ライフサイエンスコーパス: virus antigen

1 specificity for the detection of Hepatitis B virus antigen.

2 method for real-time detection of the Ebola virus antigen.

3 with the memory response stimulated by pH1N1 virus antigen.

4 r cutaneous vaccine delivery using influenza virus antigen.

5 to their content of hemagglutinin, the major virus antigen.

6 sorbent assay for antibodies to a shared MCF virus antigen.

7 d delayed-type hypersensitivity responses to virus antigen.

8 ter in vitro stimulation with purified whole virus antigens.

9 as well as durable human immune responses to virus antigens.

10 etric mean antibody titer to human influenza virus antigens.

11 phocytic choriomeningitis virus and vaccinia virus antigens.

12 cy virus type 1 (HIV-1) and type A influenza virus antigens.

13 en the vaccine immunogen and the encountered virus antigens.

14 o cytomegalovirus and human immunodeficiency virus antigens.

15 c disease without the introduction of animal virus antigens.

16 risons of similar doses of a novel influenza virus antigen administered by the intradermal route and

17 Taken together, Lassa virus antigen and IgM ELISAs were 88% (95% confidence in

18 nked immunosorbent assays (ELISAs) for Lassa virus antigen and immunoglobulin M (IgM) and G (IgG) ant

19 on; cases were confirmed by the detection of virus antigen and nucleic acid in blood, cell culture, a

20 in situ hybridization, intense Cache Valley virus antigen and RNA staining was detected in the brain

21 confirmed the colocalization of internalized virus antigen and the endosomal marker dynamin.

22 Antibody isotype responses to virus antigens and cytokine production were monitored by

23 Virus antigens and RNA were localized to the brains (cor

24 y responses, and levels of infectious virus, virus antigen, and virus RNA were similar in both groups

25 lve attempts to suppress immune responses to virus antigens, and re-targeting of viruses to favor tum

26 or the presence of antibodies to hepatitis C virus antigen (anti-HCV), hepatitis B surface antigen (H

27 Paradoxically, virus antigens are largely focused in the epithelial lay

28 sally with rM51R vectors expressing vaccinia virus antigens B5R and L1R were protected against lethal

29 se all known regulatory B subunits, or tumor virus antigens, bind stably only to the AC dimer of PP2A

30 rus infectivity was assessed by detection of virus antigen by flow cytometry together with various he

31 ected American crows was also examined by WN virus antigen capture immunoassay and TaqMan for the pre

32 The recommended WN virus antigen capture protocol, which includes a capture

33 rsensitivity (DTH) response upon intradermal virus antigen challenge.

34 ntibodies or lymphocyte proliferation to the virus antigen (class II MHC immune functions).

35 rated by continued tdTomato expression after virus antigen could no longer be detected.

36 e Directigen and VIDAS respiratory syncytial virus antigen detection assays with viral culture, the s

37 Histopathologic changes corresponded with virus antigen distribution, being largely limited to nas

38 h levels of immune cells harboring influenza virus antigen during viral infection and cell-type-speci

39 pH1N1 virus antigen elicited stronger cross-reactive memory B

40 iated immunity to two human immunodeficiency virus antigens, Env and Nef, have been examined in mice.

41 haracterized by a combination of the Grimsby virus antigen enzyme-linked immunosorbent assay, reverse

42 yelination correlated with the appearance of virus antigen expression.

43 adherence provided an important trigger for virus antigen expression.

44 method for the detection of bovine leukemia virus antigen gp51.

45 was applied to the detection of Hepatitis B virus antigen (HBsAg) in human blood plasma.

46 no acid substitutions in the major influenza virus antigen hemagglutinin (HA).

47 uito pools (n = 100), this assay detected WN virus antigen in 12 of 18 (66.7%) TaqMan-positive pools,

48 The presence of West Nile virus antigen in fixed cells or cell lysates was reveale

49 ith T3 reovirus strains and colocalizes with virus antigen in individual neurons.

50 capture immunoassay to detect West Nile (WN) virus antigen in infected mosquitoes and avian tissues h

51 re associated with the presence of influenza virus antigen in parenchymal, not endothelial cells.

52 respiratory syncytial virus and influenza A virus antigens in clinical specimens.

