| P50 | author | William E. Moerner | Q1387059 |
| P2093 | author name string | Colin J Comerci | |
| | Joanna Wysocka | |
| | Bo Gu | |
| | Saumya Saurabh | |
| | Dannielle G McCarthy | |
| P2860 | cites work | Real-time dynamics of RNA polymerase II clustering in live human cells | Q39130041 |
| | An auxin-based degron system for the rapid depletion of proteins in nonplant cells. | Q39774277 |
| | Multiple particle tracking in 3-D+t microscopy: method and application to the tracking of endocytosed quantum dots | Q40328667 |
| | Super-resolution Imaging of Live Bacteria Cells Using a Genetically Directed, Highly Photostable Fluoromodule | Q41243480 |
| | Preparation of nuclear matrices from cultured cells: subfractionation of nuclei in situ | Q41456343 |
| | A dynamic mode of mitotic bookmarking by transcription factors | Q41809452 |
| | Cohesin relocation from sites of chromosomal loading to places of convergent transcription | Q41809530 |
| | DNA Entry into and Exit out of the Cohesin Ring by an Interlocking Gate Mechanism | Q42673051 |
| | Cohesin Loss Eliminates All Loop Domains | Q46223387 |
| | Nuclear microenvironments modulate transcription from low-affinity enhancers. | Q46371048 |
| | Two independent modes of chromatin organization revealed by cohesin removal | Q47035974 |
| | Topologically associating domains and chromatin loops depend on cohesin and are regulated by CTCF, WAPL, and PDS5 proteins. | Q47317900 |
| | Mapping molecular assemblies with fluorescence microscopy and object-based spatial statistics. | Q49958799 |
| | Cohesin is positioned in mammalian genomes by transcription, CTCF and Wapl | Q51046963 |
| | HMGB2 Loss upon Senescence Entry Disrupts Genomic Organization and Induces CTCF Clustering across Cell Types | Q52692063 |
| | Super-resolution chromatin tracing reveals domains and cooperative interactions in single cells | Q58550718 |
| | Transcription Elongation Can Affect Genome 3D Structure | Q59353868 |
| | Whole-Cell, 3D, and Multicolor STED Imaging with Exchangeable Fluorophores | Q60364951 |
| | Quantification of very low-abundant proteins in bacteria using the HaloTag and epi-fluorescence microscopy | Q64464908 |
| | Mediator and RNA polymerase II clusters associate in transcription-dependent condensates | Q89180976 |
| | Enhancer hubs and loop collisions identified from single-allele topologies | Q89486296 |
| | Distinct Classes of Chromatin Loops Revealed by Deletion of an RNA-Binding Region in CTCF | Q90114569 |
| | RNA Interactions Are Essential for CTCF-Mediated Genome Organization | Q90114572 |
| | Revealing Nanoscale Morphology of the Primary Cilium Using Super-Resolution Fluorescence Microscopy | Q90831666 |
| | Guided nuclear exploration increases CTCF target search efficiency | Q91621689 |
| | Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency | Q92382497 |
| | The structural basis for cohesin-CTCF-anchored loops | Q92439389 |
| | CTCF mediates chromatin looping via N-terminal domain-dependent cohesin retention | Q92642154 |
| | Differential contribution of steady-state RNA and active transcription in chromatin organization | Q92862114 |
| | An efficient auxin-inducible degron system with low basal degradation in human cells | Q92883066 |
| | An improved auxin-inducible degron system preserves native protein levels and enables rapid and specific protein depletion | Q92992938 |
| | Molecular architecture of SMC proteins and the yeast cohesin complex | Q24296209 |
| | Association of chromatin proteins high mobility group box (HMGB) 1 and HMGB2 with mitotic chromosomes | Q24316385 |
| | Organization, inducible-expression and chromosome localization of the human HMG-I(Y) nonhistone protein gene | Q24631920 |
| | CTCF-dependent enhancer-blocking by alternative chromatin loop formation | Q24646679 |
| | Malachite Green Mediates Homodimerization of Antibody VL Domains to Form a Fluorescent Ternary Complex with Singular Symmetric Interfaces | Q27679807 |
| | Crystallographic structure of an intact IgG1 monoclonal antibody | Q27748871 |
| | Chromatin modifications and their function | Q27861067 |
| | Comprehensive mapping of long-range interactions reveals folding principles of the human genome | Q28131819 |
| | CTCF tethers an insulator to subnuclear sites, suggesting shared insulator mechanisms across species | Q28242132 |
| | Control of cell identity genes occurs in insulated neighborhoods in mammalian chromosomes | Q28249527 |
| | Topological domains in mammalian genomes identified by analysis of chromatin interactions | Q28264221 |
| | Wapl is an essential regulator of chromatin structure and chromosome segregation | Q28585430 |
| | CTCF mediates long-range chromatin looping and local histone modification in the beta-globin locus | Q28590210 |
| | Spatial partitioning of the regulatory landscape of the X-inactivation centre | Q29614999 |
| | A 3D map of the human genome at kilobase resolution reveals principles of chromatin looping | Q29615814 |
| | Oncogene-induced senescence is a DNA damage response triggered by DNA hyper-replication | Q29617915 |
| | Beyond co-localization: inferring spatial interactions between sub-cellular structures from microscopy images | Q30495968 |
| | CTCF regulates the human p53 gene through direct interaction with its natural antisense transcript, Wrap53. | Q33588115 |
| | The Cohesin Release Factor WAPL Restricts Chromatin Loop Extension | Q33649701 |
| | Organization of the mitotic chromosome | Q33693950 |
| | CTCF and cohesin regulate chromatin loop stability with distinct dynamics | Q33732376 |
| | Cotranslational folding increases GFP folding yield | Q33767764 |
| | Revealing the high-resolution three-dimensional network of chromatin and interchromatin space: a novel electron-microscopic approach to reconstructing nuclear architecture | Q35001224 |
| | A general method to improve fluorophores for live-cell and single-molecule microscopy | Q35130677 |
| | Probing protein heterogeneity in the plasma membrane using PALM and pair correlation analysis | Q36103862 |
| | Crystal Structure of a Transcribing RNA Polymerase II Complex Reveals a Complete Transcription Bubble | Q36274934 |
| | Chromatin extrusion explains key features of loop and domain formation in wild-type and engineered genomes | Q36331962 |
| | Self-organization of domain structures by DNA-loop-extruding enzymes | Q36478028 |
| | Formation of Chromosomal Domains by Loop Extrusion. | Q36957773 |
| | Releasing Activity Disengages Cohesin's Smc3/Scc1 Interface in a Process Blocked by Acetylation. | Q38655683 |
| | Irreversible APC(Cdh1) Inactivation Underlies the Point of No Return for Cell-Cycle Entry. | Q38760436 |
| | Targeted Degradation of CTCF Decouples Local Insulation of Chromosome Domains from Genomic Compartmentalization. | Q38774302 |
| P921 | main subject | superresolution | Q957423 |
| P577 | publication date | 2020-10-21 | |
| P1433 | published in | Molecular Cell | Q3319468 |
| P1476 | title | Opposing Effects of Cohesin and Transcription on CTCF Organization Revealed by Super-resolution Imaging | |