ライフサイエンスコーパス: lymphocyte subpopulation

1 considered to be the prototypical cytotoxic lymphocyte subpopulation.

2 lymph node structures and therefore specific lymphocyte subpopulations.

3 hocyte compartment and influences recovering lymphocyte subpopulations.

4 pha and PPARgamma are expressed in different lymphocyte subpopulations.

5 Safety assessments included analysis of lymphocyte subpopulations.

6 animals, causing marked alteration in thymic lymphocyte subpopulations.

7 and nelfinavir, plasma HIV-1 RNA levels, and lymphocyte subpopulations.

8 is widely expressed on all freshly isolated lymphocyte subpopulations.

9 se in the number of the reactive Vbeta+ CD4+ lymphocyte subpopulations.

10 e liver, on the cytotoxicity of intrahepatic lymphocyte subpopulations.

11 rect chromosomal context, in resting human T lymphocyte subpopulations.

12 g genetically modified mice and depletion of lymphocyte subpopulations.

13 nt subsets have also been described in other lymphocyte subpopulations.

14 ed the levels of differential leukocytes and lymphocyte subpopulations.

15 Analysis of lymphocyte subpopulations after exposure to IAV showed t

16 However, CD16 was detected only on a lymphocyte subpopulation and on monocytes in macaques an

17 -presenting cells and depletion of important lymphocyte subpopulations and also suggests a role for N

18 (I/R) injury, the contributions of specific lymphocyte subpopulations and lymphocyte-derived interfe

19 randomization of immune cell traits suggests lymphocyte subpopulations and lymphocytic surface molecu

20 virus infection of proximal hepatocytes and lymphocyte subpopulations and may be essential for the e

21 We compared pre-PP and post-PP lymphocyte subpopulations and plasma neopterin in 37, an

22 er elucidate the effects of ECP on activated lymphocyte subpopulations and the interaction between ef

23 ins and complement factors, peripheral blood lymphocyte subpopulations, and whole blood EBVd were det

24 altered proportions and absolute numbers of lymphocyte subpopulations as well as changes in the repe

25 abeling and delabeling in memory and naive T lymphocyte subpopulations as well as in NK (natural kill

26 ns of cytokine expression, redistribution of lymphocyte subpopulations, cell dysfunction, and cell de

27 reductions in LPS-induced lung neutrophils, lymphocyte subpopulations, collagen content, and vimenti

28 These results suggested that both lymphocyte subpopulations contribute to viral clearance,

29 certed and nonredundant action of two innate lymphocyte subpopulations, conventional natural killer c

30 Lymphocyte subpopulation counts and ratios including CD4

31 cyte repopulation was fast and pretransplant lymphocyte subpopulation counts recovered within 2-4 wk.

32 The CD4 and CD8 T-lymphocyte subpopulations decreased to levels in the ran

33 In vivo lymphocyte subpopulation depletion experiments demonstra

34 In addition, significant increases in other lymphocyte subpopulations (e.g., NKT, T, and B cells) th

35 (+)FOXP3(+) Tregs constitute a heterogeneous lymphocyte subpopulation essential for curtailing effect

36 28(W135,) we observed an expansion of CD8(+)-lymphocyte subpopulations expressing reduced CD8 beta-ch

37 Lymphocyte subpopulation expression of major histocompat

38 ted by identifying and enumerating the CD4 T-lymphocyte subpopulation in human whole blood.

39 ed a specific and nonredundant role for each lymphocyte subpopulation in indirect ALI pathophysiology

40 We found that a CD4(+) T lymphocyte subpopulation in peripheral blood, phenotypic

41 report a flow cytometric investigation of B lymphocyte subpopulations in blood, lymph nodes (LNs), a

42 To define the dynamics of the CD4(+) T lymphocyte subpopulations in breast milk during acute HI

43 The altered distribution of lymphocyte subpopulations in L-selectin-deficient mice r

44 in vivo SEB superantigen-mediated effect on lymphocyte subpopulations in macaques is complex, sugges

45 n of the proliferative response of different lymphocyte subpopulations in NIDHRs.

