scholarly article | Q13442814 |
P50 | author | Karolin Luger | Q6373153 |
Sheena D'Arcy | Q56992242 | ||
P2093 | author name string | Francesca Mattiroli | |
P2860 | cites work | Crystal structure of the nucleosome core particle at 2.8 A resolution | Q22122355 |
Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres | Q24292850 | ||
Histone variant H2A.Bbd is associated with active transcription and mRNA processing in human cells | Q24293198 | ||
Structure of human nucleosome containing the testis-specific histone variant TSH2B | Q24293590 | ||
Dimerization of the CENP-A assembly factor HJURP is required for centromeric nucleosome deposition | Q24295179 | ||
Transcription in the absence of histone H3.2 and H3K4 methylation. | Q50776226 | ||
Dynamics of histone H3 deposition in vivo reveal a nucleosome gap-filling mechanism for H3.3 to maintain chromatin integrity. | Q51543312 | ||
Regions of variant histone His2AvD required for Drosophila development. | Q52571223 | ||
Histone H2A.Z inheritance during the cell cycle and its impact on promoter organization and dynamics. | Q53138242 | ||
Chromosome-wide nucleosome replacement and H3.3 incorporation during mammalian meiotic sex chromosome inactivation. | Q53576128 | ||
Expression and prognostic significance of centromere protein A in human lung adenocarcinoma. | Q54312442 | ||
Histone macroH2A isoforms predict the risk of lung cancer recurrence | Q57263888 | ||
HJURP Involvement in De Novo CenH3CENP-A and CENP-C Recruitment | Q57898678 | ||
The essential histone variant H2A.Z regulates the equilibrium between different chromatin conformational states | Q77649147 | ||
Histone H2A.Z prepares the prostate specific antigen (PSA) gene for androgen receptor-mediated transcription and is upregulated in a model of prostate cancer progression | Q82357114 | ||
Structure of a CENP-A-histone H4 heterodimer in complex with chaperone HJURP | Q24299299 | ||
Structures of human nucleosomes containing major histone H3 variants | Q24305314 | ||
Nucleosome assembly by a complex of CAF-1 and acetylated histones H3/H4 | Q24313176 | ||
H3.3/H2A.Z double variant-containing nucleosomes mark 'nucleosome-free regions' of active promoters and other regulatory regions | Q24317641 | ||
Centromere-specific assembly of CENP-a nucleosomes is mediated by HJURP. | Q24321321 | ||
HJURP is a cell-cycle-dependent maintenance and deposition factor of CENP-A at centromeres | Q24321377 | ||
ANP32E is a histone chaperone that removes H2A.Z from chromatin | Q24323053 | ||
The macro domain is an ADP-ribose binding module | Q24529134 | ||
Preferential occupancy of histone variant H2AZ at inactive promoters influences local histone modifications and chromatin remodeling | Q24535638 | ||
Concerted and birth-and-death evolution of multigene families | Q24544285 | ||
Nucleosomes containing the histone variant H2A.Bbd organize only 118 base pairs of DNA | Q24563396 | ||
Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas | Q24629777 | ||
A protein complex containing the conserved Swi2/Snf2-related ATPase Swr1p deposits histone variant H2A.Z into euchromatin | Q24801790 | ||
Every amino acid matters: essential contributions of histone variants to mammalian development and disease | Q27008522 | ||
Chromosomes. CENP-C reshapes and stabilizes CENP-A nucleosomes at the centromere. | Q27331790 | ||
Crystal structure of a nucleosome core particle containing the variant histone H2A.Z | Q27628748 | ||
Structure of the yeast histone H3-ASF1 interaction: implications for chaperone mechanism, species-specific interactions, and epigenetics | Q27640732 | ||
NMR structure of chaperone Chz1 complexed with histones H2A.Z-H2B | Q27651273 | ||
The nucleosomal core histone octamer at 3.1 A resolution: a tripartite protein assembly and a left-handed superhelix | Q27655585 | ||
Structural basis for recognition of centromere histone variant CenH3 by the chaperone Scm3 | Q27667279 | ||
