| Q43155322 | A canonical promoter organization of the transcription machinery and its regulators in the Saccharomyces genome |
| Q41936960 | A conserved acidic patch in the Myb domain is required for activation of an endogenous target gene and for chromatin binding |
| Q37829707 | A modified epigenetics toolbox to study histone modifications on the nucleosome core. |
| Q24294901 | A zinc finger HIT domain-containing protein, ZNHIT-1, interacts with orphan nuclear hormone receptor Rev-erbbeta and removes Rev-erbbeta-induced inhibition of apoCIII transcription |
| Q27692030 | ATP dependent chromatin remodeling enzymes in embryonic stem cells |
| Q35865561 | ATP-dependent chromatin remodeling factors and DNA damage repair |
| Q35651278 | Access to DNA establishes a secondary target site bias for the yeast retrotransposon Ty5. |
| Q39414538 | Acetylation of H3 K56 is required for RNA polymerase II transcript elongation through heterochromatin in yeast. |
| Q27937452 | Acetylation of the SUN protein Mps3 by Eco1 regulates its function in nuclear organization. |
| Q33564388 | Actin-related protein Arp6 influences H2A.Z-dependent and -independent gene expression and links ribosomal protein genes to nuclear pores |
| Q34299231 | Activity of a C-terminal Plant Homeodomain (PHD) of Msc1 Is Essential for Function |
| Q40541541 | An RNA polymerase II-coupled function for histone H3K36 methylation in checkpoint activation and DSB repair |
| Q24671488 | Analysis of human histone H2AZ deposition in vivo argues against its direct role in epigenetic templating mechanisms |
| Q27682061 | Anp32e, a higher eukaryotic histone chaperone directs preferential recognition for H2A.Z |
| Q27658459 | Asf1-like structure of the conserved Yaf9 YEATS domain and role in H2A.Z deposition and acetylation |
| Q43179790 | Asymmetric nucleosomes flank promoters in the budding yeast genome |
| Q33568422 | Chapter 5. Nuclear actin-related proteins in epigenetic control |
| Q30437379 | Characterization of the histone H2A.Z-1 and H2A.Z-2 isoforms in vertebrates |
| Q36177486 | Chd1 and yFACT act in opposition in regulating transcription. |
| Q37704663 | Chd1 remodelers maintain open chromatin and regulate the epigenetics of differentiation. |
| Q26799305 | Chromatin Dynamics in Vivo: A Game of Musical Chairs |
| Q35748234 | Chromatin and transcription in yeast |
| Q39539723 | Chromatin remodeling by imitation switch (ISWI) class ATP-dependent remodelers is stimulated by histone variant H2A.Z. |
| Q41864430 | Chromatin structure and expression of a gene transcribed by RNA polymerase III are independent of H2A.Z deposition. |
| Q37398600 | Connection between histone H2A variants and chromatin remodeling complexes |
| Q34402955 | Control of embryonic stem cell identity by nucleosome remodeling enzymes |
| Q27939957 | Cse4 is part of an octameric nucleosome in budding yeast |
| Q50561900 | DNA Replication Is Required for Circadian Clock Function by Regulating Rhythmic Nucleosome Composition. |
| Q34022215 | Decoding the Epigenetic Language of Plant Development |
| Q28484353 | Deposition of histone variant H2A.Z within gene bodies regulates responsive genes |
| Q36748104 | Different genetic functions for the Rpd3(L) and Rpd3(S) complexes suggest competition between NuA4 and Rpd3(S) |
| Q38808036 | Different phosphoisoforms of RNA polymerase II engage the Rtt103 termination factor in a structurally analogous manner. |
| Q33414877 | Discriminating nucleosomes containing histone H2A.Z or H2A based on genetic and epigenetic information |
| Q47332390 | Downstream promoter interactions of TFIID TAFs facilitate transcription reinitiation |
| Q34794271 | Drosophila histone H2A variant (H2Av) controls poly(ADP-ribose) polymerase 1 (PARP1) activation in chromatin |
| Q37128008 | Dynamic histone variant exchange accompanies gene induction in T cells |
