ライフサイエンスコーパス: surface protein

1 biosynthesis, and a microalgal lipid droplet surface protein.

2 region of the influenza A hemagglutinin (HA) surface protein.

3 es with antibody titers to the hemagglutinin surface protein.

4 hage, carrying gene encoding a putative cell-surface protein.

5 principally on the hemagglutinin (HA) viral surface protein.

6 une responses, and regulating other Bb outer surface proteins.

7 o hepatitis D viruses pseudotyped with CSHBV surface proteins.

8 gnificance of MgrA regulation of capsule and surface proteins.

9 n factors and different combinations of cell surface proteins.

10 ntrolled by the concentration of immobilized surface proteins.

11 L-4 and analyzed for expression of >300 cell-surface proteins.

12 es targeting conserved elements on influenza surface proteins.

13 ling medical devices using a variety of cell-surface proteins.

14 es of interactions between host and parasite surface proteins.

15 cell progenitor cells to Abs targeted to 176 surface proteins.

16 tins was in the range of that to these viral surface proteins.

17 es for the functional analysis of these cell surface proteins.

18 ng merozoite proteins as well as erythrocyte surface proteins.

19 ctions with the transmembrane regions of the surface proteins.

20 t with their surrounding environment through surface proteins.

21 ion and for correct functioning of merozoite surface proteins.

22 cterization of ligand interactions with cell surface proteins.

23 ogenic autoantibodies that target neuroglial surface proteins.

24 such as polysaccharides, fimbriae, and outer surface proteins.

25 n (CSP) and the 42-kDa fragment of merozoite surface protein 1 (MSP-1(42)) of P. vivax and P. falcipa

26 the C-terminal 19-kDa fragment of merozoite surface protein 1 (MSP119) to P. falciparum MSP8 (PfMSP8

27 he 19 kDa fragment of the P. vivax Merozoite Surface Protein 1 (PvMSP119) is one of the most promisin

28 at antibodies to 5 proteins of the Merozoite Surface Protein 1 complex were differentially acquired b

29 The Plasmodium vivax merozoite surface protein 1 paralog (PvMSP1P), which has epidermal

30 ainst circumsporozoite protein and merozoite surface protein 1 were significantly higher in participa

31 e circumsporozoite protein and the merozoite surface protein 1.

32 and vaccine-induced antibodies to merozoite surface protein 2 (MSP2) are associated with resistance

33 endent on the sequential generation of major surface protein 2 (Msp2) outer membrane variants to esta

34 e-binding antigen [EBA] 175RIII-V, merozoite surface protein 2 [MSP-2], and MSP-142) and opsonic phag

35 ong to tryptophan-rich antigen and merozoite surface protein 3 (MSP3) families that were more abundan

36 entified PfMSP3.1, a member of the merozoite surface protein 3 family of merozoite surface proteins,

37 against Plasmodium falciparum (Pf) merozoite surface protein-3 and glutamate-rich protein.

38 P. vivax merozoite surface protein 3alpha (PvMSP3alpha) is a target of acqu

39 d on the use of highly immunogenic merozoite surface protein 8 (MSP8) as a vaccine carrier protein.

40 th FH and FHL-1 was identified as neisserial surface protein A (NspA), which has previously been iden

41 ive protein antigens, including pneumococcal surface protein A (PspA) and pneumolysin (Ply).

42 nosensor for rapid detection of pneumococcal surface protein A (PspA) peptide and SP lysate from synt

43 d toxins and virulence factors but increased surface protein A abundance.

44 cence assays that combined monoclonal (outer surface protein A) and polyclonal antibodies were perfor

45 ded 109 variants of the diverse pneumococcal surface proteins A and C (PspA and PspC) and zinc metall

46 These outputs included an immunogenic cell-surface protein, a cytokine, a chemokine, and a checkpoi

47 COMP interacts directly with the ubiquitous surface protein A2 of M. catarrhalis.

48 49) through interaction with the ubiquitous surface protein A2/A2H.

49 ith deep neural network (cTP-net), to impute surface protein abundances from scRNA-seq data by learni

50 phospholipases C (PLCs; PlcA and PlcB) and a surface protein (ActA).

