The 4D nucleome: Evidence for a dynamic nuclear landscape based on co-aligned active and inactive nuclear compartments

scientific article

The 4D nucleome: Evidence for a dynamic nuclear landscape based on co-aligned active and inactive nuclear compartments is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P356DOI10.1016/J.FEBSLET.2015.05.037
P698PubMed publication ID26028501
P5875ResearchGate publication ID277560224

P50authorKarsten RippeQ38800586
P2093author name stringBarbara Hübner
Marion Cremer
Thomas Cremer
Yolanda Markaki
Christoph Cremer
Michael Sterr
Hilmar Strickfaden
Daniel Smeets
Jens Popken
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Nuclear lamins are not required for lamina-associated domain organization in mouse embryonic stem cellsQ40557089
Cohesin-mediated interactions organize chromosomal domain architectureQ41470387
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Does the interchromatin compartment contain actin?Q45802027
Histone acetylation increases chromatin accessibilityQ46827175
Better imaging through chemistryQ48057083
Focused ion beam (FIB) combined with high resolution scanning electron microscopy: a promising tool for 3D analysis of chromosome architectureQ50455654
LBR and lamin A/C sequentially tether peripheral heterochromatin and inversely regulate differentiation.Q52633974
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Nuclear architecture by RNA.Q37979013
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Transcription in the context of the 3D nucleusQ38188767
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Live cell immunogold labelling of RNA polymerase II.Q30619924
Direct imaging of DNA in living cells reveals the dynamics of chromosome formationQ31232677
Spatial and temporal dynamics of DNA replication sites in mammalian cellsQ31955494
High-precision structural analysis of subnuclear complexes in fixed and live cells via spatially modulated illumination (SMI) microscopyQ33332209
In vivo chromatin organization of mouse rod photoreceptors correlates with histone modificationsQ33603017
Stable C0T-1 repeat RNA is abundant and is associated with euchromatic interphase chromosomesQ33620505
HSP70 transgene directed motion to nuclear speckles facilitates heat shock activationQ33648700
Chromatin as dynamic 10-nm fibersQ33651467
Chromosome territoriesQ33693822
TET enzymes, TDG and the dynamics of DNA demethylation.Q33715010
Double-strand break-induced transcriptional silencing is associated with loss of tri-methylation at H3K4.Q34045935
Single molecule localization microscopy of the distribution of chromatin using Hoechst and DAPI fluorescent probes.Q34122738
Functional nuclear organization of transcription and DNA replication: a topographical marriage between chromatin domains and the interchromatin compartment.Q34176028
Chromosome order in HeLa cells changes during mitosis and early G1, but is stably maintained during subsequent interphase stages.Q34179664
Perspective: transposable elements, parasitic DNA, and genome evolutionQ34192362
Gene gating: a hypothesisQ34192811
Fine structural organization of the interphase nucleus in some mammalian cellsQ34240227
Condensed chromatin domains in the mammalian nucleus are accessible to large macromoleculesQ34250385
Electron microscope tomography: transcription in three dimensionsQ34271343
Intracellular electric field and pH optimize protein localization and movement.Q34279738
Depletion of the chromatin looping proteins CTCF and cohesin causes chromatin compaction: insight into chromatin folding by polymer modellingQ34314868
Exploring the three-dimensional organization of genomes: interpreting chromatin interaction dataQ34343663
Recruitment kinetics of DNA repair proteins Mdc1 and Rad52 but not 53BP1 depend on damage complexityQ34364324
An archaeal origin of eukaryotes supports only two primary domains of lifeQ34391778
Topological organization of multichromosomal regions by the long intergenic noncoding RNA FirreQ34400074
Models of chromosome structureQ34419157
Chromatin domains and the interchromatin compartment form structurally defined and functionally interacting nuclear networks.Q34582972
Dynamic genome architecture in the nuclear space: regulation of gene expression in three dimensionsQ34603234
Chromosomes without a 30-nm chromatin fiberQ34640698
Activation of DNA damage response signaling by condensed chromatinQ34713712
Origins of major archaeal clades correspond to gene acquisitions from bacteriaQ34848019
Nuclear architecture of rod photoreceptor cells adapts to vision in mammalian evolution.Q34976799
Specificity, propagation, and memory of pericentric heterochromatinQ34986658
Revealing the high-resolution three-dimensional network of chromatin and interchromatin space: a novel electron-microscopic approach to reconstructing nuclear architectureQ35001224
Recollections of a scientific journey published in human genetics: from chromosome territories to interphase cytogenetics and comparative genome hybridizationQ35087959
Distinct properties of human HMGN5 reveal a rapidly evolving but functionally conserved nucleosome binding protein.Q35096592
Multicolor CRISPR labeling of chromosomal loci in human cells.Q35190002
Retrieving the intracellular topology from multi-scale protein mobility mapping in living cells.Q35212323
Reprogramming of fibroblast nuclei in cloned bovine embryos involves major structural remodeling with both striking similarities and differences to nuclear phenotypes of in vitro fertilized embryosQ35497293
Predictive polymer modeling reveals coupled fluctuations in chromosome conformation and transcriptionQ35592856
Form follows function: The genomic organization of cellular differentiationQ35806109
"Nanosized voltmeter" enables cellular-wide electric field mappingQ35906108
Internal organisation of the nucleus: assembly of compartments by macromolecular crowding and the nuclear matrix modelQ35935638
Eukaryogenesis, how special really?Q35990022
The International Nucleome ConsortiumQ36189603
Replicon clusters are stable units of chromosome structure: evidence that nuclear organization contributes to the efficient activation and propagation of S phase in human cellsQ36255115
Complexity of chromatin folding is captured by the strings and binders switch modelQ36342953
Evidence for a nuclear compartment of transcription and splicing located at chromosome domain boundariesQ36745903
Ultrastructural analysis of transcription and splicing in the cell nucleus after bromo-UTP microinjectionQ36837831
Polymer models of chromatin organizationQ36941824
Transcription forms and remodels supercoiling domains unfolding large-scale chromatin structuresQ36946305
The hierarchy of the 3D genomeQ37090603
Superresolution imaging of transcription units on newt lampbrush chromosomesQ37144079
Elucidating chromatin and nuclear domain architecture with electron spectroscopic imagingQ37156597
Radial chromatin positioning is shaped by local gene density, not by gene expressionQ37208453
Open chromatin in pluripotency and reprogrammingQ37477736
Higher order nuclear organization: three-dimensional distribution of small nuclear ribonucleoprotein particlesQ37660535
Chromatin structure: does the 30-nm fibre exist in vivo?Q37719900
Genome-nuclear lamina interactions and gene regulationQ37742889
P433issue20 Pt A
P407language of work or nameEnglishQ1860
P304page(s)2931-2943
P577publication date2015-05-28
P1433published inFEBS LettersQ1388051
P1476titleThe 4D nucleome: Evidence for a dynamic nuclear landscape based on co-aligned active and inactive nuclear compartments
P478volume589

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