Poly(dA.dT) sequences exist as rigid DNA structures in nucleosome-free yeast promoters in vivo.
about
Gene promoters show chromosome-specificity and reveal chromosome territories in humansEukaryotic genomes may exhibit up to 10 generic classes of gene promotersPrediction of Saccharomyces cerevisiae replication originsHomopolymer tract length dependent enrichments in functional regions of 27 eukaryotes and their novel dependence on the organism DNA (G+C)% compositionComparative analysis of chromatin landscape in regulatory regions of human housekeeping and tissue specific genesChromatin and epigenetic regulation of pre-mRNA processingDNA binding and gene activation properties of the Nmp4 nuclear matrix transcription factors.Intrinsic flexibility of B-DNA: the experimental TRX scale.A nucleosome-guided map of transcription factor binding sites in yeast.GT‐rich promoters can drive RNA pol II transcription and deposition of H2A.Z in African trypanosomesMining housekeeping genes with a Naive Bayes classifier.Prediction and analysis of nucleosome exclusion regions in the human genome.Distinct modes of regulation by chromatin encoded through nucleosome positioning signalsGenome-wide nucleosome mapping of Plasmodium falciparum reveals histone-rich coding and histone-poor intergenic regions and chromatin remodeling of core and subtelomeric genesG+C content dominates intrinsic nucleosome occupancyDrosophila ORC localizes to open chromatin and marks sites of cohesin complex loadingDNA-encoded nucleosome occupancy is associated with transcription levels in the human malaria parasite Plasmodium falciparum.Diversity of eukaryotic DNA replication origins revealed by genome-wide analysis of chromatin structure.Coregulation of transcription factor binding and nucleosome occupancy through DNA features of mammalian enhancers.Single-cell nucleosome mapping reveals the molecular basis of gene expression heterogeneityRNA polymerase I transcription factors in active yeast rRNA gene promoters enhance UV damage formation and inhibit repair.Modulation of cyclobutane thymine photodimer formation in T11-tracts in rotationally phased nucleosome core particles and DNA minicirclesChromatin-mediated epigenetic regulation in the malaria parasite Plasmodium falciparum.Repetitive sequence variations in the promoter region of the adhesin-encoding gene sabA of Helicobacter pylori affect transcriptionA bioinformatics-based strategy identifies c-Myc and Cdc25A as candidates for the Apmt mammary tumor latency modifiersA compendium of nucleosome and transcript profiles reveals determinants of chromatin architecture and transcription.Dynamic nucleosome organization at hox promoters during zebrafish embryogenesis.Rapid accessibility of nucleosomal DNA in yeast on a second time scale.Archaeal nucleosome positioning in vivo and in vitro is directed by primary sequence motifsGenome-wide identification of chromatin transitional regions reveals diverse mechanisms defining the boundary of facultative heterochromatinPoly(dA:dT)-rich DNAs are highly flexible in the context of DNA looping.Nucleosome positioning signals in genomic DNAA widespread role of the motif environment in transcription factor binding across diverse