ライフサイエンスコーパス: non-receptor

1 1 (ACK1; also known as Tnk2, tyrosine kinase non-receptor 2) as a novel binding partner of SLP-76.

2 monstrated that protein tyrosine phosphatase non-receptor 22 (PTPN22), variants in which are associat

3 ow that inositol hexakisphosphate (IP6) is a non-receptor activator of arrestin-3 and report the stru

4 Although several non-receptor activators of heterotrimeric G proteins hav

5 view has been challenged by the discovery of non-receptor activators of trimeric G proteins.

6 Non-receptor and receptor tyrosine kinases, such as Src

7 A non-receptor assisted toxin, melittin, was selected for

8 oteins as well as by receptor-associated and non-receptor-associated tyrosine kinases.

9 nce that G proteins can also be activated by non-receptor binding partners, and they can signal from

10 IgE-Fc mutant that is trapped in the closed, non-receptor binding state via an engineered disulfide a

11 A non-receptor-binding mutant of EtxB failed to prevent di

12 , an octamer capped peptide derived from the non-receptor-binding region of urokinase plasminogen act

13 Thus, multiple residues on the non-receptor-binding side of arrestin-3 are crucial for

14 We and others have recently cloned a non-receptor, calcium-dependent tyrosine kinase (CADTK;

15 oth receptor (light-activated rhodopsin) and non-receptor (casein and phosvitin) substrates.

16 (TPA) transforms cells that overexpress the non-receptor class tyrosine kinase c-Src.

17 in-tyrosine phosphatases (RPTPs), like their non-receptor counterparts, regulate the level of phospho

18 The third describes the function of a non-receptor, cytoplasmic activator of G protein signali

19 ing AP-driven Ca(2+) influx in receptor- and non-receptor-depolarized cells.

20 proteins can bind these motifs, and they are non-receptor factors.

21 anism of G-protein activation by a family of non-receptor GEFs containing a Galpha-binding and -activ

22 Mechanistically, GIV serves as a non-receptor guanine nucleotide exchange factor (GEF) th

23 ing vesicle-associated protein) is the first non-receptor guanine nucleotide exchange factor (GEF) th

24 The non-receptor guanine nucleotide exchange factor Ric-8A c

25 We have previously demonstrated that the non-receptor guanine nucleotide exchange factor RIC8 act

26 More specifically, we found that GIV is a non-receptor guanine nucleotide exchange factor that act

27 s on members of a newly identified family of non-receptor guanine nucleotide exchange factors (GEFs),

28 i is activated in the Golgi by GIV/Girdin, a non-receptor guanine-nucleotide exchange factor (GEF).

29 out by G-protein-coupled receptors (GPCRs), non-receptor guanine-nucleotide exchange factors (GEFs)

30 -2 receptor contrasts with CAM-1 action as a non-receptor in other C. elegans Wnt pathways.

31 The non-receptor isoform of protein-tyrosine phosphatase (cy

32 rectly stimulates the activity of a purified non-receptor kinase, Bruton's tyrosine kinase (Btk), whe

33 on and subsequent putative activation of the non-receptor kinase, focal adhesion kinase (FAK).

34 ns play key regulatory roles in receptor and non-receptor kinase-initiated signaling pathways.

35 Moreover, HECL is the first non-receptor-like C-type lectin to map near the natural

36 member of a large family of sperm-expressed non-receptor-like protein-tyrosine kinases.

37 PGHS-2 gene expression through activation of non-receptor-linked protein tyrosine kinase in MC.

38 PTEN also sensitized cells to non-receptor mediated apoptosis induced by a kinase inhi

39 vation of feedback mechanisms resulting from non-receptor mediated displacement of intraneuronal dopa

40 In mammalian cells, non receptor-mediated apoptosis occurs via the cytochrom

41 in the two xenografts are consistent with a non-receptor-mediated distribution.

42 stimulus and provides a framework for other non-receptor-mediated pathways of MAPK activation.

43 s are taken up by both receptor-mediated and non-receptor-mediated pathways.

44 gests that, at least in the intestine, other non-receptor-mediated uptake systems exist.

