ライフサイエンスコーパス: glycosylphosphatidylinositol

1 lycans that are bound to the cell surface by glycosylphosphatidylinositol.

2 that tethers GPIHBP1 to the cell membrane by glycosylphosphatidylinositol.

3 (ScN2a, ScGT1, or SMB cells) with synthetic glycosylphosphatidylinositol analogues, glucosamine-phos

4 9167), glutathione metabolism (P = 0.01281), glycosylphosphatidylinositol anchor (P = 0.01949), adher

5 in the form of water-soluble domain lacking glycosylphosphatidylinositol anchor (ws-LYNX1;) revealed

6 ell-surface molecules, MAM domain-containing glycosylphosphatidylinositol anchor 1 (MDGA1) and 2 (MDG

7 ptor protein tyrosine phosphatase mu) domain glycosylphosphatidylinositol anchor 1 (MDGA1), a unique

8 finger proteins, is membrane-tethered with a glycosylphosphatidylinositol anchor and modulates the ac

9 GPAA1 (glycosylphosphatidylinositol anchor attachment 1) is an

10 chondrial structure and function, as well as glycosylphosphatidylinositol anchor biosynthesis.

11 Membrane attachment via a C-terminal glycosylphosphatidylinositol anchor is critical for conv

12 her associated with cell membranes through a glycosylphosphatidylinositol anchor or released as a sol

13 lta-1 constructs truncated at their putative glycosylphosphatidylinositol anchor site, located before

14 ular prion protein, PrP(C), is attached by a glycosylphosphatidylinositol anchor to the outer leaflet

15 PrPC is tethered to the plasma membrane by a glycosylphosphatidylinositol anchor, topological variant

16 ke (LE) domains and a C' region containing a glycosylphosphatidylinositol anchor.

17 ts because it is attached to membranes via a glycosylphosphatidylinositol anchor.

18 of endogenous ephrinAs by cleavage of their glycosylphosphatidylinositol anchor.

19 lacks a predicted transmembrane domain or a glycosylphosphatidylinositol anchor.

20 to APC-activated serum due to deficiency of glycosylphosphatidylinositol- anchored complement regula

21 rP) is a highly conserved, widely expressed, glycosylphosphatidylinositol-anchored (GPI-anchored) cel

22 ow failure caused by defective expression of glycosylphosphatidylinositol-anchored (GPI-anchored) com

23 Collectively, these studies indicate that glycosylphosphatidylinositol-anchored AGPs function to l

24 ART1 synthesized in Escherichia coli, glycosylphosphatidylinositol-anchored ART1 released with

25 a soluble N-terminal fragment (PrPN1) and a glycosylphosphatidylinositol-anchored C-terminal fragmen

26 d transient axonal glycoprotein-1 (TAG-1), a glycosylphosphatidylinositol-anchored cell adhesion mole

27 l wall re-modeling by removal and release of glycosylphosphatidylinositol-anchored cell wall proteins

28 Here we demonstrate that glycosylphosphatidylinositol-anchored cell-surface recep

29 ntified COBRA-LIKE2 (COBL2), a member of the glycosylphosphatidylinositol-anchored COBRA-LIKE gene fa

30 However, delivery of glycosylphosphatidylinositol-anchored endolyn was inhibi

31 GPIHBP1, a glycosylphosphatidylinositol-anchored endothelial cell p

32 GPIHBP1, a glycosylphosphatidylinositol-anchored endothelial cell p

33 ion, and showed that carbonic anhydrase 4, a glycosylphosphatidylinositol-anchored enzyme, functions

34 al through receptor tyrosine kinase TrkA and glycosylphosphatidylinositol-anchored glial cell-derived

35 GPIHBP1, a glycosylphosphatidylinositol-anchored glycoprotein of mi

36 ulticomplex receptor system in which CD14, a glycosylphosphatidylinositol-anchored glycoprotein, and

37 update on the structure of GPIHBP1, a 28-kDa glycosylphosphatidylinositol-anchored glycoprotein, and

38 llular prion protein (PrP(c)), a ubiquitous, glycosylphosphatidylinositol-anchored glycoprotein.

