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

1 ors on the orexin promoter, as determined by chromatin immunoprecipitation.

2 emaker, we identified UNF target genes using chromatin immunoprecipitation.

3 ication involving histone H3 acetylation via chromatin immunoprecipitation.

4 d by Y1H, electrophoretic mobility assay and chromatin immunoprecipitation.

5 ns of "standard" chromatin assays, including chromatin immunoprecipitation.

6 rse transcriptase (qRT)-PCR, zymography, and chromatin immunoprecipitation.

7 GC-1alpha promoter was examined in NAc using chromatin immunoprecipitation after repeated cocaine.

8 To determine direct targets, we performed a chromatin immunoprecipitation against Lmx1b in mouse lim

9 Chromatin immunoprecipitation analyses demonstrated that

10 Chromatin immunoprecipitation analyses of liver tissue s

11 Notably, biochemical and chromatin immunoprecipitation analyses reveal constituti

12 ation of bioinformatics, reporter assay, and chromatin immunoprecipitation analyses, we found that NF

13 Chromatin immunoprecipitation analysis confirmed that cl

14 Finally, chromatin immunoprecipitation analysis confirmed that Ly

15 Chromatin immunoprecipitation analysis demonstrated that

16 Chromatin immunoprecipitation analysis demonstrates bind

17 Chromatin immunoprecipitation analysis determined GATA-3

18 Chromatin immunoprecipitation analysis identified putati

19 However, chromatin immunoprecipitation analysis in embryonic stem

20 Chromatin immunoprecipitation analysis in vivo and elect

21 Electrophoretic mobility shift assay and chromatin immunoprecipitation analysis indicated that Kl

22 o and in vitro gene profiling, together with chromatin immunoprecipitation analysis of macrophages, r

23 Chromatin immunoprecipitation analysis of the hypomorphi

24 Furthermore, chromatin immunoprecipitation analysis revealed that OA-

25 Chromatin immunoprecipitation analysis showed that this

26 for Elk-1-mediated transcription activation (chromatin immunoprecipitation analysis) of the miR-17-92

27 Chromatin changes were studied by chromatin immunoprecipitation analysis, nucleosome posit

28 EBF1 promoter was demonstrated by EMSAs and chromatin immunoprecipitation analysis, suggesting trans

29 BP1) in liver regeneration using genome-wide chromatin immunoprecipitation analysis.

30 In chromatin immunoprecipitation and co-immunoprecipitation

31 Using chromatin immunoprecipitation and EMSA, we found that ST

32 o two locations in the tru1 gene as shown by chromatin immunoprecipitation and gel shifts.

33 We have combined chromatin immunoprecipitation and gene expression profil

34 s of chromatin conformation, allele-specific chromatin immunoprecipitation and genome editing, we sho

35 Using chromatin immunoprecipitation and high-resolution microa

36 lopment of G4 ChIP-seq, an antibody-based G4 chromatin immunoprecipitation and high-throughput sequen

37 We confirmed the candidacy of DNAJB1 through chromatin immunoprecipitation and luciferase assays whil

38 Chromatin immunoprecipitation and luciferase reporter as

39 Chromatin immunoprecipitation and NNMT promoter lucifera

40 ce, western blot, reverse-transcriptase PCR, chromatin immunoprecipitation and promoter reporter assa

41 ntroduce a novel molecular assay, ChIPnQASO (Chromatin Immunoprecipitation and Quantitative Allele-Sp

42 Chromatin immunoprecipitation and reporter assays reveal

43 body of literature, based on next generation chromatin immunoprecipitation and RNA sequencing of rewa

44 Interestingly, genome-wide chromatin immunoprecipitation and RNA sequencing results

45 However, conventional chromatin immunoprecipitation and sequencing (ChIP-seq)

46 Chromatin immunoprecipitation and sequencing analysis re

47 ogy integrates data from 295 prostate cancer chromatin immunoprecipitation and sequencing experiments

48 Chromatin immunoprecipitation and sequencing experiments

49 mical approaches including quantitative PCR, chromatin immunoprecipitation, and 3,3'-diaminobenzidine

50 Using luciferase reporters, chromatin immunoprecipitation, and expression studies, w

51 uantitative real-time PCR, Western blotting, chromatin immunoprecipitation, and functional assays.

52 iology of TOP2B, we used proteomics (BioID), chromatin immunoprecipitation, and high-throughput chrom

53 c analyses such as RNA sequencing (RNA-Seq), chromatin immunoprecipitation, and ribosome profiling.

