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Genome Organization in and around the Nucleolus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/stem.1825openalex-snapshot
Biosynthesis of Ribosomal RNA in Nucleoli Regulates Pluripotency and Differentiation Ability of Pluripotent Stem Cells
inferredcites →https://doi.org/10.1007/978-3-319-46503-6_9openalex-snapshot
Structure and Function of RNA Polymerases and the Transcription Machineries
inferredcites →https://doi.org/10.1007/bf00329389openalex-snapshot
Visualization of nucleolar organizer regions in mammalian chromosomes using silver staining
inferredcites →https://doi.org/10.1007/bf00360550openalex-snapshot
Chromosomal locations of Ag-NORs and clusters of ribosomal DNA in laboratory strains of mice
inferredcites →https://doi.org/10.1007/s10577-018-09603-9openalex-snapshot
The chromatin landscape of the ribosomal RNA genes in mouse and human
inferredcites →https://doi.org/10.1007/s10577-018-9587-yopenalex-snapshot
Dosage effects of human ribosomal genes (rDNA) in health and disease
inferredcites →https://doi.org/10.1016/0022-2836(79)90483-2openalex-snapshot
The genetic behaviour of a cloned mouse ribosomal DNA segment mimics mouse ribosomal gene evolution
inferredcites →https://doi.org/10.1016/0092-8674(77)90053-8openalex-snapshot
Heterogeneity of the ribosomal genes in mice and men
inferredcites →https://doi.org/10.1016/0092-8674(89)90790-3openalex-snapshot
Two different chromatin structures coexist in ribosomal RNA genes throughout the cell cycle
inferredcites →https://doi.org/10.1016/j.bbrc.2004.07.083openalex-snapshot
Effects of chromatin structure on the enzymatic and DNA binding functions of DNA methyltransferases DNMT1 and Dnmt3a in vitro
inferredcites →https://doi.org/10.1016/j.bpj.2008.11.075openalex-snapshot
Spatio-Temporal Plasticity in Chromatin Organization in Mouse Cell Differentiation and during Drosophila Embryogenesis
inferredcites →https://doi.org/10.1016/j.ceb.2014.03.001openalex-snapshot
Nucleolus and nuclear periphery: Velcro for heterochromatin
inferredcites →https://doi.org/10.1016/j.ceb.2014.03.003openalex-snapshot
Mechanisms and dynamics of nuclear lamina–genome interactions
inferredcites →https://doi.org/10.1016/j.ceb.2017.03.004openalex-snapshot
Nucleolar reorganization in response to rDNA damage
inferredcites →https://doi.org/10.1016/j.cell.2007.03.036openalex-snapshot
Perinucleolar Targeting of the Inactive X during S Phase: Evidence for a Role in the Maintenance of Silencing
inferredcites →https://doi.org/10.1016/j.cell.2008.03.030openalex-snapshot
Epigenetic Control of rDNA Loci in Response to Intracellular Energy Status
inferredcites →https://doi.org/10.1016/j.cell.2013.02.028openalex-snapshot
Single-Cell Dynamics of Genome-Nuclear Lamina Interactions
inferredcites →https://doi.org/10.1016/j.cell.2014.11.021openalex-snapshot
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
inferredcites →https://doi.org/10.1016/j.cell.2015.08.040openalex-snapshot
Genome-wide Maps of Nuclear Lamina Interactions in Single Human Cells
inferredcites →https://doi.org/10.1016/j.cell.2016.04.047openalex-snapshot
Coexisting Liquid Phases Underlie Nucleolar Subcompartments
inferredcites →https://doi.org/10.1016/j.cell.2018.05.024openalex-snapshot
Higher-Order Inter-chromosomal Hubs Shape 3D Genome Organization in the Nucleus
inferredcites →https://doi.org/10.1016/j.celrep.2016.07.016openalex-snapshot
Identification of Nucleolus-Associated Chromatin Domains Reveals a Role for the Nucleolus in 3D Organization of the A. thaliana Genome
inferredcites →https://doi.org/10.1016/j.cub.2005.06.057openalex-snapshot
The PHD Finger/Bromodomain of NoRC Interacts with Acetylated Histone H4K16 and Is Sufficient for rDNA Silencing
inferredcites →https://doi.org/10.1016/j.cub.2015.11.065openalex-snapshot
Nucleation by rRNA Dictates the Precision of Nucleolus Assembly
inferredcites →https://doi.org/10.1016/j.jsb.2007.06.012openalex-snapshot
Positioning of NORs and NOR-bearing chromosomes in relation to nucleoli
inferredcites →https://doi.org/10.1016/j.molcel.2006.03.028openalex-snapshot
Intergenic Transcripts Regulate the Epigenetic State of rRNA Genes
inferredcites →https://doi.org/10.1016/j.molcel.2007.06.021openalex-snapshot
Activation of RNA Polymerase I Transcription by Cockayne Syndrome Group B Protein and Histone Methyltransferase G9a
inferredcites →https://doi.org/10.1016/j.molcel.2009.07.008openalex-snapshot
Loss of Human Ribosomal Gene CpG Methylation Enhances Cryptic RNA Polymerase II Transcription and Disrupts Ribosomal RNA Processing
inferredcites →https://doi.org/10.1016/j.molcel.2010.03.016openalex-snapshot
Molecular Maps of the Reorganization of Genome-Nuclear Lamina Interactions during Differentiation
inferredcites →https://doi.org/10.1016/j.molcel.2010.09.024openalex-snapshot
The Nucleolus under Stress
inferredcites →https://doi.org/10.1016/j.molcel.2012.01.024openalex-snapshot
Inheritance of Silent rDNA Chromatin Is Mediated by PARP1 via Noncoding RNA
inferredcites →https://doi.org/10.1016/j.molcel.2016.09.034openalex-snapshot
High-Resolution Mapping of RNA-Binding Regions in the Nuclear Proteome of Embryonic Stem Cells
inferredcites →https://doi.org/10.1016/j.molmed.2013.07.005openalex-snapshot
The nucleolus: an emerging target for cancer therapy
inferredcites →https://doi.org/10.1016/j.stem.2008.03.021openalex-snapshot