45 endovesiculation can be achieved by simple (non-receptor-mediated) mechanical perturbation of the er

46 ors coupled to membrane receptors or through non-receptor pathways by stimuli such as heat shock, UV

47 BRK is a recently described non receptor protein tyrosine kinase whose mRNA was foun

48 GIV (a.k.a Girdin) was the first non-receptor protein for which the GEF activity was ascr

49 The c-fes locus encodes a 93-kDa non-receptor protein tyrosine kinase (Fes) that regulate

50 (interleukin-2 inducible T cell kinase) is a non-receptor protein tyrosine kinase expressed primarily

51 Tnk1/Kos1 is a non-receptor protein tyrosine kinase found to be a tumor

52 Tnk1/Kos1 is a non-receptor protein tyrosine kinase implicated in negat

53 Focal adhesion kinase (FAK) is a non-receptor protein tyrosine kinase localized at focal

54 LCK is a non-receptor protein tyrosine kinase required for signal

55 The brk gene encodes a non-receptor protein tyrosine kinase that consists of si

56 ton's tyrosine kinase (Btk), a hematopoietic non-receptor protein tyrosine kinase that is critical fo

57 Etk/BMX is a non-receptor protein tyrosine kinase that requires a fun

58 Src is a non-receptor protein tyrosine kinase, the expression and

59 CR cross-linking activates three families of non-receptor protein tyrosine kinases (PTKs) and these a

60 addition, the activity of both receptor and non-receptor protein tyrosine kinases along with numerou

61 timulating Factor (G-CSF) receptor activates non-receptor protein tyrosine kinases Lyn and Jak2.

62 dermal growth factor receptor (EGFR) and the non-receptor protein tyrosine kinases Src and Pyk2 have

63 ll antigen receptor (TCR) activates a set of non-receptor protein tyrosine kinases that assist in del

64 otein Dab1, Src and Fyn of the Src-family of non-receptor protein tyrosine kinases, and CrkL) are loc

65 osine phosphatase (HePTP) is a 38kDa class I non-receptor protein tyrosine phosphatase (PTP) that is

66 in physically associates with and degrades a non-receptor protein tyrosine phosphatase (PTPN13), and

67 Shp2 is a non-receptor protein tyrosine phosphatase containing two

68 of Corkscrew, the drosophila ortholog of the non-receptor protein tyrosine phosphatase type II (SHP2)

69 The focal adhesion (FAK) non-receptor protein-tyrosine kinase (PTK) links both ex

70 The human c-fes locus encodes a non-receptor protein-tyrosine kinase implicated in myelo

71 c-Abl is a non-receptor protein-tyrosine kinase lacking a clear phy

72 rtners and suggest a general role for BCR in non-receptor protein-tyrosine kinase regulation and sign

73 osine kinases suggests a novel mechanism for non-receptor protein-tyrosine kinase regulation.

74 gene encoding a member of the Csk family of non-receptor protein-tyrosine kinases (PTKs) in the earl

75 monstrate here that US28 signals through the non-receptor protein-tyrosine kinases Src and focal adhe

76 sion kinase (FAK) is a member of a family of non-receptor protein-tyrosine kinases that regulates int

77 an be activated by a variety of receptor and non-receptor protein-tyrosine kinases.

78 PTPN22 (Lyp), a non-receptor protein-tyrosine phosphatase, is expressed

79 decrease in the activity of the receptor and non-receptor protein-tyrosine phosphatases that down-reg

80 However, some non-receptor proteins are also GEFs.

81 ted Akt stimulation is regulated by multiple non-receptor PTK families which regulate Akt both proxim

82 ns, whose boundaries are distinct from other non-receptor PTK family members, again indicating a stru

83 differences that place it on its own amongst non-receptor PTKs.

84 le proteins, while the fusion of receptor or non-receptor sequences upstream of 537-673 afforded stab

85 s that a WW domain-mediated process, such as non-receptor signaling, protein degradation or pre-mRNA

86 , we employed pharmacological inhibitors for non-receptor Src homology-2 domain-containing protein ty

87 Here we report that non-receptor Src tyrosine kinase and the membrane protei

88 nal palmitoylation motif of proteins such as non-receptor Src-related tyrosine kinases.

89 The molecular initiators of MAPKs by non-receptor stimuli have not been described.

90 ad wild type activity in phosphorylating the non-receptor substrate tubulin.

91 by, a wide variety of nuclear receptors and non-receptor transcription factors.

