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Biogenesis and function of nuclear bodies
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/excr.1993.1218openalex-snapshot
Intranuclear Distribution of Poly(A) RNA Determined by Electron Microscope in Situ Hybridization
inferredcites →https://doi.org/10.1006/jsbi.2000.4247openalex-snapshot
Review: Perinucleolar Structures
inferredcites →https://doi.org/10.1007/s00418-007-0359-6openalex-snapshot
Nucleolus: the fascinating nuclear body
inferredcites →https://doi.org/10.1007/s00424-007-0286-3openalex-snapshot
Regulation of the actin cytoskeleton by phosphatidylinositol 4-phosphate 5 kinases
inferredcites →https://doi.org/10.1007/s10577-008-1218-6openalex-snapshot
The nuclear organization of Polycomb/Trithorax group response elements in larval tissues of Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.ceb.2006.04.007openalex-snapshot
Chromosome territories – a functional nuclear landscape
inferredcites →https://doi.org/10.1016/j.ceb.2010.03.009openalex-snapshot
Nucleolar dominance and ribosomal RNA gene silencing
inferredcites →https://doi.org/10.1016/j.cell.2005.08.033openalex-snapshot
Regulating Gene Expression through RNA Nuclear Retention
inferredcites →https://doi.org/10.1016/j.cell.2006.01.036openalex-snapshot
RNAi Components Are Required for Nuclear Clustering of Polycomb Group Response Elements
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.2008.03.004openalex-snapshot
Chromatin Dynamics and Gene Positioning
inferredcites →https://doi.org/10.1016/j.cell.2009.02.006openalex-snapshot
Evolution and Functions of Long Noncoding RNAs
inferredcites →https://doi.org/10.1016/j.cell.2009.08.020openalex-snapshot
A Vertebrate Polycomb Response Element Governs Segmentation of the Posterior Hindbrain
inferredcites →https://doi.org/10.1016/j.cell.2009.11.030openalex-snapshot
Nuclear Receptor-Induced Chromosomal Proximity and DNA Breaks Underlie Specific Translocations in Cancer
inferredcites →https://doi.org/10.1016/j.cell.2009.12.022openalex-snapshot
A Region of the Human HOXD Cluster that Confers Polycomb-Group Responsiveness
inferredcites →https://doi.org/10.1016/j.cell.2010.02.007openalex-snapshot
Lin28: A MicroRNA Regulator with a Macro Role
inferredcites →https://doi.org/10.1016/j.cell.2010.12.026openalex-snapshot
Polycomb-Dependent Regulatory Contacts between Distant Hox Loci in Drosophila
inferredcites →https://doi.org/10.1016/j.cell.2011.03.014openalex-snapshot
No-Nonsense Functions for Long Noncoding RNAs
inferredcites →https://doi.org/10.1016/j.cell.2011.03.032openalex-snapshot
Live-Cell Chromosome Dynamics and Outcome of X Chromosome Pairing Events during ES Cell Differentiation
inferredcites →https://doi.org/10.1016/j.devcel.2009.10.017openalex-snapshot
Nuclear Bodies: Random Aggregates of Sticky Proteins or Crucibles of Macromolecular Assembly?
inferredcites →https://doi.org/10.1016/j.febslet.2010.10.008openalex-snapshot
MALAT‐1 enhances cell motility of lung adenocarcinoma cells by influencing the expression of motility‐related genes
inferredcites →https://doi.org/10.1016/j.febslet.2011.01.030openalex-snapshot
Control of RNA processing by a large non-coding RNA over-expressed in carcinomas
inferredcites →https://doi.org/10.1016/j.gde.2006.02.001openalex-snapshot
Actin and myosin as transcription factors
inferredcites →https://doi.org/10.1016/j.gde.2006.08.005openalex-snapshot
Polycomb response elements and targeting of Polycomb group proteins in Drosophila
inferredcites →https://doi.org/10.1016/j.gde.2009.02.007openalex-snapshot
Nuclear neighborhoods and gene expression
inferredcites →https://doi.org/10.1016/j.gde.2009.07.005openalex-snapshot
Nuclear organization in the 3D space of the nucleus — cause or consequence?
