ライフサイエンスコーパス: heparan sulfate proteoglycan

1 yndecan 4 as well as that of an unidentified heparan sulfate proteoglycan.

2 EGF188, that differ in their ability to bind heparan sulfate proteoglycan.

3 ers in the secretory pathway, namely LRP and heparan sulfate proteoglycan.

4 by T lymphocytes, TNF-like molecule 1A, and heparan sulfate proteoglycans.

5 creas), is in part dependent on sulfation of heparan sulfate proteoglycans.

6 ccurs after the initial binding of HMPV F to heparan sulfate proteoglycans.

7 TACI), and also interacts independently with heparan sulfate proteoglycans.

8 lphosphatidylinositol-anchored, cell-surface heparan sulfate proteoglycans.

9 ifferentiated ligand binding and activity of heparan sulfate proteoglycans.

10 lphosphatidylinositol-anchored, cell-surface heparan sulfate proteoglycans.

11 hesis, even after inhibition of sulfation of heparan sulfate proteoglycans.

12 its carboxyl terminus with lipoproteins and heparan sulfate proteoglycans.

13 do not require cell surface sialic acids or heparan sulfate proteoglycans.

14 ion in vitro, which depended on cell-surface heparan sulfate proteoglycans.

15 inoglycans are the oligosaccharide chains of heparan sulfate proteoglycans.

16 conditions depends entirely on cell surface heparan sulfate proteoglycans.

17 -sulfation states of cell-surface and matrix heparan sulfate proteoglycans.

18 is modulated by extrinsic cofactors such as heparan sulfate proteoglycans.

19 ular attachment through binding cell surface heparan sulfate proteoglycans.

20 on through binding to integrin receptors and heparan sulfate proteoglycans.

21 cells requires its interaction with surface heparan sulfate proteoglycans.

22 lular trapping mediated by membrane-proximal heparan sulfate proteoglycans.

23 sistent with a previously described role for heparan sulfate proteoglycans.

24 ude laminins, type IV collagen, nidogens and heparan sulfate proteoglycans.

25 the endothelial receptors for IE binding are heparan sulfate proteoglycans.

26 Here, we focused on the syndecan-1 heparan sulfate proteoglycan, a highly conserved, multif

27 ary domains: a charged N terminus that binds heparan sulfate proteoglycans, a central NANP repeat dom

28 a conserved member of the glypican family of heparan sulfate proteoglycans, a family with several mem

29 was reduced approximately 60% by binding to heparan sulfate proteoglycans, a prominent component of

30 ng the MEK/ERK pathway is likely to modulate heparan sulfate proteoglycan activity, which in turn may

31 It is shown in this study that the heparan sulfate proteoglycan agrin is overexpressed in T

32 ine protease neurotrypsin, which cleaves the heparan sulfate proteoglycan agrin.

33 transduction activity requires cell surface heparan sulfate proteoglycans, although AAV(VR-942) lack

34 e two modules on Thy1(+) oval cells required heparan sulfate proteoglycan and integrin alpha(5)beta(1

35 at reduce its expression and ability to bind heparan sulfate proteoglycan and LRP4 coreceptors involv

36 Of the 11 well-characterized AAV serotypes, heparan sulfate proteoglycan and sialic acid have been s

37 nalization of Tat requires interactions with heparan sulfate proteoglycans and cholesterol-enriched l

38 Heparan sulfate proteoglycans and heparin derivatives fu

39 lpha C protein interaction involves multiple heparan sulfate proteoglycans and impairs bacterial kill

40 eins, thereby increasing viral attachment to heparan sulfate proteoglycans and inducing cell migratio

41 Heparin/heparan sulfate proteoglycans and neuropilin-1 (NRP-1) h

42 This DC-mediated transfer of HTLV-1 involves heparan sulfate proteoglycans and neuropilin-1 and resul

43 glucosamine 6-O-sulfate modifications within heparan sulfate proteoglycans and regulate their interac

44 by apoE's ability to bind with cell surface heparan sulfate proteoglycans and to lipoprotein recepto

45 tion of haptotactic gradients on endothelial heparan sulfate proteoglycans and, hence, integrin-media