92 s in the protein tyrosine phosphatase (PTP), non-receptor type 11 (PTPN11) gene that encodes the SH2

93 per was from a protein tyrosine phosphatase, non-receptor type 11 (Ptpn11) mutated allele encoding Sh

94 : a pathogenic protein tyrosine phosphatase, non-receptor type 11 (PTPN11) variant and variants of un

95 e reported that tyrosine-protein phosphatase non-receptor type 11 (SHP-2) and phosphatidylinositol 3-

96 Here, we demonstrate that PTP non-receptor type 12 (PTPN12) protects cells against abe

97 n expression of tyrosine-protein phosphatase non-receptor type 13 or FAS associated phosphatase 1 (FA

98 locus encoding protein-tyrosine phosphatase non-receptor type 2 (PTPN2) has been associated with inf

99 nase FYN (FYN), protein tyrosine phosphatase non-receptor type 2 (PTPN2), and adenylate cyclase-assoc

100 tor (IL23R) and protein tyrosine phosphatase non-receptor type 22 (PTPN22) pathways.

101 holipase D, and protein tyrosine phosphatase non-receptor type 22.

102 The human protein tyrosine phosphatase non-receptor type 4 (PTPN4) prevents cell death inductio

103 he Ptpn6 gene (protein tyrosine phosphatase, non-receptor type 6; also known as Shp-1).

104 In this study, we demonstrate that the non-receptor type protein tyrosine phosphatase 14 (PTPN1

105 e c-Yes proto-oncogene (pp62c-Yes) encodes a non-receptor-type protein tyrosine kinase (NRPTK) of the

106 t mutations in PTPN11, the gene encoding the non-receptor-type protein tyrosine phosphatase SHP-2 (sr

107 brary screening and identified Fer kinase, a non-receptor-type tyrosine kinase, as a key regulator of

108 ed receptor may initiate the cross-talk with non-receptor-type tyrosine kinases, thereby activating p

109 ion, among those the catalytically inactive, non-receptor-type tyrosine phosphatase PTPN23/HD-PTP.

110 ent or not dependent on ABL proto-oncogene 1 non-receptor tyrosine kinase (c-Abl).

111 The c-fes proto-oncogene encodes a non-receptor tyrosine kinase (Fes) that has been implica

112 The V617F mutation in the JAK2 non-receptor tyrosine kinase (JAK2V617F) is present as a

113 The emergence of a non-receptor tyrosine kinase (non-RTK), ACK1 (also known

114 Pcs is predicted to be a novel regulator of non-receptor tyrosine kinase (NRTK) signaling.

115 orylated in vitro by representatives of many non-receptor tyrosine kinase (NRTK) sub-families, sugges

116 The isolated catalytic domain of the non-receptor tyrosine kinase Abl does not show a prefere

117 Deregulation of the non-receptor tyrosine kinase ACK1 (Activated Cdc42-assoc

118 We show here that the non-receptor tyrosine kinase Ack1, previously implicated

119 We have previously shown that the Arg/Abl2 non-receptor tyrosine kinase acts downstream of the EGF

120 nism by which an adaptor protein activates a non-receptor tyrosine kinase by SH2 domain displacement.

121 Caspase-9 phosphorylation by the non-receptor tyrosine kinase c-Abl at Tyr-153 reportedly

122 The non-receptor tyrosine kinase c-Abl is activated in respo

123 The non-receptor tyrosine kinase c-Abl is also activated by

124 ronal morphogenesis, we demonstrate that the non-receptor tyrosine kinase c-Abl is an intermediary fo

125 Here, we show that the stress-signaling non-receptor tyrosine kinase c-Abl links parkin to spora

126 receptor tyrosine kinase and the downstream non-receptor tyrosine kinase c-Abl.

127 phosphorylation can also be catalyzed by the non-receptor tyrosine kinase c-Abl.

128 n by primary sperm cells was mediated by the non-receptor tyrosine kinase c-Abl.

129 pe-selective small molecule inhibitor of the non-receptor tyrosine kinase c-Src (IC(50) = 64 nM).

130 determined that tTG forms a complex with the non-receptor tyrosine kinase c-Src and PI3-kinase, and t

131 e G proteins through a pathway involving the non-receptor tyrosine kinase c-Src and the G protein Ras

132 macrophage colony-stimulating factor and the non-receptor tyrosine kinase c-Src play critical roles i

133 ubiquitination of another protooncogene, the non-receptor tyrosine kinase c-Src, as well as of itself

134 The non-receptor tyrosine kinase c-Src, hereafter referred t

135 Breast tumor kinase (Brk) is a non-receptor tyrosine kinase distantly related to the Sr

136 reviously showed that targeted expression of non-receptor tyrosine kinase Etk/BMX in mouse prostate i

137 Protein tyrosine kinase 6 (PTK6) is a non-receptor tyrosine kinase expressed in epithelial can

138 The non-receptor tyrosine kinase FAK plays a key role at sit

139 Three non-receptor tyrosine kinase families (Src, ZAP-70 and T

140 tyrosine kinase (BTK) is a member of the Tec non-receptor tyrosine kinase family that is involved in

141 ffectors for Tec and Bmx, members of the Tec non-receptor tyrosine kinase family.

