| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Raffaella Santoro | |
| Filomena De Lucia | |||
| P2860 | cites work | Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals | Q22122053 |
| DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at replication foci | Q22254582 | ||
| Human DNA-(Cytosine-5) Methyltransferase-PCNA Complex as a Target for p21WAF1 | Q22299424 | ||
| NoRC--a novel member of mammalian ISWI-containing chromatin remodeling machines | Q24291631 | ||
| WSTF-ISWI chromatin remodeling complex targets heterochromatic replication foci | Q24295285 | ||
| Methyl-CpG binding domain 1 (MBD1) interacts with the Suv39h1-HP1 heterochromatic complex for DNA methylation-based transcriptional repression | Q24300386 | ||
| Histone H3.1 and H3.3 complexes mediate nucleosome assembly pathways dependent or independent of DNA synthesis | Q24304348 | ||
| Human SirT1 interacts with histone H1 and promotes formation of facultative heterochromatin | Q24306469 | ||
| An ACF1-ISWI chromatin-remodeling complex is required for DNA replication through heterochromatin | Q24318717 | ||
| Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex | Q24324026 | ||
| The chromatin remodeling complex NoRC targets HDAC1 to the ribosomal gene promoter and represses RNA polymerase I transcription | Q24534353 | ||
| The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase | Q24678267 | ||
| The Methyl-CpG Binding Protein MBD1 Interacts with the p150 Subunit of Chromatin Assembly Factor 1 | Q24682856 | ||
| A protein complex containing the conserved Swi2/Snf2-related ATPase Swr1p deposits histone variant H2A.Z into euchromatin | Q24801790 | ||
| Two different chromatin structures coexist in ribosomal RNA genes throughout the cell cycle | Q43477524 | ||
| Chromosome dynamics in the yeast interphase nucleus | Q43820233 | ||
| Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component | Q43890842 | ||
| Phosphorylation of linker histones regulates ATP-dependent chromatin remodeling enzymes | Q43911613 | ||
| Dependence of heterochromatic histone H3 methylation patterns on the Arabidopsis gene DDM1. | Q44037194 | ||
| Interplay between two epigenetic marks. DNA methylation and histone H3 lysine 9 methylation | Q44113626 | ||
| Enforcement of late replication origin firing by clusters of short G-rich DNA sequences | Q45007488 | ||
| Association of the origin recognition complex with heterochromatin and HP1 in higher eukaryotes | Q46408897 | ||
| ATP-dependent histone octamer sliding mediated by the chromatin remodeling complex NURF. | Q47070794 | ||
| Aberrant replication timing induces defective chromosome condensation in Drosophila ORC2 mutants | Q47071017 | ||
| Removal of promoter nucleosomes by disassembly rather than sliding in vivo | Q47401543 | ||
| Maintenance of genomic methylation requires a SWI2/SNF2-like protein | Q47964889 | ||
| Chromatin transitions during early Xenopus embryogenesis: changes in histone H4 acetylation and in linker histone type | Q49129010 | ||
| Mis16 and Mis18 are required for CENP-A loading and histone deacetylation at centromeres | Q50335532 | ||
| Nucleosomes unfold completely at a transcriptionally active promoter. | Q51599596 | ||
| Replication dynamics of the yeast genome. | Q52053905 | ||
| The units of DNA replication in Drosophila melanogaster chromosomes. | Q52471119 | ||
| A functional enhancer suppresses silencing of a transgene and prevents its localization close to centrometric heterochromatin. | Q52536957 | ||
| Nucleosomes positioned by ORC facilitate the initiation of DNA replication. | Q52542122 | ||
| Alterations in titer and distribution of high mobility group proteins during embryonic development of Drosophila melanogaster. | Q52578971 | ||
| A deletion of the human beta-globin locus activation region causes a major alteration in chromatin structure and replication across the entire beta-globin locus. | Q54314374 | ||
| HIRA Is Critical for a Nucleosome Assembly Pathway Independent of DNA Synthesis | Q57549500 | ||
| Conserved Histone Variant H2A.Z Protects Euchromatin from the Ectopic Spread of Silent Heterochromatin | Q58212661 | ||
| Initiation of DNA replication in chromosomes of Chinese hamster ovary cells | Q39904300 | ||
| Phosphorylation of H1 and H5 histones by cyclic AMP-dependent protein kinase reduces DNA binding | Q40257659 | ||
| Epigenetic mechanism of rRNA gene silencing: temporal order of NoRC-mediated histone modification, chromatin remodeling, and DNA methylation | Q40446676 | ||
| The chromatin remodeling complex NoRC controls replication timing of rRNA genes | Q40485184 | ||