inferredcites →https://doi.org/10.1016/j.jmb.2009.10.031openalex-snapshot
A Model for all Genomes: The Role of Transcription Factories
inferredcites →https://doi.org/10.1016/j.molcel.2004.06.001openalex-snapshot
The C. elegans Polycomb Gene sop-2 Encodes an RNA Binding Protein
inferredcites →https://doi.org/10.1016/j.molcel.2007.07.017openalex-snapshot
Structural and Functional Characterization of Human Telomerase RNA Processing and Cajal Body Localization Signals
inferredcites →https://doi.org/10.1016/j.molcel.2008.08.022openalex-snapshot
Kcnq1ot1 Antisense Noncoding RNA Mediates Lineage-Specific Transcriptional Silencing through Chromatin-Level Regulation
inferredcites →https://doi.org/10.1016/j.molcel.2009.01.026openalex-snapshot
An Architectural Role for a Nuclear Noncoding RNA: NEAT1 RNA Is Essential for the Structure of Paraspeckles
inferredcites →https://doi.org/10.1016/j.molcel.2009.06.027openalex-snapshot
Altered Nuclear Retention of mRNAs Containing Inverted Repeats in Human Embryonic Stem Cells: Functional Role of a Nuclear Noncoding RNA
inferredcites →https://doi.org/10.1016/j.molcel.2010.08.011openalex-snapshot
The Nuclear-Retained Noncoding RNA MALAT1 Regulates Alternative Splicing by Modulating SR Splicing Factor Phosphorylation
inferredcites →https://doi.org/10.1016/j.molcel.2010.09.024openalex-snapshot
The Nucleolus under Stress
inferredcites →https://doi.org/10.1016/j.molcel.2011.02.022openalex-snapshot
Structural and Functional Roles of Daxx SIM Phosphorylation in SUMO Paralog-Selective Binding and Apoptosis Modulation
inferredcites →https://doi.org/10.1016/j.tcb.2005.11.005openalex-snapshot
Subnuclear organelles: new insights into form and function
inferredcites →https://doi.org/10.1016/j.tcb.2009.10.001openalex-snapshot
Polycomb group complexes – many combinations, many functions
inferredcites →https://doi.org/10.1016/s0092-8674(03)00159-4openalex-snapshot
The Polycomb Protein Pc2 Is a SUMO E3
inferredcites →https://doi.org/10.1016/s0168-9525(00)02113-2openalex-snapshot
The epigenetics of nucleolar dominance
inferredcites →https://doi.org/10.1016/s0955-0674(03)00049-8openalex-snapshot
The nucleolus: a site of ribonucleoprotein maturation
inferredcites →https://doi.org/10.1016/s0960-9822(02)00695-4openalex-snapshot
Chromatin Motion Is Constrained by Association with Nuclear Compartments in Human Cells
inferredcites →https://doi.org/10.1038/19992openalex-snapshot
Regulation of alternative splicing by RNA editing
inferredcites →https://doi.org/10.1038/35007077openalex-snapshot
High mobility of proteins in the mammalian cell nucleus
inferredcites →https://doi.org/10.1038/cr.2010.75openalex-snapshot
PHF8 is a histone H3K9me2 demethylase regulating rRNA synthesis
inferredcites →https://doi.org/10.1038/emboj.2010.199openalex-snapshot
A long nuclear‐retained non‐coding RNA regulates synaptogenesis by modulating gene expression
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/nature06255openalex-snapshot
JHDM1B/FBXL10 is a nucleolar protein that represses transcription of ribosomal RNA genes
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/ncb1637openalex-snapshot
Polycomb response elements mediate the formation of chromosome higher-order structures in the bithorax complex
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/ncb2140openalex-snapshot
Direct visualization of the co-transcriptional assembly of a nuclear body by noncoding RNAs
inferredcites →https://doi.org/10.1038/ng1336openalex-snapshot
SUMO modification is required for in vivo Hox gene regulation by the Caenorhabditis elegans Polycomb group protein SOP-2
inferredcites →https://doi.org/10.1038/nrg2083openalex-snapshot
Genome-wide transcription and the implications for genomic organization
inferredcites →https://doi.org/10.1038/nrg2521openalex-snapshot
Long non-coding RNAs: insights into functions
inferredcites →https://doi.org/10.1038/nrg2592openalex-snapshot
Transcription factories: gene expression in unions?
inferredcites →https://doi.org/10.1038/nrm2124openalex-snapshot
Non-coding RNAs: lessons from the small nuclear and small nucleolar RNAs
inferredcites →https://doi.org/10.1038/nrm2277openalex-snapshot
Structure, dynamics and functions of promyelocytic leukaemia nuclear bodies
inferredcites →https://doi.org/10.1038/nrm2763openalex-snapshot
Mechanisms of Polycomb gene silencing: knowns and unknowns
inferredcites →https://doi.org/10.1038/nsmb.1778openalex-snapshot
PHF8 activates transcription of rRNA genes through H3K4me3 binding and H3K9me1/2 demethylation
inferredcites →https://doi.org/10.1038/nsmb.1783openalex-snapshot
Coilin-dependent snRNP assembly is essential for zebrafish embryogenesis
inferredcites →https://doi.org/10.1073/pnas.0807899106openalex-snapshot
MENε/β noncoding RNAs are essential for structural integrity of nuclear paraspeckles
inferredcites →https://doi.org/10.1073/pnas.0810634105openalex-snapshot
Enhancing nuclear receptor-induced transcription requires nuclear motor and LSD1-dependent gene networking in interchromatin granules
inferredcites →https://doi.org/10.1074/jbc.c500017200openalex-snapshot
Silencing Near tRNA Genes Requires Nucleolar Localization
inferredcites →https://doi.org/10.1083/jcb.112.5.785openalex-snapshot
Identification of a novel nuclear domain.
inferredcites →https://doi.org/10.1083/jcb.115.5.1191openalex-snapshot
Discrete nuclear domains of poly(A) RNA and their relationship to the functional organization of the nucleus.
inferredcites →https://doi.org/10.1083/jcb.126.4.877openalex-snapshot
In vivo analysis of the stability and transport of nuclear poly(A)+ RNA.
inferredcites →https://doi.org/10.1083/jcb.129.5.1181openalex-snapshot
A perinucleolar compartment contains several RNA polymerase III transcripts as well as the polypyrimidine tract-binding protein, hnRNP I [published erratum appears in J Cell Biol 1995 Jul;130(2):497-500]
inferredcites →https://doi.org/10.1083/jcb.137.5.965openalex-snapshot
The Dynamic Organization of the Perinucleolar Compartment in the Cell Nucleus
inferredcites →https://doi.org/10.1083/jcb.142.4.887openalex-snapshot
The Human Polycomb Group Complex Associates with Pericentromeric Heterochromatin to Form a Novel Nuclear Domain
inferredcites →https://doi.org/10.1083/jcb.153.1.169openalex-snapshot
Nucleolar Components Involved in Ribosome Biogenesis Cycle between the Nucleolus and Nucleoplasm in Interphase Cells
inferredcites →https://doi.org/10.1083/jcb.200303131openalex-snapshot
Clustering of multiple specific genes and gene-rich R-bands around SC-35 domains
inferredcites →https://doi.org/10.1083/jcb.200310138openalex-snapshot
Human telomerase RNA and box H/ACA scaRNAs share a common Cajal body–specific localization signal
inferredcites →https://doi.org/10.1083/jcb.200507073openalex-snapshot
Coregulated human globin genes are frequently in spatial proximity when active
inferredcites →https://doi.org/10.1083/jcb.200706060openalex-snapshot
A genetic locus targeted to the nuclear periphery in living cells maintains its transcriptional competence
inferredcites →https://doi.org/10.1083/jcb.200709082openalex-snapshot
As functional nuclear actin comes into view, is it globular, filamentous, or both?
