ライフサイエンスコーパス: mesenchymal progenitor cell

1 context of chondrogenic differentiation of a mesenchymal progenitor cell.

2 so regulates the differentiation of resident mesenchymal progenitor cells.

3 ing in smooth muscle cell differentiation of mesenchymal progenitor cells.

4 A-184 was predominantly expressed in cardiac mesenchymal progenitor cells.

5 d/or osteoblast differentiation of endosteal mesenchymal progenitor cells.

6 ng microRNAs in human OS cells compared with mesenchymal progenitor cells.

7 skeleton by inhibiting Hedgehog signaling in mesenchymal progenitor cells.

8 ochondrocytic differentiation of multipotent mesenchymal progenitor cells.

9 dipocytes arise from resident adipose tissue mesenchymal progenitor cells.

10 ication, but with massively dying neural and mesenchymal progenitor cells.

11 al transition and recruitment of circulating mesenchymal progenitor cells.

12 om resident adipose tissue preadipocytes and mesenchymal progenitor cells.

13 BMP-9-induced osteogenic differentiation of mesenchymal progenitor cells.

14 th the outermost tunica adventitia harboring mesenchymal progenitor cells.

15 lies on proliferation and differentiation of mesenchymal progenitor cells.

16 Knockdown of Pkp2 in cardiac mesenchymal progenitor cells also reduced miR-184 levels

17 ar remodeling and trafficking of circulating mesenchymal progenitor cells (also known as fibrocytes)

18 al analysis of IPF lung tissue revealed that mesenchymal progenitor cells and cells with the characte

19 ater stages of differentiation can transform mesenchymal progenitor cells and generate tumors resembl

20 36M) mutation impairs the differentiation of mesenchymal progenitor cells and generates undifferentia

21 Functionally, H3R26C-expressing mesenchymal progenitor cells and murine embryonic stem c

22 modulation regulated the differentiation of mesenchymal progenitor cells and promoted fibrocartilage

23 Wilms' tumor-1 (Wt1) leads to a reduction in mesenchymal progenitor cells and their derivatives.

24 n potential, hFOB has been compared to human mesenchymal progenitor cells and used to investigate bon

25 MCs induced alkaline phosphatase activity in mesenchymal progenitor cells, and this was abrogated by

26 Here, we examine bone marrow-derived mesenchymal progenitor cells (BM-MPCs) that have previou

27 expression and HA production in bone marrow mesenchymal progenitor cells (bmMPCs) derived from multi

28 tated the osteogenic differentiation of bone mesenchymal progenitor cells (BMSCs).

29 ing evidence that proliferating, multipotent mesenchymal progenitor cells can be programmed to yield

30 Our findings identify a population of mesenchymal progenitor cells capable of giving rise to a

31 and direct variant to gene mapping in human mesenchymal progenitor cell-derived osteoblasts employin

32 rate a critical role for Pod1 in controlling mesenchymal progenitor cell differentiation into SM and

33 r, identifying these cells as pivotal dental mesenchymal progenitor cells driving tooth root formatio

34 ulations, regulates lineage specification of mesenchymal progenitor cells during BMP-induced differen

35 n profile of all known 27 human TRP genes in mesenchymal progenitors cells during white or brown adip

36 r developmental ancestry by Tie2-expressing (mesenchymal?) progenitor cells during development.

37 Adult mesenchymal progenitor cells expressed CHL2, and its lev

38 In murine 10T1/2 mesenchymal progenitor cells, expression of mutant IDH2

39 The perivascular environment is populated by mesenchymal progenitor cells, fibroblasts, myofibroblast

40 appears to be derived from proliferation of mesenchymal progenitor cells followed by differentiation

41 tion factors, induces the differentiation of mesenchymal progenitor cells from the bone marrow into a

42 During organogenesis, neural and mesenchymal progenitor cells give rise to many cell line

43 ogenic young, senescent, and progeroid human mesenchymal progenitor cells (hMPCs), we delineate a hie

44 of ribosome-associated genes (RAGs) in human mesenchymal progenitor cells (hMPCs).

45 ailed characterization of the most primitive mesenchymal progenitor cells in the adult murine bone ma

46 ed a significant reduction in colony-forming mesenchymal progenitor cells in the bone marrow of Apc(M

47 Dental mesenchymal progenitor cells in the dental follicle lie

48 vate scleraxis expression in a population of mesenchymal progenitor cells in the dorsal sclerotome.

49 Moreover, inactivation of beta-catenin in mesenchymal progenitor cells in vitro causes chondrocyte

50 tation can lead to engraftment of functional mesenchymal progenitor cells, indicating the feasibility

51 Knockdown of miR-184 in HL-1 cells and mesenchymal progenitor cells induced and, conversely, it

52 o promote the differentiation of multipotent mesenchymal progenitor cells into osteoblasts.

