ライフサイエンスコーパス: bone marrow stroma

1 a signalling-induced gene expression in aged bone marrow stroma.

2 BCR-ABL ALL cells only when co-cultured with bone marrow stroma.

3 ting interactions between leukemic cells and bone marrow stroma.

4 urvival of AML cells also in the presence of bone marrow stroma.

5 direct, stable contact with CXCL12-producing bone marrow stroma.

6 n de novo formation of cartilage or bone and bone marrow stroma.

7 er, ibrutinib inhibited AML cell adhesion to bone marrow stroma.

8 bone via a neurohormonal effect on the host bone marrow stroma.

9 d result in transcriptional variation within bone marrow stroma.

10 ant role in myeloma cell survival within the bone marrow stroma.

11 itutive expression in all tissues, including bone marrow stroma.

12 olling the growth and recovery of hMSCs from bone marrow stroma.

13 e bone marrow, and an impaired growth of the bone marrow stroma.

14 fferentiation by human adult stem cells from bone marrow stroma.

15 senchymal stem cells (MSCs) found within the bone marrow stroma.

16 sis by infecting human CD34+ cells and human bone marrow stroma.

17 hrough the interaction of trauma plasma with bone marrow stroma.

18 U-E and CFU-GM colony growth was mediated by bone marrow stroma.

19 not normal plasma induced TGF-beta1 mRNA in bone marrow stroma.

20 ssential for the control of hematopoiesis in bone marrow stroma.

21 ractions of stem/progenitor cells with their bone marrow stroma.

22 acilitating the adhesion of CD34(+) cells to bone marrow stroma and by negatively regulating CD34(+)

23 ory factor (LIF), like SDF-1, is secreted by bone marrow stroma and directs the regeneration of skele

24 omycin phosphotransferase in the presence of bone marrow stroma and in the absence of exogenous cytok

25 ) to define a cellular taxonomy of the mouse bone marrow stroma and its perturbation by malignancy.

26 ctions that highlights the complexity of the bone marrow stroma and paves the way for future in vivo

27 Furthermore, we found that C3 is secreted by bone marrow stroma and that, although C3a does not influ

28 tients with precursor B ALL were cultured on bone marrow stroma and were treated with CCI-779, a seco

29 the major hemopoietic supporting cells, the bone marrow stroma, and addresses the consequence to hem

30 fetal liver stroma, cultured primary murine bone marrow stroma, and in stromal cell lines.

31 ues, including bone, cartilage, tendon, fat, bone marrow stroma, and muscle.

32 TGF-beta1 production by bone marrow stroma appears to plays an important role in

33 Within the bone marrow stroma are multipotential cells which are ca

34 provide a comprehensive atlas of the mouse bone marrow stroma based on single-cell RNA-sequencing d

35 . provide a comprehensive atlas of the mouse bone marrow stroma based on single-cell RNA-sequencing d

36 ha and stem cell factor (SCF) stimulation of bone marrow stroma because both cytokines induce endogen

37 en hematopoietic progenitor cells (HPCs) and bone marrow stroma (BMS).

38 en hematopoietic progenitor cells (HPCs) and bone marrow stroma (BMS).

39 ter radiation exposure, impaired adhesion to bone marrow stroma cell and decreased bone marrow stroma

40 c activity in the supernatants of the murine bone marrow stroma cell line MS-5 which attracts 10-fold

41 we found that caspase-3 is activated in L88 bone marrow stroma cell-derived exosomes and identified

42 ion to bone marrow stroma cell and decreased bone marrow stroma cell-induced proliferation.

43 rted by stromal niches, and we now find that bone marrow stroma cells (BMSCs) are severely and perman

44 nt human cell lines as well as primary human bone marrow stroma cells at frequencies of greater than

45 pression patterns after exposure of CD34 and bone marrow stroma cells derived from normal bone marrow

46 feration of MM cells even in the presence of bone marrow stroma cells, and overcomes bortezomib resis

47 Experiments with human bone marrow stroma cocultures confirm the role of fibron

48 to form colonies after long-term culture on bone marrow stroma, coincident with their conversion to

49 MAPCs are believed to be derived from the bone marrow stroma compartment as they are isolated with

50 mTOR is required for the bone marrow stroma-dependent maintenance of protein tran

51 Here, we observed that hypoxic bone marrow stroma-derived transforming growth factor-be

52 Furthermore, bone marrow stroma expresses the transcription factors r

53 Bone marrow stroma failed to grow to confluence by day 1

54 In contrast, bone marrow stroma from volunteers always reached conflu

55 Studies of the bone marrow stroma have defined individual populations i

56 Adult human mesenchymal stem cells from bone marrow stroma (hMSCs) differentiate into numerous m

57 In addition, the role of the bone marrow stroma in regulating clinical responses to D

58 F-1alpha levels above baseline production in bone marrow stroma induce the production of substance P

59 Conditioned media from bone marrow stroma induced receptor activation and chemo

60 mmary differentiation factor abundant in the bone marrow stroma, induces growth arrest of relatively

61 We demonstrate that bone marrow stroma is capable of inducing Mcl-1 dependen

62 Many studies indicate that the bone marrow stroma is damaged following bone marrow tran

63 xpression of osteopontin (OPN) in the murine bone marrow stroma is reduced.

64 died, but their ability to contribute to the bone marrow stroma is still under debate.

65 /ABL-expressing myeloid progenitor cells and bone marrow stroma may be of therapeutic value for human

66 210(BCR-ABL)-expressing progenitor cells and bone marrow stroma may provide external signals that fac

67 ween mouse and human leukemic blasts and the bone marrow stroma, mobilizing blasts to the peripheral

68 0.4% to 6% Reh cells), transduction on human bone marrow stroma monolayers (3.2% to 13.3% for Nalm-6

69 The effect of HIV infection of bone marrow stroma on support of uninfected CD34 progeni

70 unterparts, CML progenitors adhere poorly to bone marrow stroma or fibronectin (FN).

71 ng B cells but did not affect the ability of bone marrow stroma to support B lymphopoiesis.

72 nding microenvironment, rather than specific bone marrow stroma, to combat the invasion by and surviv

73 eads to a shift in the balance of endogenous bone marrow stroma, towards a composition associated wit

74 Jagged2 was also found to be upregulated in bone marrow stroma under hypoxia and promoted the growth

75 quiescent phenotype of BCCs on contact with bone marrow stroma was partly explained by decreased NF-

76 Results show that HIV-infected bone marrow stroma was unable to adequately support CD34

77 10(6) of each cell type, isolated from bone marrow stroma, was injected into the transected art

78 ft (CTA) is the vascularized bone marrow and bone marrow stroma, which when transplanted could create

79 HIV infection of bone marrow stroma, while reducing the production of non

80 ction of PBPCs was supported with autologous bone marrow stroma without additional cytokines, and a c