about
Continued stabilization of the nuclear higher-order structure of post-mitotic neurons in vivoInsights into the MCM functional mechanism: lessons learned from the archaeal MCM complex.The Mediator complex and transcription regulationMammalian sperm nuclear organization: resiliencies and vulnerabilitiesEfficient recombinant production in mammalian cells using a novel IR/MAR gene amplification methodNuclear scaffold attachment sites within ENCODE regions associate with actively transcribed genes.Global regulation of genome duplication in eukaryotes: an overview from the epifluorescence microscope.Determination of the in vivo structural DNA loop organization in the genomic region of the rat albumin locus by means of a topological approach.Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell linesNuclear matrix proteome analysis of Drosophila melanogasterThe chromatin remodeling factor SMARCB1 forms a complex with human cytomegalovirus proteins UL114 and UL44BRCA1-IRIS overexpression promotes formation of aggressive breast cancers.The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndromeNew centromeric component CENP-W is an RNA-associated nuclear matrix protein that interacts with nucleophosmin/B23 protein.Proteomic and protein interaction network analysis of human T lymphocytes during cell-cycle entry3D chromatin conformation correlates with replication timing and is conserved in resting cellsRecent knowledge concerning mammalian sperm chromatin organization and its potential weaknesses when facing oxidative challengeTREX1 acts in degrading damaged DNA from drug-treated tumor cells.Anchoring the genome.Memoirs of an insult: sperm as a possible source of transgenerational epimutations and genetic instability.The sperm nucleus: chromatin, RNA, and the nuclear matrix.Possible role of H1 histone in replication timing.Cell-type-specific organization of nuclear DNA into structural looped domains.Why Cortical Neurons Cannot Divide, and Why Do They Usually Die in the Attempt?The alphaherpesvirus US3/ORF66 protein kinases direct phosphorylation of the nuclear matrix protein matrin 3Structural and biophysical characterization of murine rif1 C terminus reveals high specificity for DNA cruciform structures.A structural basis for cellular senescence.DNA moves sequentially towards the nuclear matrix during DNA replication in vivo.The post-mitotic state in neurons correlates with a stable nuclear higher-order structure.The nuclear form of glutathione peroxidase 4 colocalizes and directly interacts with protamines in the nuclear matrix during mouse sperm chromatin assembly.The Set of Structural DNA-Nuclear Matrix Interactions in Neurons Is Cell-Type Specific and Rather Independent of Functional Constraints.Chronic cyclophosphamide exposure alters the profile of rat sperm nuclear matrix proteins.Dynamics of nuclear matrix proteome during embryonic development in Drosophila melanogaster.Reorganization of the DNA-nuclear matrix interactions in a 210 kb genomic region centered on c-myc after DNA replication in vivo.Nuclear Integrity but Not Topology of Mouse Sperm Chromosome is Affected by Oxidative DNA Damage
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Nuclear matrix support of DNA replication.
@ast
Nuclear matrix support of DNA replication.
@en
type
label
Nuclear matrix support of DNA replication.
@ast
Nuclear matrix support of DNA replication.
@en
prefLabel
Nuclear matrix support of DNA replication.
@ast
Nuclear matrix support of DNA replication.
@en
P2093
P356
P1476
Nuclear matrix support of DNA replication.
@en
P2093
Boyka Anachkova
V Djeliova
P2860
P304
P356
10.1002/JCB.20610
P577
2005-12-01T00:00:00Z