scholarly article | Q13442814 |
P50 | author | Ulrich Karl Lämmli | Q13365499 |
P2093 | author name string | U. K. Laemmli | |
E. Käs | |||
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Preferential, cooperative binding of DNA topoisomerase II to scaffold-associated regions | Q33589210 | ||
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The organisation of chromatin loops: characterization of a scaffold attachment site. | Q33879560 | ||
Periodicity of DNA folding in higher order chromatin structures | Q33919425 | ||
Chromosomal loop anchorage of the kappa immunoglobulin gene occurs next to the enhancer in a region containing topoisomerase II sites | Q34161702 | ||
Organization of the higher-order chromatin loop: specific DNA attachment sites on nuclear scaffold | Q34245431 | ||
The locus of sequence-directed and protein-induced DNA bending | Q34255559 | ||
Dysfunction of chromosomal loop attachment sites: illegitimate recombination linked to matrix association regions and topoisomerase II. | Q34291465 | ||
Mammalian topoisomerase II activity is modulated by the DNA minor groove binder distamycin in simian virus 40 DNA. | Q34450649 | ||
DNA topoisomerase II is required at the time of mitosis in yeast | Q34564154 | ||
Topoisomerase II is a structural component of mitotic chromosome scaffolds. | Q34684254 | ||
Induction of nuclear envelope breakdown, chromosome condensation, and spindle formation in cell-free extracts | Q34694399 | ||
The structure of histone-depleted metaphase chromosomes | Q34741905 | ||
Nucleosome positioning as a critical determinant for the DNA cleavage sites of mammalian DNA topoisomerase II in reconstituted simian virus 40 chromatin. | Q35854016 | ||
A consensus sequence for cleavage by vertebrate DNA topoisomerase II. | Q36010020 | ||
Drosophila topoisomerase II double-strand DNA cleavage: analysis of DNA sequence homology at the cleavage site | Q36135719 | ||
Mechanism of antitumor drug action: poisoning of mammalian DNA topoisomerase II on DNA by 4'-(9-acridinylamino)-methanesulfon-m-anisidide | Q36251195 | ||
DNA topoisomerase II mutant of Saccharomyces cerevisiae: topoisomerase II is required for segregation of daughter molecules at the termination of DNA replication | Q36258619 | ||
Map of distamycin, netropsin, and actinomycin binding sites on heterogeneous DNA: DNA cleavage-inhibition patterns with methidiumpropyl-EDTA.Fe(II) | Q36311672 | ||
Protein D1 preferentially binds A + T-rich DNA in vitro and is a component of Drosophila melanogaster nucleosomes containing A + T-rich satellite DNA. | Q36322448 | ||
Developmental regulation of topoisomerase II sites and DNase I-hypersensitive sites in the chicken beta-globin locus | Q36710521 | ||
DNase I hypersensitivity is independent of endogenous topoisomerase II activity during chicken erythrocyte differentiation | Q36844631 | ||
In vivo localization of DNA topoisomerase II cleavage sites on Drosophila heat shock chromatin | Q36911574 | ||
Structure of amplified DNA in different Syrian hamster cell lines resistant to N-(phosphonacetyl)-L-aspartate | Q36980509 | ||
A protein that preferentially binds Drosophila satellite DNA | Q37314610 | ||
Transvection and long-distance gene regulation | Q37606302 | ||
In situ localization of DNA topoisomerase II, a major polypeptide component of the Drosophila nuclear matrix fraction | Q37691913 | ||
Position effect variegation in Drosophila: towards a genetics of chromatin assembly | Q38233398 | ||
Specific inhibition of DNA binding to nuclear scaffolds and histone H1 by distamycin. The role of oligo(dA).oligo(dT) tracts | Q38342812 | ||
Recent studies of DNA topoisomerases | Q39509135 | ||
Molecular arrangement and evolution of heterochromatic DNA | Q40123878 | ||
Sequence and sequence variation within the 1.688 g/cm3 satellite DNA of Drosophila melanogaster | Q40289815 | ||
Investigations into the sequence-selective binding of mithramycin and related ligands to DNA. | Q40456474 | ||
DNA structural variations produced by actinomycin and distamycin as revealed by DNAase I footprinting. | Q40463335 | ||
Chromatin fine structure of the histone gene complex of Drosophila melanogaster | Q40490049 | ||
Cloning and characterization of a complex satellite DNA from drosophila melanogaster | Q41291765 | ||
Analysis of histone messenger RNA of Drosophila melanogaster by two-dimensional gel electrophoresis | Q41368157 | ||
Isolation of type I and II DNA topoisomerase mutants from fission yeast: single and double mutants show different phenotypes in cell growth and chromatin organization | Q41577155 | ||
