ライフサイエンスコーパス: serum immunoglobulin G

1 proliferation in the presence of respective serum immunoglobulin G.

2 SCI patients also revealed constantly lower serum immunoglobulin G [-0.27 (95% CI: -0.45; -0.10)] an

3 e deficiency, characterized by low levels of serum immunoglobulin G, A, and/or M with loss of antibod

4 ly correlated with the level of prechallenge serum immunoglobulin G against the O127 lipopolysacchari

5 l aplasia, several vaccine/pathogen-specific serum immunoglobulin G and A (IgG and IgA) titers remain

6 Neutralizing antibody responses, serum immunoglobulin G and A, and nasal wash specimen im

7 Antral gastritis, anti-H. pylori serum immunoglobulin G, and atrophy all increased, but w

8 or, CVD 915(pTETlpp) elicited high titers of serum immunoglobulin G anti-fragment C.

9 Only conjugates with O acetyls elicited serum immunoglobulin G anti-LPS with bactericidal activi

10 ith the level of protection correlating with serum immunoglobulin G anti-protective antigen titers.

11 l immunoglobulin A antiamebic antibodies and serum immunoglobulin G antiamebic antibodies.

12 VRP resulted in high levels of DENV-specific serum immunoglobulin G antibodies and significant titers

13 Although serum immunoglobulin G antibodies are significantly high

14 ll-length block 2 antigens showed that human serum immunoglobulin G antibodies induced by infection c

15 orbent assays (ELISAs) for quantification of serum immunoglobulin G antibodies specific for N. mening

16 uced specific secretory immunoglobulin A and serum immunoglobulin G antibodies that persisted at subs

17 concentrations and neutralizing activity of serum immunoglobulin G antibodies to the RSV prefusion (

18 tion, as well as the specificity, of anti-P1 serum immunoglobulin G antibodies were demonstrated in g

19 It was shown that serum immunoglobulin G antibodies were produced against

20 d formation, an impaired ability to generate serum immunoglobulin G antibodies, and significant inhib

21 treated patients with LA have high levels of serum immunoglobulin G antibodies, and sometimes low lev

22 cator of inflammation), or edentulism and 2) serum immunoglobulin G antibody response to Aggregatibac

23 e also developed sustained anti-H. hepaticus serum immunoglobulin G antibody responses and elevated a

24 Less marked, but significant, anti-SREHP serum immunoglobulin G antibody responses were also indu

25 d animalls developed sustained anti-H. felis serum immunoglobulin G antibody responses.

26 PI) owing to the presence of highly elevated serum immunoglobulin G antibody titers with a high avidi

27 cant levels of salivary immunoglobulin A and serum immunoglobulin G antibody to the respective inject

28 A serum immunoglobulin G autoantibody (NMO-IgG) serves as

29 All conjugates elicited high levels of serum immunoglobulin G both to the polysaccharides and t

30 Serum immunoglobulin G demonstrated a strong discriminat

31 There was a slight increase in serum immunoglobulin G (IgG) against the MS11 strain and

32 Serologic markers such as serum immunoglobulin G (IgG) and antinuclear antibody le

33 although FspA1 induced the highest levels of serum immunoglobulin G (IgG) and fecal IgA.

34 elivery of VXA-G1.1-NN elicited VP1-specific serum immunoglobulin G (IgG) and IgA and functional anti

35 ity to S. typhimurium severely depressed the serum immunoglobulin G (IgG) and IgA anti-FrgC response

36 -CAT construct induced significant levels of serum immunoglobulin G (IgG) and IgA antibody to both pa

37 Recall responses were seen in serum immunoglobulin G (IgG) and IgA following boosting

38 with Invaplex was found to enhance anti-OVA serum immunoglobulin G (IgG) and IgA responses and induc

39 oximately 2-week intervals and evaluated for serum immunoglobulin G (IgG) and IgG subclass and for sa

40 Despite production of serum immunoglobulin G (IgG) and IgM (median titers of 1

41 throughout the experiment and evaluated for serum immunoglobulin G (IgG) and IgM and salivary IgA an

42 In mice i.n. challenged with H10407, serum immunoglobulin G (IgG) and IgM antibodies were mea

43 or no bacteria in the liver and lungs, high serum immunoglobulin G (IgG) and IgM antibody titers, an

44 lpha stimulated strong antigen (Ag)-specific serum immunoglobulin G (IgG) and IgM responses, while MI

45 ion of mice with CVLPs induced gp41-specific serum immunoglobulin G (IgG) and intestinal secretory Ig

46 lones were found to stimulate high levels of serum immunoglobulin G (IgG) and mucosal IgA antibodies

47 luenza virus showed significant increases in serum immunoglobulin G (IgG) and mucosal IgA antibodies

48 oxin (CT) A2 and B subunits (CTA2/B) develop serum immunoglobulin G (IgG) and mucosal IgA antibody re

49 hesizing either PspA fusion protein elicited serum immunoglobulin G (IgG) and mucosal IgA responses a

50 The levels of antigen-specific serum immunoglobulin G (IgG) and mucosal IgA were higher

51 cific gamma interferon-producing T cells and serum immunoglobulin G (IgG) and mucosal IgA.