39 terstitial spaces; it then binds to GPIHBP1 (glycosylphosphatidylinositol-anchored high density lipop

40 Glycosylphosphatidylinositol-anchored high density lipop

41 e of either heparan sulfate proteoglycans or glycosylphosphatidylinositol-anchored high density lipop

42 Glycosylphosphatidylinositol-anchored high density lipop

43 To summarize recent data indicating that glycosylphosphatidylinositol-anchored high density lipop

44 However, in vivo LPL is often complexed to glycosylphosphatidylinositol-anchored high density lipop

45 nt new developments include the discovery of glycosylphosphatidylinositol-anchored high-density lipop

46 dulates lipoprotein metabolism by binding to glycosylphosphatidylinositol-anchored high-density lipop

47 lycerol-rich lipoproteins in the vicinity of glycosylphosphatidylinositol-anchored high-density lipop

48 h a soluble variant of its accessory protein glycosylphosphatidylinositol-anchored high-density lipop

49 form 1:1 complexes with the LPL transporter glycosylphosphatidylinositol-anchored high-density lipop

50 Lateral mobility of the glycosylphosphatidylinositol-anchored HpHbR, and a appro

51 Here, we identify TaMs5 as a glycosylphosphatidylinositol-anchored lipid transfer pro

52 ly restores fertility to ms1d, and encodes a glycosylphosphatidylinositol-anchored lipid transfer pro

53 matrix metalloproteinase (MMP) (MMP25) is a glycosylphosphatidylinositol-anchored matrix metalloprot

54 MMP25 (MT6-MMP) is one of the two glycosylphosphatidylinositol-anchored matrix metalloprot

55 CD160, a glycosylphosphatidylinositol-anchored member of the immu

56 Here we show that DRAGON, a glycosylphosphatidylinositol-anchored member of the repu

57 Decay-accelerating factor (DAF) is a glycosylphosphatidylinositol-anchored membrane protein t

58 While PrPC is principally a glycosylphosphatidylinositol-anchored membrane protein,

59 that LORELEI (LRE), which encodes a putative glycosylphosphatidylinositol-anchored membrane protein,

60 prion protein (PrP(C)) is a widely expressed glycosylphosphatidylinositol-anchored membrane protein.

61 n in the PIGA gene leads to membrane loss of glycosylphosphatidylinositol-anchored membrane proteins,

62 nsmembrane serine protease, and prostasin, a glycosylphosphatidylinositol-anchored membrane serine pr

63 ht the common and distinct properties of the glycosylphosphatidylinositol-anchored membrane type-matr

64 creted collagenases MMP-1 and MMP-13 and the glycosylphosphatidylinositol-anchored membrane-type MMPs

65 Members of the IgLON family of glycosylphosphatidylinositol-anchored neural cell adhesi

66 Glycosylphosphatidylinositol-anchored neurotoxin-like re

67 t axon regeneration in vitro and bind to the glycosylphosphatidylinositol-anchored Nogo receptor (NgR

68 ts identify gangliosides (GD1a and GT1b) and glycosylphosphatidylinositol-anchored Nogo receptors (Ng

69 report that the female gametophyte-expressed glycosylphosphatidylinositol-anchored protein (GPI-AP) L

70 We show that LYSIN MOTIF DOMAIN-CONTAINING GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED PROTEIN 2 (LYM2),

71 using cyan/yellow fluorescent protein-tagged glycosylphosphatidylinositol-anchored protein and vesicu

72 al PM area by the addition of membrane via a glycosylphosphatidylinositol-anchored protein compartmen

73 CD14 is a glycosylphosphatidylinositol-anchored protein expressed

74 erived neurotrophic factor family, binds the glycosylphosphatidylinositol-anchored protein GFRalpha3

75 l surface marker for human fetal liver HSCs, glycosylphosphatidylinositol-anchored protein GPI-80, th

