ライフサイエンスコーパス: remodeling activity

1 ion resulting from lack of Swi/Snf chromatin remodeling activity).

2 er highly purified Rdh54 possesses chromatin-remodeling activity.

3 ains both histone deacetylase and nucleosome remodeling activity.

4 quired to couple ATP hydrolysis to chromatin-remodeling activity.

5 F2 family of helicase/ATPases with chromatin remodeling activity.

6 h nicely explains its recently described DNA remodeling activity.

7 cture and was dependent on SWI/SNF chromatin remodeling activity.

8 hosphatase in KO mice confirmed reduced bone remodeling activity.

9 es with barrier element-associated chromatin remodeling activity.

10 omplex from human cells displaying chromatin-remodeling activity.

11 acidic activation domains can target SWI/SNF remodeling activity.

12 n in the absence of ATP-dependent nucleosome remodeling activity.

13 nf may antagonize Ssn6p-Tup1p by controlling remodeling activity.

14 nteract with RAD54 and enhance its chromatin remodeling activity.

15 ding transcripts encoding kinases with Actin remodeling activity.

16 hese mutations demonstrated markedly reduced remodeling activity.

17 uitment of Brg1-associated SWI-SNF chromatin remodeling activity.

18 sses protein domains with intrinsic membrane remodeling activity.

19 gement of diseases characterized by high ECM remodeling activity.

20 reconstitutes a NuRD complex with nucleosome remodeling activity.

21 hoinositide requirement and exert a membrane remodeling activity.

22 several OM-localized enzymes with cell wall remodeling activity.

23 mily disaggregases possess intrinsic amyloid remodeling activity.

24 as an allosteric effector of ALC1 nucleosome remodeling activity.

25 DNA binding protein 1 (Chd1), capable of the remodeling activity.

26 absence of two distinct types of nucleosome remodeling activity.

27 how Hsp70/Hsp40 is coupled to Hsp104 protein remodeling activity.

28 s, and that Sgs1 itself possesses nucleosome remodeling activity.

29 mbly via a potential ATP-dependent chromatin remodeling activity.

30 e heterohexamers surprisingly gained protein remodeling activity.

31 tions in either causing attenuated chromatin remodeling activities.

32 to the change of mechanical stimulus by bone remodeling activities.

33 migration activity while blocking other DNA remodeling activities.

34 esting tight control of its powerful protein-remodeling activities.

35 ucaryotic gene expression requires chromatin-remodeling activities.

36 ng of both histone acetylation and chromatin remodeling activities.

37 core of a subset of ATP-dependent chromatin-remodeling activities.

38 vel pathway for the recruitment of chromatin remodeling activities.

39 on or by directly inhibiting their chromatin remodeling activities.

40 e deacetylation and ATP-dependent nucleosome remodeling activities.

41 ared to the IL group, suggesting higher bone remodeling activities.

42 ariation of hormone and extracellular matrix remodeling activities.

43 directly inhibits BRG1 ATPase and chromatin remodeling activities.

44 fications to the DNA and histones as well as remodeling activities.

45 r insulators in cells with reduced chromatin-remodeling activities.

46 but here we describe its DNA binding and DNA remodeling activities.

47 ted transcriptional regulation and chromatin remodeling activities act in the VPCs to antagonize Ras

48 ress is associated with extracellular matrix remodeling activity after myocardial infarction (MI).

49 classes that may differ in their biochemical remodeling activities and biological roles.

50 readers of histone modifications, chromatin remodeling activities and DNA methylation.