46 senchyme, likely presented in the context of heparan sulfate proteoglycans, and effector molecules in

47 Angiogenin uptake into astroglia requires heparan sulfate proteoglycans, and engages clathrin-medi

48 ation of MuSK by agrin, a neuronally derived heparan-sulfate proteoglycan, and LRP4 (low-density lipo

49 we demonstrate that surfen, a small molecule heparan sulfate proteoglycan antagonist, inhibits both S

50 Heparan sulfate proteoglycans are an important and abund

51 Heparan sulfate proteoglycans are critical binding partn

52 Heparan sulfate proteoglycans are essential for biologic

53 Heparan sulfate proteoglycans are ubiquitously located o

54 can-1, the predominant intestinal epithelial heparan sulfate proteoglycan, are essential in maintaini

55 Here, we identified heparan sulfate proteoglycan as a major cellular attachm

56 activity, GAG incorporation of (35)SO4, and heparan sulfate proteoglycan assembly.

57 Heparan sulfate proteoglycans bind to and regulate many

58 glycosophosphotidylinositol (GPI)-anchored, heparan-sulfate proteoglycans bind ligands of several ot

59 secretoneurin stimulates binding of VEGF to heparan sulfate proteoglycan binding sites.

60 ting effect of apoA-V has been attributed to heparan sulfate proteoglycan binding, as confirmed by st

61 ovel role for toutvelu (ttv), a regulator of heparan sulfate proteoglycan biosynthesis during this pr

62 of potential multistep processes involved in heparan-sulfate proteoglycans-bound FGF2 release, intern

63 boat, can mediate trans signaling through a heparan sulfate proteoglycan co-receptor in S2 cells.

64 tate to produce Acetyl-CoA, and secretion of heparan sulfate proteoglycan (component of syndecan-1).

65 HSulf-1 modulates the sulfation states of heparan sulfate proteoglycans critical for heparin bindi

66 monstrate a potential mechanism by which the heparan sulfate proteoglycan Dally-like (Dlp) promotes W

67 fects of RAP were significantly decreased in heparan sulfate proteoglycan-deficient Chinese hamster o

68 xclusive ligand of dendritic cell-associated heparan sulfate proteoglycan-dependent integrin ligand (

69 ered that the dendritic cell (DC)-associated heparan sulfate proteoglycan-dependent integrin ligand (

70 a patients express dendritic cell-associated heparan sulfate proteoglycan-dependent integrin ligand,

71 leagues show that dendritic cell-associated, heparan sulfate proteoglycans-dependent integrin ligand

72 Syndecan-1 is a common heparan sulfate proteoglycan expressed by many natural t

73 We found that Glypican-3 (GPC3), a heparan sulfate proteoglycan expressed on murine as well

74 Glypicans are conserved cell surface heparan sulfate proteoglycans expressed in a spatiotempo

75 ze glycosaminoglycans, and more specifically heparan sulfate proteoglycans, for their attachment to h

76 e ectodomain shedding of syndecan-1, a major heparan sulfate proteoglycan found in epithelial cells.

77 enous hypertension, and the specific loss of heparan sulfate proteoglycans from the basolateral surfa

78 Conducted research showed that heparan sulfate proteoglycans function as adhesion molec

79 ems reflect the molecular characteristics of heparan sulfate proteoglycan functions observed previous

80 ayed comprehension of the molecular basis of heparan sulfate proteoglycan functions.

81 e includes only three characterized membrane heparan sulfate proteoglycan genes.

82 We previously found that the heparan sulfate proteoglycan glypican 1 (GPC1) is univer

83 The heparan sulfate proteoglycan Glypican 4 (Gpc4) is strong

84 roteoglycan neurocan, the growth-stimulating heparan sulfate proteoglycan glypican, or the chondroiti

85 The heparan sulfate proteoglycan glypican-1 (GPC1) is a core

86 The heparan sulfate proteoglycan glypican-1 (GPC1) is involv

87 vate EGL-mediated NO production and that the heparan sulfate proteoglycan glypican-1 is a primary mec

88 g protein on the Schwann cell surface is the heparan sulfate proteoglycan glypican-1.