54 a combination of gene expression profiling, chromatin immunoprecipitation, and targeted proteomics v

55 Here, using knockout mice, chromatin immunoprecipitations, and cellular and molecul

56 Chromatin immunoprecipitation assay confirmed an enhance

57 A chromatin immunoprecipitation assay confirmed that hyper

58 Moreover, a chromatin immunoprecipitation assay demonstrated that MY

59 Chromatin immunoprecipitation assay identified HIF-1alph

60 ies using the luciferase reporter system and chromatin immunoprecipitation assay revealed that IFNalp

61 HNF4alpha to Agxt2 promoter was confirmed by chromatin immunoprecipitation assay.

62 Chromatin immunoprecipitation assays and PCR analysis co

63 Chromatin immunoprecipitation assays confirmed that hype

64 Furthermore, DNA affinity and chromatin immunoprecipitation assays demonstrated that A

65 Luciferase reporter and chromatin immunoprecipitation assays demonstrated that T

66 Chromatin immunoprecipitation assays from NAP1L1-deplete

67 reaction, Western blots, flow cytometry, and chromatin immunoprecipitation assays in ERalpha- and HER

68 Chromatin immunoprecipitation assays indicated that KAT8

69 Chromatin immunoprecipitation assays indicated that PAF-

70 Chromatin immunoprecipitation assays of BCBL-1 and BC-3

71 Gel shift and chromatin immunoprecipitation assays revealed that HspBP

72 In silico analysis and chromatin immunoprecipitation assays revealed that the d

73 ncing of BRD4, an important BET protein, and chromatin immunoprecipitation assays showed that JQ1 alt

74 Using chromatin immunoprecipitation assays we demonstrate that

75 Mutation analysis of the promoter and chromatin immunoprecipitation assays were performed to i

76 tadpoles treated with or without T3 and for chromatin immunoprecipitation assays with these chips, w

77 In chromatin immunoprecipitation assays, 25-hydroxyvitamin

78 s, small GTPase activity, luciferase assays, chromatin immunoprecipitation assays, and network analys

79 In chromatin immunoprecipitation assays, p65 bound directly

80 quencing-mediated transcriptome analysis and chromatin immunoprecipitation assays, suggesting that MY

81 E promoter and demonstrated, using EMSAs and chromatin immunoprecipitation assays, that AP-2alpha cou

82 ow, using electrophoretic mobility shift and chromatin immunoprecipitation assays, that phosphorylati

83 Using luciferase and chromatin immunoprecipitation assays, we demonstrate tha

84 Using chromatin immunoprecipitation assays, we discovered that

85 ivity and studied in immunoprecipitation and chromatin immunoprecipitation assays.

86 -kappaB subunit p65 in cells was analyzed in chromatin immunoprecipitation assays.

87 ion of the EDNRB gene in transactivation and chromatin immunoprecipitation assays; results were valid

88 ernative splicing and performed quantitative chromatin immunoprecipitation at downstream targets in N

89 ated for expression, transposition activity, chromatin immunoprecipitation at the target loci, and ta

90 Using chromatin immunoprecipitation-based sequencing (ChIP-seq

91 determination of elongation rate in vivo by chromatin immunoprecipitation can be confounded by the k

92 o TOT preferential genomic binding sites, by chromatin immunoprecipitation (ChIP) analyses.

93 Genome-wide chromatin immunoprecipitation (ChIP) analysis and gene-e

94 Chromatin immunoprecipitation (ChIP) analysis of the CCN

95 Chromatin immunoprecipitation (ChIP) analysis showed tha

96 ce recovery experiments in living cells, and chromatin immunoprecipitation (ChIP) analysis, measured

97 We show through chromatin immunoprecipitation (ChIP) and chemical inhibi

98 Chromatin immunoprecipitation (ChIP) and chromatin isola

99 pitation (IP) for epigenetic assays, such as chromatin immunoprecipitation (ChIP) and methylated DNA

100 Chromatin immunoprecipitation (ChIP) and micrococcal nuc

101 A electrophoretic mobility shift assay and a chromatin immunoprecipitation (ChIP) assay, while the fi

102 Chromatin immunoprecipitation (ChIP) assays demonstrate

103 Chromatin immunoprecipitation (ChIP) assays established

104 ulates SALL4 transcription, we quantified by chromatin immunoprecipitation (ChIP) assays RNA polymera

105 s of our Affymetrix microarray profiling and chromatin immunoprecipitation (ChIP) assays, we found th

106 In chromatin immunoprecipitation (ChIP) assays, we showed a

107 s shown by DNM3os transcription reporter and chromatin immunoprecipitation (ChIP) assays.

