scholarly article | Q13442814 |
P2093 | author name string | J. Hurwitz | |
P. A. Bullock | |||
Y. S. Seo | |||
P2860 | cites work | DNA helicase activity of SV40 large tumor antigen | Q24531720 |
A third essential DNA polymerase in S. cerevisiae | Q28241341 | ||
The cell-cycle regulated proliferating cell nuclear antigen is required for SV40 DNA replication in vitro | Q28282848 | ||
Mechanism of elongation of primed DNA by DNA polymerase delta, proliferating cell nuclear antigen, and activator 1 | Q28610318 | ||
Purification and characterization of replication protein A, a cellular protein required for in vitro replication of simian virus 40 DNA. | Q33566767 | ||
Multiple replication factors augment DNA synthesis by the two eukaryotic DNA polymerases, alpha and delta | Q33609947 | ||
An inhibitor of the in vitro elongation reaction of simian virus 40 DNA replication is overcome by proliferating-cell nuclear antigen. | Q33684799 | ||
Simian virus 40 (SV40) large tumor antigen causes stepwise changes in SV40 origin structure during initiation of DNA replication | Q33864964 | ||
Initiation of simian virus 40 DNA replication in vitro: pulse-chase experiments identify the first labeled species as topologically unwound | Q33865002 | ||
T antigen and template requirements for SV40 DNA replication in vitro | Q33931898 | ||
Studies on the DNA elongation inhibitor and its proliferating cell nuclear antigen-dependent control in simian virus 40 DNA replication in vitro | Q34285138 | ||
Synthesis of DNA containing the simian virus 40 origin of replication by the combined action of DNA polymerases alpha and delta | Q34306463 | ||
Simian virus 40 large tumor antigen requires three core replication origin domains for DNA unwinding and replication in vitro | Q34369024 | ||
ATP-dependent formation of a specialized nucleoprotein structure by simian virus 40 (SV40) large tumor antigen at the SV40 replication origin. | Q34377926 | ||
Simian virus 40 (SV40) DNA replication: SV40 large T antigen unwinds DNA containing the SV40 origin of replication. | Q34583809 | ||
Roles of DNA topoisomerases in simian virus 40 DNA replication in vitro | Q34595603 | ||
Replication of simian virus 40 origin-containing DNA in vitro with purified proteins | Q34607996 | ||
Initiation of simian virus 40 DNA replication in vitro: large-tumor-antigen- and origin-dependent unwinding of the template | Q34626874 | ||
Unique primed start of phage phi X174 DNA replication and mobility of the primosome in a direction opposite chain synthesis | Q35299043 | ||
The distribution and properties of RNA primed initiation sites of DNA synthesis at the replication origin of Escherichia coli chromosome | Q35561525 | ||
Role of DNA polymerase alpha and DNA primase in simian virus 40 DNA replication in vitro | Q35602324 | ||
Simian virus 40 DNA replication in vitro: study of events preceding elongation of chains | Q35613480 | ||
The 245 base-pairoriCsequence of theE. colichromosome directs bidirectional replication at an adjacent region | Q35674986 | ||
Cellular factors required for multiple stages of SV40 DNA replication in vitro | Q35981213 | ||
Localized melting and structural changes in the SV40 origin of replication induced by T-antigen. | Q35989217 | ||
Territorial limits and functional anatomy of the simian virus 40 replication origin | Q36277048 | ||
Characterization of proliferating cell nuclear antigen recognized by autoantibodies in lupus sera | Q36348625 | ||
Formation of an RNA primer for initiation of replication of ColE1 DNA by ribonuclease H | Q36386816 | ||
Physical mapping of primary and secondary origins of bacteriophage T7 DNA replication | Q36388479 | ||
Construction and analysis of simian virus 40 origins defective in tumor antigen binding and DNA replication | Q36414498 | ||
Simian virus 40 DNA replication in vitro: identification of multiple stages of initiation | Q36760381 | ||
Mapping in vivo topoisomerase I sites on simian virus 40 DNA: asymmetric distribution of sites on replicating molecules | Q36765809 | ||
