| P50 | author | Peter König | Q41048973 |
| P2093 | author name string | David A Agard | |
| | John W Sedat | |
| | Michael B Braunfeld | |
| P2860 | cites work | Crystal structure of the nucleosome core particle at 2.8 A resolution | Q22122355 |
| | Chromosome condensation by a human condensin complex in Xenopus egg extracts | Q24290686 |
| | The structural maintenance of chromosomes (SMC) family of proteins in mammals | Q24291165 |
| | Differential contributions of condensin I and condensin II to mitotic chromosome architecture in vertebrate cells | Q24297107 |
| | EM measurements define the dimensions of the "30-nm" chromatin fiber: evidence for a compact, interdigitated structure | Q24542512 |
| | Solenoidal model for superstructure in chromatin | Q24561840 |
| | Nucleosomes, linker DNA, and linker histone form a unique structural motif that directs the higher-order folding and compaction of chromatin | Q24652372 |
| | Histone H1 is essential for mitotic chromosome architecture and segregation in Xenopus laevis egg extracts | Q24678815 |
| | Involvement of histone H1 in the organization of the nucleosome and of the salt-dependent superstructures of chromatin | Q24681606 |
| | Improved methods for building protein models in electron density maps and the location of errors in these models | Q26776980 |
| | Crystal structure of the SMC head domain: an ABC ATPase with 900 residues antiparallel coiled-coil inserted | Q27629557 |
| | UCSF Chimera--a visualization system for exploratory research and analysis | Q27860666 |
| | Condensin binding at distinct and specific chromosomal sites in the Saccharomyces cerevisiae genome | Q27930572 |
| | Structural maintenance of chromosomes protein C-terminal domains bind preferentially to DNA with secondary structure | Q27937303 |
| | Condensin and cohesin display different arm conformations with characteristic hinge angles | Q28216842 |
| | Condensins, chromosome condensation protein complexes containing XCAP-C, XCAP-E and a Xenopus homolog of the Drosophila Barren protein | Q28238784 |
| | Chromosome structure: improved immunolabeling for electron microscopy | Q28273312 |
| | Phosphorylation and activation of 13S condensin by Cdc2 in vitro | Q28285478 |
| | ELECTRON STAINS: I. Chemical Studies on the Interaction of DNA with Uranyl Salts | Q29041571 |
| | Reorganization of chromatin in Xenopus egg extracts: electron microscopic studies | Q33183235 |
| | Direct detection of linker DNA bending in defined-length oligomers of chromatin | Q33821984 |
| | Cryo-electron microscopy of vitrified chromosomes in situ. | Q33879953 |
| | Structures and interactions of the core histone tail domains | Q34187133 |
| | A model for chromosome structure during the mitotic and meiotic cell cycles | Q34237078 |
| | Assembly of chromatin fibers into metaphase chromosomes analyzed by transmission electron microscopy and scanning electron microscopy | Q34258032 |
| | Proteolysis of mitotic chromosomes induces gradual and anisotropic decondensation correlated with a reduction of elastic modulus and structural sensitivity to rarely cutting restriction enzymes | Q34298302 |
| | Automated electron microscope tomography of frozen-hydrated chromatin: the irregular three-dimensional zigzag architecture persists in compact, isolated fibers | Q39459139 |
| | Condensin but not cohesin SMC heterodimer induces DNA reannealing through protein-protein assembly | Q39758831 |
| | Deoxyribonucleic acid loop domain tertiary structure in mammalian spermatozoa | Q40819404 |
| | The distribution of topoisomerase II on mammalian chromosomes | Q41252778 |
| | Use of surface affinity enrichment and cryo-embedding to prepare in vitro reconstituted mitotic chromosomes for EM tomography | Q41627285 |
| | Histone H1 and chromatin higher-order structure | Q41661744 |
| | Modulation of the higher-order folding of chromatin by deletion of histone H3 and H4 terminal domains. | Q42982373 |
| | Nucleoplasmin remodels sperm chromatin in Xenopus egg extracts | Q43443780 |
| | Efficient supercoiling of DNA by a single condensin complex as revealed by electron spectroscopic imaging | Q44042955 |
| | A Two-Step Scaffolding Model for Mitotic Chromosome Assembly | Q44399616 |
| | Chromatin assembly | Q44405396 |
| | Multiple chromosomal populations of topoisomerase II detected in vivo by time-lapse, three-dimensional wide-field microscopy | Q46125653 |
| | Large-scale chromatin structural domains within mitotic and interphase chromosomes in vivo and in vitro | Q46871282 |
| | Toward fully automated high-resolution electron tomography | Q46892441 |
| | The mitotic chromosome is an assembly of rigid elastic axes organized by structural maintenance of chromosomes (SMC) proteins and surrounded by a soft chromatin envelope | Q47336365 |
| | Chromosome length and DNA loop size during early embryonic development of Xenopus laevis. | Q47391022 |
| | Dinucleosomes show compaction by ionic strength, consistent with bending of linker DNA. | Q47708879 |
| | Chromosome condensation in Xenopus mitotic extracts without histone H1. | Q52220944 |
