diverse classes of cell-surface glycoproteins, which form homophilic or het

203 es released from intracellular organelle and cell surface glycoproteins, while maintaining histopatho

204 CD44 is a widely distributed cell surface glycoprotein whose principal ligand has bee

205 CD44 and CD24 are important cell surface glycoproteins whose relative expression lev

206 Mesothelin is a cell-surface glycoprotein whose expression in normal hum

207 ratus sea urchin egg receptor for sperm is a cell surface glycoprotein with a molecular mass of 350 k

208 g strategy has yielded a cDNA that encodes a cell surface glycoprotein with a restricted pattern of e

209 CD44 is an important leukocyte cell surface glycoprotein with diverse functions includi

210 Interaction of cell surface glycoproteins with endogenous lectins on th

211 These findings suggest that cell surface glycoproteins with N-linked oligosaccharide