ライフサイエンスコーパス: cell surface protein

1 ypes, with a binding activity for a specific cell surface protein.

2 of transport activity followed by decreased cell surface protein.

3 polymorphism and are transcribed to express cell surface protein.

4 ecifically up-regulated HNSCC ULBP1 mRNA and cell surface protein.

5 ween an oncoprotein and an immunosuppressive cell-surface protein.

6 ain shedding, a well-known process in animal cell surface proteins.

7 ion and invasiveness through modification of cell surface proteins.

8 eam of cadherin adhesion molecules and other cell surface proteins.

9 n through bidirectional signals mediated via cell surface proteins.

10 M, most of its product was attached to other cell surface proteins.

11 in the signaling cascade for this family of cell surface proteins.

12 he steady-state organisation and dynamics of cell surface proteins.

13 at interacts with type-II cohesin-containing cell surface proteins.

14 hereas MIR2 can downregulate a wide range of cell surface proteins.

15 with 24 proteins, including 10 kinases and 2 cell surface proteins.

16 hrough its interactions with various ECM and cell surface proteins.

17 ol (GPI)-anchored proteins or representative cell surface proteins.

18 is essential for the proper glycosylation of cell surface proteins.

19 roteinase that mediates shedding of multiple cell surface proteins.

20 es the homo- and hetero-association of these cell surface proteins.

21 eraction with other extracellular matrix and cell surface proteins.

22 ell surface receptors whose ligands are also cell surface proteins.

23 ligands often presented in large numbers as cell surface proteins.

24 domain shedding of metalloprotease-sensitive cell surface proteins.

25 teins that regulate endosomal trafficking of cell surface proteins.

26 lls is able to recognize and degrade damaged cell surface proteins.

27 were 2, NOTCH2 and FLT3, that encode myeloid cell surface proteins.

28 ME) is vital for the internalization of most cell-surface proteins.

29 ill region, and express their VLRs solely as cell-surface proteins.

30 ndwelling medical devices using a variety of cell-surface proteins.

31 in the expression and membrane insertion of cell-surface proteins.

32 t pathways for the recycling of internalized cell-surface proteins.

33 tibody to carcinoembryonic antigen) to label cell-surface proteins.

34 of IL-4 and analyzed for expression of >300 cell-surface proteins.

35 rates the downregulation of a broad range of cell-surface proteins.

36 following proteinase K-mediated clearance of cell-surface proteins.

37 s and antibody-drug conjugates targeting the cell surface protein 6 transmembrane epithelial antigen

38 Interestingly, FACIN is a nonclassical cell surface protein, a cytosolic enzyme acetylornithine

39 These outputs included an immunogenic cell-surface protein, a cytokine, a chemokine, and a che

40 idermidis and Staphylococcus aureus requires cell-surface proteins (Aap and SasG) containing sequence

41 ntain the optimal complement and function of cell surface proteins according to cellular physiologica

42 Expression of the cell surface protein ActA allows L. monocytogenes to act

43 -ECD, when expressed as a membrane-anchored, cell-surface protein, affects collagen fibrillogenesis b

44 EC1 may have chaperone-like effects for many cell surface proteins along the biosynthesis pathway.

45 dividual Tpk1-repressed genes indicates that cell surface proteins Als1, Als2, Als4, Csh1 and Csp37 c

46 not influence IgG produced against specific cell-surface proteins, although a non-significant patter

47 The proteome map with corresponding cell surface protein analysis and antigen detection will

48 r protein (APP) is an ubiquitously expressed cell surface protein and a key molecule in the etiology

49 Cell surface protein and lipid molecules are organized i

50 isolated in the late 1970s by acquisition of cell surface proteins and antimicrobial resistance deter

51 associated with a dramatic reorganization of cell surface proteins and associated signaling component

52 using a method that selectively biotinylated cell surface proteins and by flow cytometry using tropho

53 i outer surface proteins in adhesion to host cell surface proteins and extracellular matrix component

54 oteomic approaches to characterize apoptotic cell surface proteins and identify candidate SUPER deter

55 Communication between cell surface proteins and the nucleus is integral to man

56 differed from US strains by acquisition of a cell-surface protein and macrolide resistance determinan

57 s critical for regulating the homeostasis of cell-surface proteins and controlling signal transductio

58 cytometry was used to evaluate expression of cell-surface proteins and the cytokine production profil