51 necrosis factor receptor superfamily of cell surface proteins, acts as a costimulatory receptor on T

52 CH2 was required for processing of the sperm surface protein ADAM3, which is required for sperm ferti

53 ll amino-acid mutations to influenza's major surface protein affect viral neutralization by polyclona

54 er specific to 8 group B Streptococcus (GBS) surface proteins among 81 HIV-uninfected and 83 HIV-infe

55 so, by simultaneous single-cell DNA and cell surface protein analysis, we illustrate both genetic and

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

57 surface fat was accompanied by a decrease in surface protein and carbohydrate contents.

58 We show that Z2 interacts with ZIKV surface protein and disrupts the integrity of the viral

59 red from US strains by acquisition of a cell-surface protein and macrolide resistance determinants vi

60 pecific and stronger binding between exosome surface protein and the aptamer displaces aptamers from

61 MSCs) are characterized by their unique cell surface proteins and aberrant signaling pathways.

62 s that express high levels of tumor-specific surface proteins and are composed of highly unsaturated

63 ion assays demonstrates fluid interaction of surface proteins and CD25 is only internalized when co-l

64 in reticulocyte binding proteins, merozoite surface proteins and exported proteins with unknown func

65 host cuticle led to a selective radiation of surface proteins and hydrolytic enzymes.

66 regulated expression of transcripts encoding surface proteins and in changes in their subcellular loc

67 - branched sugar oligomers attached to cell-surface proteins and lipids - is organized like a factor

68 ereby the cells upregulate the expression of surface proteins and secrete cytokines, both required fo

69 by the presence of specific combinations of surface proteins and their abundance, allowing exosomes

70 CITE-seq profiling of 82 surface proteins and transcriptomes of 53,201 single cel

71 focused on early infection steps, analyzing surface proteins and viral entry.

72 M protein is the most abundant GAS surface protein, and M1 serotype GAS strains are associa

73 lines, TRPM4 being the only gene encoding a surface protein, and surface proteome analysis found no

74 evolve under positive selection on the viral surface proteins, and discuss the potential role of thes

75 eHAV lacks virus-encoded surface proteins, and how it enters cells is unknown.

76 rtebrate clustered protocadherin (Pcdh) cell surface proteins are encoded by three closely linked gen

77 Rib domain-containing surface proteins are found associated with invasive stra

78 Because these surface proteins are involved in cell adherence or invas

79 valuable for studying cell populations, cell-surface proteins are often integral markers of cellular

80 During invasion, several parasite surface proteins are shed by a membrane-bound protease c

81 While surface proteins are suitable vaccine candidates and can

82 geted biocarrier that exploits the HER3 cell surface protein as a portal to sneak therapeutics into t

83 ozoite surface protein 3 family of merozoite surface proteins, as the direct interaction partner.

84 nvasion protein A (AipA), A. phagocytophilum surface protein (Asp14), and outer membrane protein A (O

85 n SMG resulted in an increased expression of surface proteins associated with maturation and interleu

86 searchers to jointly study transcriptome and surface proteins at the single cell level to make new bi

87 inins to engineer a genetically encoded cell-surface protein barcoding system.

88 roteins and transfer heme to IsdA, the final surface protein before heme-iron is transported through

89 Recently, 32 interacting cell surface proteins belonging to two newly defined families

90 d DIP immunoglobulin superfamily (IgSF) cell-surface proteins bind heterophilically and are expressed

91 valuated to assess the antigenicity of three surface proteins: BipA, BrpA, and Bta112.

92 rom S. pneumoniae TIGR4 lysates enriched for surface proteins by a chromatography step after culture

93 flammatory dermatoses were analyzed for cell surface proteins by flow cytometry and for copy number a

94 re we report comprehensive profiling of cell surface proteins by flow cytometry in naive and primed h

95 lterations in the tumor secretome and immune surface proteins by high throughput proteomic arrays.

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

97 with low titers against group 3 pneumococcal surface protein C (PspC) variants were more likely to be

98 on of the ospC and dbpA genes encoding outer surface protein C and decorin binding protein A, respect

99 hrough the overexpression of anti-phagocytic surface proteins called 'don't eat me' signals-including

100 Cell-type-specific surface proteins can be exploited as valuable markers fo

101 Antibodies against viral surface proteins can blunt the spread of viral infection

102 Cell surface protein capture is mediated by covalent tagging

103 The cell surface protein CD 138 increases with disease recurrence

104 We have investigated the utility of the cell surface protein CD26 to identify functionally distinct f

105 Here, we demonstrate that the cell-surface protein CD276/B7-H3 is broadly overexpressed by

106 s specificity for the T cell-activating cell surface protein CD3 and the B cell Ag CD19.

