ライフサイエンスコーパス: chromatin remodeling complex

1 ing complex termed ToRC (Toutatis-containing chromatin remodeling complex).

2 Cys) in INO80D, a subunit of the human INO80 chromatin remodeling complex.

3 litate the removal of nucleosomes by the RSC chromatin remodeling complex.

4 nits of the yeast SWI/SNF and vertebrate BAF chromatin remodeling complex.

5 e genesis of cancers driven by mutation of a chromatin remodeling complex.

6 ic loss of SMARCB1, a subunit of the SWI/SNF chromatin remodeling complex.

7 nucleosome remodeling and deacetylase (NuRD) chromatin remodeling complex.

8 ted protein Arp8 is a component of the INO80 chromatin remodeling complex.

9 18(Hamlet) subunit (Dmp18) of the SWR1/SRCAP chromatin remodeling complex.

10 and recruiting the Sin3-histone deacetylase chromatin remodeling complex.

11 nd ARP9, each encoding components of the RSC chromatin remodeling complex.

12 the switch-sucrose non-fermentable (SWI-SNF) chromatin remodeling complex.

13 nown to interact with hSNF2H to form an ISWI chromatin remodeling complex.

14 mo-1 protein, which is a subunit of the PBAF chromatin remodeling complex.

15 he epigenome as a core member of the SWI/SNF chromatin remodeling complex.

16 which encodes the BAF180 subunit of the PBAF chromatin remodeling complex.

17 transcription network by targeting the INO80 chromatin remodeling complex.

18 DPF3 (BAF45c) is a member of the BAF chromatin remodeling complex.

19 n remodelers, to form a variant of the ISW1a chromatin remodeling complex.

20 on with and likely regulation of the SWI/SNF chromatin remodeling complex.

21 velopmental regulation of the AN3-associated chromatin remodeling complex.

22 through a direct interaction with the INO80 chromatin remodeling complex.

23 of the Polycomb repressive complex 2 (PRC2) chromatin-remodeling complex.

24 o regulation at multiple levels in the INO80 chromatin-remodeling complex.

25 t on the structure and function of the INO80 chromatin-remodeling complex.

26 nent of the evolutionarily conserved SWI/SNF chromatin-remodeling complex.

27 integrity of a repressor form of the SWI/SNF chromatin-remodeling complex.

28 role in recruitment of an activating SWI/SNF chromatin-remodeling complex.

29 iptional repressor and component of the NuRD chromatin-remodeling complex.

30 modulate protein-protein interactions at the chromatin-remodeling complex.

31 bunit, MCRS1, is shared with the human INO80 chromatin-remodeling complex.

32 eterminant is Swi1, a subunit of the SWI/SNF chromatin-remodeling complex.

33 subunit of the switch/sucrose nonfermentable chromatin-remodeling complex.

34 modeling factor (NURF), a member of the ISWI chromatin-remodeling complex.

35 that is a putative member of the BAF swi/snf chromatin-remodeling complex.

36 turnover that are typically bound by the RSC chromatin-remodeling complex.

37 ranscription factors that recruit activating chromatin remodeling complexes.

38 histone posttranslational modifications, and chromatin remodeling complexes.

39 ogenic regulatory factors, microRNAs and BAF chromatin remodeling complexes.

40 atin propagation by transcription-associated chromatin remodeling complexes.

41 rum of human disorders caused by ablation of chromatin remodeling complexes.

42 ependent on Nap1l1-coupled SWI/SNF and INO80 chromatin remodeling complexes.

43 sine signaling kinases and components of the chromatin remodeling complexes.

44 which is a subunit of PBAF-specific Swi/Snf chromatin remodeling complexes.

45 onfigurations such as histone chaperones and chromatin remodeling complexes.

46 ion depends upon the antagonistic actions of chromatin remodeling complexes.

47 moved, however, by a class of ATP dependent chromatin remodeling complexes.

48 , RBBP1) as part of SIN3.histone deacetylase chromatin remodeling complexes.

49 c subset of transcriptional coactivators and chromatin remodeling complexes.

