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1 /SLY1-20 membranes remained sensitive to Rab GDP dissociation inhibitor.
2 either on membranes or in cytosol, bound to GDP dissociation inhibitor.
3 vating protein and ARF domains, may act as a GDP dissociation inhibitor.
4 of cultured cells is not associated with Rab GDP dissociation inhibitors.
5 horylation of Rab1 disrupts interaction with GDP dissociation inhibitor 1 (GDI1), but not guanine exc
6 beta8 integrin coimmunoprecipitates with Rho-GDP dissociation inhibitor 1 (RhoGDI1), an intracellular
11 and Rho1-GDP in vitro and that Msb3 and Rho GDP dissociation inhibitor act independently but opposit
12 acts through its two GoLoco motifs to exert GDP dissociation inhibitor activity over Galpha(i) subun
14 in cell survival and proliferation, and Rho GDP dissociation inhibitor alpha (RhoGDIalpha), a member
17 ors of Gbetagamma signaling pathways, act as GDP dissociation inhibitors and negatively regulate the
18 pase substrates poly(ADP-ribose) polymerase, GDP dissociation inhibitor, and PKCdelta was observed wh
19 gration inhibitors Nme1, Nme2, and Nme3, the GDP dissociation inhibitor Arhgdib, and the metalloprote
20 s, including beta-lactate dehydrogenase, Rho GDP dissociation inhibitor beta, ATP synthase, elongatio
21 (TORC1), by its direct association with Rab GDP dissociation inhibitor beta, which likely regulates
22 TP-binding proteins of the rab family by rab GDP dissociation inhibitor completely abolishes formatio
24 inhibition of Pak1 kinase activity and Rac1-GDP-dissociation inhibitor disassociation, and inhibitio
26 ressing Rho GDIalpha, an endogenous specific GDP dissociation inhibitor for Rho family proteins, usin
27 ieved by expressing Rho GDIalpha, a specific GDP dissociation inhibitor for Rho family proteins, usin
28 that D4-GDI, an abundant hematopoietic cell GDP dissociation inhibitor for the Ras-related Rho famil
29 ates poly(ADP ribose) polymerase and D4-GDI (GDP dissociation inhibitor for the rho family), as well
30 roteins as nucleotide exchange factors or as GDP dissociation inhibitors for Galpha have been propose
31 results suggest that GPR proteins are potent GDP dissociation inhibitors for Gialpha-like Galpha subu
33 tide exchange factor (GEF, Mon1-Ccz1), a Rab-GDP dissociation inhibitor (GDI) complex (prenylated Ypt
34 s both GTPase-accelerating protein (GAP) and GDP dissociation inhibitor (GDI) functions, and eIF2B is
39 is mediated by interaction with the protein GDP dissociation inhibitor (GDI) that binds to prenylate
42 red for Rab localization and function is Rab GDP dissociation inhibitor (GDI), which is proposed to r
45 ion and GTP hydrolysis on Cdc42Hs by the Rho GDP-dissociation inhibitor (GDI) is extremely sensitive
46 structure of the bovine alpha-isoform of Rab GDP-dissociation inhibitor (GDI), which functions in ves
49 or their function appears to be regulated by GDP-dissociation inhibitors (GDI), three of which have b
51 ns that regulate the Rab GTPase cycle-Gdi1p (GDP-dissociation inhibitor [GDI]) or Gyp1p/Gyp7p (GTPase
60 -synuclein on synaptic vesicles and that the GDP dissociation inhibitor.Hsp90 complex that controls R
61 also demonstrated modulatory roles for Rac1/GDP dissociation inhibitor in glucose-stimulated insulin
63 G protein binding region of Cavce possesses "GDP dissociation inhibitor-like activity" with the same
64 Here, we report that FeoB harbors a novel GDP dissociation inhibitor-like domain that specifically
66 Ras from the PM, in a process reminiscent of GDP dissociation inhibitor-mediated membrane recycling o
68 ficient Rab3a mutant, by a dominant-negative GDP dissociation inhibitor mutant unable to recycle Rab3
69 f Cdc42-guanosine diphosphate (GDP) from Rho GDP dissociation inhibitor or for the membrane recruitme
70 genous Cdc42 from Golgi membranes by the Rho-GDP dissociation inhibitor protein fails to solubilize I
71 s morphogenesis, we overexpressed bovine Rho GDP dissociation inhibitor (Rho GDI alpha), which serves
72 kinase 5 and consequent dissociation of Rho GDP dissociation inhibitor (Rho-GDI) from an ezrin/Rho-G
73 o GTPases activity, by overexpression of Rho GDP dissociation inhibitor (Rho-GDI), inhibited the stra
75 ous Rac1 and two known binding partners, Rho GDP dissociation inhibitor (RhoGDI) and p21-activated ki
76 nts, we found that Rac1 dissociates from Rho GDP dissociation inhibitor (RhoGDI) and translocates to
80 ned SCN1 and showed that SCN1 is a RhoGTPase GDP dissociation inhibitor (RhoGDI) that spatially restr
81 mechanisms underlying the ability of the Rho-GDP dissociation inhibitor (RhoGDI) to elicit the releas
82 XIAP depends on its interaction with the Rho GDP dissociation inhibitor (RhoGDI) via the XIAP RING do
83 ycling of the Rho GTPases is mediated by Rho GDP dissociation inhibitor (RhoGDI), which forms a stabl
85 on of both RhoA and Rac1; an increase in Rho GDP-dissociation inhibitor (RhoGDI) binding in the absen
86 ecently shown that reduced expression of the GDP dissociation inhibitor, RhoGDI2, is associated with
88 volatile anesthetic, halothane, with the Rho GDP dissociation inhibitor (RhoGDIalpha), which binds th
89 uced into the cells was shown to bind to rab GDP dissociation inhibitor, suggesting that this pool of
92 b GTPases (by preincubation of vesicles with GDP dissociation inhibitor), together with cytosol immun
94 itro extraction of rab4 (but not rab11) with GDP dissociation inhibitor was severely attenuated in NP
95 ed on Rab5a and phosphorylated EEA-1 and Rab GDP dissociation inhibitor, with the latter causing Rab5
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