ライフサイエンスコーパス: DNA-binding protein

1 protein) and a response regulator (usually a DNA binding protein).

2 A sliding clamp, and the RPA single-stranded DNA binding protein.

3 cation of RADX as an RPA-like, single-strand DNA binding protein.

4 ble to any type of yeast surface expressible DNA-binding protein.

5 c helix-loop-helix leucine zipper (bHLH-Zip) DNA-binding protein.

6 egulators (RfpB and RfpC), one of which is a DNA-binding protein.

7 that resembles a baculovirus single-stranded-DNA-binding protein.

8 g activity for disease-relevant proteins and DNA binding proteins.

9 ntially modulate the activities of unrelated DNA binding proteins.

10 ine deacetylases are selective regulators of DNA binding proteins.

11 ; CbpA lacks motifs found in other bacterial DNA binding proteins.

12 DNA-protein interactions for a wide range of DNA binding proteins.

13 A occupied by tandem arrays of high-affinity DNA binding proteins.

14 ssed by its interaction with single-stranded DNA binding proteins.

15 A (ssDNA) and interacting with several other DNA binding proteins.

16 ics on DNA in the presence of multiple other DNA binding proteins.

17 erization of transcription factors and other DNA-binding proteins.

18 ocessing of such modifications by regulatory DNA-binding proteins.

19 specific orientation are essential tasks for DNA-binding proteins.

20 ng at cognate sites may be common to various DNA-binding proteins.

21 target searches conducted by many different DNA-binding proteins.

22 despite being unrelated to any characterized DNA-binding proteins.

23 cificity for a group of structurally related DNA-binding proteins.

24 ncept that might be applied to inhibition of DNA-binding proteins.

25 direct transfer" reactions studied for other DNA-binding proteins.

26 rform accurate high-throughput prediction of DNA-binding proteins.

27 ISPR epitope tagging ChIP-seq (CETCh-seq) of DNA-binding proteins.

28 00 domain can be fused to other programmable DNA-binding proteins.

29 nd thermodynamically balanced engineering of DNA-binding proteins.

30 evelop a plant specific model for predicting DNA-binding proteins.

31 ty in patterning, notably in the behavior of DNA-binding proteins.

32 e researchers to use this method to identify DNA-binding proteins.

33 acterized demonstrating that Ml proteins are DNA-binding proteins.

34 oid in a way similar to exploration by other DNA-binding proteins.

35 ther indicated that CUL4A/B, damage-specific DNA binding protein 1 (DDB1), and cereblon (CRBN) appear

36 ) and uniform ripening (u) encode UV-DAMAGED DNA BINDING PROTEIN 1 (DDB1), DE-ETIOLATED 1 (DET1) and

37 o-SMAD1/5 and the expression of inhibitor of DNA binding protein 1 (ID1) were upregulated in HCV-infe

38 pts during acute and chronic infection was Z-DNA binding protein 1 (ZBP1).

39 Chd1 (Chromodomain Helicase DNA Binding Protein 1) is a conserved ATP-dependent chro

40 the RHIM-containing adaptor protein ZBP1 (Z-DNA binding protein 1; also known as DAI or DLM1) from a

41 Here, we show that acidic nucleoplasmic DNA-binding protein 1 (And-1) forms complexes with CtIP

42 The chromatin remodeler chomodomain helicase DNA-binding protein 1 (Chd1) promotes an elevated transc

43 For the chromodomain helicase DNA-binding protein 1 (Chd1) remodeler, nucleosome slidi

44 We have recently identified Z-DNA-binding protein 1 (ZBP1) as an innate sensor of infl

45 Z-DNA-binding protein 1 (ZBP1), initially reported as an i

46 dapter-inducing interferon-beta (TRIF) and Z-DNA-binding protein 1 (ZBP1)/DNA-dependent activator of

47 ar distribution, and a chromodomain helicase DNA binding protein 2 (CHD2) mutant affected in its DNA-