50 epressors that link transcription factors to chromatin remodeling complexes.

51 ne modifications, microRNA interactions, and chromatin remodeling complexes.

52 SMARCA2 are important components of SWI/SNF chromatin remodeling complexes.

53 on of the surrounding chromatin structure by chromatin remodeling complexes.

54 both directly and by targeting or activating chromatin-remodeling complexes.

55 al posttranslational modifications (PTMs) on chromatin-remodeling complexes.

56 catalytic subunits of the SWI/SNF family of chromatin-remodeling complexes.

57 The chromatin remodeling complex ACF helps establish the app

58 Brg1-containing SWI/SNF chromatin-remodeling complexes also play an important ro

59 The switch/sucrose non-fermentable chromatin remodeling complex, also known as the Brg1 ass

60 ATP-dependent chromatin remodeling complexes alter chromatin structure

61 ATP-dependent SWI/SNF chromatin remodeling complexes alter the structure of ch

62 ucted mammalian genetic models for the INO80 chromatin remodeling complex and investigated the impact

63 le of Mediator in recruitment of the Swi/Snf chromatin remodeling complex and its role, along with co

64 PRMT7 interacts with the BRG1-based hSWI/SNF chromatin remodeling complex and specifically methylates

65 f a "trimeric minimal RSC" (RSCt) of the RSC chromatin remodeling complex and the effect of nucleotid

66 8 genes encode proteins involved in multiple chromatin remodeling complexes and are likely to play im

67 ZNF198 and SUZ12 are components of chromatin remodeling complexes and associate with promye

68 sh a direct connection between ATP-dependent chromatin remodeling complexes and checkpoint regulation

69 and facilitates transcription by recruiting chromatin remodeling complexes and general transcription

70 These findings demonstrate interplay between chromatin remodeling complexes and histone modifications

71 functioning in a critical interface between chromatin remodeling complexes and the genome to direct

72 ar processes and are essential components of chromatin remodeling complexes and transcription factor

73 which functions as a subunit of the SWI/SNF chromatin-remodeling complex and a tumor suppressor in f

74 on is well established, but the link between chromatin-remodeling complexes and DNA repair remains un

75 eral Tat-activated kinases and by recruiting chromatin-remodeling complexes and histone-modifying enz

76 Chromatin-remodeling complexes and post-translational hi

77 tion in INO80D, a subunit of the human INO80 chromatin remodeling complex, and accelerated arterial a

78 the SWItch/Sucrose NonFermentable (SWI/SNF) chromatin remodeling complex, and analyzed its role in m

79 levant transcription factors and the SWI/SNF chromatin remodeling complex, and surprisingly, associat

80 of the nucleosome remodeling and deacetylase chromatin remodeling complex, and we demonstrate that CH

81 gh interactions with RNA-binding proteins in chromatin remodeling complexes, and modulate dynamic and

82 mutations in CHD4/Mi2b, a member of the NuRD-chromatin-remodeling complex, and TAF1, an element of th

83 cally, mitotic RCS1 associates with the NuRD chromatin-remodeling complex, and this RCS1 complex is l

84 Gene expression frequently requires chromatin-remodeling complexes, and it is assumed that t

85 ding BRG1, the ATPase subunit of the SWI/SNF chromatin remodeling complex; and appropriate genomic co

86 Subunits of the SWI/SNF chromatin remodeling complex are frequently mutated in h

87 genes encoding subunits of the SWI/SNF (BAF) chromatin remodeling complex are mutated in 20% of all h

88 ATP-dependent chromatin remodeling complexes are a notable group of ep

89 ATP-dependent SWI/SNF-like BAF chromatin remodeling complexes are emerging as key regul

90 rg/Brahma-associated factors)] ATP-dependent chromatin remodeling complexes are essential for formati

91 ATP-dependent chromatin remodeling complexes are essential for transcr

92 d that genes that encode subunits of SWI/SNF chromatin remodeling complexes are frequently mutated ac

93 nucleosome remodeling and deacetylase (NuRD) chromatin remodeling complexes are important regulators