Recognition of the centromere-specific histone Cse4 by the chaperone Scm3 | Q27667962 | ||
Crystal structure of the human centromeric nucleosome containing CENP-A | Q27670750 | ||
Structure of the variant histone H3.3–H4 heterodimer in complex with its chaperone DAXX | Q27675056 | ||
A Conserved Mechanism for Centromeric Nucleosome Recognition by Centromere Protein CENP-C | Q27678426 | ||
The Catalytic Subunit of the SWR1 Remodeler Is a Histone Chaperone for the H2A.Z-H2B Dimer | Q27681627 | ||
Anp32e, a higher eukaryotic histone chaperone directs preferential recognition for H2A.Z | Q27682061 | ||
Structural basis of histone H2A-H2B recognition by the essential chaperone FACT | Q27684683 | ||
High-resolution profiling of histone methylations in the human genome | Q27860906 | ||
ATP-driven exchange of histone H2AZ variant catalyzed by SWR1 chromatin remodeling complex | Q27929959 | ||
Binding of chromatin-modifying activities to phosphorylated histone H2A at DNA damage sites | Q27931488 | ||
Replication-independent histone deposition by the HIR complex and Asf1. | Q27931963 | ||
Scm3, an essential Saccharomyces cerevisiae centromere protein required for G2/M progression and Cse4 localization | Q27932322 | ||
Stepwise Histone Replacement by SWR1 Requires Dual Activation with Histone H2A.Z and Canonical Nucleosome | Q27932939 | ||
Chz1, a nuclear chaperone for histone H2AZ. | Q27933271 | ||
A Snf2 family ATPase complex required for recruitment of the histone H2A variant Htz1. | Q27933672 | ||
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin | Q27935829 | ||
Nonhistone Scm3 and histones CenH3-H4 assemble the core of centromere-specific nucleosomes | Q27936719 | ||
DNA damage response pathway uses histone modification to assemble a double-strand break-specific cohesin domain | Q27937364 | ||
Scm3 is essential to recruit the histone h3 variant cse4 to centromeres and to maintain a functional kinetochore | Q27939322 | ||
Cse4 is part of an octameric nucleosome in budding yeast | Q27939957 | ||
ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells | Q28114801 | ||
DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139 | Q28131715 | ||
Overexpression and mistargeting of centromere protein-A in human primary colorectal cancer | Q28184405 | ||
H2AX: the histone guardian of the genome | Q28274279 | ||
Histone macroH2A1 is concentrated in the inactive X chromosome of female mammals | Q28274301 | ||
Histone variants--ancient wrap artists of the epigenome | Q28274796 | ||
Distinct factors control histone variant H3.3 localization at specific genomic regions | Q28275277 | ||
DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors | Q28303693 | ||
Tetrameric structure of centromeric nucleosomes in interphase Drosophila cells | Q28469268 | ||
Genomic instability in mice lacking histone H2AX | Q28589826 | ||
DAXX envelops a histone H3.3-H4 dimer for H3.3-specific recognition | Q28658254 | ||
Dynamic regulation of nucleosome positioning in the human genome | Q29615046 | ||
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma | Q29616862 | ||
The histone variant H3.3 marks active chromatin by replication-independent nucleosome assembly | Q29618256 | ||
The RCAF complex mediates chromatin assembly during DNA replication and repair | Q29620048 | ||
A two-step mechanism for epigenetic specification of centromere identity and function | Q30405362 | ||
In vitro centromere and kinetochore assembly on defined chromatin templates. | Q30427862 | ||
HJURP is a CENP-A chromatin assembly factor sufficient to form a functional de novo kinetochore | Q30428662 | ||
Nap1 and Chz1 have separate Htz1 nuclear import and assembly functions | Q30433388 | ||
Chromatin assembly at kinetochores is uncoupled from DNA replication | Q30442008 | ||
CAL1 is the Drosophila CENP-A assembly factor | Q30570646 | ||
The Histone Database: a comprehensive resource for histones and histone fold-containing proteins | Q33229210 | ||