48 We also identified inhibitor of DNA binding protein 2 (ID2) as a key upstream regulator

49 Chromodomain helicase DNA-binding protein 2 (CHD2) is an ATPase and a member o

50 Damaged DNA-binding protein 2 (DDB2), a nuclear protein, partici

51 litated in the genomic context by UV-damaged DNA-binding protein 2 (DDB2), which is part of a multipr

52 Mutant or posttranslationally modified TAR DNA binding protein-32 (TDP-43) is also strongly associa

53 analysis revealed that chromodomain helicase DNA binding protein 4 (CHD4) is a potential downstream t

54 We report that chromodomain helicase DNA binding protein 4 (CHD4), an ATP-dependent chromatin

55 ow that Brg1 and CHD4 (chromodomain helicase DNA binding protein 4) coordinate to control target gene

56 Chromodomain Helicase DNA-binding protein 4 (CHD4) is a chromatin-remodeling e

57 Chromodomain helicase DNA-binding protein 4 (CHD4) is an ATP-dependent chromat

58 Chromodomain helicase DNA-binding protein 4 (CHD4) is an ATPase that alters th

59 interacted with CHD4 (chromodomain helicase DNA-binding protein 4), which is a part of the NuRD comp

60 e, most commonly CHD4 (chromodomain helicase DNA-binding protein 4).

61 Mutations in the human RBPs TAR-DNA binding protein 43 (TDP-43) and RNA-binding protein

62 TAR DNA binding protein 43 (TDP-43) is a major disease-assoc

63 TAR DNA binding protein 43 (TDP-43) is another protein linke

64 Tar DNA binding protein 43 (TDP-43) is the principal compone

65 sia (svPPA), is strongly associated with TAR-DNA binding protein 43 (TDP-43) type C pathology.

66 oral lobar degeneration-transactive response DNA binding protein 43 (TDP-43), progressive supranuclea

67 t, ubiquitinated and hyperphosphorylated Tar DNA binding protein 43 (TDP-43, encoded by TARDBP) neuro

68 The FTLD-TAR DNA binding protein 43 group had the youngest onset and

69 ocampal neurons, and reduced staining of TAR-DNA binding protein 43 in the nucleus, with concomitant

70 Aggregation of TDP-43 (transactive response DNA binding protein 43 kDa) is a hallmark of certain for

71 ith an approximately equal split between TAR DNA binding protein 43 proteinopathies and tauopathies.

72 Genetic mutations in TAR DNA-binding protein 43 (TARDBP, also known as TDP-43) ca

73 Aggregation of TAR-DNA-binding protein 43 (TDP-43) and of its fragments TDP

74 Mutations in TAR DNA-binding protein 43 (TDP-43) are associated with fami

75 however, identification of pathological TAR DNA-binding protein 43 (TDP-43) as the hallmark lesion i

76 as to determine whether the frequency of TAR DNA-binding protein 43 (TDP-43) deposition in Alzheimer'

77 icates a direct role of transactive-response DNA-binding protein 43 (TDP-43) in the pathology of ALS

78 TAR DNA-binding protein 43 (TDP-43) is a major disease prote

79 The 43-kDa trans-activating response region DNA-binding protein 43 (TDP-43) is a product of a causat

80 TAR DNA-binding protein 43 (TDP-43) is genetically and funct

81 Transactivation response element (TAR) DNA-binding protein 43 (TDP-43) misfolding is implicated

82 giopathy), Lewy bodies, transactive response DNA-binding protein 43 (TDP-43) pathology, and hippocamp

83 ymptoms, mutations in the DCTN1 gene and TAR DNA-binding protein 43 (TDP-43) pathology.

84 Transactive response DNA-binding protein 43 (TDP-43) performs multiple tasks

85 compared to transactivation response element DNA-binding protein 43 (TDP-43) proteinopathy patients w

86 ng mutant superoxide dismutase-1 (SOD1), TAR DNA-binding protein 43 (TDP-43), and fused in sarcoma (F

87 signature with numerous round, hyaline, TAR DNA-binding protein 43 (TDP-43)-positive inclusions.

88 cellular aggregation of transactive response DNA-binding protein 43 (TDP-43).