107 te that secreted ImpA cleaves the macrophage surface protein CD44, which inhibits the phagocytosis of

108 sis is normally inhibited by binding of cell surface protein CD47 to macrophage signal regulatory pro

109 modium vivax, rely on two distinct host cell surface proteins, CD81 and the Scavenger Receptor BI (SR

110 ired PanNETs characterized by increased cell-surface protein CD90 expression and aldehyde dehydrogena

111 The complement of cell surface proteins, collectively referred to as the surfac

112 hese data indicate that the Pneumocystis Msg surface protein complex can act to suppress host macroph

113 major surface glycoprotein (Msg) is a 120-kD surface protein complex on the organism with importance

114 te that Reck and Gpr124 are part of the cell surface protein complex that transduces Wnt7a- and Wnt7b

115 nd further characterized the major merozoite surface protein complex.

116 lish LD identity by defining positioning and surface-protein composition.

117 BapA from Salmonella is a ~386-kDa surface protein, comprising 27 tandem repeats predicted

118 y particle size, emulsifying activity index, surface protein concentration at the interface and by tr

119 that this can lead to the expression of cell surface proteins containing O-glycans comprised of a sin

120 Genes encoding cell-surface proteins control nervous system development and

121 ells, were characterized by co-expression of surface proteins corresponding to HLA-DQA1, HLA-DQA2, OL

122 factors (Gfi1, Cebpd, Cebpe, and Spi1), cell surface proteins (Csf3r and Gr1), and neutrophil granule

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

124 profile from our cohort, we identified cell surface proteins (CSPs) associated with the SCCB phenoty

125 n, the last step of endocytosis required for surface protein degradation.

126 ectroscopy, we introduce a method to measure surface protein density and to estimate the apparent For

127 We show that an ookinete and sporozoite surface protein designated as PIMMS43 (Plasmodium Infect

128 have identified a unique mouse Pneumocystis surface protein, designated Pneumocystis cross-reactive

129 -structural protein NS1, rather than a viral surface protein, determines IEC tropism.

130 However, specific charge modification of surface proteins did not change cell migration motility

131 scaffolds were discovered by HTS and disrupt surface protein display in intact cells and inhibit enzy

132 alciparum, RIFINs form the largest family of surface proteins displayed by erythrocytes(1).

133 nds for apical membrane antigen (AMA) family surface proteins displayed on the parasite.

134 The upregulation of naive-specific cell surface proteins during primed-to-naive resetting enable

135 detailed structure and arrangement of their surface proteins (E and prM in immature virus or M in ma

136 ectively simulate the kinetics of detectable surface proteins (e.g., CA-125) shed into the bloodstrea

137 Expression analysis of >300 surface proteins enabled identification of IL-4-upregula

138 ysaccharides via the action of multiple cell surface proteins encoded within polysaccharide utilizati

139 f these SNPs were in genes annotated as cell surface protein-encoding genes, including some essential

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

141 We prepared cell surface protein-enriched fractions from MSCs and CPCs, a

142 An array of carbohydrates masks the HIV-1 surface protein Env, contributing to the evasion of humo

143 argets ROR1, which encodes an onco-embryonic surface protein expressed on the CLL cells of over 90% o

144 unoglobulin-like lectin (Siglec)-8 is a cell-surface protein expressed selectively on human eosinophi

145 Characterisation of cell surface proteins expressed by each subset is informative

146 DLL3, although orders of magnitude lower in surface protein expression than typical oncology targets

147 Moreover, IL-33 increases NK-1 gene and surface protein expression, as well as IKbeta-alpha phos

148 to PD-L1 and PD-L2 3'UTRs to reduce PD-L1/L2 surface protein expression.

