ライフサイエンスコーパス: blood group antigen

1 -(1->3)-linked galactose units from a linear blood group antigen.

2 -3)GlcNAc, also known as the Lewis X (Le(x)) blood group antigen.

3 known to affect the expression of the Duffy blood group antigen.

4 es) as the acceptor to generate the H-type 3 blood group antigen.

5 and 0.03 may represent the antithetical Luke blood group antigen.

6 ce that ABCC4 is the gene underlying the PEL blood group antigen.

7 ve immunity toward pathogens bearing cognate blood group antigens.

8 r innate proteins that could recognize human blood group antigens.

9 ding than Gal-1 to fucose-containing A and B blood group antigens.

10 te and enhance norovirus attachment to histo-blood group antigens.

11 d different patterns of attachment to histo- blood group antigens.

12 odies to the core alpha-gal epitope in these blood group antigens.

13 a glycosphingolipid precursor of major human blood group antigens.

14 erstanding of the molecular genetics of many blood group antigens.

15 cid residues that are linked to diseases and blood group antigens.

16 ely as the carrier and coexpressor of the Rh blood group antigens.

17 the biologic function of structures bearing blood group antigens.

18 uding human milk oligosaccharides (HMOs) and blood group antigens.

19 blood group typing, NIPT now covers various blood group antigens.

20 er reducing the number of remaining unsolved blood group antigens.

21 in-4 and galectin-8 bind microbes expressing blood group antigens.

22 ut is independent of the expression of histo-blood group antigens.

23 tutions that create 9 clinically significant blood group antigens.

24 ecificity of B cell tolerance to donor/graft blood group antigens.

25 ynthesis enzymes, cell-cycle regulators, and blood group antigens.

26 up IV and VI viruses can interact with histo-blood group antigens.

27 and binds glycans, including the Lewis histo-blood group antigens.

28 milar induction of tolerance to incompatible blood-group antigens.

29 on waveguides is applied to the detection of blood group antigen A on whole erythrocytes.

30 HFE and TMPRSS6), glucose metabolism (PCK2), blood group antigens (ABO and FUT2), immune function (BA

31 Histo-blood group antigens affect incidence of all-cause diarr

32 ions of genotyping for red cell and platelet blood group antigens affecting several areas of medicine

33 On the other hand, histo-blood group antigens also present in the cell surface ca

34 ized by preferential recognition of specific blood group antigens, also validated by saturation trans

35 lence of Duffy negativity (lack of the Duffy blood group antigen) among human populations in sub-Saha

36 The H blood group antigen and the 2B8 epitope appeared at most

37 edge of molecular approaches for identifying blood group antigens and antibodies as applied to transf

38 he interaction between malaria parasites and blood group antigens and discusses how the knowledge gle

39 FUT2 participates in the production of histo-blood group antigens and has previously been implicated

40 ligosaccharides, on the basis of human histo-blood group antigens and milk oligosaccharides, against

41 ly in the understanding of the basis of many blood group antigens and phenotypes.

42 nd sialylated glycans and Gal-8C recognizing blood group antigens and polyLacNAc glycans.

43 vels of the a1-3-fucosylated Lewis X (Le(x)) blood group antigen, and that this glycan epitope is pri

44 of the alpha1-3-fucosylated Lewis X (Le(x)) blood group antigen, and that this glycan epitope is pri

45 cluding high mannose structures, fucosylated blood group antigens, and glycans with terminal 6-sulfat

46 major and minor histocompatibility antigens, blood group antigens, and tissue-specific "self" antigen

47 pe II membrane glycoprotein, carries over 20 blood group antigens, and XK, which spans the membrane 1

48 terleukin-8 receptor B (CXCR2) and the Duffy blood group antigen are expressed on subsets of neurons

49 syndrome coronavirus 2 (SARS-CoV-2), ABO(H) blood group antigens are among the most recognized predi

50 ns for red cell membrane components carrying blood group antigens are being identified.

51 Because ABO(H) blood group antigens are carbohydrates, we compared the

52 Since histo-blood group antigens are expressed on gut mucosa as well

53 e determines the secretor phenotype in which blood group antigens are found in non-blood body fluids.

