scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1009192628 |
P356 | DOI | 10.1007/S00294-005-0014-5 |
P932 | PMC publication ID | 1828632 |
P698 | PubMed publication ID | 16193328 |
P5875 | ResearchGate publication ID | 7572194 |
P2093 | author name string | Miki Ii | |
Steven J Brill | |||
P2860 | cites work | Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome | Q22009558 |
Identification and characterization of human MUS81-MMS4 structure-specific endonuclease | Q24299599 | ||
The Bloom's syndrome gene product is homologous to RecQ helicases | Q24313440 | ||
Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases | Q24317166 | ||
Mutations in the RNA polymerase II transcription machinery suppress the hyperrecombination mutant hpr1 delta of Saccharomyces cerevisiae | Q24533200 | ||
Requirement for three novel protein complexes in the absence of the Sgs1 DNA helicase in Saccharomyces cerevisiae | Q24548169 | ||
Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae | Q24548535 | ||
Structural biochemistry of a type 2 RNase H: RNA primer recognition and removal during DNA replication | Q27630668 | ||
RNase H2 of Saccharomyces cerevisiae is a complex of three proteins | Q27930321 | ||
Saccharomyces cerevisiae RNase H(35) functions in RNA primer removal during lagging-strand DNA synthesis, most efficiently in cooperation with Rad27 nuclease | Q27930354 | ||
Dna2 mutants reveal interactions with Dna polymerase alpha and Ctf4, a Pol alpha accessory factor, and show that full Dna2 helicase activity is not essential for growth | Q27930620 | ||
The absence of ribonuclease H1 or H2 alters the sensitivity of Saccharomyces cerevisiae to hydroxyurea, caffeine and ethyl methanesulphonate: implications for roles of RNases H in DNA replication and repair | Q27931541 | ||
Mutations in homologous recombination genes rescue top3 slow growth in Saccharomyces cerevisiae. | Q27931991 | ||
A novel Rap1p-interacting factor, Rif2p, cooperates with Rif1p to regulate telomere length in Saccharomyces cerevisiae. | Q27932204 | ||
Accelerated aging and nucleolar fragmentation in yeast sgs1 mutants | Q27933022 | ||
Yeast Tdp1 and Rad1-Rad10 function as redundant pathways for repairing Top1 replicative damage | Q27933291 | ||
RPA regulates telomerase action by providing Est1p access to chromosome ends | Q27933681 | ||
SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination | Q27935480 | ||
Functional overlap between Sgs1-Top3 and the Mms4-Mus81 endonuclease | Q27935913 | ||
Mcm1 regulates donor preference controlled by the recombination enhancer in Saccharomyces mating-type switching | Q27936567 | ||
MUS81 encodes a novel helix-hairpin-helix protein involved in the response to UV- and methylation-induced DNA damage in Saccharomyces cerevisiae | Q27939646 | ||
Sgs1: a eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation | Q27939683 | ||
5-Fluoroorotic acid as a selective agent in yeast molecular genetics | Q28131614 | ||
Elevated recombination rates in transcriptionally active DNA | Q28131616 | ||
Systematic genetic analysis with ordered arrays of yeast deletion mutants | Q28131618 | ||
The Bloom's syndrome gene product interacts with topoisomerase III | Q28139703 | ||
The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase | Q28170377 | ||
Potential role for the BLM helicase in recombinational repair via a conserved interaction with RAD51 | Q28207894 | ||
Failure to produce mitochondrial DNA results in embryonic lethality in Rnaseh1 null mice | Q28592636 | ||
Regulation of telomerase by telomeric proteins | Q29616133 | ||
RecQ helicases: caretakers of the genome | Q29618390 | ||
Positional cloning of the Werner's syndrome gene | Q29618393 | ||
Srs2 and Sgs1-Top3 suppress crossovers during double-strand break repair in yeast | Q29618612 | ||
Mus81-Eme1 are essential components of a Holliday junction resolvase | Q29619843 | ||