108 FBSbank' which houses the annotation of 1870 chromatin immunoprecipitation (ChIP) datasets of 585 TFs

109 of maize, sorghum and rice, as evidenced by Chromatin immunoprecipitation (ChIP) experiments.

110 protein associates with RNA polymerase, and chromatin immunoprecipitation (ChIP) followed by high-th

111 y all GR binding sites (GBSs) captured using chromatin immunoprecipitation (ChIP) in A549 cells.

112 mine H3NT-cleaved regions in mammals, called chromatin immunoprecipitation (ChIP) of acetylated chrom

113 The validation with the chromatin immunoprecipitation (ChIP) sequencing (ChIP-Se

114 Unlike other 3C-based methods, it includes a chromatin immunoprecipitation (ChIP) step that enriches

115 Chromatin immunoprecipitation (ChIP) studies illustrated

116 Chromatin immunoprecipitation (ChIP) studies reveal geno

117 se STAT5A is a transcription factor, we used chromatin immunoprecipitation (ChIP) to assess PDC's abi

118 of protein-protein interactions, comparative chromatin immunoprecipitation (ChIP) with sequencing, to

119 Western blotting, chromatin immunoprecipitation (ChIP), and luciferase ass

120 electrophoretic mobility shift assay (EMSA), chromatin immunoprecipitation (ChIP), promoter cloning,

121 ctrophoretic mobility shift assay (EMSA) and chromatin immunoprecipitation (ChIP), we found evidence

122 Unlike Chromatin Immunoprecipitation (ChIP), which fragments an

123 lated genes, including Lin28b and Hmga2, and chromatin immunoprecipitation (ChIP)-quantitative PCR (q

124 -responsive and ERG-dependent genes, and ERG chromatin immunoprecipitation (ChIP)-seq revealed the pr

125 Here, we analyze 85 RNA polymerase II chromatin immunoprecipitation (ChIP)-sequencing experime

126 d to bind the respective promoter regions by chromatin immunoprecipitation (ChIP).

127 ter, as revealed by mutagenesis analysis and chromatin immunoprecipitation (ChIP).

128 Chromatin immunoprecipitation (ChIP-seq) is the omics te

129 Using in silico/chromatin-immunoprecipitation (ChIP) analysis we identif

130 Chromatin-immunoprecipitation (ChIP-seq) revealed BAZ1B

131 ChIP-seq (chromatin immunoprecipitation [ChIP] combined with high-

132 Here, we leveraged p53 ChIP-seq (chromatin immunoprecipitation [ChIP] combined with high-

133 ChIP-seq (chromatin immunoprecipitation [ChIP] combined with high-

134 ChIP-seq (chromatin immunoprecipitation [ChIP] followed by deep se

135 By combining gene expression profiling and chromatin immunoprecipitation coupled to deep sequencing

136 Using histone mark chromatin immunoprecipitation coupled with deep sequenci

137 renal cell carcinoma (RCC) cell lines using chromatin immunoprecipitation coupled with high-throughp

138 Chromatin immunoprecipitation coupled with next-generati

139 ave been implemented into the core ChIP-seq (chromatin immunoprecipitation coupled with next-generati

140 ors showed decreased H3K27me3 as revealed by chromatin immunoprecipitation coupled with quantitative

141 ghput technologies including RNA sequencing, chromatin-immunoprecipitation-coupled sequencing, mass-s

142 In silico analysis in conjunction with chromatin immunoprecipitation demonstrated MADS-RIN prot

143 Chromatin immunoprecipitation demonstrates dynamic RBP-J

144 Chromatin immunoprecipitation, DNase I hypersensitivity

145 Engineered DNA-binding molecule-mediated chromatin immunoprecipitation (enChIP), coupled with mas

146 tered gene expression, the magnitude of SHB1 chromatin immunoprecipitation enrichment and the over-re

147 Analysis by the chromatin immunoprecipitation-exonuclease (ChIP-exo) met

148 transcription factor-DNA-binding arrays and chromatin immunoprecipitation experiments identified the

