scholarly article | Q13442814 |
P50 | author | Florian A Steiner | Q56489551 |
Steven Henikoff | Q28033746 | ||
P2860 | cites work | Induced ectopic kinetochore assembly bypasses the requirement for CENP-A nucleosomes | Q24300684 |
A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension | Q24304199 | ||
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Functional genomics identifies a Myb domain-containing protein family required for assembly of CENP-A chromatin | Q24683353 | ||
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Cse4 is part of an octameric nucleosome in budding yeast | Q27939957 | ||
HCP-4, a CENP-C-like protein in Caenorhabditis elegans, is required for resolution of sister centromeres | Q36364884 | ||
An inverse relationship to germline transcription defines centromeric chromatin in C. elegans | Q36511978 | ||
The CCAN recruits CENP-A to the centromere and forms the structural core for kinetochore assembly | Q36525667 | ||
The chromatin structure of centromeres from fission yeast: differentiation of the central core that correlates with function | Q36529127 | ||
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Mislocalization of the centromeric histone variant CenH3/CENP-A in human cells depends on the chaperone DAXX. | Q39023712 | ||
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HOT regions function as patterned developmental enhancers and have a distinct cis-regulatory signature | Q41766976 | ||
HIRA dependent H3.3 deposition is required for transcriptional reprogramming following nuclear transfer to Xenopus oocytes | Q41963250 | ||
"Point" centromeres of Saccharomyces harbor single centromere-specific nucleosomes | Q42561272 | ||
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A histone-H3-like protein in C. elegans | Q47068912 | ||
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Genome-scale profiling of histone H3.3 replacement patterns. | Q52660778 | ||
CENP-C is a structural platform for kinetochore assembly. | Q52716239 | ||
CENP-A-containing nucleosomes: easier disassembly versus exclusive centromeric localization. | Q53550799 | ||
The kinetochores of Caenorhabditis elegans | Q70598101 | ||
Distinct factors control histone variant H3.3 localization at specific genomic regions | Q28275277 | ||
Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project | Q28301622 | ||
Tetrameric structure of centromeric nucleosomes in interphase Drosophila cells | Q28469268 | ||
MEME SUITE: tools for motif discovery and searching | Q29547204 | ||
The histone variant H3.3 marks active chromatin by replication-independent nucleosome assembly | Q29618256 | ||
Efficient yeast ChIP-Seq using multiplex short-read DNA sequencing | Q33401685 | ||
Partitioning the C. elegans genome by nucleosome modification, occupancy, and positioning | Q33587754 | ||
A native chromatin purification system for epigenomic profiling in Caenorhabditis elegans | Q33700093 | ||
Perinuclear P granules are the principal sites of mRNA export in adult C. elegans germ cells | Q33761242 | ||
Dual recognition of CENP-A nucleosomes is required for centromere assembly | Q33950286 | ||
Epigenome characterization at single base-pair resolution. | Q34057123 | ||
Chromosome engineering allows the efficient isolation of vertebrate neocentromeres. | Q34333350 | ||
The octamer is the major form of CENP-A nucleosomes at human centromeres | Q34342975 | ||
Overlapping Regulation of CenH3 Localization and Histone H3 Turnover by CAF-1 and HIR Proteins in Saccharomyces cerevisiae | Q34477448 | ||
Broad chromosomal domains of histone modification patterns in C. elegans | Q34548272 | ||
Centromere-like regions in the budding yeast genome | Q34561899 | ||
Diverse transcription factor binding features revealed by genome-wide ChIP-seq in C. elegans | Q34625961 | ||
Isolation of a yeast centromere and construction of functional small circular chromosomes | Q34714350 | ||
Neocentromeres: new insights into centromere structure, disease development, and karyotype evolution | Q34746589 | ||
Genomewide analysis of Drosophila GAGA factor target genes reveals context-dependent DNA binding | Q34807363 | ||
Synthetic heterochromatin bypasses RNAi and centromeric repeats to establish functional centromeres. | Q34989114 | ||
Hotspots of transcription factor colocalization in the genome of Drosophila melanogaster | Q35033165 | ||
Heat shock reduces stalled RNA polymerase II and nucleosome turnover genome-wide | Q35569664 | ||
Rapid de novo centromere formation occurs independently of heterochromatin protein 1 in C. elegans embryos | Q35645091 | ||
Tripartite organization of centromeric chromatin in budding yeast | Q35657537 | ||
Nucleosome stability mediated by histone variants H3.3 and H2A.Z. | Q35840889 | ||
Cell-type-specific nuclei purification from whole animals for genome-wide expression and chromatin profiling. | Q35864744 | ||
Centromere identity is specified by a single centromeric nucleosome in budding yeast | Q35990276 | ||
Morphologically distinct microtubule ends in the mitotic centrosome of Caenorhabditis elegans | Q36324773 | ||
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e02025 | |
P577 | publication date | 2014-01-01 | |
P1433 | published in | eLife | Q2000008 |
P1476 | title | Holocentromeres are dispersed point centromeres localized at transcription factor hotspots | |
P478 | volume | 3 |
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Q48364377 | CENP-A and topoisomerase-II antagonistically affect chromosome length. |
Q35186792 | CENP-A nucleosomes localize to transcription factor hotspots and subtelomeric sites in human cancer cells |
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Q64923274 | H3.3K27M-induced chromatin changes drive ectopic replication through misregulation of the JNK pathway in C. elegans. |
Q36676559 | H3K23me2 is a new heterochromatic mark in Caenorhabditis elegans |
Q35799797 | High evolutionary turnover of satellite families in Caenorhabditis. |
Q52589500 | Histone H3K9 and H4 Acetylations and Transcription Facilitate the Initial CENP-AHCP-3 Deposition and De Novo Centromere Establishment in Caenorhabditis elegans Artificial Chromosomes. |
Q38928957 | Holocentromere identity: from the typical mitotic linear structure to the great plasticity of meiotic holocentromeres. |
Q36268643 | Holocentromeres in Rhynchospora are associated with genome-wide centromere-specific repeat arrays interspersed among euchromatin. |
Q36132266 | Inner Kinetochore Protein Interactions with Regional Centromeres of Fission Yeast |
Q26775369 | Insights into epigenetic landscape of recombination-free regions |
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Q38355891 | Recent advances in plant centromere biology |
Q35176510 | Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects |
Q33364777 | Regulation of Plant Cellular and Organismal Development by SUMO. |
Q41673553 | Satellite DNA: An Evolving Topic |
Q34465647 | Sequence features and transcriptional stalling within centromere DNA promote establishment of CENP-A chromatin. |
Q36071249 | Stable Patterns of CENH3 Occupancy Through Maize Lineages Containing Genetically Similar Centromeres |
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Q35882309 | The Genetic Map Enters Its Second Century |
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Q53477429 | The ultrastructure of mono- and holocentric plant centromeres: an immunological investigation by structured illumination microscopy and scanning electron microscopy. |
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