High-mobility group 1/2 proteins are essential for initiating rolling-circle-type DNA replication at a parvovirus hairpin origin.
about
HMG2 interacts with the nucleosome assembly protein SET and is a target of the cytotoxic T-lymphocyte protease granzyme AEvolutionary dynamics of viral attenuationPossible active origin of replication in the double stranded extended form of the left terminus of LuIII and its implication on the replication model of the parvovirus.Recombination in eukaryotic single stranded DNA virusesRoles of adeno-associated virus Rep protein and human chromosome 19 in site-specific recombinationDNA unwinding functions of minute virus of mice NS1 protein are modulated specifically by the lambda isoform of protein kinase C.Neoplastic transformation-associated stimulation of the in vitro resolution of concatemer junction fragments from minute virus of mice DNARegulation of DNA-dependent activities by the functional motifs of the high-mobility-group chromosomal proteins.Genome packaging sense is controlled by the efficiency of the nick site in the right-end replication origin of parvoviruses minute virus of mice and LuIIITwo widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin.H-1 parvovirus-associated replication bodies: a distinct virus-induced nuclear structure.Factors affecting the terminal resolution site endonuclease, helicase, and ATPase activities of adeno-associated virus type 2 Rep proteinsRep-mediated nicking of the adeno-associated virus origin requires two biochemical activities, DNA helicase activity and transesterification.Effect of ATP binding and hydrolysis on dynamics of canine parvovirus NS1In vivo accumulation of cyclin A and cellular replication factors in autonomous parvovirus minute virus of mice-associated replication bodies.Initiation of minute virus of mice DNA replication is regulated at the level of origin unwinding by atypical protein kinase C phosphorylation of NS1.Minute virus of mice initiator protein NS1 and a host KDWK family transcription factor must form a precise ternary complex with origin DNA for nicking to occur.NS1- and minute virus of mice-induced cell cycle arrest: involvement of p53 and p21(cip1)Detection of head-to-tail DNA sequences of human bocavirus in clinical samplesHMGB1 in health and disease.Resolution of parvovirus dimer junctions proceeds through a novel heterocruciform intermediateNovel PKCeta is required to activate replicative functions of the major nonstructural protein NS1 of minute virus of mice.Reverse genetic system for the analysis of parvovirus telomeres reveals interactions between transcription factor binding sites in the hairpin stemTumor Selectivity of Oncolytic Parvoviruses: From in vitro and Animal Models to Cancer Patients.Structures of minute virus of mice replication initiator protein N-terminal domain: Insights into DNA nicking and origin bindingMolecular characterization of infectious clones of the minute virus of canines reveals unique features of bocaviruses.Human HMGB1 directly facilitates interactions between nucleotide excision repair proteins on triplex-directed psoralen interstrand crosslinksMutations in DNA binding and transactivation domains affect the dynamics of parvovirus NS1 protein.A heterogeneous nuclear ribonucleoprotein A/B-related protein binds to single-stranded DNA near the 5' end or within the genome of feline parvovirus and can modify virus replication.Promoter-Targeted Histone Acetylation of Chromatinized Parvoviral Genome Is Essential for the Progress of Infection.Segregation of a single outboard left-end origin is essential for the viability of parvovirus minute virus of mice.Genome replication and postencapsidation functions mapping to the nonstructural gene restrict the host range of a murine parvovirus in human cells.Protoparvovirus Knocking at the Nuclear Door.Induction of high mobility group box-1 in vitro and in vivo by respiratory syncytial virus.
P2860
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P2860
High-mobility group 1/2 proteins are essential for initiating rolling-circle-type DNA replication at a parvovirus hairpin origin.
description
1998 nî lūn-bûn
@nan
1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
High-mobility group 1/2 protei ...... t a parvovirus hairpin origin.
@ast
High-mobility group 1/2 protei ...... t a parvovirus hairpin origin.
@en
type
label
High-mobility group 1/2 protei ...... t a parvovirus hairpin origin.
@ast
High-mobility group 1/2 protei ...... t a parvovirus hairpin origin.
@en
prefLabel
High-mobility group 1/2 protei ...... t a parvovirus hairpin origin.
@ast
High-mobility group 1/2 protei ...... t a parvovirus hairpin origin.
@en
P2860
P1433
P1476
High-mobility group 1/2 protei ...... at a parvovirus hairpin origin
@en
P2093
P Tattersall
S F Cotmore
P2860
P304
P577
1998-11-01T00:00:00Z