Chromatin higher-order structures and gene regulation

Crystal structure of the nucleosome core particle at 2.8 Å resolution

Luger, K., Mäder, A. W., Richmond, R. K., Sargent, D. F., & Richmond, T. J. (1997) · Nature · doi:10.1038/38444 · Cited by 9,466 · see citing works

High-Resolution Profiling of Histone Methylations in the Human Genome

Barski, A., Cuddapah, S., Cui, K., Roh, T.-Y., Schones, D. E., Wang, Z., Wei, G., Chepelev, I., & Zhao, K. (2007) · Cell · doi:10.1016/j.cell.2007.05.009 · Cited by 6,845 · see citing works

Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions

Guelen, L., Pagie, L., Brasset, É., Meuleman, W. R. A., Faza, M. B., Talhout, W., Eussen, B. H. J., de Klein, A., Wessels, L. F. A., de Laat, W. L., et al. (2008) · Nature · doi:10.1038/nature06947 · Cited by 1,959 · see citing works

Mediator and cohesin connect gene expression and chromatin architecture

Kagey, M. H., Newman, J. J., Bilodeau, S., Zhan, Y., Orlando, D. A., van Berkum, N. L., Ebmeier, C. C., Goossens, J., Rahl, P. B., Levine, S. S., et al. (2010) · Nature · doi:10.1038/nature09380 · Cited by 1,939 · see citing works

Histone H4-K16 Acetylation Controls Chromatin Structure and Protein Interactions

Shogren‐Knaak, M. A., Ishii, H., Sun, J.-M., Pazin, M. J., Davie, J., & Peterson, C. L. (2006) · Science · doi:10.1126/science.1124000 · Cited by 1,876 · see citing works

Genome-Wide Evolutionary Analysis of Eukaryotic DNA Methylation

Zemach, A., McDaniel, I. E., Silva, P., & Zilberman, D. (2010) · Science · doi:10.1126/science.1186366 · Cited by 1,796 · see citing works

Estrogen Receptor-α Directs Ordered, Cyclical, and Combinatorial Recruitment of Cofactors on a Natural Target Promoter

Métivier, R., Penot, G., Hübner, M. R., Reid, G., Brand, H., Koš, M., & Gannon, F. (2003) · Cell · doi:10.1016/s0092-8674(03)00934-6 · Cited by 1,431 · see citing works

Distinct Factors Control Histone Variant H3.3 Localization at Specific Genomic Regions

Goldberg, A. D., Banaszynski, L. A., Noh, K., Lewis, P. W., Elsässer, S. J., Stadler, S. C., Dewell, S. B., Law, M. J., Guo, X., Li, X., et al. (2010) · Cell · doi:10.1016/j.cell.2010.01.003 · Cited by 1,281 · see citing works

Role of the polycomb protein EED in the propagation of repressive histone marks

Margueron, R., Justin, N., Ohno, K., Sharpe, M. L., Son, J., Drury, W. J., Voigt, P., Martin, S. R., Taylor, W. R., Marco, V. D., et al. (2009) · Nature · doi:10.1038/nature08398 · Cited by 1,203 · see citing works

Opening of Compacted Chromatin by Early Developmental Transcription Factors HNF3 (FoxA) and GATA-4

Cirillo, L. A., Lin, F. R., Cuesta, I., Friedman, D., Jarník, M., & Zaret, K. S. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00459-8 · Cited by 1,188 · see citing works

A stem cell–like chromatin pattern may predispose tumor suppressor genes to DNA hypermethylation and heritable silencing

Ohm, J. E., McGarvey, K. M., Yu, X., Cheng, L., Schuebel, K. E., Cope, L., Mohammad, H. P., Chen, W., Daniel, V. C., Yu, W., et al. (2007) · Nature Genetics · doi:10.1038/ng1972 · Cited by 1,130 · see citing works

Subdiffraction Multicolor Imaging of the Nuclear Periphery with 3D Structured Illumination Microscopy

Schermelleh, L., Carlton, P. M., Haase, S., Shao, L., Winoto, L., Kner, P., Burke, B. E., Cardoso, M. C., Agard, D. A., Gustafsson, M. G. L., et al. (2008) · Science · doi:10.1126/science.1156947 · Cited by 1,126 · see citing works

