ライフサイエンスコーパス: remodeling factor

1 no requirement for ATP-dependent nucleosome remodeling factors).

2 quence) and extrinsic forces (i.e. chromatin remodeling factors).

3 ith the proposed role for PKL as a chromatin remodeling factor.

4 et locus, which encodes a putative chromatin remodeling factor.

5 egative roles in the activity of the Swi-Snf-remodeling factor.

6 ACF, an ATP-utilizing chromatin assembly and remodeling factor.

7 gh lipid-dependent sequestration of an actin-remodeling factor.

8 CHD7 encodes an ATP-dependent chromatin remodeling factor.

9 found that it is an ATP-dependent nucleosome remodeling factor.

10 s between DNA-binding proteins and chromatin remodeling factors.

11 article, and its interactions with chromatin remodeling factors.

12 highly regulated by chromatin modifying and remodeling factors.

13 junction with the PKL-related CHD3 chromatin-remodeling factors.

14 and CHD families of ATP-dependent chromatin-remodeling factors.

15 domain, a motif commonly found in chromatin-remodeling factors.

16 C terminus, a motif often found in chromatin remodeling factors.

17 in a variety of transcription and chromatin-remodeling factors.

18 t the aid of histone-modifying or nucleosome-remodeling factors.

19 ents in the field of ATP-dependent chromatin remodeling factors.

20 ion, suggesting the involvement of chromatin remodeling factors.

21 ase subunit of three ATP-dependent chromatin remodeling factors.

22 e involvement of energy-dependent nucleosome remodeling factors.

23 by cells secrete pro-inflammatory and tissue-remodeling factors.

24 rs, and how they are influenced by chromatin remodeling factors.

25 as well as frequent aberrations in chromatin remodeling factors.

26 to the SWI/SNF and CHD families of chromatin remodeling factors.

27 lpain 2 and of P-TEFb-dependent cytoskeletal remodeling factors.

28 eages is coordinately regulated by chromatin-remodeling factors.

29 k between MADS-domain proteins and chromatin remodeling factors.

30 itation Switch (ISWI) subfamily of chromatin-remodeling factors.

31 ACF1 (ATP-utilizing chromatin assembly and remodeling factor 1) and an ISWI isoform, SNF2H (sucrose

32 sophila ATP-utilizing chromatin assembly and remodeling factor (ACF), Drosophila nucleosome assembly

33 mbinant ATP-utilizing chromatin assembly and remodeling factor (ACF), purified recombinant nucleosome

34 -1, and ATP-dependent chromatin assembly and remodeling factor (ACF).

35 Hand1 and Smyd1, transcription and chromatin remodeling factors; Acta1, Acta2, Myl3, and Myom1, myofi

36 spontaneous nucleosomal site exposure, with remodeling factor action required downstream to lock in

37 t that Ikaros targets two types of chromatin-remodeling factors-activators (SWI/SNF) and repressors (

38 lesion in the nucleosome core by a chromatin-remodeling factor and contrasts with the ACF remodeling

39 a provide new insights into how a nucleosome remodeling factor and insulator proteins cooperatively c

40 uses on the roles of ATP-dependent chromatin-remodeling factors and chromatin-modifying enzymes in th

41 s including transcription factors, chromatin remodeling factors and components of the gene-silencing

42 nces of reduced expression of some chromatin-remodeling factors and histone acetylation in maize (Zea

43 ncing, as well as the discovery of chromatin-remodeling factors and histone modification activities.

44 by controlling the recruitment of nucleosome remodeling factors and histone modifying enzymes.

45 ner with coactivators that recruit chromatin remodeling factors and interact with the basal transcrip

46 lly interacts with repressive NuRD chromatin remodeling factors and promotes hPSC differentiation, wh

47 ific nuclear protein that recruits chromatin-remodeling factors and regulates numerous genes during t

48 structural proteins, nucleoporins, chromatin remodeling factors and several novel proteins that were

49 est that through interactions with chromatin-remodeling factors and specialized DNA-binding proteins,

50 xpression is in part controlled by chromatin remodeling factors and the acetylation state of nucleoso

51 c interactions revealed that these chromatin remodeling factors and the Rad53 phosphatases function i

52 ), which codes for a putative CHD3 chromatin remodeling factor, and gibberellin (GA), a plant growth

53 suggest that Chd1p functions as a nucleosome remodeling factor, and that Chd1p may share overlapping

54 s of interphase chromatin, fibers subject to remodeling factors, and regulatory DNA sequences.

