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1 ions between the Na,K-ATPase and Src kinase (non-receptor tyrosine kinase).
2 al membrane 34) and SRC (SRC proto-oncogene, non-receptor tyrosine kinase).
3 chanism for the regulation of this important non-receptor tyrosine kinase.
4 that currently appears to be unique for this non-receptor tyrosine kinase.
5 bodies and require the function of the dBtk non-receptor tyrosine kinase.
6 s III phosphatidylinositol-3-kinase, and Src non-receptor tyrosine kinase.
7 3 is able to repress the activity of the Brk non-receptor tyrosine kinase.
8 um-dependent, focal adhesion kinase-related, non-receptor tyrosine kinase.
9 rged as a negative regulator of receptor and non-receptor tyrosine kinases.
10 ith a vertebrate signaling pathway involving non-receptor tyrosine kinases.
11 y ErbB-2 requires the participation of other non-receptor tyrosine kinases.
12 n signaling between these two highly related non-receptor tyrosine kinases.
13 le docking protein downstream of receptor or non-receptor tyrosine kinases.
14 s a novel negative regulator of receptor and non-receptor tyrosine kinases.
15 ways triggered by activation of receptor and non-receptor tyrosine kinases.
17 main containing proteins, including specific non-receptor tyrosine kinases-Abl via pY251 and C-termin
21 tudy, we have identified SAM domain-carrying non-receptor tyrosine kinase, activated Cdc42-associated
22 We have previously shown that the Arg/Abl2 non-receptor tyrosine kinase acts downstream of the EGF
24 ein kinase IIdelta2 (CaMKIIdelta2) activates non-receptor tyrosine kinases and EGF receptor, with a S
25 receptor tyrosine kinases, the Src family of non-receptor tyrosine kinases and the Eph receptor tyros
26 members of the Janus kinase (Jak) family of non-receptor tyrosine kinases and the signal transducers
27 d p160(v-Abl) are plasma membrane-associated non-receptor tyrosine kinases and the transforming activ
30 ts with the SH3 domain of Fyn, an Src family non-receptor tyrosine kinase, and is tyrosine-phosphoryl
31 nsistent with genetic studies placing Abl, a non-receptor tyrosine kinase, and the Drosophila ortholo
32 kinase Itk is a member of the Tec family of non-receptor tyrosine kinases, and is required for signa
33 exposure of CD3 ITAMs to phosphorylation by non-receptor tyrosine kinases, and phase separation of s
36 substrate of all the three major classes of non-receptor tyrosine kinases associated with the IL-2R,
37 ted conformations that provide access to the non-receptor tyrosine kinases, BCR-ABL and Src, which ph
38 nism by which an adaptor protein activates a non-receptor tyrosine kinase by SH2 domain displacement.
42 ronal morphogenesis, we demonstrate that the non-receptor tyrosine kinase c-Abl is an intermediary fo
47 pe-selective small molecule inhibitor of the non-receptor tyrosine kinase c-Src (IC(50) = 64 nM).
48 determined that tTG forms a complex with the non-receptor tyrosine kinase c-Src and PI3-kinase, and t
49 e G proteins through a pathway involving the non-receptor tyrosine kinase c-Src and the G protein Ras
50 macrophage colony-stimulating factor and the non-receptor tyrosine kinase c-Src play critical roles i
51 ubiquitination of another protooncogene, the non-receptor tyrosine kinase c-Src, as well as of itself
55 t of the vesicular regulator, dynamin 2, the non-receptor tyrosine kinase, c-Abl, and the NADPH oxida
56 ough members from three distinct families of non-receptor tyrosine kinases can phosphorylate PLCgamma
57 Herein we demonstrate that activity of the non-receptor tyrosine kinase dBtk protein is required wi
61 reviously showed that targeted expression of non-receptor tyrosine kinase Etk/BMX in mouse prostate i
65 tyrosine kinase (BTK) is a member of the Tec non-receptor tyrosine kinase family that is involved in
67 nase-1 (FRK-1), an ortholog of the mammalian non-receptor tyrosine kinase Fer, is necessary for embry
71 long cytoskeletal filaments and activate the non-receptor tyrosine kinase focal adhesion kinase, whic
74 Herein, we identified a novel role for the non-receptor tyrosine kinase Fyn in regulating neuroinfl
75 ngest interaction was between MAP-2c and the non-receptor tyrosine kinase Fyn; however, MAP-2b and MA
79 eptor tyrosine kinases and the Abl family of non-receptor tyrosine kinases have both been implicated
80 inases (SrcFKs), a multi-functional group of non-receptor tyrosine kinases highly expressed in vascul
81 , PF-4618433) reveals a distinct subclass of non-receptor tyrosine kinases identifiable by the gateke
82 h tyrosine kinase 2 (PYK2) is a cytoplasmic, non-receptor tyrosine kinase implicated in multiple sign
83 lopment and represents an emerging family of non-receptor tyrosine kinases implicated in signal trans
84 we provide evidence for a selective role of non-receptor tyrosine kinases in specific aspects of hip