89 d host glycosaminoglycan-anchoring proteins (heparan sulfate proteoglycans) has limited the understan

90 Syndecan 4, a heparan sulfate proteoglycan, has been associated with o

91 Glypican-3 (GPC3) is a cell-surface heparan sulfate proteoglycan highly expressed in hepatoc

92 Heparan sulfate proteoglycans (HS-PGs) regulate several

93 Indeed, expression of heparan sulfate proteoglycans (HS-PGs), normally involve

94 Two endocytic receptors, the syndecan-1 heparan sulfate proteoglycan (HSPG) and the LDL receptor

95 Binding of AAV to heparan sulfate proteoglycan (HSPG) at the ILM may allow

96 We show that SLC35B2, as a key regulator of heparan sulfate proteoglycan (HSPG) biosynthesis, is ess

97 Glypican-3 (Gpc3) is a heparan sulfate proteoglycan (HSPG) expressed widely dur

98 Heparan sulfate proteoglycan (HSPG) has also been implic

99 Heparan sulfate proteoglycan (HSPG) is required for this

100 odes the phylogenetically conserved secreted heparan sulfate proteoglycan (HSPG) perlecan, a componen

101 misrouting phenotype in mutants defective in heparan sulfate proteoglycan (HSPG) production and avoid

102 ine protease (SP) domains and bury potential heparan sulfate proteoglycan (HSPG) receptor binding res

103 ce lacking lipoprotein lipase (LPL), hepatic heparan sulfate proteoglycan (HSPG) receptors, LDLR, or

104 The heparan sulfate proteoglycan (HSPG) syndecan-1 (SDC1) ac

105 -2 mutants, which affect enzymes involved in heparan sulfate proteoglycan (HSPG) synthesis.

106 Although binding of CXCL12gamma to heparan sulfate proteoglycan (HSPG) was 10-fold higher t

107 l synaptogenesis, including the GPI-anchored heparan sulfate proteoglycan (HSPG) Wnt co-receptor Dall

108 attachment factors (HAFs), such as DC-SIGN, heparan sulfate proteoglycan (HSPG), and alpha4beta7 int

109 Dally-like (Dlp) is a glypican-type heparan sulfate proteoglycan (HSPG), containing a protei

110 To confirm this finding, we prepared heparan sulfate proteoglycan (HSPG)-knockout (KO) cells

111 atases (Sulf-1 and Sulf-2) are extracellular heparan sulfate proteoglycan (HSPG)-specific 6-O-endosul

112 sly shown to confer binding of the virion to heparan sulfate proteoglycan (HSPG).

113 its receptors, the proto-oncogene c-Met and heparan sulfate proteoglycan (HSPG).

114 accumulation is mediated through binding to heparan sulfate proteoglycans (HSPG) allowing for possib

115 It damages cell surface heparan sulfate proteoglycans (HSPG) and activates LOX-1

116 Here, we provide evidence of a novel role of heparan sulfate proteoglycans (HSPG) in the adaptive res

117 Binding to lipid and heparan sulfate proteoglycans (HSPG) induces apoE to ado

118 Heparan sulfate proteoglycans (HSPG) play a critical rol

119 Cleavage of heparan sulfate proteoglycans (HSPG) with heparinase III

120 y RTK pathways is regulated by extracellular heparan sulfate proteoglycans (HSPG), suggesting these m

121 step of virus-cell interaction by mimicking heparan sulfate proteoglycans (HSPG), the highly conserv

122 3 spreads extracellularly and interacts with heparan sulfate proteoglycans (HSPG).

123 We now show that heparan sulfate proteoglycans (HSPGs) act as alternative

124 Heparan sulfate proteoglycans (HSPGs) act as binding rec

125 Heparan sulfate proteoglycans (HSPGs) act as coreceptors

126 Once released by HIV(+) cells, p17 binds heparan sulfate proteoglycans (HSPGs) and CXCR1 on leuko

127 bacterial surface binds to host cell surface heparan sulfate proteoglycans (HSPGs) and facilitates en

128 Binding studies with heparan sulfate proteoglycans (HSPGs) and neuropilin-1 (

129 enzyme that removes 6-O sulfate groups from heparan sulfate proteoglycans (HSPGs) and suppresses upt