| Q26851348 | Dynamics of histone variant H3.3 and its coregulation with H2A.Z at enhancers and promoters |
| Q41579365 | Eaf1 Links the NuA4 Histone Acetyltransferase Complex to Htz1 Incorporation and Regulation of Purine Biosynthesis |
| Q36981211 | Epigenetic regulation of centromeric chromatin: old dogs, new tricks? |
| Q37053543 | Epigenetic regulation of the ribosomal cistron seasonally modulates enrichment of H2A.Z and H2A.Zub in response to different environmental inputs in carp (Cyprinus carpio) |
| Q38891308 | Expression of Non-acetylatable H2A.Z in Myoblast Cells Blocks Myoblast Differentiation through Disruption of MyoD Expression |
| Q36579359 | Five repair pathways in one context: chromatin modification during DNA repair |
| Q35004993 | Full and partial genome-wide assembly and disassembly of the yeast transcription machinery in response to heat shock |
| Q30427610 | Genetic analysis implicates the Set3/Hos2 histone deacetylase in the deposition and remodeling of nucleosomes containing H2A.Z. |
| Q42278134 | Genome-wide analysis of chromatin status using tiling microarrays |
| Q37077306 | Genome-wide approaches to studying chromatin modifications |
| Q36567360 | Genome-wide patterns of histone modifications in yeast. |
| Q92088931 | Genome-wide reconstitution of chromatin transactions reveals that RSC preferentially disrupts H2AZ-containing nucleosomes |
| Q33611702 | Genome-wide views of chromatin structure |
| Q36082186 | Genome-wide, as opposed to local, antisilencing is mediated redundantly by the euchromatic factors Set1 and H2A.Z. |
| Q36471383 | Genomic distribution and functional analyses of potential G-quadruplex-forming sequences in Saccharomyces cerevisiae. |
| Q33954563 | Genomic organization of H2Av containing nucleosomes in Drosophila heterochromatin |
| Q33864143 | Global analysis for functional residues of histone variant Htz1 using the comprehensive point mutant library |
| Q47155918 | Global inhibition of transcription causes an increase in histone H2A.Z incorporation within gene bodies |
| Q36798739 | Global investigation of protein-protein interactions in yeast Saccharomyces cerevisiae using re-occurring short polypeptide sequences. |
| Q34419379 | Global turnover of histone post-translational modifications and variants in human cells |
| Q34477589 | H2A.Z (Htz1) controls the cell-cycle-dependent establishment of transcriptional silencing at Saccharomyces cerevisiae telomeres |
| Q48032398 | H2A.Z and H2B.Z double-variant nucleosomes define intergenic regions and dynamically occupy var gene promoters in the malaria parasite Plasmodium falciparum |
| Q41179603 | H2A.Z controls the stability and mobility of nucleosomes to regulate expression of the LH genes |
| Q35576229 | H2A.Z marks antisense promoters and has positive effects on antisense transcript levels in budding yeast |
| Q33279444 | H2A.Z-mediated localization of genes at the nuclear periphery confers epigenetic memory of previous transcriptional state |
| Q39989822 | H2AZ is enriched at polycomb complex target genes in ES cells and is necessary for lineage commitment |
| Q37362553 | H3.3 actively marks enhancers and primes gene transcription via opening higher-ordered chromatin. |
| Q24317641 | H3.3/H2A.Z double variant-containing nucleosomes mark 'nucleosome-free regions' of active promoters and other regulatory regions |
| Q33653254 | HAT2 mediates histone H4K4 acetylation and affects micrococcal nuclease sensitivity of chromatin in Leishmania donovani |
| Q40335328 | Histone Chaperone Nap1 Is a Major Regulator of Histone H2A-H2B Dynamics at the Inducible GAL Locus |
| Q33371693 | Histone H2A.Z and DNA methylation are mutually antagonistic chromatin marks |
| Q37352034 | Histone H2A.Z cooperates with RNAi and heterochromatin factors to suppress antisense RNAs |
| Q37247116 | Histone H2A.Z is essential for estrogen receptor signaling |
