scholarly article | Q13442814 |
P2093 | author name string | Kleckner N | |
Schwacha A | |||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | meiotic joint molecule formation | Q22294532 |
P304 | page(s) | 783-791 | |
P577 | publication date | 1995-12-01 | |
P1433 | published in | Cell | Q655814 |
P1476 | title | Identification of double Holliday junctions as intermediates in meiotic recombination. | |
P478 | volume | 83 |
Q35058154 | A DNA binding motif of meiotic recombinase Rec12 (Spo11) defined by essential glycine-202, and persistence of Rec12 protein after completion of recombination |
Q42410408 | A Two-Pathway Analysis of Meiotic Crossing Over and Gene Conversion in Saccharomyces cerevisiae |
Q36574006 | A histone octamer blocks branch migration of a Holliday junction |
Q91603727 | A mutant form of Dmc1 that bypasses the requirement for accessory protein Mei5-Sae3 reveals independent activities of Mei5-Sae3 and Rad51 in Dmc1 filament stability |
Q37272918 | A mutation in the FHA domain of Coprinus cinereus Nbs1 Leads to Spo11-independent meiotic recombination and chromosome segregation |
Q38243395 | A non-sister act: recombination template choice during meiosis |
Q36091145 | A novel, topologically constrained DNA molecule containing a double Holliday junction: design, synthesis, and initial biochemical characterization |
Q27935770 | A role for MMS4 in the processing of recombination intermediates during meiosis in Saccharomyces cerevisiae |
Q42175369 | A simple DNA-based translation system |
Q41434983 | A super new twist on the initiation of meiotic recombination |
Q53184441 | Altered distribution of MLH1 foci is associated with changes in cohesins and chromosome axis compaction in an asynaptic mutant of tomato. |
Q24624117 | An overview of structural DNA nanotechnology |
Q40300957 | Analysis of one-sided marker segregation patterns resulting from mammalian gene targeting |
Q27301695 | Analysis of the Intrinsically Disordered N-Terminus of the DNA Junction-Resolving Enzyme T7 Endonuclease I: Identification of Structure Formed upon DNA Binding |
Q35209022 | AtGEN1 and AtSEND1, two paralogs in Arabidopsis, possess holliday junction resolvase activity |
Q74297579 | Atomic force microscopy of parallel DNA branched junction arrays |
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 |
Q33604620 | Biochemistry of Meiotic Recombination: Formation, Processing, and Resolution of Recombination Intermediates |
Q58883735 | Branch Migrating Sister Chromatid Junctions Form at Replication Origins through Rad51/Rad52-Independent Mechanisms |
Q40826594 | Branch migration and Holliday junction resolution catalyzed by activities from mammalian cells |
Q35221144 | Branch migration prevents DNA loss during double-strand break repair |
Q47112510 | Break-induced replication promotes formation of lethal joint molecules dissolved by Srs2. |
Q34606685 | CYS3, a hotspot of meiotic recombination in Saccharomyces cerevisiae. Effects of heterozygosity and mismatch repair functions on gene conversion and recombination intermediates. |
Q40464973 | Cdc14 targets the Holliday junction resolvase Yen1 to the nucleus in early anaphase |
Q22121990 | Cellular roles of dna topoisomerases: a molecular perspective |
Q36857361 | Characterization of the structural and protein recognition properties of hybrid PNA-DNA four-way junctions |
Q41625134 | Chiasmata, crossovers, and meiotic chromosome segregation. |
Q39859965 | Close, stable homolog juxtaposition during meiosis in budding yeast is dependent on meiotic recombination, occurs independently of synapsis, and is distinct from DSB-independent pairing contacts |
Q27321712 | Combinatorial regulation of meiotic holliday junction resolution in C. elegans by HIM-6 (BLM) helicase, SLX-4, and the SLX-1, MUS-81 and XPF-1 nucleases |
Q41077128 | Conservative inheritance of newly synthesized DNA in double-strand break-induced gene conversion |