Purification of a cellular replication factor, RF-C, that is required for coordinated synthesis of leading and lagging strands during simian virus 40 DNA replication in vitro | Q36766121 | ||
Three domains in the simian virus 40 core origin orchestrate the binding, melting, and DNA helicase activities of T antigen | Q36800201 | ||
Topoisomerase I sites cluster asymmetrically at the ends of the simian virus 40 core origin of replication | Q36832169 | ||
Expression and complex formation of simian virus 40 large T antigen and mouse p53 in insect cells | Q36872197 | ||
An Okazaki piece of simian virus 40 may be synthesized by ligation of shorter precursor chains | Q36878892 | ||
The T-antigen-binding domain of the simian virus 40 core origin of replication | Q36889666 | ||
Replication and supercoiling of simian virus 40 DNA in cell extracts from human cells | Q36892208 | ||
Initiation of simian virus 40 DNA replication in vitro: aphidicolin causes accumulation of early-replicating intermediates and allows determination of the initial direction of DNA synthesis | Q36899181 | ||
Purification of simian virus 40 large T antigen by immunoaffinity chromatography | Q36899874 | ||
ATP stimulates the binding of simian virus 40 (SV40) large tumor antigen to the SV40 origin of replication | Q37479573 | ||
Bidirectional replication of Simian Virus 40 DNA | Q37498375 | ||
In vitro replication of duplex circular DNA containing the simian virus 40 DNA origin site | Q37529881 | ||
Simian virus 40 DNA replication in vitro | Q37576758 | ||
Multiple initiation sites of DNA replication flanking the origin region of lambda dv genome | Q37578718 | ||
Binding and unwinding--how T antigen engages the SV40 origin of DNA replication | Q37870911 | ||
Animal virus DNA replication | Q38286735 | ||
Initiation of eukaryotic DNA replication in vitro | Q38311464 | ||
Autoantibody to a nuclear antigen in proliferating cells | Q39634451 | ||
Two DNA polymerases may be required for synthesis of the lagging DNA strand of simian virus 40. | Q40105722 | ||
The binding site on SV40 DNA for a T antigen-related protein | Q40122756 | ||
Replication of polyoma DNA in isolated nuclei. Synthesis and distribution of initiator RNA | Q40178765 | ||
RNA-primed initiation sites of DNA replication in the origin region of bacteriophage lambda genome | Q40553906 | ||
An auxiliary protein for DNA polymerase-delta from fetal calf thymus | Q43717148 | ||
The unwinding of duplex regions in DNA by the simian virus 40 large tumor antigen-associated DNA helicase activity | Q44313808 | ||
Coordinated leading and lagging strand synthesis during SV40 DNA replication in vitro requires PCNA. | Q45081970 | ||
Simian virus 40 large T antigen DNA helicase. Characterization of the ATPase-dependent DNA unwinding activity and its substrate requirements | Q45842219 | ||
Unwinding of duplex DNA from the SV40 origin of replication by T antigen | Q46566766 | ||
Initiation of SV40 DNA replication in vivo: Location and structure of 5′ ends of DNA synthesized in the ori region | Q48405329 | ||
ATP-dependent assembly of double hexamers of SV40 T antigen at the viral origin of DNA replication | Q59098660 | ||
An immunoaffinity purification procedure for SV40 large T antigen | Q64380345 | ||
Complete enzymatic synthesis of DNA containing the SV40 origin of replication | Q69844485 | ||
Identification of multiple cellular factors required for SV40 replication in vitro | Q69914693 | ||
Replication of pBR322 DNA in vitro with purified proteins. Requirement for topoisomerase I in the maintenance of template specificity | Q70093088 | ||
The initiation of SV40 DNA synthesis is not unique to the replication origin | Q72855548 | ||
Sequential initiation of lagging and leading strand synthesis by two different polymerase complexes at the SV40 DNA replication origin | Q95816567 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell biology | Q7141 |
DNA replication | Q130996 | ||
