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1 d YY1 from the FCER1A promotor, evaluated by chromatin immunoprecipitation.
2 ranscriptional modifications (PTMs) by micro-chromatin immunoprecipitation.
3 odulin (TM), as shown by reporter assays and chromatin immunoprecipitation.
4 nuclease cleavage and release is followed by chromatin immunoprecipitation.
5 mus at the onset of puberty as determined by chromatin immunoprecipitation.
6 eering, genome imaging, genetic screens, and chromatin immunoprecipitation.
7 ssessed using luciferase reporter assays and chromatin immunoprecipitation.
8 o E-cadherin promoter was investigated using chromatin immunoprecipitation.
9 actions that can be authenticated in vivo by chromatin immunoprecipitation.
10 d by Y1H, electrophoretic mobility assay and chromatin immunoprecipitation.
11 YC to the promoter of two candidate genes by chromatin immunoprecipitation.
12 To determine direct targets, we performed a chromatin immunoprecipitation against Lmx1b in mouse lim
25 EBF1 promoter was demonstrated by EMSAs and chromatin immunoprecipitation analysis, suggesting trans
38 rigins through LANA was demonstrated through chromatin immunoprecipitation and isolation of proteins
39 gate the mechanisms of NS1 function, we used chromatin immunoprecipitation and laser-microdissection
40 ect transcriptional target of SOX9, based on chromatin immunoprecipitation and luciferase reporter as
52 patterns of human primary bladder tumours by chromatin immunoprecipitations and next-generation seque
53 The Cancer Genome Atlas (TCGA) dataset, (b) chromatin immunoprecipitation, and (c) determination of
54 c analyses such as RNA sequencing (RNA-Seq), chromatin immunoprecipitation, and ribosome profiling.
55 methods for TF-occupancy profiling, such as chromatin immunoprecipitation, are limited by requiremen
56 Electrophoretic mobility shift assays and chromatin immunoprecipitation assay quantitative polymer
60 he neuronal Pomc enhancers nPE1 and nPE2 and chromatin immunoprecipitation assays detected in vivo bi
62 clear receptor corepressor 2 repression, and chromatin immunoprecipitation assays identified peroxiso
70 cipitation, yeast two-hybrid, gel shift, and chromatin immunoprecipitation assays) to identify and co
71 ow, using electrophoretic mobility shift and chromatin immunoprecipitation assays, that phosphorylati
72 east two-hybrid, co-immunoprecipitation, and chromatin immunoprecipitation assays, we show that Like
73 ernative splicing and performed quantitative chromatin immunoprecipitation at downstream targets in N
78 inding of p53 as well as HIF-1alpha to Zp in chromatin immunoprecipitation (ChIP) assays, but only wh
80 g reverse protein array, immunoblotting, and chromatin immunoprecipitation (ChIP) coupled with sequen
82 ation capture technology in combination with chromatin immunoprecipitation (ChIP) has provided a syst
89 promoter of NFKB inhibitor beta (NFKBIB) by chromatin immunoprecipitation (ChIP) sequencing and ChIP
91 tional profiling by means of RNA-sequencing, chromatin immunoprecipitation (ChIP) sequencing, and ass
92 , ovary, kidney, and heart with existing p53 chromatin immunoprecipitation (ChIP) sequencing, we iden
94 identify HIF transcriptional targets in IEC, chromatin immunoprecipitation (ChIP) was performed in Ca
95 otein-DNA crosslinking patterns by combining chromatin immunoprecipitation (ChIP) with 5' -> 3' exonu
96 ing (ChIP-seq) is a technology that combines chromatin immunoprecipitation (ChIP) with next generatio
101 ription polymerase chain reaction (qRT-PCR), chromatin immunoprecipitation (ChIP)-PCR and EMSA were u
102 and monitored the formation of gamma-H2AX by chromatin immunoprecipitation (ChIP)-qPCR in order to un
105 ability of thousands of genome-wide coupling chromatin immunoprecipitation (ChIP)-Seq datasets across
106 Here, we have used RNA sequencing (RNA-seq), chromatin immunoprecipitation (ChIP)-seq, and genome-wid
110 ntrolled TF nuclear import using time-series chromatin immunoprecipitation (ChIP-seq) and/or DNA aden
115 ing events in micrococcal nuclease ChIP-seq (chromatin immunoprecipitation [ChIP] combined with high-
123 cherichia coli and Salmonella revealed using chromatin immunoprecipitation coupled with next-generati
125 viously, we described a novel alternative to chromatin immunoprecipitation, CUT&RUN, in which unfixed
126 mmunity and evaluate their performance using chromatin immunoprecipitation data sets for 40 TFs.