Q34645078 | Conserved and nonconserved proteins for meiotic DNA breakage and repair in yeasts |
Q45345101 | Control of cross-over by single-strand DNA resection |
Q21144863 | Controlling meiotic recombinational repair - specifying the roles of ZMMs, Sgs1 and Mus81/Mms4 in crossover formation |
Q48177373 | Coordination of Double Strand Break Repair and Meiotic Progression in Yeast by a Mek1-Ndt80 Negative Feedback Loop. |
Q42546714 | Crossing over is rarely associated with mitotic intragenic recombination in Schizosaccharomyces pombe |
Q27934346 | Crossover assurance and crossover interference are distinctly regulated by the ZMM proteins during yeast meiosis |
Q34035751 | Crossover localisation is regulated by the neddylation posttranslational regulatory pathway |
Q27936900 | Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis |
Q27765700 | Crystal structure of an octameric RuvA-Holliday junction complex |
Q27650328 | Crystal structure of the Mus81-Eme1 complex |
Q27931695 | Csm4-dependent telomere movement on nuclear envelope promotes meiotic recombination |
Q27937782 | Cyclin‐dependent kinase promotes formation of the synaptonemal complex in yeast meiosis |
Q64113513 | DNA Motifs Are Not General Predictors of Recombination in Two Drosophila Sister Species |
Q35898808 | DNA damage response clamp 9-1-1 promotes assembly of ZMM proteins for formation of crossovers and synaptonemal complex |
Q34835417 | DNA double-strand break repair by homologous recombination |
Q33747009 | DNA engineering and its application to nanotechnology |
Q37417016 | DNA intermediates of meiotic recombination in synchronous S. pombe at optimal temperature. |
Q24795194 | DNA loops and semicatenated DNA junctions |
Q40400277 | DNA methylation epigenetically silences crossover hot spots and controls chromosomal domains of meiotic recombination in Arabidopsis |
Q43628396 | DNA replication-dependent formation of joint DNA molecules in Physarum polycephalum |
Q34931255 | DNA strand exchange and RecA homologs in meiosis |
Q34603838 | Damage control: the pleiotropy of DNA repair genes in Drosophila melanogaster |
Q28264475 | Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase |
Q34750771 | Design and self-assembly of two-dimensional DNA crystals |
Q28207440 | Differential timing and control of noncrossover and crossover recombination during meiosis |
Q37109365 | Direct evidence for spontaneous branch migration in antiparallel DNA Holliday junctions |
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 |
Q90616013 | Distinct Functions in Regulation of Meiotic Crossovers for DNA Damage Response Clamp Loader Rad24(Rad17) and Mec1(ATR) Kinase |
Q35212663 | Distribution of meiotic recombination sites |
Q34567177 | Does crossover interference count in Saccharomyces cerevisiae? |
Q39957722 | Double Holliday junctions are intermediates of DNA break repair. |
Q64389569 | Dynamic Architecture of DNA Repair Complexes and the Synaptonemal Complex at Sites of Meiotic Recombination |
Q64387930 | Dynamic Processing of Displacement Loops during Recombinational DNA Repair |
Q36560215 | Effects of terminal nonhomology and homeology on double-strand-break-induced gene conversion tract directionality. |
Q34133607 | Eliminating both canonical and short-patch mismatch repair in Drosophila melanogaster suggests a new meiotic recombination model |
Q39530440 | Evidence for biased holliday junction cleavage and mismatch repair directed by junction cuts during double-strand-break repair in mammalian cells |
Q33994800 | Expansions and contractions in a tandem repeat induced by double-strand break repair |
Q36434484 | From early homologue recognition to synaptonemal complex formation |
Q35208023 | FtsK functions in the processing of a Holliday junction intermediate during bacterial chromosome segregation. |
Q35566393 | Functional Validation of Rare Human Genetic Variants Involved in Homologous Recombination Using Saccharomyces cerevisiae |