89 Hyperphosphorylated transactive response DNA-binding protein 43 (TDP-43, encoded by TARDBP ) prot

90 ns, including fused in sarcoma (FUS) and TAR DNA-binding protein 43 (TDP-43, encoded by TARDBP), are

91 tangles, and fused in sarcoma (FUS) and TAR DNA-binding protein 43 (TDP43) inclusions.

92 scores, presence of alpha-synuclein and TAR DNA-binding protein 43 aggregates, and additional vascul

93 Transactive response DNA-binding protein 43 kD (TDP-43) is an aggregation-pro

94 ed in sarcoma (FUS) and transactive response DNA-binding protein 43 kDa (TDP-43), are responsible for

95 ), SOD1 (superoxide dismutase 1), TDP43 (TAR DNA-binding protein 43), and tau.

96 ) and Hsp104(A503V/N728A) rescue TDP-43 (TAR DNA-binding protein 43), FUS (fused in sarcoma), and alp

97 ontained phosphorylated transactive response DNA-binding protein 43, ubiquitin, microtubule-associate

98 cally by the RNA binding protein TDP-43 (TAR DNA binding protein-43 kDa).

99 Tat-activating regulatory DNA-binding protein-43 (TDP-43) acts as an InSAC scaffol

100 Transfected CHD5 (chromodomain helicase DNA-binding protein 5) and NUT (nuclear protein in testi

101 s in the gene encoding chromodomain helicase DNA binding protein 7 (CHD7), which is an ATP-dependent

102 function mutations in chromodomain helicase DNA-binding protein 7 (CHD7(LOF)) and lysine (K) methylt

103 n demonstrate that the chromodomain helicase DNA-binding protein 7 (Chd7), frequently associated with

104 encoding ATP-dependent chromodomain helicase DNA-binding protein 7, in CHARGE syndrome lead to multip

105 tly, it was shown that chromodomain helicase DNA-binding protein-7 (CHD7) interacts with RUNX1 and su

106 runcating mutations of chromodomain helicase DNA-binding protein 8 (CHD8), and of many other genes wi

107 atin remodeling factor chromodomain helicase DNA-binding protein 8 (CHD8), and the DNA methyltransfer

108 we found that ATPases chromodomain helicase DNA-binding protein 9 (CHD9) and Brahma homologue (BRM,

109 Curved DNA binding protein A (CbpA) is a co-chaperone and nucle

110 DNA binding protein A (DbpA) is a member of the human co

111 nteracting with an ensemble of (multivalent) DNA-binding proteins able to switch between an "on" (bin

112 tibility, agt and Taf1 Both encode unrelated DNA-binding proteins, agt for an alkyl-cysteine-S-alkylt

113 y define the genome-wide binding profiles of DNA-binding proteins, allowing for a straightforward met

114 RPA, the eukaryotic single-stranded DNA binding protein, also inhibits telomere resection.

115 topoisomerase, a non-specific mitochondrial DNA binding protein and a type II restriction endonuclea

116 expansion of novel potential targets of both DNA binding proteins and sRNA regulators.

117 cterize the cell-to-cell transmission of TAR DNA-binding protein and alpha-synuclein, involved in amy

118 RadA is a DNA-dependent ATPase, a DNA-binding protein and can stimulate the branch migrati

119 a proxy for examining interactions between a DNA-binding protein and its substrate.

120 conclude that OsARID3 is an AT-rich specific DNA-binding protein and that it plays a major role in SA

121 be genetically encoded by binding sites for DNA-binding proteins and can also involve changes in chr

122 Both DNA-binding proteins and changes in chromatin structure

123 he acetyl-lysine occupancy of several ApiAP2 DNA-binding proteins and related transcriptional protein

124 romatin accessibility, nucleosome occupancy, DNA-binding proteins, and DNA methylation, primarily foc

125 DNA-binding proteins are an important class of proteins

126 The experimental methods used to identify DNA-binding proteins are expensive and time consuming an

127 We found that single-stranded DNA-binding proteins are recruited to these LIM complexe

128 These three DNA-binding proteins are very different in their structu

129 We found that expression of the DNA-binding protein, ARID3a, in mouse stem cells was imp

130 terility, and strongly reinforce the role of DNA-binding proteins as a class of genes contributing to

131 n of translin (trsn), a highly conserved RNA/DNA binding protein, as essential for starvation-induced

132 ce screen and identify ZNF304, a zinc-finger DNA-binding protein, as the pivotal factor required for

133 ales, from sub-genic regions associated with DNA-binding proteins at the order of tens or hundreds of

134 and topology, and its competition with other DNA-binding proteins at the single-DNA-molecule level.

