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1 context of chondrogenic differentiation of a mesenchymal progenitor cell.
2 d/or osteoblast differentiation of endosteal mesenchymal progenitor cells.
3 ng microRNAs in human OS cells compared with mesenchymal progenitor cells.
4 skeleton by inhibiting Hedgehog signaling in mesenchymal progenitor cells.
5 ing in smooth muscle cell differentiation of mesenchymal progenitor cells.
6 ochondrocytic differentiation of multipotent mesenchymal progenitor cells.
7 dipocytes arise from resident adipose tissue mesenchymal progenitor cells.
8 ication, but with massively dying neural and mesenchymal progenitor cells.
9 al transition and recruitment of circulating mesenchymal progenitor cells.
10 om resident adipose tissue preadipocytes and mesenchymal progenitor cells.
11  BMP-9-induced osteogenic differentiation of mesenchymal progenitor cells.
12 A-184 was predominantly expressed in cardiac mesenchymal progenitor cells.
13                 Knockdown of Pkp2 in cardiac mesenchymal progenitor cells also reduced miR-184 levels
14 ar remodeling and trafficking of circulating mesenchymal progenitor cells (also known as fibrocytes)
15 al analysis of IPF lung tissue revealed that mesenchymal progenitor cells and cells with the characte
16 ater stages of differentiation can transform mesenchymal progenitor cells and generate tumors resembl
17 36M) mutation impairs the differentiation of mesenchymal progenitor cells and generates undifferentia
18 Wilms' tumor-1 (Wt1) leads to a reduction in mesenchymal progenitor cells and their derivatives.
19 MCs induced alkaline phosphatase activity in mesenchymal progenitor cells, and this was abrogated by
20         Here, we examine bone marrow-derived mesenchymal progenitor cells (BM-MPCs) that have previou
21  expression and HA production in bone marrow mesenchymal progenitor cells (bmMPCs) derived from multi
22 ing evidence that proliferating, multipotent mesenchymal progenitor cells can be programmed to yield
23        Our findings identify a population of mesenchymal progenitor cells capable of giving rise to a
24 rate a critical role for Pod1 in controlling mesenchymal progenitor cell differentiation into SM and
25 ulations, regulates lineage specification of mesenchymal progenitor cells during BMP-induced differen
26 n profile of all known 27 human TRP genes in mesenchymal progenitors cells during white or brown adip
27 r developmental ancestry by Tie2-expressing (mesenchymal?) progenitor cells during development.
28                                        Adult mesenchymal progenitor cells expressed CHL2, and its lev
29                             In murine 10T1/2 mesenchymal progenitor cells, expression of mutant IDH2
30  appears to be derived from proliferation of mesenchymal progenitor cells followed by differentiation
31 tion factors, induces the differentiation of mesenchymal progenitor cells from the bone marrow into a
32             During organogenesis, neural and mesenchymal progenitor cells give rise to many cell line
33 ailed characterization of the most primitive mesenchymal progenitor cells in the adult murine bone ma
34 ed a significant reduction in colony-forming mesenchymal progenitor cells in the bone marrow of Apc(M
35 vate scleraxis expression in a population of mesenchymal progenitor cells in the dorsal sclerotome.
36    Moreover, inactivation of beta-catenin in mesenchymal progenitor cells in vitro causes chondrocyte
37 tation can lead to engraftment of functional mesenchymal progenitor cells, indicating the feasibility
38       Knockdown of miR-184 in HL-1 cells and mesenchymal progenitor cells induced and, conversely, it
39 o promote the differentiation of multipotent mesenchymal progenitor cells into osteoblasts.
40 e by coimplantation of human endothelial and mesenchymal progenitor cells isolated from blood and bon
41 profiling mRNA expression in the bone marrow mesenchymal progenitor cell line ST2, we discover that B
42 otch pathway has recently been implicated in mesenchymal progenitor cell (MPC) differentiation from b
43 human endothelial colony forming cell (ECFC)/mesenchymal progenitor cell (MPC)-derived bioengineered
44  endothelial colony forming cells (ECFC) and mesenchymal progenitor cells (MPC) form vascular network
45 gineering platform for the delivery of human mesenchymal progenitor cells (MPCs) by a fully biologica
46 ifferent developmental stages and in primary mesenchymal progenitor cells (MPCs) reveals that bone ma
47 covered that the IPF lung harbors fibrogenic mesenchymal progenitor cells (MPCs) that serve as a cell
48                                              Mesenchymal progenitor cells (MPCs) transformed with the
49 rentiation potential of adult tissue-derived mesenchymal progenitor cells (MPCs), such as those from
50 (RNAseq) analysis on primary pediatric human mesenchymal progenitor cells (pMPCs) expressing EWS-FLI1
51 between differentiation and maintenance of a mesenchymal progenitor cell population determines the fi
52 three different cell types (C3H10T1/2 murine mesenchymal progenitor cells, primary human adipose tiss
53 enitors isolated from nonfibrotic lungs, IPF mesenchymal progenitor cells produce daughter cells mani
54             Removal of beta-catenin early in mesenchymal progenitor cells promoted chondrocyte differ
55 romoting the mobilization and trafficking of mesenchymal progenitor cells such as fibrocytes.
56       SoxC genes therefore ensure neural and mesenchymal progenitor cell survival, and function in pa
57 gs of patients with IPF contain pathological mesenchymal progenitor cells that are cells of origin fo
58                 Postnatal bone marrow houses mesenchymal progenitor cells that are osteoblast precurs
59 ese amphibians form a "blastema", a group of mesenchymal progenitor cells that specifically directs t
60        Moreover, BMP7 triggers commitment of mesenchymal progenitor cells to a brown adipocyte lineag
61 formation, from their initial induction from mesenchymal progenitor cells to their terminal maturatio
62 ricted to the luminal aspect of the vessels; mesenchymal progenitor cells were adjacent to lumens, co
63    Fibrocytes, which are bone marrow-derived mesenchymal progenitor cells, were increased to a greate
64             In principle, transplantation of mesenchymal progenitor cells would attenuate or possibly

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