Q33737790 | GEN1/Yen1 and the SLX4 complex: Solutions to the problem of Holliday junction resolution. |
Q34567183 | Gene conversion and crossing over along the 405-kb left arm of Saccharomyces cerevisiae chromosome VII. |
Q33995776 | Gene conversion tracts from double-strand break repair in mammalian cells |
Q40695823 | Gene repeat expansion and contraction by spontaneous intrachromosomal homologous recombination in mammalian cells |
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 |
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 |
Q58696735 | HO Endonuclease-Initiated Recombination in Yeast Meiosis Fails To Promote Homologous Centromere Pairing and Is Not Constrained To Utilize the Dmc1 Recombinase |
Q33688880 | Hemicatenanes form upon inhibition of DNA replication |
Q27929751 | Heterodimeric complexes of Hop2 and Mnd1 function with Dmc1 to promote meiotic homolog juxtaposition and strand assimilation |
Q35844854 | Heteroduplex DNA in meiotic recombination in Drosophila mei-9 mutants |
Q26797303 | Hold your horSSEs: controlling structure-selective endonucleases MUS81 and Yen1/GEN1 |
Q39722627 | Holliday junction resolvase in Schizosaccharomyces pombe has identical endonuclease activity to the CCE1 homologue YDC2. |
Q27929886 | Holliday junctions accumulate in replication mutants via a RecA homolog-independent mechanism |
Q35559727 | Holliday junctions in the eukaryotic nucleus: resolution in sight? |
Q64461701 | Holliday junctions, heteroduplex DNA and map expansion: a commentary on ‘A mechanism for gene conversion in fungi’ by Robin Holliday |
Q93375413 | Homologous Recombination and the Formation of Complex Genomic Rearrangements |
Q41199030 | Human Holliday junction resolvase GEN1 uses a chromodomain for efficient DNA recognition and cleavage |
Q36978345 | Impaired resection of meiotic double-strand breaks channels repair to nonhomologous end joining in Caenorhabditis elegans |
Q28586376 | Infertility and aneuploidy in mice lacking a type IA DNA topoisomerase III beta |
Q42917873 | Inhibition of the Smc5/6 complex during meiosis perturbs joint molecule formation and resolution without significantly changing crossover or non-crossover levels. |
Q38313261 | Interaction of HMG proteins and H1 with hybrid PNA-DNA junctions |
Q63965500 | Interchromosomal Transfer of Epigenetic States in Ascobolus: Transfer of DNA Methylation Is Mechanistically Related to Homologous Recombination |
Q35950053 | Interchromosomal crossover in human cells is associated with long gene conversion tracts |
Q42566665 | Interchromosomal recombination in Zea mays |
Q27936249 | Interhomolog bias during meiotic recombination: meiotic functions promote a highly differentiated interhomolog-only pathway |
Q58486283 | Intermediates of Yeast Meiotic Recombination Contain Heteroduplex DNA |
Q43387197 | Investigating DNA supercoiling in eukaryotic genomes. |
Q37362826 | Ipl1/Aurora B kinase coordinates synaptonemal complex disassembly with cell cycle progression and crossover formation in budding yeast meiosis |
Q35530032 | Juxtaposition of heterozygous and homozygous regions causes reciprocal crossover remodelling via interference during Arabidopsis meiosis |
Q26863356 | Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models |
Q40281319 | Low-resolution reconstruction of a synthetic DNA holliday junction. |
Q33984265 | Lucky breaks: analysis of recombination in Saccharomyces |
Q29618789 | Mechanism and control of meiotic recombination initiation |
Q28259452 | Mechanism of homologous recombination: mediators and helicases take on regulatory functions |
Q33769217 | Mechanisms of recombination between diverged sequences in wild-type and BLM-deficient mouse and human cells |
Q37394575 | Meiosis: how could it work? |
Q36198265 | Meiosis: inducing variation by reduction |
Q38618828 | Meiotic Recombination: The Essence of Heredity |
Q36878569 | Meiotic and mitotic recombination in meiosis |
Q33984282 | Meiotic chromosome behavior in Saccharomyces cerevisiae and (mostly) mammals |
