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1 of Itk via coordinate action of PI 3-K and a src family tyrosine kinase.
2 th factor (EGF) receptor and activation of a Src family tyrosine kinase.
3 lls and specifically activated Lyn kinase, a src family tyrosine kinase.
4 ant c-Src tyrosine kinase and Fyn, a related Src family tyrosine kinase.
5 ponses can be mimicked through inhibition of Src family tyrosine kinases.
6 ned from mouse embryos carrying mutations in Src family tyrosine kinases.
7 interaction with Fc Rgamma, calmodulin, and Src family tyrosine kinases.
8 many different signaling molecules including src family tyrosine kinases.
9 Unc119, that associates with IL-5Ralpha and Src family tyrosine kinases.
10 s the first receptor-associated activator of Src family tyrosine kinases.
11 abrogated by PP2, a selective inhibitor for Src family tyrosine kinases.
12 hibited by PP1, a selective inhibitor of the Src family tyrosine kinases.
13 0) and Tyr(129), which are phosphorylated by Src family tyrosine kinases.
14 on of Dok was mediated, at least in part, by Src family tyrosine kinases.
15 eins (G proteins) requires the activation of Src family tyrosine kinases.
16 e found that E6AP can bind to several of the Src family tyrosine kinases.
17 tivation motif (ITAM), which signals through Src family tyrosine kinases.
18 1 (SH1) domain is transphosphorylated by the Src family tyrosine kinases.
19 its well-established role as an activator of src family tyrosine kinases.
20 ide ligand specific to the SH3 domain of the Src family tyrosine kinases.
21 ha subunits, H-Ras, c-Src, and other related Src family tyrosine kinases.
22 x with normal cellular Src (c-Src) and other Src family tyrosine kinases.
23 and functional interaction of caveolin with Src family tyrosine kinases.
24 receptor complex and various members of the src family tyrosine kinases.
25 veolin interacts directly or indirectly with Src family tyrosine kinases.
26 emblance to the known recognition motifs for Src family tyrosine kinases.
27 ated enveloped virions (CEV) require Abl and Src family tyrosine kinases.
28 reversal is dependent upon the activation of Src family tyrosine kinases.
29 nt by signaling through the Dab1 adaptor and Src family tyrosine kinases.
30 ion to tubulin, including the SH3 domains of Src family tyrosine kinases.
31 ells and are dependent on CD36 activation of Src family tyrosine kinases.
32 sly implicated in the activation of Cdk2 and Src family tyrosine kinases.
33 nels are physiologically relevant targets of Src family tyrosine kinases.
34 nase (Csk) phosphorylates and down-regulates Src family tyrosine kinases.
35 osine phosphorylation, but not activation of Src-family tyrosine kinases.
36 ai similarly modulate Hck, another member of Src-family tyrosine kinases.
37 in situ prevents the oncogenic actions of a SRC: family tyrosine kinase.
41 e have shown that this event is dependent on Src family tyrosine kinase activity and the subsequent a
43 AM-1 cytoplasmic domain antibodies, required Src family tyrosine kinase activity, was independent of
44 udies indicated that leflunomide can inhibit src-family tyrosine kinase activity, more recent studies
45 tase inhibition, and negatively regulated by Src-family tyrosine kinase activity, which restricts the
46 the catalytic site, can be phosphorylated by Src family tyrosine kinases, although endogenous phospho
47 monstrated that soluble E-selectin activated Src family tyrosine kinases, an effect that was upstream
48 face expression of TrkB that is inhibited by Src family tyrosine kinase and A2A receptor antagonists.
