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1 predicted alpha and beta subunits of chicken macrophage stimulating protein.
2 rotein and an antisera raised against murine macrophage stimulating protein.
3 ific activity than the wild type recombinant macrophage stimulating protein.
4 RTK activation, using RON, the receptor for macrophage-stimulating protein.
5 yze other plasminogen-like proteins, such as macrophage-stimulating protein and plasminogen itself.
6 and the specific Cys to Ala form of chicken macrophage stimulating protein as recombinant proteins.
7 modeling of the serine proteinase domain of macrophage stimulating protein based on homology to huma
8 COS cells transfected with the C665A chicken macrophage stimulating protein, but not from wild type c
9 on homology to human trypsin suggested that macrophage stimulating protein, but not plasminogen or h
11 were fully disulfide linked, and the mutant macrophage stimulating protein had 10-20-fold higher spe
12 human hepatocyte growth factor-like protein/macrophage stimulating protein (HGFL), our laboratory ha
13 and identified hepatocyte growth factor-like/macrophage-stimulating protein (HGFL/MSP) in injured lun
15 receptor phosphorylation, the C665A chicken macrophage-stimulating protein induced phosphorylation o
19 ation of this pathway in response to ligand (macrophage-stimulating protein) is abolished in the abse
20 ibited hepatocyte growth factor-mediated and macrophage-stimulating protein-mediated signaling and ce
22 reported that the transcription of the human macrophage stimulating protein (MSP) gene was positively
26 atocyte growth factor-like protein (HGFL) or macrophage stimulating protein (MSP), induces crucial ce
29 To analyze the promotor region of the human macrophage-stimulating protein (MSP) gene, the 5'-flanki
30 ition to its effects on macrophage function, macrophage-stimulating protein (MSP) is a growth and mot
34 ine nantais), a tyrosine kinase receptor for macrophage-stimulating protein (MSP) was implicated in t
35 rowth factor (PDGF), stem cell factor (SCF), macrophage-stimulating protein (MSP), fibroblast growth
36 lpha signaling or neutralizing antibodies to macrophage-stimulating protein (MSP), HGF, or c-Met.
37 In primary macrophages, the ligand for Ron, macrophage-stimulating protein (MSP), inhibits the expre
38 ceptor tyrosine kinase and its ligand, serum macrophage-stimulating protein (MSP), play important rol
40 ur lab and others have previously shown that macrophage-stimulating protein (MSP), through activation
43 ectively blocks interaction with its ligand, macrophage-stimulating protein (MSP; IC50 = 2 nmol/L).
44 ting protein, but not from wild type chicken macrophage-stimulating protein, or control vector, was d
45 e model of breast cancer, we discovered that macrophage-stimulating protein promoted breast tumor gro
46 nditioned media containing the C665A chicken macrophage-stimulating protein readily caused Sea phosph
47 pression of fully activatible human or mouse macrophage stimulating protein required a specific Cys t
48 on of suppressor of cytokine signaling 1 via macrophage-stimulating protein/RON signaling provide a p
50 ation of primary peritoneal macrophages with macrophage-stimulating protein, the ligand for RON, inhi
51 ioned media containing the wild type chicken macrophage-stimulating protein was only effective at ind
52 n activation, the subunits of Cys672 --> Ala macrophage stimulating protein were fully disulfide link
53 ut in our hands, the subunits of recombinant macrophage stimulating protein were mostly not disulfide
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