ライフサイエンスコーパス: membrane glycoprotein

1 t two transmembrane spans; PIG-T is a type I membrane glycoprotein.

2 ruses, is mediated by the hemagglutinin (HA) membrane glycoprotein.

3 ored in the membrane by TgGAP50, an integral membrane glycoprotein.

4 n could functionally replace the rhLCV major membrane glycoprotein.

5 predicted to encode a 383-amino acid type 2 membrane glycoprotein.

6 peptide, yet otherwise behaves like a type I membrane glycoprotein.

7 ll-specific Golgi-localized type II integral membrane glycoprotein.

8 membranes indicated that HCLL is an integral membrane glycoprotein.

9 rects the synthesis of TibA, a 104-kDa outer membrane glycoprotein.

10 ystin-2 as an approximately 110-kDa integral membrane glycoprotein.

11 e ecto-apyrase of chicken stomach, an 80-kDa membrane glycoprotein.

12 hemical engineering of glycans on a distinct membrane glycoprotein.

13 ndoplasmic reticulum (ER)-localized integral membrane glycoprotein.

14 ment proteins and the cytoplasmic domains of membrane glycoproteins.

15 ytosolic viral components and viral integral membrane glycoproteins.

16 no acid transporters associated with type II membrane glycoproteins.

17 th the VSV G protein and the influenza virus membrane glycoproteins.

18 ivation, degranulation, and loss of platelet membrane glycoproteins.

19 nds N- and O-linked oligosaccharides of cell membrane glycoproteins.

20 the degradation of both soluble and integral membrane glycoproteins.

21 least two unique peptides, of which 219 are membrane glycoproteins.

22 ubset of the N-glycans identified from renal membrane glycoproteins.

23 t, US9 colocalized with capsids and not with membrane glycoproteins.

24 ly and interactions between MA and the viral membrane glycoproteins.

25 ty of the ATP-hydrolyzing enzyme plasma cell membrane glycoprotein 1 (PC-1) to increase chondrocyte P

26 e pyrophosphatase (PDNP) family: plasma cell membrane glycoprotein 1 (PC-1, or PDNP1), autotaxin (ATX

27 osome-like compartments containing lysosomal membrane glycoprotein 1 and the proton pump, but lacking

28 (transcription factor Dp1), Lamp1 (lysosomal membrane glycoprotein 1) and Gas6 (growth arrest specifi

29 KBalpha translocated to lysosomal-associated membrane glycoprotein 1- and cathepsin B-containing vesi

30 by a failure to acquire lysosome-associated membrane glycoprotein 1.

31 factor beta (TGFbeta)-inducible plasma cell membrane glycoprotein-1 (PC-1) and the closely related B

32 alkaline phosphatase (TNAP) and plasma cell membrane glycoprotein-1 (PC-1) are involved in this proc

33 The membrane protein plasma cell membrane glycoprotein-1 (PC-1) has been identified as an

34 Plasma cell membrane glycoprotein-1 (PC-1) inhibits insulin receptor

35 r two of these proteins, lysosome-associated membrane glycoprotein-1 and transmembrane glycoprotein N

36 hway and reroutes it to lysosomal associated membrane glycoprotein-1+ compartments.

37 l acid phosphatase, and lysosomal-associated membrane glycoprotein-1, each fused to the transmembrane

38 Using similar criteria, the lysosomal membrane glycoprotein 120 was not found accumulated in a

39 c approach to identify the secretory granule membrane glycoprotein 2 as a marker for PDX1+/NKX6-1+ PP

40 Epstein-Barr virus (EBV) membrane glycoprotein 42 (gp42) is required for viral en

41 , via a disulfide bond, to the other type II membrane glycoprotein, 4F2hc (4F2 heavy chain).