49 on of focal adhesion kinase (FAK) and Lyn, a Src family tyrosine kinase and substrate of FAK, was up-
50 e transphosphorylation of Y551 by endogenous Src family tyrosine kinases and autophosphorylation at t
51 y, but they differ in that invasion requires Src family tyrosine kinases and calcium-calmodulin activ
52 ated SS RBC adhesion absolutely requires the Src family tyrosine kinases and is also enhanced by trea
53 se of CEV from the cell requires Abl but not Src family tyrosine kinases and is blocked by imatinib m
54 en produces a rapid, transient activation of src-family tyrosine kinases and tyrosine phosphorylation
55 f GDNF are inhibited by PP2, an inhibitor of Src family tyrosine kinases, and by LY29003, an inhibito
56 epends on GTPase RhoA, the RhoA ROCK kinase, Src family tyrosine kinases, and NADPH, and is modulated
57 calization requires phosphotyrosine, Abl and Src family tyrosine kinases, and neural Wiskott-Aldrich
58 the core dimer of protein phosphatase 2A, an src-family tyrosine kinase, and via phosphotyrosines, Sh
59 e of CEV from the cell requires Abl- but not Src-family tyrosine kinases, and is blocked by STI-571 (
65 this study, we show for the first time that Src family tyrosine kinases are physically and functiona
66 In vitro studies indicate that activities of Src family tyrosine kinases are regulated by tyrosine ph
69 in hemopoietic cells leads to activation of Src family tyrosine kinases as well as Syk or ZAP-70.
70 s recognized by an antibody directed against Src family tyrosine kinases associate with PLC-gamma SH2
71 to study the phosphorylation of caveolin by Src family tyrosine kinases both in vitro and in vivo.
72 sensitive to the pharmacologic inhibition of Src family tyrosine kinases but was not affected by inhi
73 which was dependent on activation of a p60c-Src family tyrosine kinase, but not the epidermal growth
74 signaling requires activation of Zap-70 and Src family tyrosine kinases, but requirements for other
77 We further demonstrate that these events are Src family tyrosine kinase-dependent and specifically id
78 ta indicate that hypotonic stress results in Src family tyrosine kinase-dependent tyrosine phosphoryl
79 he endogenous PDGFbeta-R tyrosine kinase and Src family tyrosine kinases, differing results when the
80 c transmembrane proteins bearing syk but not src family tyrosine kinase domains are capable of autono
81 ) begins to address how one such pathway, an Src family tyrosine kinase, enhances cytoskeletal linkag
86 and 1 (PSGL1), alpha(L)beta(2) integrin, the Src family tyrosine kinase FGR and spleen tyrosine kinas
87 ociated enveloped virions (CEV) use Abl- and Src-family tyrosine kinases for actin motility, and that
88 st growth factor receptor (FGFR), Flk-1, and src family tyrosine kinases from 1996 through mid-1997.
89 we show that Tim-3 can directly bind to the Src family tyrosine kinase Fyn and the p85 phosphatidyli
90 In this study, we show evidence that the Src family tyrosine kinase Fyn helps regulate this Th17/
92 trafficking caused by downregulation of the Src family tyrosine kinase Fyn was confirmed in more-det
98 ndothelial isoform of nitric-oxide synthase, Src-family tyrosine kinases, Galphaq and the insulin rec
99 shown that Cbl forms in vivo complexes with Src family tyrosine kinases, Grb2 adaptor protein, and t
102 reported that mice deficient in the myeloid Src-family tyrosine kinases Hck, Fgr, and Lyn (Src tripl
104 ses suggest the involvement of c-Met and the Src family tyrosine kinases in mediating UV-induced Gab1
106 osphorylation was blocked by addition of the Src family tyrosine kinase inhibitor 4-amino-5-(4-chloro
112 istein, a tyrosine kinase inhibitor; PP2, an Src family tyrosine kinase inhibitor; AIDA, a group I me
116 f Fyn activation on differentiation, we used Src family tyrosine kinase inhibitors, PP1 and PP2, in c
118 n of tyrosine 876 on the GluR2 C terminus by Src family tyrosine kinases is important for the regulat
119 ur residues are present in p56lyn, the other src family tyrosine kinase known to bind to the ITAM, su