149 We also report on a family of nonvariant surface proteins (Fam10) and demonstrate surface localiz

150 Members of several variant surface protein families are expressed on infected blood

151 hese parasites have evolved specialized cell-surface protein families, overlaid on a well-conserved c

152 We screened Leptospira outer membrane/surface proteins for their ability to activate/inhibit T

153 GR1) and neurotrimin (NTM) are abundant cell-surface proteins found in the brain and form part of the

154 Here, we show that surface proteins from serum extracellular vesicles label

155 prevaccination concentrations of IL-10 (RV5 surface proteins G1 and P1) and IFNgamma (G1) in the HIV

156 In this study, the FbaA surface protein gene was found to be present in most ski

157 ental contributions to fitness of individual surface protein genes and the multifactorial nature of G

158 DNA PCR positive; (3) positive for merozoite surface protein genes by PCR or positive by loop-mediate

159 involved in capsule biosynthesis and repress surface protein genes.

160 The EBV surface protein gp350 is a major target for antibodies.

161 In particular, streptococcal surface proteins have been implicated as potent neutroph

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

163 d on expression of multiple variant-specific surface proteins have been reported, but poorly defined

164 arum circumsporozoite protein (CSP), a major surface protein implicated in the structural strength, m

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

166 AS alters the expression of a myriad of cell-surface proteins implicated in diverse biological functi

167 we report synthesis of core-shell structured surface protein-imprinted nanoparticles with reversible

168 dy conjugated with graphene quantum dot with surface protein in Campylobacter jejuni cell membrane.

169 ggest the importance of lateral diffusion of surface proteins in contributing to a gradual increase i

170 ceptors belong to the largest family of cell surface proteins in eukaryotes, the G protein-coupled re

171 r HVEM is one of the most frequently mutated surface proteins in germinal center (GC)-derived B cell

172 Surface proteins in Gram-positive bacteria are incorpora

173 whole-cell metabolites, and analysis of cell surface proteins in human B cells suggested that this tr

174 tein transgene, and CD46, CD55 and CD71 cell-surface proteins in human cells.

175 large populations of apical and basolateral surface proteins in Madin-Darby canine kidney (MDCK) cel

176 port a sensor platform that profiles exosome surface proteins in minutes by the naked eye.

177 cal basis for molecular recognition of viral surface proteins in order to build predictive molecular

178 monoclonal antibodies (mAbs) targeting cell surface proteins in their native conformation.

179 metalloprotease ADAM10 sheds a range of cell surface proteins, including ligands and receptors of the

180 pB) to block ubiquitylation of the bacterial surface proteins, including OmpA, and subsequent recogni

181 pulation is proliferative and marked by cell-surface proteins, including PDGFRalpha, Sca1, and CD81.

182 ract with both HPR and alternate trypanosome surface proteins, including variant surface glycoprotein

183 Two interacting pairs of cell surface proteins independently promote fasciculation bet

184 ted endocytosis is a major regulator of cell-surface protein internalization.

185 orating antibodies against cancer associated surface proteins into the click-chemistry, we were able

186 ll death protein 1 receptor (PD-1) is a cell surface protein involved in immune response regulation.

187 n leukocyte antigen (HLA) system encode cell-surface proteins involved in regulation of immune respon

188 The preS1 domain of the large HBV surface protein is the major viral attachment site on he

189 Endocytic down-regulation of cell-surface proteins is a fundamental cellular process for c

190 teins to reveal how a collection of some 700 surface proteins is dramatically remodeled in an isogeni

191 ependent endocytosis and degradation of cell-surface proteins is extensively documented, the features

192 d a comparative study of the density of cell surface proteins (known to be involved with antigen pres

193 his study, we show that the Egr2-driven cell surface proteins LAG-3 and 4-1BB can identify dysfunctio

194 Surface protein layers (S-layers) often form the only st

195 sing a monoclonal antibody against a hepatic surface protein, leucine amino peptidase (LAP).

196 e upregulation of PD-L1 transcripts and cell surface protein levels in GBM cells.

197 ltage-gated sodium current I (Na) and Nav1.5 surface protein levels in rabbit cardiomyocytes and in H

198 provide phenotypic information such as cell-surface protein levels.

199 velope proteins containing large hepatitis B surface protein (LHBs) was increased.

200 en candidates for vaccines, we reasoned that surface proteins may provide an enriched source of such

201 e DBM), to identify sets of upregulated cell surface protein mRNAs in an LMO2-mediated T-ALL mouse mo

202 ons between nanotubes and AMB-1 via the cell surface protein MSP-1 and flagellin.

