| scholarly article | Q13442814 |
| P50 | author | Juan Lucas Argueso | Q55457091 |
| P2093 | author name string | Eric Alani | |
| Zekeriyya Gemici | |||
| Jennifer Wanat | |||
| P2860 | cites work | 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 | ||
| Genetic and physical maps of Saccharomyces cerevisiae | Q24599455 | ||
| MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice | Q24606421 | ||
| Meiotic double-strand breaks at the interface of chromosome movement, chromosome remodeling, and reductional division | Q24646919 | ||
| Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family | Q27930009 | ||
| Saccharomyces cerevisiae Mer3 is a DNA helicase involved in meiotic crossing over | Q27930902 | ||
| Conserved properties between functionally distinct MutS homologs in yeast | Q27931606 | ||
| The budding yeast Msh4 protein functions in chromosome synapsis and the regulation of crossover distribution | Q27931846 | ||
| The MER3 DNA helicase catalyzes the unwinding of holliday junctions | Q27932618 | ||
| Supercomplex formation between Mlh1-Mlh3 and Sgs1-Top3 heterocomplexes in meiotic yeast cells | Q27933098 | ||
| Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis | Q27934770 | ||
| A role for MMS4 in the processing of recombination intermediates during meiosis in Saccharomyces cerevisiae | Q27935770 | ||
| Functional overlap between Sgs1-Top3 and the Mms4-Mus81 endonuclease | Q27935913 | ||
| Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis | Q27936900 | ||
| Functional specificity of MutL homologs in yeast: evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction | Q27939611 | ||
| Zip3 provides a link between recombination enzymes and synaptonemal complex proteins | Q27939710 | ||
| New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae | Q28131599 | ||
| Three new dominant drug resistance cassettes for gene disruption in Saccharomyces cerevisiae | Q28131610 | ||
| Caenorhabditis elegans msh-5 is required for both normal and radiation-induced meiotic crossing over but not for completion of meiosis | Q28140164 | ||
| Exo1 roles for repair of DNA double-strand breaks and meiotic crossing over in Saccharomyces cerevisiae | Q28140402 | ||
| MSH4 acts in conjunction with MLH1 during mammalian meiosis | Q28142773 | ||
| Differential timing and control of noncrossover and crossover recombination during meiosis | Q28207440 | ||
| The time course and chromosomal localization of recombination-related proteins at meiosis in the mouse are compatible with models that can resolve the early DNA-DNA interactions without reciprocal recombination | Q28214583 | ||
| Mammalian MutS homologue 5 is required for chromosome pairing in meiosis | Q28295022 | ||
| Chromosomal influence on meiotic spindle assembly: abnormal meiosis I in female Mlh1 mutant mice | Q28506066 | ||
| Meiotic pachytene arrest in MLH1-deficient mice | Q28510650 | ||
| Meiotic arrest and aneuploidy in MLH3-deficient mice | Q28593875 | ||
| The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination | Q29618523 | ||
| Mechanism and control of meiotic recombination initiation | Q29618789 | ||
| The Analysis of Tetrad Data | Q31095632 | ||
| Distributive disjunction of authentic chromosomes in Saccharomyces cerevisiae | Q33531635 | ||
| Crossing over during Caenorhabditis elegans meiosis requires a conserved MutS-based pathway that is partially dispensable in budding yeast | Q33878802 | ||
| The lethal(1)TW-6cs mutation of Drosophila melanogaster is a dominant antimorphic allele of nod and is associated with a single base change in the putative ATP-binding domain | Q33958531 | ||
| Genetic evidence that the meiotic recombination hotspot at the HIS4 locus of Saccharomyces cerevisiae does not represent a site for a symmetrically processed double-strand break | Q33960929 | ||
| A test of the double-strand break repair model for meiotic recombination in Saccharomyces cerevisiae | Q33968364 | ||
| Biochemical Mutants in the Smut Fungus Ustilago Maydis. | Q33975198 | ||
| The many faces of mismatch repair in meiosis | Q33984289 | ||
| Crossover and noncrossover recombination during meiosis: timing and pathway relationships | Q33988127 | ||
| A meiotic mutant defective in distributive disjunction in Drosophila melanogaster | Q33988736 | ||