Molecular Maps of the Reorganization of Genome-Nuclear Lamina Interactions during Differentiation

Peric-Hupkes, D., Meuleman, W., Pagie, L., Bruggeman, S. W. M., Solovei, I., Brugman, W., Gräf, S., Flicek, P., Kerkhoven, R. M., van Lohuizen, M., et al. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.03.016 · Cited by 1,050 · see citing works

Systematic Protein Location Mapping Reveals Five Principal Chromatin Types in Drosophila Cells

Filion, G. J. P., van Bemmel, J. G., Braunschweig, U., Talhout, W., Kind, J., Ward, L. D., Brugman, W., de Castro, I. J., Kerkhoven, R. M., Bussemaker, H. J., et al. (2010) · Cell · doi:10.1016/j.cell.2010.09.009 · Cited by 963 · see citing works

Human SirT1 interacts with histone H1 and promotes formation of facultative heterochromatin.

Vaquero, A., Scher, M., Lee, D., Erdjument-Bromage, H., Tempst, P., & Reinberg, D. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.08.031 · Cited by 916 · see citing works

Ezh1 and Ezh2 Maintain Repressive Chromatin through Different Mechanisms

Margueron, R., Li, G., Sarma, K., Blais, A., Zavadil, J., Woodcock, C. L. F., Dynlacht, B. D., & Reinberg, D. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.11.004 · Cited by 889 · see citing works

Comprehensive analysis of the chromatin landscape in Drosophila melanogaster

Kharchenko, P. V., Alekseyenko, A. A., Schwartz, Y. B., Minoda, A., Riddle, N. C., Ernst, J., Sabo, P. J., Larschan, E., Gorchakov, A. A., Gu, T., et al. (2010) · Nature · doi:10.1038/nature09725 · Cited by 853 · see citing works

Chromatin Compaction by a Polycomb Group Protein Complex

Francis, N. J., Kingston, R. E., & Woodcock, C. L. F. (2004) · Science · doi:10.1126/science.1100576 · Cited by 841 · see citing works

X-ray structure of a tetranucleosome and its implications for the chromatin fibre

Schalch, T., Duda, S., Sargent, D. F., & Richmond, T. J. (2005) · Nature · doi:10.1038/nature03686 · Cited by 839 · see citing works

Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres

Lewis, P., Elsaesser, S. J., Noh, K., Stadler, S., & Allis, C. (2010) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1008850107 · Cited by 830 · see citing works

Transcriptional repression mediated by repositioning of genes to the nuclear lamina

Reddy, K. L., Zullo, J., Bertolino, E., & Singh, H. (2008) · Nature · doi:10.1038/nature06727 · Cited by 785 · see citing works

Chromatin structure and the inheritance of epigenetic information

Margueron, R., & Reinberg, D. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2752 · Cited by 733 · see citing works

Histone H2B Monoubiquitination Functions Cooperatively with FACT to Regulate Elongation by RNA Polymerase II

Pavri, R., Zhu, B., Li, G., Trojer, P., Mandal, S. S., Shilatifard, A., & Reinberg, D. (2006) · Cell · doi:10.1016/j.cell.2006.04.029 · Cited by 708 · see citing works

Characterization of the Drosophila melanogaster genome at the nuclear lamina

Pickersgill, H., Kalverda, B., de Wit, E., Talhout, W., Fornerod, M., & van Steensel, B. (2006) · Nature Genetics · doi:10.1038/ng1852 · Cited by 656 · see citing works

Genome-wide analysis of Polycomb targets in Drosophila melanogaster

Schwartz, Y. B., Kahn, T. G., Nix, D. A., Li, X., Bourgon, R., Biggin, M. D., & Pirrotta, V. (2006) · Nature Genetics · doi:10.1038/ng1817 · Cited by 610 · see citing works

Histone H2A.Z and DNA methylation are mutually antagonistic chromatin marks

Zilberman, D., Coleman-Derr, D., Ballinger, T., & Henikoff, S. (2008) · Nature · doi:10.1038/nature07324 · Cited by 593 · see citing works

