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1 exposed cells on the surface of a disrupted mesenchymal tissue.
2 ase (MMP)2 are present and active in cushion mesenchymal tissue.
3 re but diverse malignant tumors derived from mesenchymal tissue.
4 een axons, Schwann cells and the surrounding mesenchymal tissue.
5 hese cells, luminal bacteria, and underlying mesenchymal tissue.
6 arrest of epithelial invasion into the cecal mesenchymal tissue.
7 helial wall hosting taste buds and a core of mesenchymal tissue.
8 yclin D1 (n = 7; RQ 1 vs. 0.61, P < 0.05) in mesenchymal tissue.
9 ustaining epithelial stem cells and adjacent mesenchymal tissues.
10 ion factor that regulates the development of mesenchymal tissues.
11 in for ALT immortalization in cell lines and mesenchymal tissues.
12 ate growth signals in various epithelial and mesenchymal tissues.
13 ute to the regeneration of multiple types of mesenchymal tissues.
14 cells (MSC) can differentiate into multiple mesenchymal tissues.
15 hat was dependent upon midline cartilaginous/mesenchymal tissues.
16 would benefit from this sparing of skin and mesenchymal tissues.
17 es a specific contribution to distinct molar mesenchymal tissues.
19 an increase in apoptosis in both condensing mesenchymal tissues and cartilage of the nasal region in
20 h due to a splicing switch express Fgfr2b in mesenchymal tissues and manifest Apert syndrome-like phe
21 HIKV antigen was most frequently detected in mesenchymal tissues and mononuclear cells including tiss
22 can be induced to differentiate into various mesenchymal tissues and trans-differentiate into some no
23 gene that is expressed during development in mesenchymal tissues and ventrally derived structures wit
26 rapy in sarcoma and additional cancers where mesenchymal tissues are at risk, including head and neck
27 isms by which these undifferentiated cushion mesenchymal tissues are remodeled "post-EMT" into mature
29 the basement membrane lying between this and mesenchymal tissues, both of which express Fli1 at the t
30 dying cells and debris, many epithelial and mesenchymal tissue cells can digest nearby apoptotic cor
34 ction in lung volume was due to loss of lung mesenchymal tissue correlating with a decrease in cell p
37 ic trafficking network controlled by Rab8 to mesenchymal tissue differentiation has not been fully de
40 often called "laminopathies," mainly affect mesenchymal tissues (e.g., striated muscle, bone, and fi
41 tic value not only for the repair of damaged mesenchymal tissues following hematopoietic stem cell tr
42 nolytic activities required in collagen-rich mesenchymal tissues for extracellular matrix remodeling
43 this study we have recombined epithelial and mesenchymal tissues from normal and LEF-1-deficient embr
44 we show that the sensory nerve is vital for mesenchymal tissue homeostasis and maintenance of MSCs i
47 co-expressed at high levels in neuronal and mesenchymal tissues in the developing mouse, and at vari
48 differentiate into mature cells of multiple mesenchymal tissues including fat, bone, and cartilage.
49 irway epithelial cells, but also in adjacent mesenchymal tissues, including airway smooth muscle cell
50 in patients with genetic disorders affecting mesenchymal tissues, including bone, cartilage, and musc
51 he potential to differentiate to lineages of mesenchymal tissues, including bone, cartilage, fat, ten
52 d in vivo to differentiate into a variety of mesenchymal tissues, including bone, cartilage, tendon,
54 stinct mechanisms: direct differentiation to mesenchymal tissues, including skeletal and smooth muscl
55 e the capacity to differentiate into several mesenchymal tissues, including the components of the hem
56 ontext in the absence of direct contact with mesenchymal tissue, indicating that the program for bran
57 n at 28, 52, 104, 132-weeks (W) demonstrated mesenchymal tissue ingrowth into implant wall at 28 W, w
59 However, a bud of undifferentiated cecal mesenchymal tissue is maintained throughout development.
60 w stroma (hMSCs) differentiate into numerous mesenchymal tissue lineages and are attractive candidate
61 ced cells that can regenerate epithelial and mesenchymal tissues may potentially be utilized in limb
62 al allelic expression (DAE) of BMP5 in human mesenchymal tissues obtained from 16 donors undergoing j
64 embrane-type 3 MMP, MT3-MMP, is expressed in mesenchymal tissues of the skeleton and in peri-skeletal
65 er between the kidney and ureter forms where mesenchymal tissues originating in two different areas o
67 s include adaptive immune system activation, mesenchymal tissue priming and so-called 'remote' (non-i
68 iver regeneration in host animals by forming mesenchymal tissue, progenitor cells, hepatocytes, and c
72 related processes in tumors originating from mesenchymal tissues, such as bone and soft-tissues sarco
74 d basement membrane-less compartments within mesenchymal tissue that were mechanically primed to driv
75 (day 10.5-18.5), TIMP-2 mRNA was abundant in mesenchymal tissues that surrounded developing epithelia
76 ) is a tyrosine kinase receptor expressed in mesenchymal tissues, the ligand of which is fibrillar co
78 enetic protein (BMP) antagonist expressed in mesenchymal tissues whose function in development of the