149 Chromatin immunoprecipitation experiments reveal increas

150 Chromatin immunoprecipitation experiments revealed that

151 Chromatin immunoprecipitation experiments revealed that

152 Transcriptional analysis and chromatin immunoprecipitation experiments revealed that

153 Chromatin immunoprecipitation experiments showed that th

154 We performed co-immunoprecipitation and chromatin immunoprecipitation experiments.

155 Chromatin-immunoprecipitation experiments showed that HE

156 We applied high-resolution ChIP-exo (chromatin immunoprecipitation followed by 5'-to-3' exonu

157 idelines for efficient generation of histone chromatin immunoprecipitation followed by deep sequencin

158 eated with dexamethasone, TNF, or both using chromatin immunoprecipitation followed by deep sequencin

159 in status on DNA barcodes is interrogated by chromatin immunoprecipitation followed by deep sequencin

160 Chromatin immunoprecipitation followed by deep sequencin

161 of nucleic acid sequencing datasets such as chromatin immunoprecipitation followed by deep sequencin

162 Chromatin immunoprecipitation followed by deep sequencin

163 x2 in mouse and human nephron progenitors by chromatin immunoprecipitation followed by DNA sequencing

164 Chromatin immunoprecipitation followed by DNA sequencing

165 the genome-wide direct targets of SVP2 using chromatin immunoprecipitation followed by high-throughpu

166 hich were essentially confirmed by ChIP-seq (chromatin immunoprecipitation followed by massively para

167 Chromatin immunoprecipitation followed by massively para

168 linical pathology specimens severely hampers chromatin immunoprecipitation followed by next-generatio

169 Using chromatin immunoprecipitation followed by next-generatio

170 Histone H3 phosphorylation was analyzed by chromatin immunoprecipitation followed by promotor-speci

171 Chromatin immunoprecipitation followed by sequencing (Ch

172 nd analyzed 214 public datasets representing chromatin immunoprecipitation followed by sequencing (Ch

173 e H3 located in eukaryote centromeres) using chromatin immunoprecipitation followed by sequencing (Ch

174 ranscription factor (TF) binding sites using chromatin immunoprecipitation followed by sequencing (Ch

175 e analysis of transcription factors (TFs) by chromatin immunoprecipitation followed by sequencing (Ch

176 Chromatin immunoprecipitation followed by sequencing (Ch

177 Chromatin immunoprecipitation followed by sequencing (Ch

178 lation at lysine 27 of histone H3 (H3K27me3) chromatin immunoprecipitation followed by sequencing ide

179 he more common scenario of ERG upregulation, chromatin immunoprecipitation followed by sequencing ind

180 Genetic perturbations and chromatin immunoprecipitation followed by sequencing rev

181 Chromatin immunoprecipitation followed by sequencing rev

182 Genome-wide analysis of chromatin immunoprecipitation followed by sequencing rev

183 rophages (BDMs) with L. pneumophila and used chromatin immunoprecipitation followed by sequencing to

184 6 and 48 hours after surgery and analyzed by chromatin immunoprecipitation followed by sequencing.

185 ochemical and crystal structural studies and chromatin-immunoprecipitation followed by sequencing ana

186 Through chromatin immunoprecipitation, followed by RT-PCR analys

187 ium Synechocystis sp. PCC 6803, we performed chromatin immunoprecipitation, followed by sequencing (C

188 estern blotting, co-immunoprecipitation, and chromatin immunoprecipitation following abstinence from

189 By chromatin immunoprecipitation FOXO1 was shown to bind to

190 Chromatin immunoprecipitation high-throughput sequencing

191 Klf13 gene and its function was verified by chromatin immunoprecipitation in HL-1 cells and mouse he

192 sposase-accessible chromatin sequencing, and chromatin immunoprecipitation in human umbilical vein en

193 yces cerevisiae Mediator from chromatin with chromatin immunoprecipitation in order to reveal Mediato

194 n Yang 1 (YY1), confirmed by allele-specific chromatin immunoprecipitation in primary adipocytes.

195 -318 to +54 of Dspp promoter was verified by chromatin immunoprecipitation in vivo.

196 al, in situ hybridization, RNA sequence, and chromatin immunoprecipitation methods.

197 Here, using chromatin immunoprecipitation/next generation sequencing

198 duction by TcREG Furthermore, we show, using chromatin immunoprecipitation, NF-kappaB enrichment in t

199 We used chromatin immunoprecipitation of histone H3 and RNA poly

200 We performed chromatin immunoprecipitation on reporter genes containi

201 were direct targets of RFX2, as revealed by chromatin immunoprecipitation-PCR assays.

