Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis. - Test2 - elhamkhani - TriplyDB

Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis.

Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis.

http://www.wikidata.org/entity/Q36861158

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Complementation of defective translesion synthesis and UV light sensitivity in xeroderma pigmentosum variant cells by human and mouse DNA polymerase eta UV-induced replication arrest in the xeroderma pigmentosum variant leads to DNA double-strand breaks, gamma -H2AX formation, and Mre11 relocalization Misinsertion and bypass of thymine-thymine dimers by human DNA polymerase iota Mechanisms of accurate translesion synthesis by human DNA polymerase eta Functional Role of NBS1 in Radiation Damage Response and Translesion DNA Synthesis Requirement of Nse1, a subunit of the Smc5-Smc6 complex, for Rad52-dependent postreplication repair of UV-damaged DNA in Saccharomyces cerevisiae.Yeast Rad5 protein required for postreplication repair has a DNA helicase activity specific for replication fork regression.The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta Genomic structure, chromosomal localization and identification of mutations in the xeroderma pigmentosum variant (XPV) gene Preferential misincorporation of purine nucleotides by human DNA polymerase eta opposite benzo[a]pyrene 7,8-diol 9,10-epoxide deoxyguanosine adducts Minding the gap: the underground functions of BRCA1 and BRCA2 at stalled replication forks Polymerase eta deficiency in the xeroderma pigmentosum variant uncovers an overlap between the S phase checkpoint and double-strand break repair.Molecular genetics of Xeroderma pigmentosum variant.The role of RPA2 phosphorylation in homologous recombination in response to replication arrest Cell cycle control, checkpoint mechanisms, and genotoxic stress.High mobility of flap endonuclease 1 and DNA polymerase eta associated with replication foci in mammalian S-phase nucleus.Architecture of the replication fork stalled at the 3' end of yeast ribosomal genes.Coordinated protein and DNA remodeling by human HLTF on stalled replication fork Synthesis of site-specific DNA-protein conjugates and their effects on DNA replication Participation of recombination proteins in rescue of arrested replication forks in UV-irradiated Escherichia coli need not involve recombination.Escherichia coli RNA and DNA polymerase bypass of dihydrouracil: mutagenic potential via transcription and replication.Error-prone translesion synthesis past DNA-peptide cross-links conjugated to the major groove of DNA via C5 of thymidine Accuracy of thymine-thymine dimer bypass by Saccharomyces cerevisiae DNA polymerase eta Xeroderma pigmentosum variant: from a human genetic disorder to a novel DNA polymerase.Biochemical reconstitution of abasic DNA lesion replication in Xenopus extracts Bridging the gap: a family of novel DNA polymerases that replicate faulty DNA.Genetic control of translesion synthesis on leading and lagging DNA strands in plasmids derived from Epstein-Barr virus in human cells.Requirement of RAD52 group genes for postreplication repair of UV-damaged DNA in Saccharomyces cerevisiae.Mutational specificity and genetic control of replicative bypass of an abasic site in yeast p53 suppression overwhelms DNA polymerase eta deficiency in determining the cellular UV DNA damage response RECQ1 is required for cellular resistance to replication stress and catalyzes strand exchange on stalled replication fork structures.Inhibition of DNA replication fork progression and mutagenic potential of 1, N6-ethenoadenine and 8-oxoguanine in human cell extracts.Human DNA polymerase eta activity and translocation is regulated by phosphorylation.Rescue of stalled replication forks by RecG: simultaneous translocation on the leading and lagging strand templates supports an active DNA unwinding model of fork reversal and Holliday junction formation The block of DNA polymerase delta strand displacement activity by an abasic site can be rescued by the concerted action of DNA polymerase beta and Flap endonuclease 1.Domain structure, localization, and function of DNA polymerase eta, defective in xeroderma pigmentosum variant cells.Fidelity of eucaryotic DNA polymerase delta holoenzyme from Schizosaccharomyces pombe.Eukaryotic Translesion DNA Synthesis on the Leading and Lagging Strands: Unique Detours around the Same Obstacle Abnormal, error-prone bypass of photoproducts by xeroderma pigmentosum variant cell extracts results in extreme strand bias for the kinds of mutations induced by UV light.Impaired translesion synthesis in xeroderma pigmentosum variant extracts.

P2860

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P2860

Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis.

http://www.wikidata.org/entity/Q36861158

description

1997 nî lūn-bûn

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1997年の論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年论文

@wuu

1997年论文

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1997年论文

@zh-cn

name

Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis.

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type

label

Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis.

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prefLabel

Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis.

@en

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Journal of Biological Chemistry

P1476

Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis.

@en

P2093

Cordeiro-Stone M

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Kaufmann WK

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Price LK

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Zaritskaya LS

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P2860

Anatomy of a DNA replication fork revealed by reconstitution of SV40 DNA replication in vitro

Requirement of proliferating cell nuclear antigen in RAD6-dependent postreplicational DNA repair.

The localization of replication origins on ARS plasmids in S. cerevisiae

Replication initiation sites are distributed widely in the amplified CHO dihydrofolate reductase domain.

Differential replication of a single, UV-induced lesion in the leading or lagging strand by a human cell extract: fork uncoupling or gap formation.

Fidelity of a human cell DNA replication complex.

Inhibition of DNA replication by ultraviolet light.

Pyrimidine dimers in UV-irradiated poly dI:dC.

Photoproduct frequency is not the major determinant of UV base substitution hot spots or cold spots in human cells

Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation

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13945-13954

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272

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