| scholarly article | Q13442814 |
| P2093 | author name string | Chunyang Zheng | |
| Jeffrey J. Hayes | |||
| P2860 | cites work | Translating the Histone Code | Q22065840 |
| Crystal structure of the nucleosome core particle at 2.8 A resolution | Q22122355 | ||
| Structure of the yeast nucleosome core particle reveals fundamental changes in internucleosome interactions | Q24535791 | ||
| Nucleosomes, linker DNA, and linker histone form a unique structural motif that directs the higher-order folding and compaction of chromatin | Q24652372 | ||
| Involvement of histone H1 in the organization of the nucleosome and of the salt-dependent superstructures of chromatin | Q24681606 | ||
| Asymmetries in the nucleosome core particle at 2.5 A resolution | Q27628657 | ||
| Crystal structure of a nucleosome core particle containing the variant histone H2A.Z | Q27628748 | ||
| Solvent mediated interactions in the structure of the nucleosome core particle at 1.9 a resolution | Q27639217 | ||
| The nucleosomal core histone octamer at 3.1 A resolution: a tripartite protein assembly and a left-handed superhelix | Q27655585 | ||
| Crystal structure of globular domain of histone H5 and its implications for nucleosome binding | Q27732024 | ||
| 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 | ||
| The language of covalent histone modifications | Q27860931 | ||
| Histone acetylation in chromatin structure and transcription | Q28131749 | ||
| Signaling network model of chromatin | Q28202952 | ||
| The structure of histone H1 and its location in chromatin | Q28283435 | ||
| Persistent interactions of core histone tails with nucleosomal DNA following acetylation and transcription factor binding | Q31998516 | ||
| Disruption of higher-order folding by core histone acetylation dramatically enhances transcription of nucleosomal arrays by RNA polymerase III | Q33775383 | ||
| Direct detection of linker DNA bending in defined-length oligomers of chromatin | Q33821984 | ||
| Histone tails modulate nucleosome mobility and regulate ATP-dependent nucleosome sliding by NURF | Q33951814 | ||
| Kinetics of core histones in living human cells: little exchange of H3 and H4 and some rapid exchange of H2B. | Q33953079 | ||
| Conformational dynamics of the chromatin fiber in solution: determinants, mechanisms, and functions | Q33958912 | ||
| DNA-dependent divalent cation binding in the nucleosome core particle | Q34037316 | ||
| Nucleosomes and the chromatin fiber | Q34183804 | ||
| Effects of core histone tail domains on the equilibrium constants for dynamic DNA site accessibility in nucleosomes | Q73675481 | ||
| Hybrid trypsinized nucleosomal arrays: identification of multiple functional roles of the H2A/H2B and H3/H4 N-termini in chromatin fiber compaction | Q73701975 | ||
| The N tails of histones H3 and H4 adopt a highly structured conformation in the nucleosome | Q73842763 | ||
| Acetylation increases the alpha-helical content of the histone tails of the nucleosome | Q74152760 | ||
| The tail does not always wag the dog | Q74817619 | ||
| Linker histones stabilize the intrinsic salt-dependent folding of nucleosomal arrays: mechanistic ramifications for higher-order chromatin folding | Q77431249 | ||
| Targeted cross-linking and DNA cleavage within model chromatin complexes | Q77892535 | ||
| Structures and interactions of the core histone tail domains | Q34187133 | ||
| In vitro reconstitution and analysis of mononucleosomes containing defined DNAs and proteins | Q34427572 | ||
| Visualization of G1 chromosomes: a folded, twisted, supercoiled chromonema model of interphase chromatid structure | Q34724862 | ||
| A role for histones H2A/H2B in chromatin folding and transcriptional repression | Q35108136 | ||
| Reversible histone modification and the chromosome cell cycle | Q35225904 | ||
| Rearrangement of the histone H2A C-terminal domain in the nucleosome | Q35599382 | ||
| Laser-induced crosslinking of histones to DNA in chromatin and core particles: implications in studying histone-DNA interactions | Q35645235 | ||
| Histories H1 and H5: one or two molecules per nucleosome? | Q35745519 | ||
