コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 f the neurofibromatosis type 1 (NF1) gene, a Ras GTPase activating protein.
2 th high levels of RAS-GTP had loss of NF1, a RAS GTPase activating protein.
3 directed against either pp60(src), RhoA, or Ras GTPase-activating protein.
4 n the NF1 gene that encodes neurofibromin, a RAS GTPase-activating protein.
5 The DAB2IP tumor suppressor encodes a RAS GTPase-activating protein.
6 the NF1 gene, which encodes neurofibromin, a RAS GTPase-activating protein.
7 hoprotein reported to bind the SH3 domain of Ras GTPase-activating protein.
8 that binds to the pleckstrin domain of p120 Ras GTPase-activating protein.
9 ppressor postulated to function in part as a Ras GTPase-activating protein.
10 nositol 3'-kinase, phospholipase Cgamma, and Ras-GTPase activating protein.
11 ed CAPRI and RASAL as related Ca2+-triggered Ras GTPase-activating proteins.
13 otein (CREB) phosphorylation via RASA1 (p120 Ras GTPase-activating protein 1) down-regulation, wherea
14 rat homolog, but not its mutant defective in Ras GTPase activating protein activity, reverses miR-431
15 al known properties and functions, including Ras GTPase-activating protein activity, adenylyl cyclase
17 gene product, neurofibromin, functions as a Ras GTPase-activating protein, and has been proposed to
18 F receptors including phospholipase C gamma, Ras GTPase-activating protein, and phosphotyrosine phosp
19 The NF1 gene encodes for neurofibromin, a RAS GTPase-activating protein, and thus negatively regul
20 HB4 (ephrin receptor B4) and the RASA1 (p120 Ras GTPase-activating protein) are necessary for the dev
21 rategy and demonstrate its implementation on Ras GTPase-activating protein-binding protein 1 (G3BP1)
22 Stress granule (SG) formation mediated by Ras GTPase-activating protein-binding protein 1 (G3BP1)
23 ss granules are formed through the switch of Ras GTPase-activating protein-binding protein 1 (G3BP1)
24 s were enriched, including the SG-nucleating Ras GTPase-activating protein-binding protein 1 (G3BP1).
29 completely rescued by expression of the GAP (RAS-GTPase activating protein) domain of neurofibromin.
31 (AIP1), a recently identified member of the Ras GTPase-activating protein family, is highly expresse
34 emonstrates that the loss of DAB2IP, a novel Ras-GTPase activating protein frequently found in many c
35 calcium-promoted Ras inactivator (CAPRI), a Ras GTPase-activating protein, functions as an adaptor f
36 sential for signaling and contains a R-Ras/M-Ras GTPase activating protein (GAP) domain that is divid
38 la mutation on the interaction of H-Ras with Ras GTPase activating protein (GAP), neurofibromin 1 (NF
40 The NF1-encoded protein neurofibromin is a Ras GTPase-activating protein (GAP) and can directly lim
41 t their effects via an intracellular R-Ras/M-Ras GTPase-activating protein (GAP) domain or by activat
44 DAB2 interacting protein) is a member of the Ras GTPase-activating protein (GAP) family that has been
45 at Ras, through an effector-like function of Ras GTPase-activating protein (GAP) in neonatal cardiac
48 romoted Ras inactivator), a Ca(2+)-dependent Ras GTPase-activating protein (GAP) that switches off th
49 To distinguish between inhibition of Ras by Ras GTPase-activating protein (GAP) versus a potential e
52 ere we report that sphingosine can stimulate Ras-GTPase activating protein (GAP) activity in vitro, a
53 coded protein, neurofibromin, functions as a Ras-GTPase activating protein (GAP), nothing is known ab
54 ity of, Bruton's tyrosine kinase (Btk) and a Ras GTPase-activating protein, Gap1m, in vitro and in vi
57 he tyrosine phosphorylation of two important Ras GTPase-activating proteins (GAPs), p120 Ras-GAP and
58 ced wild-type TC21 activity in vivo and that Ras GTPase-activating proteins (GAPs; p120-GAP and NF1-G
61 novel GTPase-activating protein containing a Ras GTPase-activating protein homology domain (N terminu