Global Transcription in Pluripotent Embryonic Stem Cells
inferredcites →https://doi.org/10.1016/j.stem.2014.05.017openalex-snapshot
The 3D Genome in Transcriptional Regulation and Pluripotency
inferredcites →https://doi.org/10.1016/j.stem.2014.10.005openalex-snapshot
lncRNA Maturation to Initiate Heterochromatin Formation in the Nucleolus Is Required for Exit from Pluripotency in ESCs
inferredcites →https://doi.org/10.1016/j.tcb.2018.03.007openalex-snapshot
Nucleolar Function in Lifespan Regulation
inferredcites →https://doi.org/10.1016/j.tig.2016.05.004openalex-snapshot
On TADs and LADs: Spatial Control Over Gene Expression
inferredcites →https://doi.org/10.1016/s0022-5320(79)90134-5openalex-snapshot
Ribosomal transcriptional complexes in subnuclear fractions of chinese hamster ovary cells after short-term actinomycin D treatment
inferredcites →https://doi.org/10.1016/s0092-8674(00)80515-2openalex-snapshot
Termination of Mammalian rDNA Replication: Polar Arrest of Replication Fork Movement by Transcription Termination Factor TTF-I
inferredcites →https://doi.org/10.1016/s1097-2765(01)00317-3openalex-snapshot
Molecular Mechanisms Mediating Methylation-Dependent Silencing of Ribosomal Gene Transcription
inferredcites →https://doi.org/10.1016/s1097-2765(04)00064-4openalex-snapshot
A Concerted DNA Methylation/Histone Methylation Switch Regulates rRNA Gene Dosage Control and Nucleolar Dominance
inferredcites →https://doi.org/10.1023/a:1025016828544openalex-snapshot
Three-dimensional arrangements of centromeres and telomeres in nuclei of human and murine lymphocytes
inferredcites →https://doi.org/10.1038/374276a0openalex-snapshot
Replication of transcriptionally active chromatin
inferredcites →https://doi.org/10.1038/emboj.2010.17openalex-snapshot
The NoRC complex mediates the heterochromatin formation and stability of silent rRNA genes and centromeric repeats
inferredcites →https://doi.org/10.1038/embor.2008.109openalex-snapshot
The structure of NoRC‐associated RNA is crucial for targeting the chromatin remodelling complex NoRC to the nucleolus
inferredcites →https://doi.org/10.1038/embor.2009.254openalex-snapshot
Intergenic transcripts originating from a subclass of ribosomal DNA repeats silence ribosomal RNA genes in trans
inferredcites →https://doi.org/10.1038/embor.2013.87openalex-snapshot
The chromatin remodelling complex NoRC safeguards genome stability by heterochromatin formation at telomeres and centromeres
inferredcites →https://doi.org/10.1038/ncb1514openalex-snapshot
H3K9 methylation and RNA interference regulate nucleolar organization and repeated DNA stability
inferredcites →https://doi.org/10.1038/ncb1914openalex-snapshot
Reversible acetylation of the chromatin remodelling complex NoRC is required for non-coding RNA-dependent silencing
inferredcites →https://doi.org/10.1038/ng1010openalex-snapshot
The nucleolar remodeling complex NoRC mediates heterochromatin formation and silencing of ribosomal gene transcription
inferredcites →https://doi.org/10.1038/nrc.2017.104openalex-snapshot
Ribosome biogenesis in cancer: new players and therapeutic avenues
inferredcites →https://doi.org/10.1038/nrm1938openalex-snapshot
Chromatin in pluripotent embryonic stem cells and differentiation
inferredcites →https://doi.org/10.1038/nrm3036openalex-snapshot
Open chromatin in pluripotency and reprogramming
inferredcites →https://doi.org/10.1038/nsmb.2939openalex-snapshot
Noncoding RNAs in eukaryotic ribosome biogenesis and function
inferredcites →https://doi.org/10.1038/s41586-019-1233-0openalex-snapshot
Genome–lamina interactions are established de novo in the early mouse embryo
inferredcites →https://doi.org/10.1038/s41588-018-0139-3openalex-snapshot
MiCEE is a ncRNA-protein complex that mediates epigenetic silencing and nucleolar organization
inferredcites →https://doi.org/10.1038/s42003-019-0284-yopenalex-snapshot
Changes in long-range rDNA-genomic interactions associate with altered RNA polymerase II gene programs during malignant transformation
inferredcites →https://doi.org/10.1038/sj.emboj.7600492openalex-snapshot
The chromatin remodeling complex NoRC controls replication timing of rRNA genes
inferredcites →https://doi.org/10.1038/sj.emboj.7601454openalex-snapshot
NoRC‐dependent nucleosome positioning silences rRNA genes
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.7020273.xopenalex-snapshot
Use of RFLPs larger than 100 kbp to map the position and internal organization of the nucleolus organizer region on chromosome 2 in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0906811106openalex-snapshot
Ribosomal DNA contributes to global chromatin regulation
inferredcites →https://doi.org/10.1073/pnas.1201262109openalex-snapshot
The chromatin remodeling complex NuRD establishes the poised state of rRNA genes characterized by bivalent histone modifications and altered nucleosome positions
inferredcites →https://doi.org/10.1073/pnas.69.11.3394openalex-snapshot
Location of Ribosomal DNA in the Human Chromosome Complement
inferredcites →https://doi.org/10.1073/pnas.76.1.410openalex-snapshot
Yeast ribosomal DNA genes are located on chromosome XII.
inferredcites →https://doi.org/10.1073/pnas.92.13.5827openalex-snapshot
Molecular coevolution of mammalian ribosomal gene terminator sequences and the transcription termination factor TTF-I.