| Systematic mutagenesis of the Saccharomyces cerevisiae MLH1 gene reveals distinct roles for Mlh1p in meiotic crossing over and in vegetative and meiotic mismatch repair | Q34463536 | ||
| Chromosome size-dependent control of meiotic reciprocal recombination in Saccharomyces cerevisiae: the role of crossover interference | Q34607409 | ||
| The Mus81/Mms4 Endonuclease Acts Independently of Double-Holliday Junction Resolution to Promote a Distinct Subset of Crossovers During Meiosis in Budding Yeast | Q34617616 | ||
| Patterns of Heteroduplex Formation Associated With the Initiation of Meiotic Recombination in the Yeast Saccharomyces cerevisiae | Q34618616 | ||
| A deficiency screen of the major autosomes identifies a gene (matrimony) that is haplo-insufficient for achiasmate segregation in Drosophila oocytes. | Q34618637 | ||
| Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis | Q35190411 | ||
| The Mus81 solution to resolution: generating meiotic crossovers without Holliday junctions | Q35643073 | ||
| Early decision; meiotic crossover interference prior to stable strand exchange and synapsis | Q35739105 | ||
| Meiotic recombination and segregation of human-derived artificial chromosomes in Saccharomyces cerevisiae | Q37053699 | ||
| Meiotic disjunction of circular minichromosomes in yeast does not require DNA homology | Q37394988 | ||
| Exchanges are not equally able to enhance meiotic chromosome segregation in yeast | Q37611056 | ||
| The Saccharomyces cerevisiae MER3 gene, encoding a novel helicase-like protein, is required for crossover control in meiosis | Q38319411 | ||
| Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis | Q38344945 | ||
| The synaptonemal complex and the distribution of meiotic recombination events | Q40461968 | ||
| Requiem for distributive segregation: achiasmate segregation in Drosophila females. | Q40778432 | ||
| Crossover Interference in Saccharomyces cerevisiae Requires a TID1/RDH54- and DMC1-Dependent Pathway | Q42123510 | ||
| Repair of specific base pair mismatches formed during meiotic recombination in the yeast Saccharomyces cerevisiae | Q43182601 | ||
| Saccharomyces cerevisiae Mer3 helicase stimulates 3'-5' heteroduplex extension by Rad51; implications for crossover control in meiotic recombination | Q46127945 | ||
| Genetic and physical maps of Saccharomyces cerevisiae, Edition 11. | Q46883158 | ||
| Imposition of crossover interference through the nonrandom distribution of synapsis initiation complexes | Q47910491 | ||
| Meiotic segregation of a homeologous chromosome pair | Q48015429 | ||
| Mutation of a meiosis-specific MutS homolog decreases crossing over but not mismatch correction | Q48076989 | ||
| Direct allelic variation scanning of the yeast genome. | Q54127504 | ||
| Intermediates of Yeast Meiotic Recombination Contain Heteroduplex DNA | Q58486283 | ||
| Letter: The need for a chiasma binder | Q68895594 | ||
| An alternative pathway for meiotic chromosome segregation in yeast | Q68913680 | ||
| Gene conversion, recombination nodules, and the initiation of meiotic synapsis | Q69114349 | ||
| Genetic control of chromosome synapsis in yeast meiosis | Q69557796 | ||
| MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair | Q71919357 | ||
| Chromosome pairing via multiple interstitial interactions before and during meiosis in yeast | Q72034931 | ||
| Crossover interference is abolished in the absence of a synaptonemal complex protein | Q72790781 | ||
| EXO1 and MSH4 differentially affect crossing-over and segregation | Q73899517 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Saccharomyces cerevisiae | Q719725 |
| P304 | page(s) | 1805-1816 | |
| P577 | publication date | 2004-12-01 | |
| P1433 | published in | Genetics | Q3100575 |
| P1476 | title | Competing crossover pathways act during meiosis in Saccharomyces cerevisiae | |
| P478 | volume | 168 |
| Q42410408 | A Two-Pathway Analysis of Meiotic Crossing Over and Gene Conversion in Saccharomyces cerevisiae |
| Q36724317 | A mutation in the putative MLH3 endonuclease domain confers a defect in both mismatch repair and meiosis in Saccharomyces cerevisiae |
| Q27934521 | Analysis of the proteins involved in the in vivo repair of base-base mismatches and four-base loops formed during meiotic recombination in the yeast Saccharomyces cerevisiae |
| Q49911835 | Arabidopsis thaliana FANCD2 Promotes Meiotic Crossover Formation |