Q30827295 | Meiotic chromosome synapsis-promoting proteins antagonize the anti-crossover activity of sgs1. |
Q74460912 | Meiotic crossing-over in the regions of homology between homologous chromosomes V |
Q27940335 | Meiotic crossover control by concerted action of Rad51-Dmc1 in homolog template bias and robust homeostatic regulation |
Q29618405 | Meiotic prophase arrest with failure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog |
Q38450160 | Meiotic recombination hotspots - a comparative view. |
Q28279936 | Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis |
Q41285976 | Meiotic recombination in yeast: coronation of the double-strand-break repair model |
Q33921194 | Meiotic recombination intermediates are resolved with minimal crossover formation during return-to-growth, an analogue of the mitotic cell cycle |
Q24597411 | Meiotic versus mitotic recombination: two different routes for double-strand break repair: the different functions of meiotic versus mitotic DSB repair are reflected in different pathway usage and different outcomes |
Q34340732 | Mek1 kinase governs outcomes of meiotic recombination and the checkpoint response |
Q35950096 | Mek1 kinase is regulated to suppress double-strand break repair between sister chromatids during budding yeast meiosis |
Q52532214 | Migration of a Holliday junction through a nucleosome directed by the E. coli RuvAB motor protein. |
Q42150238 | Minisatellite variants generated in yeast meiosis involve DNA removal during gene conversion |
Q21563347 | Mitotic recombination: why? when? how? where? |
Q28305501 | Mlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonuclease |
Q27930146 | Mnd1/Hop2 facilitates Dmc1-dependent interhomolog crossover formation in meiosis of budding yeast |
Q34067772 | Mnd1p: an evolutionarily conserved protein required for meiotic recombination |
Q48174147 | Modulation of meiotic homologous recombination by DNA helicases |
Q36226840 | Molecular aspects of meiotic chromosome synapsis and recombination |
Q39700513 | Molecular dissection of mitotic recombination in the yeast Saccharomyces cerevisiae |
Q50420122 | Monitoring Recombination During Meiosis in Budding Yeast |
Q28512386 | Mouse HFM1/Mer3 is required for crossover formation and complete synapsis of homologous chromosomes during meiosis |
Q92258646 | Moving forward one step back at a time: reversibility during homologous recombination |
Q37283116 | Mph1 and Mus81-Mms4 prevent aberrant processing of mitotic recombination intermediates |
Q34570971 | MuDR transposase increases the frequency of meiotic crossovers in the vicinity of a Mu insertion in the maize a1 gene |
Q52724127 | Multi-Invasion-Induced Rearrangements as a Pathway for Physiological and Pathological Recombination. |
Q27933164 | Multiple branches of the meiotic recombination pathway contribute independently to homolog pairing and stable juxtaposition during meiosis in budding yeast |
Q28776215 | Multiple functions of MutS- and MutL-related heterocomplexes |
Q24548535 | Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae |
Q34707053 | Multiple pathways suppress non-allelic homologous recombination during meiosis in Saccharomyces cerevisiae |
Q34492648 | Mus81 and Yen1 promote reciprocal exchange during mitotic recombination to maintain genome integrity in budding yeast |
Q27936167 | Mus81 cleavage of Holliday junctions: a failsafe for processing meiotic recombination intermediates? |
Q52997071 | Mus81-Mms4 and Yen1 resolve a novel anaphase bridge formed by noncanonical Holliday junctions. |
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. |
Q27931736 | Mutations in Saccharomyces cerevisiae That Block Meiotic Prophase Chromosome Metabolism and Confer Cell Cycle Arrest at Pachytene Identify Two New Meiosis-Specific Genes SAE1 and SAE3 |
Q27930587 | Ndj1, a telomere-associated protein, promotes meiotic recombination in budding yeast |
Q35223901 | New and old ways to control meiotic recombination |