inferredcites →https://doi.org/10.1083/jcb.200803174openalex-snapshot
Association between active genes occurs at nuclear speckles and is modulated by chromatin environment
inferredcites →https://doi.org/10.1083/jcb.200906113openalex-snapshot
Paraspeckles: nuclear bodies built on long noncoding RNA
inferredcites →https://doi.org/10.1083/jcb.201004041openalex-snapshot
Hsp70 gene association with nuclear speckles is Hsp70 promoter specific
inferredcites →https://doi.org/10.1083/jcb.201011110openalex-snapshot
Paraspeckles are subpopulation-specific nuclear bodies that are not essential in mice
inferredcites →https://doi.org/10.1091/mbc.10.9.3015openalex-snapshot
A Role for the GSG Domain in Localizing Sam68 to Novel Nuclear Structures in Cancer Cell Lines
inferredcites →https://doi.org/10.1091/mbc.11.8.2705openalex-snapshot
Initiation of Nucleolar Assembly Is Independent of RNA Polymerase I Transcription
inferredcites →https://doi.org/10.1091/mbc.e03-06-0388openalex-snapshot
Repositioning of Muscle-specific Genes Relative to the Periphery of SC-35 Domains during Skeletal Myogenesis
inferredcites →https://doi.org/10.1091/mbc.e03-07-0525openalex-snapshot
Telomerase RNA Accumulates in Cajal Bodies in Human Cancer Cells
inferredcites →https://doi.org/10.1091/mbc.e05-09-0903openalex-snapshot
Cell Cycle-regulated Trafficking of Human Telomerase to Telomeres
inferredcites →https://doi.org/10.1091/mbc.e05-09-0904openalex-snapshot
Cell Cycle-dependent Recruitment of Telomerase RNA and Cajal Bodies to Human Telomeres
inferredcites →https://doi.org/10.1091/mbc.e05-12-1157openalex-snapshot
A Distant Coilin Homologue Is Required for the Formation of Cajal Bodies in Arabidopsis
inferredcites →https://doi.org/10.1091/mbc.e08-02-0184openalex-snapshot
Telomerase Reverse Transcriptase Is Required for the Localization of Telomerase RNA to Cajal Bodies and Telomeres in Human Cancer Cells
inferredcites →https://doi.org/10.1091/mbc.e08-05-0525openalex-snapshot
Coilin Is Essential for Cajal Body Organization in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/emboj/21.11.2746openalex-snapshot
Cajal body‐specific small nuclear RNAs: a novel class of 2′‐O‐methylation and pseudouridylation guide RNAs
inferredcites →https://doi.org/10.1093/nar/gkl711openalex-snapshot
Human sat III and Drosophila hsrω transcripts: a common paradigm for regulation of nuclear RNA processing in stressed cells
inferredcites →https://doi.org/10.1099/vir.0.81768-0openalex-snapshot
Identification and characterization of a virus-inducible non-coding RNA in mouse brain
inferredcites →https://doi.org/10.1101/cshperspect.a000653openalex-snapshot
The Cajal Body and Histone Locus Body
inferredcites →https://doi.org/10.1101/cshperspect.a000711openalex-snapshot
Biogenesis of Nuclear Bodies
inferredcites →https://doi.org/10.1101/cshperspect.a000794openalex-snapshot
Higher-order Genome Organization in Human Disease
inferredcites →https://doi.org/10.1101/cshperspect.a003756openalex-snapshot
The Long Arm of Long Noncoding RNAs: Roles as Sensors Regulating Gene Transcriptional Programs
inferredcites →https://doi.org/10.1101/gad.1436906openalex-snapshot
Nucleolar dominance: a model for rRNA gene silencing
inferredcites →https://doi.org/10.1101/gad.1800909openalex-snapshot
Long noncoding RNAs: functional surprises from the RNA world
inferredcites →https://doi.org/10.1101/gad.269503openalex-snapshot
Inheritance of Polycomb-dependent chromosomal interactions in Drosophila
inferredcites →https://doi.org/10.1101/gad.5.12a.2288openalex-snapshot
Nascent pre-mRNA transcripts are associated with nuclear regions enriched in splicing factors.