51 ession requires the recruitment of chromatin remodeling activities and general transcription factors

52 ity and/or by recruitment of other chromatin remodeling activities and that this remodeling can occur

53 by virtue of their protein reactivation and remodeling activities and their capacity to target misfo

54 h as a vehicle of and a barrier to chromatin remodeling activity and built a quantitative, nonequilib

55 ations abrogate mSWI/SNF-mediated nucleosome remodeling activity and enhancer DNA accessibility witho

56 II complex that contains chromatin structure remodeling activity and histone acetyltransferase activi

57 D4-N alone, is essential for full nucleosome remodeling activity and is important for localizing CHD4

58 s increased porosity because of osteoclastic remodeling activity and may be a source of LBP due to ab

59 biota species with specialized peptidoglycan remodeling activity and muropeptide-based therapeutics m

60 t with BAF60a in vitro has reduced chromatin-remodeling activity and reduced transcriptional activity

61 hus, Xist binding inhibits BRG1's nucleosome-remodeling activity and results in expulsion of the SWI/

62 anscriptional regulatory networks, chromatin remodeling activity and, ultimately, gene expression pro

63 domain hydrolyzes ATP to cause site release (remodeling activity) and to then drive downstream transl

64 ed enhancer by directly inhibiting chromatin remodeling activity, and address the apparent paradox of

65 hromatin after ligand activation, recruits a remodeling activity, and is then lost from the template.

66 ange from subtle to complete inactivation of remodeling activity, and that mutations leading to prote

67 absence of cystinosin primarily affects bone remodeling activity, apart from the influences of the Fa

68 emonstrates that the ATP-dependent chromatin-remodeling activities are essential for the in vivo func

69 from nucleosomes, even though its ATPase and remodeling activities are intact.

70 Coordinated membrane and cytoskeletal remodeling activities are required for membrane extensio

71 Alc1 ATPase and chromatin remodeling activities are strongly activated by Parp1 an

72 nuclear envelope localization and a membrane remodeling activity are mapped to the Atg39 lumenal doma

73 hanisms by which receptors recruit chromatin-remodeling activity are not fully elucidated.

74 G1 binding and RNA inhibition of BRG1 ATPase/remodeling activity are promiscuous, suggesting that con

75 the mutant proteins regain partial chromatin remodeling activity as well as essentially complete DNA-

76 This effect depends upon BRG1's chromatin-remodeling activity as well as the interaction between B

77 eir coregulators, and multiprotein chromatin remodeling activities at target genes.

78 we studied CSB's DNA-binding and nucleosome-remodeling activities at the single molecule level in re

79 uire nuclear-WASp to execute their chromatin-remodeling activity at promoters of WASp-target, immune

80 n different BM compartments in terms of bone-remodeling activity (BRA), blood volume fraction (BVF),

81 se, Glc7 phosphatase, and the RSC nucleosome remodeling activity, but not multiple other activities r

82 ation stress and causes fork collapse due to remodeling activities by fork reversal enzymes.

83 perone system under conditions that elicited remodeling activity by ClpB alone.

84 composition and GTP on membrane binding and remodeling activity by fluorescence confocal microscopy

85 Matrix-remodeling activity by matrix metalloproteinases (MMPs)

86 al models to explain how different chromatin remodeling activities can be functionally coupled.

87 s in B-actin levels and associated chromatin remodeling activities can not only impact local chromati

88 r this protein remodeling activity while DNA remodeling activity can tolerate defective ATP hydrolysi

89 ions that alter histone binding or chromatin remodeling activities cluster in the PHD finger or the h

90 e predominant Eed complex with the chromatin remodeling activity conducive for gene regulation during

91 n addition, we have demonstrated that Mit1's remodeling activity contributes to SHREC function indepe

92 controlled transcripts involved in chromatin remodeling activities, cytokinin and cell cycle regulati

93 in those implicated in extracellular matrix remodeling activity, cytoskeletal network and interactio

94 However, chromatin remodeling activity decreased after Brm knockdown only a

95 evels of IgCAMs are regulated during synapse remodeling--activity-dependent regulation of IgCAM clust

96 e observed inhibition of hSWI/SNF nucleosome remodeling activity depends on the structure formed by t

97 Chromatin-remodeling activities directed by SWI/SNF2 superfamily c

98 nctions to restrict BRM-dependent nucleosome remodeling activities downstream of the promoter region.