inferredcites →https://doi.org/10.1074/jbc.m310111200openalex-snapshot
Maintenance DNA Methylation of Nucleosome Core Particles
inferredcites →https://doi.org/10.1080/01913120490515595openalex-snapshot
Ultrastructure of Human Embryonic Stem Cells and Spontaneous and Retinoic Acid-Induced Differentiating Cells
inferredcites →https://doi.org/10.1083/jcb.101.5.1749openalex-snapshot
The ribosomal RNA gene cluster in aneuploid chickens: evidence for increased gene dosage and regulation of gene expression.
inferredcites →https://doi.org/10.1083/jcb.133.2.225openalex-snapshot
In vivo evidence that TATA-binding protein/SL1 colocalizes with UBF and RNA polymerase I when rRNA synthesis is either active or inactive.
inferredcites →https://doi.org/10.1083/jcb.133.2.235openalex-snapshot
The rDNA transcription machinery is assembled during mitosis in active NORs and absent in inactive NORs.
inferredcites →https://doi.org/10.1083/jcb.200805146openalex-snapshot
UBF levels determine the number of active ribosomal RNA genes in mammals
inferredcites →https://doi.org/10.1091/mbc.12.11.3563openalex-snapshot
Chromosomal G-dark Bands Determine the Spatial Organization of Centromeric Heterochromatin in the Nucleus
inferredcites →https://doi.org/10.1091/mbc.e10-06-0508openalex-snapshot
High-Resolution Whole-Genome Sequencing Reveals That Specific Chromatin Domains from Most Human Chromosomes Associate with Nucleoli
inferredcites →https://doi.org/10.1093/emboj/16.4.760openalex-snapshot
RNA polymerase I transcription on nucleosomal templates: the transcription termination factor TTF‐I induces chromatin remodeling and relieves transcriptional repression
inferredcites →https://doi.org/10.1093/emboj/20.11.2867openalex-snapshot
Human acrocentric chromosomes with transcriptionally silent nucleolar organizer regions associate with nucleoli
inferredcites →https://doi.org/10.1093/emboj/20.17.4892openalex-snapshot
NoRC—a novel member of mammalian ISWI‐containing chromatin remodeling machines
inferredcites →https://doi.org/10.1093/emboj/cdf460openalex-snapshot
The chromatin remodeling complex NoRC targets HDAC1 to the ribosomal gene promoter and represses RNA polymerase I transcription
inferredcites →https://doi.org/10.1093/genetics/113.4.1009openalex-snapshot
EVALUATING QUANTITATIVE VARIATION IN THE GENOME OF ZEA MAYS
inferredcites →https://doi.org/10.1093/genetics/86.2.389openalex-snapshot
NUCLEOLUS ORGANIZERS IN MUS MUSCULUS SUBSPECIES AND IN THE RAG MOUSE CELL LINE
inferredcites →https://doi.org/10.1093/jmcb/mju038openalex-snapshot
Hot spots of DNA double-strand breaks and genomic contacts of human rDNA units are involved in epigenetic regulation
inferredcites →https://doi.org/10.1093/nar/21.10.2331openalex-snapshot
Chromatin structures and transcription of rDNA in yeastSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1093/nar/25.9.1727openalex-snapshot
Chromatin structure and methylation of rat rRNA genes studied by formaldehyde fixation and psoralen cross-linking
inferredcites →https://doi.org/10.1093/nar/9.14.3219openalex-snapshot
Organization of ribosomal RNA gene repeats of the mouse
inferredcites →https://doi.org/10.1093/nar/gkh732openalex-snapshot
The chromatin remodeling complex NoRC and TTF-I cooperate in the regulation of the mammalian rRNA genes in vivo
inferredcites →https://doi.org/10.1093/nar/gkv1312openalex-snapshot
Nucleolar responses to DNA double-strand breaks
inferredcites →https://doi.org/10.1093/nar/gkv365openalex-snapshot
A novel RNA binding surface of the TAM domain of TIP5/BAZ2A mediates epigenetic regulation of rRNA genes
inferredcites →https://doi.org/10.1101/gad.12.24.3821openalex-snapshot
Expansion and contraction of ribosomal DNA repeats in Saccharomyces cerevisiae: requirement of replication fork blocking (Fob1) protein and the role of RNA polymerase I
inferredcites →https://doi.org/10.1101/gad.13.19.2570openalex-snapshot
The SIR2/3/4 complex and SIR2 alone promote longevity in Saccharomyces cerevisiae by two different mechanisms
inferredcites →https://doi.org/10.1101/gad.1417706openalex-snapshot
Erasure of histone acetylation by Arabidopsis HDA6 mediates large-scale gene silencing in nucleolar dominance
inferredcites →https://doi.org/10.1101/gad.182865.111openalex-snapshot
Histone methyltransferases regulating rRNA gene dose and dosage control in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.1914110openalex-snapshot
Mechanisms of HDA6-mediated rRNA gene silencing: suppression of intergenic Pol II transcription and differential effects on maintenance versus siRNA-directed cytosine methylation
inferredcites →https://doi.org/10.1101/gad.221648.113openalex-snapshot
Subnuclear partitioning of rRNA genes between the nucleolus and nucleoplasm reflects alternative epiallelic states
inferredcites →https://doi.org/10.1101/gad.273755.115openalex-snapshot
Chromosome-specific NOR inactivation explains selective rRNA gene silencing and dosage control in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.283838.116openalex-snapshot
Nucleolar organizer regions: genomic ‘dark matter’ requiring illumination
inferredcites →https://doi.org/10.1101/gad.590910openalex-snapshot
Interaction of noncoding RNA with the rDNA promoter mediates recruitment of DNMT3b and silencing of rRNA genes
inferredcites →https://doi.org/10.1101/gr.130237.111openalex-snapshot
Triplexator: Detecting nucleic acid triple helices in genomic and transcriptomic data
inferredcites →https://doi.org/10.1101/gr.157941.113openalex-snapshot
The shared genomic architecture of human nucleolar organizer regions
inferredcites →https://doi.org/10.1111/1567-1364.12133openalex-snapshot
