ライフサイエンスコーパス: hematopoietic organ

1 l adhesion even as the fetal liver becomes a hematopoietic organ.

2 died locally, whereas some also migrated to hematopoietic organs.

3 1P receptor modulation restricts egress from hematopoietic organs.

4 ntly than BM cells, but did not reconstitute hematopoietic organs.

5 t by increased lymphoid and myeloid cells in hematopoietic organs.

6 ng the developing central nervous system and hematopoietic organs.

7 umulation of monoclonal B lymphocytes in the hematopoietic organs.

8 tion, neonatal animals die due to failure of hematopoietic organs.

9 ase, and are rapidly recruited to particular hematopoietic organs.

10 ith the timing of erythropoietic activity in hematopoietic organs.

11 d differentiation mostly accomplished in the hematopoietic organs.

12 sively visualize the proliferative status of hematopoietic organs after myelosuppressive therapy.

13 is the persistence of cancer "stem" cells in hematopoietic organs after treatment.

14 mediated by adenosine signaling between the hematopoietic organ and the central metabolic control or

15 The Drosophila melanogaster lymph gland is a hematopoietic organ and, together with prospective vascu

16 rt tube as well as in associated lymph gland hematopoietic organs and alary muscles that attach the d

17 al hierarchy of the stem cell compartment in hematopoietic organs and discusses assays and phenotypic

18 tiple lineages of peripheral blood cells and hematopoietic organs and in hematopoietic stem cell (HSC

19 tremely low number of these cells in primary hematopoietic organs and the lack of culture systems tha

20 PHEMX ortholog is specifically expressed in hematopoietic organs and tissues and, in contrast to mur

21 ure blood cells, lineage distribution within hematopoietic organs, and frequencies of the most primit

22 until the liver begins to serve as the major hematopoietic organ at E11.5.

23 to form the enteric nervous system (ENS) and hematopoietic organs (bone marrow, thymus) where they pa

24 for the sequential colonization of different hematopoietic organs by blood-producing cells.

25 the extracellular matrix (ECM) found in the hematopoietic organ, called the lymph gland.

26 esis, and up-regulation of genes involved in hematopoietic organ development, lymphoid development, a

27 he potential role of the human placenta as a hematopoietic organ during embryonic and fetal developme

28 impairs control of cellular proliferation in hematopoietic organs during larval development.

29 mphocytic choriomeningitis virus (LCMV) from hematopoietic organs during persistent LCMV infection.

30 global deletion of Elavl1 induced atrophy of hematopoietic organs, extensive loss of intestinal villi

31 ells found in the developmentally successive hematopoietic organs has remained elusive.

32 In the lymph gland, an hematopoietic organ in Drosophila larva, a group of cell

33 imarily in hemocytes and the lymph glands, a hematopoietic organ in Drosophila larvae.

34 Atg6 mutants have enlarged lymph glands (the hematopoietic organ in Drosophila), possess elevated blo

35 Bone marrow (BM) is the key hematopoietic organ in mammals and is involved in the ho

36 The pronephros, the major hematopoietic organ in the adult fish, begins to develop

37 In human erythroid cells and hematopoietic organs, LIN28B and its targeted let-7 micr

38 In the Drosophila hematopoietic organ, niche-derived Hedgehog signaling ma

39 transcripts were undetectable in the lympho-hematopoietic organs of both the embryonic and adult mou

40 luciferase activity were observed in the two hematopoietic organs of mice, bone marrow (1,400 relativ

41 Blood cells derived from the hematopoietic organs of ribosomal protein S6 (RpS6air8)

42 trated the bone marrow, spleen and other non-hematopoietic organs of tumor-bearing animals, leading t

43 the acute impact of anticancer therapies on hematopoietic organs on a whole-body scale.

44 hila hemocytes from the lymph glands (larval hematopoietic organ) or hemolymph (blood equivalent).

45 gest that the human placenta is an important hematopoietic organ, raising the possibility of banking

46 em cells (HSCs) for limited "space" in fetal hematopoietic organs remains a significant barrier to su

47 transplanted OS mice in peripheral blood and hematopoietic organs, such as the BM, thymus, and spleen

48 xpression of CalDAG-GEFI and CalDAG-GEFII in hematopoietic organs suggests that such control may have

49 mpared to BM, 10-fold fewer FL CFCs homed to hematopoietic organs than those from BM.

50 show that the mouse placenta functions as a hematopoietic organ that harbors a large pool of pluripo

51 The placenta is a hematopoietic organ that supports hematopoietic stem/pro

52 acenta has been recently unveiled as a major hematopoietic organ that supports HSC development, the p

53 tissues, as demonstrated here for monitoring hematopoietic organs that recover after myelosuppressive

54 d development occurs in a specialized larval hematopoietic organ, the lymph gland (LG), within which

55 The Drosophila melanogaster larval hematopoietic organ, the lymph gland, is a model to stud

56 In the Drosophila hematopoietic organ, the lymph gland, the posterior sign

57 rs expressed on blood progenitors within the hematopoietic organ, the lymph gland.

58 rval and pupal stages and hyperplasia of the hematopoietic organ, the lymph gland.

59 To investigate whether another hematopoietic organ, the spleen, also contains monoclona

60 As the critical hematopoietic organs were not corrected without full RBC

61 growth, pituitary tumors, and hyperplasia of hematopoietic organs, yet it is unknown whether all cell