99 t system regulating these opposing chromatin remodeling activities during DSB repair.

100 Chromatin remodeling activities enacted by Chd4 are essential for

101 ng in membrane stress responses and membrane remodeling activities encompassing autophagy and beyond.

102 hromatin after ligand activation, recruits a remodeling activity, facilitates transcription factor bi

103 esults show that LIMK is required for matrix remodeling activities for path generation by leading cel

104 report the first demonstration of chromatin remodeling activity for a member of the CHD6-9 family of

105 Last, we observed a decrease in membrane remodeling activity for OPA1 in lipid compositions with

106 aken together, our data indicate a novel RNA remodeling activity for RapA, a representative of the SW

107 e role of activators in recruiting chromatin remodeling activities has been clearly demonstrated, the

108 rs, but a biochemical role for ARID1A in BAF remodeling activity has not been identified.

109 erative, transcriptional, metabolic, and DNA remodeling activities; hence, their genomes are constant

110 y roles for the nucleosomal acidic patch for remodeling activity, however a role for this nucleosomal

111 ClpB and Hsp104 possess some innate protein remodeling activities; however, they require the collabo

112 To reveal how ATP-dependent chromatin remodeling activities impact DNA repair, we constructed

113 e of Sar1 regulates its membrane-binding and remodeling activities in a concentration-dependent manne

114 bility that NF1 may participate in chromatin remodeling activities in addition to directly enhancing

115 te that the M-domain controls Hsp104 protein remodeling activities in an Hsp70/Hsp40-dependent manner

116 sight into the requirement for distinct fork remodeling activities in the cell.

117 e action of the many ATP-dependent chromatin remodeling activities in the nucleus.

118 st-microbes interplay potentially determines remodeling activities in the transplanted lung, highligh

119 To understand the role of chromatin-remodeling activities in transcription, it is necessary

120 exes have distinct yet overlapping chromatin-remodeling activities in vitro and perform different rol

121 remodeling factors exhibits potent chromatin remodeling activities in vitro.

122 rsatile factors that possess significant RNA remodeling activity in addition to their canonical RNA h

123 poses latent DNA sequence-specific chromatin remodeling activity in FOXL2.

124 structions for inferring differential matrix remodeling activity in hydrogels containing encapsulated

125 rated higher numbers of osteoclasts and bone remodeling activity in the OFP group, accompanied by gen

126 PF2 subunit and exhibits enhanced nucleosome-remodeling activity in the presence of H3K56ac.

127 We show that EGCG amyloid remodeling activity in vitro is dependent on auto-oxidat

128 Mvp1 exhibits potent membrane remodeling activity in vitro, and it promotes associatio

129 t complex that shows ATP-dependent chromatin remodeling activity in vitro.

130 it's AT-hook is required in vivo for SWI/SNF remodeling activity in yeast and mouse embryonic stem ce

131 loosely correlated with RapA's nucleic acid remodeling activity, indicating that the interaction bet

132 ion and constitute structural components and remodeling activities involved in the formation of the h

133 This phospholipid remodeling activity is also observed with egg phosphatid

134 the structural basis for caveolin's membrane remodeling activity is currently unknown.

135 s a GPI-inositol deacylase and that this GPI-remodeling activity is essential for SI.

136 and mRNA structures, yet the basis for this remodeling activity is not understood.

