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1  for mapping the conformational landscape of c-src tyrosine kinase.
2 dent on kinase activity and is not shared by c-Src tyrosine kinase.
3                     Sam68 is a target of the c-Src tyrosine kinase.
4 ) is required for coupling caveolin-1 to the c-Src tyrosine kinase.
5 es demonstrate that MUC1 associates with the c-Src tyrosine kinase.
6 effect on the catalytic activity of purified c-src tyrosine kinase.
7 s cytoplasmic signaling molecules, including c-Src tyrosine kinases.
8                                Inhibition of c-Src tyrosine kinase (4-amino-5-[4-chlorophenyl]-7-[t-b
9                                Inhibition of C-SRC tyrosine kinase activity also blocks PGE(2)-induce
10 ting that the SH1(KD) mutant did not inhibit c-SRC tyrosine kinase activity in general.
11 he remodeling of Kv4.3 channel and increased c-Src tyrosine kinase activity, a stretch-responsive kin
12 lin showed a rapid and transient decrease in c-Src tyrosine kinase activity.
13 n shown previously to cause up-regulation of c-Src tyrosine kinase activity.
14               Inhibition of raft-associating c-Src tyrosine kinase and downstream JNK kinase by pharm
15  the auto-activation of purified recombinant c-Src tyrosine kinase and Fyn, a related Src family tyro
16 e MUC1 cytoplasmic domain interacts with the c-Src tyrosine kinase and thereby increases binding of M
17 urn regulates VEGF-induced activation of the c-Src tyrosine kinase and vascular permeability.
18 ion of G-protein-independent DRD1 coupled to c-Src tyrosine kinases and required local release of neu
19 ng endothelial nitric-oxide synthase and the c-Src tyrosine kinase, are also potently inhibited by ea
20     The structure of a large fragment of the c-Src tyrosine kinase, comprising the regulatory and kin
21                                          The c-Src tyrosine kinase, Csk, physically interacts with th
22 be the principal site for recognition by the c-Src tyrosine kinase; however, little is known about th
23 ently co-expressing full-length caveolin and c-Src tyrosine kinase in 293T cells.
24               MUC1 has been shown to bind to c-Src tyrosine kinase in vitro, whereby c-Src phosphoryl
25 atory factors for coupling caveolin-1 to the c-Src tyrosine kinase in vivo.
26                      We detected the FYN and c-SRC tyrosine kinases in the flagellar mid-piece region
27 n the pathogenesis of melanoma, we show that c-Src tyrosine kinase is activated in melanoma cell line
28 uronal-specific N1-Src splice variant of the C-Src tyrosine kinase is conserved through vertebrate ev
29    The aim of this study was to test whether c-Src tyrosine kinase mediates connexin-43 (Cx43) reduct
30 gned to ask whether heat shock activates p60 c-Src tyrosine kinase or phosphatidylinositol 3-kinase (
31 ogenesis and vascular permeability, in which c-Src tyrosine kinase plays an essential role.
32 hat govern the coupling of caveolin-1 to the c-Src tyrosine kinase remain largely unknown.
33                     We studied regulation by c-Src tyrosine kinase (Src) of KCNQ1-5 channels heterolo
34 inetic mechanisms for the inhibition of pp60(c-src) tyrosine kinase (Src TK) by 4-anilinoquinazolines
35 ibroblast growth factor receptor (FGFr), and c-src tyrosine kinases (TKs).
36 s provide a molecular link that connects the c-Src tyrosine kinase transduction pathway to ER stress-
37 ound 4b inhibited the PDGFr, FGFr, EGFr, and c-src tyrosine kinases with IC50 values of 1.11, 0.13, 0

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