| Q28264465 | BLM helicase ortholog Sgs1 is a central regulator of meiotic recombination intermediate metabolism |
| Q36082370 | BLM ortholog, Sgs1, prevents aberrant crossing-over by suppressing formation of multichromatid joint molecules |
| Q27934346 | Crossover assurance and crossover interference are distinctly regulated by the ZMM proteins during yeast meiosis |
| Q37533767 | Crossover patterning by the beam-film model: analysis and implications |
| Q27931634 | Csm4, in collaboration with Ndj1, mediates telomere-led chromosome dynamics and recombination during yeast meiosis |
| Q27931695 | Csm4-dependent telomere movement on nuclear envelope promotes meiotic recombination |
| Q21134538 | Defining and detecting crossover-interference mutants in yeast |
| Q36371989 | Distinct DNA-binding surfaces in the ATPase and linker domains of MutLγ determine its substrate specificities and exert separable functions in meiotic recombination and mismatch repair |
| Q36571740 | Distinct functions of MLH3 at recombination hot spots in the mouse. |
| Q33222159 | Evidence of meiotic crossover control in Saccharomyces cerevisiae through Mec1-mediated phosphorylation of replication protein A. |
| Q35677573 | Evidence that histone H1 is dispensable for proper meiotic recombination in budding yeast |
| Q22122230 | Evolution of pathogenicity and sexual reproduction in eight Candida genomes |
| Q36324990 | Fluorescent Protein as a Tool for Investigating Meiotic Recombination in Neurospora. |
| Q36830881 | GC-biased gene conversion in yeast is specifically associated with crossovers: molecular mechanisms and evolutionary significance |
| Q33701780 | Genetic Analysis of Baker's Yeast Msh4-Msh5 Reveals a Threshold Crossover Level for Meiotic Viability |
| Q27932384 | Genetic analysis of mlh3 mutations reveals interactions between crossover promoting factors during meiosis in baker's yeast |
| Q33867674 | Genetic interference: don't stand so close to me. |
| Q43236419 | Genome Dynamics of Hybrid Saccharomyces cerevisiae During Vegetative and Meiotic Divisions. |
| Q57172482 | Genome wide analysis of meiotic recombination in yeast: For a few SNPs more |
| Q34042733 | Genome-wide analysis of heteroduplex DNA in mismatch repair-deficient yeast cells reveals novel properties of meiotic recombination pathways |
| Q34589816 | Heterozygous insertions alter crossover distribution but allow crossover interference in Caenorhabditis elegans |
| Q27938210 | High-resolution mapping of meiotic crossovers and non-crossovers in yeast |
| Q37269805 | Hot regions of noninterfering crossovers coexist with a nonuniformly interfering pathway in Arabidopsis thaliana. |
| Q27321836 | Joint molecule resolution requires the redundant activities of MUS-81 and XPF-1 during Caenorhabditis elegans meiosis |
| Q37574327 | Local chromosome context is a major determinant of crossover pathway biochemistry during budding yeast meiosis. |
| Q33369076 | MUS81 generates a subset of MLH1-MLH3-independent crossovers in mammalian meiosis |
| Q35905065 | Meiotic Recombination in Neurospora crassa Proceeds by Two Pathways with Extensive Holliday Junction Migration |
| Q36878569 | Meiotic and mitotic recombination in meiosis |
| Q30827295 | Meiotic chromosome synapsis-promoting proteins antagonize the anti-crossover activity of sgs1. |
| Q26991732 | Meiotic development in Caenorhabditis elegans |
| Q28305501 | Mlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonuclease |
| Q33667402 | Modulating Crossover Frequency and Interference for Obligate Crossovers in Saccharomyces cerevisiae Meiosis. |
| Q34471736 | Msh4 and Msh5 function in SC-independent chiasma formation during the streamlined meiosis of Tetrahymena |
| Q27933164 | Multiple branches of the meiotic recombination pathway contribute independently to homolog pairing and stable juxtaposition during meiosis in budding yeast |
| Q34492648 | Mus81 and Yen1 promote reciprocal exchange during mitotic recombination to maintain genome integrity in budding yeast |
| Q36210916 | Mus81-Mms4 functions as a single heterodimer to cleave nicked intermediates in recombinational DNA repair |
| Q27940287 | Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis. |
| Q93357415 | MutSγ-Induced DNA Conformational Changes Provide Insights into Its Role in Meiotic Recombination |
| Q33869354 | Mutation screening of mismatch repair gene Mlh3 in familial esophageal cancer |
