Dysfunction of chromosomal loop attachment sites: illegitimate recombination linked to matrix association regions and topoisomerase II.
about
Characterization of SAF-A, a novel nuclear DNA binding protein from HeLa cells with high affinity for nuclear matrix/scaffold attachment DNA elementsIsolation of cDNA clones encoding the beta isozyme of human DNA topoisomerase II and localisation of the gene to chromosome 3p24Human cells express two differentially spliced forms of topoisomerase II beta mRNADiversity of genomic breakpoints in TFG-ALK translocations in anaplastic large cell lymphomas: identification of a new TFG-ALK(XL) chimeric gene with transforming activityChromosome translocation based on illegitimate recombination in human tumorsPossible role of DNA topoisomerase II on transcription of the homeobox gene Hox-2.1 in F9 embryonal carcinoma cellsA comparative study of S/MAR prediction toolsRelated individuals with different androgen receptor gene deletions.Tandem chromosomal duplications: role of REP sequences in the recombination event at the join-point.Eukaryotic topoisomerases recognize nucleic acid topology by preferentially interacting with DNA crossoversIn vivo topoisomerase II cleavage of the Drosophila histone and satellite III repeats: DNA sequence and structural characteristicsChromosomal illegitimate recombination in mammalian cells is associated with intrinsically bent DNA elements.Genomic DNA breakpoints in AML1/RUNX1 and ETO cluster with topoisomerase II DNA cleavage and DNase I hypersensitive sites in t(8;21) leukemia.Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination.A nuclear matrix-specific factor that binds a specific segment of the negative regulatory element (NRE) of HIV-1 LTR and inhibits NF-kappa(B) activityThe recognition of DNA cleavage sites by porcine spleen topoisomerase IIStimulation of Tat-independent transcriptional processivity from the HIV-1 LTR promoter by matrix attachment regions.Sequence requirements for mammalian topoisomerase II mediated DNA cleavage stimulated by an ellipticine derivative.An overview of the lagomorph immune system and its genetic diversity.Nuclear matrix attachment occurs in several regions of the IgH locus.Nucleotide sequence of the intron of the germline human kappa immunoglobulin gene connecting the J and C regions reveals a matrix association region (MAR) next to the enhancerIdentification of VCR, a repeated sequence associated with a locus encoding a hemagglutinin in Vibrio cholerae O1Clusters of S1 nuclease-hypersensitive sites induced in vivo by DNA damageIllegitimate recombination induced by DNA double-strand breaks in a mammalian chromosome.Breakpoint junctions of chromosome 9p deletions in two human glioma cell lines.Molecular characterization of the breakpoints of an inversion fixed between Drosophila melanogaster and D. subobscura.Identification within the simian virus 40 genome of a chromosomal loop attachment site that contains topoisomerase II cleavage sitesStructural analysis of a carcinogen-induced genomic rearrangement event.Accuracy and coverage assessment of Oryctolagus cuniculus (rabbit) genes encoding immunoglobulins in the whole genome sequence assembly (OryCun2.0) and localization of the IGH locus to chromosome 20.Topoisomerase II: a fitted mechanism for the chromatin landscape.MAR-Mediated transgene integration into permissive chromatin and increased expression by recombination pathway engineeringPrecise localization of the alpha-globin gene cluster within one of the 20- to 300-kilobase DNA fragments released by cleavage of chicken chromosomal DNA at topoisomerase II sites in vivo: evidence that the fragments are DNA loops or domains.Nucleolin is a matrix attachment region DNA-binding