130 We previously showed that HMPV binds heparan sulfate proteoglycans (HSPGs) and that HMPV bind

131 Because SULF1 and SULF2 desulfate heparan sulfate proteoglycans (HSPGs) and the HSPG glypi

132 xtracellular Hh binds to cell-bound glypican heparan sulfate proteoglycans (HSPGs) and the secreted p

133 Heparan sulfate proteoglycans (HSPGs) are cell surface r

134 Heparan sulfate proteoglycans (HSPGs) are central modula

135 Heparan sulfate proteoglycans (HSPGs) are concentrated a

136 Heparan sulfate proteoglycans (HSPGs) are extracellular

137 Heparan sulfate proteoglycans (HSPGs) are extracellular

138 Heparan sulfate proteoglycans (HSPGs) are found in the b

139 Heparan sulfate proteoglycans (HSPGs) are important modu

140 evious studies in Drosophila have shown that heparan sulfate proteoglycans (HSPGs) are involved in bo

141 Heparan sulfate proteoglycans (HSPGs) are normally assoc

142 Heparan sulfate proteoglycans (HSPGs) are potent regulat

143 Heparan sulfate proteoglycans (HSPGs) are required durin

144 Heparan sulfate proteoglycans (HSPGs) are synthesised an

145 Heparan sulfate proteoglycans (HSPGs) are ubiquitous com

146 Heparan sulfate proteoglycans (HSPGs) are ubiquitously e

147 nd that of others have identified syndecan-1 heparan sulfate proteoglycans (HSPGs) as remnant lipopro

148 Heparan sulfate proteoglycans (HSPGs) bind to and regula

149 f DIDS-resistant virus became independent of heparan sulfate proteoglycans (HSPGs) but, concomitantly

150 O-sulfotransferases modify heparan sulfate proteoglycans (HSPGs) by catalyzing the

151 Heparan sulfate proteoglycans (HSPGs) control many cellu

152 Heparan sulfate proteoglycans (HSPGs) critically modulat

153 and distribution of Upd are regulated by the heparan sulfate proteoglycans (HSPGs) Dally and Dally-li

154 matosensory neurons as a model, we show that heparan sulfate proteoglycans (HSPGs) Dally and Syndecan

155 of injury and repair in the lung, fragmented heparan sulfate proteoglycans (HSPGs) from damaged extra

156 Heparan sulfate proteoglycans (HSPGs) function as a co-r

157 Heparan sulfate proteoglycans (HSPGs) function as corece

158 In addition, heparan sulfate proteoglycans (HSPGs) have also been imp

159 Heparan sulfate proteoglycans (HSPGs) have been attribut

160 Cell surface heparan sulfate proteoglycans (HSPGs) have been implicat

161 Heparan sulfate proteoglycans (HSPGs) have long been imp

162 Heparan sulfate proteoglycans (HSPGs) have long unbranch

163 llenge model, we evaluated the importance of heparan sulfate proteoglycans (HSPGs) in human papilloma

164 The importance of heparan sulfate proteoglycans (HSPGs) in neurodevelopmen

165 sly explored the role of N-glycoproteins and heparan sulfate proteoglycans (HSPGs) in P. aeruginosa-m

166 e selectivity has been attributed to anionic heparan sulfate proteoglycans (HSPGs) in the glomerular

167 Heparan sulfate proteoglycans (HSPGs) influence the sign

168 we identify that four genes associated with heparan sulfate proteoglycans (HSPGs) metabolism, specif

169 Heparan sulfate proteoglycans (HSPGs) modulate the actio

170 terminal pro region is excreted and binds to heparan sulfate proteoglycans (HSPGs) of the basement me

171 indicates that prion protein aggregates bind heparan sulfate proteoglycans (HSPGs) on the cell surfac

172 o covalently attach to core proteins to form heparan sulfate proteoglycans (HSPGs) on the cell surfac

173 Heparan sulfate proteoglycans (HSPGs) play critical role

174 Heparan sulfate proteoglycans (HSPGs) regulate a number

175 Islet amyloid also contains heparan sulfate proteoglycans (HSPGs) that may contribut

176 any microbial pathogens subvert cell surface heparan sulfate proteoglycans (HSPGs) to infect host cel