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.087775.108openalex-snapshot
MEN ε/β nuclear-retained non-coding RNAs are up-regulated upon muscle differentiation and are essential components of paraspeckles
inferredcites →https://doi.org/10.1101/sqb.2006.71.025openalex-snapshot
Biogenesis and Intranuclear Trafficking of Human Box C/D and H/ACA RNPs
inferredcites →https://doi.org/10.1126/science.1165216openalex-snapshot
De Novo Formation of a Subnuclear Body
inferredcites →https://doi.org/10.1126/science.1178124openalex-snapshot
Induced Chromosomal Proximity and Gene Fusions in Prostate Cancer
inferredcites →https://doi.org/10.1126/science.290.5490.337openalex-snapshot
A Myosin I Isoform in the Nucleus
inferredcites →https://doi.org/10.1126/science.8446902openalex-snapshot
A Three-Dimensional View of Precursor Messenger RNA Metabolism Within the Mammalian Nucleus
inferredcites →https://doi.org/10.1128/mcb.00825-08openalex-snapshot
The CTCF Insulator Protein Is Posttranslationally Modified by SUMO
inferredcites →https://doi.org/10.1128/mcb.02263-07openalex-snapshot
Kcnq1ot1/Lit1 Noncoding RNA Mediates Transcriptional Silencing by Targeting to the Perinucleolar Region
inferredcites →https://doi.org/10.1146/annurev.biochem.71.110601.135501openalex-snapshot
RNA Editing by Adenosine Deaminases That Act on RNA
inferredcites →https://doi.org/10.1146/annurev.cellbio.24.110707.175259openalex-snapshot
The Epigenetics of rRNA Genes: From Molecular to Chromosome Biology
inferredcites →https://doi.org/10.1158/0008-5472.246.65.1openalex-snapshot
Perinucleolar Compartment Prevalence Has an Independent Prognostic Value for Breast Cancer
inferredcites →https://doi.org/10.1186/1471-2164-8-39openalex-snapshot
A screen for nuclear transcripts identifies two linked noncoding RNAs associated with SC35 splicing domains
inferredcites →https://doi.org/10.1242/jcs.026104openalex-snapshot
The facultative heterochromatin of the inactive X chromosome has a distinctive condensed ultrastructure
inferredcites →https://doi.org/10.1261/rna.1165008openalex-snapshot
C. elegans and H. sapiens mRNAs with edited 3′ UTRs are present on polysomes
inferredcites →https://doi.org/10.1371/journal.pgen.1000922openalex-snapshot
Activation of Estrogen-Responsive Genes Does Not Require Their Nuclear Co-Localization
inferredcites →https://doi.org/10.1371/journal.pone.0006171openalex-snapshot
Reduced Viability, Fertility and Fecundity in Mice Lacking the Cajal Body Marker Protein, Coilin
inferredcites →https://doi.org/10.4161/cc.7.21.6927openalex-snapshot
Gene regulation by SINES and inosines: biological consequences of A-to-I editing of Alu element inverted repeats
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Determination of Polycomb Group of Protein Compartmentalization Through Chromatin Fractionation Procedure
inferred← citeshttps://doi.org/10.1007/978-1-4939-7318-7_31openalex-snapshot
Technical Review: Microscopy and Image Processing Tools to Analyze Plant Chromatin: Practical Considerations
inferred← citeshttps://doi.org/10.1007/978-1-62703-414-2_16openalex-snapshot
Agroinfiltration of Nicotiana benthamiana Leaves for Co-localization of Regulatory Proteins Involved in Jasmonate Signaling
inferred← citeshttps://doi.org/10.1007/978-1-62703-526-2_23openalex-snapshot
Nucleation of Nuclear Bodies
inferred← citeshttps://doi.org/10.1007/978-3-030-06128-9_10openalex-snapshot
Emergent Properties and Stability in Hierarchical Biosystems: There Is no Privileged Level of Causation
inferred← citeshttps://doi.org/10.1007/978-3-030-62532-0_2openalex-snapshot
Eukaryotic Genome in Three Dimensions
inferred← citeshttps://doi.org/10.1007/978-3-031-00793-4_7openalex-snapshot
On the Regulation of Mitosis by the Kinetochore, a Macromolecular Complex and Organising Hub of Eukaryotic Organisms
inferred← citeshttps://doi.org/10.1007/978-3-319-16769-5_1openalex-snapshot
All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-29073-7_3openalex-snapshot
Tethered Function Assays as Tools to Elucidate the Molecular Roles of RNA-Binding Proteins
inferred← citeshttps://doi.org/10.1007/978-3-319-38882-3_10openalex-snapshot
DNA Repair Foci Formation and Function at DNA Double-Strand Breaks
inferred← citeshttps://doi.org/10.1007/978-3-642-45198-0_5openalex-snapshot
Polycomb Complexes: Chromatin Regulators Required for Cell Diversity and Tissue Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-662-44817-5_5openalex-snapshot
Die eukaryotische Zelle und Modellorganismen
inferred← citeshttps://doi.org/10.1007/978-3-662-60909-5_5openalex-snapshot
Die eukaryotische Zelle und Modellorganismen
inferred← citeshttps://doi.org/10.1007/978-3-662-70328-1_5openalex-snapshot
Die eukaryotische Zelle und Modellorganismen
inferred← citeshttps://doi.org/10.1007/978-3-7091-1556-5_1openalex-snapshot
Cell Biology for Immune Evasion: Organizing Antigenic Variation, Surfaces, Trafficking, and Cellular Structures in Trypanosoma brucei
inferred← citeshttps://doi.org/10.1007/978-4-431-55576-6_7openalex-snapshot
Long Noncoding RNAs as Structural and Functional Components of Nuclear Bodies
inferred← citeshttps://doi.org/10.1007/978-94-007-5025-8_5openalex-snapshot
Effects of Phosphoinositides and Their Derivatives on Membrane Morphology and Function
inferred← citeshttps://doi.org/10.1007/s00018-012-0973-xopenalex-snapshot
Paraspeckle nuclear bodies—useful uselessness?
