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1 breast tumor or metastasis suppressor, SYK (spleen tyrosine kinase).
2 hways that involved the mannose receptor and spleen tyrosine kinase.
3 (GS-9973) is an oral, selective inhibitor of spleen tyrosine kinase.
4 bulin-E crosslinking, it did not require the 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
11 n Dectin-1 pathway components phosphorylated spleen tyrosine kinase and caspase recruitment domain-co
12 compromised E-selectin-induced activation of spleen tyrosine kinase and cell adhesion to intercellula
13 ind to monocyte FcgammaRIIA, which activates spleen tyrosine kinase and leads to the generation of ti
14 activated VLA-4 adhesion via phosphorylated spleen tyrosine kinase and paxillin within focal adhesio
15 es the B-cell receptor (BCR)-related kinases spleen tyrosine kinase and phosphatidylinositol 3-kinase
16 differentiated osteoclasts are dependent on spleen tyrosine kinase and phospholipase Cgamma2 phospho
17 is in turn activates the Src family kinases, spleen tyrosine kinase and PLCgamma2, and platelet integ
19 ited upregulated tyrosine phosphorylation of spleen tyrosine kinase and several other signal transduc
20 atalytic interaction between the kinase Syk (spleen tyrosine kinase) and the substrate PLCgamma2 to e
21 ing the high-affinity IgE receptor subunits, spleen tyrosine kinase, and phospholipase C), production
22 eptor, differentially activate NF-kappaB and spleen tyrosine kinase, and stimulate the production of
23 ession of several BCR kinases including LYN, spleen tyrosine kinase, Bruton tyrosine kinase and AKT.
24 kinase inhibitors that target BCR signaling (spleen tyrosine kinase, Bruton tyrosine kinase, PI3Kdelt
25 ting of the B-cell receptor tyrosine kinases spleen tyrosine kinase, Bruton's tyrosine kinase, and ph
27 emerged that Dectin-1 is one of a number of spleen tyrosine kinase-coupled C-type lectin receptors t
28 ing reactive oxygen species, thus preventing spleen tyrosine kinase dephosphorylation and perpetuatin
30 rthermore, treatment of lymphocytes with the spleen tyrosine kinase family inhibitor piceatannol redu
31 f TULA-2 resulted in hyperphosphorylation of spleen tyrosine kinase following FcgammaRIIA activation
35 with phosphatidylinositol 3-kinase delta and spleen tyrosine kinase inhibition, this phase 2 study ev
36 ion of albumin nanoparticles loaded with the spleen tyrosine kinase inhibitor, piceatannol, which blo
38 imal B-cell receptor signaling pathway (e.g. spleen tyrosine kinase inhibitors and Bruton's tyrosine
40 identification of three series of selective spleen tyrosine kinase inhibitors that support our hypot
46 The activation of NLRP3 by heme required spleen tyrosine kinase, NADPH oxidase-2, mitochondrial r
48 n used in clinical trials (eg, inhibitors of spleen tyrosine kinase, phosphatidylinositol 3-kinase, B
49 ivation via the SFK (Src family kinase)-Syk (spleen tyrosine kinase)-PLCgamma2 (phospholipase Cgamma2
50 ton's tyrosine kinase (pBtk), phosphorylated Spleen tyrosine kinase (pSyk), and nuclear receptor Nur7
51 of Bruton's tyrosine kinase, PI3Kdelta, and spleen tyrosine kinase) represent a significant therapeu
52 ng pathway that is dependent on FcRgamma and spleen tyrosine kinase, resulting in downregulation of i
53 roles in coordinating the signaling through spleen tyrosine kinase, Src family kinases, phosphatidyl
54 hly selective pharmacologic inhibitor of the spleen tyrosine kinase Syk [PRT060318; 2-((1R,2S)-2-amin
55 r differential molecular associations of the spleen tyrosine kinase Syk that preferentially binds to
59 inescence detection to the direct sensing of spleen tyrosine kinase (Syk) activity and inhibition usi
60 Antibody-mediated TREM2 stimulation enhanced spleen tyrosine kinase (SYK) activity and uptake of Stap
62 -CD14 selectively inhibits TLR4 endocytosis, spleen tyrosine kinase (Syk) and IRF3 phosphorylation, a
63 lex led to the recruitment and activation of spleen tyrosine kinase (Syk) and phosphatidylinositol-4,
65 vealed an increased basal phosphorylation of spleen tyrosine kinase (SYK) and phospholipase Cgamma2.