59 y use antibodies that are specific to tumour cell-surface proteins and, thus, have tumour specificity

60 (ASPH), a highly expressed tumor-associated cell surface protein, and (2) to determine if immunizati

61 SprB is a highly repetitive 669-kDa cell surface protein, and antibodies against SprB inhibi

62 ed that CD154 was an alpha granule and not a cell surface protein, and thereafter optimized the metho

63 h axon-specific and somatodendritic-specific cell surface proteins, and accumulation of a unique comb

64 associated with CD9 and CD151, but not other cell surface proteins, and DHHC2 knockdown diminished CD

65 ion and subsequent downregulation of several cell surface proteins, and in particular major histocomp

66 rmacological utility of aptamers directed at cell surface proteins, and it highlights an endocytosis-

67 e genes encoding toxins, adhesins, and other cell surface proteins, and over 200 BtrA-repressed genes

68 rticular, the analysis of conditioned media, cell surface proteins, and whole-cell lysates from metas

69 Hox4 proteins regulate Eph/ephrins and other cell-surface proteins, and can function in a non-cell-au

70 he vertebrate clustered protocadherin (Pcdh) cell surface proteins are encoded by three closely linke

71 Glycosylation alterations of cell surface proteins are often observed during the prog

72 method for orphan receptor ligands, in which cell-surface proteins are expressed in Drosophila embryo

73 Interestingly, the mRNAs encoding many cell-surface proteins are localized to dendrites, but wh

74 r-targeted biocarrier that exploits the HER3 cell surface protein as a portal to sneak therapeutics i

75 types often relies on the identification of cell surface proteins as differentiation markers, flow c

76 the highly conserved ephrin-B2 and ephrin-B3 cell surface proteins as their entry receptors.

77 ging host entry factors, such as CD81, a key cell surface protein associated with HCV entry.

78 then result in the recycling of internalized cell-surface proteins back to the plasma membrane.

79 In this study, we identified a new cell surface protein, BapA1, from Streptococcus parasang

80 d can be visualized by the expression of the cell surface protein BEN.

81 Using cell surface protein biotinylation coupled with immunobl

82 Using cell-surface protein biotinylation of rat cerebellar sli

83 Izumo1 is an essential sperm cell-surface protein, but its receptor on the egg has no

84 hese processes require dynamic modulation of cell surface proteins by endocytosis.

85 ic inflammatory dermatoses were analyzed for cell surface proteins by flow cytometry and for copy num

86 Here we report comprehensive profiling of cell surface proteins by flow cytometry in naive and pri

87 cific FlAsH-labeling of tetracysteine-tagged cell surface proteins by using prion protein (PrP) and a

88 Ectodomain cleavage of cell-surface proteins by A disintegrin and metalloprotei

89 The frequent modification of cell-surface proteins by N-linked glycans is known to be

90 the start of transcription of an R8-specific cell-surface protein, Capricious (Caps) that regulates R

91 Cell-surface protein CD10 is a prognostic marker for dif

92 Cells expressing the cell surface protein CD14 can be spatially distinguished

93 ription factor PAX5, and the B-cell-specific cell surface protein CD19.

94 Unlike CD8+ DCs that express the cell surface protein CD205, CD8- DCs, which are positive

95 cells strongly express the immunosuppressive cell-surface protein CD274 (PD-L1, B7-H1), as determined

96 Here, we demonstrate that the cell-surface protein CD276/B7-H3 is broadly overexpresse

97 ocytosis is normally inhibited by binding of cell surface protein CD47 to macrophage signal regulator

98 that PMN transmigration is regulated by the cell surface protein CD47.

99 t differing in their expression level of the cell surface protein CD5, were generated.

100 s ubiquitously express the immunosuppressive cell surface protein CD80 (B7-1).

101 Plasmodium vivax, rely on two distinct host cell surface proteins, CD81 and the Scavenger Receptor B

102 acquired PanNETs characterized by increased cell-surface protein CD90 expression and aldehyde dehydr

103 the intracellular region of the promyogenic cell surface protein Cdo (also known as Cdon) binds to B

104 egories of proteins were ribosomal proteins, cell surface proteins, chaperones, and uncharacterized p

105 ndicate that Reck and Gpr124 are part of the cell surface protein complex that transduces Wnt7a- and

106 enzyme which catalyzes the anchoring of many cell surface proteins conserved with the LPXTG sequence.