203 aining the scaffold protein and deficient in surface proteins needed for cell entry.

204 idence for direct interaction between the LD surface protein (NoLDSP) and AUTOPHAGY-RELATED8 (NoATG8)

205 Heparin-binding hemagglutinin (HBHA), a surface protein of Mycobacterium tuberculosis, is an att

206 the structure and function of Ail, the major surface protein of the deadly pathogen Yersinia pestis.

207 transmembrane protein 119 (Tmem119), a cell-surface protein of unknown function, as a highly express

208 olar K(d) values) and selectivity to exposed surface proteins of both laboratory parasite strains as

209 strate this novel approach by characterizing surface proteins of different cell types at the single-c

210 Secreted mucins in saliva and surface proteins of erythrocytes showed a high degree of

211 ta to estimate the fitness landscape for the surface proteins of human immunodeficiency virus and hep

212 oximity-dependent barcoding assay to profile surface proteins of individual exosomes using antibody-D

213 Two surface proteins of P. gingivalis, PGN_0294 and PGN_0806

214 Neuraminidase (NA), the second major surface protein on the influenza virus, is emerging as a

215 mAbs specific for surface proteins on APCs can serve as Ag-delivery vehicl

216 ls significantly alter glycosylation of cell-surface proteins on endothelial cells.

217 Surface proteins on exosomes carry information about the

218 d by analysis of the variable composition of surface proteins on individual exosomes, derived from hu

219 From 18 initially identified surface proteins, only SPy_2191 is conserved, surface-ex

220 in a majority of the animals, antibodies to surface proteins persisted beyond the duration of the st

221 The surface protein Pfs47 allows Plasmodium falciparum paras

222 The Plasmodium falciparum gametocyte surface protein, Pfs48/45, is a potential target for mal

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

224 Hic, a PspC-like pneumococcal surface protein, possesses vitronectin and factor H bind

225 on and colonization is the polymorphic outer surface proteins produced by Lyme borreliae.

226 M-D), to detect exosomes by exploiting their surface protein profile.

227 Cell-surface protein-protein interactions (PPIs) mediate cell

228 of techniques for the detection of reactive surfaces, protein-protein docking and molecular simulati

229 The surfaceome is critical because surface proteins provide a gateway for internal signals

230 Assessing exosome surface proteins provides a powerful means of identifyin

231 ite specific proteins, termed rhoptry apical surface proteins (RASP) that cap the extremity of the rh

232 In Gram-positive bacteria, a subset of surface proteins relies on an enzyme called sortase for

233 s into the complexity of the functional cell-surface-protein repertoire (surfaceome) have been techno

234 ceptors, one of the largest families of cell surface proteins, representing a major class of drug tar

235 charomyces pombe shu1(+) gene encodes a cell-surface protein required for assimilation of exogenous h

236 Dscam2 is a cell surface protein required for neuronal development in Dro

237 ers (Pra1 and Zrt1) and other zinc-regulated surface proteins, resulted in lower autoaggregation and

238 Rapid changes in influenza surface proteins resulting from antigenic drift and shif

239 Isolation of surface proteins revealed higher amounts of alpha4 or be

240 Staphylococcus aureus surface protein SasG promotes cell-cell adhesion during

241 We examined the ability of the surface protein SdrF to adhere to keratin, a major molec

242 neumococci express a versatile repertoire of surface proteins sequestering and interacting specifical

243 analysis of differentially regulated RNA and surface proteins showed a decrease in metabolic pathways

244 Biotinylating platelet surface proteins showed ADAMDEC1 hydrolyzed surface pro-

245 We find that, akin to extended hydrophobic surfaces, proteins situate their hydration waters at the

246 This process mediated by the CC17-specific surface protein Srr2 is enhanced by E2-P4 C(7) concentra

247 ages, and provide a substrate for binding of surface proteins such as InlB.