55 histone chaperones, ATP-dependent chromatin remodeling factors, and some histone-modifying enzymes i

56 e polycomb genes, zinc finger TFs, chromatin remodeling factors, and suppressors of signaling.

57 This is achieved by chromatin-remodeling factors, and their necessity for efficient DD

58 Mutations in specific chromatin-remodeling factors appear to be key determinants of the

59 Chromatin remodeling factors are becoming known as crucial facilit

60 e found that four highly conserved chromatin remodeling factors are global lncRNA repressors that pla

61 ver, the previous observation that chromatin remodeling factors are recruited into viral replication

62 revisiae that the Fun30p and Isw1p chromatin remodeling factors are similarly required for transcript

63 e, we identified NURF301/E(bx), a nucleosome remodeling factor, as a novel regulator of gypsy insulat

64 not result from an interaction with the Mi-2 remodeling factor, as only a small percentage of Mi-2 lo

65 with the B subunit flap domain and by the o remodeling factors AsiA and RbpA.

66 way remodeling and show lumican as a crucial remodeling factor associated with collagen organization

67 eriphery and locally concentrating this mRNA remodeling factor at the cytoplasmic face of the NPC.

68 he ACF (ATP-utilizing chromatin assembly and remodeling factor) ATP-dependent chromatin-remodeling co

69 mutations of the gene encoding the chromatin remodeling factor ATRX cause an unexpectedly severe hema

70 The H3.3 chaperone, Daxx, and the chromatin-remodeling factor, ATRX, are required for H3.3 incorpora

71 chaperone, DAXX, together with the chromatin-remodeling factor, ATRX, regulates H3.3 deposition and t

72 fly homolog of the human and yeast chromatin-remodeling factors BAF170, BAF155, and SWI3.

73 n nucleosome N2 and recruitment of chromatin remodeling factor Brahma-related gene 1 (BRG-1) to this

74 TERT) component, together with the chromatin remodeling factor BRG1 and beta-catenin, may also bind t

75 ous histone modifications and the nucleosome-remodeling factor BRG1 are found at "active" (DJ) and "i

76 Treg-specific deletion of the chromatin remodeling factor Brg1 impairs Treg cell activation and

77 Here, we show that the chromatin remodeling factor Brg1 is required for enhancer activati

78 vitro chromatin remodeling assays, chromatin remodeling factor BRG1 mutant cells, and RNA interferenc

79 A proteins act in concert with the chromatin-remodeling factor BRG1 to protect the promoters of antio

80 and BASP1 cooperate to recruit the chromatin remodeling factor BRG1 to WT1-responsive promoters and t

81 -TEFb, the co-activator GRIP1, the chromatin remodeling factor BRG1, and specific histone modificatio

82 Mutations in genes encoding chromatin-remodeling factor Brg1/SmarcA4 and its associated protei

83 nscriptional activator Sp1 and the chromatin remodeling factors Brg1 and BAF155 to this promoter, as

84 remodeling of the MOR promoter by chromatin remodeling factors (Brg1 and BAF155) from a compacted st

85 Concurrently, the chromatin-remodeling factor BRM is replaced by BRG1 and histones a

86 ORF78 tightly interacts with the spliceosome remodeling factor, BRR2, in vitro.

87 odeling in a manner similar to that of other remodeling factors but does not significantly reposition

88 or recruitment of an ATP-dependent chromatin-remodeling factor by a general transcription factor in v

89 omplement signaling pathway and the synaptic remodeling factor c1q.

90 eal the mechanism underlying how a chromatin remodeling factor can regulate oocyte meiosis.

91 Rb gene family's interaction with chromatin remodeling factors can influence DNA repair dynamics.

92 ACF (ATP-utilizing chromatin assembly and remodeling factor) catalyzes the ATP-dependent assembly

93 that the Saccharomyces cerevisiae chromatin remodeling factor Chd1 functions during transcription el

94 Elimination of chromatin remodeling factor CHD1 in Drosophila embryos abolishes i

95 screen and found that loss of the nucleosome remodeling factor CHD4 confers cisplatin resistance.