| Q92223579 | Network Rewiring of Homologous Recombination Enzymes during Mitotic Proliferation and Meiosis |
| Q64065581 | Noncanonical Contributions of MutLγ to VDE-Initiated Crossovers During Meiosis |
| Q37587231 | On the role of AtDMC1, AtRAD51 and its paralogs during Arabidopsis meiosis |
| Q35911013 | Patterns of recombination and MLH1 foci density along mouse chromosomes: modeling effects of interference and obligate chiasma. |
| Q35222734 | Pch2 modulates chromatid partner choice during meiotic double-strand break repair in Saccharomyces cerevisiae. |
| Q34025948 | Processing of joint molecule intermediates by structure-selective endonucleases during homologous recombination in eukaryotes |
| Q27932985 | Rad52 promotes postinvasion steps of meiotic double-strand-break repair |
| Q63965511 | Regulated Crossing-Over Requires Inactivation of Yen1/GEN1 Resolvase during Meiotic Prophase I |
| Q36900915 | Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis. |
| Q92634185 | Resolvases, Dissolvases, and Helicases in Homologous Recombination: Clearing the Road for Chromosome Segregation |
| Q36540776 | Roles for mismatch repair family proteins in promoting meiotic crossing over |
| Q35675416 | Separable Crossover-Promoting and Crossover-Constraining Aspects of Zip1 Activity during Budding Yeast Meiosis |
| Q31108050 | Sex, Scavengers, and Chaperones: Transcriptome Secrets of Divergent Symbiodinium Thermal Tolerances |
| Q58056259 | Sex, Scavengers, and Chaperones: Transcriptome Secrets of Divergent Symbiodinium Thermal Tolerances |
| Q33576921 | Single Holliday junctions are intermediates of meiotic recombination |
| Q37309109 | Structural insights into Saccharomyces cerevisiae Msh4-Msh5 complex function using homology modeling |
| Q27929908 | Sustained and rapid chromosome movements are critical for chromosome pairing and meiotic progression in budding yeast |
| Q35945625 | Synthetic lethality of Drosophila in the absence of the MUS81 endonuclease and the DmBlm helicase is associated with elevated apoptosis. |
| Q33509521 | Temperature-dependent modulation of chromosome segregation in msh4 mutants of budding yeast |
| Q34407325 | The Arabidopsis thaliana PARTING DANCERS gene encoding a novel protein is required for normal meiotic homologous recombination |
| Q28306188 | The Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions |
| Q33952127 | The Smc5-Smc6 complex is required to remove chromosome junctions in meiosis. |
| Q33691482 | The baker's yeast diploid genome is remarkably stable in vegetative growth and meiosis |
| Q90637153 | The conserved XPF:ERCC1-like Zip2:Spo16 complex controls meiotic crossover formation through structure-specific DNA binding |
| Q36416265 | The diverse roles of transverse filaments of synaptonemal complexes in meiosis |
| Q33615733 | The mismatch repair and meiotic recombination endonuclease Mlh1-Mlh3 is activated by polymer formation and can cleave DNA substrates in trans. |
| Q48081095 | The mismatch repair protein MLH1 marks a subset of strongly interfering crossovers in tomato |
| Q33486516 | The pch2Delta mutation in baker's yeast alters meiotic crossover levels and confers a defect in crossover interference |
| Q33294063 | The role of AtMUS81 in interference-insensitive crossovers in A. thaliana |
| Q34463801 | Top3-Rmi1 DNA single-strand decatenase is integral to the formation and resolution of meiotic recombination intermediates |
| Q34026349 | Topoisomerase II mediates meiotic crossover interference |
| Q33246417 | Two levels of interference in mouse meiotic recombination |
| Q90338823 | Unresolved Recombination Intermediates Cause a RAD9-Dependent Cell Cycle Arrest in Saccharomyces cerevisiae |
| Q36110079 | Use of fluorescent protein to analyse recombination at three loci in Neurospora crassa. |
| Q28253087 | Variation in crossover frequencies perturb crossover assurance without affecting meiotic chromosome segregation in Saccharomyces cerevisiae |
| Q28506423 | ZIP4H (TEX11) deficiency in the mouse impairs meiotic double strand break repair and the regulation of crossing over |
| Q36900922 | ZMM proteins during meiosis: crossover artists at work |
| Q42352313 | mlh3 mutations in baker's yeast alter meiotic recombination outcomes by increasing noncrossover events genome-wide. |
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