scholarly article | Q13442814 |
P819 | ADS bibcode | 2010PLoSO...515380A |
P356 | DOI | 10.1371/JOURNAL.PONE.0015380 |
P932 | PMC publication ID | 2976770 |
P698 | PubMed publication ID | 21085703 |
P5875 | ResearchGate publication ID | 47812992 |
P2093 | author name string | Richard M Badge | |
Rhona H Borts | |||
Robert P Mason | |||
Amit Dipak Amin | |||
Alexandre B H Chaix | |||
P2860 | cites work | Genetic analysis of the Saccharomyces cerevisiae Sgs1 helicase defines an essential function for the Sgs1-Top3 complex in the absence of SRS2 or TOP1 | Q73034734 |
Different domains of Sgs1 are required for mitotic and meiotic functions | Q73696436 | ||
Elevation of sister chromatid exchange in Saccharomyces cerevisiae sgs1 disruptants and the relevance of the disruptants as a system to evaluate mutations in Bloom's syndrome gene | Q73795297 | ||
Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases | Q73844491 | ||
Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases | Q24317166 | ||
Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae | Q24548535 | ||
Roles of RECQ helicases in recombination based DNA repair, genomic stability and aging | Q24646853 | ||
The Bloom's syndrome gene product promotes branch migration of holliday junctions | Q24674127 | ||
Versatile and open software for comparing large genomes | Q24807126 | ||
Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae | Q27861085 | ||
Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family | Q27930009 | ||
Supercomplex formation between Mlh1-Mlh3 and Sgs1-Top3 heterocomplexes in meiotic yeast cells | Q27933098 | ||
SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination | Q27935480 | ||
Purification and characterization of the Sgs1 DNA helicase activity of Saccharomyces cerevisiae. | Q27936079 | ||
Role of Polo-like kinase CDC5 in programming meiosis I chromosome segregation | Q27936086 | ||
Yeast Rmi1/Nce4 controls genome stability as a subunit of the Sgs1-Top3 complex | Q27938674 | ||
RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination | Q27939265 | ||
RMI1/NCE4, a suppressor of genome instability, encodes a member of the RecQ helicase/Topo III complex | Q27939442 | ||
Sgs1: a eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation | Q27939683 | ||
Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis. | Q27940287 | ||
New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae | Q28131599 | ||
A positive selection for mutants lacking orotidine-5'-phosphate decarboxylase activity in yeast: 5-fluoro-orotic acid resistance | Q28131606 | ||
Improved method for high efficiency transformation of intact yeast cells | Q28131608 | ||
Three new dominant drug resistance cassettes for gene disruption in Saccharomyces cerevisiae | Q28131610 | ||
The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase | Q28170377 | ||
Mechanisms and functions of DNA mismatch repair | Q28262719 | ||
Centromere-proximal crossovers are associated with precocious separation of sister chromatids during meiosis in Saccharomyces cerevisiae | Q28764746 | ||
Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae | Q29546523 | ||
The Bloom's syndrome helicase suppresses crossing over during homologous recombination | Q29547237 | ||
The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination | Q29618523 | ||
Srs2 and Sgs1-Top3 suppress crossovers during double-strand break repair in yeast | Q29618612 | ||
Major ecological transitions in wild sunflowers facilitated by hybridization | Q30004700 | ||
The yeast Sgs1p helicase acts upstream of Rad53p in the DNA replication checkpoint and colocalizes with Rad53p in S-phase-specific foci | Q30448876 | ||
Meiotic chromosome synapsis-promoting proteins antagonize the anti-crossover activity of sgs1. | Q30827295 | ||
Involvement of SGS1 in DNA damage-induced heteroallelic recombination that requires RAD52 in Saccharomyces cerevisiae | Q32048153 | ||
RecQ helicases: guardian angels of the DNA replication fork | Q33314341 | ||
The mismatch repair system reduces meiotic homeologous recombination and stimulates recombination-dependent chromosome loss | Q40020196 | ||
Synaptonemal complex and crossing-over: structural support or interference? | Q40571789 | ||
The Bloom's syndrome helicase interacts directly with the human DNA mismatch repair protein hMSH6. | Q40634607 | ||
Coming undone: how to untangle a chromosome | Q40666036 | ||
The mismatch repair system contributes to meiotic sterility in an interspecific yeast hybrid. | Q41064501 | ||
Specific pathways prevent duplication-mediated genome rearrangements | Q41927457 | ||
SGS1, a homologue of the Bloom's and Werner's syndrome genes, is required for maintenance of genome stability in Saccharomyces cerevisiae | Q42967143 | ||
The genetic consequences of ablating helicase activity and the Top3 interaction domain of Sgs1. | Q43198272 | ||
The N-terminal region of Sgs1, which interacts with Top3, is required for complementation of MMS sensitivity and suppression of hyper-recombination in sgs1 disruptants | Q43720699 | ||
Homeologous recombination between AluSx-sequences as a cause of hemophilia | Q45878501 | ||
Multiple pathways cooperate in the suppression of genome instability in Saccharomyces cerevisiae | Q46062549 | ||
The Sgs1 Helicase Regulates Chromosome Synapsis and Meiotic Crossing Over | Q47388021 | ||
The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants | Q50192890 | ||
