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1 ase (MMP)2 are present and active in cushion mesenchymal tissue.
2 re but diverse malignant tumors derived from mesenchymal tissue.
3 een axons, Schwann cells and the surrounding mesenchymal tissue.
4 hese cells, luminal bacteria, and underlying mesenchymal tissue.
5 yclin D1 (n = 7; RQ 1 vs. 0.61, P < 0.05) in mesenchymal tissue.
6 arrest of epithelial invasion into the cecal mesenchymal tissue.
7 ate growth signals in various epithelial and mesenchymal tissues.
8 in for ALT immortalization in cell lines and mesenchymal tissues.
9 ute to the regeneration of multiple types of mesenchymal tissues.
10  cells (MSC) can differentiate into multiple mesenchymal tissues.
11 hat was dependent upon midline cartilaginous/mesenchymal tissues.
12 ustaining epithelial stem cells and adjacent mesenchymal tissues.
13 ion factor that regulates the development of mesenchymal tissues.
14          The thymus represents an epithelial-mesenchymal tissue, anatomically structured into discret
15  an increase in apoptosis in both condensing mesenchymal tissues and cartilage of the nasal region in
16 h due to a splicing switch express Fgfr2b in mesenchymal tissues and manifest Apert syndrome-like phe
17 can be induced to differentiate into various mesenchymal tissues and trans-differentiate into some no
18 gene that is expressed during development in mesenchymal tissues and ventrally derived structures wit
19  of 4-day embryonic chicken wing and leg bud mesenchymal tissue, and adjacent flank mesoderm.
20                                  Dentin is a mesenchymal tissue, and, as such, is based on a collagen
21 isms by which these undifferentiated cushion mesenchymal tissues are remodeled "post-EMT" into mature
22              We show that in Kif3a-deficient mesenchymal tissues both the repressor function of Gli3
23 the basement membrane lying between this and mesenchymal tissues, both of which express Fli1 at the t
24       WISP2 is a novel secreted regulator of mesenchymal tissue cellularity.
25                            In each case, the mesenchymal tissue consisting of normal-appearing stroma
26 ction in lung volume was due to loss of lung mesenchymal tissue correlating with a decrease in cell p
27                   Analysis of the underlying mesenchymal tissue demonstrated a fibrotic response in t
28 e mouse models to address this hypothesis in mesenchymal tissue development and tumorigenesis.
29  in fibroblasts within fetal, but not adult, mesenchymal tissues during healing.
30  often called "laminopathies," mainly affect mesenchymal tissues (e.g., striated muscle, bone, and fi
31 tic value not only for the repair of damaged mesenchymal tissues following hematopoietic stem cell tr
32 nolytic activities required in collagen-rich mesenchymal tissues for extracellular matrix remodeling
33 this study we have recombined epithelial and mesenchymal tissues from normal and LEF-1-deficient embr
34 anization of cellular events in regenerating mesenchymal tissue in vivo.
35  co-expressed at high levels in neuronal and mesenchymal tissues in the developing mouse, and at vari
36  differentiate into mature cells of multiple mesenchymal tissues including fat, bone, and cartilage.
37 in patients with genetic disorders affecting mesenchymal tissues, including bone, cartilage, and musc
38 he potential to differentiate to lineages of mesenchymal tissues, including bone, cartilage, fat, ten
39 d in vivo to differentiate into a variety of mesenchymal tissues, including bone, cartilage, tendon,
40 s) include stem cells capable of forming all mesenchymal tissues, including bone.
41 stinct mechanisms: direct differentiation to mesenchymal tissues, including skeletal and smooth muscl
42 e the capacity to differentiate into several mesenchymal tissues, including the components of the hem
43 ontext in the absence of direct contact with mesenchymal tissue, indicating that the program for bran
44 ormation of organs that depend on epithelial-mesenchymal tissue interactions.
45     However, a bud of undifferentiated cecal mesenchymal tissue is maintained throughout development.
46 w stroma (hMSCs) differentiate into numerous mesenchymal tissue lineages and are attractive candidate
47 ced cells that can regenerate epithelial and mesenchymal tissues may potentially be utilized in limb
48 al allelic expression (DAE) of BMP5 in human mesenchymal tissues obtained from 16 donors undergoing j
49 embrane-type 3 MMP, MT3-MMP, is expressed in mesenchymal tissues of the skeleton and in peri-skeletal
50 er between the kidney and ureter forms where mesenchymal tissues originating in two different areas o
51       The interaction between epithelial and mesenchymal tissues plays a critical role in the develop
52 iver regeneration in host animals by forming mesenchymal tissue, progenitor cells, hepatocytes, and c
53                                 Derived from mesenchymal tissues, sarcomas occur in all parts of the
54                              We investigated mesenchymal tissue-specific requirement of BmprIa and it
55 related processes in tumors originating from mesenchymal tissues, such as bone and soft-tissues sarco
56 (day 10.5-18.5), TIMP-2 mRNA was abundant in mesenchymal tissues that surrounded developing epithelia
57 ) is a tyrosine kinase receptor expressed in mesenchymal tissues, the ligand of which is fibrillar co
58      We further discovered that two adjacent mesenchymal tissues, the periodontium and dental pulp, a
59 enetic protein (BMP) antagonist expressed in mesenchymal tissues whose function in development of the
60 with some indication of residual degenerated mesenchymal tissue within the defects.

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