DNA topoisomerase II cleaves at specific sites in the 5' flanking region of c-fos proto-oncogenes in vitro | Q42572866 | ||
In vivo mapping of DNA topoisomerase II-specific cleavage sites on SV40 chromatin. | Q44075309 | ||
Topoisomerase II cleavage in chromatin | Q44310706 | ||
Chromosomal ARS and CEN elements bind specifically to the yeast nuclear scaffold | Q44716633 | ||
Double-stranded DNA cleavage/religation reaction of eukaryotic topoisomerase II: evidence for a nicked DNA intermediate | Q45387279 | ||
Single strand DNA cleavage reaction of duplex DNA by Drosophila topoisomerase II. | Q47070885 | ||
Selective arrangement of ubiquitinated and D1 protein-containing nucleosomes within the drosophila genome | Q47071279 | ||
Cleavage of DNA by mammalian DNA topoisomerase II | Q48394076 | ||
Chromosome assembly in vitro: Topoisomerase II is required for condensation | Q50801821 | ||
Drosophila topoisomerase II-DNA interactions are affected by DNA structure | Q52446622 | ||
Characterization of a topoisomerase-like activity at specific hypersensitive sites in the Drosophila histone gene cluster. | Q52453441 | ||
Novel partitioning of DNA cleavage sites for Drosophila topoisomerase II. | Q52457339 | ||
Double strand DNA cleavage by type II DNA topoisomerase from Drosophila melanogaster | Q52518950 | ||
DNA bending and its relation to nucleosome positioning. | Q54439461 | ||
Chromomycin, mithramycin, and olivomycin binding sites on heterogeneous DNA. Footprinting with methidiumpropyl-EDTA.cntdot.iron(II) | Q55062421 | ||
Higher order metaphase chromosome structure: evidence for metalloprotein interactions. | Q55062979 | ||
DNA topoisomerase II is required for condensation and separation of mitotic chromosomes in S. pombe | Q58457397 | ||
DNA topoisomerases | Q69364784 | ||
Electrophoretic separations of large DNA molecules by periodic inversion of the electric field | Q70022520 | ||
Metaphase chromosome structure. Involvement of topoisomerase II | Q70144641 | ||
Nuclear reconstitution in vitro: stages of assembly around protein-free DNA | Q70160719 | ||
Disassembly of the nucleus in mitotic extracts: membrane vesicularization, lamin disassembly, and chromosome condensation are independent processes | Q70160721 | ||
Nonintercalative antitumor drugs interfere with the breakage-reunion reaction of mammalian DNA topoisomerase II | Q72397901 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | repetitive DNA | Q424473 |
P304 | page(s) | 705-716 | |
P577 | publication date | 1992-02-01 | |
P1433 | published in | The EMBO Journal | Q1278554 |
P1476 | title | In vivo topoisomerase II cleavage of the Drosophila histone and satellite III repeats: DNA sequence and structural characteristics | |
P478 | volume | 11 |
Q34040750 | A model for chromatin opening: stimulation of topoisomerase II and restriction enzyme cleavage of chromatin by distamycin |
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Q28476505 | An integrated Drosophila model system reveals unique properties for F14512, a novel polyamine-containing anticancer drug that targets topoisomerase II |
Q36827157 | Autosomal location of a new subtype of 1.688 satellite DNA of Drosophila melanogaster |
Q38506653 | Binding of matrix attachment regions to lamin polymers involves single-stranded regions and the minor groove |
Q38507885 | Binding of sequences from the 5'- and 3'-nontranscribed spacers of the rat rDNA locus to the nucleolar matrix |
Q41962445 | Chromatin Organization by Repetitive Elements (CORE): A Genomic Principle for the Higher-Order Structure of Chromosomes |
Q35606571 | Chromatin evolution and molecular drive in speciation |
Q35128590 | Chromosomal translocations involving the MLL gene: molecular mechanisms |
Q28481619 | Cis-by-Trans regulatory divergence causes the asymmetric lethal effects of an ancestral hybrid incompatibility gene |
Q36694090 | Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene |
Q36745813 | Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting center |
Q33770453 | Covalent protein-DNA complexes at the 5' strand termini of meiosis-specific double-strand breaks in yeast |
Q40022761 | DNA cleavage within the MLL breakpoint cluster region is a specific event which occurs as part of higher-order chromatin fragmentation during the initial stages of apoptosis |
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Q35893882 | DNA topoisomerase II selects DNA cleavage sites based on reactivity rather than binding affinity. |
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Q24676660 | Dietary bioflavonoids induce cleavage in the MLL gene and may contribute to infant leukemia |
