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1 breast tumor or metastasis suppressor, SYK (spleen tyrosine kinase).
2 bulin-E crosslinking, it did not require the spleen tyrosine kinase.
3 hways that involved the mannose receptor and spleen tyrosine kinase.
4 (GS-9973) is an oral, selective inhibitor of spleen tyrosine kinase.
5 ing protein 9 (CARD9) disturb the subsequent spleen tyrosine kinase 2-CARD9/BCL10/MALT1-driven signal
6 n an increase in tyrosine phosphorylation of spleen tyrosine kinase, a hallmark feature of the Dectin
7 mediator release, as well as Lyn kinase and spleen tyrosine kinase activation and signaling through
12 n of proximal BCR signaling, at the level of spleen tyrosine kinase and BTK, and augmented PYK2-depen
13 n Dectin-1 pathway components phosphorylated spleen tyrosine kinase and caspase recruitment domain-co
14 compromised E-selectin-induced activation of spleen tyrosine kinase and cell adhesion to intercellula
15 ind to monocyte FcgammaRIIA, which activates spleen tyrosine kinase and leads to the generation of ti
16 activated VLA-4 adhesion via phosphorylated spleen tyrosine kinase and paxillin within focal adhesio
17 es the B-cell receptor (BCR)-related kinases spleen tyrosine kinase and phosphatidylinositol 3-kinase
18 differentiated osteoclasts are dependent on spleen tyrosine kinase and phospholipase Cgamma2 phospho
19 is in turn activates the Src family kinases, spleen tyrosine kinase and PLCgamma2, and platelet integ
21 ited upregulated tyrosine phosphorylation of spleen tyrosine kinase and several other signal transduc
22 usly reported in platelets, to phosphorylate spleen tyrosine kinase and thus increased Ca2+ influx, p
23 eased ITAM signaling based on p-Syk (phospho-spleen tyrosine kinase) and p-PLCgamma2 (phospho-phospho
24 atalytic interaction between the kinase Syk (spleen tyrosine kinase) and the substrate PLCgamma2 to e
25 eased expression of the Fc epsilon receptor, spleen tyrosine kinase, and Bruton's tyrosine kinase, pl
26 ing the high-affinity IgE receptor subunits, spleen tyrosine kinase, and phospholipase C), production
27 eptor, differentially activate NF-kappaB and spleen tyrosine kinase, and stimulate the production of
28 ity biotinylation assays, we identified SYK (spleen tyrosine kinase) as a kinase involved in DEPTOR T
29 ession of several BCR kinases including LYN, spleen tyrosine kinase, Bruton tyrosine kinase and AKT.
30 kinase inhibitors that target BCR signaling (spleen tyrosine kinase, Bruton tyrosine kinase, PI3Kdelt
31 ting of the B-cell receptor tyrosine kinases spleen tyrosine kinase, Bruton's tyrosine kinase, and ph
33 emerged that Dectin-1 is one of a number of spleen tyrosine kinase-coupled C-type lectin receptors t
34 ing reactive oxygen species, thus preventing spleen tyrosine kinase dephosphorylation and perpetuatin
36 ispectral immunofluorescence, phosphorylated-spleen tyrosine kinase expression was localized to CD163
37 rthermore, treatment of lymphocytes with the spleen tyrosine kinase family inhibitor piceatannol redu
38 f TULA-2 resulted in hyperphosphorylation of spleen tyrosine kinase following FcgammaRIIA activation
39 which after phosphorylation by SFKs recruit spleen tyrosine kinase for further signal propagation.
