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1 cloning and was found to encode a Sac1p-like phosphoinositide phosphatase.
2 mechanism uncovered INP53, a gene encoding a phosphoinositide phosphatase.
3 II secreted Salmonella effector protein with phosphoinositide phosphatase activity and a distinct GTP
4                 In cell-free assays, reduced phosphoinositide phosphatase activity correlated with in
5 ty protein phosphatase and also possesses D3-phosphoinositide phosphatase activity on phosphatidylino
6 re, we show that SopB/SigD, an effector with phosphoinositide phosphatase activity, has anti-apoptoti
7 c1 proteins individually defective in either phosphoinositide phosphatase activity, or in recycling o
8                                 It acts as a phosphoinositide phosphatase and consists of an amino-te
9                In addition, we show that the phosphoinositide phosphatase and tensin homolog deleted
10 , we addressed the reverse process driven by phosphoinositide phosphatases and uncovered a key negati
11 ng enzymes, including phospholipase C (PLC), phosphoinositide phosphatase, and diacylglycerol (DAG) k
12 enzymes involved in PIP metabolism--Sac1p, a phosphoinositide phosphatase, and Vps34p and Pik1p, a PI
13 al that the main domains of VSPs and related phosphoinositide phosphatases are intrinsically modular
14 have previously identified synaptojanin 2, a phosphoinositide phosphatase, as an effector of Rac1.
15  (mtm), a Drosophila melanogaster MTM1/MTMR2 phosphoinositide phosphatase, as necessary and sufficien
16 ase (PLIP), which defines a new subfamily of phosphoinositide phosphatases clearly distinct from PTEN
17   Salmonella recruited ARNO via Arf6 and the phosphoinositide phosphatase effector SopB-induced PIP3
18 as identified and shown to encode a putative phosphoinositide phosphatase, Fig4.
19 r survival outcome in AML independent of its phosphoinositide phosphatase function.
20 tested the hypothesis that synaptojanin 1, a phosphoinositide phosphatase implicated in the endocytos
21 ng a new perspective on the function of this phosphoinositide phosphatase in health and development.
22  magnesium-activated PtdIns(3,5)P2-selective phosphoinositide phosphatase in vitro.
23    The biological relevance of most of these phosphoinositide phosphatases in acute myeloid leukemia
24 family of disease-related myotubularin (MTM) phosphoinositide phosphatases includes catalytically ina
25 ddition to recombinant versions of the Sac1p phosphoinositide-phosphatase indicated that PI(4)P was r
26 tream of PIK3CA in a manner dependent on the phosphoinositide phosphatase INPP4B.
27 ns that lack expression of synaptojanin 1, a phosphoinositide phosphatase involved in clathrin-coated
28     In LNCaP prostate cancer cells, the PTEN phosphoinositide phosphatase is inactivated, leading to
29                       Synaptojanin (Synj), a phosphoinositide phosphatase, is known to play an import
30 hosphatidylinositol 3-kinases and the PTEN 3-phosphoinositide phosphatase may coordinate G protein co
31                                    Sac1 is a phosphoinositide phosphatase of the endoplasmic reticulu
32      In contrast to previously characterized phosphoinositide phosphatases, PLIP has a preference for
33 egatively targeting the tumor suppressor and phosphoinositide phosphatase PTEN (phosphatase and tensi
34 gand found within the C-terminal tail of the phosphoinositide phosphatase PTEN revealed two discrete
35 we describe a defect in expression of the D3 phosphoinositide phosphatase, PTEN, in Jurkat and JTAg T
36                               FIG4 encodes a phosphoinositide phosphatase required for regulation of
37                  We identified the conserved phosphoinositide phosphatase Sac1 as a Drosophila VAP (D
38 functions between Sac1p and other homologous phosphoinositide phosphatases, sac1(ts) mutant cells lac
39          We analyzed the primary role of the phosphoinositide phosphatase Sac1p in Saccharomyces cere
40                                        The 5-phosphoinositide phosphatase Sac3, in which loss-of-func
41 and gene ablation in mice suggested that two phosphoinositide phosphatases, SH2 domain-containing ino
42                     Here, we report that the phosphoinositide phosphatase SopB, a Salmonella Typhimur
43 s required for proper neurotransmission, the phosphoinositide phosphatase synaptojanin 1 is a key reg
44 philin also binds the GTPase dynamin and the phosphoinositide phosphatase synaptojanin and is thought
45 ially suppressed by removing one copy of the phosphoinositide phosphatase synaptojanin, suggesting a
46 g diameters, we show that the major synaptic phosphoinositide phosphatase, synaptojanin 1 (Synj1), ac
47                  Here, we found that SopB, a phosphoinositide phosphatase that is delivered into host
48          The tumor suppressor gene PTEN is a phosphoinositide phosphatase that is inactivated by dele
49                                    FIG4 is a phosphoinositide phosphatase that is mutated in several
50                          Myotubularin is a 3-phosphoinositide phosphatase that is mutated in X-linked
51 EN suppresses tumor formation by acting as a phosphoinositide phosphatase to limit signaling by phosp

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