Q38611105 | Non-B DNA Secondary Structures and Their Resolution by RecQ Helicases. |
Q37781771 | Novel DNA materials and their applications |
Q30441651 | Novel pro- and anti-recombination activities of the Bloom's syndrome helicase |
Q33936256 | Observing spontaneous branch migration of Holliday junctions one step at a time |
Q37080083 | Paranemic crossover DNA: a generalized Holliday structure with applications in nanotechnology |
Q34618616 | Patterns of Heteroduplex Formation Associated With the Initiation of Meiotic Recombination in the Yeast Saccharomyces cerevisiae |
Q27936069 | Pch2 acts through Xrs2 and Tel1/ATM to modulate interhomolog bias and checkpoint function during meiosis |
Q38988847 | Pervasive and essential roles of the Top3-Rmi1 decatenase orchestrate recombination and facilitate chromosome segregation in meiosis |
Q34025948 | Processing of joint molecule intermediates by structure-selective endonucleases during homologous recombination in eukaryotes |
Q46734062 | Questions and Assays |
Q28509598 | RNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosis |
Q34151222 | RTEL1: an essential helicase for telomere maintenance and the regulation of homologous recombination |
Q40974663 | Rad51-dependent DNA structures accumulate at damaged replication forks in sgs1 mutants defective in the yeast ortholog of BLM RecQ helicase |
Q34712004 | Rad51/Dmc1 paralogs and mediators oppose DNA helicases to limit hybrid DNA formation and promote crossovers during meiotic recombination |
Q27932985 | Rad52 promotes postinvasion steps of meiotic double-strand-break repair |
Q35920107 | Rad52-independent accumulation of joint circular minichromosomes during S phase in Saccharomyces cerevisiae |
Q64387873 | Rad54 dissociates homologous recombination intermediates by branch migration |
Q37678703 | Rad54, the motor of homologous recombination |
Q27939265 | RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination |
Q34108141 | Recombination at double-strand breaks and DNA ends: conserved mechanisms from phage to humans. |
Q48018607 | Recombination at work for meiosis |
Q40996441 | Recombination by replication |
Q41327161 | Reduced dosage of the chromosome axis factor Red1 selectively disrupts the meiotic recombination checkpoint in Saccharomyces cerevisiae |
Q89665180 | Refined spatial temporal epigenomic profiling reveals intrinsic connection between PRDM9-mediated H3K4me3 and the fate of double-stranded breaks |
Q63965511 | Regulated Crossing-Over Requires Inactivation of Yen1/GEN1 Resolvase during Meiotic Prophase I |
Q38559892 | Regulation of recombination and genomic maintenance |
Q42007696 | Regulatory control of the resolution of DNA recombination intermediates during meiosis and mitosis |
Q24675453 | Repairing a double-strand chromosome break by homologous recombination: revisiting Robin Holliday's model |
Q37311395 | Resolution by unassisted Top3 points to template switch recombination intermediates during DNA replication |
Q64928982 | Resolution of the Holliday junction recombination intermediate by human GEN1 at the single-molecule level. |
Q29618204 | Role of RAD52 epistasis group genes in homologous recombination and double-strand break repair |
Q27931976 | Role of Saccharomyces cerevisiae Msh2 and Msh3 repair proteins in double-strand break-induced recombination |
Q36540776 | Roles for mismatch repair family proteins in promoting meiotic crossing over |
Q28583161 | SCP2: a major protein component of the axial elements of synaptonemal complexes of the rat |
Q55186299 | SHOC1 is a ERCC4-(HhH)2-like protein, integral to the formation of crossover recombination intermediates during mammalian meiosis. |
Q36217378 | Saccharomyces cerevisiae Dmc1 and Rad51 proteins preferentially function with Tid1 and Rad54 proteins, respectively, to promote DNA strand invasion during genetic recombination |