54 Blood group antigens are polymorphic, inherited structur

55 FUT2 determines whether histo-blood group antigens are secreted at mucosal surfaces.

56 at amino acid substitution sites that create blood group antigens are significant correlates and pote

57 Analogous to human leukocyte antigens, blood group antigens are surface markers on the erythroc

58 in, and the cell-surface carbohydrate, the A blood group antigen, are expressed by significantly fewe

59 malarial parasite P. knowlesi use the Duffy blood group antigen as a receptor to invade human erythr

60 Plasmodium vivax, requires the Duffy blood group antigen as an obligate receptor for invasion

61 They recognize human histo-blood group antigens as receptors in a strain-specific m

62 NVs recognize human histo-blood group antigens as receptors, but SW918 VLPs did no

63 hey have been found to recognize human histo-blood group antigens as receptors.

64 virus capture method, we characterized histo-blood group antigen attachment properties of various nor

65 throcyte proteins, we have found that the Ok blood group antigen, basigin, is a receptor for PfRh5, a

66 Some blood group antigen-bearing proteins function as major t

67 able to infect humans lacking the Duffy (Fy) blood group antigen because this receptor is critical fo

68 Expression of the Helicobacter pylori blood group antigen binding adhesin A (BabA) is more com

69 Helicobacter pylori BabA is the ABO blood group antigen binding adhesin, which has a closely

70 pylori outer membrane proteins, such as the blood group antigen-binding adhesin (BabA), are associat

71 re to the human gastric epithelium using the blood group antigen-binding adhesin (BabA).

72 denal ulcer-promoting gene, and possibly the blood group antigen-binding adhesion, are the only facto

73 oped a competitive binding assay to quantify blood group antigen-binding specificity in solution.

74 -immunoglobulin, immunoglobulin A, and histo-blood group antigen-blocking (HBGA) antibody levels amon

75 ination as panimmunoglobulin, IgA, and histo-blood group antigen-blocking antibodies against both vac

76 completely dependent on binding to the Duffy blood group antigen by the parasite Duffy binding protei

77 ly dependent on the recognition of the Duffy blood group antigen by the parasite ligand Duffy-binding

78 underlying specific recognition of HMOs and blood group antigens by human galectins, emphasizing the

79 y charged, but neutral glycans such as histo-blood group antigens can also function as receptors.

80 Identification of blood group antigens can now be performed in genetic ter

81 s in genogroups I and II interact with histo-blood group antigen carbohydrates, bovine noroviruses (g

82 The expression of ABO(H) blood group antigens causes deletion of cells that gener

83 NVs also were identified in genes regulating blood group antigens, coat color, fecundity, lactation,

84 band 3 also displayed high levels of the Wrb blood group antigen, confirming the role of band 3 in Wr

85 As expected, IgG and IgM antibody signals to blood group antigens correlated strongly with blood type

86 Previous studies utilized SPR for blood group antigen detection, however, showed poor rege

87 haran Africa due to the absence of the Duffy blood group antigen (Duffy antigen), the only known eryt

88 ssesses strong binding preference for ABO(H) blood group antigens, each domain exhibits distinct bind

89 e intestinal tract, recognize and kill human blood group antigen-expressing Escherichia coli while fa

90 dependent of their secretor status and histo-blood group antigen expression.

91 tion with a galectin that does not recognize blood group antigens failed to impact SARS-CoV-2 infecti

92 ting enzyme effects more complete removal of blood group antigens from cell surfaces, demonstrating t

93 cell's surface receptor, known as the Duffy blood-group antigen (Fy).

94 The Blood Group Antigen Gene Mutation Database (BGMUT) is an

95 ty binding of Helicobacter pylori to the ABO blood group antigen-glycosylated gastric mucosa.

96 I], 1.3-103), whereas persons with a B histo-blood group antigen had decreased risk of infection (OR,

97 ttachment of live norovirus strains to histo-blood group antigens has not been investigated to date.

98 the molecular bases of almost all the major blood group antigens have been determined.

99 Blood group antigens have been implicated in studies of

100 Human histo-blood group antigens have been regarded as receptors for

101 Many novel functions associated with blood group antigens have recently been identified.

102 icle (VLP) antigenic relationships and histo-blood group antigen (HBGA) binding profiles with strains

103 oV-like biological features, including histo-blood group antigen (HBGA) binding, rhesus enteric calic

104 nked immunosorbent assay (ELISA) and a histo-blood group antigen (HBGA) blocking assay using sera fro

105 ne GI or GII HuNoV strain when using a histo-blood group antigen (HBGA) blocking assay.