42 The multidomain integral membrane glycoprotein, a member of the adenine nucleotid

43 have measured the diffusion coefficients of membrane glycoprotein aggregates linked together by conc

44 al prostate tissue in situ using a fusogenic membrane glycoprotein along with the immune adjuvant hsp

45 lias emmprin or basigin), an integral plasma membrane glycoprotein and a member of the Ig superfamily

46 Signal regulatory protein (SIRP) alpha1 is a membrane glycoprotein and a member of the SIRP receptor

47 drugs promote tight binding of antibody to a membrane glycoprotein and cause platelet destruction in

48 we first cloned the rhesus monkey LCV major membrane glycoprotein and discovered that the binding ep

49 endoplasmic reticulum (ER)-localized, type I membrane glycoprotein and is essential for cell viabilit

50 s) reside on functionally important platelet membrane glycoproteins and are caused by single nucleoti

51 uires limited amounts of lysosome-associated membrane glycoproteins and does not acquire cathepsin D

52 alactose (alpha-gal) epitope associated with membrane glycoproteins and glycolipids represents a majo

53 The identities of viral membrane glycoproteins and tegument proteins involved in

54 cular damage by binding to specific platelet membrane glycoproteins and to constituents of exposed co

55 Soluble CD14 is derived from a membrane glycoprotein, and it enhances endothelial cytok

56 tal inhibition of radiolabeling of the inner membrane glycoprotein, and moreover, pulse-chase studies

57 ed haplotypes are significantly enriched for membrane glycoproteins, and a similar trend is seen amon

58 e choline transporter-like protein family of membrane glycoproteins, and correlates perfectly with HN

59 Overall, A antigen on platelet membranes, glycoproteins, and glycosphingolipids was lin

60 Plasma membrane glycoproteins are potential biomarkers because

61 cleocapsids devoid of the viral envelope and membrane glycoproteins are transported in axons.

62 generated by experience with viral fusogenic membrane glycoproteins as cytotoxic genes and the recogn

63 PV1 is an endothelial-specific integral membrane glycoprotein associated with the stomatal diaph

64 e structures associated with the erythrocyte membrane glycoprotein, band 3 (detected by sodium dodecy

65 MIR16 is an integral membrane glycoprotein, because it remained associated wi

66 tivation protein (FAP) is a type II integral membrane glycoprotein belonging to the serine protease f

67 Membrane glycoproteins bind galectins in proportion to t

68 The gene encodes a 180 kDa basement membrane glycoprotein called usherin.

69 was established as the over-expression of a membrane glycoprotein, called P-glycoprotein (Pgp), whic

70 Members of the CD1 family of membrane glycoproteins can present antigenic lipids to T

71 We demonstrate that the membrane glycoprotein carboxypeptidase S and the G prote

72 Kell, a type II membrane glycoprotein, carries over 20 blood group antig

73 e glycosylphosphatidylinositol-linked plasma-membrane glycoprotein CD14 on the surface of human macro

74 rification processes, we extracted four cell membrane glycoproteins, CD146/melanoma cell adhesion mol

75 l (DC) markers CD208/DC-lysosomal-associated membrane glycoprotein, CD205/DEC205, or CD83.

76 ed DEC-205/CD205 and DC-lysosomal-associated membrane glycoprotein/CD208 (DC-LAMP/CD208), suggesting

77 , but not mice, ADA also occurs bound to the membrane glycoprotein CD26/dipeptidyl peptidase IV.

78 The membrane glycoprotein CD36 is involved in platelet aggre

79 The recent identification of the human membrane glycoprotein, CD46, as the MV receptor allowed

80 that show limited staining for the lysosomal membrane glycoprotein CD63 and little fusion with second

81 uble cysteine motif and fused to the surface membrane glycoprotein CD8.

82 le is part of the cell surface heterodimeric membrane glycoprotein CD98 (4F2 antigen) complex known t

83 se chimeras, unlike the lysosomal-associated membrane glycoprotein chimera, were rapidly degraded in

84 Synaptic vesicle protein 2 (SV2) is a membrane glycoprotein common to all synaptic and endocri

85 be achieved by engineering a fusogenic viral membrane glycoprotein complex.

86 Axl2p is a type I membrane glycoprotein containing four cadherin-like moti

87 CD147 is a broadly expressed plasma membrane glycoprotein containing two immunoglobulin-like

88 bonds in E1 and have determined that the E1 membrane glycoprotein contains two separate sets of inte

89 e prion protein (PrP), a glycolipid-anchored membrane glycoprotein, contains a conserved hydrophobic

90 This study asked whether the EBV major membrane glycoprotein could functionally replace the rhL

91 This integral membrane glycoprotein cycles between the TGN and the cel

92 the first atomic structure of this class of membrane glycoprotein-cytoskeleton connection.