76 GPIHBP1, a glycosylphosphatidylinositol-anchored protein of capilla

77 CD59 is a glycosylphosphatidylinositol-anchored protein that inhib

78 monstrate that neogenin may stabilize HJV, a glycosylphosphatidylinositol-anchored protein that inter

79 n the UMOD gene, which encodes Uromodulin, a glycosylphosphatidylinositol-anchored protein that is ex

80 er/sleepless (qvr/sss) gene encodes a small, glycosylphosphatidylinositol-anchored protein that plays

81 D59 is a ubiquitously expressed cell-surface glycosylphosphatidylinositol-anchored protein that prote

82 We observed that Golgi, lysosomes, and glycosylphosphatidylinositol-anchored protein vesicles a

83 d Golgi exocytosis but not the exocytosis of glycosylphosphatidylinositol-anchored protein vesicles o

84 sis that a lynx family member, or indeed any glycosylphosphatidylinositol-anchored protein, could act

85 ion behavior of urokinase receptor (uPAR), a glycosylphosphatidylinositol-anchored protein, in a plan

86 Reck, a multi-domain and multi-functional glycosylphosphatidylinositol-anchored protein, specifica

87 The sleepless gene encodes a brain-enriched, glycosylphosphatidylinositol-anchored protein.

88 hy profile strongly suggested that Shu1 is a glycosylphosphatidylinositol-anchored protein.

89 Most glycosylphosphatidylinositol-anchored proteins (GPI-APs)

90 n of cholesterol-rich membranes that contain glycosylphosphatidylinositol-anchored proteins (GPI-APs)

91 tified two Arabidopsis pollen-tube-expressed glycosylphosphatidylinositol-anchored proteins (GPI-APs)

92 Both are predicted glycosylphosphatidylinositol-anchored proteins (GPI-APs)

93 pacity is saturated during stress, misfolded glycosylphosphatidylinositol-anchored proteins dissociat

94 that the defective surface expression of the glycosylphosphatidylinositol-anchored proteins is caused

95 versibly impaired the PD localization of the glycosylphosphatidylinositol-anchored proteins Plasmodes

96 cosaminoglycans, glycoproteins, glycolipids, glycosylphosphatidylinositol-anchored proteins) and the

97 Yet how nonubiquitinated proteins, such as glycosylphosphatidylinositol-anchored proteins, enter MV

98 g lipid mixtures is also applicable to other glycosylphosphatidylinositol-anchored proteins.

99 pid rates of endocytosis and lateral flow of glycosylphosphatidylinositol-anchored proteins.

100 monocytogenes ortholog, had high activity on glycosylphosphatidylinositol-anchored proteins.

101 n with other cell surface proteins including glycosylphosphatidylinositol-anchored proteins.

102 for identification of the myristoylated and glycosylphosphatidylinositol-anchored proteome with sele

103 Mammalian prions refold host glycosylphosphatidylinositol-anchored PrP(C) into beta-s

104 Recently, we identified the glycosylphosphatidylinositol-anchored repulsive guidance

105 Here we showed that testisin, a glycosylphosphatidylinositol-anchored serine protease, c

106 In skin, matriptase acts upstream of the glycosylphosphatidylinositol-anchored serine protease, p

107 mediated via its activation of prostasin, a glycosylphosphatidylinositol-anchored serine protease.

108 in is a trypsin-like serine protease that is glycosylphosphatidylinositol-anchored to the epithelial

109 orientation in the PM (transmembrane versus glycosylphosphatidylinositol-anchored), and ubiquitinati

110 n accelerated fusion rate when driven by the glycosylphosphatidylinositol-anchored, but not by the tr

111 Glypican 3 (GPC3) is a family of glycosylphosphatidylinositol-anchored, cell-surface hepa

112 Glypican 3 (GPC3) belongs to a family of glycosylphosphatidylinositol-anchored, cell-surface hepa

113 Thus native CSP appears as a glycosylphosphatidylinositol-anchored, flexible rod-like

114 LY6E is a glycosylphosphatidylinositol-anchored, IFN-inducible pro

115 eins, but we found evidence that they can be glycosylphosphatidylinositol-anchored.

