Pages that link to "Q28131828"
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The following pages link to Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome (Q28131828):
Displaying 50 items.
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (Q21061203) (← links)
- An Alu element-associated hypermethylation variant of the POMC gene is associated with childhood obesity (Q21092420) (← links)
- Chromatin Landscape Dictates HSF Binding to Target DNA Elements (Q21092435) (← links)
- The insulator binding protein CTCF positions 20 nucleosomes around its binding sites across the human genome (Q21092478) (← links)
- A user's guide to the encyclopedia of DNA elements (ENCODE) (Q21092716) (← links)
- A large fraction of extragenic RNA pol II transcription sites overlap enhancers (Q21145794) (← links)
- The GENCODE pseudogene resource (Q21183996) (← links)
- Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors (Q21183997) (← links)
- Determination of enriched histone modifications in non-genic portions of the human genome (Q21283767) (← links)
- Genome-wide analysis of KAP1 binding suggests autoregulation of KRAB-ZNFs (Q21563454) (← links)
- The histone variant macroH2A1 marks repressed autosomal chromatin, but protects a subset of its target genes from silencing (Q22001529) (← links)
- What does our genome encode? (Q22065765) (← links)
- Enhancers: five essential questions (Q22121999) (← links)
- Comparative studies of gene expression and the evolution of gene regulation (Q22122000) (← links)
- Initial impact of the sequencing of the human genome (Q22122172) (← links)
- Genomic views of distant-acting enhancers (Q22122210) (← links)
- Developmental roles of the histone lysine demethylases (Q22306162) (← links)
- Sustained JNK1 activation is associated with altered histone H3 methylations in human liver cancer (Q24170091) (← links)
- Selective anchoring of TFIID to nucleosomes by trimethylation of histone H3 lysine 4 (Q24294553) (← links)
- Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locus (Q24300588) (← links)
- Multiple Wnt/ß-Catenin Responsive Enhancers Align with the MYC Promoter through Long-Range Chromatin Loops (Q24300934) (← links)
- Bromodomain-containing protein 4 (BRD4) regulates RNA polymerase II serine 2 phosphorylation in human CD4 T cells (Q24301441) (← links)
- HERC2 rs12913832 modulates human pigmentation by attenuating chromatin-loop formation between a long-range enhancer and the OCA2 promoter (Q24301601) (← links)
- A phospho/methyl switch at histone H3 regulates TFIID association with mitotic chromosomes. (Q24303673) (← links)
- SET1 and p300 act synergistically, through coupled histone modifications, in transcriptional activation by p53 (Q24310032) (← links)
- Chromatin and transcriptional signatures for Nodal signaling during endoderm formation in hESCs (Q24312034) (← links)
- Regulation of transcription through acetylation of H3K122 on the lateral surface of the histone octamer (Q24317494) (← links)
- RNA exosome depletion reveals transcription upstream of active human promoters (Q24321777) (← links)
- The euchromatic and heterochromatic landscapes are shaped by antagonizing effects of transcription on H2A.Z deposition (Q24336460) (← links)
- Histone lysine demethylase JARID1a activates CLOCK-BMAL1 and influences the circadian clock (Q24338936) (← links)
- On the mechanism of multiple lysine methylation by the human mixed lineage leukemia protein-1 (MLL1) core complex (Q24339403) (← links)
- The accessible chromatin landscape of the human genome (Q24595581) (← links)
- Proteomic investigation of epigenetics in neuropsychiatric disorders: a missing link between genetics and behavior? (Q24603107) (← links)
- Pioneer factors in embryonic stem cells and differentiation (Q24604741) (← links)
- A minicircuitry involving REST and CREB controls miR-9-2 expression during human neuronal differentiation (Q24608565) (← links)
- Identification and characterization of Hoxa9 binding sites in hematopoietic cells (Q24610737) (← links)
- Insights from genomic profiling of transcription factors (Q24611607) (← links)
- Accurate inference of transcription factor binding from DNA sequence and chromatin accessibility data (Q24614616) (← links)
- Genome-scale DNA methylation maps of pluripotent and differentiated cells (Q24621431) (← links)
- Epigenetic priors for identifying active transcription factor binding sites (Q24623379) (← links)
- Pioneer transcription factors: establishing competence for gene expression (Q24625373) (← links)
- Histone H3K27ac separates active from poised enhancers and predicts developmental state (Q24628758) (← links)
- Epigenetic switch involved in activation of pioneer factor FOXA1-dependent enhancers (Q24630926) (← links)
- Embryonic stem cell and induced pluripotent stem cell: an epigenetic perspective (Q24633489) (← links)
- Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome (Q24634411) (← links)
- Opposing regulation of the locus encoding IL-17 through direct, reciprocal actions of STAT3 and STAT5 (Q24635387) (← links)
- Identification of 67 histone marks and histone lysine crotonylation as a new type of histone modification (Q24635918) (← links)
- FoxA1 translates epigenetic signatures into enhancer-driven lineage-specific transcription (Q24645118) (← links)
- Combinatorial patterns of histone acetylations and methylations in the human genome (Q24647290) (← links)
- Microplate-based chromatin immunoprecipitation method, Matrix ChIP: a platform to study signaling of complex genomic events (Q24648362) (← links)