93 tricted markers CD83 and lysosome-associated membrane glycoprotein (DC-LAMP) and the costimulatory mo

94 MHC class II, CD83, DC-lysosomal-associated membrane glycoprotein (DC-LAMP), and CD11c expression we

95 ous system deposition of abnormal forms of a membrane glycoprotein designated PrP (prion protein).

96 Dysadherin, a cancer-associated membrane glycoprotein, down-regulates E-cadherin and pro

97 he actin-depolymerizing factor gelsolin, the membrane glycoprotein dysadherin, the centrosomal protei

98 Sindbis virus contains two membrane glycoproteins, E1 and E2, which are organized i

99 Emmprin (CD147; basigin) is a plasma membrane glycoprotein, enriched on the surface of many c

100 As a type 1 integral membrane glycoprotein, Env is cotranslationally transloc

101 Tyrosinase is a type I membrane glycoprotein essential for melanin synthesis.

102 Peripherin/rds (P/rds) is a membrane glycoprotein essential for the photoreceptor ou

103 gulatory subunit bI (EST01644); rat integral membrane glycoprotein (EST00085); human IFNAR gene for i

104 E3-19K is a type I membrane glycoprotein expressed by adenoviruses (Ads) to

105 pp 120, a plasma membrane glycoprotein expressed by hepatocytes, is a sub

106 is a now well-characterized type 2 integral membrane glycoprotein expressed in a highly restricted m

107 BARP), a previously uncharacterized integral membrane glycoprotein expressed in neuroendocrine cells

108 GPVI is a 62-kDa membrane glycoprotein expressed in noncovalent associati

109 s studies showed that Ad37 binds to a 50-kDa membrane glycoprotein expressed on human ocular (conjunc

110 CD36 is a membrane glycoprotein expressed on platelets, monocytes,

111 CD40 ligand (CD40L), a 33-kDa type II membrane glycoprotein expressed primarily on activated C

112 based on gene transfer of a viral fusogenic membrane glycoprotein (FMG) into tumor cells, and incorp

113 Viral fusogenic membrane glycoproteins (FMGs) are candidates for gene th

114 We report here the use of viral fusogenic membrane glycoproteins (FMGs) as a new class of therapeu

115 how that IFT trains are coupled to flagellar membrane glycoproteins (FMGs) in a Ca(2+)-dependent mann

116 Expression of viral fusogenic membrane glycoproteins (FMGs) is a potent strategy for a

117 ique and powerful ability of viral fusogenic membrane glycoproteins (FMGs) to couple concentrated ant

118 Membrane glycoproteins from extracts of these organs wer

119 xpression of some MAP1B as a neuronal plasma membrane glycoprotein, further documented here by its im

120 Two viral integral membrane glycoproteins (fusion [F] and attachment [HN, H

121 Two viral integral membrane glycoproteins (fusion [F] and attachment [HN, H

122 ough its tight interaction with the integral membrane glycoprotein GAP50.

123 e is the glycosylphosphatidylinositol-linked membrane glycoprotein Gas1.

124 irus (HSV) requires the action of four viral membrane glycoproteins (gB, gD, gH, and gL) and the bind

125 x virus (HSV) entry into cells requires four membrane glycoproteins: gD is the receptor binding prote

126 The membrane glycoproteins gE and gI are encoded by pseudora

127 The viral membrane glycoprotein genes of the isolates were sequenc

128 the molecular identity of a fifth, a 38-kDa membrane glycoprotein (Glima), is unknown.

