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1 n anti-mineralization role in the peripheral connective tissue cells.
2 er cells, hyaline cells, ganglion cells, and connective tissue cells.
3 ransforming growth factor beta (TGF-beta) in connective tissue cells.
4 growth factor (LDGF), which is mitogenic for connective tissue cells.
5 cs of cultured human gingival epithelial and connective tissue cells.
6 diator expression was limited mainly to some connective tissue cells.
7 s detected in interalveolar and interlobular connective tissue cells adjacent to glandular alveolar (
9 to determine whether MMP-10 is expressed in connective tissue cells and to assess how it may contrib
10 r the wound, immunostaining for fibroblasts, connective tissue cells, and newly forming vasculature b
11 tensively in vestibular supporting cells and connective tissue cells, and the two Cxs were co-localiz
12 We find that progenitor cells derived from connective tissue cells differentiate into muscle, carti
13 deposition, inflammatory cell retention, and connective tissue cell differentiation, respectively.
14 ls involved in wound closure in vitro and in connective tissue cells during closure of gingival wound
15 served cellular response programs of derived connective tissue cells (e.g., chondroblasts and osteobl
16 f TAHD was associated with alteration of the connective tissue cell epigenetics, and DMR associated g
17 -1 and mTLL-1 in lysyl oxidase activation by connective tissue cells, fibroblasts cultured from Bmp1-
19 al bi-fated program gives rise to muscle and connective tissue cells in skeletal muscles that are dep
20 embryogenesis and (2) a layer of fibroblasts/connective tissue cells in the gastrointestinal tract, t
21 sponse initiates and what is the role of the connective tissue cells in the progression of this disea
22 trix metalloproteinases (MMPs) from resident connective tissue cells in tooth-supporting tissues (per
26 hat cytokines and growth factors produced by connective tissue cells might concentrate in BL, where t
30 ession of phenotypical markers, the emerging connective tissue cell population may originate from mic
32 what we believe to be the first evidence for connective tissue cell progenitors that reside locally w
33 nstrate that, like TGF-beta, CTGF can induce connective tissue cell proliferation and extracellular m
34 n skeletal muscle progenitors and associated connective tissue cells provides a model for examining h
37 trate distinct positional characteristics of connective tissue cells that are associated with their r
38 to create 3D open scaffolds for adhesion of connective tissue cells through well-defined adhesion pl
39 suggests that HGF secreted by interalveolar connective tissue cells traverses the acinar cells and m
40 basis for the divergence of CTGF actions on connective tissue cell types and suggest a model for fun
43 endons that contain predominantly fibroblast connective tissue cells were used to isolate fibroblast