67 ibition of SLE T cell activation by blocking spleen tyrosine kinase (Syk) and SLE T cell migration by
68 was necessary to sustain phosphorylation of spleen tyrosine kinase (SYK) and the B-cell linker prote
69 re upstream protein tyrosine kinases such as spleen tyrosine kinase (SyK) and the JAK family of kinas
70 lation of this tyrosine initiates binding of spleen tyrosine kinase (Syk) and triggers further downst
71 was abolished by pharmacological blockade of spleen tyrosine kinase (Syk) and was absent in Syk(-/-)
73 vidence for a previously unknown function of spleen tyrosine kinase (SYK) as a partner and posttransl
79 e sought to further evaluate the role of the spleen tyrosine kinase (Syk) in cGVHD in multiple murine
80 ssion of the intracellular signaling pathway spleen tyrosine kinase (Syk) in intestinal DCs from H. p
81 tagonizing the activities of RAF1, BRAF, and spleen tyrosine kinase (SYK) in normal B cells and CLL c
82 and colleagues describe the critical role of spleen tyrosine kinase (SYK) in paclitaxel resistance by
85 ort to the development of clinical trials of spleen tyrosine kinase (Syk) inhibition for more effecti
86 signaling pathway, PD98059 and U0126 and the spleen tyrosine kinase (Syk) inhibitor, Piceatannol.
88 n BMDCs from wild-type mice was inhibited by spleen tyrosine kinase (Syk) inhibitors and was abolishe
90 pment of a series of highly kinome-selective spleen tyrosine kinase (Syk) inhibitors with favorable d
107 ruitment in A. fumigatus phagosomes required spleen tyrosine kinase (Syk) kinase-dependent production
108 al numbers, exhibited unimpaired BCR-induced spleen tyrosine kinase (Syk) phosphorylation but reduced
110 of Mule phosphorylation by silencing of the Spleen Tyrosine Kinase (Syk) prevents its dissociation f
112 ctivation, as inhibition of the BCR-proximal spleen tyrosine kinase (SYK) reversed ERK hyperactivatio
113 We show that mmLDL induced recruitment of spleen tyrosine kinase (Syk) to a TLR4 signaling complex
117 M), leading to recruitment and activation of spleen tyrosine kinase (Syk), a kinase that is essential
119 In the present study, we concentrate on Spleen tyrosine kinase (Syk), a nonreceptor tyrosine kin
120 In this report, we assessed the role of spleen tyrosine kinase (SYK), a nonreceptor tyrosine kin
121 was applied to identify unique substrates of spleen tyrosine kinase (Syk), a protein-tyrosine kinase
123 cellular signaling proteins FcepsilonRgamma, spleen tyrosine kinase (SYK), and EWS/FLI1-Activated Tra
125 conjunction with Src family kinases (SFKs), spleen tyrosine kinase (Syk), and phospholipase gamma2 (
127 sphotyrosinylation and specifically recruits spleen tyrosine kinase (Syk), initiating cellular activa
128 dothelial selectins activate Src kinases and spleen tyrosine kinase (Syk), leading to alpha(L)beta(2)
129 tment of early signaling proteins, including spleen tyrosine kinase (Syk), linker for activation of T
130 macrophages and dendritic cells deficient in spleen tyrosine kinase (Syk), we identified a novel path
131 ITAM) phosphorylation, and activation of the spleen tyrosine kinase (SYK), which initiates downstream
133 hematosus (SLE) display increased amounts of spleen tyrosine kinase (Syk), which is involved in the a
134 s phosphorylation induces the recruitment of spleen tyrosine kinase (Syk), which is required for down
136 ell antigen receptor (BCR)-proximal effector spleen tyrosine kinase (SYK), which we identified as an
137 was TLR2-independent, involved sarcoma (SRC)-spleen tyrosine kinase (SYK)-Caspase recruitment domain-
138 up-regulated in GBM tissue samples through a spleen tyrosine kinase (SYK)-dependent activation of the
139 ymphoblastic leukemia (ALL) by targeting the spleen tyrosine kinase (SYK)-dependent antiapoptotic bla
140 erful platelet activation through a Src- and spleen tyrosine kinase (Syk)-dependent tyrosine phosphor
141 beta by fine-tuning pro-IL-1beta expression, spleen tyrosine kinase (SYK)-mediated NLRP3 activation a
155 ed by the equilibrium between kinases (e.g., spleen tyrosine kinase [Syk]) and phosphatases (e.g., Sh
156 META060 inhibited the activity of kinases (spleen tyrosine kinase [Syk], Bruton's tyrosine kinase [
157 signaling nodes (Src family tyrosine kinase, spleen tyrosine kinase [SYK], phospholipase Cgamma), but
159 contrast, levels of IgE receptor-associated spleen tyrosine kinase, Syk, were increased on day 4 (P
161 or macrophages treated with an inhibitor of spleen tyrosine kinase, the tyrosine kinase that signals
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