ライフサイエンスコーパス: lymphopoietic

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1 associated with osteoblastoid identity and B-lymphopoietic activity.

2 The substantial increase in lymphopoietic and hematopoietic processes in HFD mice in

3 development and hence determine the overall lymphopoietic capacity of the thymus, it is possible tha

4 While yolk sac (YS) also contained lymphopoietic cells after E9.5, CD41+ YS cells from < or

5 Lymphopoietic cells detectable in stromal co-cultures ar

6 alters the rate of production of myeloid and lymphopoietic cells or alters the degree of apoptosis or

7 IL-7 is well known as a lymphopoietic cytokine, but recent studies have also ide

8 IL-7, a powerful lymphopoietic cytokine, is elevated in rheumatoid arthri

9 members and their ligands clearly modulate T lymphopoietic decisions, evidence for their participatio

10 Rather, the T lymphopoietic defect of NZB mice is due to an impaired a

11 tein Bcl-2 is not sufficient to overcome the lymphopoietic defects observed in the absence of E2A.

12 MYSM1-inactivating mutation display similar lymphopoietic deficiencies.

13 derived from progenitors at each stage of T lymphopoietic differentiation, and the results were vali

14 est retinoids can normally contribute to the lymphopoietic environment in bone marrow.

15 the thymic microenvironment is the source of lymphopoietic factors that include interleukin-7 (IL-7).

16 9 cells showed decreased expression of key B-lymphopoietic factors, including IL-7 and CXCL12.

17 halamic-pituitary-thyroid axis, are potent B lymphopoietic factors.

18 row, suggesting that IKKbeta may mediate its lymphopoietic function via extrinsic factors.

19 sity significantly altered hematopoietic and lymphopoietic functions in the bone marrow and thymus.

20 ells and their continual replacement by host lymphopoietic mechanisms.

21 This lymphopoietic pathway is not unique to transgenic mice b

22 , db/db mice are unable to fully recover the lymphopoietic population following irradiation insult, a

23 ystem not only facilitates analysis of the T-lymphopoietic potential of progenitor cell populations;

24 Sp cells to T lymphocytes but did not confer lymphopoietic potential on YS cells.

25 eage lymphoid cells in culture, but had no T lymphopoietic potential when transplanted.

26 the marker are high on all progenitors with lymphopoietic potential, and progressive loss helps to e

27 t least two independent sites that differ in lymphopoietic potential.

28 f CD4(-)CD8(-) cells also exhibited normal T lymphopoietic potential.

29 ymopoietic response and enhanced delivery of lymphopoietic precursors from the bone marrow play an im

30 e Notch1 is absolutely required early in the lymphopoietic process, neither receptor is essential at

31 esults document the initial wave of innate B lymphopoietic progenitor cells available for seeding the

32 indicated that db/db marrow has a deficit in lymphopoietic progenitors; furthermore, db/db mice are u

33 bservation would seem to suggest that during lymphopoietic reconstitution, missing lymphoid lineages

34 erapeutic strategy for protecting uninfected lymphopoietic stem cells from HIV-1-infected patients.

35 n of hepatocyte growth factor (HGF) that had lymphopoietic stimulatory activity in vitro.

36 espite the fact that B-cell precursors and B-lymphopoietic stimuli are present in that organ.

37 ys a fundamental role in the ontogeny of the lymphopoietic system across species.

38 opment and organization of the hematopoietic/lymphopoietic system and have now been shown to be expre

39 Ikaros isoforms is highly restricted to the lymphopoietic system and is particularly enriched in mat

40 udy the role of the Ikaros gene in the human lymphopoietic system, we cloned and characterized human

41 the development and homeostasis of the mouse lymphopoietic system.

42 d B-like cells and the presence of dedicated lymphopoietic tissues emerge as ancestral vertebrate fea

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