142 nase-1 (FRK-1), an ortholog of the mammalian non-receptor tyrosine kinase Fer, is necessary for embry

143 The non-receptor tyrosine kinase focal adhesion kinase (FAK)

144 long cytoskeletal filaments and activate the non-receptor tyrosine kinase focal adhesion kinase, whic

145 ignaling protein, the ubiquitously expressed non-receptor tyrosine kinase focal adhesion kinase.

146 Herein, we identified a novel role for the non-receptor tyrosine kinase Fyn in regulating neuroinfl

147 ngest interaction was between MAP-2c and the non-receptor tyrosine kinase Fyn; however, MAP-2b and MA

148 The p56 Src family non-receptor tyrosine kinase has been shown to be critic

149 h tyrosine kinase 2 (PYK2) is a cytoplasmic, non-receptor tyrosine kinase implicated in multiple sign

150 Imatinib (Gleevec), a non-receptor tyrosine kinase inhibitor (nRTKI), is one o

151 The c-Abl protein is a non-receptor tyrosine kinase involved in many aspects of

152 en hMSH5 and c-Abl; the latter is a critical non-receptor tyrosine kinase involved in many critical c

153 The Ableson (Abl) non-receptor tyrosine kinase is also involved in the rem

154 The non-receptor tyrosine kinase is rapidly mobilized and ac

155 ed receptors, results in the activation of a non-receptor tyrosine kinase known as focal adhesion kin

156 Janus kinase 3 (Jak3) is a non-receptor tyrosine kinase known to be expressed in he

157 blished that BCR is a substrate for c-FES, a non-receptor tyrosine kinase linked to myeloid growth an

158 p59(fyn) is a non-receptor tyrosine kinase of the Src family that has

159 ase (FAK) potently, we explored whether this non-receptor tyrosine kinase participates in the activat

160 by Src64B mutants, linking Akap200 with the non-receptor tyrosine kinase pathway.

161 Non-receptor tyrosine kinase proline-rich protein tyrosi

162 n that binds to and is phosphorylated by the non-receptor tyrosine kinase PYK2, contains several modu

163 Spleen tyrosine kinase (Syk) is a non-receptor tyrosine kinase required for signaling from

164 ent focal adhesion kinase/Src proto-oncogene non-receptor tyrosine kinase signaling.

165 Here we show that Drosophila Shark, a non-receptor tyrosine kinase similar to mammalian Syk an

166 The non-receptor tyrosine kinase Src and receptor tyrosine k

167 The non-receptor tyrosine kinase Src is a major player in mu

168 d pharmacologic approaches identify that the non-receptor tyrosine kinase Src is required for FN tran

169 The non-receptor tyrosine kinase Src regulates resensitizati

170 in (LRP) was found to be a substrate for the non-receptor tyrosine kinase Src, but the physiological

171 -Cbl also acts as a ubiquitin ligase for the non-receptor tyrosine kinase Src, thereby down-regulatin

172 as ligand-independent EGFR activation by the non-receptor tyrosine kinase Src.

173 ted that integrin-mediated activation of the non-receptor tyrosine kinase Syk in hematopoietic cells

174 vated Cdc42-associated kinase-2 (ACK-2) is a non-receptor tyrosine kinase that appears to be a highly

175 Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase that has been extensively s

176 The brk gene encodes a non-receptor tyrosine kinase that has been found to be o

177 ACK1 is a non-receptor tyrosine kinase that has been shown to be i

178 ACK1 is a non-receptor tyrosine kinase that interacts with ubiquit

179 c-Abl is a non-receptor tyrosine kinase that is activated in human

180 ACK1 is a multidomain non-receptor tyrosine kinase that is an effector of the

181 c-Abl is a non-receptor tyrosine kinase that is involved in a varie

182 Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase that is regulated by integr

183 Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase that localizes to focal adh

184 uton's tyrosine kinase (Btk) is a Tec family non-receptor tyrosine kinase that plays a critical role

185 target of the enzymatic activity of c-Abl, a non-receptor tyrosine kinase that potently activated in

186 JAK2 is a non-receptor tyrosine kinase that regulates several cell

187 ivated Cdc42-associated kinase-2 (ACK2) is a non-receptor tyrosine kinase that serves as a specific e

188 and a putative substrate of the transforming non-receptor tyrosine kinase v-Src.

