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1 GAP (RASA1), a negative regulator of the Ras small GTP-binding protein.
2 ting a specific role for a Rho family member small GTP-binding protein.
3 ation of ADP-ribosylation factor 6 (ARF6), a small GTP-binding protein.
4 that acts as a negative regulator of the Ras small GTP-binding protein.
5 n about which signaling events regulate this small GTP-binding protein.
6 nvolving the transcriptional activation of a small GTP-binding protein.
7 ignal transduction initiated through the Ras small GTP-binding protein.
8 ranyl and are likely members of the numerous small GTP binding proteins.
9 GTP exchange proteins for the Rab3 family of small GTP binding proteins.
10 y oncogenic member of the Ras superfamily of small GTP binding proteins.
11 cterial toxins that target the Rho family of small GTP-binding proteins.
12 the ADP ribosylation factor (ARF) family of small GTP-binding proteins.
13 kinase cascades partly regulated by upstream small GTP-binding proteins.
14 om mammals and yeast, which are activated by small GTP-binding proteins.
15 AK family, whose activities are regulated by small GTP-binding proteins.
16 which have been implicated as regulators of small GTP-binding proteins.
17 cytoskeletal locations to activate Rho-type small GTP-binding proteins.
18 R-Ras is a member of the RAS superfamily of small GTP-binding proteins.
19 the ARF (ADP-ribosylation factor) family of small GTP-binding proteins.
20 exchange of GDP for GTP on the Arf family of small GTP-binding proteins.
21 as-related RGK (Rad, Gem, and Kir) family of small GTP-binding proteins.
22 actor (GEF) for the Arf family of eukaryotic small GTP-binding proteins.
23 e exchange factors for the Rho/Rac family of small GTP-binding proteins.
24 or the proper function and activation of the small GTP-binding proteins.
25 king to the plasma membrane, in concert with small GTP-binding proteins.
26 ude a novel member of the Ras superfamily of small GTP-binding proteins, a novel Ser/Thr kinase, and
28 GTPase that is a member of the Rho family of small GTP binding proteins, acts as a key molecular swit
29 peptide derived from the NH2 terminus of the small GTP-binding protein ADP ribosylation factor 1 (ARF
33 lathrin-independent pathway regulated by the small GTP-binding protein ADP-ribosylation factor 6 (Arf
34 iched membranes requires the activation of a small GTP-binding protein, ADP ribosylation factor (ARF)
36 and is activated by protein kinase C and the small GTP-binding proteins, ADP-ribosylation factor (ARF
37 acts specifically with myristoylated ARF1, a small GTP binding protein also located in the Golgi.
38 eukaryotic organisms is under the control of small GTP-binding proteins, although the underlying mole
40 EF, thereby regulating its activity toward a small GTP-binding protein and promoting the activation o
41 nalyzed the role of several Golgi-associated small GTP-binding proteins and found that Rab43 differen
42 Rap1 is a member of the Ras superfamily of small GTP-binding proteins and has 2 isoforms, Rap1a and
43 ate how GDIs serve as negative regulators of small GTP-binding proteins and how the isoprenoid moiety
44 not involved in the interaction of Dbl with small GTP-binding proteins and is incapable of transform
45 Rap1 is a member of the Ras superfamily of small GTP-binding proteins and is localized on pancreati
48 n cytoskeletal dynamics include the Rho-like small GTP-binding proteins and their exchange factors.
49 TC21 is a member of the Ras superfamily of small GTP-binding proteins and, like Ras, has been impli
51 Several members of the rho/rac family of small GTP-binding proteins are known to regulate the dis
58 rane, we show that cellular depletion of the small GTP-binding protein ARF6 promotes the formation of
59 a guanine nucleotide exchange factor for the small GTP-binding protein Arf6 that localizes to the pos
60 ase-activating protein in hair cells for the small GTP-binding protein ARF6, known to participate in
62 gs are consistent with the proposed roles of small GTP-binding proteins as molecular switches that re
65 sm of activation for PI3K-C2alpha and that a small GTP-binding protein can activate a class II PI3K i
66 s indicate that members of the Rho family of small GTP-binding proteins can provoke the concomitant s
67 en demonstrated recently that binding of the small GTP binding protein Cdc42 is able to activate Ste2
69 factor (EGF) promotes the activation of the small GTP-binding protein Cdc42, as well as its phosphor
72 reases in Ca2+, receptor-coupled G proteins, small GTP binding proteins, ceramide metabolisms, and pr
75 ng microarray analysis reveals that RAB38, a small GTP binding protein, demonstrates a similar expres
76 s suggest that impairment of the function of small GTP-binding proteins, due to a lovastatin-induced
77 eins (alpha s, alpha q, alpha i2, alpha i3), small GTP-binding proteins, endothelial nitric oxide syn
80 ein named Rin, an incompletely characterized small GTP-binding protein expressed only in neurons.
