| P2093 | author name string | Hongtao Yu | |
| | Yoori Kim | |
| P2860 | cites work | Human Scc4 is required for cohesin binding to chromatin, sister-chromatid cohesion, and mitotic progression | Q24336136 |
| | Cohesins: chromosomal proteins that prevent premature separation of sister chromatids | Q27934146 |
| | Comprehensive mapping of long-range interactions reveals folding principles of the human genome | Q28131819 |
| | Chromosomal cohesin forms a ring | Q28185991 |
| | CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease | Q28214592 |
| | Topological domains in mammalian genomes identified by analysis of chromatin interactions | Q28264221 |
| | Chromatin compaction protects genomic DNA from radiation damage | Q28534299 |
| | Wapl is an essential regulator of chromatin structure and chromosome segregation | Q28585430 |
| | Cohesin mediates transcriptional insulation by CCCTC-binding factor | Q29618130 |
| | Analysis of cryo-electron microscopy images does not support the existence of 30-nm chromatin fibers in mitotic chromosomes in situ | Q30485080 |
| | Human mitotic chromosomes consist predominantly of irregularly folded nucleosome fibres without a 30-nm chromatin structure | Q30512823 |
| | Intermingling of chromosome territories in interphase suggests role in translocations and transcription-dependent associations | Q33240304 |
| | The Cohesin Release Factor WAPL Restricts Chromatin Loop Extension | Q33649701 |
| | Chromosome territories | Q33693822 |
| | CTCF and cohesin regulate chromatin loop stability with distinct dynamics | Q33732376 |
| | Nonspecifically bound proteins spin while diffusing along DNA. | Q33929106 |
| | Open and closed domains in the mouse genome are configured as 10-nm chromatin fibres | Q34417217 |
| | Electron microscopic and biochemical evidence that chromatin structure is a repeating unit | Q34513851 |
| | Chromatin architecture reorganization during stem cell differentiation. | Q35889947 |
| | In vitro loading of human cohesin on DNA by the human Scc2-Scc4 loader complex | Q36066244 |
| | 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 |
| | Histone modifications for human epigenome analysis | Q38112246 |
| | The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells. | Q38494604 |
| | Genetic Tailors: CTCF and Cohesin Shape the Genome During Evolution. | Q38600010 |
| | CTCF Binding Polarity Determines Chromatin Looping. | Q38822699 |
| | Biomolecular condensates: organizers of cellular biochemistry | Q39146409 |
| | Live-cell imaging reveals a stable cohesin-chromatin interaction after but not before DNA replication | Q40247003 |
| | Hi-C 2.0: An optimized Hi-C procedure for high-resolution genome-wide mapping of chromosome conformation. | Q40463215 |
| | Timing facilitated site transfer of an enzyme on DNA | Q40531695 |
| | Chromosome territories reposition during DNA damage-repair response | Q40868345 |
| | Single-Molecule Imaging Reveals a Collapsed Conformational State for DNA-Bound Cohesin | Q40994875 |
| | Synthetic lethality between the cohesin subunits STAG1 and STAG2 in diverse cancer contexts | Q41155792 |
| | Orientation and repositioning of chromosomes correlate with cell geometry-dependent gene expression | Q41230108 |
| | Chromosome intermingling-the physical basis of chromosome organization in differentiated cells | Q41694050 |
| | Comparative Hi-C reveals that CTCF underlies evolution of chromosomal domain architecture | Q42165706 |
| | Rapid movement and transcriptional re-localization of human cohesin on DNA | Q42348483 |
| | Structural Basis for a Safety-Belt Mechanism That Anchors Condensin to Chromosomes. | Q42657177 |
| | Actin cytoskeleton differentially alters the dynamics of lamin A, HP1α and H2B core histone proteins to remodel chromatin condensation state in living cells | Q42823083 |
| | ATP hydrolysis is required for cohesin's association with chromosomes | Q44653969 |
| | Individual interphase chromosome domains revealed by in situ hybridization | Q44890622 |
| | ChromEMT: Visualizing 3D chromatin structure and compaction in interphase and mitotic cells | Q45235642 |
| | Ten principles of heterochromatin formation and function. | Q46162198 |
| | Chromatin structure influences the sensitivity of DNA to gamma-radiation | Q46427208 |
| | Two independent modes of chromatin organization revealed by cohesin removal | Q47035974 |
| | The 10-nm chromatin fiber and its relationship to interphase chromosome organization | Q47269443 |
| | Spatial organization of chromosome territories in the interphase nucleus of trisomy 21 cells | Q48120933 |
| | Chromosome territory relocation paradigm during DNA damage response: Some insights from molecular biology to physics. | Q48236249 |
| | Establishing and dissolving cohesion during the vertebrate cell cycle | Q50046814 |
| | Real-time imaging of DNA loop extrusion by condensin. | Q52374532 |
| | Cytoskeletal control of nuclear morphology and chromatin organization | Q52780036 |
| | Forces driving the three-dimensional folding of eukaryotic genomes | Q56793669 |
| | Towards a Unified Model of SMC Complex Function | Q58609851 |
| | Gain of CTCF-Anchored Chromatin Loops Marks the Exit from Naive Pluripotency | Q58615807 |
| | Chromatin organization by an interplay of loop extrusion and compartmental segregation | Q64123945 |
| | Absolute quantification of cohesin, CTCF and their regulators in human cells | Q83232109 |
| | Random Motion of Chromatin Is Influenced by Lamin A Interconnections | Q88667680 |
| | Organization of Chromatin by Intrinsic and Regulated Phase Separation | Q90204625 |
| | Histone Modifications Regulate Chromatin Compartmentalization by Contributing to a Phase Separation Mechanism | Q90205185 |
| | Nuclear condensates of the Polycomb protein chromobox 2 (CBX2) assemble through phase separation | Q90258440 |
| | Cohesion and cohesin-dependent chromatin organization | Q90451666 |
| | Chromosome territories and the global regulation of the genome | Q91140229 |
| | DNA loop extrusion by human cohesin | Q91384775 |
| | Human cohesin compacts DNA by loop extrusion | Q91525048 |
| | The Energetics and Physiological Impact of Cohesin Extrusion | Q91634085 |
| | Mechanisms and Functions of Chromosome Compartmentalization | Q92081056 |
| | Loop formation by SMC complexes: turning heads, bending elbows, and fixed anchors | Q92160394 |
| | The structural basis for cohesin-CTCF-anchored loops | Q92439389 |
| | Heterochromatin drives compartmentalization of inverted and conventional nuclei | Q92548360 |
| | Phase separation of Polycomb-repressive complex 1 is governed by a charged disordered region of CBX2 | Q92571882 |
| | CTCF mediates chromatin looping via N-terminal domain-dependent cohesin retention | Q92642154 |
| | The role of 3D genome organization in development and cell differentiation | Q92734276 |
| | Cohesin Disrupts Polycomb-Dependent Chromosome Interactions in Embryonic Stem Cells | Q92851887 |
| | Specific Contributions of Cohesin-SA1 and Cohesin-SA2 to TADs and Polycomb Domains in Embryonic Stem Cells | Q92877885 |
| P577 | publication date | 2020-12-02 | |
| P1433 | published in | Experimental and Molecular Medicine | Q15758292 |
| P1476 | title | Shaping of the 3D genome by the ATPase machine cohesin | |