ライフサイエンスコーパス: gamma-globulin

1 Ag (4-hydroxy-3-nitrophenyl) acetyl-chicken gamma globulin.

2 h 4-hydroxy-3-nitrophenylacetyl (NP) chicken gamma globulin.

3 body was affinity-purified from pooled serum gamma globulin.

4 o corticosteroids, cromolyn, and intravenous gamma globulin.

5 tonomic neuropathy responding to intravenous gamma globulin.

6 including streptavidin, IgG, fibrinogen, and gamma-globulin.

7 ophenylacetyl hapten conjugated with chicken gamma-globulin.

8 ic anhydrase, human serum albumin (HSA), and gamma-globulin.

9 with a hapten nitrophenyl coupled to chicken gamma-globulin.

10 y-3-nitrophenyl)acetyl conjugated to chicken gamma-globulin.

11 trep TSS include clindamycin and intravenous gamma-globulin.

12 roxy-3-nitrophenyl)acetyl coupled to chicken gamma-globulin.

13 erns, except for a lower mean serum level of gamma-globulin.

14 sent in human hemoglobin, serum albumin, and gamma-globulins.

15 rs (hazard rate ratio for 1 SD difference in gamma globulin, 1.14 [1.05-1.24]; P = 0.002).

16 t was associated with higher serum levels of gamma-globulin (2.4 +/- 0.2 g/dL vs. 1.7 +/- 0.1 g/dL; P

17 We examined whether serum gamma globulin, a nonspecific measure of the humoral imm

18 the presence of different proteins (albumin, gamma globulin, alpha1-acid glycoprotein, or lysozyme) a

19 y-3-nitrophenyl)acetyl conjugated to chicken gamma globulin and found a similar effect.

20 In contrast, therapeutic intravenous gamma globulin and its Fc fragments are anti-inflammator

21 Intravenous gamma globulin and selective apheresis are niche therapi

22 In addition, analysis of pooled human gamma globulin and several normal sera revealed the pres

23 cific GCs after immunization with DNP-bovine gamma-globulin and conclude that the changes at the DNA

24 Higher level of serum gamma-globulin and higher percentages of circulating pla

25 sex, concurrent immune diseases, lower serum gamma-globulin and immunoglobulin G levels, and lower ti

26 combinations of plasmapheresis, intravenous gamma-globulin and monoclonal antibodies to CD20 on B ly

27 BSA, but not gamma-globulin and myoglobin, decreased the membrane flu

28 Anticoagulants, corticosteroids, intravenous gamma globulin, and intravenous cyclophosphamide had all

29 erum levels of aspartate transaminase (AST), gamma-globulin, and immunoglobulin G; higher serum level

30 for carbonic anhydrase, human serum albumin, gamma-globulins, and thermolysin.

31 meostasis and maternofetal transfer of serum gamma-globulins, are mediated by the MHC class I-related

32 IgE reactivity to meat extract and bovine gamma globulin (BGG) was assessed by immunoblotting and

33 coupled to exogenous proteins such as bovine gamma-globulins, BSA, and human serum albumin.

34 T-cell-dependent antigen nitrophenyl-chicken gamma globulin but not to the T-cell-independent antigen

35 nactivated ovine or bovine serum depleted of gamma globulin by protein G affinity chromatography, wer

36 roxy-3-nitrophenylacetyl hapten (NP)-chicken gamma-globulin (CGG) (NP-CGG)- or NP-Ficoll-induced anti

37 DCs, (4-hydroxy-3-nitrophenyl)acetyl-chicken gamma-globulin (CGG) + anti-CGG ICs, and CGG-primed T ce

38 rimed but unmutated lambda+ B cells, chicken gamma-globulin (CGG) memory T cells, FDCs, and ICs (anti

39 Gamma globulin concentrations were familial, being posit

40 Gamma globulin concentrations were higher with greater d

41 epleted ovine serum or 25% heat-inactivated, gamma globulin-depleted bovine serum.

42 this buffer and either 25% heat-inactivated, gamma globulin-depleted ovine serum or 25% heat-inactiva

43 with (4-hydroxy-3-nitrophenyl)acetyl-chicken gamma-globulin, expression of Igamma1 switch transcripts

44 intraperitoneal or intravenous injection of gamma globulin, followed by an injection of P4.