177 stimulator of glioma growth, is regulated by heparan sulfate proteoglycans (HSPGs) via a ternary comp

178 wn to interfere with binding to cell surface heparan sulfate proteoglycans (HSPGs), also resulted in

179 Recently, a glucose transporter, GLUT-1, heparan sulfate proteoglycans (HSPGs), and neuropilin-1

180 transferases, a class of enzymes that modify heparan sulfate proteoglycans (HSPGs), are essential to

181 We demonstrated that expression of heparan sulfate proteoglycans (HSPGs), including TbetaRI

182 ein belonging to the heterogeneous family of heparan sulfate proteoglycans (HSPGs), is expressed by c

183 Heparan sulfate proteoglycans (HSPGs), located on the ce

184 We found levels of mRNAs encoding heparan sulfate proteoglycans (HSPGs), particularly SDC1

185 DS-resistant HCMV also became independent of heparan sulfate proteoglycans (HSPGs), suggesting that e

186 In contrast to the functional role of heparan sulfate proteoglycans (HSPGs), the importance of

187 ize glycosaminoglycans (GAGs), specifically, heparan sulfate proteoglycans (HSPGs), were resistant to

188 Epiblast-state transition in mESCs involves heparan sulfate proteoglycans (HSPGs), which have also b

189 LDL receptor (LDLR) family and cell-surface heparan sulfate proteoglycans (HSPGs), which have been s

190 uction by bridging the virus to cell-surface heparan sulfate proteoglycans (HSPGs).

191 as Hedgehog (Hh) and Wingless (Wg) depend on heparan sulfate proteoglycans (HSPGs).

192 his alters hepatic lipoprotein clearance via heparan sulfate proteoglycans (HSPGs).

193 n interact with the extracellular matrix and heparan sulfate proteoglycans (HSPGs).

194 aces of uninfected cells by interacting with heparan sulfate proteoglycans (HSPGs).

195 ally involves virion binding to cell surface heparan sulfate proteoglycans (HSPGs).

196 linked to core proteins collectively termed heparan sulfate proteoglycans (HSPGs).

197 cans comprise a major family of cell surface heparan sulfate proteoglycans (HSPGs).

198 ter hepatocytes in vivo through cell surface heparan sulfate proteoglycans (HSPGs).

199 thought to enter hepatocytes in vivo through heparan sulfate proteoglycans (HSPGs).

200 s with their receptors are often mediated by heparan sulfate proteoglycans (HSPGs).

201 vein (vn) and may influence binding of Vn to heparan-sulfated proteoglycans (HSPGs).

202 revealed that syndecan-4 (SD-4) is the sole heparan sulfate proteoglycan immunoprecipitated by DC-HI

203 Glypican-1 (Gpc1) is the predominant heparan sulfate proteoglycan in the developing and adult

204 wo glycosylphosphatidylinositol (GPI)-linked heparan sulfate proteoglycans in Drosophila.

205 inoglycans, we analyzed the role of membrane heparan sulfate proteoglycans in the adhesion and migrat

206 gnaling and suggest a physiological role for heparan sulfate proteoglycans in the regulation of ephri

207 ccumulate through binding to highly specific heparan-sulfate proteoglycans in the extracellular matri

208 dent replication confirms a role for GPC5, a heparan sulfate proteoglycan, in disease risk.

209 we evaluated the role of syndecan-1, a major heparan sulfate proteoglycan, in modulating inflammatory

210 we evaluated the role of syndecan-1, a major heparan sulfate proteoglycan, in modulating multiorgan h

211 as well as aberrant cellular localization of heparan sulfate proteoglycans, in all subtypes.