Ribosomal DNA and cellular senescence: new evidence supporting the connection between rDNA and aging
inferredcites →https://doi.org/10.1111/febs.14108openalex-snapshot
Integrating the genomic architecture of human nucleolar organizer regions with the biophysical properties of nucleoli
inferredcites →https://doi.org/10.1111/j.1365-2559.2008.03168.xopenalex-snapshot
What the nucleolus says to a tumour pathologist
inferredcites →https://doi.org/10.1111/j.1432-0436.2007.00192.xopenalex-snapshot
Differentiation of human embryonic stem cells induces condensation of chromosome territories and formation of heterochromatin protein 1 foci
inferredcites →https://doi.org/10.1111/j.1742-4658.2010.07892.xopenalex-snapshot
Wisely chosen paths – regulation of rRNA synthesis
inferredcites →https://doi.org/10.1126/science.1179044openalex-snapshot
Abundance of Ribosomal RNA Gene Copies Maintains Genome Integrity
inferredcites →https://doi.org/10.1126/science.1181369openalex-snapshot
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
inferredcites →https://doi.org/10.1126/science.1246384openalex-snapshot
Changes in rRNA Transcription Influence Proliferation and Cell Fate Within a Stem Cell Lineage
inferredcites →https://doi.org/10.1126/science.aaf7040openalex-snapshot
Early-life nutrition modulates the epigenetic state of specific rDNA genetic variants in mice
inferredcites →https://doi.org/10.1128/mcb.15.10.5294openalex-snapshot
Transcription in the Yeast rRNA Gene Locus: Distribution of the Active Gene Copies and Chromatin Structure of Their Flanking Regulatory Sequences
inferredcites →https://doi.org/10.1128/mcb.23.5.1558-1568.2003openalex-snapshot
In Exponentially Growing Saccharomyces cerevisiae Cells, rRNA Synthesis Is Determined by the Summed RNA Polymerase I Loading Rate Rather than by the Number of Active Genes
inferredcites →https://doi.org/10.1128/mcb.25.7.2539-2546.2005openalex-snapshot
Epigenetic Mechanism of rRNA Gene Silencing: Temporal Order of NoRC-Mediated Histone Modification, Chromatin Remodeling, and DNA Methylation
inferredcites →https://doi.org/10.1146/annurev-biochem-062917-012612openalex-snapshot
Regulation of RNA Polymerase I Transcription in Development, Disease, and Aging
inferredcites →https://doi.org/10.1177/002215540004800102openalex-snapshot
Nonrandom Distribution of Metaphase AgNOR Staining Patterns on Human Acrocentric Chromosomes
inferredcites →https://doi.org/10.1200/jco.2016.70.7836openalex-snapshot
Genetic Basis of Acute Lymphoblastic Leukemia
inferredcites →https://doi.org/10.1242/jcs.01249openalex-snapshot
Nucleolar localization of the human telomeric repeat binding factor 2 (TRF2)
inferredcites →https://doi.org/10.1242/jcs.02500openalex-snapshot
Distinctive nuclear organisation of centromeres and regions involved in pluripotency in human embryonic stem cells
inferredcites →https://doi.org/10.1242/jcs.104.2.327openalex-snapshot
Localization of the RNA polymerase I transcription factor hUBF during the cell cycle
inferredcites →https://doi.org/10.1242/jcs.112.19.3259openalex-snapshot
The mitotically phosphorylated form of the transcription termination factor TTF-1 is associated with the repressed rDNA transcription machinery
inferredcites →https://doi.org/10.1242/jcs.40.1.181openalex-snapshot
Non-nucleolar transcription complexes of rat liver as revealed by spreading isolated nuclei
inferredcites →https://doi.org/10.1371/journal.pgen.1000889openalex-snapshot
Initial Genomics of the Human Nucleolus
inferredcites →https://doi.org/10.1371/journal.pgen.1001225openalex-snapshot
Nucleolin Is Required for DNA Methylation State and the Expression of rRNA Gene Variants in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pgen.1001376openalex-snapshot
Ribosomal DNA Deletions Modulate Genome-Wide Gene Expression: “rDNA–Sensitive” Genes and Natural Variation
inferredcites →https://doi.org/10.1371/journal.pgen.1004505openalex-snapshot
Conditional Inactivation of Upstream Binding Factor Reveals Its Epigenetic Functions and the Existence of a Somatic Nucleolar Precursor Body
inferredcites →https://doi.org/10.1371/journal.pgen.1005696openalex-snapshot
New Perspectives on DNA and RNA Triplexes As Effectors of Biological Activity
inferredcites →https://doi.org/10.1371/journal.pgen.1006899openalex-snapshot
A unique enhancer boundary complex on the mouse ribosomal RNA genes persists after loss of Rrn3 or UBF and the inactivation of RNA polymerase I transcription
inferredcites →https://doi.org/10.1371/journal.pgen.1007258openalex-snapshot
The long-range interaction map of ribosomal DNA arrays
inferredcites →https://doi.org/10.1371/journal.pone.0001843openalex-snapshot
Mouse Ribosomal RNA Genes Contain Multiple Differentially Regulated Variants
inferredcites →https://doi.org/10.1371/journal.pone.0157276openalex-snapshot
The Regulation of rRNA Gene Transcription during Directed Differentiation of Human Embryonic Stem Cells
inferredcites →https://doi.org/10.1371/journal.pone.0178821openalex-snapshot
Nucleolus association of chromosomal domains is largely maintained in cellular senescence despite massive nuclear reorganisation
inferredcites →https://doi.org/10.15252/embr.201744330openalex-snapshot
The RNA helicase DHX9 establishes nucleolar heterochromatin, and this activity is required for embryonic stem cell differentiation
inferredcites →https://doi.org/10.1534/g3.113.009290openalex-snapshot
Genomic Characterization of the Mouse Ribosomal DNA Locus
inferredcites →https://doi.org/10.3390/ijms18071411openalex-snapshot
The Nucleolus: In Genome Maintenance and Repair
