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1 ion resulting from lack of Swi/Snf chromatin remodeling activity).
2 ains both histone deacetylase and nucleosome remodeling activity.
3 quired to couple ATP hydrolysis to chromatin-remodeling activity.
4 F2 family of helicase/ATPases with chromatin remodeling activity.
5 h nicely explains its recently described DNA remodeling activity.
6 cture and was dependent on SWI/SNF chromatin remodeling activity.
7 es with barrier element-associated chromatin remodeling activity.
8 omplex from human cells displaying chromatin-remodeling activity.
9 acidic activation domains can target SWI/SNF remodeling activity.
10 n in the absence of ATP-dependent nucleosome remodeling activity.
11 nf may antagonize Ssn6p-Tup1p by controlling remodeling activity.
12 uitment of Brg1-associated SWI-SNF chromatin remodeling activity.
13 mily disaggregases possess intrinsic amyloid remodeling activity.
14 reconstitutes a NuRD complex with nucleosome remodeling activity.
15 as an allosteric effector of ALC1 nucleosome remodeling activity.
16 DNA binding protein 1 (Chd1), capable of the remodeling activity.
17 absence of two distinct types of nucleosome remodeling activity.
18 how Hsp70/Hsp40 is coupled to Hsp104 protein remodeling activity.
19 mbly via a potential ATP-dependent chromatin remodeling activity.
20 e heterohexamers surprisingly gained protein remodeling activity.
21 er highly purified Rdh54 possesses chromatin-remodeling activity.
22 migration activity while blocking other DNA remodeling activities.
23 esting tight control of its powerful protein-remodeling activities.
24 ucaryotic gene expression requires chromatin-remodeling activities.
25 ng of both histone acetylation and chromatin remodeling activities.
26 core of a subset of ATP-dependent chromatin-remodeling activities.
27 vel pathway for the recruitment of chromatin remodeling activities.
28 on or by directly inhibiting their chromatin remodeling activities.
29 e deacetylation and ATP-dependent nucleosome remodeling activities.
30 directly inhibits BRG1 ATPase and chromatin remodeling activities.
31 fications to the DNA and histones as well as remodeling activities.
32 r insulators in cells with reduced chromatin-remodeling activities.
33 but here we describe its DNA binding and DNA remodeling activities.
34 ted transcriptional regulation and chromatin remodeling activities act in the VPCs to antagonize Ras
35 ress is associated with extracellular matrix remodeling activity after myocardial infarction (MI).
38 ession requires the recruitment of chromatin remodeling activities and general transcription factors
39 ity and/or by recruitment of other chromatin remodeling activities and that this remodeling can occur
40 by virtue of their protein reactivation and remodeling activities and their capacity to target misfo
41 h as a vehicle of and a barrier to chromatin remodeling activity and built a quantitative, nonequilib
42 II complex that contains chromatin structure remodeling activity and histone acetyltransferase activi
43 D4-N alone, is essential for full nucleosome remodeling activity and is important for localizing CHD4
44 t with BAF60a in vitro has reduced chromatin-remodeling activity and reduced transcriptional activity
45 anscriptional regulatory networks, chromatin remodeling activity and, ultimately, gene expression pro
46 domain hydrolyzes ATP to cause site release (remodeling activity) and to then drive downstream transl
47 ed enhancer by directly inhibiting chromatin remodeling activity, and address the apparent paradox of
48 hromatin after ligand activation, recruits a remodeling activity, and is then lost from the template.
49 ange from subtle to complete inactivation of remodeling activity, and that mutations leading to prote
50 emonstrates that the ATP-dependent chromatin-remodeling activities are essential for the in vivo func
55 G1 binding and RNA inhibition of BRG1 ATPase/remodeling activity are promiscuous, suggesting that con
56 the mutant proteins regain partial chromatin remodeling activity as well as essentially complete DNA-
57 This effect depends upon BRG1's chromatin-remodeling activity as well as the interaction between B
59 we studied CSB's DNA-binding and nucleosome-remodeling activities at the single molecule level in re
60 uire nuclear-WASp to execute their chromatin-remodeling activity at promoters of WASp-target, immune
61 n different BM compartments in terms of bone-remodeling activity (BRA), blood volume fraction (BVF),
62 se, Glc7 phosphatase, and the RSC nucleosome remodeling activity, but not multiple other activities r
64 composition and GTP on membrane binding and remodeling activity by fluorescence confocal microscopy
66 r this protein remodeling activity while DNA remodeling activity can tolerate defective ATP hydrolysi
67 e predominant Eed complex with the chromatin remodeling activity conducive for gene regulation during
68 n addition, we have demonstrated that Mit1's remodeling activity contributes to SHREC function indepe
69 in those implicated in extracellular matrix remodeling activity, cytoskeletal network and interactio
71 evels of IgCAMs are regulated during synapse remodeling--activity-dependent regulation of IgCAM clust
72 e observed inhibition of hSWI/SNF nucleosome remodeling activity depends on the structure formed by t
73 nctions to restrict BRM-dependent nucleosome remodeling activities downstream of the promoter region.