protein familiesDNA-guided establishment of nucleosome patterns within coding regions of a eukaryotic genome.Natural haplotypes of FLM non-coding sequences fine-tune flowering time in ambient spring temperatures in Arabidopsis.A comparison of nucleosome organization in Drosophila cell lines.Genomic approaches to DNA repair and mutagenesis.Formation of boundaries of transcriptionally silent chromatin by nucleosome-excluding structuresKinetochores prevent repair of UV damage in Saccharomyces cerevisiae centromeres.Determinants of nucleosome positioning
P2860
Q21093383-90299C0D-689F-43A9-92F1-9D3458C99D92Q21266696-DBD1944F-1308-40A8-A9E8-0B3D54839E73Q24791456-6C0A7471-C4C7-4A90-8DCA-5F5800D771DBQ24792585-3A45FD06-77FE-4B33-A980-92A2BFFFE899Q24815416-C420B7A9-7B6A-4FEC-A827-092F4EC5AE72Q26999294-8A28F746-9F64-4038-8820-AF8C69652ABCQ30167559-C5A095EF-800C-4EDE-B5B9-83ACB10863B2Q30493018-ECA615DB-4158-4DA1-A9AA-B2B4F90716FCQ30837896-6B74C521-8BDB-4AFF-B2BC-BEF11F375BB8Q33140157-98D374B3-96C3-411F-88D8-FFD7F31FB925Q33262100-47175021-02C5-472F-B86D-1899CE04FCCCQ33330187-7568A876-51E4-4532-BFD5-DB0B8E8E0BF1Q33383211-21A8B711-5FEF-465C-BAC9-E5A2E39DC0DBQ33518894-374D46C6-A478-4067-8F9A-5DDF264754E9Q33520380-CCDE3125-80BE-44AC-A55F-F9960F1BA0CCQ33618928-70655C48-D8A4-43A8-BA13-6C3D077B3BCAQ33669258-7F6A5798-02B6-4132-85BD-30B9E368D18AQ33686941-BA39BC68-E858-4EFF-AE71-E20194421389Q33723246-C1C48376-E297-4F41-88F5-3F4FBD0C4064Q33790088-B8193EA1-C6DE-4836-8476-1732C1274462Q33861785-0863361C-0EA7-4043-B0FD-42EEAA67DFFBQ33878067-B61ACD18-CF87-4C11-9F45-30BD6A71EEDEQ34055162-43962855-40AA-41B8-9A9B-E82C3B6E827EQ34297737-C6A6B4B5-BF31-4389-AF66-3A967D94CF94Q34411614-72828D5C-5147-4FDE-92F4-AB603FDB095DQ34711883-D80ACA06-9AF7-4C41-8C1F-4E027CFF3C4FQ34721066-E3B2ACD7-F2EB-43A0-BCCC-96FF8F8A11C9Q34767771-54BFFF46-D97E-416F-ADAC-46D221CF0A23Q34768504-24D5020A-9A6E-4E89-9CE2-865BBFB71B69Q34806568-BE3E3490-B83A-49D1-A8AE-E92D92C77376Q35022475-D216F8D7-977B-413A-8C81-E84D69A0E057Q35914766-6050169A-718E-4FCA-8CF1-1123A5DD73A2Q36032482-521A1B3E-A43E-416F-9AD2-BF36EB0C14E9Q36199591-B9CC8B06-9241-450E-8D22-5B366D1C4A2BQ36308355-B7247805-6655-4A94-85E5-ACC6C25E1F76Q36389394-4920DC03-0B0B-4EB0-AAE3-4CBD0A9354EAQ36395930-4B698D4F-57A4-491D-B027-8971A06E7146Q36420584-18AC72A7-40C1-4B30-BA77-02A792F29D9FQ36701315-3B3A29AE-FC30-4357-B733-679E3C9A0B4CQ37086686-37ED3ADB-FDB7-498E-BC20-DC267BB72037
P2860
Poly(dA.dT) sequences exist as rigid DNA structures in nucleosome-free yeast promoters in vivo.
description
2000 nî lūn-bûn
@nan
2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Poly(dA.dT) sequences exist as ...... -free yeast promoters in vivo.
@ast
Poly(dA.dT) sequences exist as ...... -free yeast promoters in vivo.
@en
type
label
Poly(dA.dT) sequences exist as ...... -free yeast promoters in vivo.
@ast
Poly(dA.dT) sequences exist as ...... -free yeast promoters in vivo.
@en
prefLabel
Poly(dA.dT) sequences exist as ...... -free yeast promoters in vivo.
@ast
Poly(dA.dT) sequences exist as ...... -free yeast promoters in vivo.
@en
P2093
P2860
P356
P1476
Poly(dA.dT) sequences exist as ...... -free yeast promoters in vivo.
@en
P2093
P2860
P304
P356
10.1093/NAR/28.21.4083
P407
P577
2000-11-01T00:00:00Z