107 Here we show that the conserved cell-surface protein CwpV provides antiphage protection

108 ablished, the TE expressed intracellular and cell-surface proteins cytokeratin-7 (CK7) and fibroblast

109 tors that specifically bind to the dendritic cell-surface protein DC-SIGN.

110 the locus AFUA_3G08990, encoding a putative cell surface protein (denoted CSP), was performed with a

111 hat VV exhibited an extremely strong bias of cell surface protein-dependent binding to monocytes, B c

112 is is the first identification of a specific cell surface protein directly involved in biofilm format

113 ntly, EpCAM (CD326) has been identified as a cell surface protein discriminating LCs from Langerin(+)

114 On Th2 cells, galectin-9 binds cell surface protein disulfide isomerase (PDI), increasi

115 s entry-triggering protein to bind the human cell surface protein DNase X.

116 to benefit their survival, and the study of cell surface proteins downregulated by viruses has provi

117 The upregulation of naive-specific cell surface proteins during primed-to-naive resetting e

118 despread downregulation of immune-modulating cell surface proteins during the initial stages of KSHV

119 ome from a wide range of proteins, including cell-surface proteins (E-cadherin, N-cadherin, and Integ

120 elatively abundant expression of Tetherin, a cell surface protein encoded by the Bone Marrow Stromal

121 d by reciprocal changes in expression of the cell surface proteins, EpCAM/CD326 and NCAM/CD56.

122 Many cell surface proteins exhibit polarized expression, bein

123 genes of WxL loci A and C encode antigenic, cell surface proteins exposed at higher levels in clinic

124 ll-specific chemotaxis receptor (ECSCR) is a cell surface protein expressed by blood endothelial cell

125 The prion protein (PrP(C)) is a cell surface protein expressed mainly in the nervous sys

126 ivated 1 (mCLCA1) as the 10.1.1 Ag, a 90-kDa cell-surface protein expressed in lymphatic endothelium

127 CD30 is a cell-surface protein expressed on certain activated T ce

128 g immunoglobulin-like lectin (Siglec)-8 is a cell-surface protein expressed selectively on human eosi

129 sing especially on the roles of secreted and cell surface proteins, expressed in a sex-specific manne

130 The CD133 cell-surface protein expresses the AC133 epitope that is

131 All complementation constructs showed cell surface protein expression and correct orientation

132 tive positions on the S1-S2 linker decreased cell surface protein expression but the N-glycan still a

133 rombin antithrombin complex), and lymphocyte cell surface protein expression during the first week of

134 ar loops are regulatory factors in total and cell surface protein expression of the alpha4beta2 nAChR

135 HIV type 1 Nef downregulates cell surface protein expression, alters signal transduct

136 eak current density without perturbing Kv4.3 cell surface protein expression.

137 mor gastric tissue samples were analyzed for cell surface protein expression.

138 ing agents, allowing quantitative imaging of cell-surface protein expression in vivo.

139 gnificant induction of IL-13Ralpha2 mRNA and cell-surface protein expression, which was dependent on

140 These include cell surface proteins, extracellular matrix proteins, an

141 een well understood because of the number of cell surface proteins, factors, and conditions found to

142 hat these parasites have evolved specialized cell-surface protein families, overlaid on a well-conser

143 s the first report of GIP recognition of the cell surface protein FAS, which belongs to the tumor nec

144 Biotinylation of MV4-11 cell surface proteins followed by immunoblotting of the

145 ed in the pericellular matrix interacts with cell surface proteins for specific cellular functions.

146 Sticks and stones (Sns), a cell surface protein found on Drosophila myoblasts, has

147 ocyte function-associated antigen (LFA)-1, a cell surface protein found on lymphocytes, and its cogna

148 ing sites on Fn-binding protein A (FnBPA), a cell surface protein from Staphylococcus aureus, are imp

149 that expresses the human KEL2 (Chellano) red cell surface protein from the Kell system on red cells,

150 alloproteinase/gamma-secretase processing of cell surface proteins function in signal transduction an

151 udies implicate three additional HH-binding, cell-surface proteins, GAS1, CDO, and BOC, as putative c

152 Proteolytic shedding of cell surface proteins generates paracrine signals involv

153 wall properties through repression of select cell surface protein genes.