inferredcites →https://doi.org/10.4161/19491034.2014.990863openalex-snapshot
Functional redundancy in the nuclear compartmentalization of the late-replicating genome
inferredcites →https://doi.org/10.4161/epi.21072openalex-snapshot
Formation of nuclear heterochromatin
inferredcites →https://doi.org/10.4161/rna.8.3.14999openalex-snapshot
Potential in vivo roles of nucleic acid triple-helices
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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An Optimized Adaptation of DamID for NGS Applications
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Senescence and the Genome
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Introduction to Epigenetics
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Epigenetic Alterations in Colorectal Cancer
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Role of Nuclear Lamins in the Regulation of the Genome: Focus on CardioLaminopathy
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Regulatory roles of nucleolus organizer region-derived long non-coding RNAs
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Nucleolus-associated chromatin domains are maintained under heat stress, despite nucleolar reorganization in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10750-026-06373-yopenalex-snapshot
Comparative nucleolar ultrastructure analysis and life-history traits in three zooplankton species
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Nucleus | Nuclear Compartmentalization
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Epigenetic change-based cancer development in the gastrointestinal gastric, pancreatic, and colorectal cancers
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Epigenetic alterations in the gastrointestinal tract: Current and emerging use for biomarkers of cancer
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PARP1 at the crossroad of cellular senescence and nucleolar processes
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.120969openalex-snapshot
Insensitivity of dental pulp stem cells migration to substrate stiffness
inferred← citeshttps://doi.org/10.1016/j.ceb.2022.01.004openalex-snapshot
Lamina-associated domains: Tethers and looseners
inferred← citeshttps://doi.org/10.1016/j.ceb.2023.102171openalex-snapshot
Methods for mapping 3D-chromosome architecture around nucleoli
inferred← citeshttps://doi.org/10.1016/j.cell.2020.11.024openalex-snapshot
High-Throughput Discovery and Characterization of Human Transcriptional Effectors
inferred← citeshttps://doi.org/10.1016/j.cis.2022.102777openalex-snapshot
Biological colloids: Unique properties of membraneless organelles in the cell
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2025.137987openalex-snapshot
Sulphur-doped carbon quantum dots with nucleolus targeting image and drug loading for photodynamic therapy of cancer cells
inferred← citeshttps://doi.org/10.1016/j.fsi.2025.110642openalex-snapshot
Extracellular proteins from Perkinsus olseni: LC-MS/MS-based proteomic profiling and functional insights into host–parasite interactions
inferred← citeshttps://doi.org/10.1016/j.gde.2021.02.003openalex-snapshot
The shifting shape of genomes: dynamics of heterochromatin interactions at the nuclear lamina
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.05.011openalex-snapshot
Non-coding RNAs at the Eukaryotic rDNA Locus: RNA–DNA Hybrids and Beyond
inferred← citeshttps://doi.org/10.1016/j.molcel.2025.05.004openalex-snapshot
The nucleolar granular component mediates genome-nucleolus interactions and establishes their repressive chromatin states
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.11.005openalex-snapshot
Chromatin domains in space and their functional implications
inferred← citeshttps://doi.org/10.1016/j.pbi.2022.102199openalex-snapshot
Organization and epigenomic control of RNA polymerase III-transcribed genes in plants
inferred← citeshttps://doi.org/10.1016/j.saa.2020.118381openalex-snapshot
RNA-responsive fluorescent carbon dots for fast and wash-free nucleolus imaging
inferred← citeshttps://doi.org/10.1016/j.sbi.2019.10.010openalex-snapshot
Chromatin structure changes during various processes from a DNA sequence view
inferred← citeshttps://doi.org/10.1016/j.schres.2020.07.022openalex-snapshot
Copy number variations of satellite III (1q12) and ribosomal repeats in health and schizophrenia
inferred← citeshttps://doi.org/10.1016/j.stemcr.2020.08.012openalex-snapshot
Regulation and Roles of the Nucleolus in Embryonic Stem Cells: From Ribosome Biogenesis to Genome Organization
inferred← citeshttps://doi.org/10.1016/j.tcb.2023.10.012openalex-snapshot
Emerging roles of nuclear bodies in genome spatial organization
inferred← citeshttps://doi.org/10.1016/j.tig.2019.06.005openalex-snapshot
Nucleolus and rRNA Gene Chromatin in Early Embryo Development
inferred← citeshttps://doi.org/10.1038/s41422-020-00458-6openalex-snapshot
Mutual dependency between lncRNA LETN and protein NPM1 in controlling the nucleolar structure and functions sustaining cell proliferation
inferred← citeshttps://doi.org/10.1038/s41467-022-29146-2openalex-snapshot
Genome-wide maps of nucleolus interactions reveal distinct layers of repressive chromatin domains
inferred← citeshttps://doi.org/10.1038/s41467-023-36021-1openalex-snapshot
Mapping nucleolus-associated chromatin interactions using nucleolus Hi-C reveals pattern of heterochromatin interactions
inferred← citeshttps://doi.org/10.1038/s41467-025-66294-7openalex-snapshot
Single-cell dynamics of genome-nucleolus interactions captured by nucleolar laser microdissection (NoLMseq)