SV40 | Q734305 | ||
P304 | page(s) | 2350-2361 | |
P577 | publication date | 1991-05-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Initiation of simian virus 40 DNA synthesis in vitro | |
P478 | volume | 11 |
Q37236627 | A 5' to 3' exonuclease functionally interacts with calf DNA polymerase epsilon |
Q38342898 | A cell-free replication system for human polyomavirus JC DNA |
Q89709677 | A model for the formation of the duplicated enhancers found in polyomavirus regulatory regions |
Q35185890 | Analyses of the interaction between the origin binding domain from simian virus 40 T antigen and single-stranded DNA provide insights into DNA unwinding and initiation of DNA replication |
Q24319018 | Anatomy of a DNA replication fork revealed by reconstitution of SV40 DNA replication in vitro |
Q28610293 | Assembly of simian virus 40 Okazaki pieces from DNA primers is reversibly arrested by ATP depletion |
Q42410390 | Bypass of a protein barrier by a replicative DNA helicase. |
Q35852375 | Cellular factors required for papillomavirus DNA replication. |
Q33583906 | Characterization of RNA primers synthesized by the human breast cancer cell DNA synthesome |
Q72055334 | Cofractionation of hela cell replication proteins with Ors‐binding activity |
Q40455939 | DNA Replication: A familiar ring to DNA polymerase processivity |
Q27929803 | DNA polymerase II, the probable homolog of mammalian DNA polymerase epsilon, replicates chromosomal DNA in the yeast Saccharomyces cerevisiae |
Q35849678 | DNA polymerase epsilon may be dispensable for SV40- but not cellular-DNA replication. |
Q41908115 | DNA polymerases delta and epsilon are required for chromosomal replication in Saccharomyces cerevisiae |
Q36566480 | DNA synthesis generally initiates outside the simian virus 40 core origin in vitro |
Q36659454 | De novo synthesis of budding yeast DNA polymerase alpha and POL1 transcription at the G1/S boundary are not required for entrance into S phase |
Q35805068 | Did an early version of the eukaryal replisome enable the emergence of chromatin? |
Q48845921 | Direct Visualization of RNA-DNA Primer Removal from Okazaki Fragments Provides Support for Flap Cleavage and Exonucleolytic Pathways in Eukaryotic Cells. |
Q24292826 | Distinctive activities of DNA polymerases during human DNA replication |
Q37687363 | Dna2 on the road to Okazaki fragment processing and genome stability in eukaryotes |
Q24798598 | Enzymatic properties of the Caenorhabditis elegans Dna2 endonuclease/helicase and a species-specific interaction between RPA and Dna2 |
Q33594119 | Error-free replicative bypass of (6-4) photoproducts by DNA polymerase zeta in mouse and human cells |
Q39182130 | Eukaryotic DNA Replication Fork. |
Q73396982 | Eukaryotic DNA replication: a model for a fixed double replisome |
Q39874875 | Evidence that replication of human neurotropic JC virus DNA in glial cells is regulated by the sequence-specific single-stranded DNA-binding protein Pur alpha |
Q37483099 | Genetic and biochemical analyses of Pfh1 DNA helicase function in fission yeast |
Q36250593 | Genetic control of translesion synthesis on leading and lagging DNA strands in plasmids derived from Epstein-Barr virus in human cells |
Q41344493 | Genetic evidence that aphidicolin inhibits in vivo DNA synthesis in Chinese hamster ovary cells |
Q37416480 | Highly error-free role of DNA polymerase eta in the replicative bypass of UV-induced pyrimidine dimers in mouse and human cells |
Q37190833 | How many pols does it take to replicate nuclear DNA? |
Q36693564 | Human Xeroderma Pigmentosum Group A Protein Interacts with Human Replication Protein A and Inhibits DNA Replication |
Q33842984 | In the simian virus 40 in vitro replication system, start site selection by the polymerase alpha-primase complex is not significantly altered by changes in the concentration of ribonucleotides |
Q40019439 | In vitro analysis of SV40 DNA replication |
Q44973230 | Insights into the oligomeric states, conformational changes, and helicase activities of SV40 large tumor antigen |