129 ct was specific for Mpl, as 2 other platelet membrane glycoproteins, glycoprotein IIb and multimerin,

130 von Willebrand factor (VWF) to the platelet membrane glycoprotein (GP) Ib-IX-V complex initiates a s

131 von Willebrand factor (VWF) to the platelet membrane glycoprotein (GP) Ib-IX-V complex on platelets

132 initiated by the interaction of the platelet membrane glycoprotein (GP) Ib-IX-V complex with its adhe

133 The factor XI receptor is the platelet membrane glycoprotein (GP) Ib-IX-V complex, a significan

134 part, by interaction of the platelet plasma membrane glycoprotein (GP) Ib/V/IX complex with von Will

135 n, the extracellular portion of the platelet membrane glycoprotein (GP) Ibalpha (the ligand binding s

136 e the binding of these organisms to platelet membrane glycoprotein (GP) Ibalpha.

137 rmine whether a common variant (PIA2) of the membrane glycoprotein (GP) IIIa gene is associated with

138 The platelet membrane glycoprotein (GP)Ib-V-IX complex is the recepto

139 selves but bind tightly to specific platelet membrane glycoproteins (GP) when soluble drug is present

140 sequence from the third variable loop of the membrane glycoprotein gp120.

141 s phosphorylation of p80 and a novel 140-kDa membrane glycoprotein, gp140.

142 n CR2 is also the receptor for the EBV viral membrane glycoprotein gp350/220.

143 vaccine development has focused on the major membrane glycoprotein, gp350, since it is the major targ

144 dy-dependent immunity against the melanosome membrane glycoprotein gp75/tyrosinase-related protein-1

145 s caused by antibodies that bind to platelet membrane glycoproteins (GPs) only when the sensitizing d

146 This plasma membrane glycoprotein has a wide range of ligands includ

147 Two viral integral membrane glycoproteins (hemagglutinin tetramers and fusi

148 The herpes simplex virus (HSV) membrane glycoprotein heterodimer gE/gI and the US9 prot

149 inuous surface translocation mediated by the membrane glycoprotein Ib alpha.

150 von Willebrand factor (VWF) to the platelet membrane glycoprotein Ib-IX (GPIb-IX) results in platele

151 i that bind sialic acid moieties on platelet membrane glycoprotein Ibalpha.

152 ue focus on blockade of the platelet surface membrane glycoprotein IIb/IIIa receptor, which binds cir

153 Platelet membrane glycoprotein IIIa (GPIIIa) is the most polymorp

154 al regulatory protein alpha (SIRPalpha) is a membrane glycoprotein immunoreceptor abundant in cells o

155 Laminin-1 is a basement membrane glycoprotein implicated in tumor-host adhesion,

156 or the presence of an intact N-linked type I membrane glycoprotein in the cytosol.

157 rds gene encodes rds/peripherin, an integral membrane glycoprotein in the outer segments of rod and c

158 The rds gene encodes rds/peripherin (rds), a membrane glycoprotein in the rims of rod and cone outer

159 In addition, membrane glycoproteins in platelets obtained at these ti

160 IFT-driven movement of adherent flagella membrane glycoproteins in the model alga Chlamydomonas e

161 N-Glycans released from liver membrane glycoproteins included many glycans also identi

162 es simplex virus (HSV) expresses a number of membrane glycoproteins, including gB, gD, and gH/gL, tha

163 slational maturation process for the type II membrane glycoprotein influenza neuraminidase (NA) was i

164 Human lactadherin, a milk fat globule membrane glycoprotein, inhibits human rotavirus infectio

165 pecific membrane antigen, a type II integral membrane glycoprotein initially characterized by the mon

166 Tapasin is a type I membrane glycoprotein involved with other accessory prot

167 v1.1 and Kv1.4 potassium channels are plasma membrane glycoproteins involved in action potential repo

168 mine how the immunoreactivity of this normal membrane glycoprotein is differentially influenced by tr

169 This membrane glycoprotein is poliovirus receptor-related pro

170 This membrane glycoprotein is required for the formation of p

171 Kell, a type II membrane glycoprotein, is a zinc endopeptidase, while XK

172 Glycoprotein Ib alpha (GpIbalpha), a trans-membrane glycoprotein, is expressed on the surface of me

173 e M, a glycosylphosphatidylinositol-anchored membrane glycoprotein, is highly expressed in Madin-Darb

174 glycosylphosphatidylinositol (GPI)-anchored membrane glycoprotein, is necessary for prion infection

175 ding a chloride channel, receptors and other membrane glycoproteins, kinases, transcription factors,

176 s embedded with hexagonal arrays of integral membrane glycoproteins known as uroplakins.