inferred← citeshttps://doi.org/10.1038/s41467-026-71213-5openalex-snapshot
Architecture and regulation of nanoscale chromatin domains
inferred← citeshttps://doi.org/10.1038/s41556-024-01512-wopenalex-snapshot
Fasting shapes chromatin architecture through an mTOR/RNA Pol I axis
inferred← citeshttps://doi.org/10.1038/s41556-025-01806-7openalex-snapshot
Hierarchical interactions between nucleolar and heterochromatin condensates are mediated by a dual-affinity protein
inferred← citeshttps://doi.org/10.1038/s41556-025-01822-7openalex-snapshot
LBR and LAP2 mediate heterochromatin tethering to the nuclear periphery to preserve genome homeostasis
inferred← citeshttps://doi.org/10.1038/s41598-020-76174-3openalex-snapshot
SMN protein promotes membrane compartmentalization of ribosomal protein S6 transcript in human fibroblasts
inferred← citeshttps://doi.org/10.1042/bst20190854openalex-snapshot
MicroRNAs and long non-coding RNAs as novel regulators of ribosome biogenesis
inferred← citeshttps://doi.org/10.1042/bst20253011openalex-snapshot
Anticancer drug development against ribosome synthesis and the nucleolus
inferred← citeshttps://doi.org/10.1053/j.gastro.2020.09.058openalex-snapshot
Epigenetic Alterations in the Gastrointestinal Tract: Current and Emerging Use for Biomarkers of Cancer
inferred← citeshttps://doi.org/10.1073/pnas.2221109120openalex-snapshot
A nucleolar long “non-coding” RNA encodes a novel protein that functions in response to stress
inferred← citeshttps://doi.org/10.1091/mbc.e20-10-0670openalex-snapshot
Increased numbers of nucleoli in a genome-wide RNAi screen reveal proteins that link the cell cycle to RNA polymerase I transcription
inferred← citeshttps://doi.org/10.1091/mbc.e22-06-0237openalex-snapshot
Nucleoli and the nucleoli–centromere association are dynamic during normal development and in cancer
inferred← citeshttps://doi.org/10.1093/brain/awad086openalex-snapshot
A homozygous POLR1A variant causes leukodystrophy and affects protein homeostasis
inferred← citeshttps://doi.org/10.1093/nar/gkaa457openalex-snapshot
Studying RNA–DNA interactome by Red-C identifies noncoding RNAs associated with various chromatin types and reveals transcription dynamics
inferred← citeshttps://doi.org/10.1093/nar/gkab662openalex-snapshot
Antisense ribosomal siRNAs inhibit RNA polymerase I-directed transcription inC. elegans
inferred← citeshttps://doi.org/10.1093/nar/gkad1235openalex-snapshot
Discovery of novel microRNA mimic repressors of ribosome biogenesis
inferred← citeshttps://doi.org/10.1093/nar/gkag615openalex-snapshot
Antibody-trapping presents a widespread pitfall for microscopy and genomics in the nucleus
inferred← citeshttps://doi.org/10.1093/nargab/lqaf012openalex-snapshot
Ribosomal DNA arrays are the most H-DNA rich element in the human genome
inferred← citeshttps://doi.org/10.1093/plcell/koab020openalex-snapshot
Gene dosage compensation of rRNA transcript levels inArabidopsis thalianalines with reduced ribosomal gene copy number
inferred← citeshttps://doi.org/10.1101/2020.01.24.917823openalex-snapshot
Low ribosomal RNA genes copy number provoke genomic instability and chromosomal segment duplication events that modify global gene expression and plant-pathogen response
inferred← citeshttps://doi.org/10.1101/2020.11.23.395020openalex-snapshot
Co-surveillance of ribosomal RNA by the exosome complex and nucleolar RNAi in C. elegans
inferred← citeshttps://doi.org/10.1101/2021.09.06.458940openalex-snapshot
Promyelocytic leukemia nuclear body (PML-NB) -free intranuclear milieu facilitates development of oocytes in mice
inferred← citeshttps://doi.org/10.1101/2022.11.14.516489openalex-snapshot
rRNA transcription is integral to liquid-liquid phase separation and maintenance of nucleolar structure
inferred← citeshttps://doi.org/10.1101/2024.07.03.601885openalex-snapshot
NPM1 mediates genome-nucleolus interactions and the establishment of their repressive chromatin states
inferred← citeshttps://doi.org/10.1101/2024.10.01.615958openalex-snapshot
mRNA expression is co-regulated by non-nucleolar RNA polymerase I
inferred← citeshttps://doi.org/10.1101/gad.351979.124openalex-snapshot
LINE1 elements at distal junctions of rDNA repeats regulate nucleolar organization in human embryonic stem cells
inferred← citeshttps://doi.org/10.1101/gr.261586.120openalex-snapshot
Large tandem duplications affect gene expression, 3D organization, and plant–pathogen response
inferred← citeshttps://doi.org/10.1111/gtc.12807openalex-snapshot
The SUN1 splicing variants SUN1_888 and SUN1_916 differentially regulate nucleolar structure
inferred← citeshttps://doi.org/10.1134/s0006297920060012openalex-snapshot
The Role of Liquid–Liquid Phase Separation in the Compartmentalization of Cell Nucleus and Spatial Genome Organization
inferred← citeshttps://doi.org/10.1186/s12860-022-00411-yopenalex-snapshot
Nucleolar localization of the ErbB3 receptor as a new target in glioblastoma
inferred← citeshttps://doi.org/10.1186/s13059-020-02003-5openalex-snapshot
Lamina-associated domains: peripheral matters and internal affairs
inferred← citeshttps://doi.org/10.1186/s40246-025-00830-wopenalex-snapshot
Deletions in (CCCT)n repeat regions belonging to the human pRNA gene inhibit its expression
inferred← citeshttps://doi.org/10.1242/dev.204696openalex-snapshot
Emerging roles for the nucleolus in development and stem cells
inferred← citeshttps://doi.org/10.1364/boe.462493openalex-snapshot
Combined optical fluorescence microscopy and X-ray tomography reveals substructures in cell nuclei in 3D
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010854openalex-snapshot