Histone variants: emerging players in cancer biology | Q33630867 | ||
HJURP binds CENP-A via a highly conserved N-terminal domain and mediates its deposition at centromeres | Q33667469 | ||
H2A.Bbd: an X-chromosome-encoded histone involved in mammalian spermiogenesis | Q33760193 | ||
Nucleosome stability mediated by histone variants H3.3 and H2A.Z. | Q35840889 | ||
Towards a mechanism for histone chaperones | Q35861914 | ||
Ubinuclein-1 confers histone H3.3-specific-binding by the HIRA histone chaperone complex | Q35878397 | ||
p21 transcription is regulated by differential localization of histone H2A.Z. | Q35917048 | ||
Stepwise assembly of chromatin during DNA replication in vitro | Q35923880 | ||
DNA repair factor APLF is a histone chaperone | Q36238038 | ||
Centromere protein-A, an essential centromere protein, is a prognostic marker for relapse in estrogen receptor-positive breast cancer | Q36245350 | ||
The basic linker of macroH2A stabilizes DNA at the entry/exit site of the nucleosome | Q36280768 | ||
Topography of the histone octamer surface: repeating structural motifs utilized in the docking of nucleosomal DNA | Q36657548 | ||
Cell-cycle-dependent structural transitions in the human CENP-A nucleosome in vivo | Q36669215 | ||
Genomic analysis of estrogen cascade reveals histone variant H2A.Z associated with breast cancer progression | Q36671809 | ||
CENP-A confers a reduction in height on octameric nucleosomes | Q36912565 | ||
Histone H2A.Z is essential for estrogen receptor signaling | Q37247116 | ||
Nucleosome-free region dominates histone acetylation in targeting SWR1 to promoters for H2A.Z replacement | Q37274135 | ||
Genome-wide dynamics of Htz1, a histone H2A variant that poises repressed/basal promoters for activation through histone loss | Q37458741 | ||
The budding yeast Centromere DNA Element II wraps a stable Cse4 hemisome in either orientation in vivo | Q37698353 | ||
Reconciling the positive and negative roles of histone H2A.Z in gene transcription | Q37723982 | ||
The chaperone-histone partnership: for the greater good of histone traffic and chromatin plasticity | Q37952956 | ||
The role of the nucleosome acidic patch in modulating higher order chromatin structure | Q38085143 | ||
Mechanisms and functions of ATP-dependent chromatin-remodeling enzymes | Q38126255 | ||
Structural biology-based insights into combinatorial readout and crosstalk among epigenetic marks | Q38205661 | ||
Histone chaperones: assisting histone traffic and nucleosome dynamics | Q38218235 | ||
Placing the HIRA histone chaperone complex in the chromatin landscape. | Q38607892 | ||
Removal of H2A.Z by INO80 promotes homologous recombination | Q38856752 | ||
Phosphorylation and DNA binding of HJURP determine its centromeric recruitment and function in CenH3(CENP-A) loading | Q38977427 | ||
Mislocalization of the centromeric histone variant CenH3/CENP-A in human cells depends on the chaperone DAXX. | Q39023712 | ||
Transcription recovery after DNA damage requires chromatin priming by the H3.3 histone chaperone HIRA. | Q39090477 | ||
FACT-mediated exchange of histone variant H2AX regulated by phosphorylation of H2AX and ADP-ribosylation of Spt16. | Q39992783 | ||
Activation of Holliday junction recognizing protein involved in the chromosomal stability and immortality of cancer cells | Q40083781 | ||
Reconstitution of chromatin: assembly of the nucleosome | Q40572714 | ||
The histone chaperone Nap1 promotes nucleosome assembly by eliminating nonnucleosomal histone DNA interactions | Q40889167 | ||
Chromatin assembly coupled to DNA repair: a new role for chromatin assembly factor I. | Q41166774 | ||
CENP-A K124 Ubiquitylation Is Required for CENP-A Deposition at the Centromere | Q41333170 | ||
Cell-cycle-coupled structural oscillation of centromeric nucleosomes in yeast | Q41811815 | ||