42 arious surface molecules, phosphorylation of spleen tyrosine kinase, induction of cytokines, and hist
44 with phosphatidylinositol 3-kinase delta and spleen tyrosine kinase inhibition, this phase 2 study ev
49 ion of albumin nanoparticles loaded with the spleen tyrosine kinase inhibitor, piceatannol, which blo
51 imal B-cell receptor signaling pathway (e.g. spleen tyrosine kinase inhibitors and Bruton's tyrosine
53 identification of three series of selective spleen tyrosine kinase inhibitors that support our hypot
59 ucing peroxisome stress and attenuating SYK (spleen tyrosine kinase)-mTOR (mammalian target of rapamy
60 The activation of NLRP3 by heme required spleen tyrosine kinase, NADPH oxidase-2, mitochondrial r
61 many cytoplasmic signaling molecules such as spleen tyrosine kinase, other kinases like Bruton's tyro
64 n used in clinical trials (eg, inhibitors of spleen tyrosine kinase, phosphatidylinositol 3-kinase, B
65 ivation via the SFK (Src family kinase)-Syk (spleen tyrosine kinase)-PLCgamma2 (phospholipase Cgamma2
66 ays validated GSK986310C as a candidate SYK (spleen tyrosine kinase) probe and X-ray crystallography
67 ton's tyrosine kinase (pBtk), phosphorylated Spleen tyrosine kinase (pSyk), and nuclear receptor Nur7
68 of Bruton's tyrosine kinase, PI3Kdelta, and spleen tyrosine kinase) represent a significant therapeu
69 ng pathway that is dependent on FcRgamma and spleen tyrosine kinase, resulting in downregulation of i
70 molecular patterns, heme training depends on spleen tyrosine kinase signal transduction pathway actin
72 002 is an oral inhibitor of the Janus kinase/spleen tyrosine kinase signaling pathways, targeting sev
74 roles in coordinating the signaling through spleen tyrosine kinase, Src family kinases, phosphatidyl
75 hly selective pharmacologic inhibitor of the spleen tyrosine kinase Syk [PRT060318; 2-((1R,2S)-2-amin
76 r differential molecular associations of the spleen tyrosine kinase Syk that preferentially binds to
78 results were obtained with mice lacking the spleen-tyrosine kinase Syk in platelets, an essential co
81 er, in macrophages, IL-17RA was required for spleen tyrosine kinase (Syk) activation upon fungal-indu
83 inescence detection to the direct sensing of spleen tyrosine kinase (Syk) activity and inhibition usi
84 Antibody-mediated TREM2 stimulation enhanced spleen tyrosine kinase (SYK) activity and uptake of Stap
85 from human basophils and mast cells requires spleen tyrosine kinase (SYK) activity, but SYK expressio
87 ovarian cancers identified hyperactivity of spleen tyrosine kinase (SYK) and EGFR, which mutually ph
88 -CD14 selectively inhibits TLR4 endocytosis, spleen tyrosine kinase (Syk) and IRF3 phosphorylation, a
89 lex led to the recruitment and activation of spleen tyrosine kinase (Syk) and phosphatidylinositol-4,
91 vealed an increased basal phosphorylation of spleen tyrosine kinase (SYK) and phospholipase Cgamma2.
93 ibition of SLE T cell activation by blocking spleen tyrosine kinase (Syk) and SLE T cell migration by
94 was necessary to sustain phosphorylation of spleen tyrosine kinase (SYK) and the B-cell linker prote
95 re upstream protein tyrosine kinases such as spleen tyrosine kinase (SyK) and the JAK family of kinas
96 lation of this tyrosine initiates binding of spleen tyrosine kinase (Syk) and triggers further downst
97 was abolished by pharmacological blockade of spleen tyrosine kinase (Syk) and was absent in Syk(-/-)
100 vidence for a previously unknown function of spleen tyrosine kinase (SYK) as a partner and posttransl
101 Using a proteomics approach, we identified spleen tyrosine kinase (Syk) as a potential target in ac
103 e used to compare WBNs to LDNs and delineate spleen tyrosine kinase (SYK) expression across neutrophi
104 l surface IgE and FceRI expression, cellular spleen tyrosine kinase (SYK) expression, IgE-mediated hi
109 e sought to further evaluate the role of the spleen tyrosine kinase (Syk) in cGVHD in multiple murine
110 estigated the implication of FcgammaRIIa and spleen tyrosine kinase (Syk) in DC activation and showed
111 ssion of the intracellular signaling pathway spleen tyrosine kinase (Syk) in intestinal DCs from H. p
112 tagonizing the activities of RAF1, BRAF, and spleen tyrosine kinase (SYK) in normal B cells and CLL c
113 and colleagues describe the critical role of spleen tyrosine kinase (SYK) in paclitaxel resistance by
115 asari et al. find a role for the nonreceptor spleen tyrosine kinase (SYK) in upstream signaling leadi
117 ort to the development of clinical trials of spleen tyrosine kinase (Syk) inhibition for more effecti
118 1) antagonists, B-adrenergic agonists, and a spleen tyrosine kinase (Syk) inhibitor were best at indi
119 antagonists, beta-adrenergic agonists, and a spleen tyrosine kinase (Syk) inhibitor were best at indi
120 signaling pathway, PD98059 and U0126 and the spleen tyrosine kinase (Syk) inhibitor, Piceatannol.