85 resent study, we examined the role of Fyn, a non-receptor tyrosine kinase, in microglial activation a
86 Thus, these studies strongly suggest that non-receptor tyrosine kinases, in particular c-Src, may
88 The Janus tyrosine kinase (JAK) family of non-receptor tyrosine kinases includes four isoforms (JA
90 or TNK2, an ubiquitously expressed oncogenic non-receptor tyrosine kinase, integrates signals from li
92 en hMSH5 and c-Abl; the latter is a critical non-receptor tyrosine kinase involved in many critical c
94 inase (Lyn) is a member of the Src family of non-receptor tyrosine kinases involved in immune signali
95 for its proviral activity, and the family of non-receptor tyrosine kinases involved in this process,
96 stimulation of VGSC, engagement of these two non-receptor tyrosine kinases involves distinct signalin
99 osine phosphorylation of GIV by receptor and non-receptor-tyrosine kinases is a key step that is requ
107 motes signaling by causing activation of the non-receptor tyrosine kinase, JAK2, which associates wit
109 ed receptors, results in the activation of a non-receptor tyrosine kinase known as focal adhesion kin
111 blished that BCR is a substrate for c-FES, a non-receptor tyrosine kinase linked to myeloid growth an
113 e of signaling nodes Itk and Txk, Tec family non-receptor tyrosine kinases, mice exhibit a significan
116 orylated in vitro by representatives of many non-receptor tyrosine kinase (NRTK) sub-families, sugges
117 und heterozygous deleterious variants in the non-receptor tyrosine kinases (NRTKs) ACK1 and BRK.
118 belson family kinases (AFKs; Abl1, Abl2) are non-receptor tyrosine kinases (NRTKs) implicated in canc
122 to-oncogenes encode 60 000 and 62 000 Dalton non-receptor tyrosine kinases of the Src family, pp60c-s
123 SHP-1 antagonizes the action of receptor and non-receptor-tyrosine kinases on GIV and down-regulates
124 orylation of cellular proteins including the non-receptor tyrosine kinases p125fak and Src and the ad
125 ase (FAK) potently, we explored whether this non-receptor tyrosine kinase participates in the activat
127 canonical signaling mechanisms such as Src (non-receptor tyrosine kinase), PI3K, ERK, or MAPK pathwa
129 e reported previously that Janus kinase 3, a non-receptor tyrosine kinase, plays a crucial role in AJ
132 n that binds to and is phosphorylated by the non-receptor tyrosine kinase PYK2, contains several modu
133 increase in tyrosine phosphorylation of the non-receptor tyrosine kinase, PYK2, in A7r5 cells treate
135 nsights into the mechanisms by which Abelson non-receptor tyrosine kinases relay information from axo
137 eelin activates members of the Src family of non-receptor tyrosine kinases (SFKs) and that this activ
142 d pharmacologic approaches identify that the non-receptor tyrosine kinase Src is required for FN tran
143 ownstream signalling mechanisms, such as the non-receptor tyrosine kinase Src or N-methyl-D-aspartate
146 in (LRP) was found to be a substrate for the non-receptor tyrosine kinase Src, but the physiological
147 -Cbl also acts as a ubiquitin ligase for the non-receptor tyrosine kinase Src, thereby down-regulatin
150 hysically interacts with SRC proto-oncogene, non-receptor tyrosine kinase (SRC) protein to regulate F
152 relationship between Notch and either of the non-receptor tyrosine kinases Src42A and Src64B to promo
155 ted that integrin-mediated activation of the non-receptor tyrosine kinase Syk in hematopoietic cells
156 h collagen induced a rapid activation of the non-receptor tyrosine kinase, Syk, as measured by an inc
157 vated Cdc42-associated kinase-2 (ACK-2) is a non-receptor tyrosine kinase that appears to be a highly
167 uton's tyrosine kinase (Btk) is a Tec family non-receptor tyrosine kinase that plays a critical role
168 target of the enzymatic activity of c-Abl, a non-receptor tyrosine kinase that potently activated in
171 ivated Cdc42-associated kinase-2 (ACK2) is a non-receptor tyrosine kinase that serves as a specific e
174 kinase (FAK) and its close relative Pyk2 are non-receptor tyrosine kinases that mediate adhesion sign
175 d gene) protein belongs to the Abl family of non-receptor tyrosine kinases that regulate cell motilit
176 s a novel negative regulator of receptor and non-receptor tyrosine kinases through currently undefine
177 eration, we asked whether the recruitment of non-receptor tyrosine kinases to the cytoskeleton might
181 protein Hck is a member of the Src family of non-receptor tyrosine kinases which is preferentially ex
182 he identification of cellular Src (c-Src), a non-receptor tyrosine kinase, which has since been impli
183 Btk family kinases represent new members of non-receptor tyrosine kinases, which include Btk/Atk, It
184 , encoded by the TNK2 gene, is a cytoplasmic non-receptor tyrosine kinase whose aberrant activation c