81 idium botulinum C3 exoenzyme inactivates the small GTP-binding protein family Rho by ADP-ribosylating
87 rs of integrin activation, we identified the small GTP-binding protein, H-Ras, and its effector kinas
88 n as well as proliferation, the role of this small GTP-binding protein has not been addressed in the
91 ed by cytosolic signaling pathways involving small GTP-binding proteins, heterotrimeric G proteins, i
93 odification of a variety of proteins such as small GTP binding proteins implicated in intracellular s
94 oratories has established a role for certain small GTP-binding proteins in controlling the enzymatic
95 ba myosin I, yeast myosin I, STE20, PAK, and small GTP-binding proteins in membrane- and cytoskeleton
96 1 activation, suggesting a critical role for small GTP-binding proteins in PKD1-mediated signaling.
97 ses as a subfamily of the Ras-superfamily of small GTP-binding proteins in the development of various
99 Several laboratories have demonstrated that small GTP-binding proteins including ADP-ribosylation fa
104 ft agar, indicating that activation of these small GTP-binding proteins is required for fibroblast tr
108 ings support the concept that dysfunction of small GTP-binding proteins lead to statin-induced muscle
111 istics between heterotrimeric G proteins and small GTP binding proteins of the Ras superfamily is tha
112 These data demonstrate that one or more small GTP binding proteins of the Rho family has a centr
115 vents guanine nucleotide exchange on RhoA, a small GTP-binding protein of the rho subfamily, which is
116 Membrane trafficking is regulated in part by small GTP-binding proteins of the ADP-ribosylation facto
118 d in guanine nucleotide-exchange factors for small GTP-binding proteins of the Ras and Rho families,
120 ngers but that result from the activation of small GTP-binding proteins of the Rho family and their d
126 ctin depolymerization, we considered whether small GTP-binding proteins of the rho subfamily might pa
130 er of the GTPase-activating proteins for the small GTP-binding protein p21Rac, possesses a single cys
132 ADP-ribosylation factor (Arf) family of small GTP-binding proteins plays a central role in membr
135 ce similarity to mammalian and plant Rab2, a small GTP-binding protein, possessing several conserved
136 Rem, Rem2, Rad, and Gem/Kir (RGK) family of small GTP-binding proteins potently inhibits high voltag
137 a calcium-dependent manner, and to Tem1p, a small GTP-binding protein previously found to be require
139 the Rad, Rem, Rem2, Gem/Kir (RGK) family of small GTP-binding proteins profoundly inhibit L-type Ca(
140 This structure of a GAP-like domain for small GTP-binding proteins provides a framework for anal
141 ubcellular distribution and interaction with small GTP-binding proteins provides a mechanism to regul
142 In contrast, to H-Ras, a closely related small GTP-binding protein R-Ras has the opposite activit
148 a was concomitant with the appearance of the small GTP-binding protein Rab7 on the vacuolar membrane.