Nucleosome Arrays Reveal the Two-Start Organization of the Chromatin Fiber

Dorigo, B., Schalch, T., Kulangara, A., Duda, S., Schroeder, R. R., & Richmond, T. J. (2004) · Science · doi:10.1126/science.1103124 · Cited by 562 · see citing works

Dynamics of Replication-Independent Histone Turnover in Budding Yeast

Dion, M. F., Kaplan, T., Kim, M., Buratowski, S., Friedman, N., & Rando, O. J. (2007) · Science · doi:10.1126/science.1134053 · Cited by 556 · see citing works

Ring1B Compacts Chromatin Structure and Represses Gene Expression Independent of Histone Ubiquitination

Eskeland, R., Leeb, M., Grimes, G. R., Kress, C., Boyle, S., Sproul, D., Gilbert, N., Fan, Y., Skoultchi, A. I., Wutz, A., et al. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.02.032 · Cited by 553 · see citing works

Nucleosome stability mediated by histone variants H3.3 and H2A.ZPreprint

Jin, C., & Felsenfeld, G. (2007) · Genes & Development · doi:10.1101/gad.1547707 · Cited by 544 · see citing works

Chromatin Fiber Folding: Requirement for the Histone H4 N-terminal Tail

Dorigo, B., Schalch, T., Bystricky, K., & Richmond, T. J. (2003) · Journal of Molecular Biology · doi:10.1016/s0022-2836(03)00025-1 · Cited by 527 · see citing works

EM measurements define the dimensions of the “30-nm” chromatin fiber: Evidence for a compact, interdigitated structure

Robinson, P. J. J., Fairall, L., Huynh, V. A. T., & Rhodes, D. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601212103 · Cited by 517 · see citing works

A Method for Genetically Installing Site-Specific Acetylation in Recombinant Histones Defines the Effects of H3 K56 Acetylation

Neumann, H., Hancock, S. M., Buning, R., Routh, A. L., Chapman, L., Somers, J., Owen‐Hughes, T., van Noort, J., Rhodes, D., & Chin, J. W. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.07.027 · Cited by 498 · see citing works

Nucleosome dynamics define transcriptional enhancers

He, H. H., Meyer, C. A., Shin, H., Bailey, S. T., Wei, G., Wang, Q., Zhang, Y., Xu, K., Ni, M., Lupien, M., et al. (2010) · Nature Genetics · doi:10.1038/ng.545 · Cited by 476 · see citing works

Perinuclear localization of chromatin facilitates transcriptional silencing

Andrulis, E. D., Neiman, A. M., Zappulla, D. C., & Sternglanz, R. (1998) · Nature · doi:10.1038/29100 · Cited by 468 · see citing works

The nuclear envelope and transcriptional control

Akhtar, A., & Gasser, S. M. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2122 · Cited by 443 · see citing works

Chromatin-Bound Nuclear Pore Components Regulate Gene Expression in Higher Eukaryotes

Capelson, M., Liang, Y. X., Schulte, R. J., Mair, W. B., Wagner, U., & Hetzer, M. W. (2010) · Cell · doi:10.1016/j.cell.2009.12.054 · Cited by 443 · see citing works

Nucleoporins Directly Stimulate Expression of Developmental and Cell-Cycle Genes Inside the Nucleoplasm

Kalverda, B., Pickersgill, H., Shloma, V. V., & Fornerod, M. W. J. (2010) · Cell · doi:10.1016/j.cell.2010.01.011 · Cited by 442 · see citing works

PHF8 mediates histone H4 lysine 20 demethylation events involved in cell cycle progression.

Liu, W., Tanasa, B., Tyurina, O. V., Zhou, T. Y., Gassmann, R., Liu, W. T., Ohgi, K. A., Benner, C., Garcia-Bassets, I., Aggarwal, A. K., et al. (2010) · Nature · doi:10.1038/nature09272 · Cited by 441 · see citing works

Theoretical Analysis of Epigenetic Cell Memory by Nucleosome Modification

Dodd, I. B., Micheelsen, M. A., Sneppen, K., & Thon, G. (2007) · Cell · doi:10.1016/j.cell.2007.02.053 · Cited by 436 · see citing works

ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cellsPreprint

Wong, L. H., McGhie, J. D. R., Sim, M., Anderson, M. A., Ahn, S., Hannan, R. D., George, A. J., Morgan, K. A., Mann, J. R., & Choo, K. H. A. (2010) · Genome Research · doi:10.1101/gr.101477.109 · Cited by 415 · see citing works

Composition and histone substrates of polycomb repressive group complexes change during cellular differentiation

Kuzmichev, A., Margueron, R., Vaquero, A., Preissner, T. S., Scher, M. B., Kirmizis, A., Ouyang, X., Brockdorff, N., Abate-Shen, C. T., Farnham, P., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409875102 · Cited by 406 · see citing works

Analysis of cryo-electron microscopy images does not support the existence of 30-nm chromatin fibers in mitotic chromosomes in situ

Eltsov, M., MacLellan‐Gibson, K., Maeshima, K., Frangakis, A. S., & Dubochet, J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810057105 · Cited by 404 · see citing works

H2A.Z-Mediated Localization of Genes at the Nuclear Periphery Confers Epigenetic Memory of Previous Transcriptional State

Brickner, D. G., Cajigas, I., Fondufe‐Mittendorf, Y. N., Ahmed, S. A. A., Lee, P., Widom, J., & Brickner, J. H. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050081 · Cited by 390 · see citing works

Chromatin Higher-order Structure and Dynamics

Woodcock, C. L., & Ghosh, R. P. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000596 · Cited by 384 · see citing works

Genome-wide profiling of PRC1 and PRC2 Polycomb chromatin binding in Drosophila melanogaster

Tolhuis, B., Muijrers, I., de Wit, E., Teunissen, H., Talhout, W., van Steensel, B., & van Lohuizen, M. (2006) · Nature Genetics · doi:10.1038/ng1792 · Cited by 380 · see citing works

Nucleosome repeat length and linker histone stoichiometry determine chromatin fiber structure

Routh, A. L., Sandin, S., & Rhodes, D. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802336105 · Cited by 372 · see citing works

Partitioning of Histone H3-H4 Tetramers During DNA Replication–Dependent Chromatin Assembly

Xu, M., Long, C., Chen, X., Huang, C., Chen, S., & Zhu, B. (2010) · Science · doi:10.1126/science.1178994 · Cited by 351 · see citing works

Gene loops juxtapose promoters and terminators in yeast

O'Sullivan, J. M., Tan‐Wong, S. M., Morillon, A., Lee, B., Coles, J., Mellor, J., & Proudfoot, N. J. (2004) · Nature Genetics · doi:10.1038/ng1411 · Cited by 346 · see citing works

Higher-Order Structures of Chromatin: The Elusive 30 nm Fiber

Tremethick, D. J. (2007) · Cell · doi:10.1016/j.cell.2007.02.008 · Cited by 344 · see citing works

L3MBTL1, a Histone-Methylation-Dependent Chromatin Lock

Trojer, P., Li, G., Sims, R. J., Vaquero, A., Kalakonda, N., Boccuni, P., Lee, D., Erdjument‐Bromage, H., Tempst, P., Nimer, S. D., et al. (2007) · Cell · doi:10.1016/j.cell.2007.03.048 · Cited by 343 · see citing works

H2AZ Is Enriched at Polycomb Complex Target Genes in ES Cells and Is Necessary for Lineage Commitment

Creyghton, M. P., Markoulaki, S., Levine, S. S., Hanna, J. H., Lodato, M. A., Sha, K., Young, R. A., Jaenisch, R., & Boyer, L. A. (2008) · Cell · doi:10.1016/j.cell.2008.09.056 · Cited by 340 · see citing works

Structure of the ‘30nm’ chromatin fibre: A key role for the linker histone

Robinson, P. J., & Rhodes, D. (2006) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2006.05.007 · Cited by 314 · see citing works

H2A.Z Alters the Nucleosome Surface to Promote HP1α-Mediated Chromatin Fiber Folding

Fan, J. Y., Rangasamy, D., Luger, K., & Tremethick, D. J. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.10.023 · Cited by 305 · see citing works

Chromatin Compaction by Human MeCP2

Georgel, P. T., Horowitz-Scherer, R. A., Adkins, N., Woodcock, C. L., Wade, P. A., & Hansen, J. C. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305308200 · Cited by 305 · see citing works