154 P96 serves as an essential chaperone for the cell-surface protein glycoprotein A repetitions predomin

155 (+) bacteria, including one that encodes the cell-surface protein gp130, as well as several genes tha

156 dentified the LapA protein, another enormous cell surface protein (> 8000 aa), as a key requirement f

157 that can be found in gram-positive bacterial cell surface proteins, has previously been used to devel

158 atocytes is mediated at least in part by the cell-surface protein Heart of glass and contributes to t

159 ed to an in-house database of genes encoding cell surface proteins (herein referred to as the surface

160 irus entry mediator (HVEM) is one of several cell surface proteins herpes simplex virus (HSV) uses fo

161 machinery for both insertion and removal of cell surface proteins, highlighting a novel role for the

162 tigen of the prostate-1 (STEAP-1) is a novel cell surface protein highly expressed in primary prostat

163 CD2, a T cell surface protein highly expressed on Tem cells, is t

164 Fc receptor-like 3 (FCRL3) is a cell surface protein homologous to Fc receptors.

165 Hh signaling is regulated by two conserved cell-surface proteins: Ig/fibronectin superfamily member

166 Neuropilins are a class of cell surface proteins implicated in cell migration and a

167 PGF-CTERM proteins include the major cell surface protein in Halobacterium, a glycoprotein wi

168 ar mechanism driving polar localization of a cell surface protein in plants.

169 epithelial (HCLE) cells and to biotinylated cell surface protein in static and liquid phase adhesion

170 ne receptors belong to the largest family of cell surface proteins in eukaryotes, the G protein-coupl

171 ions and is, in principle, extendable to all cell surface proteins in the synapse.

172 cell surface, suggesting the involvement of cell surface proteins in this process.

173 ng the mechanical strain exerted by specific cell-surface proteins in living cells.

174 To determine the biological role of these cell-surface proteins in reproduction, Cre/LoxP technolo

175 zophrenia are likely to be those directed to cell surface proteins, in which the likelihood of pathog

176 or for nuclear factor kappaB ligand, and FAS cell-surface proteins, in combination with increased lev

177 n plasma membrane via interaction with other cell surface proteins including glycosylphosphatidylinos

178 alpha2-macroglobulin (55%), as well as some cell surface proteins including talin-1 (21%), fascin (4

179 hoblastic leukemia (BCP-ALL) surfaceome; 713 cell surface proteins, including 181 CD proteins, were d

180 for proteolytic maturation of signaling and cell surface proteins, including amyloid precursor prote

181 capacity, as well as expression of FOXP3 and cell surface proteins, including CD39 and CTLA-4.

182 rane metalloprotease ADAM10 sheds a range of cell surface proteins, including ligands and receptors o

183 ssibility that extracellular LOX may oxidize cell surface proteins, including the PDGF receptor-beta

184 ells and induced a set of immune-suppressive cell-surface proteins, including BTLA, IRF4, and Siglec

185 Two interacting pairs of cell surface proteins independently promote fasciculatio

186 this study, we show that Abs against cancer cell surface proteins induce complement-dependent cytoly

187 interactions among pancreatic beta-cells via cell surface proteins inhibit basal and enhance stimulat

188 lation of PMN chemotactic transmigration and cell surface protein interactions.

189 mediated endocytosis is a major regulator of cell-surface protein internalization.

190 es for genes encoding transcription factors, cell-surface proteins, intracellular signaling molecules

191 of iron toxicity; (iii) higher expression of cell surface proteins involved in immune evasion and str

192 human leukocyte antigen (HLA) system encode cell-surface proteins involved in regulation of immune r

193 ated by trypsin treatment, indicating that a cell surface protein is directly involved.

194 r heterodimers, but GPCR regulation by other cell surface proteins is not well understood.

195 The complement of fungal cell surface proteins is widely regulated by ubiquitinat

196 Endocytic down-regulation of cell-surface proteins is a fundamental cellular process

197 protein to maintain ER homeostasis, and as a cell surface protein, is known to regulate the phosphati

198 Regenerating afferents expressed the cell surface proteins lachesin and fasciclin I.

199 In this study, we show that the Egr2-driven cell surface proteins LAG-3 and 4-1BB can identify dysfu

200 r and structural characterization of a novel cell-surface protein, Lar_0958 from Lactobacillus reuter

201 perfamily lectins or Siglecs are a family of cell surface proteins largely expressed in hematopoietic

202 s followed by interactions with more limited cell surface proteins, leading to fusion with cellular m

203 nfirmed numerous of these differences at the cell surface protein level.