| | Three-dimensional reconstruction of a human metaphase chromosome from electron micrographs. | Q52609938 |
| | Disassembly of the mammalian metaphase chromosome into its subunits: studies with ultraviolet light and repair synthesis inhibitors. | Q53531369 |
| | Radial loops and helical coils coexist in metaphase chromosomes. | Q53703047 |
| | High-order structure of metaphase chromosomes: evidence for a multiple coiling model | Q69567736 |
| | Metaphase chromosome structure. Involvement of topoisomerase II | Q70144641 |
| | Transitions between in situ and isolated chromatin | Q70501386 |
| | Subdivision of the mitotic cycle into eleven stages, on the basis of the chromosomal changes observed in mouse duodenal crypt cells stained by the DNA-specific Feulgen reaction | Q71622963 |
| | Globular and fibrous structure in barley chromosomes revealed by high-resolution scanning electron microscopy | Q73685817 |
| | Resolving the role of topoisomerase II in chromatin structure and function | Q75294399 |
| | Spatial and temporal regulation of Condensins I and II in mitotic chromosome assembly in human cells. | Q34321072 |
| | Nucleosome arrays reveal the two-start organization of the chromatin fiber | Q34371762 |
| | Mitotic chromosomes are chromatin networks without a mechanically contiguous protein scaffold | Q34386361 |
| | X-ray structure of a tetranucleosome and its implications for the chromatin fibre | Q34431881 |
| | DNA renaturation activity of the SMC complex implicated in chromosome condensation | Q34438003 |
| | ATP-dependent positive supercoiling of DNA by 13S condensin: a biochemical implication for chromosome condensation | Q34438428 |
| | 13S condensin actively reconfigures DNA by introducing global positive writhe: implications for chromosome condensation | Q34504401 |
| | The making of the mitotic chromosome: modern insights into classical questions | Q34532415 |
| | Condensin is required for nonhistone protein assembly and structural integrity of vertebrate mitotic chromosomes | Q34536233 |
| | Visualization of early chromosome condensation: a hierarchical folding, axial glue model of chromosome structure | Q34550665 |
| | Cell cycle extracts | Q34590228 |
| | A heterodimeric coiled-coil protein required for mitotic chromosome condensation in vitro | Q34725116 |
| | Mitotic chromosome condensation. | Q34737023 |
| | Phosphorylation of serine 10 in histone H3, what for? | Q35199083 |
| | From DNA structure to gene expression: mediators of nuclear compartmentalization and dynamics. | Q35217751 |
| | Dual roles of the 11S regulatory subcomplex in condensin functions | Q35359850 |
| | Intercalary heterochromatin and genetic silencing | Q35568150 |
| | Multiple roles of Condensins: a complex story. | Q35795403 |
| | Visualization of nucleosomes in thin sections by stereo electron microscopy. | Q36202003 |
| | Localization of topoisomerase II in mitotic chromosomes | Q36213345 |
| | A three-dimensional approach to mitotic chromosome structure: evidence for a complex hierarchical organization | Q36218032 |
| | Topoisomerase II does not play a scaffolding role in the organization of mitotic chromosomes assembled in Xenopus egg extracts | Q36232430 |
| | The three-dimensional architecture of chromatin in situ: electron tomography reveals fibers composed of a continuously variable zig-zag nucleosomal ribbon | Q36234105 |
| | Elasticity measurements show the existence of thin rigid cores inside mitotic chromosomes. | Q36256431 |
| | A role of topoisomerase II in linking DNA replication to chromosome condensation | Q36324263 |
| | Role of linker histone in chromatin structure and function: H1 stoichiometry and nucleosome repeat length | Q36408581 |
| | Stereoscopic scanning electron microscopy of the chromosomes in Vicia faba (broad beans). | Q36632995 |
| | Nucleosome arcs and helices | Q36638552 |
| | Topoisomerase II forms multimers in vitro: effects of metals, beta-glycerophosphate, and phosphorylation of its C-terminal domain | Q36668278 |
| | DNA changes involved in the formation of metaphase chromosomes, as observed in mouse duodenal crypt cells stained by osmium-ammine. I. New structures arise during the S phase and condense at prophase into "chromomeres," which fuse at prometaphase in | Q36670730 |
| | IVE (Image Visualization Environment): a software platform for all three-dimensional microscopy applications | Q36811607 |
| | Nucleosome positioning is determined by the (H3-H4)2 tetramer | Q37631358 |
| | Mammalian SMC3 C-terminal and coiled-coil protein domains specifically bind palindromic DNA, do not block DNA ends, and prevent DNA bending | Q38317132 |
| | Structure of nucleosome core particles of chromatin | Q38560180 |
| P433 | issue | 4 | |
| P921 | main subject | African clawed frog | Q654718 |
| | tomography | Q841267 |
| P304 | page(s) | 349-372 | |
| P577 | publication date | 2007-02-28 | |
| P1433 | published in | Chromosoma | Q15765851 |
| P1476 | title | The three-dimensional structure of in vitro reconstituted Xenopus laevis chromosomes by EM tomography | |
| P478 | volume | 116 | |