Histone H4K20/H3K9 demethylase PHF8 regulates zebrafish brain and craniofacial development

Qi, H. H., Sarkissian, M., Hu, G., Wang, Z., Bhattacharjee, A., Gordon, D. B., Gonzales, M., Lan, F., Ongusaha, P. P., Huarte, M., et al. (2010) · Nature · doi:10.1038/nature09261 · Cited by 303 · see citing works

Heterochromatin formation in the mouse embryo requires critical residues of the histone variant H3.3

Santenard, A., Ziegler-Birling, C., Koch, M., Tora, L., Bannister, A. J., & Torres‐Padilla, M. (2010) · Nature Cell Biology · doi:10.1038/ncb2089 · Cited by 301 · see citing works

DNA Methylation Increases Nucleosome Compaction and Rigidity

Choy, J. S., Wei, S., Lee, J. Y., Tan, S., Chu, S., & Lee, T.-H. (2010) · Journal of the American Chemical Society · doi:10.1021/ja910264z · Cited by 279 · see citing works

The Histone Variant MacroH2A Interferes with Transcription Factor Binding and SWI/SNF Nucleosome Remodeling

Angelov, D., Molla, A., Perche, P.-Y., Hans, F., Côté, J., Khochbin, S., Bouvet, P., & Dimitrov, S. I. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00100-x · Cited by 273 · see citing works

Structure of the 3000Å chromatin filament: X-ray diffraction from oriented samples

Widom, J. (1985) · Cell · doi:10.1016/0092-8674(85)90025-x · Cited by 269 · see citing works

A role for the CPF 3′-end processing machinery in RNAP II-dependent gene loopingPreprint

Ansari, A., & Hampsey, M. (2005) · Genes & Development · doi:10.1101/gad.1362305 · Cited by 257 · see citing works

The essential histone variant H2A.Z regulates the equilibrium between different chromatin conformational states

Fan, J. Y., Gordon, F., Luger, K., Hansen, J. C., & Tremethick, D. J. (2002) · Nature Structural Biology · doi:10.1038/nsb767 · Cited by 248 · see citing works

Reversible Oligonucleosome Self-Association: Dependence on Divalent Cations and Core Histone Tail Domains

Schwarz, P. M., Felthauser, A. M., Fletcher, T. M., & Hansen, J. C. (1996) · Biochemistry · doi:10.1021/bi9525684 · Cited by 247 · see citing works

Chromosomal Distribution of PcG Proteins during Drosophila Development

Negre, N. N., Hennetin, J., Sun, L. V., Lavrov, S. A., Bellis, M., White, K. P., & Cavalli, G. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040170 · Cited by 246 · see citing works

Chromatin fibers are left-handed double helices with diameter and mass per unit length that depend on linker length

Williams, S. P., Athey, B. D., Muglia, L. J., et al. (1986) · Biophysical Journal · doi:10.1016/s0006-3495(86)83637-2 · Cited by 244 · see citing works

Nuclear Pore Proteins Nup153 and Megator Define Transcriptionally Active Regions in the Drosophila Genome

Vaquerizas, J. M., Suyama, R., Kind, J., Miura, K., Luscombe, N. M., & Akhtar, A. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000846 · Cited by 243 · see citing works

Chromatin loops in gene regulation

Kadauke, S., & Blobel, G. A. (2008) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2008.07.002 · Cited by 237 · see citing works

Mass Spectrometric Mapping of Linker Histone H1 Variants Reveals Multiple Acetylations, Methylations, and Phosphorylation as Well as Differences between Cell Culture and Tissue

Wiśniewski, J. R., Zougman, A., Krüger, S., & Mann, M. (2006) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m600255-mcp200 · Cited by 233 · see citing works

A New Fluorescence Resonance Energy Transfer Approach Demonstrates That the Histone Variant H2AZ Stabilizes the Histone Octamer within the Nucleosome

Park, Y., Dyer, P. N., Tremethick, D. J., & Luger, K. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313152200 · Cited by 231 · see citing works

HP1 Binds Specifically to Lys26-methylated Histone H1.4, whereas Simultaneous Ser27 Phosphorylation Blocks HP1 Binding