62 Ras-GRF mutant containing the PH domain from Ras-GTPase-activating protein in place of its own N-term
67 ith PLCgamma, phosphatidylinositol 3-kinase, Ras GTPase-activating protein, or protein tyrosine phosp
70 -back' mutants in which association with the Ras GTPase-activating protein, phosphatidylinositol 3-ki
71 992 receptors were associated with more SOS, Ras-GTPase activating protein, phosphatidylinositol 3-ki
72 n as DAB2IP), a novel member of the Ras-GAP (Ras-GTPase-activating protein) protein family, opens its
73 ells while the phosphorylation/activation of Ras GTPase activating protein (Ras GAP) and mitogen acti
75 In the present study, we identified a novel Ras GTPase-activating protein (Ras-GAP) as an ASK1-inter
77 l abolished the association of PDGFalphar to Ras GTPase-activating protein (Ras-GAP), but it did not
78 ongly reduced by silencing expression of the Ras-GTPase activating protein (Ras-GAP) neurofibromin, a
80 we demonstrate that RASAL2, which encodes a RAS-GTPase-activating protein (RAS-GAP), is a functional
81 an include functional alteration of GTPases, Ras GTPase-activating proteins, Ras guanine exchange fac
84 effect found in our previous studies of the Ras GTPase activating protein (RasGAP) and the elongatio
86 n (G125V) in the scat Rasa3 gene, encoding a Ras GTPase activating protein (RasGAP), and elucidate th
87 One key regulator of this cascade is the Nf1 Ras GTPase activating protein (RasGAP), which attenuates
90 acted with the SH3 domain and phosphorylated Ras GTPase-activating protein (RasGAP) and upregulated R
91 aptor Grb2-associated binder-1 (GAB1) on its RAS GTPase-activating protein (RASGAP) binding sites and
92 orylation of Dok-1, augmented recruitment of Ras GTPase-activating protein (RasGAP) by Dok-1, and inh
93 AP1 as a human protein related to a putative Ras GTPase-activating protein (RasGAP) from the fission
97 of activated Ras by blocking recruitment of Ras GTPase-activating protein (RasGAP) to the plasma mem
98 otifs in the C terminus and does not bind to Ras GTPase-activating protein (RasGAP) upon phosphorylat
99 y, including Nck adaptor protein (Nck), p120-Ras GTPase-activating protein (RasGAP), and the alpha- a
101 predicted, growth-related targets, including Ras GTPase-activating protein (RasGAP), cyclin-dependent
102 peptide derived from the N2 fragment of p120 Ras GTPase-activating protein (RasGAP), sensitizes tumor
108 precisely controlled by mechanisms involving Ras GTPase activating proteins (RasGAPs) responsible for
111 Rasal, belonging to the GAP1 subfamily of Ras GTPase-activating proteins (RasGAPs) with dual RasGA
112 Nf1, a tumor suppressor gene that encodes a Ras-GTPase-activating protein, results in hyperactivity
113 We further show that nsp1 interacts with Ras GTPase-activating protein SH3 domain-binding protein
114 tors (HERs), induced expression of G3BP, the Ras GTPase-activating protein SH3 domain-binding protein
117 resis and identified by mass spectrometry as Ras-GTPase-activating protein SH3 domain-binding protein
118 teins (p85 (phosphoinositide 3-kinase), Vav, Ras-GTPase-activating protein SH3 domain-binding protein
119 that members of the Ras network of proteins, Ras-GTPase activating protein-SH3-domain-binding protein
120 Here, we describe the isolation of a novel Ras-GTPase activating protein, SynGAP, that interacts wi
122 to citron, p135 SynGAP, an abundant synaptic Ras GTPase-activating protein that can bind to all three
125 e we report the characterisation of RASAL, a Ras GTPase-activating protein that senses the frequency
127 ating protein (SynGAP) is a neuronal RasGAP (Ras GTPase-activating protein) that is selectively expre
128 as, suggesting that it may also compete with Ras GTPase-activating protein, thus contributing to the
130 alyzed GTP hydrolysis in water, Ras, and Ras.Ras-GTPase-activating protein using quantum mechanics/mo
133 ing protein homologous to mammalian synaptic Ras GTPase-activating protein, which modify daf-7 expres