177 lineages carry an incompletely glycosylated membrane glycoprotein, known as the Tn antigen.

178 are known to produce soluble forms of viral membrane glycoproteins lacking the transmembrane domain.

179 mediated cleavage of the epithelial basement membrane glycoprotein laminin-5 as a model to evaluate m

180 nal zone (MZ), characterized by the basement membrane glycoproteins, laminin alpha5 and agrin, that p

181 he transferrin receptor and to the lysosomal membrane glycoprotein LAMP 1 did not.

182 sitive vesicles contain lysosomal-associated membrane glycoprotein (LAMP-1), a recognized lysosomal m

183 g vacuoles are associated with the lysosomal membrane glycoprotein, LAMP-1.

184 g its acquisition of the lysosome-associated membrane glycoproteins (LAMPs) CD63 and LAMP1 and the ac

185 nvelope protein E and the much more abundant membrane glycoprotein M are both necessary and sufficien

186 CD40 ligand (CD40L) is a 33-kDa type II membrane glycoprotein mainly expressed on activated CD4(

187 Platelet membrane glycoproteins mediate binding to subendothelial

188 Syncytia activate macrophages and fusogenic membrane glycoprotein-mediated cell killing very efficie

189 Here, we show that neural (N)-cadherin, a membrane glycoprotein mediating strong homophilic adhesi

190 irus m02 gene family encodes putative type I membrane glycoproteins named m02 through m16.

191 ciated membrane protein 1), a major integral membrane glycoprotein of lysosomes, thereby accelerating

192 The E1 membrane glycoprotein of Sindbis virus contains structur

193 CD40L is a type II membrane glycoprotein of the TNF family that is found on

194 tin-2, the PKD2 gene product, is an integral membrane glycoprotein of unknown function.

195 or-1 (havcr-1), a mucin-like type 1 integral-membrane glycoprotein of unknown natural function.

196 Membrane glycoproteins of alphavirus play a critical rol

197 concerning the structural difference between membrane glycoproteins of normal epithelial cells and ep

198 hemagglutinin (HA) is one of the major spike membrane glycoproteins of the influenza virus.

199 asmic domain, non-covalently associates with membrane glycoproteins of the killer-cell inhibitory rec

200 ug-induced antibody that binds to a platelet membrane glycoprotein only when the drug is present.

201 MDR1-encoded transporter is a 170-kDa plasma membrane glycoprotein [P-glycoprotein (P-gp)] capable of

202 hosphorylates tyrosine residues on an 80-kDa membrane glycoprotein, p80.

203 racterized by the overexpression of a 95-kDa membrane glycoprotein (p95) and by marked reduction in i

204 n this chromosomal region is the plasma cell-membrane glycoprotein PC-1 (6q22-q23).

205 osine phosphorylation, and protein levels of membrane glycoprotein PC-1 were determined in rectus abd

206 r necrosis factor-alpha or overexpression of membrane glycoprotein PC-1.

207 gene Prph2 encodes a photoreceptor-specific membrane glycoprotein, peripherin-2 (also known as perip

208 Membrane glycoproteins play vital roles in many fundamen

209 CD4, an integral membrane glycoprotein, plays a critical role in the immu

210 Several platelet membrane glycoprotein polymorphisms have been identified

211 f T cells and mature (DC-lysosome-associated membrane glycoprotein positive (DC-LAMP+)) DCs, but with

212 ved by proteolytic processing of an integral membrane glycoprotein precursor (pro TGF alpha).