RPA governs endonuclease switching during processing of Okazaki fragments in eukaryotes | Q30704734 | ||
Isolation and characterization of a second RNase H (RNase HII) of Escherichia coli K-12 encoded by the rnhB gene | Q31022160 | ||
The protein components and mechanism of eukaryotic Okazaki fragment maturation | Q31034204 | ||
Involvement of SGS1 in DNA damage-induced heteroallelic recombination that requires RAD52 in Saccharomyces cerevisiae | Q32048153 | ||
DNA topoisomerase-targeting antitumor drugs can be studied in yeast | Q33654182 | ||
Defending genome integrity during DNA replication: a proposed role for RecQ family helicases | Q33666386 | ||
Mutational spectrum analysis of RNase H(35) deficient Saccharomyces cerevisiae using fluorescence-based directed termination PCR. | Q33786781 | ||
The essential role of yeast topoisomerase III in meiosis depends on recombination | Q33890637 | ||
The hyper-gene conversion hpr5-1 mutation of Saccharomyces cerevisiae is an allele of the SRS2/RADH gene | Q33957478 | ||
Use of a chromosomal inverted repeat to demonstrate that the RAD51 and RAD52 genes of Saccharomyces cerevisiae have different roles in mitotic recombination | Q33963818 | ||
Identification and characterization of the human mus81-eme1 endonuclease | Q34193657 | ||
Excision of misincorporated ribonucleotides in DNA by RNase H (type 2) and FEN-1 in cell-free extracts | Q34429499 | ||
Alternate pathways involving Sgs1/Top3, Mus81/ Mms4, and Srs2 prevent formation of toxic recombination intermediates from single-stranded gaps created by DNA replication | Q34430247 | ||
A genome-wide screen for methyl methanesulfonate-sensitive mutants reveals genes required for S phase progression in the presence of DNA damage | Q34430366 | ||
Identification of the genes encoding Mn2+-dependent RNase HII and Mg2+-dependent RNase HIII from Bacillus subtilis: classification of RNases H into three families | Q34487534 | ||
A postsynaptic role for Rhp55/57 that is responsible for cell death in Deltarqh1 mutants following replication arrest in Schizosaccharomyces pombe | Q34575480 | ||
Bipartite structure of the SGS1 DNA helicase in Saccharomyces cerevisiae | Q34608894 | ||
Disruption of theCrithidia fasciculata RNH1gene results in the loss of two active forms of ribonuclease H | Q34761035 | ||
The Mechanism of Mus81-Mms4 Cleavage Site Selection Distinguishes It from the Homologous Endonuclease Rad1-Rad10 | Q35148358 | ||
Role of DNA replication proteins in double-strand break-induced recombination in Saccharomyces cerevisiae | Q36701282 | ||
The severe slow growth of Deltasrs2 Deltarqh1 in Schizosaccharomyces pombe is suppressed by loss of recombination and checkpoint genes | Q39682063 | ||
Homologous recombination is required for the viability of rad27 mutants | Q39726024 | ||
Role for the fission yeast RecQ helicase in DNA repair in G2. | Q39787542 | ||
Role of Schizosaccharomyces pombe RecQ homolog, recombination, and checkpoint genes in UV damage tolerance | Q40023980 | ||
DNA repair by a Rad22-Mus81-dependent pathway that is independent of Rhp51. | Q40249048 | ||
The involvement of Srs2 in post-replication repair and homologous recombination in fission yeast | Q40773146 | ||
A hyper-recombination mutation in S. cerevisiae identifies a novel eukaryotic topoisomerase | Q42641816 | ||
SGS1, a homologue of the Bloom's and Werner's syndrome genes, is required for maintenance of genome stability in Saccharomyces cerevisiae | Q42967143 | ||
DNA helicase gene interaction network defined using synthetic lethality analyzed by microarray | Q43446083 | ||
Inactivation of homologous recombination suppresses defects in topoisomerase III-deficient mutants | Q44267600 | ||
Budding yeast mms4 is epistatic with rad52 and the function of Mms4 can be replaced by a bacterial Holliday junction resolvase | Q44290859 | ||