135 The DNA binding protein BAF (barrier to autointegration fact

136 monstrated to target a shared substrate, the DNA binding protein BAF, elucidating a signaling pathway

137 t the role of intragenic DNA methylation and DNA binding protein BORIS in cancer-specific splicing an

138 ivate the fluorescence of only those labeled DNA-binding proteins bound to the DNA.

139 hesis with the specificity of a programmable DNA-binding protein by using protein trans-splicing to l

140 (b) altered homeostasis of critical RNA- and DNA-binding proteins, (c) impaired cytoskeleton function

141 otential target site, which may be how other DNA binding proteins can steer selection of advantageous

142 he high-mobility group protein B1 (HMGB1), a DNA-binding protein capable of inducing secretion of TNF

143 In particular, mutants of the RNA-guided DNA binding protein Cas9 that have lost their DNA cleava

144 complex, incorporating the sequence-specific DNA-binding protein Cep3 together with regulatory subuni

145 sively assesses the influence on contacts of DNA-binding proteins, cis-regulatory elements and DNA co

146 ends on the concentration of the periplasmic DNA-binding protein ComE, indicating that ComE is direct

147 A) is a co-chaperone and nucleoid associated DNA binding protein conserved in most gamma-proteobacter

148 modifiers, chromatin remodelers, and methyl-DNA binding proteins contribute to neurodevelopmental de

149 the growth-suppressing activity of the bHLH DNA-binding protein Daughterless (Da).

150 ion of chromatin loops is mainly mediated by DNA-binding proteins (DBPs) that bind to the interacting

151 ificity and ease of targeting the RNA-guided DNA-binding protein dCas9 to any 20 bp user-defined DNA

152 Here, we report that the damage-specific DNA-binding protein DDB2 is critical for beta-catenin-me

153 imes per base pair site reported for various DNA-binding proteins during 1D diffusion on DNA.

154 tools to help increase annotation levels of DNA-binding proteins encoded in plant genomes.

155 excess heterogeneous DNA, sequence-specific DNA-binding proteins execute various translocation mecha

156 onstrated that Hop1 is a structure-selective DNA-binding protein exhibiting high affinity for the Hol

157 nriched within the Apicomplexan AP2 (ApiAP2) DNA-binding protein family.

158 Many cellular functions rely on DNA-binding proteins finding and associating to specific

159 Open chromatin provides access to DNA-binding proteins for the correct spatiotemporal regu

160 (TALE) proteins are a class of programmable DNA-binding proteins for which the fundamental mechanism

161 We report a novel design for a fluorescent, DNA-binding protein (FP-DBP) that completely 'paints' en

162 of stress and starvation, an NAP called Dps (DNA-binding protein from starved cells) becomes highly u

163 cterium Deinococcus radiodurans contains two DNA-binding proteins from starved cells (Dps): Dps1 (DR2

164 Mutations in the RNA- and DNA-binding proteins, fused in sarcoma (FUS) and transac

165 lification requires only the single-stranded DNA-binding protein gp32 from bacteriophage T4 and a str

166 tively-bound clusters of the single-stranded DNA binding protein (gp32) of the T4 DNA replication com

167 The replication protein A (RPA) DNA-binding protein has a pivotal role in DNA metabolism

168 These sequence-specific DNA binding proteins have been primarily characterized a

169 Recent advances in the field of programmable DNA-binding proteins have led to the development of faci

170 inding and stabilizing the mRNA encoding the DNA binding protein HMGA1, a known oncogene.