52 hK63 or LThR72 exhibited high titers of both serum immunoglobulin G (IgG) and mucosal secretory IgA a

53 between the concentration of vaccine-induced serum immunoglobulin G (IgG) and protection against colo

54 ed animals demonstrated significantly higher serum immunoglobulin G (IgG) and salivary IgA antibody l

55 Both peptides readily induced serum immunoglobulin G (IgG) and salivary IgA antipeptid

56 astric tissue, histology, and measurement of serum immunoglobulin G (IgG) and salivary IgA.

57 The specificity of anti-P1 serum immunoglobulin G (IgG) and secretory IgA antibodie

58 enuation elicited higher Salmonella-specific serum immunoglobulin G (IgG) and/or mucosal secretory-Ig

59 later, significant reductions were seen for serum immunoglobulin G (IgG) antibodies at week 14 and f

60 Serum immunoglobulin G (IgG) antibodies have been implic

61 recombinant proteins were reacted with human serum immunoglobulin G (IgG) antibodies in Western immun

62 We investigated the ability of serum immunoglobulin G (IgG) antibodies to periodontal b

63 Serum immunoglobulin G (IgG) antibodies to spike subunit

64 Low maternally derived serum immunoglobulin G (IgG) antibodies to Streptococcus

65 ta provide evidence that a critical level of serum immunoglobulin G (IgG) antibodies to the surface p

66 were found to be immunogenic since elevated serum immunoglobulin G (IgG) antibodies without a specif

67 Oral and i.p. vaccines elicited O11-specific serum immunoglobulin G (IgG) antibodies, but IgA was obs

68 isms are found and the induction of specific serum immunoglobulin G (IgG) antibodies, we examined the

69 ay was used to measure the seroprevalence of serum immunoglobulin G (IgG) antibody among NHANES parti

70 We determined pneumococcal serum immunoglobulin G (IgG) antibody concentrations aga

71 ria during the study interval, and increased serum immunoglobulin G (IgG) antibody levels substantiat

72 nce of P. gingivalis in dental plaque and of serum immunoglobulin G (IgG) antibody levels to P. gingi

73 GFPuv-specific serum immunoglobulin G (IgG) antibody responses were ana

74 oPn produced greater titers of MoPn-specific serum immunoglobulin G (IgG) antibody than mice that rec

75 zed by enzyme-linked immunosorbent assay for serum immunoglobulin G (IgG) antibody to Aggregatibacter

76 Levels of serum immunoglobulin G (IgG) antibody to GTF or CAT in t

77 Serum immunoglobulin G (IgG) antibody, induced by subcut

78 rticular) demonstrated significantly reduced serum immunoglobulin G (IgG) antibody, salivary IgA anti

79 train RB51 (SRB51) produced small amounts of serum immunoglobulin G (IgG) but no IgM antibody to smoo

80 Ribi had the highest levels of PorB-specific serum immunoglobulin G (IgG) by enzyme-linked immunosorb

81 New serum immunoglobulin G (IgG) detected by whole-cell enzy

82 We studied the prognostic relevance of serum immunoglobulin G (IgG) elevated above the upper li

83 mean titer (GMTs) and 4-fold rise of anti-Vi serum immunoglobulin G (IgG) enzyme-linked immunosorbent

84 ntigenic MDI-albumin products, as defined by serum immunoglobulin G (IgG) from MDI-exposed workers, w

85 ale C57BL/6 mice treated daily with purified serum immunoglobulin G (IgG) from patients with longstan

86 Aberrant serum immunoglobulin G (IgG) glycosylation and its immun

87 immunosorbent assay to measure beta-specific serum immunoglobulin G (IgG) levels and used it to compa

88 To investigate this, we measured serum immunoglobulin G (IgG) levels to 55 pneumococcal p

89 Significant anti-GLU serum immunoglobulin G (IgG) levels were seen in groups

90 Smoking is also known to reduce serum immunoglobulin G (IgG) levels.

91 haride (PS) conjugate vaccines may prime for serum immunoglobulin G (IgG) memory responses to meningo

92 transplantations indicate that low levels of serum immunoglobulin G (IgG) negatively impact outcomes.

93 Overall, 23% of patients developed either a serum immunoglobulin G (IgG) response (9%) or sputum IgA

94 . denticola induced a significant (400-fold) serum immunoglobulin G (IgG) response compared to that i

95 Serum immunoglobulin G (IgG) responses were analyzed lon

96 Anamnestic anti-SEB serum immunoglobulin G (IgG) responses were elicited in

97 ized with replication-defective HSV, durable serum immunoglobulin G (IgG) responses were elicited.