| The Generation and Propagation of Variegated Chromosome Structures | Q40545200 | ||
| Relevance of histone acetylation and replication timing for deposition of centromeric histone CENP-A | Q40653599 | ||
| Establishment of transcriptional competence in early and late S phase | Q40689976 | ||
| Centromeres are specialized replication domains in heterochromatin | Q40815256 | ||
| The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote | Q40903819 | ||
| X-Inactivation and histone H4 acetylation in embryonic stem cells | Q41145161 | ||
| Replication structure of the human beta-globin gene domain | Q41509399 | ||
| A histone H3 methyltransferase controls DNA methylation in Neurospora crassa | Q42664087 | ||
| Dnmt3a and Dnmt3b are transcriptional repressors that exhibit unique localization properties to heterochromatin | Q42827600 | ||
| The replication timing program of the Chinese hamster beta-globin locus is established coincident with its repositioning near peripheral heterochromatin in early G1 phase | Q24812133 | ||
| Crystal structure of a nucleosome core particle containing the variant histone H2A.Z | Q27628748 | ||
| Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins | Q27860456 | ||
| Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain | Q27860477 | ||
| Worms gang up on bacteria | Q27860588 | ||
| ATP-driven exchange of histone H2AZ variant catalyzed by SWR1 chromatin remodeling complex | Q27929959 | ||
| Histone acetylation regulates the time of replication origin firing | Q27930649 | ||
| Pathways mediating the nuclear import of histones H3 and H4 in yeast | Q27930782 | ||
| A role for the yeast SWI/SNF complex in DNA replication | Q27930838 | ||
| A Snf2 family ATPase complex required for recruitment of the histone H2A variant Htz1. | Q27933672 | ||
| Spt16 and Pob3 of Saccharomyces cerevisiae form an essential, abundant heterodimer that is nuclear, chromatin-associated, and copurifies with DNA polymerase alpha | Q27934795 | ||
| Histone acetyltransferase HBO1 interacts with the ORC1 subunit of the human initiator protein | Q28116036 | ||
| Dynamic binding of histone H1 to chromatin in living cells | Q28141055 | ||
| DNA methyltransferase Dnmt1 associates with histone deacetylase activity | Q28141500 | ||
| Chromatin remodeling, histone modifications, and DNA methylation-how does it all fit together? | Q28203279 | ||
| Functional differences between the human ATP-dependent nucleosome remodeling proteins BRG1 and SNF2H | Q28204516 | ||
| Replication factors MCM2 and ORC1 interact with the histone acetyltransferase HBO1 | Q28208502 | ||
| Histone H1 variants differentially inhibit DNA replication through an affinity for chromatin mediated by their carboxyl-terminal domains | Q28214739 | ||
| Influence of histone H1 on chromatin structure | Q28254229 | ||
| On the mechanism of DNA replication in mammalian chromosomes | Q28255203 | ||
| Structural determinants for generating centromeric chromatin | Q28274742 | ||
| Methyl-CpG binding protein MBD1 couples histone H3 methylation at lysine 9 by SETDB1 to DNA replication and chromatin assembly | Q28278522 | ||
| Lsh, a member of the SNF2 family, is required for genome-wide methylation | Q28364248 | ||
| The nucleolar remodeling complex NoRC mediates heterochromatin formation and silencing of ribosomal gene transcription | Q28508771 | ||
| MSX1 cooperates with histone H1b for inhibition of transcription and myogenesis | Q28591024 | ||
| Different EZH2-containing complexes target methylation of histone H1 or nucleosomal histone H3 | Q28609869 | ||
| Heterochromatin Dynamics in Mouse Cells | Q29012057 | ||
| Epigenetics in human disease and prospects for epigenetic therapy | Q29547437 | ||
| Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription | Q29547568 | ||
| Role of histone H3 lysine 9 methylation in epigenetic control of heterochromatin assembly | Q29614718 | ||
| Nucleosome disruption and enhancement of activator binding by a human SW1/SNF complex | Q29617854 | ||
| The histone variant H3.3 marks active chromatin by replication-independent nucleosome assembly | Q29618256 | ||
| Histone H3.3 is enriched in covalent modifications associated with active chromatin | Q33196967 | ||
| Modulation of ISWI function by site-specific histone acetylation | Q33757651 | ||
| Normal spermatogenesis in mice lacking the testis-specific linker histone H1t. | Q33786969 | ||
| Nucleosome movement by CHRAC and ISWI without disruption or trans-displacement of the histone octamer. | Q33867495 | ||
| Activation of silent replication origins at autonomously replicating sequence elements near the HML locus in budding yeast | Q33959297 | ||