Q27935123 | Saccharomyces cerevisiae Dmc1 protein promotes renaturation of single-strand DNA (ssDNA) and assimilation of ssDNA into homologous super-coiled duplex DNA. |
Q38293464 | Saccharomyces cerevisiae Mus81-Mms4 is a catalytic, DNA structure-selective endonuclease |
Q35675416 | Separable Crossover-Promoting and Crossover-Constraining Aspects of Zip1 Activity during Budding Yeast Meiosis |
Q33576921 | Single Holliday junctions are intermediates of meiotic recombination |
Q40429985 | Sister chromatid gene conversion is a prominent double-strand break repair pathway in mammalian cells |
Q48044829 | Spatiotemporal asymmetry of the meiotic program underlies the predominantly distal distribution of meiotic crossovers in barley |
Q29618612 | Srs2 and Sgs1-Top3 suppress crossovers during double-strand break repair in yeast |
Q36143773 | Structural DNA nanotechnology: an overview |
Q24794390 | Structural analysis of hemicatenated DNA loops. |
Q37309109 | Structural insights into Saccharomyces cerevisiae Msh4-Msh5 complex function using homology modeling |
Q35198972 | Suppression of crossing-over by DNA methylation in Ascobolus |
Q27929908 | Sustained and rapid chromosome movements are critical for chromosome pairing and meiotic progression in budding yeast |
Q37383395 | Synaptonemal complex (SC) component Zip1 plays a role in meiotic recombination independent of SC polymerization along the chromosomes |
Q41066968 | Synaptonemal complexes: structure and function |
Q21145860 | Synthesis-dependent strand annealing in meiosis |
Q33247669 | Synthetic junctions as tools to identify and characterize Holliday junction resolvases |
Q33509521 | Temperature-dependent modulation of chromosome segregation in msh4 mutants of budding yeast |
Q28301386 | Temporally and biochemically distinct activities of Exo1 during meiosis: double-strand break resection and resolution of double Holliday junctions |
Q42057649 | Testing predictions of the double-strand break repair model relating to crossing over in Mammalian cells |
Q29547237 | The Bloom's syndrome helicase suppresses crossing over during homologous recombination |
Q36384393 | The DNA replication factor RFC1 is required for interference-sensitive meiotic crossovers in Arabidopsis thaliana |
Q36631422 | The Genomes of Three Uneven Siblings: Footprints of the Lifestyles of Three Trichoderma Species |
Q27937197 | The Mnd1 protein forms a complex with hop2 to promote homologous chromosome pairing and meiotic double-strand break repair |
Q35643073 | The Mus81 solution to resolution: generating meiotic crossovers without Holliday junctions |
Q34617616 | The Mus81/Mms4 Endonuclease Acts Independently of Double-Holliday Junction Resolution to Promote a Distinct Subset of Crossovers During Meiosis in Budding Yeast |
Q36236720 | The Rad1-Rad10 nuclease promotes chromosome translocations between dispersed repeats |
Q33952127 | The Smc5-Smc6 complex is required to remove chromosome junctions in meiosis. |
Q28475013 | The Werner syndrome helicase/exonuclease processes mobile D-loops through branch migration and degradation |
Q27940329 | The budding yeast mei5 and sae3 proteins act together with dmc1 during meiotic recombination |
Q36028916 | The centenary of Janssens's chiasmatype theory |
Q34604064 | The chromosome bias of misincorporations during double-strand break repair is not altered in mismatch repair-defective strains of Saccharomyces cerevisiae. |
Q55221543 | The conserved LEM-3/Ankle1 nuclease is involved in the combinatorial regulation of meiotic recombination repair and chromosome segregation in Caenorhabditis elegans. |
Q90637153 | The conserved XPF:ERCC1-like Zip2:Spo16 complex controls meiotic crossover formation through structure-specific DNA binding |
Q34607928 | The conversion gradient at HIS4 of Saccharomyces cerevisiae. I. Heteroduplex rejection and restoration of Mendelian segregation |
Q34607889 | The conversion gradient at HIS4 of Saccharomyces cerevisiae. II. A role for mismatch repair directed by biased resolution of the recombinational intermediate. |