| Q84865644 | Histone H2A.Z regulates the expression of several classes of phosphate starvation response genes but not as a transcriptional activator |
| Q43159915 | Histone H3 lysine 36 dimethylation (H3K36me2) is sufficient to recruit the Rpd3s histone deacetylase complex and to repress spurious transcription |
| Q35025031 | Histone H3 variants and their potential role in indexing mammalian genomes: the "H3 barcode hypothesis" |
| Q92074963 | Histone Tail Dynamics in Partially Disassembled Nucleosomes During Chromatin Remodeling |
| Q27939494 | Histone variant H2A.Z and RNA polymerase II transcription elongation |
| Q89475630 | Histone variant H2A.Z deposition and acetylation directs the canonical Notch signaling response |
| Q33581966 | Histone variant H2A.Z regulates centromere silencing and chromosome segregation in fission yeast |
| Q27934483 | Histone variant Htz1 promotes histone H3 acetylation to enhance nucleotide excision repair in Htz1 nucleosomes |
| Q26827964 | Histone variants as emerging regulators of embryonic stem cell identity |
| Q33588109 | Histone variants: dynamic punctuation in transcription |
| Q33630867 | Histone variants: emerging players in cancer biology |
| Q38355887 | Histone variants: the artists of eukaryotic chromatin |
| Q37514183 | How eukaryotic genes are transcribed |
| Q33569829 | Hypoxic repression of endothelial nitric-oxide synthase transcription is coupled with eviction of promoter histones |
| Q34020211 | Identification and characterization of the two isoforms of the vertebrate H2A.Z histone variant |
| Q33426080 | Identification of novel transcriptional regulators involved in macrophage differentiation and activation in U937 cells |
| Q41889467 | Infrequently transcribed long genes depend on the Set2/Rpd3S pathway for accurate transcription |
| Q33565190 | Insights into chromatin structure and dynamics in plants |
| Q27938380 | Interaction of a DNA Zip Code with the Nuclear Pore Complex Promotes H2A.Z Incorporation and INO1 Transcriptional Memory |
| Q36579347 | Is histone loss a common feature of DNA metabolism regulation? |
| Q38409542 | Isw1 functions in parallel with the NuA4 and Swr1 complexes in stress-induced gene repression |
| Q38285917 | Key functional regions in the histone variant H2A.Z C-terminal docking domain |
| Q47550184 | Learning and Age-Related Changes in Genome-wide H2A.Z Binding in the Mouse Hippocampus. |
| Q37176820 | MYSTs mark chromatin for chromosomal functions |
| Q39318001 | Maintenance of heterochromatin boundary and nucleosome composition at promoters by the Asf1 histone chaperone and SWR1-C chromatin remodeler in Saccharomyces cerevisiae. |
| Q36738573 | Mechanisms of ATP dependent chromatin remodeling |
| Q37180651 | Mechanisms that specify promoter nucleosome location and identity |
| Q36177449 | Monoubiquitylation of H2A.Z distinguishes its association with euchromatin or facultative heterochromatin |
| Q36287862 | Msc1 acts through histone H2A.Z to promote chromosome stability in Schizosaccharomyces pombe |
| Q36208613 | Multivalent di-nucleosome recognition enables the Rpd3S histone deacetylase complex to tolerate decreased H3K36 methylation levels |
| Q31139142 | Multivalent engagement of TFIID to nucleosomes |
| Q40069093 | Myb proteins regulate expression of histone variant H2A.Z during thymocyte development |
| Q30433388 | Nap1 and Chz1 have separate Htz1 nuclear import and assembly functions |
| Q92883511 | Nascent chromatin occupancy profiling reveals locus- and factor-specific chromatin maturation dynamics behind the DNA replication fork |
| Q37629627 | NuA4 and SWR1-C: two chromatin-modifying complexes with overlapping functions and components |
| Q27936275 | NuA4-dependent acetylation of nucleosomal histones H4 and H2A directly stimulates incorporation of H2A.Z by the SWR1 complex. |
| Q27930805 | NuA4-directed chromatin transactions throughout the Saccharomyces cerevisiae genome |