171 NA colocalized with the VACV single-stranded DNA binding protein I3 in multiple puncta throughout the

172 of filament formation by the single-stranded DNA binding protein ICP8 in the formation of prereplicat

173 ad1, and the downstream genes, inhibitors of DNA binding proteins, Id1 and Id3.

174 The DNA-binding protein Ikaros is a potent tumor suppressor

175 tivator, which targets promoters via RBPJ, a DNA binding protein in the Notch signaling pathway.

176 e results reveal the role of single-stranded DNA binding proteins in controlling Exo1-catalyzed resec

177 ion followed by sequencing (ChIP-Seq) of 104 DNA binding proteins in embryonic stem cell (ESC) lines.

178 The single-stranded DNA binding proteins in mouse shelterin, POT1a and POT1b

179 nc fingers (C2H2-ZFs), the largest family of DNA-binding proteins in metazoans.

180 ineage specific models for the prediction of DNA-binding proteins in plants.

181 ly organized and assembled with histones and DNA-binding proteins in three dimensions.

182 ow that dinoflagellate nuclei have recruited DNA-binding proteins in three distinct evolutionary wave

183 or designing RNAs that competitively inhibit DNA binding proteins including transcription factors.

184 cleosomes occupy DNA targets for a subset of DNA-binding proteins, including CCCTC-binding factor (CT

185 We found that nucleosomes and specific DNA-binding proteins, including the general regulatory f

186 The T7 single-stranded DNA binding protein increases primer formation and exten

187 ctedly, a post-translational modification of DNA-binding proteins, initiating the cell response to si

188 The papillomavirus (PV) E2 protein is a DNA binding, protein interaction platform that recruits

189 hly conserved heterotrimeric single-stranded DNA-binding protein involved in DNA replication, recombi

190 ing yeast Rap1 is a specific double-stranded DNA-binding protein involved in repression and activatio

191 nge of DNA topoisomers at equilibrium with a DNA binding protein is separated into free and protein-b

192 Understanding the interactions of different DNA binding proteins is a crucial first step toward deci

193 Identification of these DNA-binding proteins is crucial to understanding the mec

194 The ribbon-helix-helix (RHH) superfamily of DNA-binding proteins is dispersed widely in procaryotes.

195 ork wherein a member of the DNABII family of DNA-binding proteins is positioned at the vertex of each

196 MuvB contains the DNA-binding protein LIN54, which directs the complex to

197 tingly, 5hmC colocalized with the methylated DNA binding protein MeCP2 and with the active chromatin

198 Once deposited, mCA is bound by the methyl-DNA-binding protein MECP2 and functions in a rheostat-li

199 Commonly, a DNA-binding protein mediates the interaction of viral DN

200 l cells in a manner that is dependent on the DNA-binding protein MRE11 and the antiviral factor IRF1

201 hin the leu-tRNA gene and is mediated by the DNA binding protein MTERF1.

202 oloenzyme, the mitochondrial single-stranded DNA binding protein mtSSB, the replicative helicase Twin

203 replisome, the mitochondrial single-stranded DNA-binding protein (mtSSB).

204 TAR DNA binding protein of 43 kDa (TDP-43) is the major path

205 2 protein (gp32) is the single-stranded (ss) DNA binding protein of the bacteriophage T4.

206 ral dementia (FTD) with transactive response DNA-binding protein of 43 kD (TDP-43)-positive inclusion

207 Trans-activation element DNA-binding protein of 43 kDa (TDP-43) characterizes ins

208 otemporal lobar degeneration (FTLD) with TAR DNA-binding protein of 43 kDa (TDP-43) pathology (FTLD-T

209 (WD repeat and high mobility group [HMG]-box DNA-binding protein), one of the genes that was upregula

210 d that could be adapted for delivering other DNA-binding proteins or functional nucleic acids.