53 e by coimplantation of human endothelial and mesenchymal progenitor cells isolated from blood and bon

54 profiling mRNA expression in the bone marrow mesenchymal progenitor cell line ST2, we discover that B

55 g these cells in vivo is challenging, making mesenchymal progenitor cell lines valuable tools to stud

56 is evidence for rare populations of putative mesenchymal progenitor cells located in the perivascular

57 Hedgehog signaling, has been identified as a mesenchymal progenitor cell marker in various tissues, i

58 otch pathway has recently been implicated in mesenchymal progenitor cell (MPC) differentiation from b

59 to examine how cell-extrinsic forces impact mesenchymal progenitor cell (MPC) fate.

60 in a temporal and spatial fashion to control mesenchymal progenitor cell (MPC) fate.

61 As such, we developed two mesenchymal progenitor cell (MPC) lines, MPC1 and MPC2,

62 human endothelial colony forming cell (ECFC)/mesenchymal progenitor cell (MPC)-derived bioengineered

63 endothelial colony forming cells (ECFC) and mesenchymal progenitor cells (MPC) form vascular network

64 exhibits accessible chromatin exclusively in mesenchymal progenitor cells (MPCs) and Ewing sarcoma ce

65 gineering platform for the delivery of human mesenchymal progenitor cells (MPCs) by a fully biologica

66 Primary mesenchymal progenitor cells (MPCs) harvested from debri

67 However, the role of TRAF3 in mesenchymal progenitor cells (MPCs) is unknown.

68 Specific knockout of miR-204/-211 in mesenchymal progenitor cells (MPCs) results in Runx2 acc

69 ifferent developmental stages and in primary mesenchymal progenitor cells (MPCs) reveals that bone ma

70 Here, we show in murine mesenchymal progenitor cells (MPCs) that Atrx deficiency

71 carring of the lung mediated by pathological mesenchymal progenitor cells (MPCs) that manifest autono

72 covered that the IPF lung harbors fibrogenic mesenchymal progenitor cells (MPCs) that serve as a cell

73 Mesenchymal progenitor cells (MPCs) transformed with the

74 characterization revealed that skin harbored mesenchymal progenitor cells (MPCs) with a similar pheno

75 ry and in peripheral neurons, we transfected mesenchymal progenitor cells (MPCs), a type of support c

76 ult mice with TRAF3 conditionally deleted in mesenchymal progenitor cells (MPCs), associated with inc

77 rentiation potential of adult tissue-derived mesenchymal progenitor cells (MPCs), such as those from

78 henotype in both human and cynomolgus monkey mesenchymal progenitor cells (MPCs).

79 (RNAseq) analysis on primary pediatric human mesenchymal progenitor cells (pMPCs) expressing EWS-FLI1

80 between differentiation and maintenance of a mesenchymal progenitor cell population determines the fi

81 iversity and distinct functionality of these mesenchymal progenitor cell populations that regulate to

82 pathways and regulates proper cell fates of mesenchymal progenitor cell populations.

83 three different cell types (C3H10T1/2 murine mesenchymal progenitor cells, primary human adipose tiss

84 enitors isolated from nonfibrotic lungs, IPF mesenchymal progenitor cells produce daughter cells mani

85 Removal of beta-catenin early in mesenchymal progenitor cells promoted chondrocyte differ

86 developing senescence (seno)-resistant human mesenchymal progenitor cells (SRCs), genetically fortifi

87 romoting the mobilization and trafficking of mesenchymal progenitor cells such as fibrocytes.

88 SoxC genes therefore ensure neural and mesenchymal progenitor cell survival, and function in pa

89 gs of patients with IPF contain pathological mesenchymal progenitor cells that are cells of origin fo

90 Postnatal bone marrow houses mesenchymal progenitor cells that are osteoblast precurs

91 ese amphibians form a "blastema", a group of mesenchymal progenitor cells that specifically directs t

92 Moreover, BMP7 triggers commitment of mesenchymal progenitor cells to a brown adipocyte lineag

93 d collaborators engineered human ESC-derived mesenchymal progenitor cells to give the ability to resi

94 formation, from their initial induction from mesenchymal progenitor cells to their terminal maturatio

95 rrow-derived MSCs (BM-MSCs) and iPSC-derived mesenchymal progenitor cells via the neural crest (NCC-M

96 ricted to the luminal aspect of the vessels; mesenchymal progenitor cells were adjacent to lumens, co

97 communicating senescent-like neutrophils and mesenchymal progenitor cells were key regulators of tiss

98 eloped a species-hybrid model in which human mesenchymal progenitor cells were used to develop white

99 Fibrocytes, which are bone marrow-derived mesenchymal progenitor cells, were increased to a greate

100 In principle, transplantation of mesenchymal progenitor cells would attenuate or possibly