94 Accordingly, ATP-dependent chromatin remodeling complexes are important regulators

95 in genes encoding subunits of SWI/SNF (BAF) chromatin remodeling complexes are particularly prevalen

96 at switching/sucrose nonfermenting (SWI/SNF) chromatin remodeling complexes are recruited to the Igh

97 one acetyltransferases and the BRM and Brg-1 chromatin remodeling complexes are recruited to viral IE

98 Genetic alterations of the mSWI/SNF chromatin remodeling complexes are the most frequent amo

99 Chromatin-remodeling complexes are assembled around a ca

100 Genes encoding subunits of SWI/SNF (BAF) chromatin-remodeling complexes are collectively mutated

101 ties are regulated by additional subunits of chromatin-remodeling complexes are less well understood.

102 tion of Schwann cells and implicate the NuRD chromatin remodeling complex as a requisite factor in ti

103 Here, we identify the yeast ISW1 chromatin remodeling complex as an unanticipated mRNP nu

104 Together, our findings identify the ACF chromatin-remodeling complex as a critical component in

105 t ATPase of the mammalian SWI/SNF (mSWI/SNF) chromatin remodeling complex, as being essential for the

106 fied BRG1, the ATPase subunit of the SWI/SNF chromatin-remodeling complex, as an E2F6 interacting pro

107 indicate that the growth-regulating SWI/SNF chromatin remodeling complex associated with ANGUSTIFOLI

108 with components of B-WICH, an ATP-dependent chromatin remodeling complex associated with rDNA transc

109 It recruited the SWI/SNF chromatin remodeling complex ATPase BRG1 to promote nucl

110 uitment of the SWItch/Sucrose NonFermentable chromatin remodeling complex ATPase enzyme SMARCA4 (also

111 ate that H3K4me1 augments association of the chromatin-remodeling complex BAF to enhancers in vivo an

112 BRD9 and BRD7 are part of the human SWI/SNF chromatin-remodeling complexes BAF and PBAF.

113 re is increasing evidence that ATP-dependent chromatin remodeling complexes based on the alternative

114 brahma (Brm), a subunit of the ATP-dependent chromatin-remodeling complex BRG/brahma-associated facto

115 ts recruitment of a component of the SWI/SNF chromatin remodeling complex, Brg1, and RNA polymerase I

116 incorporated into promoters by SWR-C-related chromatin remodeling complexes, but whether it is also a

117 SWI/SNF-like Brg/Brm-associated factor (BAF) chromatin remodeling complexes by creating distinct poly

118 enesis by demonstrating that disruption of a chromatin remodeling complex can largely, if not complet

119 nase activity and suggest that ATP-dependent chromatin remodeling complexes can regulate nonchromatin

120 Haploinsufficiency of ARID1B, a component of chromatin remodeling complex, causes intellectual disabi

121 1-GCN5L acetylase] and TFTC (GCN5 and TRRAP) chromatin remodeling complexes, causes the neurodegenera

122 re known to alter the composition of the BAF chromatin-remodeling complex, causing ejection and degra

123 r it resulted in increased expression of the chromatin remodeling complex CBP/p300, as well as decrea

124 The SWI/SNF chromatin remodeling complex changes the positions where

125 indings define a direct relationship between chromatin-remodeling complexes, chromatin structure, and

126 ll, Kubik et al. (2015) describe how the RSC chromatin remodeling complex collaborates with two DNA s

127 UNC13D intron 1 recruitment of STAT4 and the chromatin remodeling complex component BRG1, diminishing

128 associated factors-containing complex (PBAF) chromatin remodeling complex component BRG1-associated f

129 ither of the two subunits of a transcription/chromatin remodeling complex consisting of DAXX (death-d

130 Genes encoding subunits of the SWI/SNF chromatin-remodeling complex constitute, collectively, o

131 pe II NTE strain prevents the recruitment of chromatin remodeling complexes containing Brahma-related

132 (BAF250A) promotes the formation of SWI/SNF chromatin remodeling complexes containing BRG1 or BRM.