211 nvolving nonstructural proteins, such as the DNA-binding protein P1 and the genome terminal protein (

212 This system depends on a DNA-binding protein ParB, which binds specifically to th

213 starvation protein A (SspA) complex and the DNA-binding protein pathogenicity island gene regulator

214 In Francisella tularensis, the putative DNA-binding protein PigR works in concert with the SspA

215 DNA-binding proteins play a very important role in the s

216 The DNA-binding protein PRDM9 directs positioning of the dou

217 The DNA-binding protein PRDM9 has a critical role in specify

218 In this paper, we present iDNAProt-ES, a DNA-binding protein prediction method that utilizes both

219 o form t-loops or complex with single-strand DNA binding proteins, raising the question of the mechan

220 ching has been reported or proposed for many DNA-binding proteins, raising the question of how widesp

221 ICD complex is recruited to chromatin by the DNA-binding protein Rbp-J in a Tead-independent fashion.

222 NA) screening, we identified single-stranded DNA binding protein replication protein A (RPA) as a reg

223 nted the accumulation of the single-stranded DNA binding protein replication protein A (RPA) on damag

224 ncoded nuclear antigen and sequence-specific DNA binding protein required for viral origin binding an

225 Together with the single-stranded DNA binding protein RPA, TopBP1/Dpb11 binds to UFBs, and

226 n (WRN) and the heterotrimeric eukaryotic ss-DNA binding protein RPA.

227 ast LTR retrotransposon Tf1 is guided by the DNA binding protein Sap1 and that the efficiency and loc

228 ssion yeast cells carrying a mutation in the DNA-binding protein Sap1 show defects in DNA replication

229 DNA-binding proteins search for specific targets via fac

230 active phosphatase Eya1 cooperates with the DNA-binding protein Six1 to promote gene induction in re

231 The DNA-binding protein SlmA binds to FtsZ and prevents Z-ri

232 consist of binding sites for many different DNA-binding proteins, some known and others unknown.

233 feasibility of CETCh-seq by tagging several DNA-binding proteins spanning a wide range of endogenous

234 The bacterial single-stranded DNA binding protein (SSB) acts as an organizer of DNA re

235 Escherichia coli single-stranded DNA binding protein (SSB) is an essential homotetramer t

236 E. coli single strand (ss) DNA binding protein (SSB) is an essential protein that b

237 The single-stranded DNA binding protein (SSB) of Escherichia coli plays esse

238 The single-stranded DNA binding protein (SSB) participates in this process,

239 otetrameric Escherichia coli single-stranded DNA binding protein (SSB) plays a central role in DNA re

240 ce of separation in DQAMmiR on single-strand DNA binding protein (SSB) whose native structure and bin

241 During DNA replication, the single-stranded DNA binding protein (SSB) wraps single-stranded DNA (ssD

242 ch revealed a novel mode for single-stranded DNA-binding protein (SSB)-DNA binding, in which SSB inte

243 so have higher levels of the single-stranded DNA-binding protein SSB1, which has a critical role in D

244 Single-stranded DNA binding proteins (SSBs) are ubiquitous across all or

245 Single-stranded DNA binding proteins (SSBs) selectively bind single-stra

246 on protein A (RPA) and other single-stranded DNA binding proteins (SSBs).

247 Single-stranded (ss) DNA-binding proteins (SSBs) bind and protect ssDNA inter

248 Single-stranded DNA-binding proteins (SSBs) play a key role in genome ma

249 However, as a DNA-binding protein, Sso7d is highly positively charged,

250 DNA binding proteins such as chromatin remodellers, tran

251 NA specificity, outside of extremely modular DNA binding proteins such as TAL effectors, has generall

252 y widespread footprints of sequence-specific DNA-binding proteins such as CTCF, which we validate in

253 covariance between histone modifications and DNA binding proteins, such as the relationship between t

254 applied to biological phenomena that involve DNA-binding proteins, such as DNA condensation with crys

255 Interestingly, single-stranded DNA-binding protein suppresses the MtRecG- and MtRuvAB-m

256 racterization of an HRP conjugate with scCro DNA binding protein tag and its application for the dete

257 unique DNA sensing platform based on an HRP-DNA binding protein tag conjugate and a hybrid ssDNA-dsD

