ライフサイエンスコーパス: blood group antigen

1 and 0.03 may represent the antithetical Luke 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 ding than Gal-1 to fucose-containing A and B blood group antigens.

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

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

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

9 a glycosphingolipid precursor of major human blood group antigens.

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

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

12 the biologic function of structures bearing blood group antigens.

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

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

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

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

17 ve immunity toward pathogens bearing cognate blood group antigens.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

36 Blood group antigens are polymorphic, inherited structur

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 Blood group antigens have been implicated in studies of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

120 Blood group antigen immunogenicity is a crucial factor i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 Some blood group antigens reside on proteins with known recep

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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