inferred← citeshttps://doi.org/10.1007/s00018-017-2503-3openalex-snapshot
Integration of mRNP formation and export
inferred← citeshttps://doi.org/10.1007/s00018-018-2894-9openalex-snapshot
Intrinsically disordered proteins in crowded milieu: when chaos prevails within the cellular gumbo
inferred← citeshttps://doi.org/10.1007/s00109-023-02407-3openalex-snapshot
Liquid–liquid phase separation in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00412-013-0429-6openalex-snapshot
The SUMO system: a master organizer of nuclear protein assemblies
inferred← citeshttps://doi.org/10.1007/s00412-015-0561-6openalex-snapshot
Resetting a functional G1 nucleus after mitosis
inferred← citeshttps://doi.org/10.1007/s00412-018-0667-8openalex-snapshot
Imaging the dynamics of transcription loops in living chromosomes
inferred← citeshttps://doi.org/10.1007/s00418-017-1618-9openalex-snapshot
Nuclear organization during in vitro differentiation of porcine mesenchymal stem cells (MSCs) into adipocytes
inferred← citeshttps://doi.org/10.1007/s00418-025-02429-7openalex-snapshot
The O-GlcNAcylation of β-actin Ser199 controls nuclear speckle localization and is dysregulated in diabetes
inferred← citeshttps://doi.org/10.1007/s00439-017-1762-2openalex-snapshot
Compound heterozygous GATA5 mutations in a girl with hydrops fetalis, congenital heart defects and genital anomalies
inferred← citeshttps://doi.org/10.1007/s00441-015-2204-xopenalex-snapshot
Special characteristics of the transcription and splicing machinery in photoreceptor cells of the mammalian retina
inferred← citeshttps://doi.org/10.1007/s00709-014-0648-6openalex-snapshot
Functional ultrastructure of the plant nucleolus
inferred← citeshttps://doi.org/10.1007/s00709-016-0978-7openalex-snapshot
Meiosis, Balbiani body and early asymmetry of Thermobia oocyte
inferred← citeshttps://doi.org/10.1007/s00709-017-1163-3openalex-snapshot
Structure and biogenesis of ribonucleoprotein bodies in epidermal cells of Caragana arborescens L
inferred← citeshttps://doi.org/10.1007/s10565-018-9428-yopenalex-snapshot
Three-dimensional organization and dynamics of the genome
inferred← citeshttps://doi.org/10.1007/s10577-013-9391-7openalex-snapshot
Functional insights into the role of nuclear-retained long noncoding RNAs in gene expression control in mammalian cells
inferred← citeshttps://doi.org/10.1007/s10577-014-9425-9openalex-snapshot
Connecting the dots of RNA-directed DNA methylation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10577-023-09714-yopenalex-snapshot
Nuclear architecture and the structural basis of mitotic memory
inferred← citeshttps://doi.org/10.1007/s11011-020-00564-9openalex-snapshot
Molecular mechanisms underlying actions of certain long noncoding RNAs in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s11103-012-9973-3openalex-snapshot
Direct interactions of ABA-insensitive(ABI)-clade protein phosphatase(PP)2Cs with calcium-dependent protein kinases and ABA response element-binding bZIPs may contribute to turning off ABA response
inferred← citeshttps://doi.org/10.1007/s11427-019-1609-6openalex-snapshot
Evidence of constraint in the 3D genome for trans-splicing in human cells
inferred← citeshttps://doi.org/10.1007/s11427-019-1613-3openalex-snapshot
Architectural proteins for the formation and maintenance of the 3D genome
inferred← citeshttps://doi.org/10.1007/s11515-016-1433-zopenalex-snapshot
Cellular, physiological and pathological aspects of the long non-coding RNA NEAT1
inferred← citeshttps://doi.org/10.1007/s11738-015-1917-5openalex-snapshot
Localization sites of nuclear envelope SUN2-like proteins in root meristem cells of Allium cepa under hydroxyurea-induced DNA replication stress
inferred← citeshttps://doi.org/10.1007/s12154-012-0082-1openalex-snapshot
The nuclear membrane as a lipid ‘sink’—linking cell cycle progression to lipid synthesis
inferred← citeshttps://doi.org/10.1007/s12192-014-0512-9openalex-snapshot
To be or not to be: the regulation of mRNA fate as a survival strategy during mammalian hibernation
inferred← citeshttps://doi.org/10.1007/s12551-020-00761-xopenalex-snapshot
The rich inner life of the cell nucleus: dynamic organization, active flows, and emergent rheology
inferred← citeshttps://doi.org/10.1007/s13258-025-01661-8openalex-snapshot
Nuclear ribonucleoprotein condensates as platforms for gene expression regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-397920-9.00006-8openalex-snapshot
Functional Architecture of the Cell's Nucleus in Development, Aging, and Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-404613-9.00027-7openalex-snapshot
RETRACTED: References
inferred← citeshttps://doi.org/10.1016/b978-0-12-800046-5.00004-7openalex-snapshot
Crowding-Induced Formation and Structural Alteration of Nuclear Compartments
inferred← citeshttps://doi.org/10.1016/b978-0-12-800046-5.00005-9openalex-snapshot
Phase Separation as a Possible Means of Nuclear Compartmentalization
inferred← citeshttps://doi.org/10.1016/b978-0-12-800046-5.00006-0openalex-snapshot
Formation of Multiprotein Assemblies in the Nucleus
inferred← citeshttps://doi.org/10.1016/b978-0-12-803395-1.00009-5openalex-snapshot
Crosstalk Between Non-Coding RNAs and the Epigenome in Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-803480-4.00015-6openalex-snapshot
Actin in the Cell Nucleus
inferred← citeshttps://doi.org/10.1016/b978-0-12-803480-4.00021-1openalex-snapshot
Altered Nucleus and Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-823967-4.00011-7openalex-snapshot