116 a mannose donor for protein N-glycosylation, glycosylphosphatidylinositol-anchoring, and C- and O-man

117 Proteins having glycosylphosphatidylinositol anchors or single transmemb

118 are variants in MDGAs (MAM domain-containing glycosylphosphatidylinositol anchors), including multipl

119 ific phospholipase C (PI-PLC), which cleaves glycosylphosphatidylinositol anchors, or by NEP1-40, a p

120 hat form chitin, N-linked glycosylation, and glycosylphosphatidylinositol anchors, the mutant phenoty

121 At the cell surface, m157 is exclusively a glycosylphosphatidylinositol-associated protein in MCMV-

122 e morphogenetic protein (BMP) signaling, and glycosylphosphatidylinositol biosynthesis, as well as a

123 he second step of mammalian and trypanosomal glycosylphosphatidylinositol biosynthesis.

124 s of GPI anchors in humans lead to inherited glycosylphosphatidylinositol deficiency (IGD).

125 ins, and a C-terminal region that includes a glycosylphosphatidylinositol-dependent cell wall attachm

126 Thy-1 (CD90) is a 25-37 kDa glycosylphosphatidylinositol (GPI) -anchored glycoprotei

127 is dispensable for restriction, whereas the glycosylphosphatidylinositol (GPI) addition site in the

128 lacking one of the two acyl chains from its glycosylphosphatidylinositol (GPI) anchor (PrP(C)-G-lyso

129 mportant N-linked glycosylation (Asn514) and glycosylphosphatidylinositol (GPI) anchor (Ser529) sites

130 fluenza virus hemagglutinin (HA), and with a glycosylphosphatidylinositol (GPI) anchor addition seque

131 s transmembrane and cytosolic regions with a glycosylphosphatidylinositol (GPI) anchor and examined t

132 In this study, the role of the glycosylphosphatidylinositol (GPI) anchor attached to Pr

133 c differences in Rab GTPase requirements and glycosylphosphatidylinositol (GPI) anchor biosynthesis,

134 he gene encoding PIGA, which is required for glycosylphosphatidylinositol (GPI) anchor biosynthesis.

135 tive agent of African sleeping sickness) the glycosylphosphatidylinositol (GPI) anchor biosynthetic p

136 tified PIGL, the de-N-acetylase required for glycosylphosphatidylinositol (GPI) anchor formation, as

137 The glycosylphosphatidylinositol (GPI) anchor is a C-termina

138 The glycosylphosphatidylinositol (GPI) anchor is a lipid and

139 hment to the plasma membrane by linkage to a glycosylphosphatidylinositol (GPI) anchor is a mode of p

140 The glycosylphosphatidylinositol (GPI) anchor is a post-tran

141 C-terminus of many eukaryotic proteins, the glycosylphosphatidylinositol (GPI) anchor is a posttrans

142 C-terminus of many eukaryotic proteins, the glycosylphosphatidylinositol (GPI) anchor is a posttrans

143 coiled coil motif, and a putative C-terminal glycosylphosphatidylinositol (GPI) anchor motif.

144 nogalactan (AG) glycomodule, and a predicted glycosylphosphatidylinositol (GPI) anchor motif.

145 The encoded 63 kDa protein has a predicted glycosylphosphatidylinositol (GPI) anchor omega-site ((5

146 nly affects protein N-glycosylation but also glycosylphosphatidylinositol (GPI) anchor side-chain mod

147 cular weight due to changes in the procyclin glycosylphosphatidylinositol (GPI) anchor side-chains.

148 BST2 with a glycosylphosphatidylinositol (GPI) anchor signal deletio

149 ytoplasmic tail (CT) domains and appending a glycosylphosphatidylinositol (GPI) anchor signal sequenc

150 ntial N-glycosylation sites, and a predicted glycosylphosphatidylinositol (GPI) anchor site.