96 man CHARGE syndrome, ATP-dependent chromatin remodeling factor CHD7, contributes to the control of ne

97 s heterodimeric partner BACH1, the chromatin remodeling factor CHD8, and the DNA methyltransferase DN

98 Because DDM1 encodes a putative chromatin remodeling factor, chromatin structure is likely to be i

99 ranscription factor 1 (BACH1), the chromatin remodeling factor chromodomain helicase DNA-binding prot

100 G-1 and its interactor Mi-2beta, a chromatin remodeling factor commonly linked to repression, were re

101 ell's full wild-type complement of chromatin remodeling factors, competition of regulatory proteins w

102 The maize (Zea mays) nucleosome remodeling factor complex component101 (nfc101) and nfc1

103 r), a core component of the NURF (Nucleosome Remodeling Factor) complex, results in the emergence of

104 ivators TAFII250 and p300, SWI/SNF chromatin remodeling factor component BRG-1, and basal transcripti

105 issue-specific non-coding RNAs and chromatin remodeling factors confer robustness to mesodermal linea

106 ing, but little is known about how chromatin-remodeling factors contribute to plant organogenesis.

107 angiogenic, growth, and extracellular matrix remodeling factors, cytokines and chemokines, and contro

108 SSB plays the role of a remodeling factor defining the mode of RecG binding to t

109 The chromatin remodeling factor DEK is an attractive candidate as it m

110 r data indicate the involvement of chromatin remodeling factors distinct from the Swi-Snf complex in

111 t that nucleosome loss induced by nucleosome remodeling factors during gene activation enables Top2 b

112 Members of the ISWI family of chromatin remodeling factors exhibit ATP-dependent nucleosome slid

113 The ISWI class of chromatin remodeling factors exhibits potent chromatin remodeling

114 fies an interesting class of targetable bone-remodeling factors expressed by normal and malignant pla

115 This demonstrates that ATP-dependent remodeling factors facilitate covalent histone modificat

116 stone chaperones and ATP-dependent chromatin remodeling factors facilitate transitions in chromatin s

117 r Stat and the ISWI ATP-dependent nucleosome remodeling factor Falz, thereby expanding further the mS

118 possible that OXS3 might act as a chromatin remodeling factor for the stress response.

119 Chromatin remodeling factors function both in transcriptional acti

120 e and shows how a highly conserved chromatin remodeling factor has a distinct role in anti-microbial

121 report that Brg, an ATP-dependent chromatin remodeling factor, has dual functions in regulating Shh

122 The Imitation SWItch (ISWI) chromatin remodeling factors have been implicated in nucleosome po

123 Transcription factors and chromatin-remodeling factors have been implicated in regulating th

124 ATP-dependent chromatin remodeling factors have unique roles in disrupting histo

125 romatin state of the template, and chromatin remodeling factors have well-documented roles in regulat

126 ion is self-templating; and (ii) the protein-remodeling factor heat-shock protein (Hsp)104 (acting to

127 chromatin as well as ATP-dependent chromatin remodeling factors help to overcome this barrier and fac

128 AVES1 (AS1) and AS2 as well as the chromatin-remodeling factor HIRA.

129 nctions cooperatively with another chromatin remodeling factor, Histone deacetylase 3 (HDAC3) to supp

130 target chromatin assembly factors, chromatin remodeling factors, histone acetyltransferases and histo

131 Eya1 copurified REST-interacting chromatin-remodeling factors, histone deacetylase/lysine demethyla

132 Moreover, the chromatin-remodeling factor Hmga2 in the skin plays a critical rol

133 With the ACF chromatin remodeling factor, HMGN2 does not directly inhibit the A

134 tone deacetylase Clr3 and the SNF2 chromatin-remodeling factor homolog Mit1.

135 The protein-remodeling factor Hsp104 governs inheritance of [PSI+],

136 A protein-remodeling factor, Hsp104, controls the inheritance of s

137 proteins, which are ATP-dependent chromatin remodeling factors implicated in RNA polymerase II trans

138 in and may therefore function as a chromatin remodeling factor in a complex(es) involving a histone a

139 domain helicase DNA-binding 3-type chromatin remodeling factor in Arabidopsis.

140 ed chromatin, and we suggest a role for this remodeling factor in dosage compensation.

141 ancer and shows a key role of this chromatin remodeling factor in prostate cancer biology.

142 dies indicate a central role for a chromatin-remodeling factor in the SSRI/p11 signaling pathway and

143 n as initial chromatin-binding and chromatin-remodeling factors in a variety of tissues, including li

144 e kinases and their interplay with chromatin remodeling factors in cancer cells.