Biochemical and structural biology aspects of liquid–liquid phase separation: protein side of liquid–liquid phase separation, membrane-less organelles, and biomolecular condensates
inferred← citeshttps://doi.org/10.1016/b978-0-12-823967-4.00024-5openalex-snapshot
Interactions and interplay of MLOs with classical membrane-bound organelles
inferred← citeshttps://doi.org/10.1016/b978-0-323-99507-8.00084-6openalex-snapshot
Phase separation of tumor suppressor p53 and its family proteins
inferred← citeshttps://doi.org/10.1016/b978-0-443-19001-8.00019-2openalex-snapshot
Phase separation and chromatin
inferred← citeshttps://doi.org/10.1016/b978-0-443-21809-5.00001-6openalex-snapshot
The three functional states of proteins: beyond the classical “lock and key” paradigm
inferred← citeshttps://doi.org/10.1016/b978-0-443-21809-5.00012-0openalex-snapshot
Various levels of phase transitions in the protein universe and around
inferred← citeshttps://doi.org/10.1016/b978-0-443-21809-5.00020-xopenalex-snapshot
Biological complexity of the phase-separated protein states
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2020.12.007openalex-snapshot
RNA-seeded membraneless bodies: Role of tandemly repeated RNA
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2020.02.002openalex-snapshot
From mother to embryo: A molecular perspective on zygotic genome activation
inferred← citeshttps://doi.org/10.1016/bs.ctm.2021.09.003openalex-snapshot
Current methods for studying intracellular liquid-liquid phase separation
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2014.11.004openalex-snapshot
Nuclear Compartments, Genome Folding, and Enhancer-Promoter Communication
inferred← citeshttps://doi.org/10.1016/bs.irn.2024.04.009openalex-snapshot
RNP granules in ALS and neurodegeneration: From multifunctional membraneless organelles to therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/bs.mie.2018.09.035openalex-snapshot
Phase Separation of Intrinsically Disordered Proteins
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2024.03.006openalex-snapshot
Liquid-liquid phase separation as triggering factor of fibril formation
inferred← citeshttps://doi.org/10.1016/j.ajhg.2021.01.008openalex-snapshot
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
inferred← citeshttps://doi.org/10.1016/j.alcohol.2012.04.004openalex-snapshot
Chronic ethanol up-regulates the synaptic expression of the nuclear translational regulatory protein AIDA-1 in primary hippocampal neurons
inferred← citeshttps://doi.org/10.1016/j.bbagen.2025.130815openalex-snapshot
Unraveling architectural RNAs: Structural and functional blueprints of membraneless organelles and strategies for genome-scale identification
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2015.05.007openalex-snapshot
Architectural RNAs (arcRNAs): A class of long noncoding RNAs that function as the scaffold of nuclear bodies
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2015.08.009openalex-snapshot
The ins and outs of lncRNA structure: How, why and what comes next?
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2020.194641openalex-snapshot
From start to end: Phase separation and transcriptional regulation
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2014.08.016openalex-snapshot
Ki-1/57 and CGI-55 ectopic expression impact cellular pathways involved in proliferation and stress response regulation
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118650openalex-snapshot
Alteration of SC35 localization by transfection reagents
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118879openalex-snapshot
The interaction between nucleophosmin/NPM1 and the large ribosomal subunit precursors contribute to maintaining the nucleolar structure
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119058openalex-snapshot
Connecting the “dots”: RNP granule network in health and disease
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119102openalex-snapshot
Liquid-liquid phase separation as a common organizing principle of intracellular space and biomembranes providing dynamic adaptive responses
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2022.119251openalex-snapshot
State without borders: Membrane-less organelles and liquid–liquid phase transitions
inferred← citeshttps://doi.org/10.1016/j.bbapap.2013.01.003openalex-snapshot
Protein disorder, prion propensities, and self-organizing macromolecular collectives
inferred← citeshttps://doi.org/10.1016/j.bbcan.2024.189245openalex-snapshot
Biomolecular condensates: A new lens on cancer biology
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.12.150openalex-snapshot
Formation of tRNA granules in the nucleus of heat-induced human cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.02.060openalex-snapshot
Identification of a chemical inhibitor for nuclear speckle formation: Implications for the function of nuclear speckles in regulation of alternative pre-mRNA splicing
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.04.026openalex-snapshot
G-patch domain-containing protein 4 localizes to both the nucleoli and Cajal bodies and regulates cell growth and nucleolar structure
inferred← citeshttps://doi.org/10.1016/j.biocel.2013.10.009openalex-snapshot
Life without A tail: New formats of long noncoding RNAs
inferred← citeshttps://doi.org/10.1016/j.biocel.2014.03.012openalex-snapshot
Regulation of mammary epithelial cell homeostasis by lncRNAs
inferred← citeshttps://doi.org/10.1016/j.biocel.2017.06.001openalex-snapshot
Targeting proteins to RNA transcription and processing sites within the nucleus