Identification of double Holliday junctions as intermediates in meiotic recombination. | Q54599520 | ||
Differential effects of the mismatch repair genes MSH2 and MSH3 on homeologous recombination in Saccharomyces cerevisiae | Q57451646 | ||
Human homologues of yeast helicase | Q59094515 | ||
Extensive 3'-overhanging, single-stranded DNA associated with the meiosis-specific double-strand breaks at the ARG4 recombination initiation site | Q64389995 | ||
Sgs1 function in the repair of DNA replication intermediates is separable from its role in homologous recombinational repair | Q33408756 | ||
Sources and evolution of human Alu repeated sequences | Q33585405 | ||
Mapping the DNA topoisomerase III binding domain of the Sgs1 DNA helicase | Q33639225 | ||
The full-length Saccharomyces cerevisiae Sgs1 protein is a vigorous DNA helicase that preferentially unwinds holliday junctions | Q33707142 | ||
Mismatch repair proteins regulate heteroduplex formation during mitotic recombination in yeast | Q33781506 | ||
Association of yeast DNA topoisomerase III and Sgs1 DNA helicase: studies of fusion proteins. | Q33944291 | ||
Meiotic recombination frequencies are affected by nutritional states in Saccharomycescerevisiae | Q33952006 | ||
The subtelomeric Y' repeat family in Saccharomyces cerevisiae: an experimental system for repeated sequence evolution. | Q33956252 | ||
Mismatch correction acts as a barrier to homeologous recombination in Saccharomyces cerevisiae | Q33964716 | ||
Sgs1 helicase activity is required for mitotic but apparently not for meiotic functions | Q33965180 | ||
Biochemical Mutants in the Smut Fungus Ustilago Maydis. | Q33975198 | ||
Examination of the roles of Sgs1 and Srs2 helicases in the enforcement of recombination fidelity in Saccharomyces cerevisiae | Q34569374 | ||
Distinct roles for the Saccharomyces cerevisiae mismatch repair proteins in heteroduplex rejection, mismatch repair and nonhomologous tail removal | Q34570828 | ||
The role of the mismatch repair machinery in regulating mitotic and meiotic recombination between diverged sequences in yeast. | Q34606599 | ||
Regulation of mitotic homeologous recombination in yeast. Functions of mismatch repair and nucleotide excision repair genes | Q34608647 | ||
Bipartite structure of the SGS1 DNA helicase in Saccharomyces cerevisiae | Q34608894 | ||
Homologous recombination and maintenance of genome integrity: cancer and aging through the prism of human RecQ helicases | Q34772977 | ||
Chromosome choreography: the meiotic ballet | Q35195590 | ||
Heteroduplex rejection during single-strand annealing requires Sgs1 helicase and mismatch repair proteins Msh2 and Msh6 but not Pms1 | Q35318165 | ||
Early decision; meiotic crossover interference prior to stable strand exchange and synapsis | Q35739105 | ||
Roles of RecA homologues Rad51 and Dmc1 during meiotic recombination | Q35910251 | ||
BLM ortholog, Sgs1, prevents aberrant crossing-over by suppressing formation of multichromatid joint molecules | Q36082370 | ||
Chromosome evolution in eukaryotes: a multi-kingdom perspective | Q36293593 | ||
Barriers to recombination between closely related bacteria: MutS and RecBCD inhibit recombination between Salmonella typhimurium and Salmonella typhi. | Q36574936 | ||
Characterization of a highly conserved binding site of Mlh1 required for exonuclease I-dependent mismatch repair | Q37072156 | ||
Interaction of genetic and environmental factors in Saccharomyces cerevisiae meiosis: the devil is in the details. | Q37607234 | ||
Ntg2p, a Saccharomyces cerevisiae DNA N-glycosylase/apurinic or apyrimidinic lyase involved in base excision repair of oxidative DNA damage, interacts with the DNA mismatch repair protein Mlh1p. Identification of a Mlh1p binding motif. | Q38288690 | ||
Interaction between yeast sgs1 helicase and DNA topoisomerase III. | Q38311228 | ||
Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis | Q38344945 | ||
Bloom helicase and DNA topoisomerase IIIalpha are involved in the dissolution of sister chromatids. | Q38408536 | ||
Mismatch repair and the fidelity of genetic recombination | Q38730984 | ||
Top3 processes recombination intermediates and modulates checkpoint activity after DNA damage. | Q39084503 | ||
Topoisomerase III acts upstream of Rad53p in the S-phase DNA damage checkpoint | Q39528622 | ||
Mph1 requires mismatch repair-independent and -dependent functions of MutSalpha to regulate crossover formation during homologous recombination repair | Q39844167 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Saccharomyces cerevisiae | Q719725 |
P304 | page(s) | e15380 | |
P577 | publication date | 2010-11-09 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | The roles of the Saccharomyces cerevisiae RecQ helicase SGS1 in meiotic genome surveillance | |
P478 | volume | 5 |
Q35135863 | In vivo evolution of metabolic pathways by homeologous recombination in mitotic cells |
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Q38172111 | Investigations of homologous recombination pathways and their regulation |
Q47377567 | Sgs1 Binding to Rad51 Stimulates Homology-Directed DNA Repair in Saccharomyces cerevisiae |
Q59810709 | Spore-autonomous fluorescent protein expression identifies meiotic chromosome mis-segregation as the principal cause of hybrid sterility in yeast |
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