213 In this study, MKS3 was identified as a membrane glycoprotein predominantly localized to the ER.

214 lacking synaptic vesicle protein 2 (SV2), a membrane glycoprotein present in all vesicles that under

215 ic acid to radiolabel endogenous soluble and membrane glycoproteins present in the late Golgi and tra

216 The selectins are membrane glycoproteins promoting adhesive events between

217 sociated with the cystinuria-related type II membrane glycoprotein, rBAT (related to b(0,+) amino aci

218 en (TIN-Ag) is a recently described basement membrane glycoprotein reactive with autoantibodies in so

219 ss the Ad death protein (ADP), an Ad nuclear membrane glycoprotein required at late stages of infecti

220 the gE and gI genes are conserved and encode membrane glycoproteins required for efficient pathogenes

221 OX2 (CD200) is a broadly expressed membrane glycoprotein, shown here to be important for re

222 (HAVcr-1) cDNA codes for a class I integral membrane glycoprotein, termed havcr-1, of unknown natura

223 ily termed HERV-W encodes a highly fusogenic membrane glycoprotein that appears to be expressed speci

224 e report that the scavenger receptor CD36, a membrane glycoprotein that binds Abeta, is essential for

225 Hip encodes a membrane glycoprotein that binds to all three mammalian

226 Beta-secretase (BACE1) is a type I integral membrane glycoprotein that can cleave APP first to gener

227 The Na+/I- symporter (NIS), a 618-amino acid membrane glycoprotein that catalyzes the active accumula

228 myl carboxylase is a 758 amino acid integral membrane glycoprotein that catalyzes the post-translatio

229 Cvt17 is a membrane glycoprotein that contains a motif conserved in

230 glycosylphosphatidylinositol (GPI)-anchored membrane glycoprotein that contains a putative membrane-

231 We demonstrate that ITM2A is a type II membrane glycoprotein that exists as two species with ap

232 Platelet glycoprotein (GP) VI is a 62-kDa membrane glycoprotein that exists on both human and muri

233 glycosylphosphatidylinositol (GPI)-anchored membrane glycoprotein that has been shown to play an imp

234 ane cofactor protein (MCP; CD46) is a type 1 membrane glycoprotein that inhibits complement activatio

235 interacting protein of RGS16) as an integral membrane glycoprotein that interacts with regulator of G

236 Human NTPDase 2 is a cell surface integral membrane glycoprotein that is anchored to the membranes

237 nsulin receptor tyrosine kinase, is a plasma membrane glycoprotein that is expressed in the hepatocyt

238 or-II (IGF-II) receptor is a multifunctional membrane glycoprotein that is known to bind both M6P and

239 rface antigen 1 (MSA-1) is an immunodominant membrane glycoprotein that is the target of invasion-blo

240 e Na(+)/I(-) symporter (NIS) is a key plasma membrane glycoprotein that mediates active I(-) transpor

241 The Na(+)/I(-) symporter (NIS) is a plasma membrane glycoprotein that mediates active I(-) transpor

242 Transferrin receptor 2 (TfR2) is a membrane glycoprotein that mediates cellular iron uptake

243 The Na+/I- symporter (NIS) is a key plasma membrane glycoprotein that mediates Na+-dependent active

244 man chromosome 11p13 and encodes an integral membrane glycoprotein that participates in specific cell

245 receptor type 2 (CR2/CD21) is a B lymphocyte membrane glycoprotein that plays a central role in the i

246 CD59 is a 77-amino acid membrane glycoprotein that plays an important role in re

247 d its identical copy, IRL11, encode a type I membrane glycoprotein that possesses IgG Fc-binding capa

248 CD1d is an MHC class I-like membrane glycoprotein that presents lipid Ags to NKT cel

249 Prm1 is a pheromone-induced membrane glycoprotein that promotes plasma membrane fusi

250 n of the expression of tissue factor (TF), a membrane glycoprotein that promotes thrombosis, and of E

251 t receptor potential melastatin (Trpm) 4b, a membrane glycoprotein that regulates calcium influx.

252 CD59 is a membrane glycoprotein that regulates formation of the cy

253 les that are homologues of cellular CD200, a membrane glycoprotein that regulates immune responses an

254 CD44 is a widely expressed integral membrane glycoprotein that serves as a specific adhesion

255 membrane antigen (PSMA) is a type 2 integral membrane glycoprotein that serves as an attractive targe

256 alovirus (HCMV) US11 polypeptide is a type I membrane glycoprotein that targets major histocompatibil

257 embrane antigen (PSMA) is a type II integral membrane glycoprotein that was initially characterized b