202 Chromatin immunoprecipitation-PCR detected increased ETS

203 alling by the Human Phospho-Kinase Array and chromatin immunoprecipitation-PCR revealed that unlike G

204 Here, we apply permanganate treatment and chromatin immunoprecipitation (PIP-seq) of initiation fa

205 Likewise, mapping TF binding through chromatin immunoprecipitation proved less predictive of

206 Chromatin-Immunoprecipitation-qPCR and electrophoretic m

207 mmunoprecipitation sequencing (ChIP-seq) and chromatin immunoprecipitation quantitative PCR (ChIP-qPC

208 o analyses to identify targets of MIR122 and chromatin immunoprecipitation quantitative polymerase ch

209 Furthermore, chromatin immunoprecipitation-quantitative PCR assay sho

210 Moreover, ENCODE data and our chromatin immunoprecipitation results indicate that cohe

211 Chromatin immunoprecipitation results suggested that RDM

212 Chromatin immunoprecipitation revealed a significantly h

213 being detectable early in enriched pups, and chromatin immunoprecipitation revealed an increase at th

214 Chromatin immunoprecipitation revealed that H3K4me3, the

215 Chromatin immunoprecipitation revealed that Kdm5b is pre

216 Chromatin immunoprecipitation revealed that MYST3 binds

217 Chromatin immunoprecipitation reveals dynamic binding of

218 Chromatin immunoprecipitation reveals that Stat3 binds t

219 By performing promoter activity assays and chromatin immunoprecipitation, reverse transcriptase qua

220 We integrated sequencing data from chromatin immunoprecipitation, RNA expression, DNA methy

221 chromatin immunoprecipitation-seq analyses of NRSF targe

222 binding of the GC receptor (GR) detected by chromatin immunoprecipitation-Seq correlated with induct

223 Using chromatin immunoprecipitation-seq, we classified 20% of

224 Bioinformatic and chromatin immunoprecipitation sequencing (ChIP-seq) anal

225 Chromatin immunoprecipitation sequencing (ChIP-seq) and

226 Using chromatin immunoprecipitation sequencing (ChIP-seq) comb

227 Chromatin immunoprecipitation sequencing (ChIP-seq) expe

228 Chromatin immunoprecipitation sequencing (ChIP-seq) expe

229 Chromatin immunoprecipitation sequencing (ChIP-seq) reve

230 Using chromatin immunoprecipitation sequencing (ChIP-Seq) we r

231 he cytokinin primary response, making use of chromatin immunoprecipitation sequencing (ChIP-seq), pro

232 enome wide in the HNSCC model UM-SCC46 using chromatin immunoprecipitation sequencing (ChIP-seq).

233 ell as data from related experiments such as Chromatin Immunoprecipitation sequencing (ChIP-Seq).

234 st, inexpensive, and more easily scaled than chromatin immunoprecipitation sequencing (ChIP-seq).

235 Here we describe fixed-tissue chromatin immunoprecipitation sequencing (FiT-seq), a me

236 In addition, chromatin immunoprecipitation sequencing analyses showed

237 Gene profiling and chromatin immunoprecipitation sequencing analyses unrave

238 We performed Sp7 chromatin immunoprecipitation sequencing analysis identi

239 Chromatin immunoprecipitation sequencing analysis reveal

240 Chromatin immunoprecipitation sequencing analysis with i

241 Chromatin immunoprecipitation sequencing and gene expres

242 Our distribution was supported by chromatin immunoprecipitation sequencing and microarray

243 We used chromatin immunoprecipitation sequencing and RNA sequenc

244 egulates adult neural stem cells, we perform chromatin immunoprecipitation sequencing and RNA-sequenc

245 shed Arabidopsis (Arabidopsis thaliana) EIN3 chromatin immunoprecipitation sequencing data set, we in

246 Analysis of chromatin immunoprecipitation sequencing data sets for M

247 integrated these profiles with whole-animal chromatin immunoprecipitation sequencing data to deconvo

248 the identified CNSs were evaluated using TF chromatin immunoprecipitation sequencing data, resulting

249 Genome-wide chromatin immunoprecipitation sequencing experiments rev

250 Using RNA-sequencing and chromatin immunoprecipitation sequencing experiments, we

251 ole for CLOCK in human neurons by performing chromatin immunoprecipitation sequencing for endogenous