189 The c-Abl proto-oncogene is a non-receptor tyrosine kinase whose activity and localiza

190 c-Abl is a non-receptor tyrosine kinase whose activity is tightly c

191 canonical signaling mechanisms such as Src (non-receptor tyrosine kinase), PI3K, ERK, or MAPK pathwa

192 ions between the Na,K-ATPase and Src kinase (non-receptor tyrosine kinase).

193 al membrane 34) and SRC (SRC proto-oncogene, non-receptor tyrosine kinase).

194 The non-receptor tyrosine kinase, ACK1 (also known as TNK2),

195 tudy, we have identified SAM domain-carrying non-receptor tyrosine kinase, activated Cdc42-associated

196 ts with the SH3 domain of Fyn, an Src family non-receptor tyrosine kinase, and is tyrosine-phosphoryl

197 nsistent with genetic studies placing Abl, a non-receptor tyrosine kinase, and the Drosophila ortholo

198 t of the vesicular regulator, dynamin 2, the non-receptor tyrosine kinase, c-Abl, and the NADPH oxida

199 resent study, we examined the role of Fyn, a non-receptor tyrosine kinase, in microglial activation a

200 or TNK2, an ubiquitously expressed oncogenic non-receptor tyrosine kinase, integrates signals from li

201 ABI-1, a downstream target of Abl non-receptor tyrosine kinase, is a member of the WAVE re

202 Syk, a non-receptor tyrosine kinase, is an important component

203 Etk/Bmx, a member of the Tec family of non-receptor tyrosine kinase, is characterized by an N-t

204 motes signaling by causing activation of the non-receptor tyrosine kinase, JAK2, which associates wit

205 Focal adhesion kinase (FAK), a non-receptor tyrosine kinase, mediates integrin-based ce

206 e reported previously that Janus kinase 3, a non-receptor tyrosine kinase, plays a crucial role in AJ

207 increase in tyrosine phosphorylation of the non-receptor tyrosine kinase, PYK2, in A7r5 cells treate

208 However, we have reported that the non-receptor tyrosine kinase, Src, is activated by Tf to

209 h collagen induced a rapid activation of the non-receptor tyrosine kinase, Syk, as measured by an inc

210 fere with signaling by interleukin-6 and the non-receptor tyrosine kinase, v-Src.

211 he identification of cellular Src (c-Src), a non-receptor tyrosine kinase, which has since been impli

212 3 is able to repress the activity of the Brk non-receptor tyrosine kinase.

213 um-dependent, focal adhesion kinase-related, non-receptor tyrosine kinase.

214 chanism for the regulation of this important non-receptor tyrosine kinase.

215 s III phosphatidylinositol-3-kinase, and Src non-receptor tyrosine kinase.

216 Recently a number of non-receptor tyrosine kinases (for example src and abl)

217 Tec family non-receptor tyrosine kinases (Itk, Btk, Tec, Rlk and Bm

218 belson family kinases (AFKs; Abl1, Abl2) are non-receptor tyrosine kinases (NRTKs) implicated in canc

219 residues within p27 to be phosphorylated by non-receptor tyrosine kinases (NRTKs).

220 eelin activates members of the Src family of non-receptor tyrosine kinases (SFKs) and that this activ

221 ein kinase IIdelta2 (CaMKIIdelta2) activates non-receptor tyrosine kinases and EGF receptor, with a S

222 receptor tyrosine kinases, the Src family of non-receptor tyrosine kinases and the Eph receptor tyros

223 members of the Janus kinase (Jak) family of non-receptor tyrosine kinases and the signal transducers

224 d p160(v-Abl) are plasma membrane-associated non-receptor tyrosine kinases and the transforming activ

225 Recent work has shown that non-receptor tyrosine kinases and tyrosine phosphorylati

226 Abelson non-receptor tyrosine kinases are also found in mature s

227 The activities of Src-family non-receptor tyrosine kinases are regulated by structura

228 substrate of all the three major classes of non-receptor tyrosine kinases associated with the IL-2R,