133 hat functions in part through recruitment of chromatin remodeling complexes containing methyl-CpG bin

134 7ac, and H4K5ac as well as by recruitment of chromatin-remodeling complex containing BRG-1.

135 60 complex (TIP60.com) is a tumor suppressor chromatin-remodeling complex containing RVB proteins.

136 SWI/SNF ATP-dependent chromatin-remodeling complexes containing either Brahma-

137 The Rsc2 subunit of the RSC chromatin remodeling complex contains an RSC-like BAH do

138 The Swi/Snf (PBAF and BAF) chromatin-remodeling complexes contribute to DNA damage-

139 Chromatin remodeling complexes control the availability

140 Among them, the ATP-dependent chromatin remodeling complexes control the chromatin arc

141 During development, trithorax group (trxG) chromatin remodeling complexes counteract repression by

142 f these genes requires their modification by chromatin remodeling complexes (CRCs), which are recruit

143 witch (SWI)/Sucrose Nonfermenting (SNF)-type chromatin-remodeling complexes (CRCs) are involved in re

144 The composition of chromatin-remodeling complexes dictates how these enzyme

145 00, CBP, PCAF, and GCN5 or the BRM and Brg-1 chromatin remodeling complexes did not diminish IE gene

146 SNF2h-based ATP-dependent chromatin remodeling complexes diverge in composition, n

147 mutants indicate an additional role for the chromatin-remodeling complex during meiosis.

148 we explore the role of the mammalian SWI/SNF chromatin-remodeling complex during spermatogenesis usin

149 ATP-dependent Brahma-associated factor (BAF) chromatin remodeling complex (esBAF).

150 The SWI/SNF chromatin remodeling complex facilitates gene transcript

151 demonstrated that LEDGF/p75 complexes with a chromatin-remodeling complex facilitates chromatin trans

152 The mammalian SWI/SNF chromatin-remodeling complex facilitates DNA access by t

153 The SWI/SNF chromatin remodeling complex family mobilizes nucleosome

154 leukemia cells require the mammalian SWI/SNF chromatin remodeling complex for their survival and aber

155 plant SWITCH/SUCROSE NONFERMENTING (SWI/SNF) chromatin remodeling complexes formed around the ATPases

156 unifying concepts on how these two opposing chromatin remodeling complexes function selectively at t

157 The INO80 chromatin remodeling complex functions in transcriptiona

158 The Swi/Snf chromatin remodeling complex functions to alter nucleoso

159 F, an evolutionarily conserved ATP-dependent chromatin-remodeling complex, has an important role in t

160 However, whether chromatin remodeling complexes have the ability to regul

161 ch37 is also associated with the human Ino80 chromatin-remodeling complex (hINO80).

162 ormone receptors mediated the association of chromatin remodeling complexes, histone modification, an

163 Our studies of the SWI/SNF chromatin remodeling complex identified that BAF250a, a

164 itching defective/sucrose nonfermenting-type chromatin remodeling complex, (iii) transcription coacti

165 catalytic subunits of distinct ATP-dependent chromatin remodeling complexes implicated in transcripti

166 ith the chromatin remodeler BRG1 and the BAF chromatin remodeling complex in brown adipocytes.

167 RSC, an essential chromatin remodeling complex in budding yeast, is involv

168 icated the role of the SWI/SNF ATP-dependent chromatin remodeling complex in nuclear excision repair

169 Recent findings have implicated the NuRD chromatin remodeling complex in the sophisticated choreo

170 t roles of the SNR1/SNF5 subunit and the Brm chromatin remodeling complex in transcription regulation

171 n appears to be regulated by Brg1-containing chromatin remodeling complexes in a partially SRF-depend

172 important roles for BAZ1B and its associated chromatin remodeling complexes in NAc in the regulation

173 nes, regulatory interactions of histones and chromatin remodeling complexes in response to dynamic an

174 ucleosome positions, which can be changed by chromatin remodeling complexes in the cell.

