ライフサイエンスコーパス: inducer cell

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1 eptor gammat is expressed on lymphoid tissue inducer cells.

2 3 subset, which contains the lymphoid tissue inducer cells.

3 nal natural killer cells and lymphoid tissue inducer cells.

4 ound that the development of lymphoid tissue-inducer cells, a rare subset of specialized cells that h

5 atural killer (NK) cells and lymphoid tissue inducer cells after IL-23 stimulation.

6 ORgamma(t)(+)CCR6(+)NKp46(-) lymphoid tissue inducer cells after thymic injury in an IL-23-dependent

7 ntage of cells thought to be lymphoid tissue inducer cells among donor ILCs was far higher than that

8 jointly directed by Rankl(+) lymphoid tissue inducer cells and invariant Vgamma5(+) dendritic epiderm

9 ession of the CD30 ligand by lymphoid tissue inducer cells and podoplanin by T zone stroma are tempor

10 s between lymphotoxin (LT)alpha(1)beta(2) on inducer cells and the lymphotoxin beta receptor (LTbetaR

11 of these cells suggests that lymphoid tissue inducer cells are capable of providing the CD30 signals.

12 Lymphoid tissue inducer cells are members of an emerging family of innat

13 developed in the absence of lymphoid tissue-inducer cells, but required the chemokine CXCL13.

14 Lymphoid tissue inducer cells express a diverse array of tumor necrosis

15 e trafficking: CD45+CD4+CD3- lymphoid tissue inducer cells express CXCR5 and CCR7 and migrate toward

16 We found that adult but not neonatal inducer cells expressed high levels of OX40L and CD30L,

17 on CD4(+)CD3(-)CD11c(-)B220(-)IL-7Ralpha(+) inducer cells from birth to adulthood in mice.

18 organizer and hematopoietic lymphoid tissue inducer cells has been regarded as critical for these pr

19 sly unrecognized role for CD4(+)3(-)RANKL(+) inducer cells in intrathymic self-tolerance.

20 fetal liver progenitors and lymphoid tissue inducer cells in the neonatal intestine, resulting in im

21 The expression of OX40L and CD30L on inducer cells increased gradually in the first few weeks

22 During this process, haematopoietic 'inducer' cells interact with stromal 'organizer' cells,

23 Lymphoid tissue-inducer cells (LTi cells) are indispensable for the deve

24 though we found CD4(+)CD3(-) lymphoid tissue-inducer cells (LTi cells) in neonatal lungs, particularl

25 Published work links adult lymphoid tissue-inducer cells (LTi) with T cell-dependent antibody respo

26 upport the notion that human lymphoid tissue inducer cells may form in the fetus and persist througho

27 The dependence of lymphoid tissue inducer cells on vitamin A was furthermore illustrated b

28 (ILCs) type 3, also known as lymphoid tissue inducer cells, plays a major role in both the developmen

29 we demonstrate a novel role for a CD4(+)3(-) inducer cell population, previously linked to developmen

30 group 3 ILCs (ILC3s) include lymphoid tissue inducer cells, produce IL-17 and/or IL-22, and are depen

31 4beta7(-) and alpha4beta7(+) lymphoid tissue inducer cell progenitors in the fetal liver and common l

32 2% inhibition of the autologous T suppressor-inducer cell proliferation induced by UV-EC (vehicle: 21

33 ls, natural killer cells and lymphoid tissue inducer cells, the latter responsible for the generation

34 The failure of neonatal inducer cells to express the ligands that rescue T cells

35 In the absence of inducer, cell-to-cell spread of virus did not occur, des

36 ggest that CD30 signals from lymphoid tissue inducer cells were a primitive mechanism to recruit and

37 However, lymphoid tissue inducer cells were not affected in these mice nor was th

38 t avian precardiac endoderm acting as feeder/inducer cells would induce high percentage conversion of

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