137 We report that BRG1 remodeling activity is required for GR-mediated transact

138 nal regulation, and ATP-dependent nucleosome remodeling activity is required for optimal transcriptio

139 The model also shows that nucleosome remodeling activity is required to predict the correct N

140 Isw2 ATP-dependent chromatin-remodeling activity is targeted to early meiotic and MAT

141 We find that loss of CHD7 or its chromatin remodeling activity leads to complete absence of hair ce

142 eflective of ongoing local structural tissue remodeling activity likely involved during the transitio

143 fashion, suggesting that recruitment of the remodeling activity likely takes place during the initia

144 While chromatin remodeling activities may facilitate the accessibility o

145 the last two decades suggests that chromatin-remodeling activities may have emerged by adaptation of

146 for Mi2 remodeling activity, suggesting that remodeling activity may be required for both activation

147 G1, suggesting that recruitment of chromatin remodeling activity might play a role in stimulation of

148 To determine how these chromatin-remodeling activities negatively regulate the vulval cel

149 versatility is the result of the many actin-remodeling activities of actin-binding proteins, such as

150 ctin levels can directly influence chromatin remodeling activities of BAF and polycomb proteins.

151 hat DAG facilitates the membrane binding and remodeling activities of both EndoB and Drp1, thereby in

152 length and enhances the ATPase and chromatin remodeling activities of CHD2.

153 tagonizing the transcriptional and chromatin-remodeling activities of complexes similar to Myb-MuvB/d

154 Our data show that the remodeling activities of E108Q are strongly favored on p

155 data suggest that DNA damage recognition and remodeling activities of FANCM and FAAP24 cooperate with

156 s underlying the antifibrogenic and vascular remodeling activities of PPARgamma ligands will be neces

157 opose that the site-specific barrier and RNA remodeling activities of PPR10 are a consequence of its

158 e autoinhibition of the ATPase and chromatin-remodeling activities of Rhp26 via its interaction with

159 nf5p coordinates the assembly and nucleosome-remodeling activities of Snf-Swi.

160 one dynamics are influenced by the chromatin-remodeling activities of STH1/NPS1 and ISW2.

161 s a regulatory subunit to modulate chromatin remodeling activities of the Brahma complex on target ge

162 lymers that are central to the many membrane-remodeling activities of the ESCRT (endosomal sorting co

163 target the histone deacetylase and chromatin remodeling activities of the NuRD complex to specific ge

164 substantial interplay between the chromatin remodeling activity of BRG1 and histone acetylation.

165 eosome arrays are generated by the chromatin remodeling activity of Chd1.

166 cleosomes critically depend on the chromatin remodeling activity of FUN30.

167 f acetylated histone residues, the chromatin remodeling activity of hSWI/SNF has also been shown to r

168 ence of H1 partially inhibits the nucleosome remodeling activity of hSWI/SNF.

169 d the effect of histone H1 on the nucleosome remodeling activity of human SWI/SNF, an ATP-dependent c

170 The nucleosome remodeling activity of ISW1a was dependent on whether IS

171 Here, we examined the presumed nucleosome remodeling activity of Lsh on chromatin in the context o

172 macrophage MMP-10 in controlling the tissue remodeling activity of macrophages and moderating scar f

173 What was evident is the superior remodeling activity of ORF69, which could convert the ho

174 t the reduction of SUMO2/3 foci requires the remodeling activity of PICH.

175 This ATP-dependent remodeling activity of Rad54 appears to control subseque

176 ked the OTP stereoprobe reactivity and lipid remodeling activity of recombinant TLCD1.

177 by which GTP binding activates the membrane-remodeling activity of Sar1 remains unclear.

178 These results reveal the chromatin remodeling activity of shelterin and demonstrate that sh

179 The interplay between the remodeling activity of SMARCAD1 and histone acetylation

180 ed these and other models by quantifying the remodeling activity of SWI-SNF on arrays of (H3-H4)(2) t

181 ecognition, RPA, XPA, and XPC, stimulate the remodeling activity of SWI/SNF, which in turn stimulates

182 We present evidence suggesting that the remodeling activity of Tgfbr1 in the LPM and endoderm re

183 These data suggest that the chromatin remodeling activity of the BRM complex plays a general r

184 ome-stimulated ATPase activity and chromatin remodeling activity of the complex.

185 Because Arp8p is required for the chromatin remodeling activity of the INO80 complex, the complex ma

186 hat H2A.Z incorporation increases nucleosome remodeling activity of the largest class of mammalian re

187 ts is critically dependent on the nucleosome-remodeling activity of the mammalian SWI/SNF complex.