rRNA transcription is integral to phase separation and maintenance of nucleolar structure
inferred← citeshttps://doi.org/10.1371/journal.pone.0223030openalex-snapshot
Discontinuous transcription of ribosomal DNA in human cells
inferred← citeshttps://doi.org/10.1371/journal.pone.0323554openalex-snapshot
Nucleolar sequestration of cannabinoid type-2 receptors in triple-negative breast cancer cells
inferred← citeshttps://doi.org/10.1371/journal.ppat.1014682openalex-snapshot
Active transcriptome remodeling underlies antimony-induced drug tolerance in persister-like Leishmania parasites
inferred← citeshttps://doi.org/10.1515/hsz-2023-0214openalex-snapshot
Synthesis of the ribosomal RNA precursor in human cells: mechanisms, factors and regulation
inferred← citeshttps://doi.org/10.1530/rep-22-0124openalex-snapshot
Omne vivum ex ovo : the oocyte reprogramming and remodeling activities
inferred← citeshttps://doi.org/10.15407/agrisp11.01.070openalex-snapshot
Investigation of some nucleoli traits in interphase leukocytes of two rabbit breeds and their hybrid
inferred← citeshttps://doi.org/10.18093/0869-0189-2023-33-1-7-16openalex-snapshot
Study of human ribosomal gene complex in cystic fibrosis
inferred← citeshttps://doi.org/10.18699/vjgb-25-43openalex-snapshot
The effects of Non3 mutations on chromatin organization in Drosophila melanogaster
inferred← citeshttps://doi.org/10.24075/brsmu.2023.048openalex-snapshot
Genetically encoded light-inducible sensor for nucleolar visualization
inferred← citeshttps://doi.org/10.25557/2073-7998.2021.02.49-60openalex-snapshot
Variation in the number of copies of ribosomal genes in the genomes of patients with cystic fibrosis
inferred← citeshttps://doi.org/10.3103/s009545272003007xopenalex-snapshot
Epigenetic Changes of Activity of the Ribosomal Cistrons of Human Acrocentric Chromatids in Fetuses, Middle-aged (22–45 years) and Old Individuals (80–106 years)
inferred← citeshttps://doi.org/10.3389/fcell.2020.00394openalex-snapshot
The Emerging Roles of Heterochromatin in Cell Migration
inferred← citeshttps://doi.org/10.3389/fcell.2021.774719openalex-snapshot
Understanding 3D Genome Organization and Its Effect on Transcriptional Gene Regulation Under Environmental Stress in Plant: A Chromatin Perspective
inferred← citeshttps://doi.org/10.3389/fcvm.2022.1045455openalex-snapshot
Nucleolar stress: Friend or foe in cardiac function?
inferred← citeshttps://doi.org/10.3389/fgene.2021.645863openalex-snapshot
RNA Biogenesis Instructs Functional Inter-Chromosomal Genome Architecture
inferred← citeshttps://doi.org/10.3389/fgene.2021.730633openalex-snapshot
The Role of rDNA Clusters in Global Epigenetic Gene Regulation
inferred← citeshttps://doi.org/10.3389/fpls.2021.797348openalex-snapshot
Personal Perspectives on Plant Ribosomal RNA Genes Research: From Precursor-rRNA to Molecular Evolution
inferred← citeshttps://doi.org/10.3389/fpls.2022.788911openalex-snapshot
The Nuclear 35S rDNA World in Plant Systematics and Evolution: A Primer of Cautions and Common Misconceptions in Cytogenetic Studies
inferred← citeshttps://doi.org/10.3389/fpls.2024.1445097openalex-snapshot
The overlooked manipulation of nucleolar functions by plant pathogen effectors
inferred← citeshttps://doi.org/10.3390/ani15020140openalex-snapshot
The Observation of Meiotic Union Behavior of Gametophytes Provides a New Basis for Ploidy of Carassius auratus gibelio
inferred← citeshttps://doi.org/10.3390/biom14101333openalex-snapshot
Stress-Induced Evolution of the Nucleolus: The Role of Ribosomal Intergenic Spacer (rIGS) Transcripts
inferred← citeshttps://doi.org/10.3390/books978-3-0365-3162-5openalex-snapshot
Molecular Mechanisms of Leaf Morphogenesis
inferred← citeshttps://doi.org/10.3390/cancers12071813openalex-snapshot
The Nucleolus and PARP1 in Cancer Biology
inferred← citeshttps://doi.org/10.3390/cancers12103009openalex-snapshot
Dichotomous Impact of Myc on rRNA Gene Activation and Silencing in B Cell Lymphomagenesis
inferred← citeshttps://doi.org/10.3390/cells11030574openalex-snapshot
Regulation of Nucleolar Activity by MYC
inferred← citeshttps://doi.org/10.3390/cells11111846openalex-snapshot
Restructuring of Lamina-Associated Domains in Senescence and Cancer
inferred← citeshttps://doi.org/10.3390/cells9030526openalex-snapshot
Nucleolar Organization and Functions in Health and Disease
inferred← citeshttps://doi.org/10.3390/cells9102300openalex-snapshot
How Altered Ribosome Production Can Cause or Contribute to Human Disease: The Spectrum of Ribosomopathies
inferred← citeshttps://doi.org/10.3390/cells9122587openalex-snapshot
Dynamics of Whole-Genome Contacts of Nucleoli in Drosophila Cells Suggests a Role for rDNA Genes in Global Epigenetic Regulation
inferred← citeshttps://doi.org/10.3390/f14071464openalex-snapshot
Differences in the Growth of Seedlings and the Selection of Fast-Growing Species in the Gleditsia Genus
inferred← citeshttps://doi.org/10.3390/genes12070961openalex-snapshot
Antagonising Chromatin Remodelling Activities in the Regulation of Mammalian Ribosomal Transcription
inferred← citeshttps://doi.org/10.3390/genes13020343openalex-snapshot
The Psychoemotional Stress-Induced Changes in the Abundance of SatIII (1q12) and Telomere Repeats, but Not Ribosomal DNA, in Human Leukocytes
inferred← citeshttps://doi.org/10.3390/ijms21103431openalex-snapshot
Instability of Short Arm of Acrocentric Chromosomes: Lesson from Non-Acrocentric Satellited Chromosomes. Report of 24 Unrelated Cases
inferred← citeshttps://doi.org/10.3390/ijms21197314openalex-snapshot