106 or could block norovirus attachment to histo-blood group antigen (HBGA) co-factors.

107 s influenced by genetically determined histo-blood group antigen (HBGA) expression.

108 o-expression of the CAR and the type B histo-blood group antigen (HBGA) is required to convert the re

109 Histo-blood group antigen (HBGA) Lewis/secretor phenotypes pre

110 We assessed the relationship between histo-blood group antigen (HBGA) phenotypes and clinical rotav

111 Histo-blood group antigen (HBGA) phenotypes have been associat

112 Histo-blood group antigen (HBGA) phenotypes may contribute to

113 trains correlates with an individual's histo-blood group antigen (HBGA) profile, the biological basis

114 g the hinge forms a dimer and binds to histo-blood group antigen (HBGA) receptors with a low affinity

115 rus-like particle (VLP) binding to the histo-blood group antigen (HBGA) receptors.

116 e change, Q396R, is able to modify the histo-blood group antigen (HBGA) recognition pattern.

117 Histo-blood group antigen (HBGA) status may affect vaccine eff

118 Histo-blood group antigen (HBGA) typing of saliva showed that

119 strain specifically recognizes A-type histo-blood group antigen (HBGA) using a glycan array screen c

120 a region topologically similar to the histo-blood group antigen (HBGA)-binding sites of the human no

121 levels measured in neutralization and histo-blood group antigen (HBGA)-blocking assays.

122 d were compared with those measured in histo-blood group antigen (HBGA)-blocking assays.

123 including GII.4 Sydney, form distinct, histo-blood group antigen (HBGA)-dependent capsid clusters on

124 Histo-blood group antigens (HBGA) are known HuNoV susceptibili

125 vealed the involvement of type A and B histo-blood group antigens (HBGA) in TV infection.

126 ibit both strains of VLPs' bindings to histo-blood group antigens (HBGA) receptors on human cells at

127 block the interaction of VLPs with ABH histo-blood group antigens (HBGA), suggesting that multiple an

128 c profiles and altered specificity for histo-blood group antigens (HBGA), the determinants of cell at

129 ns have shown the association of human histo-blood group antigens (HBGAs) and susceptibility to infec

130 Noroviruses are known to bind to histo-blood group antigens (HBGAs) and the specific binding pa

131 Histo-blood group antigens (HBGAs) are a source of antigenic v

132 Previous studies indicated that histo-blood group antigens (HBGAs) are critical host-susceptib

133 Carbohydrate-dependent histo-blood group antigens (HBGAs) are known to be critical fo

134 Histo-blood group antigens (HBGAs) are norovirus binding ligan

135 histo-blood type, and its determinant histo-blood group antigens (HBGAs) are regarded as receptors f

136 worldwide, and interactions with human histo-blood group antigens (HBGAs) are thought to play a criti

137 taviruses are known to recognize human histo-blood group antigens (HBGAs) as a host ligand that is be

138 NoVs use histo-blood group antigens (HBGAs) as attachment factors.

139 oviruses (NoVs) are known to recognize histo-blood group antigens (HBGAs) as attachment factors.

140 demic acute gastroenteritis, recognize histo-blood group antigens (HBGAs) as host attachment factors

141 e epidemic acute gastroenteritis using histo-blood group antigens (HBGAs) as host receptors or attach

142 Human noroviruses (huNoVs) recognize histo-blood group antigens (HBGAs) as host susceptibility fact

143 ons of human noroviruses (huNoVs) with histo-blood group antigens (HBGAs) as receptors or attachment

144 The discovery of human histo-blood group antigens (HBGAs) as receptors or ligands of

145 ecent finding that NVs recognize human histo-blood group antigens (HBGAs) as receptors provided a new

146 is, have been found to recognize human histo-blood group antigens (HBGAs) as receptors.

147 Noroviruses (NVs) recognize human histo-blood group antigens (HBGAs) as receptors.

148 viruses and differential expression of histo-blood group antigens (HBGAs) between populations may con

149 Histo-blood group antigens (HBGAs) expressed on enterocytes ar

150 c/antigenic diversity, and reliance on histo-blood group antigens (HBGAs) for attachment.