212 ivation by binding dendritic cell-associated heparan sulfate proteoglycan-integrin ligand (DC-HIL) on

213 ed groups on their glycosaminoglycan chains, heparan sulfate proteoglycans interact with growth facto

214 Agrin is a key heparan sulfate proteoglycan involved in the development

215 sulfate and that N- and 6-O-sulfation of the heparan sulfate proteoglycans is required for HCV infect

216 Interaction with heparan sulfate proteoglycans is supposed to provide che

217 The biosynthesis of heparan sulfate proteoglycans is tightly regulated by mu

218 a member of the mammalian glypican family of heparan sulfate proteoglycans, is highly expressed in gl

219 d ones bind heparin - a structural analog of heparan sulfate proteoglycans known to mediate exosome e

220 of integrin alpha(6)beta(1) and cell surface heparan sulfate proteoglycans, leading to ROS-dependent

221 Here we provide evidence that heparan sulfate proteoglycans may mediate binding betwee

222 These studies suggest that heparan sulfate proteoglycans may play a critical role i

223 evious studies have suggested alterations in heparan sulfate proteoglycan metabolism in rat and mouse

224 shedding of syndecan-1, a major cell surface heparan sulfate proteoglycan, modulates molecular and ce

225 in Caenorhabditis elegans, LON-2/glypican, a heparan sulfate proteoglycan, modulates UNC-6/netrin sig

226 Expression of SP-Tatm3x in heparan sulfate proteoglycan-negative cells further impr

227 e binding of Wg to Dally, a potential target heparan sulfate proteoglycan of Sulf1.

228 on of DC-HIL, we hypothesized that a heparin/heparan sulfate proteoglycan on activated T cells is the

229 mation between FGF, FGF receptor (FGFR), and heparan sulfate proteoglycan on the cell membrane.

230 and Tec kinase, as well as membrane-proximal heparan sulfate proteoglycans on cell surfaces.

231 ) extracellular trapping of FGF2 mediated by heparan sulfate proteoglycans on cell surfaces.

232 "seeding." We have previously observed that heparan sulfate proteoglycans on the cell surface mediat

233 ctoferrin was attributable to its binding to heparan sulfate proteoglycans on the cell surface of DA

234 All recombinant Tau assemblies bound heparan sulfate proteoglycans on the cell surface, which

235 L protein mediates attachment of virions to heparan sulfate proteoglycans on the surface of hepatocy

236 ances LPL cleavage in the presence of either heparan sulfate proteoglycans or glycosylphosphatidylino

237 llografts, selective induction of the matrix heparan sulfate proteoglycan perlecan was observed, alon

238 Endorepellin, the C-terminal fragment of the heparan sulfate proteoglycan perlecan, influences variou

239 in, the angiostatic C-terminal domain of the heparan sulfate proteoglycan perlecan, inhibits angiogen

240 Endorepellin, the C-terminal fragment of the heparan sulfate proteoglycan perlecan, possesses angiost

241 t cell lines, RBL-2H3 and HMC-1, produce the heparan sulfate proteoglycan, perlecan, with a molecular

242 ), which is bound to the pericellular matrix heparan sulfate proteoglycan, perlecan.

243 vide the first genetic evidence that hepatic heparan sulfate proteoglycans play a central role in the

244 der normal physiological conditions, hepatic heparan sulfate proteoglycans play a crucial role in the

245 by high expression of syndecan-1 (CD138), a heparan sulfate proteoglycan present on the myeloma cell

246 Heparan sulfate proteoglycans, present on cell surfaces

247 Syndecan-1 is a cell surface heparan sulfate proteoglycan primarily expressed in the

248 d, Saez et al demonstrate that inhibition of heparan sulfate proteoglycan production by bone marrow o

249 r mediating the interaction of AAV2 with the heparan sulfate proteoglycan receptor.

250 air depends on interactions between cellular heparan sulfate proteoglycan receptors, syndecan-1 and -

251 t or dynamin activity or remove cell surface heparan sulfate proteoglycans reduced infection efficien

252 kdown of glycosaminoglycan polymerases or of heparan sulfate proteoglycans reduced the cellular bindi

253 Transmembrane heparan sulfate proteoglycans regulate multiple aspects

254 Heparan sulfate proteoglycans regulate various physiolog

255 Previous studies showed that Dally, a heparan sulfate proteoglycan, regulates both the distrib

256 Heparan sulfate proteoglycan(s) is present in neutrophil

257 es the interaction between TGF-beta1 and its heparan sulfate proteoglycan sequestration receptor, TGF

258 led at the cell surface level via binding to heparan sulfate proteoglycans, such as syndecans.