98 e the long-term course of H. pylori-specific serum immunoglobulin G (IgG) responses with respect to s

99 were effective in eliciting antigen-specific serum immunoglobulin G (IgG) responses, and these respon

100 s evokes large increases in antigen-specific serum immunoglobulin G (IgG) responses.

101 fold increase over the prechallenge anti-SMV serum immunoglobulin G (IgG) titer, mostly subclass IgG1

102 were consistent with significantly declined serum immunoglobulin G (IgG) titers for HHV-6 of MS pati

103 ckerboard analyses of eight plaque bacteria, serum immunoglobulin G (IgG) titers to 17 bacteria, and

104 Serum immunoglobulin G (IgG) titers to 28 pneumococcal p

105 B) toxoid in saline elicited higher anti-SEB serum immunoglobulin G (IgG) titers when the toxoid was

106 Binding activity of patient serum immunoglobulin G (IgG) to HupB did not correlate w

107 colonization, 9 of 40 patients developed new serum immunoglobulin G (IgG) to OMP CD, as measured by e

108 ollowing infection and who had developed new serum immunoglobulin G (IgG) to their infecting strain w

109 Thirty-four glycopeptides from human serum immunoglobulin G (IgG) tryptic digests were obviou

110 eleased from bovine fetuin, polyclonal human serum immunoglobulin G (IgG), and human alpha1-acid glyc

111 three types of blood isolates: plasma, total serum immunoglobulin G (IgG), and total plasma extracell

112 he most effective means of immunization: the serum immunoglobulin G (IgG), IgA, and IgM anti-fragment

113 We measured serum immunoglobulin G (IgG), IgM, and IgA antibodies to

114 increased class switched memory B cells and serum immunoglobulin G (IgG).

115 s resulted in the induction of FimA-specific serum (immunoglobulin G [IgG] and IgA) and salivary (IgA

116 adermal comparative tuberculin skin test and serum immunoglobulin G [IgG] responses) against a range

117 vated during primary infections (acute-phase serum immunoglobulin G [IgG] titers, <25), compared with

118 nses (HI, antibody-secreting cell [ASC], and serum immunoglobulin G [IgG]) in 15 LRs and 25 control H

119 minent specific anti-CtxB responses in vivo (serum immunoglobulin G [IgG], P </= 0.05; serum IgA, P <

120 Deletion carriers had a higher serum immunoglobulin G level (1370 mg/dL vs 1140 mg/dL [

121 ortal vein diameter, splenomegaly, increased serum immunoglobulin G level, and increasing number of a

122 tly improved liver histology (P = 0.005) and serum immunoglobulin G levels (P = 0.0002).

123 Serum immunoglobulin G levels and other hematological pa

124 We compared serum immunoglobulin G levels and toxin-neutralizing ant

125 ecific NCSTN variant and support the role of serum immunoglobulin G levels as a potential predictive

126 The serum immunoglobulin G levels correlated with protection

127 P. gingivalis-specific serum immunoglobulin G levels were significantly elevate

128 , with a 44% reduction in intracardiomyocyte serum immunoglobulin G localization in het-treated-8 mic

129 cination geometric mean titre of LT-specific serum immunoglobulin G of 3400.29, compared with 315.41

130 asma could not be duplicated by pooled human serum, immunoglobulin G, or fibrinogen, whether used sep

131 Serum immunoglobulin G profiling by proteome microarray

132 Serum immunoglobulin G reactivity to Hsp10 and Hsp60 ant

133 the naturally infected SCID/NCr mice had no serum immunoglobulin G response against H. hepaticus.

134 vaccine doses elicited a strong PA-specific serum immunoglobulin G response with a geometric mean ti

135 Only LAM-reactive serum immunoglobulin G responses were significantly incr

136 ufficient to decrease P. gingivalis-specific serum immunoglobulin G responses, but lower antibody tit

137 osted 4 weeks later induced higher levels of serum immunoglobulin G specific for PspA and for outer m

138 Serum immunoglobulin G subclass levels and antibody tite

139 The serum immunoglobulin G subclass profiles were indicative

140 ked immunosorbent assay (ELISA) to determine serum immunoglobulin G titers against Shigella LPS.

141 he vhs(-)/ICP8(-) mutant showed prechallenge serum immunoglobulin G titers comparable to those immuni

142 a clinical oral-health examination, and had serum immunoglobulin G titers measured against 19 period

143 of variants with ChoP correlates with higher serum immunoglobulin G titers to LPS containing this str

144 Antimeasles serum immunoglobulin G titers were quantified using enzy

145 Vi stimulates serum immunoglobulin G Vi antibodies, whereas Ty21a, whi

146 A low serum immunoglobulin G was associated with number of inf

147 Subgingival P. endodontalis levels and serum immunoglobulin G were associated with a higher EL

148 ut adjuvant stimulated induction of specific serum immunoglobulin G, whereas antigen alone or admixed