protein that specifically recognizes a region with high base-unpairing potential.In vitro evolution of preferred topoisomerase II DNA cleavage sites.Breakpoints of t(4;11) translocations in the human MLL and AF4 genes in ALL patients are preferentially clustered outside of high-affinity matrix attachment regions.Matrix attachment regions and transcription units in a polygenic mammalian locus overlapping two isochores.Interaction of the nuclear matrix-associated region (MAR)-binding proteins, SATB1 and CDP/Cux, with a MAR element (L2a) in an upstream regulatory region of the mouse CD8a gene.Mutually exclusive interaction of a novel matrix attachment region binding protein and the NF-muNR enhancer repressor. Implications for regulation of immunoglobulin heavy chain expression.The RAD5 gene product is involved in the avoidance of non-homologous end-joining of DNA double strand breaks in the yeast Saccharomyces cerevisiae.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
P2860
Q24337072-DB274B20-30BE-428E-A082-320BD8106D26Q24629023-EE8BC15E-F3B6-4C07-87DF-3802B6526E22Q24632777-4892B787-96CB-4D92-B5BF-3E6BDD2E2E6FQ24669845-E28779C0-9B8A-401A-9397-42ADFDD6F96FQ24678527-5F60A128-8F3C-4CC8-89A8-80C8357AF761Q28509477-673BAA40-2067-47BF-AC4B-70539F71F293Q33276687-36A9201E-ADB7-492B-9C31-2547C8399F98Q33893888-8D2A1944-4060-45D7-94E5-3B4C4790D196Q33918822-C53E9870-DF42-467D-A9A2-911FA553559BQ33923932-969F81B0-1F77-4CA1-9246-DDEFA5F7F056Q33937443-D4D69229-885A-420A-9839-5EA1E590DA80Q33938661-2183390D-BF81-4B82-84C1-301A4025C6DAQ34016369-D665B57B-77A2-4661-ABFA-420EAACE0C66Q34137518-0B4BD45B-A8D7-4ECE-847A-AA905F9079DCQ34597244-083CB852-3265-403E-A9A9-E54605BC44C4Q35013645-610ACFC3-41D3-4F7D-8A2B-9C81D541F609Q35107931-49E4B17B-9919-41BC-BFE3-01475E989D4FQ35765484-4F580A0F-35B4-4E65-BCE5-2E54497AC879Q35785529-3D36C387-8295-416A-BC32-7AC98854F35CQ35839296-A21EC5B0-3138-4B39-99A7-261E69B241E4Q35928971-C75EF9C7-20C5-46E4-93F4-C86BDD982774Q35974812-B2C77070-F31F-4863-988C-86CAF8901A18Q36572117-919CC6D7-0B3E-41BF-914E-A4028DC08B9BQ36664862-EE3087F7-37DC-45F6-B34B-654FAE367665Q36670180-82D94244-0704-425C-ACBF-2AB1204C2A89Q36698911-6A57A7D0-4B51-44CB-B02C-AF289EF97CBDQ36799774-59863F3E-F02A-4898-BE7D-F3AB7E176A02Q36811206-237C8901-75A1-4630-94E8-A7FD462E539BQ37191641-F4574578-829D-490E-9229-6B98D2A52455Q37342441-1B3CBCEB-03EF-49C6-B4EF-955EEC111BDBQ37560972-A5D80C32-AD41-4165-A13A-786DFD316FDDQ37598605-B94633DC-7821-45C9-9390-E62322AA03EAQ38300450-298EA203-8AA1-4F30-B727-647FB90DD4DEQ38328203-5FBF666E-09D9-4705-BCAF-F9100587A7D4Q38497781-32CBEC01-2DAA-4F9D-9C7D-7B66E8072F09Q38502337-A20E9FD7-9DB3-40F1-A954-45E015FAB9FDQ38502576-0793E44E-4FB1-4754-B0E7-EA9F8E1E9E55Q38505126-D367C2E4-D3A6-4D8B-B701-C13D17120822Q39719243-80FCCD01-2ACB-4A83-A675-7312B41A4BB5Q40022761-AACEAAB0-E797-46D1-9CFC-A51A648EC051
P2860
Dysfunction of chromosomal loop attachment sites: illegitimate recombination linked to matrix association regions and topoisomerase II.
description
1989 nî lūn-bûn
@nan
1989 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@ast
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@en
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@nl
type
label
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@ast
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@en
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@nl
prefLabel
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@ast
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@en
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@nl
P2093
P2860
P356
P1476
Dysfunction of chromosomal loo ...... regions and topoisomerase II.
@en
P2093
A O Sperry
V C Blasquez
W T Garrard
P2860
P304
P356
10.1073/PNAS.86.14.5497
P407
P577
1989-07-01T00:00:00Z