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

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

6 membranes indicated that HCLL is an integral membrane glycoprotein.

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

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

9 n could functionally replace the rhLCV major membrane glycoprotein.

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

11 oclonal antibody products targeting the EBOV 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 nds N- and O-linked oligosaccharides of cell membrane glycoproteins.

19 the degradation of both soluble and integral membrane glycoproteins.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

42 Specific to the extracellular virion membrane, glycoproteins A33, A34, and B5 are highly cons

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 sive elucidation of differentially expressed membrane glycoproteins and molecular modeling suggested

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

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

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

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

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

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

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

61 Plasma membrane glycoproteins are potential biomarkers because

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

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

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

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

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

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

68 2, CD11c, dendritic cell lysosome-associated membrane glycoprotein, beta-defensin 2, and S100A7; glob

69 Membrane glycoproteins bind galectins in proportion to t

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

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

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

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

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

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

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

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

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

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

80 The membrane glycoprotein CD36 is involved in platelet aggre

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

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

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

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

85 o interact with the late endosomal/lysosomal membrane glycoprotein CLN3 (ceroid lipofuscinosis neuron

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

119 were chemically released from isolated cell membrane glycoproteins following N-glycan and lipid/glyc

120 Membrane glycoproteins from extracts of these organs wer

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

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

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

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

125 e is the glycosylphosphatidylinositol-linked membrane glycoprotein Gas1.

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

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

128 The membrane glycoproteins gE and gI are encoded by pseudora

129 The viral membrane glycoprotein genes of the isolates were sequenc

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

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

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

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

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

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

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

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

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

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

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

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 t layilin, a C-type lectin domain-containing membrane glycoprotein, is selectively expressed on highl

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

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

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

179 the viral E3 ubiquitin ligase ICP0 and viral membrane glycoprotein L.

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

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

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

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

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

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

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

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

188 Platelet membrane glycoproteins mediate binding to subendothelial

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

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

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

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

193 The E1 membrane glycoprotein of Sindbis virus contains structur

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

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

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

197 Membrane glycoproteins of alphavirus play a critical rol

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

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

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

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

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

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

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

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

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

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

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

209 Membrane glycoproteins play vital roles in many fundamen

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

211 Human platelet membrane glycoprotein polymorphisms can be immunogenic i

212 Several platelet membrane glycoprotein polymorphisms have been identified

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

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

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

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

217 he proper functions of a cholesterol-binding membrane glycoprotein, Prominin-1 (Prom1/CD133), which c

218 The selectins are membrane glycoproteins promoting adhesive events between

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 s well as that of a co-transfected secretory membrane glycoprotein, vesicular stomatitis virus G (VSV

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

283 Membrane glycoproteins were shown to be useful biomarker

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

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

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

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 RAGE exists as a membrane glycoprotein with an ectodomain, a transmembran

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.