46 ant role in establishing the distribution of lymphocyte subpopulations in primary and secondary lymph

47 We investigated the role of different lymphocyte subpopulations in the host defense reaction a

48 in certain Vbeta-expressing peripheral blood lymphocyte subpopulations in the infected monkeys.

49 The present study was designed to examine T-lymphocyte subpopulations in the vaginal mucosae of naiv

50 s is frequently used for the purification of lymphocyte subpopulations in vitro, how lymphocytes esca

51 alcium mobilization in naive and activated T lymphocyte subpopulations in vitro.

52 mbers of human subjects, analysis of defined lymphocyte subpopulations including antigen-specific pop

53 Despite alterations in lymphocyte subpopulations, individuals with Down syndrom

54 used multicolor flow cytometry to phenotype lymphocyte subpopulations infiltrating the brain, along

55 ice with genetically targeted disruptions in lymphocyte subpopulations (knockout mice), we demonstrat

56 xpansion of an aggressive and unusual CD4(+) lymphocyte subpopulation lacking the CD28 receptor.

57 Lymphocyte subpopulation levels are used for prognosis a

58 eractions conferred by gammadelta T cells on lymphocyte subpopulations may regulate the cytokine resp

59 For lymphocyte subpopulations, NK cells (HR= 0.61, 95% CI =

60 Lymphocyte subpopulations of 40 children and adolescents

61 we explored the effect of tumor-infiltrating lymphocyte subpopulations on lung cancer biology by stud

62 to humans, CD16 expression was detected on a lymphocyte subpopulation, on monocytes, and on neutrophi

63 is known about the potential impact of CM on lymphocyte subpopulations or the role of pre-existing in

64 intersubject variance of betaAR density and lymphocyte subpopulations over time in 10 normal subject

65 significant reduction in CD4+ lamina propria lymphocyte subpopulation (p < 0.01).

66 The discovery that lymphocyte subpopulations participate in distinct compon

67 The effect of PP on lymphocyte subpopulations, plasma neopterin, and cytokin

68 rvations to determine which virus-specific T-lymphocyte subpopulations play a primary role in control

69 Lymphocyte subpopulations, protein expression, regulator

70 Some lymphocyte subpopulations required stimulation subsequen

71 made in delineating lung dendritic cell and lymphocyte subpopulations, similar advances in lung macr

72 Depletion studies of individual lymphocyte subpopulations suggested that CD4+ T cells ar

73 nd induced more marked alterations in CD8(+)-lymphocyte subpopulations than did the parent F14 strain

74 (NKT) cells constitute a highly conserved T lymphocyte subpopulation that has the potential to regul

75 The predominant CD4(+) T-lymphocyte subpopulations that became infected were acti

76 of CM and past infection exposure impact on lymphocyte subpopulations to give an indication of their

77 None of the lymphocyte subpopulations was correlated with functional

78 cTFH cells and other lymphocyte subpopulations were characterized.

79 nt proportions of the phenotypic variance of lymphocyte subpopulations were detected on chromosomes 1

80 Specifically, neutrophils and CD4(+) T lymphocyte subpopulations were increased, whereas macrop

81 study of FIV infection demonstrated that all lymphocyte subpopulations were infected by 4 weeks posti

82 cific binding of [125I]-(-)iodopindolol, and lymphocyte subpopulations were measured by flow cytometr

83 s were shown to be the IkappaBzeta-producing lymphocyte subpopulation, which also released abundant I

84 nvariant T (MAIT) cells represent peculiar T-lymphocyte subpopulations with innate-like properties th

85 ytes betaARs are unequally distributed among lymphocyte subpopulations, with the highest density on C

86 in PLN, and also altered the distribution of lymphocyte subpopulations within other tissues.