229 ough members from three distinct families of non-receptor tyrosine kinases can phosphorylate PLCgamma

230 The Abelson (Abl) family of non-receptor tyrosine kinases has an important role in c

231 Tec family non-receptor tyrosine kinases have been implicated in si

232 eptor tyrosine kinases and the Abl family of non-receptor tyrosine kinases have both been implicated

233 inases (SrcFKs), a multi-functional group of non-receptor tyrosine kinases highly expressed in vascul

234 , PF-4618433) reveals a distinct subclass of non-receptor tyrosine kinases identifiable by the gateke

235 lopment and represents an emerging family of non-receptor tyrosine kinases implicated in signal trans

236 The Abl family of mammalian non-receptor tyrosine kinases includes c-Abl and Arg.

237 stimulation of VGSC, engagement of these two non-receptor tyrosine kinases involves distinct signalin

238 to-oncogenes encode 60 000 and 62 000 Dalton non-receptor tyrosine kinases of the Src family, pp60c-s

239 orylation of cellular proteins including the non-receptor tyrosine kinases p125fak and Src and the ad

240 Members of the Src family of non-receptor tyrosine kinases play a critical role in me

241 Fes/Fer non-receptor tyrosine kinases regulate cell adhesion and

242 nsights into the mechanisms by which Abelson non-receptor tyrosine kinases relay information from axo

243 relationship between Notch and either of the non-receptor tyrosine kinases Src42A and Src64B to promo

244 They are regulated by many non-receptor tyrosine kinases such as Src, Jak, Syk and

245 d gene) protein belongs to the Abl family of non-receptor tyrosine kinases that regulate cell motilit

246 s a novel negative regulator of receptor and non-receptor tyrosine kinases through currently undefine

247 eration, we asked whether the recruitment of non-receptor tyrosine kinases to the cytoskeleton might

248 Cytoskeletal binding of non-receptor tyrosine kinases was synchronous with tyros

249 protein Hck is a member of the Src family of non-receptor tyrosine kinases which is preferentially ex

250 kinase Itk is a member of the Tec family of non-receptor tyrosine kinases, and is required for signa

251 Despite high level of homology among non-receptor tyrosine kinases, different kinase families

252 Thus, these studies strongly suggest that non-receptor tyrosine kinases, in particular c-Src, may

253 cYes, a member of the Src family of non-receptor tyrosine kinases, is highly expressed in mo

254 e of signaling nodes Itk and Txk, Tec family non-receptor tyrosine kinases, mice exhibit a significan

255 by a broad spectrum of cytokines, as well as non-receptor tyrosine kinases, such as Src.

256 Btk family kinases represent new members of non-receptor tyrosine kinases, which include Btk/Atk, It

257 main containing proteins, including specific non-receptor tyrosine kinases-Abl via pY251 and C-termin

258 rged as a negative regulator of receptor and non-receptor tyrosine kinases.

259 ith a vertebrate signaling pathway involving non-receptor tyrosine kinases.

260 y ErbB-2 requires the participation of other non-receptor tyrosine kinases.

261 n signaling between these two highly related non-receptor tyrosine kinases.

262 le docking protein downstream of receptor or non-receptor tyrosine kinases.

263 s a novel negative regulator of receptor and non-receptor tyrosine kinases.

264 ways triggered by activation of receptor and non-receptor tyrosine kinases.

265 Here we report that non-receptor tyrosine phosphatase 14 (PTPN14) interacts

266 cogenic function via direct interaction with non-receptor tyrosine phosphatase 14 (PTPN14) through th

267 The non-receptor tyrosine phosphatase Ptpn11 (Shp2) is an im

268 RNA interference (RNAi) screening identified non-receptor tyrosine phosphatases (PTPNs) required for

269 osine kinases (protein-tyrosine kinases) and non-receptor tyrosine phosphatases (PTPs) have been impl

270 Bmx/Etk non-receptor tyrosine protein kinase has been implicated

271 Members of the Src family of non-receptor tyrosine protein kinases are known to be in

272 The non-receptor-tyrosine kinase c-Src is overexpressed in >

273 and S-glutathionylation within EGFR and the non-receptor-tyrosine kinase Src.

274 Non-receptor-tyrosine kinases (protein-tyrosine kinases)

275 osine phosphorylation of GIV by receptor and non-receptor-tyrosine kinases is a key step that is requ

276 SHP-1 antagonizes the action of receptor and non-receptor-tyrosine kinases on GIV and down-regulates