151 Histo-blood group antigens (HBGAs) have been associated with r

152 ing of the RV surface protein (VP4) to histo-blood group antigens (HBGAs) in an RV genotype-dependent

153 the binding of 8 Noroviruses (NORs) to histo-blood group antigens (HBGAs) in human saliva using recom

154 Histo-blood group antigens (HBGAs) in saliva and gut recognize

155 GI VLPs bound to histo-blood group antigens (HBGAs) including fucose, Lewis, an

156 Histo-blood group antigens (HBGAs) on the intestinal epitheliu

157 rface carbohydrate structures known as histo-blood group antigens (HBGAs) prior to internalization, a

158 Recent findings demonstrate that human histo-blood group antigens (HBGAs) serve as receptors for noro

159 Histo-blood group antigens (HBGAs) such as fucosyltransferase

160 lymerase chain reaction (RT-qPCR), and histo-blood group antigens (HBGAs) were determined by phenotyp

161 that different NORs bind to different histo-blood group antigens (HBGAs), and at least four distinct

162 es that blocked the binding of VLPs to histo-blood group antigens (HBGAs), and norovirus-specific T c

163 Noroviruses bind to gut histo-blood group antigens (HBGAs), but only 70%-80% of indivi

164 nsialylated glycoconjugates, including histo-blood group antigens (HBGAs), in the infectivity of huma

165 the genus Norovirus and recognizes the histo-blood group antigens (HBGAs), similarly to human norovir

166 had no binding affinity for synthetic histo-blood group antigens (HBGAs), suggesting that PSVs could

167 ic gastroenteritis, is associated with histo-blood group antigens (HBGAs), which are also cell attach

168 olled secretor-dependent expression of histo-blood group antigens (HBGAs), which are also critical fo

169 ytes in a genotype-specific manner via histo-blood group antigens (HBGAs), which are also detectable

170 These viruses usually interact with histo-blood group antigens (HBGAs), which are considered essen

171 n cores 2, 4, and 6, as well as type 1 histo-blood group antigens (HBGAs).

172 rocess have been identified, including human blood group antigens (HBGAs).

173 otype-dependent binding to nonsecretor histo-blood group antigens (HBGAs).

174 (P[4], P[6], and P[8]) recognize human histo-blood group antigens (HBGAs).

175 human RVs interacts with the secretor histo-blood group antigens (HBGAs).

176 ith their capsid-protruding domains to histo-blood-group antigens (HBGAs), an interaction thought to

177 Blood group antigen immunogenicity is a crucial factor i

178 ivation prevents a strong immune response to blood group antigens in ABO-mismatched allograft recipie

179 diabetes insipidus and absence of the Colton blood group antigens in humans, whereas, mutation of a t

180 nonsecretors and are unable to express histo-blood group antigens in secretions and on mucosal surfac

181 to identify blood groups within 5 s for all blood group antigens including A, B, D, C, c, E, and e.

182 CR1 contains the Knops blood group antigens, including the antithetical pairs S

183 ractions between malaria parasites and other blood group antigens, including the Gerbich, MNS and Rhe

184 ical study for the detection of p53 protein, blood groups antigens, including Lewis(a) and Lewis(b),

185 digestive and respiratory epithelia of histo-blood group antigens involved in the attachment of patho

186 an only be remedied when the identity of the blood group antigen is discovered.

187 The Vel blood group antigen is expressed on the red blood cells

188 The clinically important MAM blood group antigen is present on haematopoietic cells o

189 rica where its erythrocyte ligand, the Duffy blood group antigen, is missing.

190 cosylated glycans, which are primarily histo-blood group antigens, is largely unknown.

191 genes, which encode a serologically distinct blood group antigen known as Dantu.

192 -tetraose core chains to generate Lewis (Le) blood group antigens Le(a) or Le(x), respectively, and H

193 e involvement of babA in binding to the host blood group antigen Lewis B, neither the presence of dif

194 -chain with structural homology to the human blood group antigen Lewis X (Le(x)).

195 her presynaptic proteins or the carbohydrate blood group antigen Lewis(b), but not both.

196 to examine expression of the oligosaccharide blood-group antigens Lewis(b), A, and H type 2 in taste

197 t, previously had been linked with the Duffy blood-group-antigen locus on chromosome 1q.

198 Polypeptide blood group antigens, many of which are created by singl

199 Both oligosaccharide and protein blood group antigens may act as receptors for bacterial,

200 ty problems, due to the absence of undefined blood group antigens, may cause difficulty in finding ma

201 re, we identify the peptide within the Duffy blood group antigen of human and rhesus erythrocytes to

202 gen is the most clinically important protein blood group antigen of the erythrocyte.

