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1 Rich2 was an uncharacterized Rho-GAP protein.
2 ave investigated the properties of the Giant gap protein.
3 complex in vivo with DGAP1, a Dictyostelium GAP protein.
4 ession and does not require the diffusion of gap proteins.
5 ty, which reveals a novel mode of action for GAP proteins.
6 preference was unique to DEF-1, as other ARF GAP proteins, ACAP1, ACAP2, and ARFGAP1, were able to fu
7 ediator and an integration point between the GAP proteins and HRG-mediated signaling in breast cancer
9 are binding sites for FAK, vinculin and ARF-GAP proteins, as well as tyrosine residues that when pho
10 periments provide evidence for modulation of GAP protein-dependent response turnoff, which may also p
11 The limit functional domain of the Cdc42-GAP protein did not compete with p180 or p175 for bindin
12 acting protein 1), a novel member of the Ras-GAP protein family, facilitates dephosphorylation of ASK
13 known as DAB2IP), a novel member of the Ras-GAP protein family, mediates TNF-induced activation of A
14 E6, focal adhesion kinase, and the GIT1 ARF-GAP protein for binding to paxillin are required but not
15 anti-Galphaq/11 antibody or RGS2 protein (a GAP protein for Galphaq), followed by immunostaining to
17 with the maternal repressor Capicua and the gap protein Kruppel as the principal components of a rep
18 ndent CRMs contain clusters of sites for the gap protein Kruppel, which may limit the posterior exten
20 SRC), tyrosine phosphatases (PTP-PEST), ARF-GAP proteins (p95pkl, PAG3) and papillomavirus E6 oncopr
22 focal adhesion protein paxillin via the Arf-GAP protein paxillin kinase linker (PKL) and PIX/Cool su
23 rbol ester receptor beta2-chimaerin is a Rac-GAP protein possessing a single copy of the C1 domain, a
25 t (Gtalpha)in mice lacking the photoreceptor GAP-protein RGS9, or expressing the GTPase-deficient mut
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