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1 demonstrating the function of an additional inositol 5-phosphatase.
2 inhibitory Lyn target SH2 domain-containing inositol 5' phosphatase.
3 g tyrosine phosphatase-2, and SH2-containing inositol 5'-phosphatase.
4 y enhancing Src homology 2 domain-containing inositol 5' phosphatase 1 activity or by blocking sphing
6 The phosphatase Src homology 2-containing inositol 5'-phosphatase 1 (SHIP1) is known to exert inhi
7 if phosphorylation and SH2 domain-containing inositol 5'-phosphatase 1 activation were Src-dependent,
9 the presence of SHIP1 (SH2 domain-containing inositol 5'-phosphatase 1) and involves inhibition of Mn
10 ess SHIP-1 (Src homology 2 domain-containing inositol 5'-phosphatase 1), that CRP induces SHIP-1 stim
11 esulting activation of SH2 domain-containing inositol 5'-phosphatase 1, and consistent with this mech
12 trolling the levels of SH2 domain-containing inositol 5'-phosphatase 1, miR-155 in part maintains an
14 (SOCS1) and Src homology-2 domain-containing inositol 5-phosphatase 1 (SHIP-1) and therefore could pl
16 we identify Src homology-2 domain-containing inositol 5-phosphatase 1 (SHIP1) as a direct target of m
17 mune cells, Src homology 2 domain-containing inositol 5-phosphatase 1 (SHIP1) controls the dephosphor
19 s mediated through the SH2 domain-containing inositol 5-phosphatase 1 (SHIP1)/protein kinase B (Akt)
20 r levels of Src homology-2 domain-containing inositol 5-phosphatase 1 and were more responsive to B-c
23 gnaling inositol phosphatase, SH2-containing inositol-5-phosphatase 1 (SHIP), results in the loss of
26 we show that a deficiency of SH2-containing inositol-5'-phosphatase-1 (SHIP) in a nonhematopoietic h
27 of the inhibitory phosphatase SH2-containing-inositol-5'-phosphatase-1 (SHIP1) induces acute cell dea
28 nositide phosphatases, SH2 domain-containing inositol 5'-phosphatase 2 (SHIP2) and phosphatase and te
29 , which encodes SHIP2 (SH2-domain containing inositol 5-phosphatase 2), was previously reported to in
32 We previously have identified 15 putative inositol 5-phosphatases (5PTases) from Arabidopsis and s
38 re two similar proteins comprising a central inositol 5-phosphatase domain followed by an ASH and a R
40 s strongly inhibited by coclustering with an inositol 5-phosphatase domain to decrease local PI(4,5)P
41 Moreover, in vivo recruitment of Synj1's inositol 5-phosphatase domain to endophilin-induced memb
42 f inositol polyphosphate-5-phosphatase A, an inositol 5-phosphatase downregulated in cancer and defec
43 f synaptojanin defines it as a member of the inositol-5-phosphatase family, which includes the produc
45 ino-terminal SacI homology region, a central inositol 5'-phosphatase homology region, and a carboxyl-
46 mediated by SHIP (Src homology 2-containing inositol 5' phosphatase), in particular SHIP1, which act
49 ble recruitment to the plasma membrane of an inositol 5-phosphatase module through the rapamycin/FRB/
56 conditions that result from mutations of the inositol 5-phosphatase oculocerebrorenal syndrome of Low
57 ns, including SHC, Src homology 2-containing inositol-5-phosphatase, protein kinase C-delta, and Erk2
58 osine phosphase-2 (SHP2), and SH2 containing inositol 5'-phosphatase proteins (SHIP) induce T-cell in
59 be a comparative study of two representative inositol-5-phosphatases, Schizosaccharomyces pombe synap
61 RI on mast cells leads to recruitment of the inositol 5' phosphatase SHIP and to inhibition of mast c
63 phosphorylated, recruits the SH2-containing inositol 5'- phosphatase SHIP and the SH2-containing tyr
66 ported here, Src homology-2 (SH2)-containing inositol 5-phosphatase SHIP-1 and its adaptor Dok-1 were
70 ermine the role of src-homology 2-containing inositol 5' phosphatase (SHIP) in regulating the PI3K/Ak
75 t anti-Ig and that the SH2 domain-containing inositol 5'-phosphatase (SHIP) was recruited to the same
76 his pathway is antagonized by SH2-containing inositol 5'-phosphatase (SHIP), raising the possibility
77 hatases SHP-1, SHP-2, and the SH2 containing inositol 5'phosphatase (SHIP) to the phosphorylated Fc g
79 er germline or induced SH2 domain-containing inositol 5-phosphatase (SHIP) deficiency in the host abr
80 als lacking Src homology 2 domain-containing inositol 5-phosphatase (SHIP) display a reduction in lym
81 role of the Src homology 2 domain-containing inositol 5-phosphatase (SHIP) has been invoked in a vari
84 y which the Src homology 2 domain-containing inositol 5-phosphatase (SHIP) negatively regulates phago
85 hosphatase, Src homology domain 2-containing inositol 5-phosphatase (SHIP), for FcgammaRIIB-mediated
86 mice deficient in the SH2 domain-containing inositol 5-phosphatase (SHIP), in response to collagen r
87 itol-5-phosphatase Src homology 2-containing inositol 5-phosphatase (SHIP), which has been shown by u
91 ermine that Src homology 2 domain-containing inositol-5-phosphatase (SHIP) and CCAAT enhancer-binding
92 restricted protein Src homology 2-containing inositol-5-phosphatase (SHIP) blunts phosphatidylinosito
98 Inpp5d (Src homology 2 domain-containing inositol-5-phosphatase [Ship1])-deficient mice experienc
103 h increased PM recruitment of SH2-containing inositol 5' phosphatase (SHIP2) (a key enzyme for PI(3,4
104 de lipids, the type II SH2-domain-containing inositol 5-phosphatase (SHIP2; approved gene symbol Inpp
106 om the consumption of PtdIns 3,4,5-P3 by the inositol-5-phosphatase Src homology 2-containing inosito
107 e indicates that ex vivo B cells require the inositol 5-phosphatase, Src homology domain 2-containing
109 ) is an integral membrane protein related to inositol-5-phosphatases such as synaptojanin, a protein
112 d by the activation of SH2 domain-containing inositol 5-phosphatase that inhibits WASP activation.
115 sphatase-1 (SHP-1) and SH2 domain-containing inositol 5 phosphatase were hyperphosphorylated in GC ce
116 in (synaptojanin 1) is a recently identified inositol 5'-phosphatase, which is highly enriched in ner
117 The in vivo association of SH2-containing inositol 5'-phosphatase with IL-4Ralpha was verified by
118 he presence of a family of synaptojanin-type inositol 5'-phosphatases with different tissue and subce