248 s enabled identification of IL-4-upregulated surface proteins, such as CD90, CD108, CD109, and CD200R

249 amily includes Plasmodium falciparum variant surface proteins, such as RIFINs and STEVORs, is controv

250 cofactors for antitumor Abs that target cell surface proteins, suggesting that the MARCH protein repe

251 - gestation mouse placenta as well as a cell surface protein that can be used to identify and isolate

252 Here, we identify P113 as a merozoite surface protein that directly interacts with RH5Nt.

253 ression of staphylococcus protein A (SpA), a surface protein that drives polyclonal B cell expansion

254 coded by the conjugative plasmid pCF10, is a surface protein that has been implicated to play a role

255 irus, revealing changes in the hemagglutinin surface protein that increase stability and receptor bin

256 ogen activator receptor (uPAR)(11) as a cell-surface protein that is broadly induced during senescenc

257 obacterium tuberculosis (Mtb) is a bacterial surface protein that is commonly used in nucleic acid va

258 onoclonal antibody targeting KIR3DL2, a cell surface protein that is expressed in cutaneous T-cell ly

259 tine/glutamate antiporter system xc(-), as a surface protein that is upregulated specifically in tumo

260 and especially the identity and role of cell surface proteins that are responsible for sperm-egg reco

261 The FcgammaRs are immune cell surface proteins that bind IgG and facilitate cytokine p

262 nalyses identified HPV+ and HPV- cancer cell surface proteins that can also serve as potential target

263 and viral decoys, including challenging cell surface proteins that cannot be produced using typical d

264 These include cell-surface proteins that mediate adherence of the bacterial

265 NCE Human leukocyte antigens (HLAs) are cell surface proteins that regulate innate and adaptive immun

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

267 actions between two subfamilies of IgSF cell surface proteins, the Dprs and the DIPs, provided new ca

268 heating was developed to perform a rapid on-surface protein thermal decomposition and digestion suit

269 The cargo and surface proteins they carry are considered to define the

270 has evolved from the identification of cell-surface proteins to characterizing intracellular protein

271 ing infection and reroutes a variety of cell surface proteins to disrupt host immunity and promote th

272 (HtrA) that cleaves gastric epithelial cell surface proteins to disrupt the epithelial integrity and

273 ells, VZV alters cell signaling and remodels surface proteins to enhance T cell skin trafficking.

274 Pathogens use a variety of secreted and surface proteins to interact with and manipulate their h

275 antly, we linked the quantity of each cell's surface proteins to its total transcriptome, which is a

276 panded role for Ldts in covalently attaching surface proteins to PG.

277 It requires parasite surface proteins to provide attachment to host cells and

278 ems like the GIT is through the use of their surface proteins to sense and interact with components o

279 Most of Gram-positive bacteria anchor surface proteins to the peptidoglycan cell wall by sorta

280 They include genes encoding transporters, surface proteins, transcriptional regulators, and metabo

281 IV-1 spread; critically, however, which cell surface protein triggers contact-induced polarization at

282 The presence of cell surface proteins typically associated with antigen prese

283 pression and rapid upregulation of IL7Ralpha surface protein upon transition from monocyte to macroph

284 re we report that mice lacking CD137, a cell surface protein used in several studies as a marker for

285 RTANCE The pH stability of the hemagglutinin surface protein varies between different influenza strai

286 SP4 and block the trimerization of the virus surface protein VP7, a step required for its incorporati

287 s VP7 and NSP4 and the assembly of the virus surface proteins VP7 and VP4.

288 sor, cystatin, and numerous Variant-specific Surface Proteins (VSPs).

289 cing the evolution of antigenic sites at IAV surface proteins, we show that an amino acid variant bec

290 emonstrated that many glycosylation sites on surface proteins were down-regulated in statin-treated c

291 3277 and 381 mutant strains lacking CTD cell surface proteins were more immune-stimulatory than the p

292 Cell surface proteins were quantified by flow cytometry.

293 er membrane proteins (P28/OMP) and a 120-kDa surface protein, were also recognized as necessary for t

294 y universal influenza vaccines target the HA surface protein, which is a key component of pandemic in

295 n mechanics and adhesion in a staphylococcal surface protein, which may represent a general mechanism

296 s, synaptic connectivity is dictated by cell surface proteins, which assign unique identities to neur

297 gnify a large family of structurally related surface proteins, which contribute to the ability of str

298 llate a set of AS and DE genes encoding cell surface proteins, which present promising diagnostic and

299 umsporozoite protein (PfCSP) is a sporozoite surface protein whose role in sporozoite motility and ce

300 only conferred by the interaction of a viral surface protein with a host receptor complex.