175 tudies highlight an unsuspected role for BAF chromatin remodeling complexes in the maintenance of HSC

176 ng defective/sucrose nonfermenting (SWI/SNF) chromatin-remodeling complex in regulating the behaviora

177 ssion, suggesting a key role for the SWI/SNF chromatin-remodeling complex in SCCOHT.

178 5 (ARP5) is a conserved subunit of the INO80 chromatin-remodeling complex in yeast and mammals.

179 c and mechanistic basis for the BRG1 and BRM chromatin-remodeling complexes in regulating gene expres

180 ing factors CTCF, RAD21, SMC3, and YY1/INO80 chromatin-remodeling complexes in repressor depletion an

181 ed factor (BAF) complexes (mammalian SWI/SNF chromatin remodeling complexes) in several human intelle

182 a polybromo protein in ATP-dependent SWI/SNF chromatin remodeling complexes, in coronary development.

183 We show that BAZ1B, a component of chromatin remodeling complexes, in the nucleus accumbens

184 re of chromatin), an abundant, ATP-dependent chromatin-remodeling complex, in the cellular response t

185 Among them, multiple subunits of the chromatin remodeling complexes including ISW1, ISW2, INO

186 the SWItch/Sucrose NonFermentable (SWI/SNF) chromatin remodeling complex, including all three putati

187 the nucleus and bind multiple components of chromatin-remodeling complexes, including Polycomb group

188 Every known SWI/SNF chromatin-remodeling complex incorporates an ARID DNA bi

189 Here, we report that the ATP-dependent chromatin remodeling complex INO80 is required for turno

190 up protein (HMGB) that is a component of the chromatin-remodeling complex INO80, which is involved in

191 Loss of the yeast Ino80 chromatin-remodeling complex (Ino80-C) moderately sensit

192 Here we show that the Ino80 chromatin remodeling complex (Ino80C) directly prevents

193 Here we show that Mot1, Ino80 chromatin remodeling complex (Ino80C), and NC2 co-locali

194 gulatory switch for other PTMs, and connects chromatin remodeling complexes into gene transcription a

195 e variant H2A.Z into nucleosomes by the SWR1 chromatin remodeling complex is a critical step in eukar

196 The mammalian SWI/SNF chromatin remodeling complex is a key player in multiple

197 The SWI/SNF chromatin remodeling complex is a master regulator of de

198 The INO80 chromatin remodeling complex is an evolutionarily conser

199 Here we found that the SWI/SNF chromatin remodeling complex is capable of regulating Me

200 The SWI/SNF chromatin remodeling complex is critical for AR transcri

201 macrophages, the mammalian Swi/Snf-like BAF chromatin remodeling complex is recruited to many TLR4 t

202 Here we show that the INO80 chromatin remodeling complex is required for oncogenic t

203 se observations suggest that prior action of chromatin remodeling complexes is necessary for the acti

204 ed to switch/sucrose nonfermenting (SWI/SNF) chromatin remodeling complexes is presented.

205 The mammalian SWI/SNF chromatin-remodeling complex is essential for the multip

206 SNF5, a core component of the SWI/SNF chromatin remodeling complex, is expressed as two isofor

207 ARID1A, a subunit of the SWI/SNF chromatin remodeling complex, is frequently mutated in c

208 al helicase of the mammalian SWI/SNF-related chromatin remodeling complex, is required for Schwann ce

209 Here, we show that INO80, a chromatin remodeling complex, is required for SE-mediate

210 , an accessory subunit of the ISWI family of chromatin remodeling complexes, is upregulated in the nu

211 BAF47), a core subunit of the SWI/SNF (BAF) chromatin-remodeling complex, is inactivated in nearly a

212 t of the Brg1/Brahma-associated factor (BAF) chromatin-remodeling complex, is required in NCCs to dir

213 hat BRG1, which is the core subunit of eight chromatin-remodeling complexes, is essential not only fo

214 The chromatin remodeling complex Isw2 from Saccharomyces cer

215 he composition of a SIN3.histone deacetylase chromatin remodeling complex, leads to altered gene expr

216 The SWI/SNF chromatin-remodeling complex links the positive and nega

217 s suggest that the proteasome and the hINO80 chromatin-remodeling complex may cooperate to regulate t

218 e further propose that guiding ATP-dependent chromatin-remodeling complexes may be a more general fun

219 chromatin regulators, including the neuronal chromatin remodeling complex (nBAF) component SS18L1 (al

220 activation of other individual ATP-dependent chromatin remodeling complexes negligibly affects report

221 c studies in fruit flies have implicated the chromatin remodeling complex nucleosome remodeling facto

222 TA-1, its cofactor FOG-1, and the associated chromatin remodeling complex NuRD in the developmental s

223 iral gene expression by interacting with the chromatin remodeling complex NuRD.