145 nhancers, histone acetylation, and chromatin remodeling factors in controlling accessibility are disc

146 we have studied the expression of chromatin remodeling factors in different spermatogenic stages and

147 es a restricted window for reactivating bone remodeling factors in humans.

148 Remodeling factors in murine bronchoalveolar lavage flui

149 ng the importance of ATP-dependent chromatin-remodeling factors in the cell's early response to DNA d

150 little is known about the role of chromatin remodeling factors in this process.

151 The role of chromatin-remodeling factors in transcription is well established,

152 avior and on the expression of key chromatin remodeling factors including DNA methyltransferase 1, te

153 ent upregulation of a cohort of cytoskeleton remodeling factors, including alpha-actinin-1.

154 ries motifs for binding of certain chromatin remodeling factors, including insulator proteins.

155 R45H), which has been shown to allow SWI/SNF remodeling factor-independent transcription from the yea

156 lly, suppression of IL-6, TNF-alpha, and ECM remodeling factors indicated reduced metastatic potentia

157 that it serves as a highly conserved histone remodeling factor involved in chromatin-based gene silen

158 3 proteins have been implicated as chromatin-remodeling factors involved in repression of transcripti

159 CA4 (also known as BRG1 in humans) chromatin remodeling factor is critical for establishing lineage-s

160 ant alleles and show that the CHD1 chromatin-remodeling factor is important for wing development and

161 cripts]) whose repression by these chromatin remodeling factors is required for the maintenance of no

162 to the HO promoter (in the absence of other remodeling factors), is 5k(B)T.

163 We show that SMARCA3, a chromatin-remodeling factor, is a target for the p11/annexin A2 he

164 ow in a mouse model that BAF155, a chromatin remodeling factor, is highly expressed in committed OPCs

165 ysis revealed that Phf10/Baf45a, a chromatin remodeling factor, is less phosphorylated upon Bckdk dep

166 ed gene 1 (Brg1), an ATP-dependent chromatin remodeling factor, is required for the repression of neu

167 ciency for CHD7, an ATP-dependent nucleosome remodeling factor, is the leading cause of CHARGE syndro

168 te transcription by recruiting the chromatin-remodeling factor Isw1p.

169 haromyces cerevisiae ATP-dependent chromatin remodeling factors, Isw2 and Ino80, function to attenuat

170 e adenosine triphosphate-dependent chromatin remodeling factors ISWI and DOM control germline stem ce

171 Chromatin remodeling factor LSH is critical for normal development

172 ger protein die-1 and the putative chromatin remodeling factor lss-4.

173 ed to reduce proline levels by the chromatin remodeling factor lymphoid-specific helicase (LSH), an e

174 Chromatin remodeling factor metastatic tumor protein 1 (MTA1), one

175 he zinc-finger protein p66 and the chromatin remodeling factor Mi2, were found to coelute by gel-filt

176 e proteins, which, in concert with chromatin-remodeling factors, modulate chromatin structure.

177 SGs trap mRNA coding for the DNA repair and remodeling factor MRG15 (MORF4L1), translation of which

178 ) and relationship with the master chromatin remodeling factor MTA1, continues to be poorly understoo

179 PICKLE (PKL) encodes a CHD3-chromatin-remodeling factor necessary for the repression of expres

180 hus, in a purified system lacking nucleosome remodeling factors, not only the core histone octamer bu

181 ing root cells is up-regulation of cell wall remodeling factors, notably expansins, while plant hormo

182 ting root cells is upregulation of cell wall remodeling factors, notably expansins, while plant hormo

183 The nucleosome remodeling factor NURF is a four-subunit, ISWI-containin

184 The Drosophila nucleosome remodeling factor NURF utilizes the energy of ATP hydrol

185 The nucleosome remodeling factor (NURF) alters chromatin accessibility

186 e TF OCT4 and that ZIC2 recruits the nuclear remodeling factor (NURF) complex to the OCT4 promoter, t

187 protein likely acts as part of a Nucleosome Remodeling Factor (NURF) complex with NURF-1, a nematode

188 F, the scaffolding subunit of the nucleosome remodeling factor (NURF) complex, has been implicated in

189 human ortholog of the Drosophila nucleosome-remodeling factor (NURF) complex.

