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

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

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

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

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

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

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

9 of the polymorphic BRG/BRM-associated factor chromatin remodeling complex.

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

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

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

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

14 nteraction of PRDM3 and PRDM16 with the NuRD chromatin remodeling complex.

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

16 18(Hamlet) subunit (Dmp18) of the SWR1/SRCAP chromatin remodeling complex.

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

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

19 wo mutually exclusive ATPases of the SWI/SNF chromatin remodeling complex.

20 ge (>300 kD) multidomain subunit of the NURF chromatin remodeling complex.

21 hromatin in budding yeast depends on the RSC chromatin remodeling complex.

22 y interacts with the Imitation SWItch (ISWI) chromatin remodeling complex.

23 the disease-specific recruitment of a major chromatin remodeling complex.

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

25 transcription network by targeting the INO80 chromatin remodeling complex.

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

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

28 phosites in SMARCC2, a member of the SWI/SNF chromatin-remodeling complex.

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

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

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

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

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

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

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

36 ed by BRG1, an ATPase subunit of the SWI/SNF chromatin-remodeling complex.

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

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

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

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

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

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

43 or members of the SWI/SNF (or BAF) family of chromatin remodeling complexes.

44 histone posttranslational modifications, and chromatin remodeling complexes.

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

46 atin propagation by transcription-associated chromatin remodeling complexes.

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

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

49 ved from human DNA repair proteins and yeast chromatin remodeling complexes.

50 r, there is no known link between MUC1-C and chromatin remodeling complexes.

51 ARCA4 and SMARCA2, key components of SWI/SNF chromatin remodeling complexes.

52 ranscription factors that recruit activating chromatin remodeling complexes.

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

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

55 onfigurations such as histone chaperones and chromatin remodeling complexes.

56 epressors that link transcription factors to chromatin remodeling complexes.

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

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

59 The chromatin remodeling complex ACF helps establish the app

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

61 ian Switch/Sucrose-Nonfermentable (mSWI/SNF) chromatin-remodeling complexes (also called BAF complexe

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

63 ATP-dependent chromatin remodeling complexes alter chromatin structure

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

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

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

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

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

69 8 genes encode proteins involved in multiple chromatin remodeling complexes and are likely to play im

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

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

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

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

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

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

76 connection between mutations in the SWI/SNF chromatin-remodeling complex and the tumor suppressor ge

77 Chromatin-remodeling complexes and post-translational hi

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

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

80 l deletion of Swi3, a subunit of the SWI/SNF chromatin remodeling complex, and partial loss of functi

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

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

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

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

89 ATP-dependent chromatin remodeling complexes are essential for transcr

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

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

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

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

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

95 Chromatin-remodeling complexes are assembled around a ca

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

97 Switch/sucrose-nonfermentable (SWI/SNF) chromatin-remodeling complexes are critical regulators o

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

99 utations in ARID1A, a subunit of the SWI/SNF chromatin remodeling complex, are the most common altera

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

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

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

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

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

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

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

107 ammalian SWI/SNF complexes are multi-subunit chromatin remodeling complexes associated with an ATPase

108 , 2 missense) in the BICRA (BRD4 interacting chromatin remodeling complex-associated protein) gene, a

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 romodomain-containing subunit of the SWI/SNF chromatin remodeling complex BAF.

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

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

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

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

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

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

118 ral genes encoding components of the SWI/SNF chromatin remodeling complex cause neurodevelopmental di

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

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

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

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

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

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

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

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

127 lta) forms of Swi1, a subunit of the SWI/SNF chromatin-remodeling complex, confer dramatically distin

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

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

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

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

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

133 7ac, and H4K5ac as well as by recruitment of chromatin-remodeling complex containing BRG-1.

134 60 complex (TIP60.com) is a tumor suppressor chromatin-remodeling complex containing RVB proteins.

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

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

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

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

139 that Arid1a, a key component of the SWI/SNF chromatin remodeling complex, controls liver regeneratio

140 well as other members of the LSD1-containing chromatin remodeling complex CoREST, is rapidly polyubiq

141 Mutations in the chromatin remodeling complex could thus mitigate the pro

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

143 nsin D interacts with a putative member of a chromatin-remodeling complex during development.

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

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

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

147 ched association with components of the NuRD chromatin remodeling complex, especially RBBP4.

