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1  factor Rgl2-mediated nucleotide exchange of Ral GTPase.
2 been shown to be effector targets for active Ral GTPases.
3 onserved regulation of Wnt signaling through Ral GTPases.
4 lular actions of activated EGF receptors and Ral-GTPases.
5 binding partners including the GAP domain of Ral GTPase Accelerating Protein alpha1 (RalGAPalpha1(GAP
6 of bi-allelic variants in RALGAPA1 (encoding Ral GTPase activating protein catalytic alpha subunit 1)
7  Sro7 activation of the exocyst in yeast and Ral GTPase activation of the exocyst in animal cells.
8 o Ras effector pathways cooperate to promote Ral-GTPase activation.
9                 Molecularly, upregulation of Ral GTPase activity and Sox9 expression underlies the ob
10 t transduces growth factor signaling to both Ral GTPase and Akt-mediated signaling cascades.
11 ing protein) complex, they limit activity of Ral GTPases and restrict anchorage-independent prolifera
12            Here we investigated the roles of Ral GTPases and their common effector exocyst complex in
13 interacts with the Ral signaling components, Ral GTPase, and the RalGDS family member Rlf.
14                                              Ral GTPases are critical effectors of Ras, yet the molec
15 ion of one or both Ral genes, we report that Ral GTPases are crucial for axonal radial sorting.
16                                              Ral GTPases are important mediators of transformation, t
17 atodes and mammary tumor cells, we show that Ral GTPases are involved in exosome biogenesis.
18                           Here, we show that RAL GTPases are necessary and sufficient to activate EGF
19                                              Ral GTPases are RAS effector molecules and by implicatio
20  of the activities of Ras members identified Ral GTPase as a key regulator during PMN activation and
21 gnised cellular and molecular contexts where RAL GTPases become essential mediators of adult tissue h
22 ugh the exocyst complex, a known effector of Ral GTPases, consistent with an exocyst-mediated functio
23 irectly binds to exocyst component Sec5 in a Ral GTPase-dependent manner.
24 )-adrenergic receptors, activated c-Src by a Ral-GTPase-dependent mechanism.
25 ld-type geranylgeranylated proteins and that Ral GTPases do not undergo alternative prenylation in re
26                                    RAS-like (RAL) GTPases function in Wnt signalling-dependent intest
27 alGDS, a Ras effector protein that activates Ral GTPases, has a second function that promotes Akt pho
28                                              Ral GTPases have been implicated as critical drivers of
29                                              Ral GTPases have been implicated as mediators of Ras-ind
30                                              Ral GTPases have been implicated in the regulation of a
31 nduced intestinal regeneration, this role of RAL GTPases impacts on EGFR-dependent tumourigenic growt
32 sistent with an exocyst-mediated function of Ral GTPases in Schwann cells.
33   Together, we identify a conserved role for RAL GTPases in the promotion of optimal Wnt signaling, w
34                               To investigate RAL GTPases in vivo, we generated null and conditional k
35            These results identify a role for Ral-GTPases in the activation of c-Src by EGF receptors
36  redistribution of the GEFs to their target, Ral-GTPases, in the plasma membrane.
37 nt or expression of constitutively activated Ral-GTPase led to tyrosine phosphorylation of Stat3 and
38 own a new post-translational modification of Ral GTPases: nondegradative ubiquitination.
39                                              Ral GTPases regulate exocyst-dependent vesicle trafficki
40 on vesicles and the plasma membrane and that Ral GTPases regulate the assembly interface of a full oc
41                                   Therefore, Ral GTPases represent new regulators of MVB formation an
42        These findings demonstrate a role for Ral-GTPase signaling in the modulation of the readily re
43                       While lack of only one Ral GTPase was dispensable for early peripheral nerve de
44                                              Ral GTPases were localized to the leading lamellipodia i
45                           Activities of both Ral GTPases were mediated through the exocyst.
46 specifically catalyze the GTP loading of the Ral GTPase when overexpressed in 293T cells.
47 at exhibited vastly improved selectivity for Ral GTPases when compared with the first-generation lead
48 n of 11 amino-terminal amino acids unique to Ral GTPases, which abolished the ability of RalA to prec
49 primary sequence to the Ras, Rap, R-Ras, and Ral GTPases, which regulate cell growth and differentiat