inferred← citeshttps://doi.org/10.1016/j.bpj.2012.07.007openalex-snapshot
Crowding Effects on the Formation and Maintenance of Nuclear Bodies: Insights from Molecular-Dynamics Simulations of Simple Spherical Model Particles
inferred← citeshttps://doi.org/10.1016/j.bpj.2013.11.039openalex-snapshot
Effects of Phosphoinositides and their Derivatives on Endomembrane Morphology and Function
inferred← citeshttps://doi.org/10.1016/j.bpj.2017.01.025openalex-snapshot
Ephemeral Protein Binding to DNA Shapes Stable Nuclear Bodies and Chromatin Domains
inferred← citeshttps://doi.org/10.1016/j.bpj.2018.03.011openalex-snapshot
Formation of Chromatin Subcompartments by Phase Separation
inferred← citeshttps://doi.org/10.1016/j.bpj.2018.05.023openalex-snapshot
Do Cellular Condensates Accelerate Biochemical Reactions? Lessons from Microdroplet Chemistry
inferred← citeshttps://doi.org/10.1016/j.bpj.2021.10.008openalex-snapshot
Assembly of model postsynaptic densities involves interactions auxiliary to stoichiometric binding
inferred← citeshttps://doi.org/10.1016/j.bpj.2021.11.1933openalex-snapshot
Chromatin network retards droplet coalescence
inferred← citeshttps://doi.org/10.1016/j.bpj.2022.05.039openalex-snapshot
Simulating the chromatin-mediated phase separation of model proteins with multiple domains
inferred← citeshttps://doi.org/10.1016/j.bpj.2023.09.012openalex-snapshot
Understanding the free-energy landscape of phase separation in lipid bilayers using molecular dynamics
inferred← citeshttps://doi.org/10.1016/j.brainres.2020.146672openalex-snapshot
Increased level of NEAT1 long non-coding RNA is detectable in peripheral blood cells of patients with Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.ceb.2012.03.010openalex-snapshot
Nuclear bodies: multifunctional companions of the genome
inferred← citeshttps://doi.org/10.1016/j.ceb.2013.08.005openalex-snapshot
Long non-coding RNAs: modulators of nuclear structure and function
inferred← citeshttps://doi.org/10.1016/j.cell.2012.05.022openalex-snapshot
Getting RNA and Protein in Phase
inferred← citeshttps://doi.org/10.1016/j.cell.2015.10.040openalex-snapshot
The LC Domain of hnRNPA2 Adopts Similar Conformations in Hydrogel Polymers, Liquid-like Droplets, and Nuclei
inferred← citeshttps://doi.org/10.1016/j.cell.2016.06.010openalex-snapshot
Compositional Control of Phase-Separated Cellular Bodies
inferred← citeshttps://doi.org/10.1016/j.cell.2016.11.054openalex-snapshot
Spatiotemporal Control of Intracellular Phase Transitions Using Light-Activated optoDroplets
inferred← citeshttps://doi.org/10.1016/j.cell.2017.02.007openalex-snapshot
A Phase Separation Model for Transcriptional Control
inferred← citeshttps://doi.org/10.1016/j.cell.2017.04.022openalex-snapshot
Lamina-Associated Domains: Links with Chromosome Architecture, Heterochromatin, and Gene Repression
inferred← citeshttps://doi.org/10.1016/j.cell.2018.09.013openalex-snapshot
CRISPR-Mediated Programmable 3D Genome Positioning and Nuclear Organization
inferred← citeshttps://doi.org/10.1016/j.cell.2018.10.057openalex-snapshot
Liquid Nuclear Condensates Mechanically Sense and Restructure the Genome
inferred← citeshttps://doi.org/10.1016/j.cell.2020.03.050openalex-snapshot
Competing Protein-RNA Interaction Networks Control Multiphase Intracellular Organization
inferred← citeshttps://doi.org/10.1016/j.cellsig.2024.111156openalex-snapshot
Unravelling the molecular interplay: SUMOylation, PML nuclear bodies and vascular cell activity in health and disease
inferred← citeshttps://doi.org/10.1016/j.cellsig.2025.112190openalex-snapshot
Current mechanistic insights into biochemical properties and cellular functions of human Caf1 deadenylases
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.01.022openalex-snapshot
Formation of Subnuclear Foci Is a Unique Spatial Behavior of Mating MAPKs during Hyperosmotic Stress
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.03.089openalex-snapshot
PARN and TOE1 Constitute a 3′ End Maturation Module for Nuclear Non-coding RNAs
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111263openalex-snapshot
A small RNA-guided PRC2 complex eliminates DNA as an extreme form of transposon silencing
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115826openalex-snapshot
De novo assembly of RNA m6A modification factors into viral genome-associated nuclear bodies drives HCMV RNA accumulation
inferred← citeshttps://doi.org/10.1016/j.chembiol.2023.08.010openalex-snapshot
RNA G-quadruplex in functional regulation of noncoding RNA: Challenges and emerging opportunities
inferred← citeshttps://doi.org/10.1016/j.chempr.2020.09.022openalex-snapshot
Programmable ATP-Fueled DNA Coacervates by Transient Liquid-Liquid Phase Separation
inferred← citeshttps://doi.org/10.1016/j.cis.2016.06.011openalex-snapshot
Experimental models for dynamic compartmentalization of biomolecules in liquid organelles: Reversible formation and partitioning in aqueous biphasic systems
inferred← citeshttps://doi.org/10.1016/j.cocis.2021.101457openalex-snapshot
Polyampholyte physics: Liquid–liquid phase separation and biological condensates
inferred← citeshttps://doi.org/10.1016/j.crtox.2024.100161openalex-snapshot
Cigarette smoking inhibits myoblast regeneration by promoting proteasomal degradation of NPAT protein and hindering cell cycle progression
inferred← citeshttps://doi.org/10.1016/j.csbj.2022.05.004openalex-snapshot
DisPhaseDB: An integrative database of diseases related variations in liquid–liquid phase separation proteins
inferred← citeshttps://doi.org/10.1016/j.csbj.2022.07.002openalex-snapshot
