| P50 | author | Joshua C Black | Q42252415 |
| P2093 | author name string | Johnathan R Whetstine | |
| P2860 | cites work | Determination of enriched histone modifications in non-genic portions of the human genome | Q21283767 |
| | Human Orc2 localizes to centrosomes, centromeres and heterochromatin during chromosome inheritance | Q24297783 |
| | Reversal of histone lysine trimethylation by the JMJD2 family of histone demethylases | Q24315937 |
| | Dynamic Histone H1 Isotype 4 Methylation and Demethylation by Histone Lysine Methyltransferase G9a/KMT1C and the Jumonji Domain-containing JMJD2/KDM4 Proteins | Q24316425 |
| | Covalent histone modifications--miswritten, misinterpreted and mis-erased in human cancers | Q24605342 |
| | Genome-wide maps of chromatin state in pluripotent and lineage-committed cells | Q24632506 |
| | Combinatorial patterns of histone acetylations and methylations in the human genome | Q24647290 |
| | EZH2 is a marker of aggressive breast cancer and promotes neoplastic transformation of breast epithelial cells | Q24672969 |
| | High-resolution profiling of histone methylations in the human genome | Q27860906 |
| | Chromatin modifications and their function | Q27861067 |
| | Comprehensive mapping of long-range interactions reveals folding principles of the human genome | Q28131819 |
| | Localization and phosphorylation of HP1 proteins during the cell cycle in mammalian cells | Q28142902 |
| | Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma | Q28237604 |
| | Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions | Q28279406 |
| | Male rats fed methyl- and folate-deficient diets with or without niacin develop hepatic carcinomas associated with decreased tissue NAD concentrations and altered poly(ADP-ribose) polymerase activity | Q28304100 |
| | Dynamic Regulation of Histone Lysine Methylation by Demethylases | Q29036779 |
| | The polycomb group protein EZH2 is involved in progression of prostate cancer | Q29614514 |
| | Heterochromatin revisited | Q29614716 |
| | Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability | Q29620365 |
| | Rb-mediated heterochromatin formation and silencing of E2F target genes during cellular senescence | Q29620428 |
| | Genomic study of replication initiation in human chromosomes reveals the influence of transcription regulation and chromatin structure on origin selection | Q30436435 |
| | The spatio-temporal organization of DNA replication sites is identical in primary, immortalized and transformed mammalian cells | Q31112880 |
| | Lamin A/C is a risk biomarker in colorectal cancer | Q33361579 |
| | Global reorganization of replication domains during embryonic stem cell differentiation | Q33374614 |
| | Sequencing newly replicated DNA reveals widespread plasticity in human replication timing | Q33591861 |
| | Drosophila ORC localizes to open chromatin and marks sites of cohesin complex loading | Q33618928 |
| | Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome. | Q33760054 |
| | Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer | Q33865946 |
| | Long-distance control of origin choice and replication timing in the human beta-globin locus are independent of the locus control region | Q33964800 |
| | The hinge and chromo shadow domain impart distinct targeting of HP1-like proteins | Q33967856 |
| | EZH2 is downstream of the pRB-E2F pathway, essential for proliferation and amplified in cancer | Q34268216 |
| | Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging | Q34652089 |
| | Histone modification patterns associated with the human X chromosome | Q34683351 |
| | Molecular biology. Chromatin higher order folding--wrapping up transcription | Q34849091 |
| | Linking cell cycle to histone modifications: SBF and H2B monoubiquitination machinery and cell-cycle regulation of H3K79 dimethylation | Q35568111 |
| | Nuclear structure in cancer cells | Q35877173 |
| | The function of nuclear architecture: a genetic approach | Q35965838 |
| | Facultative heterochromatin: is there a distinctive molecular signature? | Q36971377 |
| | The heterochromatin protein 1 (HP1) family: put away a bias toward HP1. | Q37229600 |
| | Temporal regulation of DNA replication in mammalian cells. | Q37603332 |
| | Epigenetic regulation of cancer growth by histone demethylases | Q37770486 |
| | Genome-wide kinetics of nucleosome turnover determined by metabolic labeling of histones | Q38343707 |
| | Downregulation of histone H3 lysine 9 methyltransferase G9a induces centrosome disruption and chromosome instability in cancer cells. | Q39986966 |
| | Plasticity of HP1 proteins in mammalian cells. | Q40081037 |
| | Dissociation of heterochromatin protein 1 from lamin B receptor induced by human polyomavirus agnoprotein: role in nuclear egress of viral particles | Q40111017 |
| | Histone H3 lysine 9 methylation and HP1gamma are associated with transcription elongation through mammalian chromatin | Q40390690 |
| | Nuclear localization and histone acetylation: a pathway for chromatin opening and transcriptional activation of the human beta-globin locus | Q40442851 |
| | Nuclear organization of DNA replication in primary mammalian cells. | Q40445454 |
| | Heterochromatin protein 1 (HP1) modulates replication timing of the Drosophila genome | Q40784286 |
| | Coordination of replication and transcription along a Drosophila chromosome. | Q41711507 |
| | Large histone H3 lysine 9 dimethylated chromatin blocks distinguish differentiated from embryonic stem cells | Q41868578 |
| | H3K27me3 forms BLOCs over silent genes and intergenic regions and specifies a histone banding pattern on a mouse autosomal chromosome | Q42076431 |
| | The HP1-p150/CAF-1 interaction is required for pericentric heterochromatin replication and S-phase progression in mouse cells | Q42803821 |
| | Stability of histone modifications across mammalian genomes: implications for 'epigenetic' marking | Q44407647 |
| | HP1-beta mobilization promotes chromatin changes that initiate the DNA damage response. | Q46625510 |
| | Oncogene-induced senescence as an initial barrier in lymphoma development | Q46634165 |
| | Cell cycle control of centromeric repeat transcription and heterochromatin assembly | Q46793624 |
| | Unique and redundant functions of C. elegans HP1 proteins in post-embryonic development | Q47069207 |
| | The heterochromatin protein Swi6/HP1 activates replication origins at the pericentromeric region and silent mating-type locus. | Q64883396 |
| P433 | issue | 1 | |
| P304 | page(s) | 9-15 | |
| P577 | publication date | 2011-01-01 | |
| P1433 | published in | Epigenetics | Q15753739 |
| P1476 | title | Chromatin landscape: methylation beyond transcription | |
| P478 | volume | 6 | |