224 d cells and MK requires interaction with the chromatin remodeling complex NuRD.

225 ssembly and remodeling factor) ATP-dependent chromatin-remodeling complex, occurring in the nucleus a

226 cleosome remodeling and deacetylation (NuRD) chromatin remodeling complex opposes this transcriptiona

227 This activity is provided by chromatin remodeling complexes, or remodelers, which are

228 nteractions between individual ATP-dependent chromatin remodeling complexes play critical role in bot

229 Here we show that the SWI/SNF chromatin-remodeling complex plays a critical role in or

230 We also identified that the BAP chromatin-remodeling complex probably functions cooperat

231 iochemical and structural studies of the RSC chromatin-remodeling complex prompt a proposal for the r

232 ATP-dependent chromatin remodeling complexes rearrange nucleosomes by

233 Here we show that the RSC chromatin remodeling complex recruits budding yeast Scc2

234 However, how chromatin remodeling complexes regulate DNA damage check

235 ied that the Osa-containing SWI/SNF (Brahma) chromatin-remodeling complex regulates Drosophila midgut

236 The mammalian SWI/SNF chromatin-remodeling complex regulates nucleosome packag

237 ons, cells have evolved a set of specialized chromatin remodeling complexes (remodelers).

238 t that the combined action of activators and chromatin remodeling complexes remove the -1 nucleosome

239 nnel, and ataxin-7 (ATXN7), a component of a chromatin-remodeling complex, respectively.

240 H3K14ac have a higher affinity for purified chromatin remodeling complex RSC (Remodels the Structure

241 protein interacts with SNF2H to form an ISWI chromatin remodeling complex, RSF.

242 us loss-of-function mutations in the SWI/SNF chromatin-remodeling complex subunit gene SMARCE1.

243 ATP-dependent chromatin remodeling complexes such as INO80 have been i

244 ATP-dependent chromatin remodeling complexes, such as SWI/SNF, are req

245 TP binding proteins that are part of various chromatin-remodeling complexes, such as Ino80, SNF2-rela

246 FR-regulated microRNA pathway in the SWI/SNF chromatin remodeling complex suggests that EGFR-mediated

247 y sensor AMPKs, mitochondrial biogenesis and chromatin remodeling complex SWI/SNF activation, which m

248 The ATP-dependent chromatin remodeling complex SWI/SNF regulates transcrip

249 e yeast PHO8 gene was found to depend on the chromatin-remodeling complex SWI/SNF, whereas activation

250 tin ligase adds an enzymatic function to the chromatin-remodeling complex SWI/SNF-A.

251 1, a subunit of the evolutionarily conserved chromatin-remodeling complex SWI/SNF.

252 The ATP-dependent chromatin-remodeling complex SWR1 exchanges a variant hi

253 SWI/SNF is a chromatin remodeling complex that affects transcription

254 ew set of genes encoding subunits of the BAF chromatin remodeling complex that exhibited Ras-mediated

255 the polycomb repressive complex 2 (PRC2), a chromatin remodeling complex that mediates silencing of

256 nting protein 2 homologue (hSNF2H) to form a chromatin remodeling complex that participates in severa

257 The SWI/SNF complex is an ATP-dependent chromatin remodeling complex that plays pivotal roles in

258 several nuclear proteins including SIN3:HDAC chromatin remodeling complexes that are involved in repr

259 ctivity of the SWI/SNF-related ATP-dependent chromatin remodeling complexes that control the accessib