53 infection on the presentation of hepatitis C virus antigens in cultured chimpanzee cells were examine

54 Immunohistochemistry identified West Nile virus antigens in the brainstem and spinal cord.

55 ally due to lack of data on the detection of virus antigens in tissues.

56 Titers to avian influenza virus antigens increased with age and with geometric mea

57 a cells induced to express late Epstein-Barr virus antigens indicated that expression of BZLF2 did no

58 While the majority of virus antigen is detected in central nervous system macr

59 response during the peak of infection, when virus antigen is maximal.

60 Virus antigen levels within the kidney were highest in d

61 Evolution of influenza virus antigens means that vaccines must be updated to ma

62 with a DNA vaccine encoding immunodeficiency virus antigens mixed with ligands for TLR9 or TLR7/8.

63 ession studies in virus antigen-positive and virus antigen-negative live cells in the lungs of Color-

64 Clearance of virus antigen occurred preferentially from the gray matt

65 Detection of Ebola virus antigens or virus isolation appears to be the most

66 for differential gene expression studies in virus antigen-positive and virus antigen-negative live c

67 re paralyzed and had increased inflammation, virus antigen-positive cells, and TMEV-specific lymphopr

68 Furthermore, our data suggest that influenza virus antigens prepared via systems not reliant on egg a

69 tant, containing high-titered recombinant WN virus antigen, proved to be an excellent alternative to

70 of a monoclonal antibody, recombinant Mexico virus antigen (rMXV)-based IgM capture enzyme-linked imm

71 Based on lack of virus antigen shedding and disease induction, the murine

72 The duration of virus antigen shedding following infection was considera

73 was evaluated by (i) clinical findings, (ii) virus antigen shedding or infectious virus titers in the

74 ocytes into Ccr2(-/-)Ccl2(-/-) mice impaired virus antigen-specific clearance.

75 Virus antigen-specific lymphoproliferation was vigorous

76 of CD8(+) T cells specific for two different virus antigens stimulated ex vivo using either autologou

77 (HA)-specific memory B cell responses after virus antigen stimulation in nose-associated lymphoid ti

78 TL lines are used against genetically stable virus antigens, suggests that escape mutants may be a se

79 ccuracy of positive QuickVue rapid influenza virus antigen test results.

80 cted cells revealed a filamentous pattern of virus antigen, the appearance of which was sensitive to

81 imulation by overlapping peptide pools of BK virus antigen to determine frequency of CD8+ and CD4+ T

82 lan et al. conclude that transport of herpes-virus antigens to lymph nodes by dendritic cells is cruc

83 the more traditional suckling-mouse brain WN virus antigen used in the immunoglobulin M (IgM) antibod

84 e tested for antibodies to 5 avian influenza virus antigens, using a protein microarray.

85 A multivalent Dengue virus antigen was designed and shown to bind antibodies

86 Rabies virus antigen was detected in archived autopsy brain tis

87 The low detection limit for Hepatitis B virus antigen was estimated to be 0.01IU/mL.

88 Varicella-zoster virus antigen was found in 45 of 70 GCA-negative TAs (64

89 In contrast, by immunohistochemistry virus antigen was found in liver, intestine, kidney, spl

90 Varicella-zoster virus antigen was frequently found in perineurial cells

91 Virus antigen was localized predominantly to anterior ho

92 Virus antigen was localized predominantly to anterior ho

93 Virus antigen was more abundant and infectious virus inc

94 Virus antigen was observed in airway epithelia, pneumocy

95 Virus antigen was partially controlled during the early

96 The virus antigen was prepared from the KS-1 cell line, whic

97 mbinant human monoclonal antibodies to Ebola virus antigens was isolated from phage display libraries

98 zoster antigen (also called varicella-zoster virus antigen) was detectable in temporal artery biopsie

99 ys using a new ELISA for EBO (subtype Zaire) virus antigen were conducted to assess the prevalence of

100 es virus neutralizing antibodies, and rabies virus antigens were conducted on available specimens, in

101 Respiratory syncytial virus antigens were detected in circulating CD4+ and CD8

102 ls directed against both cell- and egg-grown virus antigens, whereas egg-grown virus vaccine induced

103 r epithelium, with extensive distribution of virus antigen within tracheal, bronchial, bronchiolar, a

104 lded influenza H1N1 or respiratory syncitial virus antigens yielded reduced or unchanged reactivity i