259 neuronal connectivity, recent studies of the heparan sulfate proteoglycans suggest that these ancient

260 t this activity requires the shedding of the heparan sulfate proteoglycan syndecan-1 (Sdc1) from the

261 When shed from the cell surface, the heparan sulfate proteoglycan syndecan-1 can facilitate t

262 Furthermore, we identified the heparan sulfate proteoglycan syndecan-1 in complexes wit

263 The heparan sulfate proteoglycan syndecan-1 is expressed by

264 The cell surface heparan sulfate proteoglycan syndecan-1 is induced in st

265 The heparan sulfate proteoglycan syndecan-1 is proteolytical

266 We recently showed that the heparan sulfate proteoglycan syndecan-1 mediates hepatic

267 ncreasing the expression and shedding of the heparan sulfate proteoglycan syndecan-1, a molecule know

268 s have shown that postsynaptic expression of heparan sulfate proteoglycan syndecan-2 (SDC2) induces d

269 The interaction of TG2 with the heparan sulfate proteoglycan syndecan-4 (Sdc4) regulates

270 n sulfate (HS)/heparin and reported that the heparan sulfate proteoglycan syndecan-4 acts as a recept

271 The heparan sulfate proteoglycan syndecan-4 is important in

272 nascin-C, was dependent on expression of the heparan sulfate proteoglycan syndecan-4, which also bind

273 The cell surface heparan sulfate proteoglycan, syndecan-1, has been repor

274 ia low density lipoprotein receptors and the heparan sulfate proteoglycan, syndecan-1.

275 PAPST1 is a sulfotransferase involved in heparan sulfate proteoglycan synthesis encoded by the so

276 Heparan sulfate proteoglycans take part in crucial event

277 Syndecan-2 is a heparan sulfate proteoglycan that has a cell adhesion re

278 Syndecan-2 is a heparan sulfate proteoglycan that is known to be importa

279 wth factors (HBGFs) and glypican-1 (GPC1), a heparan sulfate proteoglycan that promotes efficient sig

280 ne copy of GPC1, which encodes glypican 1, a heparan sulfate proteoglycan that regulates Hedgehog sig

281 Syndecans are a family of four transmembrane heparan sulfate proteoglycans that act as coreceptors fo

282 Glypicans are heparan sulfate proteoglycans that are bound to the cell

283 cur in a manner dependent on the presence of heparan sulfate proteoglycans that are expressed ubiquit

284 Heparin, an analog of the heparan sulfate proteoglycans that are receptors for den

285 Glypicans are heparan sulfate proteoglycans that modulate the signalin

286 Animal cells express heparan sulfate proteoglycans that perform many importan

287 Glypicans are a family of cell-surface heparan sulfate proteoglycans that regulate growth-facto

288 the enzyme heparanase (HPSE), which degrades heparan sulfate proteoglycans, the main components of EC

289 inding domain that mediates interaction with heparan sulfate proteoglycans, thereby targeting LPA pro

290 of HPV type 16 (HPV16) (pseudo)virions with heparan sulfate proteoglycans triggers a conformational

291 he PSC requires expression of the Dally-like heparan-sulfate proteoglycan, under the control of the C

292 In addition, eliminating heparan sulfate proteoglycans using heparinase completel

293 The direct Ad binding to hepatic heparan sulfate proteoglycans via the KKTK motif within

294 olecule-3-grabbing nonintegrin (DC-SIGN) and heparan sulfate proteoglycan were implicated as corecept

295 rosarcoma and a murine osteoblast cell line, heparan sulfate proteoglycans were identified as the cel

296 Ps Dpp and Gbb through its Vg domain, and to heparan sulfate proteoglycans, which are well-known for

297 T beta RIII is a heparan sulfate proteoglycan with a short cytoplasmic ta

298 hanosensitive complex contains an endogenous heparan sulfate proteoglycan with HS chains that is crit

299 We review recent genetic evidence that heparan sulfate proteoglycans work in concert with the L

300 modifications of glycosaminoglycan chains on heparan sulfate proteoglycans, yet their biological func