252 sing both whole-transcriptome sequencing and chromatin immunoprecipitation sequencing pinpointed onco

253 ar cell in vivo Transcriptome sequencing and chromatin immunoprecipitation sequencing results showed

254 Chromatin immunoprecipitation sequencing revealed H3K27m

255 Furthermore, chromatin immunoprecipitation sequencing revealed that t

256 Furthermore, microarray and chromatin immunoprecipitation sequencing screens led to

257 We used RNA sequencing coupled with chromatin immunoprecipitation sequencing to identify gen

258 t approaches for the study of the epigenome (chromatin immunoprecipitation sequencing) and transcript

259 s in Arabidopsis seedlings were generated by chromatin immunoprecipitation sequencing, and changes in

260 hole-genome bisulfite sequencing and H3K27Ac chromatin-immunoprecipitation sequencing of primary tumo

261 However, most chromatin immunoprecipitation-sequencing (ChIP-seq) anal

262 The method can be used in parallel with chromatin immunoprecipitation-sequencing (ChIP-seq) expe

263 for continuous functional genomic data (e.g. chromatin immunoprecipitation-sequencing (ChIP-seq) peak

264 d de novo using epigenetic data derived from chromatin immunoprecipitation-sequencing (ChIP-Seq).

265 Genome-wide chromatin immunoprecipitation-sequencing analysis reveal

266 uced genes were identified by integration of chromatin immunoprecipitation-sequencing and RNA-sequenc

267 Moreover, chromatin immunoprecipitation-sequencing reveals BRG1 bi

268 ng on the integration of DNA methylation and chromatin immunoprecipitation-sequencing technologies in

269 Chromatin-immunoprecipitation-sequencing (ChIP-seq)-repo

270 Chromatin immunoprecipitation showed PPAR-gamma binding

271 Chromatin immunoprecipitation showed that C/EBPbeta was

272 Chromatin immunoprecipitation showed that further induct

273 Chromatin immunoprecipitation showed the presence of HDA

274 This is supported by chromatin immunoprecipitation showing IRF1 recruitment t

275 Chromatin immunoprecipitation shows that DUX4 recruits p

276 paB to DNA demethylation was tested by using chromatin immunoprecipitation, small interfering RNA-med

277 By chromatin immunoprecipitation, STAT1 bound a putative re

278 The complexity and inefficiency of chromatin immunoprecipitation strategies restrict their

279 pression of TP53 and CC-regulated genes with chromatin immunoprecipitation studies for TP53, RB1, E2F

280 Chromatin immunoprecipitation studies further demonstrat

281 Chromatin immunoprecipitation studies revealed both Jagg

282 Chromatin immunoprecipitation studies revealed that the

283 By chromatin immunoprecipitation studies, we found decrease

284 kely due to methodological weakness in early chromatin immunoprecipitation studies.

285 ther analyses using luciferase reporters and chromatin immunoprecipitation suggested that the -70 kb

286 We confirmed by chromatin immunoprecipitation that P4 recruits PR to the

287 Here we show, by chromatin immunoprecipitation, that UV-B exposure of Ara

288 LPS silencing of Rgs10 Furthermore, we used chromatin immunoprecipitation to demonstrate that H3 his

289 forward and reverse genetic approaches with chromatin immunoprecipitation to identify centromeres of

290 qRT-PCR, Western blotting, ELISA, and ChIP (chromatin immunoprecipitation) to characterize Pb-induce

291 ctivation were determined in both sexes, and chromatin immunoprecipitation was used to determine tran

292 Using dual-luciferase reporter assay and Chromatin immunoprecipitation, we demonstrate there is a

293 nitin treatment, transcriptome profiling and chromatin immunoprecipitation, we found that TFI gene ex

294 alyses, as well as targeted metabolomics and chromatin immunoprecipitation, were performed on the liv

295 urther mechanistic insights were provided by chromatin immunoprecipitation, Western blot, and immunos

296 Chromatin immunoprecipitation with anti-KNL2 antibodies

297 By using chromatin immunoprecipitation with CRISPR/Cas9 knockin o

298 Chromatin immunoprecipitation with massively parallel DN

299 Here, by combining studies using chromatin immunoprecipitation with sequencing and RNA se

300 nding in gel shift assays and as assessed by chromatin immunoprecipitation with the -14-kb Pu.1 or +3