| H2A.Z is required for global chromatin integrity and for recruitment of RNA polymerase II under specific conditions | Q33969518 | ||
| Human DNA polymerase epsilon colocalizes with proliferating cell nuclear antigen and DNA replication late, but not early, in S phase | Q34104931 | ||
| Epigenetic codes for heterochromatin formation and silencing: rounding up the usual suspects | Q34120020 | ||
| Mice develop normally without the H1(0) linker histone | Q34126573 | ||
| Coordinated methyl and RNA binding is required for heterochromatin localization of mammalian HP1alpha | Q34196189 | ||
| Chromatin assembly factor 1 is essential and couples chromatin assembly to DNA replication in vivo | Q34266465 | ||
| Separation of basal histone synthesis from S-phase histone synthesis in dividing cells | Q34281289 | ||
| Lashings of DNA methylation, forkfuls of chromatin remodeling. | Q34467396 | ||
| Replication timing and transcriptional control: beyond cause and effect | Q34688494 | ||
| Replicating by the clock | Q35038281 | ||
| Telomeric chromatin modulates replication timing near chromosome ends | Q35187055 | ||
| Maintaining Transcriptional States Through DNA Replication | Q35540957 | ||
| Drosophila NURF-55, a WD repeat protein involved in histone metabolism | Q35669441 | ||
| Chromatin remodeling by RNA polymerases | Q35683447 | ||
| HP1 and the dynamics of heterochromatin maintenance | Q35741016 | ||
| Histone chaperone ASF1 cooperates with the Brahma chromatin-remodelling machinery | Q35804570 | ||
| Facts about FACT and transcript elongation through chromatin | Q35804601 | ||
| Those interfering little RNAs! Silencing and eliminating chromatin. | Q35804616 | ||
| Histone variants, nucleosome assembly and epigenetic inheritance | Q35818464 | ||
| Early-replicating heterochromatin | Q35963910 | ||
| Asynchronous replication timing of imprinted loci is independent of DNA methylation, but consistent with differential subnuclear localization | Q35964571 | ||
| Lsh, a modulator of CpG methylation, is crucial for normal histone methylation | Q36097628 | ||
| Duplication and maintenance of heterochromatin domains | Q36313402 | ||
| Histone H1 reduces the frequency of initiation in Xenopus egg extract by limiting the assembly of prereplication complexes on sperm chromatin | Q36871689 | ||
| A CAF-1 dependent pool of HP1 during heterochromatin duplication | Q37513828 | ||
| Chromosomal landscape of nucleosome-dependent gene expression and silencing in yeast. | Q38317749 | ||
| Involvement of putative SNF2 chromatin remodeling protein DRD1 in RNA-directed DNA methylation | Q38341855 | ||
| Evidence for DNA translocation by the ISWI chromatin-remodeling enzyme | Q38357160 | ||
| Specific binding of high-mobility-group I (HMGI) protein and histone H1 to the upstream AT-rich region of the murine beta interferon promoter: HMGI protein acts as a potential antirepressor of the promoter | Q39445206 | ||
| SWI-SNF-mediated nucleosome remodeling: role of histone octamer mobility in the persistence of the remodeled state | Q39452532 | ||
| A critical epitope for substrate recognition by the nucleosome remodeling ATPase ISWI. | Q39530698 | ||
| Genomic targeting of methylated DNA: influence of methylation on transcription, replication, chromatin structure, and histone acetylation | Q39540147 | ||
| Ku complex controls the replication time of DNA in telomere regions. | Q39864326 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 332-343 | |
| P577 | publication date | 2005-06-01 | |
| P1433 | published in | Biochemistry and Cell Biology | Q4914719 |
| P1476 | title | Many players, one goal: how chromatin states are inherited during cell division | |
| P478 | volume | 83 |
| Q34178082 | Architectural epigenetics: mitotic retention of mammalian transcriptional regulatory information |
| Q33334253 | Control of trichome branching by chromatin assembly factor-1. |
| Q37108842 | Epigenetic regulation of hepatic stellate cell activation |
| Q34505232 | Epigenetics of prostate cancer: beyond DNA methylation |
| Q38722379 | Fluctuations of pol I and fibrillarin contents of the nucleoli. |
| Q38409875 | Histone H3 acetylation and H3 K4 methylation define distinct chromatin regions permissive for transgene expression |
| Q38723565 | Nucleolar DNA: the host and the guests. |
| Q37087570 | Polycomb group proteins and long-range gene regulation |
| Q36692156 | RNA interference guides histone modification during the S phase of chromosomal replication. |
| Q33407823 | Transcriptional interaction-assisted identification of dynamic nucleosome positioning |
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