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 new phage, carrying gene encoding a putative cell-surface protein.

6 eraction with other extracellular matrix and cell surface proteins.

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

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

9 domain shedding of metalloprotease-sensitive cell surface proteins.

10 teins that regulate endosomal trafficking of cell surface proteins.

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

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

13 uctures for the functional analysis of these cell surface proteins.

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

15 ion and invasiveness through modification of cell surface proteins.

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

17 n through bidirectional signals mediated via cell surface proteins.

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

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

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

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

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

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

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

25 characterization of ligand interactions with cell surface proteins.

26 iption factors and different combinations of cell surface proteins.

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

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

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

30 ill region, and express their VLRs solely as 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 of IL-4 and analyzed for expression of >300 cell-surface proteins.

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

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

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

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

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

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

40 umor necrosis factor receptor superfamily of cell surface proteins, acts as a costimulatory receptor

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

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

43 Also, by simultaneous single-cell DNA and cell surface protein analysis, we illustrate both geneti

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

45 yR7 PRs express the Dpr11 cell surface protein and are presynaptic to Dm8 amacrine

46 Cell surface protein and lipid molecules are organized i

47 lls (MSCs) are characterized by their unique cell surface proteins and aberrant signaling pathways.

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

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

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

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

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

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

54 ycans - branched sugar oligomers attached to cell-surface proteins and lipids - is organized like a f

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

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

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

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

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

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

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

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

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

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

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

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

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

68 is invaluable for studying cell populations, cell-surface proteins are often integral markers of cell

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

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

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

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

73 gglutinins to engineer a genetically encoded cell-surface protein barcoding system.

74 Recently, 32 interacting cell surface proteins belonging to two newly defined fam

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

76 pr and DIP immunoglobulin superfamily (IgSF) cell-surface proteins bind heterophilically and are expr

77 Using cell-surface protein biotinylation of rat cerebellar sli

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

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

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

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

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

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

84 Cell surface protein capture is mediated by covalent tag

85 The cell surface protein CD 138 increases with disease recur

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

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

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

89 We have investigated the utility of the cell surface protein CD26 to identify functionally disti

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

91 e, has specificity for the T cell-activating cell surface protein CD3 and the B cell Ag CD19.

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

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

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

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

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

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

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

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

100 The complement of cell surface proteins, collectively referred to as the s

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

102 and that this can lead to the expression of cell surface proteins containing O-glycans comprised of

103 Genes encoding cell-surface proteins control nervous system development

104 tion factors (Gfi1, Cebpd, Cebpe, and Spi1), cell surface proteins (Csf3r and Gr1), and neutrophil gr

105 Here, we dissect its cell-surface protein (CSP) composition to discover novel

106 ional profile from our cohort, we identified cell surface proteins (CSPs) associated with the SCCB ph

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

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

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

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

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

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

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

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

117 e polysaccharides via the action of multiple cell surface proteins encoded within polysaccharide util

118 38% of these SNPs were in genes annotated as cell surface protein-encoding genes, including some esse

119 prostate-specific membrane antigen (PSMA), a cell-surface protein enriched in prostate cancer and the

120 We prepared cell surface protein-enriched fractions from MSCs and CP

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 Characterisation of cell surface proteins expressed by each subset is inform

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

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

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

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

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

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

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

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

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

146 1 (NEGR1) and neurotrimin (NTM) are abundant cell-surface proteins found in the brain and form part o

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

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

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

150 Proteolytic shedding of cell surface proteins generates paracrine signals involv

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

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

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

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

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

156 The transmembrane (TM) anchors of cell surface proteins have been one of the 'blind spots'

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

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

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

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

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

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

163 ic KRAS alters the expression of a myriad of cell-surface proteins implicated in diverse biological f

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

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

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

167 g of whole-cell metabolites, and analysis of cell surface proteins in human B cells suggested that th

168 ry of monoclonal antibodies (mAbs) targeting cell surface proteins in their native conformation.

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

170 t protein transgene, and CD46, CD55 and CD71 cell-surface proteins in human cells.

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

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

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

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

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

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

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

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

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

180 PC population is proliferative and marked by cell-surface proteins, including PDGFRalpha, Sca1, and C

181 Two interacting pairs of cell surface proteins independently promote fasciculatio

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

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

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

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

186 ed cell death protein 1 receptor (PD-1) is a cell surface protein involved in immune response regulat

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

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

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

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

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

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

193 tin-dependent endocytosis and degradation of cell-surface proteins is extensively documented, the fea

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

195 formed a comparative study of the density of cell surface proteins (known to be involved with antigen

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

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

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

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

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

201 ed the upregulation of PD-L1 transcripts and cell surface protein levels in GBM cells.

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

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

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

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

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

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

208 aceome DBM), to identify sets of upregulated cell surface protein mRNAs in an LMO2-mediated T-ALL mou

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

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

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

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

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

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

215 signals significantly alter glycosylation of cell-surface proteins on endothelial cells.

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

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

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

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

220 8102 (clade III) to test the hypothesis that cell surface proteins play a role in defence against pre

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

222 To achieve this, we first identified a cell-surface protein, PLPPR3, that allowed purification

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

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

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

226 Cell-surface protein-protein interactions (PPIs) mediate

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

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

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

230 sights into the complexity of the functional cell-surface-protein repertoire (surfaceome) have been t

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

232 Dscam2 is a cell surface protein required for neuronal development i

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

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

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

236 Biotinylation of cell surface proteins revealed decreased surface localiz

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

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

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

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

241 t as cofactors for antitumor Abs that target cell surface proteins, suggesting that the MARCH protein

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

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

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

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

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

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

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

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

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

251 ass monoclonal antibody targeting KIR3DL2, a cell surface protein that is expressed in cutaneous T-ce

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

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

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

255 own, and especially the identity and role of cell surface proteins that are responsible for sperm-egg

256 The FcgammaRs are immune cell surface proteins that bind IgG and facilitate cytok

257 her analyses identified HPV+ and HPV- cancer cell surface proteins that can also serve as potential t

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

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

260 The cell surface proteins that mediate polyamine transport i

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

262 Ephrins are cell surface proteins that regulate diverse biological p

263 PORTANCE Human leukocyte antigens (HLAs) are cell surface proteins that regulate innate and adaptive

264 Repulsive guidance molecules (RGMs) are cell surface proteins that regulate the development and

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

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

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

268 asminogen activator receptor (uPAR)(11) as a cell-surface protein that is broadly induced during sene

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

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

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

272 These include cell-surface proteins that mediate adherence of the bact

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

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

275 interactions between two subfamilies of IgSF cell surface proteins, the Dprs and the DIPs, provided n

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

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

278 d during infection and reroutes a variety of cell surface proteins to disrupt host immunity and promo

279 ent A (HtrA) that cleaves gastric epithelial cell surface proteins to disrupt the epithelial integrit

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

281 ethod has evolved from the identification of cell-surface proteins to characterizing intracellular pr

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

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 The presence of cell surface proteins typically associated with antigen

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

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

289 Here we report that mice lacking CD137, a cell surface protein used in several studies as a marker

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

291 re, 33277 and 381 mutant strains lacking CTD cell surface proteins were more immune-stimulatory than

292 Cell surface proteins were quantified by flow cytometry.

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

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

295 tworks, synaptic connectivity is dictated by cell surface proteins, which assign unique identities to

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

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

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

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

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