188 esses that might be opposed by the chromatin remodeling activity of the SWI/SNF complexes.

189 urvival, migratory, inflammatory, and matrix remodeling activity of vessel wall macrophages.

190 te the importance of ATP-dependent chromatin remodeling activity on inducible gene expression mediate

191 gene expression and that these two chromatin remodeling activities perform independent and overlappin

192 This novel actin remodeling activity progressively healed multiple micro-

193 egradation and suggest that INO80 nucleosome remodeling activity promotes the dissociation of ubiquit

194 event repositioning, implicating a chromatin remodeling activity recruited by Ace1p.

195 FOXL2C134W-dependent chromatin remodeling activity redirected glucocorticoid receptor c

196 res that govern their nucleosome binding and remodeling activities remain unknown.

197 of WhyD during exponential growth directs PG remodeling activity required for proper cell elongation

198 Many Snf2 enzymes possess chromatin-remodeling activity, requiring a functional ATPase domai

199 hyltransferase- and ATP-dependent nucleosome remodeling activities, respectively.

200 Loss of Mit1 remodeling activity results in nucleosome depletion at s

201 CHD class II nucleosome remodeling activity (specifically CHD3.1) retained by KA

202 genes encoding plasma membrane and cell wall-remodeling activities suggested a link between two separ

203 was isolated that displays robust nucleosome remodeling activity, suggesting a separate essential rol

204 deacetylase activity is not required for Mi2 remodeling activity, suggesting that remodeling activity

205 ontaining histone deacetylase and nucleosome remodeling activities suggests a role for chromatin reor

206 e displacement from the DNA by the chromatin remodeling activity, SW1-SNF, or the histone chaperone,

207 epigenetic silencing complex, with chromatin remodeling activities that repress transcription of the

208 We conclude that Hsp104 has a protein remodeling activity that acts on trapped, aggregated pro

209 in is emerging as a protein complex with DNA remodeling activity that acts together with several asso

210 possesses a cryptic ATP-dependent nucleosome remodeling activity that is potently activated in the pr

211 ium has unique peptidoglycan composition and remodeling activity through SagA, which generates smalle

212 chanisms by which NKX2-1 acts with chromatin remodeling activities to regulate gene expression progra

213 the PIP2-dependent recruitment of chromatin remodeling activities to the promoter.

214 f INI1, BAF155, and BAF170 to BRG1 increases remodeling activity to a level comparable to that of the

215 d that couples the activity of a nucleosome 'remodeling' activity to restriction endonuclease activit

216 However, our data on inflammatory and remodeling activity triggered by smoke differed signific

217 th motifs stimulate the ATPase and chromatin-remodeling activities upon binding of BRG1 to nucleosome

218 rized the amyloid binding and conformational remodeling activities using an array of techniques, incl

219 suggest that PELP1 participates in chromatin remodeling activity via displacement of histone 1 in can

220 Although its remodeling activity was characterized in vitro decades a

221 n recruitment of MEF2-SWI/SNF complex, whose remodeling activity was compromised in the absence of My

222 d histone acetylation), suggesting that BRG1 remodeling activity was directly responsible for changes

223 nhancer accessibility through its nucleosome remodeling activities, we investigated the role of the c

224 activation and RIPK1/BAF-mediated chromatin-remodeling activity were found in cells expressing non-c

225 iated ECM shows high collagen deposition and remodeling activity, which results in an increased amoun

226 thin a hexamer are required for this protein remodeling activity while DNA remodeling activity can to

227 TAT peptide is able to combine cytoskeletal remodeling activity with membrane translocation activity

228 complexes displaying chromatin modifier and remodeling activities, with the capacity to alter chroma

229 otent inhibitors of bone resorption and bone remodeling activity, with limited potential for side-eff

230 ation-recognition and non-covalent chromatin remodeling activities within a single human protein.