| Q37548517 | Nucleosome fragility is associated with future transcriptional response to developmental cues and stress in C. elegans |
| Q38885861 | Nucleosome mobility and the regulation of gene expression: Insights from single-molecule studies. |
| Q37326387 | Nucleosome organization in the Drosophila genome. |
| Q37885611 | Nucleosome positioning in Saccharomyces cerevisiae. |
| Q35840889 | Nucleosome stability mediated by histone variants H3.3 and H2A.Z. |
| Q24672606 | Opposing roles for Set2 and yFACT in regulating TBP binding at promoters |
| Q38072728 | Organizing the genome with H2A histone variants |
| Q34199248 | PICH and BLM limit histone association with anaphase centromeric DNA threads and promote their resolution |
| Q42510780 | Physical and functional interactions between Drosophila homologue of Swc6/p18Hamlet subunit of the SWR1/SRCAP chromatin-remodeling complex with the DNA repair/transcription factor TFIIH. |
| Q26852536 | Post-translational modifications of histones that influence nucleosome dynamics |
| Q38169520 | Post-translational modifications of the histone variant H2AZ. |
| Q36865040 | Pyrosequencing positions nucleosomes precisely |
| Q27938414 | RSC exploits histone acetylation to abrogate the nucleosomal block to RNA polymerase II elongation |
| Q28472344 | RSF governs silent chromatin formation via histone H2Av replacement |
| Q35959575 | Regulation of Budding Yeast CENP-A levels Prevents Misincorporation at Promoter Nucleosomes and Transcriptional Defects. |
| Q54188370 | Regulation of chromatin states and gene expression during HSN neuronal maturation is mediated by EOR-1/PLZF, MAU-2/cohesin loader, and SWI/SNF complex. |
| Q37398628 | Regulation of gene expression and cellular proliferation by histone H2A.Z. |
| Q58924948 | Repression of flowering in Arabidopsis requires activation of FLOWERING LOCUS C expression by the histone variant H2A.Z |
| Q27348721 | Restricting dosage compensation complex binding to the X chromosomes by H2A.Z/HTZ-1 |
| Q36579373 | Reuniting the contrasting functions of H2A.Z. |
| Q51563325 | Revealing epigenetic patterns in gene regulation through integrative analysis of epigenetic interaction network. |
| Q33416352 | Role of the histone variant H2A.Z/Htz1p in TBP recruitment, chromatin dynamics, and regulated expression of oleate-responsive genes |
| Q33617819 | Roles for H2A.Z and its acetylation in GAL1 transcription and gene induction, but not GAL1-transcriptional memory |
| Q90163871 | Roles of the INO80 and SWR1 Chromatin Remodeling Complexes in Plants |
| Q43259704 | SAS-mediated acetylation of histone H4 Lys 16 is required for H2A.Z incorporation at subtelomeric regions in Saccharomyces cerevisiae |
| Q38698612 | SETD2 and histone H3 lysine 36 methylation deficiency in advanced systemic mastocytosis |
| Q27934592 | SWI/SNF-like chromatin remodeling factor Fun30 supports point centromere function in S. cerevisiae. |
| Q42064469 | SWR-C and INO80 chromatin remodelers recognize nucleosome-free regions near +1 nucleosomes. |
| Q33826542 | SWR1 complex poises heterochromatin boundaries for antisilencing activity propagation. |
| Q34752031 | Scm3 is a centromeric nucleosome assembly factor |
| Q27932939 | Stepwise Histone Replacement by SWR1 Requires Dual Activation with Histone H2A.Z and Canonical Nucleosome |
| Q24339519 | TIP48/Reptin and H2A.Z requirement for initiating chromatin remodeling in estrogen-activated transcription |
| Q34918097 | Targeting of the SUN protein Mps3 to the inner nuclear membrane by the histone variant H2A.Z. |
| Q47288294 | Temporal regulation of chromatin during myoblast differentiation. |
| Q33258828 | Temporal regulation of foregut development by HTZ-1/H2A.Z and PHA-4/FoxA |
| Q35823742 | The 19S proteasome subcomplex promotes the targeting of NuA4 HAT to the promoters of ribosomal protein genes to facilitate the recruitment of TFIID for transcriptional initiation in vivo |