148 The SWI/SNF chromatin remodeling complex facilitates gene transcript

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

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

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

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

153 The INO80 chromatin remodeling complex functions in transcriptiona

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

155 The SWItch/Sucrose non-fermentable (SWI/SNF) chromatin remodeling complex has also emerged as a criti

156 The SWI/SNF chromatin remodeling complex has been found mutated in a

157 In addition, chromatin remodeling complexes have an impact on the abu

158 an switch/sucrose non-fermentable (mSWI/SNF) chromatin remodeling complexes have been widely implicat

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

160 Eukaryotes encode a plethora of chromatin-remodeling complexes, histone-modification enz

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

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

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

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

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

166 TF NANOG is highly dependent on the SWI/SNF chromatin remodeling complex in individual blastocysts b

167 the role of the mammalian SWI/SNF (mSWI/SNF) chromatin remodeling complex in NEPC.

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

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

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

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

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

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

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

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

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

177 ttractive strategy to target mutated SWI/SNF chromatin-remodeling complexes in cancer.

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

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

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

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

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

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

184 ch/sucrose non-fermentable (mSWI/SNF or BAF) chromatin remodeling complex, including its core catalyt

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

186 rs with mutations in subunits of the SWI/SNF chromatin remodeling complex, inclusive of most epitheli

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

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

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

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

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

192 Chromatin remodeling complexes instruct cellular differe

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

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

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

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

197 The INO80 chromatin remodeling complex is an evolutionarily conser

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

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

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

201 ADP-ribosylation of BAF170, a subunit of BAF chromatin remodeling complex, is critical for activation

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

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

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

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

206 Atxn7, a subunit of SAGA chromatin remodeling complex, is subject to polyglutamin

207 of SMARCB1, encoding a member of the SWI/SNF chromatin remodeling complex, is the hallmark genetic ab

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

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

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

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

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

213 of the BRAF-histone deacetylase (HDAC) (BHC) chromatin-remodeling complex (LSD1, RCOR1, HMG20A, HMG20

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

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

216 anied by release of the repressive nucleolar chromatin remodeling complex (NoRC) from rDNA, together

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

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

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

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

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

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

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

224 This decondensation is mediated through chromatin-remodeling complex PBAP, as PBAP is both robus

225 The BAF (SWI/SNF) chromatin remodeling complex plays a crucial role in mod

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

227 d properties potentially by interacting with chromatin remodeling complex PRC2 and downregulation of

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

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

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

231 However, how chromatin remodeling complexes regulate DNA damage check

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

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

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

235 n BRG1, the catalytic subunit of the SWI/SNF chromatin remodeling complex, results in a meiotic arres

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

237 principle, the nucleosome preference of the chromatin remodeling complex, RSC.

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

239 e show that BAF60a, a subunit of the SWI/SNF chromatin-remodeling complexes, serves an indispensable

240 minichromosome maintenance (MCM) protein and chromatin-remodeling complex SMARCB1 and SMARCC2 to be L

241 , the Arabidopsis homolog of the yeast INO80 chromatin remodeling complex subunit IES6 (INO EIGHTY SU

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 SWI/SNF-family chromatin remodeling complexes, such as S. cerevisiae RS

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

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

247 d the phosphorylated FgSR interacts with the chromatin remodeling complex SWI/SNF at the target genes

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

249 ors is BRG1, the major ATPase subunit of the chromatin remodeling complex SWI/SNF, establishing a rel

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

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

252 1, a subunit of the evolutionarily conserved chromatin-remodeling complex SWI/SNF.

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

254 one variant H2A.Z by the SWI2/SNF2-Related 1 chromatin remodeling complex (SWR1-C) is important for g

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

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

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

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

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

260 ammalian SWI/SNF complexes are ATP-dependent chromatin remodeling complexes that regulate genomic arc

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

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

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

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

265 nd pathways, including HMGB1 and the SWI/SNF chromatin remodeling complex, that are SARS lineage and

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

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

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

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

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

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

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

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

274 nucleosome arrays, which are repositioned by chromatin remodeling complexes to control DNA accessibil

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

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

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

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

279 0s) that tether SWITCH/SUCROSE NONFERMENTING chromatin remodeling complexes to transcription factors

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

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

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

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

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

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

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

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

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

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

290 (Pygo) and the Osa/ARID1A subunit of the BAF chromatin remodeling complex, which could synergize with

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

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

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

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

300 recently identified subunit of SWI/SNF(BAF) chromatin remodeling complexes, yet its function is poor