204 tibodies (BsAbs) is affected by the relative cell-surface protein levels of the respective targets.

205 s not provide phenotypic information such as cell-surface protein levels.

206 igations revealed that the expression of the cell surface protein LRIG1, a negative regulator of rece

207 It is well-known as a clinical cell surface protein marker for study of HIV progression

208 ial versus endocardial titin and noncollagen cell surface proteins may be responsible for the increas

209 mic and/or transmembrane domain (TMD) of the cell surface protein MHC-I K(d).

210 ractions between nanotubes and AMB-1 via the cell surface protein MSP-1 and flagellin.

211 y provides in vivo genetic evidence that the cell-surface protein N-cadherin represents a promising t

212 1 or TIM-1) is an immunoglobulin superfamily cell-surface protein not expressed by cells of the myelo

213 n is a tumor-associated antigen displayed on cell surface proteins of a high percentage of human carc

214 , has been shown to cleave a wide variety of cell surface proteins of immunological importance.

215 A sample preparation technique to enrich for cell surface proteins of the intrahepatic cholangiocarci

216 ntify transmembrane protein 119 (Tmem119), a cell-surface protein of unknown function, as a highly ex

217 R gene comprises a diverse array of neuronal cell-surface proteins of the cadherin superfamily, altho

218 antibodies to target functionally important cell-surface proteins on bone-resorbing osteoclasts repr

219 p32/gC1qR/C1QBP/HABP1 is a mitochondrial/cell surface protein overexpressed in certain cancer cel

220 ercellular adhesion molecule 1 (ICAM-1) is a cell-surface protein overexpressed in many diseases and

221 n receptor 1 (ANTXR1), is a highly conserved cell-surface protein overexpressed on tumor-infiltrating

222 and of immunosuppressive cytokine IL-10 and cell-surface protein PD-L1/CD274.

223 8102 (clade III) to test the hypothesis that cell surface proteins play a role in defence against pre

224 udies have suggested that CD47, an essential cell-surface protein, plays an important role in polymor

225 e snake venom toxin rhodocytin and the tumor cell surface protein podoplanin.

226 Autotransporters are a large superfamily of cell surface proteins produced by Gram-negative bacteria

227 CD8(+) T cells become exhausted, inducing cell surface protein programmed cell death-1 (PD-1) as c

228 in diseases; they arise from misfolding of a cell surface protein, PrP(C) to a form called PrP(Sc).

229 f the ABar blastomere, indicating that these cell surface proteins redundantly regulate multiple deve

230 specific expression of sensory receptors and cell-surface proteins regulating synaptic target specifi

231 ings provide unique structural insights into cell-surface protein repeats involved in adhesion of Gra

232 ed receptors, one of the largest families of cell surface proteins, representing a major class of dru

233 Dscam encodes a family of cell surface proteins required for establishing neural c

234 zosaccharomyces pombe shu1(+) gene encodes a cell-surface protein required for assimilation of exogen

235 nents of the extracellular matrix as well as cell surface proteins resulting in degradation or releas

236 approach is generalizable to many mammalian cell surface proteins, results in the generation of func

237 Biotinylation of cell surface proteins revealed decreased surface localiz

238 infection, this pathogen may interact with a cell surface protein(s) to selectively impede the comple

239 The Streptococcus pyogenes cell-surface protein Scl2 contains a globular N-terminal

240 omposed of the type-II cohesin module of the cell surface protein SdbA bound to a trimodular C-termin

241 ll-specific chemotaxis receptor (ECSCR) is a cell-surface protein selectively expressed by endothelia

242 tor cells, induced by BMP2 and marked by the cell surface protein, stage-specific embryonic antigen 1

243 al trafficking and polarized distribution of cell surface proteins such as megalin and E-cadherin and

244 ls to chemoattractants by oxidizing specific cell surface proteins, such as PDGFR-beta.

245 Cell surface proteins tagged with a 15-amino acid peptid

246 We aimed to identify novel cell surface proteins targeted for downregulation by HIV

247 late- gestation mouse placenta as well as a cell surface protein that can be used to identify and is

248 er, we identify CD73 as a TCR ligand-induced cell surface protein that distinguishes gammadeltaTCR-ex

249 igin-2 (NL2), an inhibitory synapse-specific cell surface protein that functions in cell adhesion and

250 ansposon insertions in remA, which encodes a cell surface protein that has a lectin domain and appear

251 CD38 is a multifunctional cell surface protein that has receptor as well as enzyme

252 -specific angiogenesis inhibitor (BAI3) as a cell surface protein that interacts with ELMO.