258 These results show that the HRP-DNA binding protein tag conjugate can be used as an alte

259 equence-specific double- and single-stranded DNA-binding proteins, Taz1 and Pot1, respectively, bridg

260 egeneration (FTLD) with transactive response DNA-binding protein (TDP) inclusions in 40.5%, FTLD-tau

261 poral lobar degeneration (FTLD) with longTAR DNA-binding protein (TDP)-43-positive neuropil threads a

262 l aggregation and mutation of the 43-kDa TAR DNA-binding protein (TDP-43) are strongly implicated in

263 TAR DNA-binding protein (TDP-43) is a highly conserved and e

264 logical 43-kDa transactive response sequence DNA-binding protein (TDP-43) were also analysed.

265 cluding the telomeric repeat single-stranded DNA-binding protein Teb1 and its heterotrimer partners T

266 complex (TEB) with single-stranded telomere DNA-binding protein Teb1, paralogous to heterotrimeric r

267 other related homing endonucleases or other DNA-binding protein templates.

268 ARID3B is a DNA binding protein that is overexpressed in neuroblasto

269 Cdc13, a single-stranded DNA binding protein that recruits telomerase to endogeno

270 This system provides a model for any DNA-binding protein that can be posttranslationally modi

271 MECP2 encodes a methyl-DNA-binding protein that has been proposed to function a

272 EBNA1 is a sequence-specific DNA-binding protein that is consistently expressed in EB

273 ication of Combgap (Cg), a sequence-specific DNA-binding protein that is involved in recruitment of P

274 In the absence of MatP, a DNA-binding protein that links ZapB to the chromosomal t

275 E STATEMENT CCCTC-binding factor (CTCF) is a DNA-binding protein that organizes nuclear chromatin top

276 PA over RPA (replication protein A), another DNA-binding protein that participates in the nucleotide

277 ication protein A (RPA) is a single-stranded DNA-binding protein that plays an essential role in DNA

278 Ikaros is a zinc finger DNA-binding protein that regulates chromatin remodeling

279 Here we describe a role for RefZ, a DNA-binding protein that regulates FtsZ, and its cognate

280 a risk locus for schizophrenia and encodes a DNA-binding protein that regulates higher-order chromati

281 nesis, and SOX5 and SOX6 are closely related DNA-binding proteins that critically enhance its functio

282 occluding the underlying DNA sequences from DNA-binding proteins that must act on it.

283 ential to distinguish nucleosomes from other DNA-binding proteins that protect against MNase.

284 We propose that DNA-binding proteins that rapidly re-associate post-repl

285 temperature, encode closely related AP2/ERF DNA-binding proteins that recognize the C-repeat (CRT)/d

286 anscription factors is a conserved family of DNA-binding proteins that responds to a diverse set of c

287 be a general mechanism used by site-specific DNA-binding proteins to minimize time-consuming interrog

288 f genes, including the gene encoding the RNA/DNA-binding protein translocated in liposarcoma or fused

289 X1-SLX4 is negatively regulated by telomeric DNA-binding proteins TRF1 and TRF2 and is suppressed by

290 rts focus on affinity and specificity of the DNA-binding proteins, typically overlooking the kinetic

291 G colocalized with the viral single-stranded DNA binding protein UL57, but colocalization became less

292 show that in vivo delivery of an engineered DNA-binding protein uncoupled from the repressor domain

293 Many DNA binding proteins utilize one-dimensional (1D) diffus

294 specifically measuring target site search by DNA-binding proteins via intersegmental translocation.

295 evertants, the thrR gene encoding a putative DNA-binding protein was inactivated, also resulting in c

296 unders of a new structural family of dimeric DNA-binding proteins with C-terminal, flexible, effector

297 Bacteria use a set of DNA-binding proteins with low sequence specificity calle

298 In Drosophila, the DNA-binding protein Zelda (also known as Vielfaltig) is

299 -of-function mutations we engineered the ZF6-DNA-binding protein (ZF6-DB) that targets 20 base pairs

300 to various DNA-binding modules: full-length DNA binding proteins, zinc fingers (ZFs), transcription