122 n BMDCs from wild-type mice was inhibited by spleen tyrosine kinase (Syk) inhibitors and was abolishe
124 pment of a series of highly kinome-selective spleen tyrosine kinase (Syk) inhibitors with favorable d
149 ruitment in A. fumigatus phagosomes required spleen tyrosine kinase (Syk) kinase-dependent production
151 oteins (total tyrosine phosphorylation), and spleen tyrosine kinase (Syk) phosphorylation after antig
152 ibits antigen-induced, FcepsilonRI-dependent spleen tyrosine kinase (Syk) phosphorylation and downstr
153 al numbers, exhibited unimpaired BCR-induced spleen tyrosine kinase (Syk) phosphorylation but reduced
156 of Mule phosphorylation by silencing of the Spleen Tyrosine Kinase (Syk) prevents its dissociation f
159 ctivation, as inhibition of the BCR-proximal spleen tyrosine kinase (SYK) reversed ERK hyperactivatio
160 xploring autoimmune diseases have shown that spleen tyrosine kinase (SYK) signalling is involved in t
161 We show that mmLDL induced recruitment of spleen tyrosine kinase (Syk) to a TLR4 signaling complex
165 M), leading to recruitment and activation of spleen tyrosine kinase (Syk), a kinase that is essential
167 In the present study, we concentrate on Spleen tyrosine kinase (Syk), a nonreceptor tyrosine kin
168 In this report, we assessed the role of spleen tyrosine kinase (SYK), a nonreceptor tyrosine kin
169 was applied to identify unique substrates of spleen tyrosine kinase (Syk), a protein-tyrosine kinase
171 cellular signaling proteins FcepsilonRgamma, spleen tyrosine kinase (SYK), and EWS/FLI1-Activated Tra
173 conjunction with Src family kinases (SFKs), spleen tyrosine kinase (Syk), and phospholipase gamma2 (
174 e, siRNA depletion of Mincle and its adaptor spleen tyrosine kinase (Syk), and Syk pharmacological in
176 ntral role of a nonreceptor tyrosine kinase, spleen tyrosine kinase (SYK), in mediating osteomyelitis
177 sphotyrosinylation and specifically recruits spleen tyrosine kinase (Syk), initiating cellular activa
178 dothelial selectins activate Src kinases and spleen tyrosine kinase (Syk), leading to alpha(L)beta(2)
179 tment of early signaling proteins, including spleen tyrosine kinase (Syk), linker for activation of T
180 arrow-derived macrophages exhibited elevated spleen tyrosine kinase (SYK), lysine methyltransferase 5
181 Inhibitors of sarcome (Src) tyrosine kinase, spleen tyrosine kinase (Syk), phosphoinositide 3-kinase
182 macrophages and dendritic cells deficient in spleen tyrosine kinase (Syk), we identified a novel path
183 ITAM) phosphorylation, and activation of the spleen tyrosine kinase (SYK), which initiates downstream
185 lipid-SH2 domain interaction inhibitors for spleen tyrosine kinase (Syk), which is implicated in hem
186 hematosus (SLE) display increased amounts of spleen tyrosine kinase (Syk), which is involved in the a
187 s phosphorylation induces the recruitment of spleen tyrosine kinase (Syk), which is required for down
189 ell antigen receptor (BCR)-proximal effector spleen tyrosine kinase (SYK), which we identified as an
190 was TLR2-independent, involved sarcoma (SRC)-spleen tyrosine kinase (SYK)-Caspase recruitment domain-
191 e lectin member 5a (Clec5a), which encodes a spleen tyrosine kinase (SYK)-coupled surface receptor, a
192 up-regulated in GBM tissue samples through a spleen tyrosine kinase (SYK)-dependent activation of the
193 ymphoblastic leukemia (ALL) by targeting the spleen tyrosine kinase (SYK)-dependent antiapoptotic bla
194 erful platelet activation through a Src- and spleen tyrosine kinase (Syk)-dependent tyrosine phosphor
195 beta by fine-tuning pro-IL-1beta expression, spleen tyrosine kinase (SYK)-mediated NLRP3 activation a
213 ed by the equilibrium between kinases (e.g., spleen tyrosine kinase [Syk]) and phosphatases (e.g., Sh
214 META060 inhibited the activity of kinases (spleen tyrosine kinase [Syk], Bruton's tyrosine kinase [
215 signaling nodes (Src family tyrosine kinase, spleen tyrosine kinase [SYK], phospholipase Cgamma), but
217 contrast, levels of IgE receptor-associated spleen tyrosine kinase, Syk, were increased on day 4 (P
219 or macrophages treated with an inhibitor of spleen tyrosine kinase, the tyrosine kinase that signals
220 n the involvement of protein tyrosine kinase spleen tyrosine kinase, they point to the role of recept