45 superior to that achieved with pooled immune gamma globulin from human volunteers inoculated with liv

46 inactivated ovine or bovine serum from which gamma globulin had been depleted by protein G affinity c

47 e induction of peripheral tolerance to human gamma-globulin (HGG).

48 s involved in both the transcytosis of serum gamma-globulins (IgGs) and in regulating their serum per

49 3-nitrophenyl acetyl (NP)-conjugated chicken gamma globulin in alum.

50 ent studies addressed the use of intravenous gamma globulin in JRA.

51 nization with nitrophenol-conjugated chicken gamma-globulin in alum.

52 ession analysis is used to determine HSA and gamma-globulin in binary mixtures without previous separ

53 3-nitrophenyl)acetyl (NP) coupled to chicken gamma-globulin, in a cell transfer system.

54 d of measurement, and the IgA content of the gamma globulin infusion and its route of administration.

55 otal protein concentration of up to 400 g/L. gamma-Globulin is found to have a stronger influence as

56 cardial fibroelastosis following intravenous gamma globulin (IVIG) and corticosteroid therapy.

57 Intravenous gamma globulin (IVIG) has been used to suppress alloanti

58 he anti-inflammatory property of intravenous gamma globulin (IVIG) was investigated in a murine model

59 ment or treatment with high dose intravenous gamma-globulin (IVIG) to down-regulate FcgammaRIV while

60 apy were distinguished only by a lower serum gamma-globulin level at entry.

61 Thus, gamma globulin levels predict increased risk of diabetes

62 Higher gamma globulin levels predicted risk of diabetes.

63 hepatitis is made on the basis of increased gamma-globulin levels and the presence of circulating au

64 enylacetyl hapten (NP) conjugated to chicken gamma globulin lysine (NP-CGG) or heat-killed Streptococ

65 trol), and no patients receiving intravenous gamma globulin (n = 13) or normal blood donors (n = 20).

66 oxy-3-nitrophenyl) acetyl coupled to chicken gamma globulin (NP-CGG) in alum.

67 with (4-hydroxy-3-nitrophenyl)acetyl-chicken gamma globulin (NP-CGG) or Ars-CGG mounted robust spleni

68 roxy-3-nitrophenyl-acetyl coupled to chicken gamma-globulin (NP-CGG) and the adjuvant aluminum-hydrox

69 rrier conjugate, nitrophenyl-coupled chicken gamma-globulin (NP-CGG), the mutant mice had a diminishe

70 Passive administration of human gamma globulin or mouse serum prior to WNV infection pro

71 This effect was not mimicked by gamma-globulin or myoglobin (both 1 mg . mL-1) in intact

72 In therapeutic postexposure studies, human gamma globulin partially protected against WNV-induced m

73 tic agents, intravenous heparin, intravenous gamma globulin, plasmapheresis, and/or antiproliferative

74 Intravenous gamma globulin remains the mainstay of the acute phase t

75 roxy-3-nitrophenyl)acetyl coupled to chicken gamma globulin showed that long-lived beta-gal+ B cells

76 obtained from patients receiving therapeutic gamma-globulin) showed complete saturation of monocyte F

77 roxy-3-nitrophenyl)acetyl coupled to chicken gamma-globulin than in those from neonates immunized wit

78 t in either delay or omission of intravenous gamma globulin therapy and higher incidence of coronary

79 phylaxis in IgA-deficient patients receiving gamma globulin therapy is still controversial.

80 cifically the presence of elevated levels of gamma-globulins, to be determined.

81 Gamma globulin was also associated in univariate analysi

82 In univariate analysis, a 1 SD difference in gamma globulin was associated with a 20% higher incidenc

83 Cross-sectionally, gamma globulin was positively related to age (r = 0.08,

84 enylacetyl (NP) hapten conjugated to chicken gamma globulin were delayed in IL-21R.KO mice, but reach

85 responses to NP hapten conjugated to chicken gamma globulin were significantly impaired.

86 Bovine serum albumin and gamma-Globulin were chosen as molecular crowders and as