| A new procedure for purifying histone pairs H2A+H2B and H3+H4 from chromatin using hydroxylapatite | Q35749964 | ||
| Acetylation of histone H4 plays a primary role in enhancing transcription factor binding to nucleosomal DNA in vitro. | Q35850301 | ||
| Participation of core histone "tails" in the stabilization of the chromatin solenoid | Q36208922 | ||
| Preferential and asymmetric interaction of linker histones with 5S DNA in the nucleosome | Q36411435 | ||
| The N-terminal tail of histone H2A binds to two distinct sites within the nucleosome core | Q36544944 | ||
| Topography of the histone octamer surface: repeating structural motifs utilized in the docking of nucleosomal DNA | Q36657548 | ||
| Histone contributions to the structure of DNA in the nucleosome | Q37567894 | ||
| A positive role for nucleosome mobility in the transcriptional activity of chromatin templates: restriction by linker histones | Q37621095 | ||
| Toward a unified model of chromatin folding | Q38648054 | ||
| The H3-H4 N-terminal tail domains are the primary mediators of transcription factor IIIA access to 5S DNA within a nucleosome | Q39584897 | ||
| Proteases as structural probes for chromatin: The domain structure of histones | Q40179478 | ||
| Use of selectively trypsinized nucleosome core particles to analyze the role of the histone "tails" in the stabilization of the nucleosome | Q41307889 | ||
| Histone H2A.Z acetylation modulates an essential charge patch | Q43656797 | ||
| Dinucleosomes show compaction by ionic strength, consistent with bending of linker DNA. | Q47708879 | ||
| Asymmetric linker histone association directs the asymmetric rearrangement of core histone interactions in a positioned nucleosome containing a thyroid hormone response element | Q47968842 | ||
| Linker DNA and H1-dependent reorganization of histone-DNA interactions within the nucleosome | Q47968852 | ||
| The histone tails of the nucleosome | Q48018656 | ||
| Characterization of two xenopus somatic 5S DNAs and one minor oocyte-specific 5S DNA | Q48413653 | ||
| Electrostatic mechanism of chromatin folding. | Q52484628 | ||
| Structure of nucleosomes, chromatin, and RNA polymerase-promoter complex as revealed by DNA-protein cross-linking. | Q52522821 | ||
| Nucleosome remodeling induced by RNA polymerase II: loss of the H2A/H2B dimer during transcription. | Q52545774 | ||
| Linker DNA bending induced by the core histones of chromatin. | Q54290296 | ||
| Eukaryotic RNA polymerase II binds to nucleosome cores from transcribed genes | Q59079465 | ||
| Chromatin | Q60060525 | ||
| Chromatin Fiber Folding: Requirement for the Histone H4 N-terminal Tail | Q61041700 | ||
| In vivo studies on the dynamics of histone-DNA interaction: evidence for nucleosome dissolution during replication and transcription and a low level of dissolution independent of both | Q67658601 | ||
| Roles of H1 domains in determining higher order chromatin structure and H1 location | Q68726073 | ||
| Deposition of newly synthesized histones: new histones H2A and H2B do not deposit in the same nucleosome with new histones H3 and H4 | Q69200945 | ||
| Homogeneous reconstituted oligonucleosomes, evidence for salt-dependent folding in the absence of histone H1 | Q69415462 | ||
| Differential dissociation of histone tails from core chromatin | Q70703383 | ||
| Reversible oligonucleosome self-association: dependence on divalent cations and core histone tail domains | Q71165591 | ||
| Core Histone Tail Domains Mediate Oligonucleosome Folding and Nucleosomal DNA Organization through Distinct Molecular Mechanisms | Q71823623 | ||
| Modulation of chromatin folding by histone acetylation | Q71941995 | ||
| Quantitative agarose gel electrophoresis of chromatin: nucleosome-dependent changes in charge, sharp, and deformability at low ionic strength | Q72266514 | ||
| Major role of the histones H3-H4 in the folding of the chromatin fiber | Q73038816 | ||
| P433 | issue | 26 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | biochemistry | Q7094 |
| cell biology | Q7141 | ||
| P304 | page(s) | 24217-24224 | |