Transcriptional and developmental functions of the H3.3 histone variant in Drosophila | Q41960228 | ||
Partitioning of histone H3-H4 tetramers during DNA replication-dependent chromatin assembly | Q43111741 | ||
Centromere identity maintained by nucleosomes assembled with histone H3 containing the CENP-A targeting domain | Q46132923 | ||
Evolution of histone H3: emergence of variants and conservation of post-translational modification sites. | Q47266768 | ||
A retroviral gene trap insertion into the histone 3.3A gene causes partial neonatal lethality, stunted growth, neuromuscular deficits and male sub-fertility in transgenic mice | Q47912968 | ||
Dynamic phosphorylation of CENP-A at Ser68 orchestrates its cell-cycle-dependent deposition at centromeres | Q48392345 | ||
Imaging the fate of histone Cse4 reveals de novo replacement in S phase and subsequent stable residence at centromeres | Q33795322 | ||
The expression level of HJURP has an independent prognostic impact and predicts the sensitivity to radiotherapy in breast cancer | Q33889488 | ||
Structural characterization of the histone variant macroH2A. | Q33925060 | ||
Dual recognition of CENP-A nucleosomes is required for centromere assembly | Q33950286 | ||
Automodification switches PARP-1 function from chromatin architectural protein to histone chaperone | Q34144527 | ||
Histone variants in metazoan development | Q34149623 | ||
Altered telomeres in tumors with ATRX and DAXX mutations | Q34196696 | ||
QKI-mediated alternative splicing of the histone variant MacroH2A1 regulates cancer cell proliferation | Q34208257 | ||
Structural basis for the histone chaperone activity of Asf1 | Q34312157 | ||
The octamer is the major form of CENP-A nucleosomes at human centromeres | Q34342975 | ||
Chaperone Nap1 shields histone surfaces used in a nucleosome and can put H2A-H2B in an unconventional tetrameric form. | Q34366314 | ||
A network of players in H3 histone variant deposition and maintenance at centromeres | Q34390431 | ||
Purification and characterization of CAF-I, a human cell factor required for chromatin assembly during DNA replication in vitro | Q34451628 | ||
MacroH2A1.1 and PARP-1 cooperate to regulate transcription by promoting CBP-mediated H2B acetylation | Q34458110 | ||
Purification of a human SRCAP complex that remodels chromatin by incorporating the histone variant H2A.Z into nucleosomes | Q34516925 | ||
Histone chaperones in nucleosome assembly and human disease | Q34647041 | ||
The histone variant macroH2A suppresses melanoma progression through regulation of CDK8. | Q34676833 | ||
The nucleosome surface regulates chromatin compaction and couples it with transcriptional repression | Q34707393 | ||
Histone mRNA expression: multiple levels of cell cycle regulation and important developmental consequences | Q35021205 | ||
Structure and Scm3-mediated assembly of budding yeast centromeric nucleosomes | Q35038924 | ||
Mislocalization of the Drosophila centromere-specific histone CID promotes formation of functional ectopic kinetochores | Q35335808 | ||
Phylogenomics of the nucleosome | Q35570334 | ||
Structural transitions of centromeric chromatin regulate the cell cycle-dependent recruitment of CENP-N | Q35635462 | ||
Acetylation of H2A.Z is a key epigenetic modification associated with gene deregulation and epigenetic remodeling in cancer | Q35694399 | ||
The Histone Chaperones FACT and Spt6 Restrict H2A.Z from Intragenic Locations | Q35762777 | ||
Histone chaperone Anp32e removes H2A.Z from DNA double-strand breaks and promotes nucleosome reorganization and DNA repair | Q35764396 | ||
P433 | issue | 11 | |
P921 | main subject | molecular chaperones | Q422496 |
P304 | page(s) | 1454-1466 | |
P577 | publication date | 2015-10-12 | |
P1433 | published in | EMBO Reports | Q5323356 |
P1476 | title | The right place at the right time: chaperoning core histone variants | |
P478 | volume | 16 |
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