Q34806472 | Different topoisomerase II antitumor drugs direct similar specific long-range fragmentation of an amplified c-MYC gene locus in living cells and in high-salt-extracted nuclei. |
Q34676566 | Displacement of D1, HP1 and topoisomerase II from satellite heterochromatin by a specific polyamide |
Q39724816 | Distinct frequency-distributions of homopolymeric DNA tracts in different genomes |
Q34629963 | Distribution of topoisomerase II-mediated cleavage sites and relation to structural and functional landmarks in 830 kb of Drosophila DNA |
Q92354850 | Diversification and collapse of a telomere elongation mechanism |
Q34994228 | Genome-wide mapping of matrix attachment regions in Drosophila melanogaster |
Q34016369 | Genomic DNA breakpoints in AML1/RUNX1 and ETO cluster with topoisomerase II DNA cleavage and DNase I hypersensitive sites in t(8;21) leukemia. |
Q41839378 | Hairpin structures formed by alpha satellite DNA of human centromeres are cleaved by human topoisomerase IIalpha |
Q47674081 | Higher order chromatin structures in maize and Arabidopsis |
Q37622596 | Human matrix attachment regions are necessary for the establishment but not the maintenance of transgene insulation in Drosophila melanogaster |
Q33781807 | Identification of a class of chromatin boundary elements |
Q34764322 | Identification of a novel "chromosome scaffold" protein that associates with Tec elements undergoing en masse elimination in Euplotes crassus |
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Q33888626 | In vivo analysis of scaffold-associated regions in Drosophila: a synthetic high-affinity SAR binding protein suppresses position effect variegation |
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Q38507546 | Isolation of matrices from maize leaf nuclei: identification of a matrix-binding site adjacent to the Adh1 gene |
Q39584139 | Loss of drug-stimulated topoisomerase II DNA breaks in living cells is different at two unrelated loci |
Q34189725 | Maintenance of a functional higher order chromatin structure: The role of the nuclear matrix in normal and disease states. |
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Q37218253 | Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17 |
Q56899481 | New nucleotide sequence data on the EMBL File Server |
Q40416660 | Nucleosomal DNA sequence database |
Q35221459 | Nucleotide-resolution mapping of topoisomerase-mediated and apoptotic DNA strand scissions at or near an MLL translocation hotspot |
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Q34057694 | SAR-dependent mobilization of histone H1 by HMG-I/Y in vitro: HMG-I/Y is enriched in H1-depleted chromatin |
Q37207512 | SUMO modification of DNA topoisomerase II: trying to get a CENse of it all |
Q28368229 | Selective inhibition of topoisomerases from Pneumocystis carinii compared with that of topoisomerases from mammalian cells |
Q40789703 | Sequence non-specific double-strand breaks and interhomolog interactions prior to double-strand break formation at a meiotic recombination hot spot in yeast |
Q37119617 | Sequencing human-gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites |
Q35656363 | Sex Differences in Drosophila melanogaster Heterochromatin Are Regulated by Non-Sex Specific Factors |
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Q35117867 | Structure-specific DNA-binding proteins as the foundation for three-dimensional chromatin organization |
Q36739019 | Study of the cell cycle-dependent assembly of the DNA pre-replication centres in Xenopus egg extracts. |
Q34300558 | The AT-hook protein D1 is essential for Drosophila melanogaster development and is implicated in position-effect variegation |
Q42214954 | The C-terminal domain of Saccharomyces cerevisiae DNA topoisomerase II. |
Q34394858 | The analysis of mutant alleles of different strength reveals multiple functions of topoisomerase 2 in regulation of Drosophila chromosome structure. |
Q24532883 | The novel SAR-binding domain of scaffold attachment factor A (SAF-A) is a target in apoptotic nuclear breakdown. |
Q40789437 | The nucleotide mapping of DNA double-strand breaks at the CYS3 initiation site of meiotic recombination in Saccharomyces cerevisiae |
Q38320271 | The sequence-specific nuclear matrix binding factor F6 is a chicken GATA-like protein |
Q42135175 | The structure of an endogenous Drosophila centromere reveals the prevalence of tandemly repeated sequences able to form i-motifs |
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