Reply to: Pitfalls in using phenanthroline to study the causal relationship between promoter nucleosome acetylation and transcription
- PMID: 35768425
- PMCID: PMC9243053
- DOI: 10.1038/s41467-022-30351-2
Reply to: Pitfalls in using phenanthroline to study the causal relationship between promoter nucleosome acetylation and transcription
Conflict of interest statement
The authors declare no competing interests.
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Comment on
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Transcription shapes genome-wide histone acetylation patterns.Nat Commun. 2021 Jan 11;12(1):210. doi: 10.1038/s41467-020-20543-z. Nat Commun. 2021. PMID: 33431884 Free PMC article.
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Pitfalls in using phenanthroline to study the causal relationship between promoter nucleosome acetylation and transcription.Nat Commun. 2022 Jun 29;13(1):3726. doi: 10.1038/s41467-022-30350-3. Nat Commun. 2022. PMID: 35768402 Free PMC article. No abstract available.
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Pitfalls in using phenanthroline to study the causal relationship between promoter nucleosome acetylation and transcription.Nat Commun. 2022 Jun 29;13(1):3726. doi: 10.1038/s41467-022-30350-3. Nat Commun. 2022. PMID: 35768402 Free PMC article. No abstract available.
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Histone H3 acetylated at lysine 9 in promoter is associated with low nucleosome density in the vicinity of transcription start site in human cell.Chromosome Res. 2006;14(2):203-11. doi: 10.1007/s10577-006-1036-7. Epub 2006 Mar 17. Chromosome Res. 2006. PMID: 16544193
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25 years after the nucleosome model: chromatin modifications.Trends Biochem Sci. 2000 Dec;25(12):619-23. doi: 10.1016/s0968-0004(00)01718-7. Trends Biochem Sci. 2000. PMID: 11116189 Review.
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