75 hromatin after ligand activation, recruits a remodeling activity, facilitates transcription factor bi
76 esults show that LIMK is required for matrix remodeling activities for path generation by leading cel
77 report the first demonstration of chromatin remodeling activity for a member of the CHD6-9 family of
78 aken together, our data indicate a novel RNA remodeling activity for RapA, a representative of the SW
79 e role of activators in recruiting chromatin remodeling activities has been clearly demonstrated, the
80 ClpB and Hsp104 possess some innate protein remodeling activities; however, they require the collabo
82 bility that NF1 may participate in chromatin remodeling activities in addition to directly enhancing
83 te that the M-domain controls Hsp104 protein remodeling activities in an Hsp70/Hsp40-dependent manner
86 st-microbes interplay potentially determines remodeling activities in the transplanted lung, highligh
88 exes have distinct yet overlapping chromatin-remodeling activities in vitro and perform different rol
90 rsatile factors that possess significant RNA remodeling activity in addition to their canonical RNA h
91 rated higher numbers of osteoclasts and bone remodeling activity in the OFP group, accompanied by gen
95 loosely correlated with RapA's nucleic acid remodeling activity, indicating that the interaction bet
96 ion and constitute structural components and remodeling activities involved in the formation of the h
99 nal regulation, and ATP-dependent nucleosome remodeling activity is required for optimal transcriptio
101 fashion, suggesting that recruitment of the remodeling activity likely takes place during the initia
103 the last two decades suggests that chromatin-remodeling activities may have emerged by adaptation of
104 for Mi2 remodeling activity, suggesting that remodeling activity may be required for both activation
105 G1, suggesting that recruitment of chromatin remodeling activity might play a role in stimulation of
108 tagonizing the transcriptional and chromatin-remodeling activities of complexes similar to Myb-MuvB/d
110 data suggest that DNA damage recognition and remodeling activities of FANCM and FAAP24 cooperate with
111 s underlying the antifibrogenic and vascular remodeling activities of PPARgamma ligands will be neces
112 opose that the site-specific barrier and RNA remodeling activities of PPR10 are a consequence of its
113 e autoinhibition of the ATPase and chromatin-remodeling activities of Rhp26 via its interaction with
116 s a regulatory subunit to modulate chromatin remodeling activities of the Brahma complex on target ge
117 lymers that are central to the many membrane-remodeling activities of the ESCRT (endosomal sorting co
118 target the histone deacetylase and chromatin remodeling activities of the NuRD complex to specific ge
120 f acetylated histone residues, the chromatin remodeling activity of hSWI/SNF has also been shown to r
122 d the effect of histone H1 on the nucleosome remodeling activity of human SWI/SNF, an ATP-dependent c
124 Here, we examined the presumed nucleosome remodeling activity of Lsh on chromatin in the context o
125 macrophage MMP-10 in controlling the tissue remodeling activity of macrophages and moderating scar f
130 ed these and other models by quantifying the remodeling activity of SWI-SNF on arrays of (H3-H4)(2) t
131 ecognition, RPA, XPA, and XPC, stimulate the remodeling activity of SWI/SNF, which in turn stimulates
134 Because Arp8p is required for the chromatin remodeling activity of the INO80 complex, the complex ma
135 hat H2A.Z incorporation increases nucleosome remodeling activity of the largest class of mammalian re
136 ts is critically dependent on the nucleosome-remodeling activity of the mammalian SWI/SNF complex.
139 te the importance of ATP-dependent chromatin remodeling activity on inducible gene expression mediate
140 gene expression and that these two chromatin remodeling activities perform independent and overlappin
142 egradation and suggest that INO80 nucleosome remodeling activity promotes the dissociation of ubiquit
147 genes encoding plasma membrane and cell wall-remodeling activities suggested a link between two separ
148 was isolated that displays robust nucleosome remodeling activity, suggesting a separate essential rol
149 deacetylase activity is not required for Mi2 remodeling activity, suggesting that remodeling activity
150 ontaining histone deacetylase and nucleosome remodeling activities suggests a role for chromatin reor
151 e displacement from the DNA by the chromatin remodeling activity, SW1-SNF, or the histone chaperone,
153 in is emerging as a protein complex with DNA remodeling activity that acts together with several asso
154 possesses a cryptic ATP-dependent nucleosome remodeling activity that is potently activated in the pr
155 chanisms by which NKX2-1 acts with chromatin remodeling activities to regulate gene expression progra
157 f INI1, BAF155, and BAF170 to BRG1 increases remodeling activity to a level comparable to that of the
158 d that couples the activity of a nucleosome 'remodeling' activity to restriction endonuclease activit
159 rized the amyloid binding and conformational remodeling activities using an array of techniques, incl
160 suggest that PELP1 participates in chromatin remodeling activity via displacement of histone 1 in can
161 n recruitment of MEF2-SWI/SNF complex, whose remodeling activity was compromised in the absence of My
162 d histone acetylation), suggesting that BRG1 remodeling activity was directly responsible for changes
163 thin a hexamer are required for this protein remodeling activity while DNA remodeling activity can to
164 TAT peptide is able to combine cytoskeletal remodeling activity with membrane translocation activity
165 complexes displaying chromatin modifier and remodeling activities, with the capacity to alter chroma
166 otent inhibitors of bone resorption and bone remodeling activity, with limited potential for side-eff
167 ation-recognition and non-covalent chromatin remodeling activities within a single human protein.
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