253 In this study, we show that THY-1, a cell surface protein that is critical for the early stag

254 Thy-1 is a cell surface protein that is expressed during the differ

255 c enzyme, we provide evidence that LipC is a cell surface protein that is present in both the cell wa

256 Complement receptor type 2 (CR2, CD21) is a cell surface protein that links the innate and adaptive

257 Dystroglycan is a prominent cell surface protein that mediates attachment to the ext

258 CD47 is a cell surface protein that transmits an anti-phagocytic s

259 nds, and viral decoys, including challenging cell surface proteins that cannot be produced using typi

260 ENOX (ECTO-NOX) proteins are growth-related cell surface proteins that catalyze both hydroquinone or

261 ex post-translational modifications (PTM) on cell surface proteins that govern adhesion, migration, a

262 Fas (APO-1/CD95) is one of the key cell surface proteins that mediate AICD in CD4(+) and CD

263 The cell surface proteins that mediate polyamine transport i

264 d colleagues now show that Beat and Side are cell surface proteins that physically interact with each

265 is a network of interacting circulatory and cell surface proteins that recognizes, marks, and facili

266 Ephrins are cell surface proteins that regulate diverse biological p

267 Receptor tyrosine kinases (RTKs) are cell surface proteins that tightly regulate a variety of

268 CD47 is a widely distributed cell-surface protein that acts a marker of self through

269 four primary tumors, and showed that CD47, a cell-surface protein that acts as a "don't eat me" signa

270 of cytolethal distending toxin, including a cell-surface protein that interacts with the toxin.

271 ial cell adhesion molecule (EpCAM; CD326), a cell-surface protein that is characteristic of some epit

272 l of fms-related tyrosine kinase 1 (FLT1), a cell-surface protein that sequesters vascular endothelia

273 responses to extracellular signals depend on cell-surface proteins that are internalized and recycled

274 B7 family consists of structurally related, cell-surface proteins that regulate immune responses by

275 class B G-protein-coupled receptors (GPCRs), cell-surface proteins that respond to peptide hormones,

276 nscribes genes encoding the parasite's major cell-surface proteins-the variant surface glycoprotein (

277 s NK cell detection of changes to endogenous cell-surface proteins through inhibitory receptors.

278 s a Type V system, using a long beta-helical cell surface protein to contact receptors in target cell

279 activity and expressed a similar pattern of cell surface proteins to IL-17-producing cells.

280 tive targeting approach based on patterns of cell surface proteins to rationally develop small, synth

281 of >8,000 cellular proteins, including 1,200 cell-surface proteins to manipulate signaling pathways a

282 at the BTB was assessed by biotinylation of cell surface proteins, to be followed by tracking the en

283 olarized epithelial cells, newly synthesized cell surface proteins travel in carrier vesicles from th

284 and HIV-1 spread; critically, however, which cell surface protein triggers contact-induced polarizati

285 The cell surface protein Trop2 is expressed on immature stem

286 s, the sec49K receptor was identified as the cell surface protein tyrosine phosphatase CD45.

287 We observed a loss of Clr-b cell-surface protein upon VV and ectromelia virus infect

288 Like most cell surface proteins, VEGF-R2 is glycosylated, although

289 HCLE cell surface proteins were biotinylated to measure the e

290 Cell surface proteins were quantified by flow cytometry.

291 Following cleavage from the cell surface, proteins were complexed in solution and su

292 allele resulted in increased localization of cell surface proteins, whereas reduced levels of Mon1a s

293 tm) consists of five highly sequence-related cell surface proteins, which are implicated in diverse c

294 so collate a set of AS and DE genes encoding cell surface proteins, which present promising diagnosti

295 Tetherin (Bst-2 CD317) is a cell-surface protein whose expression is induced by IFNa

296 Thy1 (CD90), a cell surface protein with an enigmatic function, is expr

297 a simple and efficient way to label specific cell surface proteins with biophysical probes on mammali

298 coaggregation factor A (CafA), is one of 14 cell surface proteins with the LPXTG motif predicted in

299 alternative splicing to produce a family of cell-surface proteins with over 19,000 different ectodom

300 ied to monitor fluorescent ligand binding on cell-surface proteins with time-resolved Forster resonan