Q39776560 | Large T antigen promotes JC virus replication in G2-arrested cells by inducing ATM- and ATR-mediated G2 checkpoint signaling |
Q36662300 | Mapping initiation sites for simian virus 40 DNA synthesis events in vitro |
Q61446988 | Mechanism of Bidirectional Leading-Strand Synthesis Establishment at Eukaryotic DNA Replication Origins |
Q37483304 | Modulation of mutagenesis in eukaryotes by DNA replication fork dynamics and quality of nucleotide pools |
Q24619923 | Molecular biology, epidemiology, and pathogenesis of progressive multifocal leukoencephalopathy, the JC virus-induced demyelinating disease of the human brain |
Q36651448 | Mutation of the cyclin-dependent kinase phosphorylation site in simian virus 40 (SV40) large T antigen specifically blocks SV40 origin DNA unwinding |
Q41083928 | Mutation pattern of immunoglobulin transgenes is compatible with a model of somatic hypermutation in which targeting of the mutator is linked to the direction of DNA replication |
Q71405574 | On the presence of DNA polymerase alpha in human lymphocyte nuclei and chromosomes |
Q34360447 | Peptides containing cyclin/Cdk-nuclear localization signal motifs derived from viral initiator proteins bind to DNA when unphosphorylated |
Q36682339 | Primer-DNA formation during simian virus 40 DNA replication in vitro |
Q31625778 | Protein-protein interactions of the primase subunits p58 and p48 with simian virus 40 T antigen are required for efficient primer synthesis in a cell-free system |
Q28205766 | Reconstitution of human DNA polymerase delta using recombinant baculoviruses: the p12 subunit potentiates DNA polymerizing activity of the four-subunit enzyme |
Q30718522 | Replication protein A modulates its interface with the primed DNA template during RNA-DNA primer elongation in replicating SV40 chromosomes |
Q36687824 | Roles of DNA polymerases in replication, repair, and recombination in eukaryotes. |
Q40853044 | SV40 DNA replication intermediates: analysis of drugs which target mammalian DNA replication |
Q90019146 | SV40 T antigen interactions with ssDNA and replication protein A: a regulatory role of T antigen monomers in lagging strand DNA replication |
Q34070113 | SV40 large T antigen functions in DNA replication and transformation |
Q38308533 | Species-specific functional interactions of DNA polymerase alpha-primase with simian virus 40 (SV40) T antigen require SV40 origin DNA |
Q40017972 | Species-specific replication of simian virus 40 DNA in vitro requires the p180 subunit of human DNA polymerase alpha-primase |
Q44984556 | Structure and activity associated with multiple forms of Schizosaccharomyces pombe DNA polymerase delta |
Q36811814 | Studies on the initiation of simian virus 40 replication in vitro: RNA primer synthesis and its elongation |
Q35898933 | The N-terminal side of the origin-binding domain of simian virus 40 large T antigen is involved in A/T untwisting. |
Q24321288 | The evolutionarily conserved zinc finger motif in the largest subunit of human replication protein A is required for DNA replication and mismatch repair but not for nucleotide excision repair |
Q31998506 | The middle subunit of replication protein A contacts growing RNA-DNA primers in replicating simian virus 40 chromosomes |
Q40015894 | The mouse DNA polymerase alpha-primase subunit p48 mediates species-specific replication of polyomavirus DNA in vitro |
Q31034204 | The protein components and mechanism of eukaryotic Okazaki fragment maturation |
Q31976778 | The replication protein A binding site in simian virus 40 (SV40) T antigen and its role in the initial steps of SV40 DNA replication. |
Q42467404 | The role of DNA polymerase alpha in the control of mutagenesis in Saccharomyces cerevisiae cells starved for nutrients |
Q38185572 | To peep into Pif1 helicase: multifaceted all the way from genome stability to repair-associated DNA synthesis |
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