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 contrast, BiPN fusion proteins containing a glycosylphosphatidylinositol anchor instead of the ISG65

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

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

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

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

16 hat, in agreement with its substitution by a glycosylphosphatidylinositol anchor, COB was polarly tar

17 t of HJV, hemojuvelin, contains a C-terminal glycosylphosphatidylinositol anchor, suggesting that it

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

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

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

21 of endogenous ephrinAs by cleavage of their glycosylphosphatidylinositol anchor.

22 lacks a predicted transmembrane domain or a glycosylphosphatidylinositol anchor.

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

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

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

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

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

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

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

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

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

32 However, delivery of glycosylphosphatidylinositol-anchored endolyn was inhibi

33 GPIHBP1, a glycosylphosphatidylinositol-anchored endothelial cell p

34 GPIHBP1, a glycosylphosphatidylinositol-anchored endothelial cell p

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

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

37 GPIHBP1, a glycosylphosphatidylinositol-anchored glycoprotein of mi

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

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

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

41 Glycosylphosphatidylinositol-anchored high density lipop

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

43 Glycosylphosphatidylinositol-anchored high density lipop

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

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

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

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

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

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

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

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

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

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

54 CD160, a glycosylphosphatidylinositol-anchored member of the immu

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

56 Decay-accelerating factor ([DAF] CD55) is a glycosylphosphatidylinositol-anchored membrane inhibitor

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

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

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

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

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

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

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

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

65 Glycosylphosphatidylinositol-anchored neurotoxin-like re

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

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

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

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

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

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

72 CD14 is a glycosylphosphatidylinositol-anchored protein expressed

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

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

75 GPIHBP1, a glycosylphosphatidylinositol-anchored protein of capilla

76 CD59 is a glycosylphosphatidylinositol-anchored protein that inhib

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

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

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

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

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

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

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

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

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

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

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

88 Most glycosylphosphatidylinositol-anchored proteins (GPI-APs)

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

90 king transmembrane or intracellular domains, glycosylphosphatidylinositol-anchored proteins can modul

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

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

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

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

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

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

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

98 not require heparan sulfate proteoglycan- or glycosylphosphatidylinositol-anchored proteins.

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

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

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

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

103 Recently, we identified the glycosylphosphatidylinositol-anchored repulsive guidance

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

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

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

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

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

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

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

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

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

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

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

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

116 Proteins having glycosylphosphatidylinositol anchors or single transmemb

117 Furthermore, engineered CEACAMs appended to glycosylphosphatidylinositol anchors partitioned with TX

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 Glycosylphosphatidylinositol biosynthesis is essential f

123 The second step in glycosylphosphatidylinositol biosynthesis is the de-N-ac

124 he second step of mammalian and trypanosomal glycosylphosphatidylinositol biosynthesis.

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

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

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

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

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

134 ttached to the cell membrane in humans via a glycosylphosphatidylinositol (GPI) anchor but in mouse v

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

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

137 The glycosylphosphatidylinositol (GPI) anchor is a lipid and

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

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

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

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

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

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

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

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

146 BST2 with a glycosylphosphatidylinositol (GPI) anchor signal deletio

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

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

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

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

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

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

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

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

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

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

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

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

159 Glycosylphosphatidylinositol (GPI) anchor-directed membr

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

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

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

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

164 ferase that is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor.

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

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

167 Glycosylphosphatidylinositol (GPI) anchoring of proteins

168 Glycosylphosphatidylinositol (GPI) anchoring of proteins

169 Glycosylphosphatidylinositol (GPI) anchoring of the prio

170 (PIG-U), a transamidase complex unit in the glycosylphosphatidylinositol (GPI) anchoring pathway), a

171 Besides glycosylphosphatidylinositol (GPI) anchors and N-glycosy

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

173 The glycosylphosphatidylinositol (GPI) anchors of Plasmodium

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

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

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

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

178 has been suggested that compounds affecting glycosylphosphatidylinositol (GPI) biosynthesis in blood

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

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

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

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

183 Glycosylphosphatidylinositol (GPI) is a glycolipid that

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

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

186 This strategy mimics the natural glycosylphosphatidylinositol (GPI) linkage found in many

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

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

189 e expressing prion protein (PrP) lacking the glycosylphosphatidylinositol (GPI) membrane anchor, abno

190 Glycosylphosphatidylinositol (GPI) membrane anchoring of

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

192 The glycosylphosphatidylinositol (GPI) of Plasmodium falcipa

193 Yeast and human glycosylphosphatidylinositol (GPI) precursors differ in

194 Glycosylphosphatidylinositol (GPI) transamidase (GPIT),

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

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

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

198 The VSG glycosylphosphatidylinositol (GPI)-anchor strongly influ

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

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

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

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

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

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

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

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

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

208 SRV) receptor, hyaluronidase 2 (Hyal2), is a glycosylphosphatidylinositol (GPI)-anchored molecule con

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

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

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

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

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

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

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

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

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

218 Glycosylphosphatidylinositol (GPI)-anchored proteins are

219 Glycosylphosphatidylinositol (GPI)-anchored proteins are

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

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

222 Glycosylphosphatidylinositol (GPI)-anchored proteins ser

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

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

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

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

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

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

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

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

231 Western blotting revealed that glycosylphosphatidylinositol (GPI)-anchored ULBP3 but no

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

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

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

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

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

237 tor (GDNF) receptor alpha-1 (GFRalpha1), the glycosylphosphatidylinositol (GPI)-linked coreceptor for

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

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

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

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

242 Glypicans, a family of glycosylphosphatidylinositol (GPI)-linked HSPGs, are exp

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

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

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

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

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

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

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

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

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

252 Glycosylphosphatidylinositols (GPIs) serve as membrane a

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

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

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

256 a mutant containing the CD43 ectodomain on a glycosylphosphatidylinositol linkage was ineffective.

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

258 Glycosylphosphatidylinositol-linked and transmembrane ma

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

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

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

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

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

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

265 HJV is a glycosylphosphatidylinositol-linked membrane protein tha

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

267 ene, because its inactivation causes lack of glycosylphosphatidylinositol-linked membrane proteins.

268 h the normal and abnormal prion proteins are glycosylphosphatidylinositol-linked membrane proteins.

269 Incorporation of a glycosylphosphatidylinositol-linked protein (placental a

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

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

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

273 Because aggregation of glycosylphosphatidylinositol-linked proteins activates S

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

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

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

277 S1 ectodomain (ED), as ectopic expression of glycosylphosphatidylinositol-linked S1ED enhances alpha(

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

279 FcgammaRIIIb is a glycosylphosphatidylinositol-linked, low affinity recept

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

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

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

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

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

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

286 The procyclins contain glycosylphosphatidylinositol membrane anchors with large

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

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

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

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

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

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

293 In mammals, P. falciparum glycosylphosphatidylinositols (PfGPIs) can induce NOS ex

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

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

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

297 an of hyphae by the C terminus of Hwp1 via a glycosylphosphatidylinositol remnant anchor.

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

299 two of the five subunits of the ER-localized glycosylphosphatidylinositol transamidase complex, are r

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