Q34282411 | The crystal structures of DNA Holliday junctions. |
Q36416265 | The diverse roles of transverse filaments of synaptonemal complexes in meiosis |
Q53322003 | The double life of Holliday junctions. |
Q33968416 | The efficiency of meiotic recombination between dispersed sequences in Saccharomyces cerevisiae depends upon their chromosomal location. |
Q79120277 | The endogenous Mus81-Eme1 complex resolves Holliday junctions by a nick and counternick mechanism |
Q33890637 | The essential role of yeast topoisomerase III in meiosis depends on recombination |
Q34181483 | The flexibility of DNA double crossover molecules |
Q36974995 | The homologous recombination system of Ustilago maydis |
Q36300927 | The hotspot conversion paradox and the evolution of meiotic recombination |
Q33984289 | The many faces of mismatch repair in meiosis |
Q64388083 | The meiotic-specific Mek1 kinase in budding yeast regulates interhomolog recombination and coordinates meiotic progression with double-strand break repair |
Q41064501 | The mismatch repair system contributes to meiotic sterility in an interspecific yeast hybrid. |
Q41822890 | The mitotic DNA damage checkpoint proteins Rad17 and Rad24 are required for repair of double-strand breaks during meiosis in yeast |
Q33957081 | The msh2 gene of Schizosaccharomyces pombe is involved in mismatch repair, mating-type switching, and meiotic chromosome organization. |
Q33486516 | The pch2Delta mutation in baker's yeast alters meiotic crossover levels and confers a defect in crossover interference |
Q34684345 | The resistance of DMC1 D-loops to dissociation may account for the DMC1 requirement in meiosis |
Q33294063 | The role of AtMUS81 in interference-insensitive crossovers in A. thaliana |
Q33750279 | The roles of the Saccharomyces cerevisiae RecQ helicase SGS1 in meiotic genome surveillance |
Q29618523 | The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination |
Q43936941 | The synaptonemal complex protein ZYP1 is required for imposition of meiotic crossovers in barley |
Q37263332 | Thermodynamics of forming a parallel DNA crossover |
Q34055346 | Three structure-selective endonucleases are essential in the absence of BLM helicase in Drosophila |
Q41665531 | Three-dimensional microscopy of the Rad51 recombination protein during meiotic prophase |
Q24648825 | Tid1/Rdh54 promotes colocalization of rad51 and dmc1 during meiotic recombination |
Q28474239 | Topoisomerase 3alpha and RMI1 suppress somatic crossovers and are essential for resolution of meiotic recombination intermediates in Arabidopsis thaliana |
Q42107861 | Trans events associated with crossovers are revealed in the absence of mismatch repair genes in Saccharomyces cerevisiae |
Q33728150 | Trying to Avoid Your Sister |
Q29615266 | Un ménage à quatre: the molecular biology of chromosome segregation in meiosis |
Q31155692 | Understanding and Manipulating Meiotic Recombination in Plants. |
Q27938589 | Yeast spt6-140 mutation, affecting chromatin and transcription, preferentially increases recombination in which Rad51p-mediated strand exchange is dispensable |
Q27313630 | ZHP-3 acts at crossovers to couple meiotic recombination with synaptonemal complex disassembly and bivalent formation in C. elegans |
Q36900922 | ZMM proteins during meiosis: crossover artists at work |
Q27934770 | Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis |
Q35082997 | c(3)G encodes a Drosophila synaptonemal complex protein |
Q34615978 | mei-P22 encodes a chromosome-associated protein required for the initiation of meiotic recombination in Drosophila melanogaster. |
Q35209608 | mei-W68 in Drosophila melanogaster encodes a Spo11 homolog: evidence that the mechanism for initiating meiotic recombination is conserved |
Q42352313 | mlh3 mutations in baker's yeast alter meiotic recombination outcomes by increasing noncrossover events genome-wide. |
Q58486287 | γ-H2AX illuminates meiosis |
Search more.