127 ng results were aligned with those of pol II chromatin immunoprecipitation-deep sequencing across the
129 l II dynamics and gene expression, the FoxO1 chromatin immunoprecipitation-deep sequencing results we
130 in the SV40 chromatin found in virions using chromatin immunoprecipitation-DNA sequencing (ChIP-Seq).
131 chain reaction, luciferase reporter assays, chromatin immunoprecipitation, docking and molecular dyn
133 high-throughput genomic analyses, including chromatin immunoprecipitation experiments and genome-wid
141 ers marked by extraordinarily high and broad chromatin immunoprecipitation followed by deep sequencin
142 of nucleic acid sequencing datasets such as chromatin immunoprecipitation followed by deep sequencin
144 binding affinity by observing differences in chromatin immunoprecipitation followed by deep sequencin
145 lysis of Treg cells by RNA-sequencing, Foxp3 chromatin immunoprecipitation followed by high-throughpu
146 NA Elements) project, data and analyses from chromatin immunoprecipitation followed by high-throughpu
147 28p in response to chronic beta-AR stress by chromatin immunoprecipitation followed by massive genomi
150 the precise recruitment of MRE11 to DSBs by chromatin immunoprecipitation followed by next-generatio
152 such as position weight matrices (PWMs) and chromatin immunoprecipitation followed by sequencing (Ch
153 We have undertaken a transcriptomic and chromatin immunoprecipitation followed by sequencing (Ch
155 Using RNA sequencing (RNA-seq), histone chromatin immunoprecipitation followed by sequencing (Ch
156 important for inferring target genes from TF chromatin immunoprecipitation followed by sequencing (Ch
158 on of microfluidic oscillatory washing-based chromatin immunoprecipitation followed by sequencing (MO
161 ng epigenetic profiling for enhancer H3K27ac chromatin immunoprecipitation followed by sequencing in
162 he more common scenario of ERG upregulation, chromatin immunoprecipitation followed by sequencing ind
166 e latter, recent work has utilized ChIP-seq (chromatin immunoprecipitation followed by sequencing) to
168 6 and 48 hours after surgery and analyzed by chromatin immunoprecipitation followed by sequencing.
169 s that express individual FXR isoforms using chromatin immunoprecipitation, followed by sequencing an
170 orted by chromosome conformation capture and chromatin immunoprecipitation for cells after transcript
171 r to fully active ESs as determined by using chromatin immunoprecipitation for multiple epigenetic ma
173 anogaster by combining long-read sequencing, chromatin immunoprecipitation for the centromeric histon
186 o analyses to identify targets of MIR122 and chromatin immunoprecipitation quantitative polymerase ch
187 cells that expressed the FXR isoforms using chromatin immunoprecipitation, quantitative polymerase c
188 and MtCCS52A in roots and nodule primordia, chromatin immunoprecipitation-quantitative PCR and proto
189 group H3K4-methyl-transferases in StMSI1-OE Chromatin immunoprecipitation-quantitative PCR confirmed
190 epigenetic histone mark H3K27me3 in vivo and chromatin immunoprecipitation-quantitative PCR results s
191 together with the Tandem Mass Tag approach, chromatin immunoprecipitation-quantitative polymerase ch
192 a proximity ligation assay (PLA) and double chromatin immunoprecipitation (ReCHIP) that Omomyc prefe
194 ss-response transcription factor NF-kappaB1, chromatin immunoprecipitation revealed reduced gammaH2A.