260 mportant lineage-specific role for a SWI/SNF chromatin-remodeling complex that collaborates with core

261 the Foxp transcription factors and the NuRD chromatin-remodeling complex that modulates transcriptio

262 SWI/SNF is a multisubunit chromatin-remodeling complex that performs fundamental r

263 d from yeast to man and many are subunits of chromatin-remodeling complexes that facilitate transcrip

264 he remodels the structure of chromatin (RSC) chromatin remodeling complex, the nuclear motor Kip1, th

265 The Mi2/NuRD chromatin remodeling complex tightly associates with act

266 which EBF2 cooperates with a tissue-specific chromatin remodeling complex to activate brown fat ident

267 acts with and recruits a tissue-specific BAF chromatin remodeling complex to brown fat gene enhancers

268 o signaling pathways that direct the SWI/SNF chromatin remodeling complex to cardiomyogenic loci in m

269 l enhancers and recruiting the SWI/SNF (BAF) chromatin remodeling complex to establish accessible chr

270 Nucleosome Remodeling and Deacetylase (NuRD) chromatin remodeling complex to regulate gene transcript

271 We show that recruitment of the Swi/Snf chromatin remodeling complex to the induced CHA1 promote

272 dentified, but the contributions of specific chromatin remodeling complexes to peripheral nerve myeli

273 f bromodomain proteins, directs multisubunit chromatin remodeling complexes to specific acetyl-nucleo

274 ppear to act as scaffolds to further recruit chromatin remodeling complexes to specific target genes.

275 et is associated with its failure to recruit chromatin remodeling complexes to the Ifng gene promoter

276 d by recruiting both histone deacetylase and chromatin remodeling complexes to their promoters by the

277 0s) that tether SWITCH/SUCROSE NONFERMENTING chromatin remodeling complexes to transcription factors

278 We show that recruitment of the SWI/SNF chromatin-remodeling complex to both RSSs increases coup

279 HJURP selectively recruits the condensin II chromatin-remodeling complex to facilitate CENP-A deposi

280 t locus, we show that Oct1 recruits the NuRD chromatin-remodeling complex to promote a repressed stat

281 recruiting and interacting with the SWI/SNF chromatin-remodeling complex to specifically mediate Neu

282 a growing list of nuclear proteins including chromatin remodeling complexes, transcription factors an

283 , a component of the WICH complex (WSTF-ISWI chromatin-remodeling complex), under basal conditions in

284 The conserved SWI/SNF chromatin remodeling complex uses the energy from ATP hy

285 tial ATPase subunit of the mammalian SWI/SNF chromatin remodeling complex, uses the energy from ATP h

286 ATP-dependent chromatin-remodeling complexes utilize the energy from A

287 y elements in the histone promoters, the RSC chromatin-remodeling complex, various histone chaperones

288 The SWI/SNF chromatin remodeling complex was found to cooperate with

289 Smarca4 -encoded BRG1 subunit of the SWI/SNF chromatin remodeling complex, we employed in vitro model

290 ow that the BRG1/BRM-associated factor (BAF) chromatin remodeling complex, which is mutated in over 2

291 asymmetric nucleosomes are bound by the RSC chromatin remodeling complex, which is required for main

292 the nucleus and is a component of the INO80 chromatin remodeling complex, which is responsible for t

293 es and is an essential component of the SWR1 chromatin remodeling complex, which regulates transcript

294 RCA4 is the catalytic subunit of the SWI/SNF chromatin-remodeling complex, which alters the interacti

295 lly, EcR genetically interacts with the NURF chromatin-remodeling complex, which we previously showed

296 ecialized and novel cardiac-enriched SWI/SNF chromatin-remodeling complexes, which are required for h

297 dentified and purified a human ATP-dependent chromatin remodeling complex with similarity to the Sacc

298 proposing that distinct associations of the chromatin remodeling complex with specific GRFs tightly

299 is a unique and defining subunit of the BAF chromatin remodeling complex with the potential to facil

300 of BRG1-associated factors (BAF), an SWI/SNF chromatin-remodeling complex with known repressive funct