120 nd apoEr2, we examined the effect of Fyn, an Src family-tyrosine kinase known to interact with and ph
121 phosphorylation was dependent upon both the Src family tyrosine kinase Lck and the tyrosine phosphat
124 In this report, the crystal structure of the Src family tyrosine kinase Lck was used to guide the cre
129 hosphatase has been reported to activate the src family tyrosine kinases Lck and Fyn by dephosphoryla
130 how that KIR CYT, once phosphorylated by the src-family tyrosine kinase LCK, additionally bind the p8
131 , whereas consistent with work done with the Src-family tyrosine kinase Lck, the presence of helix al
134 to guide the dissection of two kinases [the Src-family tyrosine kinase, Lck, and the heme-regulated
135 usly demonstrated that mice deficient in the Src family tyrosine kinase Lyn developed a mild lupus-li
137 (IgE), FcepsilonRI, is phosphorylated by the Src family tyrosine kinase Lyn to initiate mast cell sig
138 study, we provide the first evidence that a Src family tyrosine kinase, Lyn, plays a key role in inh
143 hrough the phosphorylation and activation of Src family tyrosine kinase members, such as Fyn, that ph
144 osine phosphorylated in vitro and in vivo by Src family tyrosine kinases on tyrosine 876 near its C t
147 be blocked by pharmacological inhibitors of Src family tyrosine kinases or the epidermal growth fact
148 T cell antigen receptor (TCR) activates the Src family tyrosine kinase p56 Lck, which, in turn, phos
150 Furthermore, we find that activation of the src-family tyrosine kinase, p56lck is an upstream mediat
151 l cell adhesion molecule (NCAM) requires the src family tyrosine kinase p59(fyn) in nerve growth cone
154 ) that specifically inhibits the activity of Src family tyrosine kinases, PDGF did not activate Stat3
159 horylation was sensitive to the inhibitor of Src family tyrosine kinases, PP1, in a dose-dependent fa
161 the hippocampus, the combined activation of SRC family tyrosine kinases, protein kinase A, protein k
162 ced PKD activation was mediated primarily by Src family tyrosine kinases rather than protein kinase C
163 or Btk (Bruton's tyrosine kinase) family and Src family tyrosine kinases, respectively, PDGF can stim
166 ies suggest that TCR signaling downstream of Src family tyrosine kinase(s) but upstream of calcineuri
168 nd biochemical data clearly demonstrate that Src-family tyrosine kinases serve as a critical signal r
169 ) and Caveolin-1 (Cav-1) in the mechanism of Src family tyrosine kinase (SFK) inhibition by Csk.
172 an oral small molecule inhibitor of Abl and Src family tyrosine kinases (SFK), including p56(Lck) (L
181 gh EGF receptor was abolished by blockade of Src family tyrosine kinase signaling but not inhibition
182 rough its downstream, intracellular Dab1 and Src family tyrosine kinase signaling cascade, is essenti
183 Pyrazolopyrimidine, a selective inhibitor of Src family tyrosine kinases, significantly blocked the V
184 n of p130Cas was also dependent on an active Src family tyrosine kinase, since it could be blocked by
185 phosphorylated forms of BCR-signaling nodes (Src family tyrosine kinase, spleen tyrosine kinase [SYK]
187 rations (50-250 microM) markedly inactivated Src family tyrosine kinases temporally and spatially in
191 mbryonic fibroblast (MEF) cells deficient in Src family tyrosine kinases to examine the role of Src i
192 y kinases (Fyn, Src, and Lck) and Fes, a non-Src-family tyrosine kinase, to alter Na,K-ATPase activit
193 te binds only the active conformation of the Src family tyrosine kinase, unlike the ATP cofactor, whi
194 autophosphorylation and activity of Fyn, an Src family tyrosine kinase, was observed in LAR(-/-) cel
195 dence that IL-13 induces the activation of a Src family tyrosine kinase, which is required for IL-13
196 osine phosphorylation of Cas proteins; then, Src family tyrosine kinases, which are recruited to phos
197 uated ERK1/2 activation, while inhibition of Src family tyrosine kinases with PP2 abolished the respo
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