151 f the mutant cells revealed that a defect in glycosylphosphatidylinositol (GPI) anchor synthesis lead

152 equencing on all exons of known genes of the glycosylphosphatidylinositol (GPI) anchor synthesis path

153 e TSHR ECD tethered to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that multimeri

154 e eukaryotic hallmark is the attachment of a glycosylphosphatidylinositol (GPI) anchor to C-terminal

155 lusively to lipid rafts by the addition of a glycosylphosphatidylinositol (GPI) anchor to its ectodom

156 marker, we chose monomeric GFP linked via a glycosylphosphatidylinositol (GPI) anchor to the cell me

157 transmembrane topology and carboxy-terminal glycosylphosphatidylinositol (GPI) anchor, BST2 represen

158 C-terminus that directs the attachment of a glycosylphosphatidylinositol (GPI) anchor, but whether T

159 se effects of PrP(Sc) are dependent upon its glycosylphosphatidylinositol (GPI) anchor, suggesting th

160 mine phosphate (EtN-P) from mannose 2 of the glycosylphosphatidylinositol (GPI) anchor, thus permitti

161 ectodomain of the protein, which includes a glycosylphosphatidylinositol (GPI) anchor, was sufficien

162 Glycosylphosphatidylinositol (GPI) anchor-directed membr

163 full-length tetherin, but not the C-terminal glycosylphosphatidylinositol (GPI) anchor-truncated form

164 rP-sen is attached to the cell membrane by a glycosylphosphatidylinositol (GPI) anchor.

165 s is anchored to the cell membrane through a glycosylphosphatidylinositol (GPI) anchor.

166 and the lipid and glycan composition of its glycosylphosphatidylinositol (GPI) anchor.

167 ified with N-linked glycans and a sialylated glycosylphosphatidylinositol (GPI) anchor.

168 CPG15-2 is glycosylphosphatidylinositol (GPI) anchored to the cell

169 Glycosylphosphatidylinositol (GPI) anchoring of proteins

170 Glycosylphosphatidylinositol (GPI) anchoring of proteins

171 Glycosylphosphatidylinositol (GPI) anchoring of the prio

172 Glycosylphosphatidylinositol (GPI) anchoring plays key r

173 Besides glycosylphosphatidylinositol (GPI) anchors and N-glycosy

174 Glycosylphosphatidylinositol (GPI) anchors attach nearly

175 s that are localized to the cell surface via glycosylphosphatidylinositol (gpi) anchors have been pro

176 e lipids that also share a known function as glycosylphosphatidylinositol (GPI) anchors in different

177 d HSPCs and their progeny lack expression of glycosylphosphatidylinositol (GPI) anchors on their cell

178 w that GDE2, unlike classical GDPDs, cleaves glycosylphosphatidylinositol (GPI) anchors.

179 tor-like kinases and proteins with predicted glycosylphosphatidylinositol (GPI) anchors.

180 rv1 cells harbor defects in sphingolipid and glycosylphosphatidylinositol (GPI) biosyntheses and may

181 ss A (PIGA) is involved in the first step of glycosylphosphatidylinositol (GPI) biosynthesis.

182 ription factor (TF) Sp1 and causes inherited glycosylphosphatidylinositol (GPI) deficiency (IGD).

183 Several peptides/small proteins and glycosylphosphatidylinositol (GPI) derivatives were synt

184 coded neuropeptides covalently tethered to a glycosylphosphatidylinositol (GPI) glycolipid anchor on

185 Glycosylphosphatidylinositol (GPI) is a glycolipid that

186 Parasite-derived glycosylphosphatidylinositol (GPI) is believed to be a m

187 the biosynthesis of the glycolipid molecule glycosylphosphatidylinositol (GPI) is disrupted in hemat

188 Biosynthesis of glycosylphosphatidylinositol (GPI) is required for ancho

189 hored to the plasma membrane by a C-terminal glycosylphosphatidylinositol (GPI) linkage.