200 lution of ligands by exponential enrichment, chromatin immunoprecipitation-seq, and cross-linking imm
201 phorylation, mass spectrometry analysis, and chromatin immunoprecipitation sequencing (ChIP-seq) anal
205 SA2 binding and R-loops sites extracted from Chromatin Immunoprecipitation sequencing (ChIP-seq) and
208 e report the genomic landscape of REC8 using chromatin immunoprecipitation sequencing (ChIP-seq) in A
213 onad development among species, we performed chromatin immunoprecipitation sequencing (ChIP-seq) usin
214 mics by performing RNA sequencing (RNA-seq), chromatin immunoprecipitation sequencing (ChIP-seq), and
216 alyses of R-loop data with existing RNA-seq, chromatin immunoprecipitation sequencing (ChIP-seq), DNa
217 he cytokinin primary response, making use of chromatin immunoprecipitation sequencing (ChIP-seq), pro
218 ponential enrichment sequencing (SELEX-seq), chromatin immunoprecipitation sequencing (ChIP-seq), RNA
219 s likely functionally relevant, validated by chromatin immunoprecipitation sequencing (ChIP-seq).
220 now report the successful adaptation of this chromatin immunoprecipitation sequencing (ChIPseq) appro
222 ic targets in CIC-DUX4 sarcoma, we performed chromatin immunoprecipitation sequencing analysis using
227 -inducible isogenic cell lines and performed chromatin immunoprecipitation sequencing and transcripto
229 ds/degradome reads, RNA sequencing, and even chromatin immunoprecipitation sequencing data; it also p
231 ole for CLOCK in human neurons by performing chromatin immunoprecipitation sequencing for endogenous
234 AL1 oncogene, a finding validated in vivo by chromatin immunoprecipitation sequencing of a patient-de
241 e-wide mapping of FOXA2 binding intervals by chromatin immunoprecipitation sequencing was performed u
242 cing, genome-wide RNA polymerase II (RNPII), chromatin immunoprecipitation sequencing, and DNase sequ
243 ted and analyzed by RNA sequencing, H3K27me3 chromatin immunoprecipitation sequencing, and sonication
244 rioritized candidate SNPs were examined with chromatin immunoprecipitation sequencing, RNA sequencing
246 ontrol and desiccation stress conditions via chromatin immunoprecipitation-sequencing (ChIP-seq) appr
251 d de novo using epigenetic data derived from chromatin immunoprecipitation-sequencing (ChIP-Seq).
256 s determined by RNA-sequencing combined with chromatin immunoprecipitation-sequencing analysis reveal
258 lved in AVM formation, we performed RNA- and chromatin immunoprecipitation-sequencing experiments on
264 cription and expression were demonstrated by chromatin immunoprecipitation, small interfering RNA kno
268 1s-induced upregulation of the promoter, and chromatin immunoprecipitation studies provide evidence t
276 romosome conformation capture, Hi-C)(2), and chromatin immunoprecipitation techniques (such as chroma
277 to attenuated DNA binding, and we show using chromatin immunoprecipitation that MftR binds directly t
280 forward and reverse genetic approaches with chromatin immunoprecipitation to identify centromeres of
282 qRT-PCR, Western blotting, ELISA, and ChIP (chromatin immunoprecipitation) to characterize Pb-induce
284 Using dual-luciferase reporter assay and Chromatin immunoprecipitation, we demonstrate there is a
285 everse transcriptase PCR (qRT-PCR) array and chromatin immunoprecipitation, we elucidated the role of
288 otein-DNA crosslinking patterns by combining chromatin immunoprecipitation with 5' to 3' exonuclease
289 riptomes and mapped putative enhancers using chromatin immunoprecipitation with an antibody against H
291 kdown hearts at 5 weeks of age combined with chromatin immunoprecipitation with deep sequencing and f
292 tion approach using sequence composition and chromatin immunoprecipitation with high-throughput seque
295 ssible chromatin with sequencing (ATAC-seq), chromatin immunoprecipitation with sequencing (ChIP-seq)
299 of nuclei and ribosomes with RNA sequencing, chromatin immunoprecipitation with sequencing, assay for
300 sible chromatin using sequencing (ATAC-seq), chromatin immunoprecipitation with sequencing, whole-gen