Daujat, S., Zeißler, U., Waldmann, T., Happel, N., & Schneider, R. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.c500229200 · Cited by 230 · see citing works

The C-terminal Domain Is the Primary Determinant of Histone H1 Binding to Chromatin in Vivo

Hendzel, M. J., Lever, M. A., Crawford, E., & Th'ng, J. P. H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m400070200 · Cited by 225 · see citing works

The nucleosome surface regulates chromatin compaction and couples it with transcriptional repression

Zhou, J., Fan, J. Y., Rangasamy, D., & Tremethick, D. J. (2007) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1323 · Cited by 205 · see citing works

PcG Proteins, DNA Methylation, and Gene Repression by Chromatin Looping

Tiwari, V. K., McGarvey, K. M., Licchesi, J. D. F., Ohm, J. E., Herman, J. G., Schübeler, D., & Baylin, S. B. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060306 · Cited by 205 · see citing works

Nucleosomes containing the histone variant H2A.Bbd organize only 118 base pairs of DNA

Bao, Y., Konesky, K. L., Park, Y., Rosu, S., Dyer, P. N., Rangasamy, D., Tremethick, D. J., Laybourn, P. J., & Luger, K. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600316 · Cited by 202 · see citing works

Dynamic Histone H1 Isotype 4 Methylation and Demethylation by Histone Lysine Methyltransferase G9a/KMT1C and the Jumonji Domain-containing JMJD2/KDM4 Proteins

Trojer, P., Zhang, J., Yonezawa, M., Schmidt, A., Zheng, H., Jenuwein, T., & Reinberg, D. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m807818200 · Cited by 201 · see citing works

Acetylation Mimics within Individual Core Histone Tail Domains Indicate Distinct Roles in Regulating the Stability of Higher-Order Chromatin Structure

Wang, X., & Hayes, J. J. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01245-07 · Cited by 186 · see citing works

Polycomb Proteins Remain Bound to Chromatin and DNA during DNA Replication In Vitro

Francis, N. J., Follmer, N. E., Simon, M. D., Aghia, G., & Butler, J. D. (2009) · Cell · doi:10.1016/j.cell.2009.02.017 · Cited by 181 · see citing works

The H4 Tail Domain Participates in Intra- and Internucleosome Interactions with Protein and DNA during Folding and Oligomerization of Nucleosome Arrays

Kan, P., Caterino, T. L., & Hayes, J. J. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01343-08 · Cited by 178 · see citing works

Core Histone Tail Domains Mediate Oligonucleosome Folding and Nucleosomal DNA Organization through Distinct Molecular Mechanisms

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The Core Histone N-terminal Tail Domains Function Independently and Additively during Salt-dependent Oligomerization of Nucleosomal Arrays

Gordon, F., Luger, K., & Hansen, J. C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507048200 · Cited by 162 · see citing works

Mechanism of Polymerase II Transcription Repression by the Histone Variant macroH2A

Doyen, C.-M., An, W., Angelov, D., Bondarenko, V., Mietton, F., Studitsky, V. M., Hamiche, A., Roeder, R. G., Bouvet, P., & Dimitrov, S. I. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.3.1156-1164.2006 · Cited by 154 · see citing works

Errata: The essential histone variant H2A.Z regulates the equilibrium between different chromatin conformational states

Fan, J. Y., Gordon, F., Luger, K., Hansen, J. C., & Tremethick, D. J. (2002) · Nature Structural Biology · doi:10.1038/nsb0402-316b · Cited by 154 · see citing works

Determinants of histone H1 mobility and chromatin binding in living cells

Catez, F., Ueda, T., & Bustin, M. (2006) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1077 · Cited by 153 · see citing works

Histone H2A.Z is essential for estrogen receptor signalingPreprint

Gévry, N. Y., Hardy, S., Jacques, P., Laflamme, L., Svotelis, A., Robert, F., & Gaudreau, L. R. (2009) · Genes & Development · doi:10.1101/gad.1787109 · Cited by 147 · see citing works

Dynamic interactions between the promoter and terminator regions of the mammalian BRCA1 gene

Tan‐Wong, S. M., French, J. D., Proudfoot, N. J., & Brown, M. A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801048105 · Cited by 146 · see citing works