190 ing of the extracellular portion without the glycosylphosphatidylinositol (GPI) linker was highly act

191 heterologously expressed BrPGIP3 fused to a glycosylphosphatidylinositol (GPI) membrane anchor, immo

192 Glycosylphosphatidylinositol (GPI) membrane anchoring of

193 re anchored to the membrane via a C-terminal glycosylphosphatidylinositol (GPI) moiety.

194 The glycosylphosphatidylinositol (GPI) of Plasmodium falcipa

195 Proteins anchored to the cell surface via glycosylphosphatidylinositol (GPI) play various key role

196 Glycosylphosphatidylinositol (GPI) transamidase (GPIT),

197 d the role of two additional subunits of the glycosylphosphatidylinositol (GPI) transamidase complex

198 ficking, glycosaminoglycan biosynthesis, and glycosylphosphatidylinositol (GPI)-anchor biosynthesis.

199 omain can be functionally substituted by the glycosylphosphatidylinositol (GPI)-anchor of MT6-MMP.

200 The VSG glycosylphosphatidylinositol (GPI)-anchor strongly influ

201 that are tethered on the cell membrane via a glycosylphosphatidylinositol (GPI)-anchor.

202 obstacles that slow the lateral diffusion of glycosylphosphatidylinositol (GPI)-anchored and transmem

203 e is known to contain chitin, and a putative glycosylphosphatidylinositol (GPI)-anchored chitin deace

204 We report that glycosylphosphatidylinositol (GPI)-anchored ephrin-As fu

205 ypanosoma brucei is a heterodimer comprising glycosylphosphatidylinositol (GPI)-anchored expression s

206 mals culminated in the identification of the glycosylphosphatidylinositol (GPI)-anchored glycoprotein

207 eficiency virus (SIV) VLPs containing either glycosylphosphatidylinositol (GPI)-anchored granulocyte-

208 Prion protein (PrP), a host-encoded glycosylphosphatidylinositol (GPI)-anchored membrane gly

209 Cripto-1 (CR-1) is a glycosylphosphatidylinositol (GPI)-anchored membrane gly

210 or, although CR-1 is primarily produced as a glycosylphosphatidylinositol (GPI)-anchored membrane pro

211 Concomitant expression of glycosylphosphatidylinositol (GPI)-anchored nonsignaling

212 CrRLK1L FERONIA (FER) and LORELEI (LRE)-LIKE GLYCOSYLPHOSPHATIDYLINOSITOL (GPI)-ANCHORED PROTEIN 1 (L

213 in COS-7 cells, and show dramatic changes in glycosylphosphatidylinositol (GPI)-anchored protein arra

214 Recently, the glycosylphosphatidylinositol (GPI)-anchored protein DRAG

215 CD177 is a glycosylphosphatidylinositol (GPI)-anchored protein expr

216 (lre-5) of LORELEI, which encodes a putative glycosylphosphatidylinositol (GPI)-anchored protein impl

217 L), named LETUM2/MEDOS1 (LET2/MDS1), and the glycosylphosphatidylinositol (GPI)-anchored protein LLG1

218 Ly6G is a glycosylphosphatidylinositol (GPI)-anchored protein of u

219 The urokinase receptor (uPAR) is a glycosylphosphatidylinositol (GPI)-anchored protein that

220 novel B-cell epitope, Meu10, which encodes a glycosylphosphatidylinositol (GPI)-anchored protein thou

221 membrane expression and gene promoter of the glycosylphosphatidylinositol (GPI)-anchored protein Thy1

222 different cellular proteins, such as CD14, a glycosylphosphatidylinositol (GPI)-anchored protein to t

223 y prion diseases involve the misfolding of a glycosylphosphatidylinositol (GPI)-anchored protein.

