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1 25 (OH)(2) vitamin D(3) (Vit D) to stimulate osteoclast-like cell (OCL) formation in cocultures of sp
2 f soluble factors produced by these cells on osteoclast-like cell differentiation.
3 ine kidney cell line (MDCT209) and a chicken osteoclast-like cell line (HD-11EM), whereas promoter P3
4 ), whereas promoter P3 is active only in the osteoclast-like cell line.
5                                              Osteoclast-like cell numbers and acid phosphatase levels
6                                 Using murine osteoclast-like cells (OCLs) and their mononuclear precu
7 equired for activation of Src by cyt-PTPe in osteoclast-like cells (OCLs) in culture.
8 ity exists that pro-B cells can give rise to osteoclast-like cells (OCLs) in vitro and in vivo.
9                  In vitro bone resorption by osteoclast-like cells (OCLs) is inhibited by both c-src
10                                     Atp6i-/- osteoclast-like cells (OCLs) lose the function of extrac
11                                 Using murine osteoclast-like cells (OCLs) or their mononuclear precur
12  mononuclear precursors as well as in mature osteoclast-like cells (OCLs).
13 mediators of arterial mineral resorption are osteoclast-like cells (OLCs) derived from hematopoietic
14                                    The human osteoclast-like cells also expressed another isoform den
15 matory), leading to suppressed maturation of osteoclast-like cells and enhanced maturation of osteobl
16    This correlated with fewer multinucleated osteoclast-like cells and more trabecular bone volume an
17                                              Osteoclast-like cells are generated readily from PTPepsi
18                             In cell culture, osteoclast-like cells displayed no changes in p65*(536)
19 cer cells with elevated phosphate demand, in osteoclast-like cells during bone reabsorption, and in h
20 oteins colocalize only within adherent avian osteoclast-like cells examined by double antibody immuno
21                           Indeed, KO derived osteoclast-like cells exhibited increased Syk tyrosine p
22 xamined avian osteoclast and human and mouse osteoclast-like cells for androgen responsiveness.
23 tartrate-resistant acid phosphatase-positive osteoclast-like cells formed from hemopoietic precursors
24  at high levels in authentic osteoclasts and osteoclast-like cells formed in an in vitro co-culture s
25                                        Using osteoclast-like cells generated by coculturing mouse bon
26 d directly with an increase in the number of osteoclast-like cells generated in marrow cultures.
27 only mdc9 and mdc15 mRNAs were detectable in osteoclast-like cells generated in vitro.
28 ry splenocytes readily aggregated and formed osteoclast-like cells in chemically defined osteoclastog
29    The identification of osteoblast-like and osteoclast-like cells in human tissue has led to a major
30  cell lines inhibited the differentiation of osteoclast-like cells in mouse bone marrow cultures.
31 stant acid phosphatase-positive multinuclear osteoclast-like cells in response to RANKL in a dose-dep
32 sed macrophage infiltration and formation of osteoclast-like cells in the calcified lesions.
33 ymes and other proteins suggested a role for osteoclast-like cells in the host response to microliths
34 ligand, and the appearance of multinucleated osteoclast-like cells in the MPS bone marrow.
35 e number and activity of bone marrow-derived osteoclast-like cells in vitro, suggesting that the rest
36 nd glutathione and thioredoxin reductases in osteoclast-like cells in vitro.
37  silica induces differentiation of pulmonary osteoclast-like cells leading to progressive lung injury
38 ha treatment leads to the rare appearance of osteoclast-like cells near the site of injection.
39 ated from the conditioned media of RAW 264.7 osteoclast-like cells or primary osteoclasts were charac
40                                       Murine osteoclast-like cells or their mononuclear precursors we
41   This work reveals that Npt2b and pulmonary osteoclast-like cells play key roles in pulmonary homeos
42 ages of Me(v)/Me(v) mice generated much more osteoclast-like cells than that of littermate controls i
43  bone height and 4-fold increased numbers of osteoclast-like cells versus wild type at 24 wk, consist
44 ty and resorbing activity of mu-calpain(-/-) osteoclast-like cells were also reduced, indicating that
45 e marrow mononuclear cells and RAW 264.7 pre-osteoclast-like cells were treated with RANKL to induce
46 er of osteoclasts and the formation of giant osteoclast-like cells within the alveolar bone.
47 um (10% for osteoblast-like cells and 2% for osteoclast-like cells).
48 irectly stimulated HBMC differentiation into osteoclast-like cells, IL-8, but not MCP-1, induced bone
49 on of several cellular proteins in cultured, osteoclast-like cells, including c-fms, c-src, and an 85
50 lcification is coupled with the formation of osteoclast-like cells, paralleling the bone remodeling p
51 402F)) markedly inhibited bone resorption by osteoclast-like cells, whereas kinase-dead Pyk2 had litt
52 ed their differentiation into multinucleated osteoclast-like cells.
53 and cJun, followed by increased formation of osteoclast-like cells.
54 acrophages into the calcified lesion to form osteoclast-like cells.
55  promote differentiation of macrophages into osteoclast-like cells.
56  were found in wild-type BM monocyte derived osteoclast-like cells.
57 tartrate-resistant acid phosphatase-positive osteoclast-like cells.
58 staining was used to identify multinucleated osteoclast-like cells.
59  restore bone-resorbing activity to Src(-/-) osteoclast-like cells.
60 pressed together with the more common C1a in osteoclast-like cells.
61 ntially expressed in highly purified chicken osteoclast-like cells.
62  coincides with the presence of multinuclear osteoclast-like cells.
63 ed cadherin-6/2 from a cDNA library of human osteoclast-like cells.
64 is significantly less phosphorylated in src- osteoclast-like cells.
65 antibody treatment suppressed silica-induced osteoclast-like differentiation in the lung and attenuat
66                                 Interrupting osteoclast-like differentiation may therefore constitute
67 osis, intratracheal silica challenge induced osteoclast-like differentiation of alveolar macrophages
68 ry M2 macrophages, could potentially display osteoclast-like functions.
69              Undifferentiated carcinoma with osteoclast-like giant cells (UCOGCs) is a rare and aggre
70  cells in an undifferentiated carcinoma with osteoclast-like giant cells could be a marker of a poor
71 ontaining an undifferentiated carcinoma with osteoclast-like giant cells have been described in the l
72  benign osteolytic tumor featuring prominent osteoclast-like giant cells, mononuclear osteoclast prec
73 eoplasm containing an area of carcinoma with osteoclast-like giant cells.
74 ponent of an undifferentiated carcinoma with osteoclast-like giant cells.
75 esent in the undifferentiated carcinoma with osteoclast-like giant cells.
76 n undifferentiated pancreatic carcinoma with osteoclast-like giant cells.
77 sed by mammalian cells significantly reduced osteoclast-like MNC formation induced by 1,25-dihydroxyv
78 one was identified and isolated from a human osteoclast-like multinucleated cell (MNC) cDNA library,
79  completely inhibited the differentiation of osteoclast-like multinucleated cell formation in the pre
80 es of authentic osteoclasts and suggest that osteoclast-like multinucleated cells can arise in synovi