203 is dependent on the expression of the Duffy blood group antigen on erythrocytes.

204 that binds to the fucosylated Lewis b histo-blood group antigen on the surface of gastric epithelial

205 inomas express sialylated, fucosylated Lewis blood group antigens on cell surface and secreted mucins

206 ess the BabA adhesin, which binds to ABO/Leb blood group antigens on gastric mucin and epithelial cel

207 g made in understanding the effects of other blood group antigens on malaria.

208 It is not known whether the expression of blood group antigens on platelet proteins alters platele

209 pean descent affects the expression of histo-blood group antigens on the mucosal epithelia of human r

210 ress abnormally high or low levels of A or B blood group antigens on their platelet surfaces (high ex

211 igen from donor RBCs without affecting other blood group antigens or reducing the circulatory life sp

212 in particular terminal fucosylated Lewis and blood group antigens present on N- and O-glycans.

213 These adhesins bind to the Dr(a) blood-group antigen present on decay-accelerating factor

214 ichia coli recognize as a receptor the Dr(a) blood-group antigen present on the complement regulatory

215 ysis suggested pathways related to the histo-blood group antigen production, and the regulation of io

216 At least two erythrocyte blood group antigen proteins have complement regulatory

217 The interplay between malaria parasites and blood group antigens remains a fascinating subject with

218 The Indian (In) blood group antigens reside on CD44, and most individual

219 Finally, some blood group antigens reside on proteins that serve cruci

220 Some blood group antigens reside on proteins with known recep

221 The presence of histo-blood group antigens (secretor, ABO, and Lewis type) was

222 These histo-blood group antigens serve as host receptor sites necess

223 In comparison to blood group antigen-specific IA, nonantigen-specific IA

224 d cost of nonantigen-specific as compared to blood group antigen-specific IA.

225 of Helicobacter pylori binds to fucosylated blood group antigens, such as the Lewis(b) antigens in h

226 ave various capacities for binding ABH histo-blood group antigens, suggesting that different mechanis

227 nificantly more likely to be nonsecretors of blood group antigens than are women without such a histo

228 inity to glycophorin A, a well-studied human blood group antigen that forms TM homodimers.

229 Fy is an important minor blood-group antigen that has two immunologically distinc

230 d the salivary agglutinin also present Lewis blood group antigens, the exact repertoire varying on an

231 We report the molecular bases of 5 Er blood group antigens: the recognized Era, Erb, and Er3 a

232 P. vivax binds the Duffy blood group antigen through its Duffy-binding protein 1

233 ibute to the expression of the MN and Wright blood group antigens, to act as a receptor for the malar

234 cases will become apparent and accurate NIPT blood group antigen typing results are crucial for guidi

235 Lewis(y-6) and H (Le(y)/H) are blood group antigens up-regulated on RA synovial endothe

236 panel of oligosaccharides including HMOs and blood group antigens using a complementary approach base

237 ve calculated the immunogenicities of common blood group antigens using data collected on clinically

238 fants, we found that lack of the Lewis histo-blood group antigen was associated with increased suscep

239 milligram scale biosynthesis of the H-type 3 blood group antigen was explored using purified recombin

240 Historically, a blood group antigen was identified when an immune respon

241 of Piezo1 as the carrier molecule for the Er blood group antigens was demonstrated using immunoprecip

242 -like particles (VLPs) to specific ABH histo-blood group antigens was investigated by using human sal

243 r-positive and 8 secretor-negative for histo-blood group antigens) were challenged with ascending dos

244 ssociated with expression of the D and Cc/Ee blood group antigens, were synthesized and screened for

245 essing syntaxin-1 (82%) also expressed the A blood group antigen, whether or not they expressed alpha

246 ide epitope homologous to the human Lewis(b) blood group antigen, which adopts a relatively well-defi

247 One such variant is the Dantu blood group antigen, which is associated with 74% protec

248 nsfected with either vector expressed the P1 blood group antigen, which was absent from untransfected

249 ifferent patterns of attachment to ABH histo-blood group antigens, which are carbohydrate epitopes pr

250 Both viruses recognize and bind to histo-blood group antigens, which are expressed by the fucosyl

251 ra, are predominantly negative for the Duffy blood-group antigen, which mediates invasion of reticulo

252 confined to the major histocompatibility and blood group antigens, xenotransplantation is confronted