224 Glycosylphosphatidylinositol (GPI)-anchored proteins are

225 Glycosylphosphatidylinositol (GPI)-anchored proteins are

226 Glycosylphosphatidylinositol (GPI)-anchored proteins are

227 ar differentiation via their ability to shed glycosylphosphatidylinositol (GPI)-anchored proteins fro

228 In nature, many glycosylphosphatidylinositol (GPI)-anchored proteins loc

229 for CD59 and not a general feature of other glycosylphosphatidylinositol (GPI)-anchored proteins or

230 Glycosylphosphatidylinositol (GPI)-anchored proteins ser

231 The absence of two glycosylphosphatidylinositol (GPI)-anchored proteins, CD

232 phospholipase C specific for the cleavage of glycosylphosphatidylinositol (GPI)-anchored proteins, di

233 thought to be in part due to several surface glycosylphosphatidylinositol (GPI)-anchored proteins, li

234 s in the transport to the plasma membrane of glycosylphosphatidylinositol (GPI)-anchored proteins.

235 ll wall integrity by altering the sorting of glycosylphosphatidylinositol (GPI)-anchored proteins.

236 nocytogenes enzyme has very weak activity on glycosylphosphatidylinositol (GPI)-anchored proteins.

237 n hamsters or transgenic mice overexpressing glycosylphosphatidylinositol (GPI)-anchored PrP(C).

238 rrier-protective activity is linked with the glycosylphosphatidylinositol (GPI)-anchored serine prote

239 T. gondii has a superfamily of glycosylphosphatidylinositol (GPI)-anchored surface anti

240 LRE encodes a putative glycosylphosphatidylinositol (GPI)-anchored surface prot

241 alpha2deltas are a family of glycosylphosphatidylinositol (GPI)-anchored VGCC-associa

242 In the present study, we constructed glycosylphosphatidylinositol (GPI)-anchored VHH JM2 and

243 It has several glycosylphosphatidylinositol (GPI)-anchored virulence fa

244 proteins, except for RAET1E and RAET1G, are glycosylphosphatidylinositol (GPI)-anchored.

245 ed the delivery of GM1 ganglioside (GM1) and glycosylphosphatidylinositol (GPI)-GFP (but not vesicula

246 tor tyrosine kinase EphA2 interacts with its glycosylphosphatidylinositol (GPI)-linked ephrin-A1 liga

247 Reverse signaling via glycosylphosphatidylinositol (GPI)-linked Ephrins may he

248 was capable of detecting hemifusion, we used glycosylphosphatidylinositol (GPI)-linked hemagglutinin

249 ion abnormally delayed (Dally) is one of two glycosylphosphatidylinositol (GPI)-linked heparan sulfat

250 EphrinA1 is a glycosylphosphatidylinositol (GPI)-linked ligand for the

251 Prnd encodes the glycosylphosphatidylinositol (GPI)-linked protein doppel

252 s a small, variably and highly glycosylated, glycosylphosphatidylinositol (GPI)-linked protein, is ex

253 lobinuria (PNH), hematopoietic cells lacking glycosylphosphatidylinositol (GPI)-linked proteins on th

254 Endocytosis of glycosylphosphatidylinositol (GPI)-linked proteins via a

255 ne candidate plasticity gene 15, is a small, glycosylphosphatidylinositol (GPI)-linked, extracellular

256 Here, we employed a glycosylphosphatidylinositol (GPI)-scFv X5 approach to c

257 Plasma concentrations of glycosylphosphatidylinositol (GPI)-specific phospholipas

258 /and anchored to the plasma membrane through glycosylphosphatidylinositol (GPI).

259 osphoglycan portion of the Toxoplasma gondii glycosylphosphatidylinositol (GPI1) for the detection of

260 y responses induced by Plasmodium falciparum glycosylphosphatidylinositols (GPIs) are thought to be i

261 lycan corresponding to Plasmodium falciparum glycosylphosphatidylinositols (GPIs) has been proposed a

262 otoxin that is tethered to the membrane by a glycosylphosphatidylinositol linkage (GPIalpha btx) in c

263 Membrane tethering but not specifically the glycosylphosphatidylinositol linkage characteristic of g

264 biphasic response, regardless of whether its glycosylphosphatidylinositol linkage to the membrane can

265 lerating factor (DAF, also known as CD55), a glycosylphosphatidylinositol-linked (GPI-linked) plasma

266 ne family (YPS genes) encoding extracellular glycosylphosphatidylinositol-linked aspartyl proteases.