190 the chromatin remodeling complex nucleosome remodeling factor (NURF) in immunity, but it has yet to

191 The Drosophila nucleosome remodeling factor (NURF) is a protein complex consisting

192 The Drosophila nucleosome remodeling factor (NURF) is a protein complex of four di

193 The Drosophila nucleosome remodeling factor (NURF) is a protein complex of four su

194 Nucleosome Remodeling Factor (NURF) is an ATP-dependent nucleosome

195 The Drosophila nucleosome remodeling factor (NURF) is an imitation switch (ISWI)-c

196 The Drosophila nucleosome remodeling factor (NURF) is an ISWI-containing chromatin

197 Drosophila nucleosome remodeling factor (NURF) is an ISWI-containing protein c

198 The nucleosome remodeling factor (NURF) is one of several ISWI-containi

199 omatin factors, we identified the nucleosome-remodeling factor (NURF) subunit BPTF as an essential re

200 (BPTF) is the largest subunit of nucleosome remodeling factor (NURF), a member of the ISWI chromatin

201 re both present, we find that the nucleosome remodeling factor (NURF), an ISWI-dependent chromatin re

202 sential and unique subunit of the nucleosome-remodeling factor (NURF), predominantly regulates the ex

203 1 and ISWI, key components of the nucleosome-remodeling factor (NURF), synergistically disrupted the

204 ive selection is dependent on the nucleosome remodeling factor (NURF).

205 tional regulation by ATP-dependent chromatin remodeling factors occurs in concert with histone modify

206 Hsp104, a yeast protein-remodeling factor of the AAA+ (ATPases associated with v

207 ATP-dependent chromatin remodeling factors of SWI/SNF2 family including ISWI, SN

208 As dysfunction of other chromatin remodeling factors often has severe effects on developme

209 ents overloading of activators and chromatin remodeling factors on nascent DNA and thereby mediates p

210 Unique chromatin remodeling factors orchestrate dramatic changes in nucle

211 dditional factors such as the CHD3 chromatin remodeling factor PICKLE (PKL) act to restrict meristema

212 Chromatin remodeling factors play an active role in the DNA damage

213 NA-binding family of ATP-dependent chromatin remodeling factors play essential roles during eukaryote

214 x group protein Brahma and related chromatin-remodeling factors, providing further evidence that alte

215 regulated epigenetically through a chromatin remodeling factor, Pygo2.

216 ibute to elongation by transporting junction remodeling factors, rather than having a mechanical role

217 Under DNA damage, the RSF1 chromatin remodeling factor recruits HDAC1 to DSB sites.

218 In Arabidopsis a SWI2/SNF2 chromatin remodeling factor-related protein DDM1 and a cytosine me

219 r data identifies cofilin-1 and ADF as actin remodeling factors required for fast amoeboid migration.

220 homologous recombination (HR) and chromatin remodeling factors required for HR are essential for qiR

221 kpoint protein, MDC1, and H2AX are chromatin remodeling factors required for the recruitment of DNA r

222 ne H3(K36) methyltransferase and a chromatin remodeling factor, respectively.

223 y enriched for nuclear components, chromatin remodeling factors, RNA splicing factors, RNA granule co

224 specific function for the general chromatin remodeling factor Rpd3 in regulating dendrite targeting

225 We identify the chromatin-remodeling factor Satb2 as a partner of Ski, and show th

226 antidepressant protein p11 and the chromatin remodeling factor SMARCA3 mediate this delayed response

227 AP2C, EOMES, ETS2, and GATA3-and a chromatin remodeling factor, SMARCA4.

228 that the ISWI family ATP-dependent chromatin remodeling factor SMARCA5 (SNF2H) plays a critical role

229 validated in this manner were the chromatin-remodeling factors SMARCA5 and SMARCD1 and the growth re

230 In addition, loss of the nuclear chromatin-remodeling factor SMARCB1 in rhabdoid tumors led to incr

231 R-7 suppresses the coupling of the chromatin remodeling factor SMARCD1 with p53, resulting in increas

232 nes, RNAi silencing of the SWI/SNF chromatin-remodeling factor Smarcd3/Baf60c in EpCAM- breast cancer

233 demonstrate that the ATP-dependent chromatin remodeling factor Snf2h (also known as Smarca5) plays a

234 The ATP-dependent chromatin-remodeling factor SNF2h was also recruited to DS in late

235 The miRNAs target the SWI/SNF chromatin remodeling factor SNF2H/SMARCA5, a component of the ACF1

236 Another remodeling factor, SNF2h, is constitutively present at t

237 This allows recruitment of the nucleosome remodeling factor Snf5 and subsequent transcription.

238 e (Jhd2), and a mutated form of a nucleosome-remodeling factor (Spt6) that have never been reported t