Roles of ASYMMETRIC LEAVES2 (AS2) and Nucleolar Proteins in the Adaxial–Abaxial Polarity Specification at the Perinucleolar Region in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms21249738openalex-snapshot
Non-Coding RNA-Driven Regulation of rRNA Biogenesis
inferred← citeshttps://doi.org/10.3390/ijms222111403openalex-snapshot
Analyses of the Updated “Animal rDNA Loci Database” with an Emphasis on Its New Features
inferred← citeshttps://doi.org/10.3390/ijms222313095openalex-snapshot
Phase Separation of Intrinsically Disordered Nucleolar Proteins Relate to Localization and Function
inferred← citeshttps://doi.org/10.3390/ijms25021230openalex-snapshot
New Functional Motifs for the Targeted Localization of Proteins to the Nucleolus in Drosophila and Human Cells
inferred← citeshttps://doi.org/10.3390/life11040342openalex-snapshot
The “Genomic Code”: DNA Pervasively Moulds Chromatin Structures Leaving no Room for “Junk”
inferred← citeshttps://doi.org/10.3390/ncrna7030050openalex-snapshot
Zooming in: PAGE-Northern Blot Helps to Analyze Anti-Sense Transcripts Originating from Human rIGS under Transcriptional Stress
inferred← citeshttps://doi.org/10.3844/ojbsci.2022.18.25openalex-snapshot
Analysis of Nucleoli in Intact Lymphocytes in Different Mammalian Species and Hybrids
inferred← citeshttps://doi.org/10.5483/bmbrep.2021.54.10.098openalex-snapshot
Visualization of chromatin higher-order structures and dynamics in live cells
inferred← citeshttps://doi.org/10.6084/m9.figshare.19321019openalex-snapshot
Additional file 1 of Nucleolar localization of the ErbB3 receptor as a new target in glioblastoma
inferred← citeshttps://doi.org/10.6084/m9.figshare.19321022openalex-snapshot
Additional file 2 of Nucleolar localization of the ErbB3 receptor as a new target in glioblastoma
inferred← citeshttps://doi.org/10.6084/m9.figshare.19321025openalex-snapshot
Additional file 3 of Nucleolar localization of the ErbB3 receptor as a new target in glioblastoma
inferred← citeshttps://doi.org/10.6084/m9.figshare.19321028openalex-snapshot
Additional file 4 of Nucleolar localization of the ErbB3 receptor as a new target in glioblastoma
inferred← citeshttps://doi.org/10.6084/m9.figshare.19321031openalex-snapshot
Additional file 5 of Nucleolar localization of the ErbB3 receptor as a new target in glioblastoma
inferred← citeshttps://doi.org/10.6084/m9.figshare.19321034openalex-snapshot
Additional file 6 of Nucleolar localization of the ErbB3 receptor as a new target in glioblastoma
inferred← citeshttps://doi.org/10.6084/m9.figshare.19321037openalex-snapshot
Additional file 7 of Nucleolar localization of the ErbB3 receptor as a new target in glioblastoma
inferred← citeshttps://doi.org/10.6084/m9.figshare.19321040openalex-snapshot
Additional file 8 of Nucleolar localization of the ErbB3 receptor as a new target in glioblastoma
inferred← citeshttps://doi.org/10.64898/2026.02.13.705825openalex-snapshot
Cell Ploidy Modulates Nucleolar Size via Dosage of Nucleolar Organizing Regions
inferred← citeshttps://doi.org/10.64898/2026.04.13.718322openalex-snapshot
The dynamics of nucleolus-centromeres interaction in living cells
inferred← citeshttps://doi.org/10.64898/2026.05.29.726936openalex-snapshot
Active Transcriptome Remodeling and Epigenetic Adaptations Underlie Persistence in Leishmania parasites
inferred← citeshttps://doi.org/10.64898/2026.06.23.733628openalex-snapshot
Chromatin topology control by a muscle-specific ribosomal protein
inferred← citeshttps://doi.org/10.70675/217850a9z3e46z4daazadc6zb1bce2ccfe54openalex-snapshot
Analyse de données et modèle pour l'étude de la chromatine, des G-quadruplexes et de la réparation de l'ADN
inferred← citeshttps://doi.org/10.70675/37a54d4bzd7f4z45d9zadf8z7f69bffedebaopenalex-snapshot
Organisation du génome par le complexe cohésine chez la levure Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.70675/89769afeza443z495cz9933z31ab8621510eopenalex-snapshot
Effet de position télomérique : implications dans la régulation du génome et les maladies rares
inferred← citeshttps://doi.org/10.70675/b29d142fzed1az4785zbb11z225e807d15e5openalex-snapshot
Analyse d'interactions Hox/Cofacteur à l'échelle super-résolutive et contrôle transcriptionnel de l'autophagie chez la drosophile
inferred← citeshttps://doi.org/10.70675/c349f8ecz721ez40f7z8ff6zd0754e9a03ebopenalex-snapshot
Entre silence, naissance et dégradation : vers la caractérisation de nouveaux mécanismes relatifs à la biologie des ARN de transfert et assurant l'homéostasie de la cellule végétale.
inferred← citeshttps://doi.org/10.70675/cbab8417z11f2z4456zb805z9876e7d9b073openalex-snapshot
Régulation de la chromatine par SMCHD1 : implication dans la dystrophie facio-scapulo-humérale et le syndrome d'arhinie et de microphtalmie de Bosma
inferred← citeshttps://doi.org/10.7554/elife.104295openalex-snapshot
Meioc-Piwil1 complexes regulate rRNA transcription for differentiation of spermatogonial stem cells
inferred← citeshttps://doi.org/10.7554/elife.104295.1openalex-snapshot
Meioc-Piwil1 complexes regulate rRNA transcription for differentiation of spermatogonial stem cells
inferred← citeshttps://doi.org/10.7554/elife.104295.2openalex-snapshot
Meioc-Piwil1 complexes regulate rRNA transcription for differentiation of spermatogonial stem cells
inferred← citeshttps://doi.org/10.7554/elife.104295.3openalex-snapshot
Meioc-Piwil1 complexes regulate rRNA transcription for differentiation of spermatogonial stem cells
inferred← citeshttps://doi.org/10.7554/elife.76421openalex-snapshot
Probe-free optical chromatin deformation and measurement of differential mechanical properties in the nucleus
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