150 ion of cells requires activation of both the small GTP-binding protein Rac and Jun N-terminal kinase;
152 a signal transduction pathway involving the small GTP-binding protein Rac that leads to JNK activati
154 es are regulated in vitro and in vivo by the small GTP-binding proteins Rac and Cdc42 and lipids, suc
157 trate here that members of the Rho family of small GTP binding proteins, Rac and CDC42, act downstrea
158 such as the early growth response 1 (Egr1), small GTP binding protein Rac1 (Rac1), neurogranin (Nrgn
160 ion of a constitutively active mutant of the small GTP-binding protein rac1 (V12rac1) leads to a sign
162 P-1 production during ischemia, and that the small GTP-binding protein Rac1 and reactive oxygen speci
163 or loss of TRPC5 prevented activation of the small GTP-binding protein Rac1 and stabilized synaptopod
166 expressing a dominant negative allele of the small GTP-binding protein Rac1, which is required for ox
168 recently observed that in certain cells, the small GTP-binding proteins Rac1 and Cdc42 but not Rho re
172 to selected members of the Rho subfamily of small GTP binding proteins (Rac1, but not RhoA or Cdc42)
173 served that two members of the Rho family of small GTP-binding proteins, Rac1 and Cdc42, regulate the
174 signal transduction pathway mediated by the small GTP-binding proteins RalA and RhoA but independent
175 ress conditions requires the activity of the small GTP binding protein Ran-GSP1, but not the NLS-bind
176 a guanine nucleotide exchange factor for the small GTP-binding protein Ran, seven beta-repeat domains
179 scribes the effect of high glucose (HG) on a small GTP-binding protein, Rap1b, expression and activat
182 of NF-kappaB by osteopontin depended on the small GTP-binding protein Ras and the tyrosine kinase Sr
183 of Erk2 is preceded by the activation of the small GTP-binding protein Ras in fibronectin-adherent ce
185 l growth factor (EGF) receptor activates the small GTP-binding protein Ras, which in turn, mediates E
189 Moreover, the Ser(863) mutant prevented small GTP-binding protein Rheb from enhancing the phosph
190 ation by insulin or by overexpression of the small GTP-binding protein RheB under nutrient starvation
193 eceptors activate TRPC3 channels through the small GTP-binding protein Rho and subsequent phospholipa
194 anisms that require the participation of the small GTP-binding protein Rho and the integrity of the a
195 tidic acid (LPA) are thought to activate the small GTP-binding protein Rho based on their ability to
196 al inactivation by C. botulinum toxin of the small GTP-binding protein Rho caused a 41 +/- 12% decrea
198 ) Lbc oncoprotein specifically activates the small GTP-binding protein Rho in mammalian fibroblasts t
199 t evidence that altering the activity of the small GTP-binding protein Rho induces cadherin-mediated
201 botulinum C3 exoenzyme which inactivates the small GTP-binding protein rho p21, also inhibited tyrosi
202 protein target for the activated form of the small GTP-binding protein Rho, preferentially binds the
208 es strong evidence that m1, Galpha12 and the small GTP-binding protein RhoA are components of a novel
209 a yeast two-hybrid screen, we identified the small GTP-binding protein RhoA as a necessary component
212 rtex, directly induces the expression of the small GTP-binding protein Rnd2 in newly generated mouse
213 plasmic reticulum and the Golgi requires the small GTP-binding proteins Sar1 and Arf1 and that its gl
214 f the related Rab proteins, but not on other small GTP binding proteins such as Ran or R-Ras2/TC21.
217 thway, the post-translational prenylation of small GTP-binding proteins such as Rho and Rac, and thei
220 nd muscle cell surface is thought to involve small GTP-binding proteins such as the Rab4 protein.
221 plexes that form in response to signals from small GTP-binding proteins, such as Cdc42, Rho, and Ras.
226 ane dissociation rate of GFP-tagged K-ras, a small GTP binding protein that localizes to plasma membr
229 factors (ARFs), members of the RAS family of small GTP binding proteins that regulate various cellula
234 alian ADP-ribosylation factor 1 (mARF1) is a small GTP-binding protein that is activated by a Golgi g
236 d with the transferrin receptor and Rab11, a small GTP-binding protein that is concentrated in the pe
241 dies have shown that YPT1, which encodes the small GTP-binding protein that regulates membrane traffi
244 c42 (cell division cycle 42) is a Rho family small GTP-binding protein that works as a molecular swit
245 Rop belongs to the RHO family of Ras-related small GTP-binding proteins that are key molecular switch
247 example of a regulator of the Rho family of small GTP-binding proteins that exhibits binding to a pr
253 Gem and Rad are members of another family of small GTP binding proteins (the Rad, Gem, and Kir family
254 ering this diversity of target molecules for small GTP-binding proteins, their likely tissue specific
255 e factor that specifically activates the Rho small GTP binding protein, thus resulting in biologicall
256 nucleus makes it only the second of over 100 small GTP-binding proteins to be identified in the nucle
258 el MLK family of highly related kinases link small GTP-binding proteins to the JNK signaling pathway.
259 ther guanine nucleotide exchange factors for small GTP-binding proteins, together with the recent ide
260 Clostridium difficile toxin B (a Rho family small GTP-binding protein toxin) directly correlated wit
261 ross-talk between two distinct regulators of small GTP-binding proteins using structural and biochemi
262 NK), downstream effectors of Ras or Ras-like small GTP-binding proteins, we evaluated the role of the
263 features of cell shape rearrangement involve small GTP-binding proteins, we examined the contribution
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