| Q36631422 | The Genomes of Three Uneven Siblings: Footprints of the Lifestyles of Three Trichoderma Species |
| Q27930026 | The Isw2 chromatin-remodeling ATPase cooperates with the Fkh2 transcription factor to repress transcription of the B-type cyclin gene CLB2 |
| Q37085208 | The MSL3 chromodomain directs a key targeting step for dosage compensation of the Drosophila melanogaster X chromosome |
| Q33658624 | The SWR1 histone replacement complex causes genetic instability and genome-wide transcription misregulation in the absence of H2A.Z. |
| Q30884260 | The Schizosaccharomyces pombe JmjC-protein, Msc1, prevents H2A.Z localization in centromeric and subtelomeric chromatin domains |
| Q58751869 | The Swr1 chromatin-remodeling complex prevents genome instability induced by replication fork progression defects |
| Q27936207 | The Tup1 corepressor directs Htz1 deposition at a specific promoter nucleosome marking the GAL1 gene for rapid activation |
| Q35070913 | The X and Y chromosomes assemble into H2A.Z-containing [corrected] facultative heterochromatin [corrected] following meiosis. |
| Q34092981 | The current state of chromatin immunoprecipitation |
| Q24336460 | The euchromatic and heterochromatic landscapes are shaped by antagonizing effects of transcription on H2A.Z deposition |
| Q84414718 | The evolution of epitype |
| Q37038673 | The gamma-H2A.X: is it just a surrogate marker of double-strand breaks or much more? |
| Q33369072 | The genomic distribution and function of histone variant HTZ-1 during C. elegans embryogenesis |
| Q36352391 | The histone variant H2A.W defines heterochromatin and promotes chromatin condensation in Arabidopsis |
| Q64899742 | The histone variant H2A.Z in gene regulation. |
| Q37288973 | The histone variant His2Av is required for adult stem cell maintenance in the Drosophila testis |
| Q36226790 | The influence of DNA sequence on epigenome-induced pathologies |
| Q21092478 | The insulator binding protein CTCF positions 20 nucleosomes around its binding sites across the human genome |
| Q93088380 | The repressive role of Arabidopsis H2A.Z in transcriptional regulation depends on AtBMI1 activity |
| Q36270857 | The right place at the right time: chaperoning core histone variants |
| Q36579354 | The role of chromatin structure in regulating stress-induced transcription in Saccharomyces cerevisiae |
| Q37687220 | The role of histone modifications and variants in regulating gene expression in breast cancer. |
| Q34082953 | Threonine-4 of the budding yeast RNAP II CTD couples transcription with Htz1-mediated chromatin remodeling. |
| Q37325705 | Toxoplasma H2A variants reveal novel insights into nucleosome composition and functions for this histone family |
| Q42911076 | Transcription alters chromosomal locations of cohesin in Saccharomyces cerevisiae |
| Q42244178 | Transcription factor CTF1 acts as a chromatin domain boundary that shields human telomeric genes from silencing |
| Q38043829 | Transcription-associated histone modifications and cryptic transcription |
| Q37398592 | Transcriptional and epigenetic functions of histone variant H2A.Z. |
| Q52663127 | Transcriptional regulation mediated by H2A.Z via ANP32e-dependent inhibition of protein phosphatase 2A. |
| Q34613479 | Translational and rotational settings of H2A.Z nucleosomes across the Saccharomyces cerevisiae genome. |
| Q34947175 | USP10 deubiquitylates the histone variant H2A.Z and both are required for androgen receptor-mediated gene activation |
| Q35720902 | Ubiquitylation of histone H2B controls RNA polymerase II transcription elongation independently of histone H3 methylation |
| Q41767877 | Yeast H2A.Z, FACT complex and RSC regulate transcription of tRNA gene through differential dynamics of flanking nucleosomes. |
| Q35917048 | p21 transcription is regulated by differential localization of histone H2A.Z. |