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1 ast strains carrying mutations in individual phosphoinositide kinases.
2 tidylinositol and its derivatives are termed phosphoinositide kinases.
3  A2 (PLA2), but its action is independent of phosphoinositide kinase 3 (PI3K) and PI4K.
4 B2s did not result in hyperactivation of the phosphoinositide kinase-3/AKT or mitogen-activated prote
5 uction of prosurvival pathways, most notably phosphoinositide kinase-3/Akt, after oxaliplatin.
6               These two chimeras also showed phosphoinositide kinase activity in vitro when immunoads
7 most abundant and widely expressed mammalian phosphoinositide kinase activity is contributed by phosp
8 a co-factor which stimulates the activity of phosphoinositide kinases and phospholipase C (PLC) by pr
9  site of use by the concerted actions of the phosphoinositide kinases and PLC.
10       GTP-binding proteins, protein kinases, phosphoinositide kinases, and protein phosphatases all p
11 e ATP-binding core and demonstrates that all phosphoinositide kinases belong to one superfamily.
12 membrane-bound substrate and ATP shows how a phosphoinositide kinase can phosphorylate its substrate
13                         We show that diverse phosphoinositide kinases can be assayed using this appro
14      Finally, we show that several different phosphoinositide kinases colocalize with PTP-MEG2, thus
15 eceptor responsiveness, we overexpressed the phosphoinositide kinase domain of PI3K (which disrupts b
16 about the substrate selectivity of different phosphoinositide kinase families.
17  is phosphorylated by protein kinases of the phosphoinositide kinase family, including ATM, ATR or DN
18 PtdIns(3,5)P(2)-synthesizing enzyme PIKfyve (phosphoinositide kinase for position 5 containing a FYVE
19                       Our data indicate that phosphoinositide kinases have multiple roles in the regu
20 plasma membranes, where it can interact with phosphoinositide kinases implicated in actin assembly re
21 y tetanus toxin and by phenylarsine oxide, a phosphoinositide kinase inhibitor.
22                      SMG1 is a member of the phosphoinositide kinase-like kinase family of proteins t
23                  Recent studies suggest that phosphoinositide kinases may participate in intracellula
24                          Adenoviral-mediated phosphoinositide kinase overexpression significantly inc
25 hair cells and that, in conjunction with the phosphoinositide kinase PI-4Kbeta1, RHD4 regulates the a
26 ublications have reported the implication of phosphoinositide kinase PI3Kbeta in PTEN-deficient cell
27     By interacting with betaARK1 through the phosphoinositide kinase (PIK) domain, phosphoinositide 3
28  three other cortical structures, eisosomes, phosphoinositide kinase (PIK) patches, and the TORC2 com
29 itment of multiple copies of the kinase into phosphoinositide kinase (PIK) patches.
30                                The mammalian phosphoinositide kinase PIKfyve catalyzes the synthesis
31         Here we have examined whether the 5'-phosphoinositide kinase PIKfyve, reported previously to
32 rotein) in yeast-two hybrid screens with the phosphoinositide kinase PIKfyve.
33  carcinoma cell line (TCCSUP) identified the phosphoinositide kinase, PIKfyve, as a potential compone
34                                              Phosphoinositide kinases play central roles in signal tr
35 fying enzymes including sphingomyelinase and phosphoinositide kinases regulate the generation and deg
36 known as mTOR and RAFT-1) is a member of the phosphoinositide kinase related kinase family.
37                                              Phosphoinositide kinases such as PI3-kinase synthesize l
38 linositol 5-phosphate 4-kinase (dPIP4K) as a phosphoinositide kinase that regulates growth during lar
39            Here we report that PI5P4Kbeta, a phosphoinositide kinase that regulates PI(5)P levels, de
40 otein determines an important novel class of phosphoinositide kinases that seems to be targeted to sp
41 ce that cell volume increases also stimulate phosphoinositide kinases, the purpose of these studies w

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