Histone H1 Subtypes Differentially Modulate Chromatin Condensation without Preventing ATP-Dependent Remodeling by SWI/SNF or NURF

Clausell, J., Happel, N., Hale, T. K., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007243 · Cited by 142 · see citing works

MeCP2 Binds Cooperatively to Its Substrate and Competes with Histone H1 for Chromatin Binding Sites

Ghosh, R. P., Horowitz-Scherer, R. A., Tv, N., Shlyakhtenko, L. S., & Woodcock, C. L. F. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00379-10 · Cited by 142 · see citing works

Linker histone binding and displacement: versatile mechanism for transcriptional regulation

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Cyclical Chromatin Looping and Transcription Factor Association on the Regulatory Regions of the p21 (CDKN1A) Gene in Response to 1α,25-Dihydroxyvitamin D3

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Salt-dependent Intra- and Internucleosomal Interactions of the H3 Tail Domain in a Model Oligonucleosomal Array

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Histone H1 variant-specific lysine methylation by G9a/KMT1C and Glp1/KMT1D

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Chromatin fiber structure: Where is the problem now?

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The Interaction of NSBP1/HMGN5 with Nucleosomes in Euchromatin Counteracts Linker Histone-Mediated Chromatin Compaction and Modulates Transcription

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Highly Compacted Chromatin Formed In Vitro Reflects the Dynamics of Transcription Activation In Vivo

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Reconstitution of Heterochromatin-Dependent Transcriptional Gene Silencing

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PR‐Set7‐mediated monomethylation of histone H4 lysine 20 at specific genomic regions induces transcriptional repression

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SWI/SNF remodeling and p300‐dependent transcription of histone variant H2ABbd nucleosomal arrays

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HMGN5/NSBP1: A new member of the HMGN protein family that affects chromatin structure and function

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Protein–Protein Förster Resonance Energy Transfer Analysis of Nucleosome Core Particles Containing H2A and H2A.Z

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Structural characterization of H3K56Q nucleosomes and nucleosomal arrays

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EZH2-dependent chromatin looping controls INK4a and INK4b, but not ARF, during human progenitor cell differentiation and cellular senescence

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Role of the M-loop and Reactive Center Loop Domains in the Folding and Bridging of Nucleosome Arrays by MENT

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The Silent Information Regulator 3 Protein, SIR3p, Binds to Chromatin Fibers and Assembles a Hypercondensed Chromatin Architecture in the Presence of Salt

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New chaps in the histone chaperone arenaPreprint

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Determinants of Histone H4 N-terminal Domain Function during Nucleosomal Array Oligomerization

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Global Changes in and Characterization of Specific Sites of Phosphorylation in Mouse and Human Histone H1 Isoforms upon CDK Inhibitor Treatment Using Mass Spectrometry

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Inheriting nuclear organization: can nuclear lamins impart spatial memory during post-mitotic nuclear assembly?

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Chromatin accessibility and the regulatory epigenome

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Epigenetic mechanisms in neurological disease

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Prime, Repair, Restore: The Active Role of Chromatin in the DNA Damage Response

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Long-Range Chromatin Interactions

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An epigenetic framework for neurodevelopmental disorders: From pathogenesis to potential therapy

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Focus on UV-Induced DNA Damage and Repair—Disease Relevance and Protective Strategies

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Epigenome Maintenance in Response to DNA Damage

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ZBTB33 binds unmethylated regions of the genome associated with actively expressed genes

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Chromatin architecture defines the glucocorticoid response

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Epigenetic aberration of gene expression in endometriosis

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Histone H3 phosphorylation near the nucleosome dyad alters chromatin structure

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Chromatin Dynamics during Nucleotide Excision Repair: Histones on the Move

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ESRP2–microRNA-122 axis promotes the postnatal onset of liver polyploidization and maturation

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Chromatin remodeling by nuclear receptors

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Characterizing the Role of AIF4 in Saccharomyces Cerevisiae

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A Network Model of the Molecular Organization of Chromatin in Drosophila

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Genome-Wide Views of Chromatin Structure

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Evolution of the Drosophila melanogaster Chromatin Landscape and Its Associated Proteins

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