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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 actions between L1CAM and two populations of cytoskeleton proteins.
5 ownregulated genes encoded cell adhesion and cytoskeleton proteins.
6  and identified the network of Rho-recruited cytoskeleton proteins.
7 elective isoform of the erythrocyte membrane cytoskeleton protein 4.1R.
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
10 et cell interaction and rearrangement of the cytoskeleton proteins actin and tubulin.
11 d organization of the three major eukaryotic cytoskeleton proteins, actin, microtubules, and intermed
12 re, we found that BAG3 co-localized with the cytoskeleton protein, alpha-Tubulin, and depolymerizatio
13 erent neurotransmitters, and neuron-specific cytoskeleton proteins, among others.
14 k cortical cytoskeleton and are deficient in cytoskeleton proteins and devoid of microvilli.
15 ls induces aberrant disulfide bonds in actin cytoskeleton proteins and F-actin collapse in a SLC7A11-
16 roteoglycan that can regulate orientation of cytoskeleton proteins and improve function of dystrophic
17  that interacts with both membrane-bound and cytoskeleton proteins and with Arp2/3.
18  signaling pathway, downregulate cancer cell cytoskeleton proteins, and block adenovirus trafficking
19 on of the long isoform of a single gene, the cytoskeleton protein Ankyrin.
20 ers of synaptic activity [activity-regulated cytoskeleton protein (Arc), CaMKII and phospho-CaMKII, r
21 ular localization of signal transduction and cytoskeleton proteins as well as of specific regions of
22 NC complexes resulted in loss of microtubule cytoskeleton proteins at the nucleus and changes in nucl
23 upted, both the adaptor Protein 4.1B and the cytoskeleton protein betaII spectrin are mislocalized in
24                           In the screen, the cytoskeleton protein C27H5.2 was found to be involved in
25 ith nsP3/GFP contain a high concentration of cytoskeleton proteins, chaperones, elongation factor 1A,
26 teractions between various components of the cytoskeleton proteins controlling liver and bile duct de
27                     Adducins are a family of cytoskeleton proteins encoded by three genes (alpha, bet
28 nt protein synthesis, polysome profiles, and cytoskeleton protein expression, with minimal effects on
29  protein, probably mediating a modulation of cytoskeleton protein expression.
30 mains and a C-terminal domain that binds the cytoskeleton proteins ezrin, radixin, moesin, and merlin
31 ssed in M2 melanoma cells, lacking the actin cytoskeleton protein filamin A and in A7, a subclone of
32 h as glucose metabolism, regulation of actin cytoskeleton, protein folding, translation/ribosome, spl
33 )-spectrin, encoded by the gene Sptbn4, is a cytoskeleton protein found at nodes and the axon initial
34 ell wall synthesis proteins is guided by the cytoskeleton protein FtsZ, which assembles at mid-cell a
35 occus pneumoniae interacts directly with the cytoskeleton protein FtsZ, which places CcrZ in the midd
36            YeeV interacts with two essential cytoskeleton proteins, FtsZ and MreB.
37 n channel (LGIC) function and trafficking by cytoskeleton proteins has been the topic of recent resea
38 mpartments, described their interaction with cytoskeleton proteins, identified their ability to activ
39              Yeast Abp1p is a cortical actin cytoskeleton protein implicated in cytoskeletal regulati
40 ation causes a decrease in the expression of cytoskeleton proteins in dendrites and spines.
41 n integrate the activities of multiple actin cytoskeleton proteins in response to varying environment
42                               These putative cytoskeleton proteins include the major portions of a 43
43 gent pathways, including pyrin and the actin cytoskeleton, protein misfolding and cellular stress, NF
44  (Gp) 0.6, that interacts with the essential cytoskeleton protein MreB and inhibits its function.
45                     Normally, inhibiting the cytoskeleton protein MreB forces E. coli cells to grow a
46 r suppressor gene encodes merlin, a membrane/cytoskeleton protein necessary for the maintenance of co
47 ity, one of which is Arc (activity-regulated cytoskeleton protein or Arg3.1).
48 sts, of which 635 proteins were either known cytoskeleton proteins or cytoskeleton-interacting protei
49                                              Cytoskeleton proteins play important roles in regulating
50         Absence of the large multifunctional cytoskeleton protein plectin can simultaneously account
51 t report that tubulin, a stable and abundant cytoskeleton protein required for cell cycle progression
52 to glial fibrillary acidic protein (GFAP), a cytoskeleton protein specifically expressed in astrocyte
53 bronectin; linker-mediated elasticity of the cytoskeleton protein spectrin; and elasticity of ankyrin
54 on and evolution of dynein compared to other cytoskeleton proteins such as actin, myosin, and tubulin
55     The interaction of Tax with small GTPase-cytoskeleton proteins, such as ras GAP1m, Rac1, Cdc42, R
56 Nestin has been shown to interact with other cytoskeleton proteins, suggesting a role in regulating c
57 t through miR-194-mediated downregulation of cytoskeleton protein talin2 in HER2-overexpressing human
58 ogy to protein-tyrosine phosphatases and the cytoskeleton protein tensin.
59                       Profilin 1 (PFN1) is a cytoskeleton protein that modulates actin dynamics throu
60  the peptidoglycan exoskeleton together with cytoskeleton proteins that regulate septum formation and
61 mentous structures similar to the eukaryotic cytoskeleton, proteins that mediate polar chromosome anc
62  these findings identified TCoB as the third cytoskeleton protein to be nitrated and suggest a previo
63 of STMP molecules enhanced the resistance of cytoskeleton proteins to cold-temperature stress.
64 Our study identified genes that regulate the cytoskeleton, protein trafficking and secretion, barrier
65  interactions and the consequent decrease of cytoskeleton protein turnover.
66  enzymes involved in pectin modification and cytoskeleton proteins was observed at fibre initiation s
67 al, or slightly above normal, and additional cytoskeleton proteins were upregulated.
68                                 Centrins are cytoskeleton proteins with key roles in cell division, i
69                            Spectrins are key cytoskeleton proteins with roles in membrane integrity,