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1 ted antibody to fodrin, an abundant neuronal cytoskeleton protein.
2 , an evolutionarily conserved cortical actin cytoskeleton protein.
3 association of RAFTK with paxillin, a 68-kDa cytoskeleton protein.
4 and identified the network of Rho-recruited cytoskeleton proteins.
5 actions between L1CAM and two populations of cytoskeleton proteins.
6 ownregulated genes encoded cell adhesion and cytoskeleton proteins.
8 the green fluorescent protein (GFP) and the cytoskeleton proteins Act1p (actin), Sac6p (yeast fimbri
9 tional regulator Tata-binding protein/TFIID, cytoskeleton proteins actin and 68-kD neurofilament, and
11 d organization of the three major eukaryotic cytoskeleton proteins, actin, microtubules, and intermed
14 roteoglycan that can regulate orientation of cytoskeleton proteins and improve function of dystrophic
16 signaling pathway, downregulate cancer cell cytoskeleton proteins, and block adenovirus trafficking
17 ular localization of signal transduction and cytoskeleton proteins as well as of specific regions of
18 upted, both the adaptor Protein 4.1B and the cytoskeleton protein betaII spectrin are mislocalized in
19 ith nsP3/GFP contain a high concentration of cytoskeleton proteins, chaperones, elongation factor 1A,
20 teractions between various components of the cytoskeleton proteins controlling liver and bile duct de
23 mains and a C-terminal domain that binds the cytoskeleton proteins ezrin, radixin, moesin, and merlin
24 ssed in M2 melanoma cells, lacking the actin cytoskeleton protein filamin A and in A7, a subclone of
25 h as glucose metabolism, regulation of actin cytoskeleton, protein folding, translation/ribosome, spl
27 n channel (LGIC) function and trafficking by cytoskeleton proteins has been the topic of recent resea
28 mpartments, described their interaction with cytoskeleton proteins, identified their ability to activ
30 n integrate the activities of multiple actin cytoskeleton proteins in response to varying environment
34 r suppressor gene encodes merlin, a membrane/cytoskeleton protein necessary for the maintenance of co
36 sts, of which 635 proteins were either known cytoskeleton proteins or cytoskeleton-interacting protei
39 t report that tubulin, a stable and abundant cytoskeleton protein required for cell cycle progression
40 to glial fibrillary acidic protein (GFAP), a cytoskeleton protein specifically expressed in astrocyte
41 bronectin; linker-mediated elasticity of the cytoskeleton protein spectrin; and elasticity of ankyrin
42 The interaction of Tax with small GTPase-cytoskeleton proteins, such as ras GAP1m, Rac1, Cdc42, R
43 Nestin has been shown to interact with other cytoskeleton proteins, suggesting a role in regulating c
44 t through miR-194-mediated downregulation of cytoskeleton protein talin2 in HER2-overexpressing human
46 the peptidoglycan exoskeleton together with cytoskeleton proteins that regulate septum formation and
47 mentous structures similar to the eukaryotic cytoskeleton, proteins that mediate polar chromosome anc
48 these findings identified TCoB as the third cytoskeleton protein to be nitrated and suggest a previo
50 enzymes involved in pectin modification and cytoskeleton proteins was observed at fibre initiation s
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