239 g initiates the recruitment of the chromatin remodeling factor, SRCAP, followed by the replacement of

240 re mammalian homologues of SWI/SNF chromatin-remodeling factor subunits that can regulate both transc

241 n correlated with the induction of genes for remodeling factors such as vascular endothelial growth f

242 e data suggest that aberrations in chromatin-remodeling factors, such as ARID1B, might contribute to

243 ught to involve the recruitment of chromatin-remodeling factors, such as histone deacetylases, to met

244 show that esBAF, a SWI/SNF family nucleosome remodeling factor, suppresses transcription of ncRNAs fr

245 ption factor IIS), and a number of chromatin remodeling factors (Swi/Snf and Spt6).

246 e recently reported that the yeast chromatin-remodeling factor Swi1 can exist as a prion, [SWI(+)], d

247 [SWI+], a prion of the chromatin remodeling factor Swi1p, was also proposed to benefit it

248 omeotic genes related to the yeast chromatin remodeling factor SWI2/SNF2.

249 We propose that Mit1 is a chromatin remodeling factor that cooperates with the Clr3 histone

250 a Cas9 construct fused to PRDM9, a chromatin remodeling factor that deposits histone methylations H3K

251 mplex, has been characterized as a chromatin remodeling factor that enhances accessibility of the tra

252 BRG1 is a chromatin-remodeling factor that interacts with BRCA1 and pRB.

253 T-bet, a transcription and chromatin remodeling factor that is required to direct the differe

254 PICKLE (PKL) codes for a CHD3 chromatin remodeling factor that plays multiple roles in Arabidops

255 eat-shock protein 104 (Hsp104p) is a protein-remodeling factor that promotes survival after extreme s

256 uiting different transcription and chromatin remodeling factors that are expressed in a cell-specific

257 This is achieved by chromatin remodeling factors that can locally slide, evict, or cha

258 ment the ability of FGFR2 to recruit histone-remodeling factors that epigenetically activate transcri

259 is one of the major ATP-dependent, chromatin remodeling factors that regulate nucleosome positioning

260 isms (DNA methylation plus related chromatin remodeling factors) that cause the down-regulation of re

261 P-1 and ATP-utilizing chromatin assembly and remodeling factor; this effect was dependent in part on

262 uring, which may be mediated by the putative remodeling factor TIP49, appears to be linked to nucleol

263 ustrate how cancer cells utilize a chromatin remodeling factor to engage a core survival pathway to s

264 histone acetyltransferases, and/or chromatin remodeling factors to a promoter region to facilitate th

265 stem cell types can use different chromatin remodeling factors to control cell self-renewal.

266 lized DNA sequences and recruiting chromatin remodeling factors to control gene transcription.

267 nts, which inappropriately recruit chromatin-remodeling factors to elicit the aberrant transcriptiona

268 The importance of chromatin remodeling factors to enhancer activation is highlighted

269 cription factors, coactivators and chromatin remodeling factors to promoter and enhancer regions gene

270 on by TR involves the targeting of chromatin remodeling factors to repressed genes by the HDAC activi

271 ferase 1 (CARM1) methylates Pontin chromatin-remodeling factor under glucose starvation, and methylat

272 c regulation of gene expression by chromatin remodeling factors underlies cell fate determination.

273 omplex (ATP-utilizing chromatin assembly and remodeling factor), we have named this factor human ACF

274 hromatin assembly also function as chromatin remodeling factors, we investigated the relationship bet

275 t recombinant Mi2 is an efficient nucleosome remodeling factor when compared to that of the native Nu

276 related to the ATPase subunits of chromatin-remodeling factors, whereas Rad51 is related to bacteria

277 ata highlight Eps15 as an important membrane-remodeling factor, which acts in a partially redundant m

278 remodeling factor and contrasts with the ACF remodeling factor, which stimulates the removal of lesio

279 Smarcad1 is a conserved chromatin remodeling factor with a poorly understood tissue functi

280 tudy, we discovered that CHD5 is a chromatin remodeling factor with a unique enzymatic activity.

281 lymerases, different types of TFs, chromatin-remodeling factors with ATPase or helicase activity, and

282 the ULT proteins function to link chromatin-remodeling factors with DNA binding transcription factor

283 This association of ATP-remodeling factors with HMT CARM1 defines a new componen

284 Recently, three chromatin remodeling factors with roles in transcriptional regulat