The ability of Sgs1 to interact with DNA topoisomerase III is essential for damage-induced recombination | Q45182071 | ||
Drosophila RNase H1 is essential for development but not for proliferation | Q46138782 | ||
Cleavage of model replication forks by fission yeast Mus81-Eme1 and budding yeast Mus81-Mms4. | Q53661726 | ||
Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases | Q73844491 | ||
Functional domains required for the Saccharomyces cerevisiae Mus81-Mms4 endonuclease complex formation and nuclear localization | Q79328396 | ||
P433 | issue | 4 | |
P921 | main subject | Saccharomyces cerevisiae | Q719725 |
P304 | page(s) | 213-225 | |
P577 | publication date | 2005-10-01 | |
P1433 | published in | Current Genetics | Q15765847 |
P1476 | title | Roles of SGS1, MUS81, and RAD51 in the repair of lagging-strand replication defects in Saccharomyces cerevisiae | |
P478 | volume | 48 |
Q42108506 | A cell cycle-regulated Slx4-Dpb11 complex promotes the resolution of DNA repair intermediates linked to stalled replication. |
Q37149779 | A junction branch point adjacent to a DNA backbone nick directs substrate cleavage by Saccharomyces cerevisiae Mus81-Mms4. |
Q37713613 | A saccharomyces cerevisiae RNase H2 interaction network functions to suppress genome instability |
Q27933571 | An N-terminal acidic region of Sgs1 interacts with Rpa70 and recruits Rad53 kinase to stalled forks |
Q24652448 | Contributions of the two accessory subunits, RNASEH2B and RNASEH2C, to the activity and properties of the human RNase H2 complex |
Q35182121 | Epistasis analysis between homologous recombination genes in Saccharomyces cerevisiae identifies multiple repair pathways for Sgs1, Mus81-Mms4 and RNase H2 |
Q36990200 | Flexibility of eukaryotic Okazaki fragment maturation through regulated strand displacement synthesis |
Q34368094 | Genetic and functional interactions between Mus81-Mms4 and Rad27. |
Q34895210 | Homologous recombination is required for genome stability in the absence of DOG-1 in Caenorhabditis elegans |
Q37472978 | Incision of damaged DNA in the presence of an impaired Smc5/6 complex imperils genome stability |
Q43077169 | Large-scale expansions of Friedreich's ataxia GAA repeats in yeast |
Q33369076 | MUS81 generates a subset of MLH1-MLH3-independent crossovers in mammalian meiosis |
Q36573932 | Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability |
Q28469182 | Multiple-pathway analysis of double-strand break repair mutations in Drosophila |
Q34492648 | Mus81 and Yen1 promote reciprocal exchange during mitotic recombination to maintain genome integrity in budding yeast |
Q27666608 | PCNA directs type 2 RNase H activity on DNA replication and repair substrates |
Q34025948 | Processing of joint molecule intermediates by structure-selective endonucleases during homologous recombination in eukaryotes |
Q35683347 | RNase H and postreplication repair protect cells from ribonucleotides incorporated in DNA |
Q37507641 | Rad51 and Rad54 promote noncrossover recombination between centromere repeats on the same chromatid to prevent isochromosome formation |
Q40540204 | Roles of DNA helicases in the mediation and regulation of homologous recombination |
Q89093963 | Separable roles for Mec1/ATR in genome maintenance, DNA replication, and checkpoint signaling |
Q33594452 | Sgs1 and exo1 redundantly inhibit break-induced replication and de novo telomere addition at broken chromosome ends |
Q35130760 | Template disruptions and failure of double Holliday junction dissolution during double-strand break repair in Drosophila BLM mutants |
Q33698561 | The Mus81-Mms4 structure-selective endonuclease requires nicked DNA junctions to undergo conformational changes and bend its DNA substrates for cleavage |
Q58730668 | The topoisomerase 3α zinc-finger domain T1 of Arabidopsis thaliana is required for targeting the enzyme activity to Holliday junction-like DNA repair intermediates |