Chromatin Hubs: A biological and computational outlook
inferred← citeshttps://doi.org/10.1016/j.csbj.2023.02.028openalex-snapshot
Mini-review: Gene regulatory network benefits from three-dimensional chromatin conformation and structural biology
inferred← citeshttps://doi.org/10.1016/j.cub.2014.03.070openalex-snapshot
Gene Regulation: The HSP70 Gene Jumps When Shocked
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.05.019openalex-snapshot
Nuclear GPS for Interchromosomal Clustering
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.09.024openalex-snapshot
Translation Repressors, an RNA Helicase, and Developmental Cues Control RNP Phase Transitions during Early Development
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.06.003openalex-snapshot
CDK-Regulated Phase Separation Seeded by Histone Genes Ensures Precise Growth and Function of Histone Locus Bodies
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.09.005openalex-snapshot
Biomolecular Condensates and Gene Activation in Development and Disease
inferred← citeshttps://doi.org/10.1016/j.dnarep.2024.103779openalex-snapshot
53BP1-the ‘Pandora’s box’ of genome integrity
inferred← citeshttps://doi.org/10.1016/j.expneurol.2017.03.011openalex-snapshot
RNAi of arcRNA hsrω affects sub-cellular localization of Drosophila FUS to drive neurodiseases
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.05.035openalex-snapshot
Nuclear translocation of DJ-1 during oxidative stress-induced neuronal cell death
inferred← citeshttps://doi.org/10.1016/j.gde.2011.11.004openalex-snapshot
A view of nuclear Polycomb bodies
inferred← citeshttps://doi.org/10.1016/j.gde.2011.12.005openalex-snapshot
Nuclear architecture by RNA
inferred← citeshttps://doi.org/10.1016/j.gde.2013.11.021openalex-snapshot
Genome regulation at the peripheral zone: lamina associated domains in development and disease
inferred← citeshttps://doi.org/10.1016/j.gde.2024.102176openalex-snapshot
RNA in chromatin organization and nuclear architecture
inferred← citeshttps://doi.org/10.1016/j.gene.2019.144276openalex-snapshot
Role of non-coding RNA in the pathogenesis of depression
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145716openalex-snapshot
Establishment of lncRNA-mRNA network in bovine oocyte between germinal vesicle and metaphase II stage
inferred← citeshttps://doi.org/10.1016/j.isci.2024.109732openalex-snapshot
Long noncoding RNAs heat shock RNA omega nucleates TBPH and promotes intestinal stem cell differentiation upon heat shock
inferred← citeshttps://doi.org/10.1016/j.isci.2026.115152openalex-snapshot
Elastic enhancer network tunes equilibrium thermodynamics of liquid liquid phase separation in super enhancers
inferred← citeshttps://doi.org/10.1016/j.jbc.2026.111352openalex-snapshot
Forces that shape the transcriptome: Linking cellular mechanosensing to mRNA splicing
inferred← citeshttps://doi.org/10.1016/j.jid.2016.04.040openalex-snapshot
The Molecular Revolution in Cutaneous Biology: Chromosomal Territories, Higher-Order Chromatin Remodeling, and the Control of Gene Expression in Keratinocytes
inferred← citeshttps://doi.org/10.1016/j.jmb.2018.08.005openalex-snapshot
Multiple Modes of Protein–Protein Interactions Promote RNP Granule Assembly
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.04.015openalex-snapshot
Repetitive RNAs as Regulators of Chromatin-Associated Subcompartment Formation by Phase Separation
inferred← citeshttps://doi.org/10.1016/j.jmb.2021.167151openalex-snapshot
Nuclear Protein Condensates and Their Properties in Regulation of Gene Expression
inferred← citeshttps://doi.org/10.1016/j.jtbi.2017.04.006openalex-snapshot
On the origin of non-membrane-bound organelles, and their physiological function
inferred← citeshttps://doi.org/10.1016/j.mcpro.2024.100715openalex-snapshot
Nuclear Phosphoproteome Reveals Prolyl Isomerase PIN1 as a Modulator of Oncogene-Induced Senescence
inferred← citeshttps://doi.org/10.1016/j.micres.2024.127627openalex-snapshot
Liquid-Liquid phase separation in bacteria
inferred← citeshttps://doi.org/10.1016/j.mocell.2025.100240openalex-snapshot
RNA-associated nuclear condensates: Where the nucleus keeps its RNAs in check
inferred← citeshttps://doi.org/10.1016/j.molcel.2012.07.022openalex-snapshot
Nuclear Retention Prevents Premature Cytoplasmic Appearance of mRNA
inferred← citeshttps://doi.org/10.1016/j.molcel.2014.01.009openalex-snapshot
Long Noncoding RNA NEAT1-Dependent SFPQ Relocation from Promoter Region to Paraspeckle Mediates IL8 Expression upon Immune Stimuli
inferred← citeshttps://doi.org/10.1016/j.molcel.2014.07.012openalex-snapshot
The Long Noncoding RNAs NEAT1 and MALAT1 Bind Active Chromatin Sites
inferred← citeshttps://doi.org/10.1016/j.molcel.2014.10.004openalex-snapshot
The Coilin Interactome Identifies Hundreds of Small Noncoding RNAs that Traffic through Cajal Bodies
inferred← citeshttps://doi.org/10.1016/j.molcel.2018.10.036openalex-snapshot
A Systems-Level Study Reveals Regulators of Membrane-less Organelles in Human Cells
inferred← citeshttps://doi.org/10.1016/j.molcel.2020.07.003openalex-snapshot
Advances in Chromatin and Chromosome Research: Perspectives from Multiple Fields
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.10.009openalex-snapshot
Hybridization-proximity labeling reveals spatially ordered interactions of nuclear RNA compartments
inferred← citeshttps://doi.org/10.1016/j.molcel.2022.05.027openalex-snapshot
Integrated lncRNA function upon genomic and epigenomic regulation
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