267 e gene to C. albicans PGA59, which encodes a glycosylphosphatidylinositol-linked cell wall protein.

268 rosine kinase receptor (cRET) and a specific glycosylphosphatidylinositol-linked co-receptor (GFRalph

269 ding preferences, that interact with the six glycosylphosphatidylinositol-linked ephrin-A ligands and

270 guidance molecule c (RGMc or hemojuvelin), a glycosylphosphatidylinositol-linked glycoprotein express

271 herpes simplex virus glycoprotein D and the glycosylphosphatidylinositol-linked Ig domain protein CD

272 HJV is a glycosylphosphatidylinositol-linked membrane protein tha

273 e plasminogen activator receptor (uPAR) is a glycosylphosphatidylinositol-linked membrane protein wit

274 Incorporation of a glycosylphosphatidylinositol-linked protein (placental a

275 Hemojuvelin (HJV) is a glycosylphosphatidylinositol-linked protein and binds bo

276 Our results indicate that HJV is a glycosylphosphatidylinositol-linked protein and undergoe

277 flow cytometry using antibodies specific for glycosylphosphatidylinositol-linked proteins (e.g., CD48

278 however, examined mainly ganglioside GM1 and glycosylphosphatidylinositol-linked proteins as lipid ra

279 itol-specific phospholipase C targets PI and glycosylphosphatidylinositol-linked proteins of eukaryot

280 in, nitric oxide depletion, absence of other glycosylphosphatidylinositol-linked proteins such as uro

281 that are either single-pass, multi-pass, or glycosylphosphatidylinositol-linked proteins.

282 somatic mutations result in a deficiency of glycosylphosphatidylinositol-linked surface proteins, in

283 FcgammaRIIIb is a glycosylphosphatidylinositol-linked, low affinity recept

284 embrane and cytoplasmic tail domains or by a glycosylphosphatidylinositol linker in membrane-type MMP

285 amino acid sequences, (2) signal peptide and glycosylphosphatidylinositol lipid anchor addition seque

286 CPO was modified by attachment of a glycosylphosphatidylinositol membrane anchor to the C te

287 o recent data from transgenic mice lacking a glycosylphosphatidylinositol membrane anchor to the norm

288 ement plasma membrane via a carboxy-terminal glycosylphosphatidylinositol membrane anchor.

289 nctions of glypican-4 are independent of its glycosylphosphatidylinositol membrane anchorage, as a no

290 the biosynthesis of N- and O-linked glycans, glycosylphosphatidylinositol membrane anchors, beta1,3-

291 nce factors promote infection, including the glycosylphosphatidylinositol membrane-anchored major sur

292 that are anchored to the cell surface via a glycosylphosphatidylinositol moiety.

293 and is anchored to the plasma membrane via a glycosylphosphatidylinositol or is covalently linked to

294 ound to glycan moieties within P. falciparum glycosylphosphatidylinositol (PfGPI) molecules on the pa

295 previously shown that Plasmodium falciparum glycosylphosphatidylinositols (PfGPIs) can induce A. ste

296 o (Lycopersicon esculentum) AGP containing a glycosylphosphatidylinositol plasma membrane anchor sequ

297 ylceramide; in contrast, it had no effect on glycosylphosphatidylinositol production.

298 positional specificity of callose-modifying glycosylphosphatidylinositol proteins at PD.

299 P)-tagged proteins at the cell surface via a glycosylphosphatidylinositol tail.

300 tion signal (e.g., green fluorescent protein-glycosylphosphatidylinositol) were found in the cilium,