258 Transferrin receptor (TfR1) is a type II membrane glycoprotein that, as a cell surface homodimer,

259 CD22 is a B cell membrane glycoprotein that, upon Ag receptor engagement,

260 isiae, Bud8p and Bud9p are homologous plasma membrane glycoproteins that appear to mark the distal an

261 Human cytomegalovirus encodes at least 25 membrane glycoproteins that are found in the viral envel

262 D200 and its receptor CD200R are both type I membrane glycoproteins that contain two Ig-like domains.

263 ts pinpoint RhCG and Rhcg as novel polytopic membrane glycoproteins that may function as epithelial t

264 n-dependent MPR (CD-MPR) are type I integral membrane glycoproteins that play a critical role in the

265 les and beta(2)-microglobulin (beta(2)m) are membrane glycoproteins that present peptide Ags to TCRs,

266 The TLR family comprises membrane glycoproteins that recognize pathogen-associate

267 CD5 is a 67-kDa membrane glycoprotein the expression of which in murine

268 to reduce steric hindrance imposed by large membrane glycoproteins the time constant was short and C

269 ral myelin protein 22 (PMP22) is a tetraspan membrane glycoprotein, the misexpression of which is ass

270 Paramyxoviruses require two viral membrane glycoproteins, the attachment protein variously

271 A homologous set of beta 2 m-associated membrane glycoproteins, the CD1 molecules, appears to bi

272 t viral-cell membrane fusion mediated by two membrane glycoproteins: the attachment protein (G) and t

273 Abs immunoprecipitated a hydrophobic, plasma membrane glycoprotein (thymic stromal cotransporter, TSC

274 rus hemagglutinin (HA) as a generic integral membrane glycoprotein to distinguish global versus speci

275 Relocation of a membrane glycoprotein to the cytosol via signal sequence

276 onal maturation pathway for the human type I membrane glycoprotein tyrosinase.

277 The human cytomegalovirus (HCMV) membrane glycoprotein, UL16, binds to three of the five

278 e of the drug but bind tightly to a platelet membrane glycoprotein, usually alpha(IIb)/beta3 integrin

279 This solvent solubilized the integral membrane glycoproteins very effectively even after serio

280 ells were transfected with a viral fusogenic membrane glycoprotein (vesicular stomatitis virus G glyc

281 d a chimeric rhLCV in which the native major membrane glycoprotein was replaced with EBV gp350.

282 Membrane glycoproteins were shown to be useful biomarker

283 antibodies that react with specific platelet-membrane glycoproteins when the provoking drug is presen

284 B5R is a type I integral membrane glycoprotein, whereas F13L is an unglycosylated

285 ng protein-1 (CRSBP-1) is a newly identified membrane glycoprotein which is hypothesized to be respon

286 dium-dependent and highly hydrophobic plasma membrane glycoproteins which maintain low levels of glut

287 Human CD23 is a 45-kD type II membrane glycoprotein, which functions as a low-affinity

288 bile acid transporter (Asbt) is a polytopic membrane glycoprotein, which is specifically expressed o

289 Tyrosinase is a type I membrane glycoprotein whose activity is essential for me

290 yloid precursor protein (APP) is an integral membrane glycoprotein whose cleavage products, particula

291 , was originally predicted to be an integral membrane glycoprotein with 11 transmembrane (TM) domains

292 Gaa1 is a polytopic membrane glycoprotein with a cytoplasmic N terminus and

293 ) Gaa1 is an endoplasmic reticulum-localized membrane glycoprotein with a cytoplasmically oriented N

294 gE is a type 1 membrane glycoprotein with a large ectodomain that is ex

295 of the appropriate Mr = 85,000-95,000 plasma membrane glycoprotein with core of Mr = 42,000 was estab

296 kidney disease (ADPKD), encodes an integral membrane glycoprotein with similarity to calcium channel

297 Tetherin is an unusual membrane glycoprotein with two membrane anchors and an e

298 nins belong to a family of trimeric basement membrane glycoproteins with multiple domains, structures

299 f the membrane-spanning domain of one of the membrane glycoproteins with the membrane bilayer and wit

300 d a mutant influenza hemagglutinin (a type I membrane glycoprotein) with a C-terminal extension.