| P577 | publication date | 2003-04-15 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Intra- and inter-nucleosomal protein-DNA interactions of the core histone tail domains in a model system | |
| Intra- and Inter-nucleosomal Protein-DNA Interactions of the Core Histone Tail Domains in a Model System | |||
| P478 | volume | 278 |
| Q33719316 | A cassette of N-terminal amino acids of histone H2B are required for efficient cell survival, DNA repair and Swi/Snf binding in UV irradiated yeast |
| Q34245171 | A distinct switch in interactions of the histone H4 tail domain upon salt-dependent folding of nucleosome arrays |
| Q36926047 | A two-state activation mechanism controls the histone methyltransferase Suv39h1. |
| Q90067785 | Accessibility of promoter DNA is not the primary determinant of chromatin-mediated gene regulation |
| Q37314859 | Acetylation Mimics Within a Single Nucleosome Alter Local DNA Accessibility In Compacted Nucleosome Arrays |
| Q28829535 | Chemical and biological tools for the preparation of modified histone proteins |
| Q37175650 | Chemically ubiquitylated histone H2B stimulates hDot1L-mediated intranucleosomal methylation |
| Q37733528 | Chromatin as an expansive canvas for chemical biology |
| Q90160401 | DNA-Protein Cross-Link Formation in Nucleosome Core Particles Treated with Methyl Methanesulfonate |
| Q34977877 | Determinants of histone H4 N-terminal domain function during nucleosomal array oligomerization: roles of amino acid sequence, domain length, and charge density |
| Q30499101 | Effects of histone acetylation by Piccolo NuA4 on the structure of a nucleosome and the interactions between two nucleosomes |
| Q42184197 | Electrostatic Origin of Salt-Induced Nucleosome Array Compaction |
| Q52367201 | Free energy profiles for unwrapping the outer superhelical turn of nucleosomal DNA. |
| Q36567360 | Genome-wide patterns of histone modifications in yeast. |
| Q33559830 | Groucho-mediated repression may result from a histone deacetylase-dependent increase in nucleosome density |
| Q83364389 | H2A.Z stabilizes chromatin in a way that is dependent on core histone acetylation |
| Q51278763 | Histone Acetylation Regulates Chromatin Accessibility: Role of H4K16 in Inter-nucleosome Interaction. |
| Q36973671 | Histone N-terminal tails interfere with nucleosome traversal by RNA polymerase II. |
| Q33960896 | Histone variant innovation in a rapidly evolving chordate lineage |
| Q35229609 | Histones: at the crossroads of peptide and protein chemistry |
| Q36016884 | Internucleosomal interactions mediated by histone tails allow distant communication in chromatin |
| Q64957242 | Ion counting demonstrates a high electrostatic field generated by the nucleosome. |
| Q42957995 | Multiscale modeling of nucleosome dynamics |
| Q24626585 | New insights into nucleosome and chromatin structure: an ordered state or a disordered affair? |
| Q86246092 | Nucleosome structure and function |
| Q47592143 | Organization of telomeric nucleosomes: atomic force microscopy imaging and theoretical modeling |
| Q44760951 | Probing core histone tail-DNA interactions in a model dinucleosome system |
| Q41895677 | Regulation of gene transcription by the histone H2A N-terminal domain |
| Q36222333 | Structural features of transcription factor IIIA bound to a nucleosome in solution |
| Q38305529 | The H3 tail domain participates in multiple interactions during folding and self-association of nucleosome arrays |
| Q41888720 | The H4 tail domain participates in intra- and internucleosome interactions with protein and DNA during folding and oligomerization of nucleosome arrays |
| Q35656781 | The amino-terminal tails of histones H2A and H3 coordinate efficient base excision repair, DNA damage signaling and postreplication repair in Saccharomyces cerevisiae |
| Q40516553 | The divalent cations Ca2+ and Mg2+ play specific roles in stabilizing histone-DNA interactions within nucleosomes that are partially redundant with the core histone tail domains |
| Q33563883 | The effect of epigenetic modifications on the secondary structures and possible binding positions of the N-terminal tail of histone H3 in the nucleosome: a computational study |
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