| scholarly article | Q13442814 |
| P2093 | author name string | Yumi Kim | |
| Abby F Dernburg | |||
| Zhouliang Yu | |||
| P2860 | cites work | C. elegans mre-11 is required for meiotic recombination and DNA repair but is dispensable for the meiotic G(2) DNA damage checkpoint | Q24602472 |
| A link between meiotic prophase progression and crossover control | Q25257844 | ||
| The multifaceted roles of the HORMA domain in cellular signaling | Q26776388 | ||
| Identification of DSB-1, a protein required for initiation of meiotic recombination in Caenorhabditis elegans, illuminates a crossover assurance checkpoint | Q27320869 | ||
| DNA methylation restrains transposons from adopting a chromatin signature permissive for meiotic recombination | Q27323102 | ||
| Matefin/SUN-1 phosphorylation is part of a surveillance mechanism to coordinate chromosome synapsis and recombination with meiotic progression and chromosome movement | Q27324259 | ||
| COM-1 promotes homologous recombination during Caenorhabditis elegans meiosis by antagonizing Ku-mediated non-homologous end joining | Q27324477 | ||
| Caenorhabditis elegans histone methyltransferase MET-2 shields the male X chromosome from checkpoint machinery and mediates meiotic sex chromosome inactivation | Q27336177 | ||
| Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis | Q27345390 | ||
| Mutant rec-1 eliminates the meiotic pattern of crossing over in Caenorhabditis elegans. | Q41905539 | ||
| Condensins regulate meiotic DNA break distribution, thus crossover frequency, by controlling chromosome structure | Q41948641 | ||
| Recombination between small X chromosome duplications and the X chromosome in Caenorhabditis elegans | Q41963640 | ||
| Meiotic chromosome homology search involves modifications of the nuclear envelope protein Matefin/SUN-1. | Q43242461 | ||
| C. elegans HIM-17 links chromatin modification and competence for initiation of meiotic recombination | Q45021539 | ||
| A family of zinc-finger proteins is required for chromosome-specific pairing and synapsis during meiosis in C. elegans. | Q45933828 | ||
| HTP-3 links DSB formation with homolog pairing and crossing over during C. elegans meiosis | Q47068681 | ||
| Overlapping mechanisms promote postsynaptic RAD-51 filament disassembly during meiotic double-strand break repair. | Q47068714 | ||
| Polo kinases establish links between meiotic chromosomes and cytoskeletal forces essential for homolog pairing | Q47069168 | ||
| A conserved checkpoint pathway mediates DNA damage--induced apoptosis and cell cycle arrest in C. elegans | Q47069275 | ||
| Genetic and cytological characterization of the recombination protein RAD-51 in Caenorhabditis elegans | Q47069371 | ||
| The nuclear envelope protein Matefin/SUN-1 is required for homologous pairing in C. elegans meiosis | Q47069536 | ||
| Synaptonemal complex assembly in C. elegans is dispensable for loading strand-exchange proteins but critical for proper completion of recombination | Q47069553 | ||
| Caenorhabditis elegans Chk2-like gene is essential for meiosis but dispensable for DNA repair | Q47813081 | ||
| Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11. | Q50720785 | ||
| The fidelity of synaptonemal complex assembly is regulated by a signaling mechanism that controls early meiotic progression. | Q52998112 | ||
| Tel1(ATM)-mediated interference suppresses clustered meiotic double-strand-break formation. | Q53659612 | ||
| A mutation in Caenorhabditis elegans that increases recombination frequency more than threefold | Q59090188 | ||
| Spo11-accessory proteins link double-strand break sites to the chromosome axis in early meiotic recombination | Q64386697 | ||
| The effect of gamma radiation on recombination frequency in Caenorhabditis elegans | Q69132341 | ||
| Genetic control of chromosome synapsis in yeast meiosis | Q69557796 | ||
| Meiotic cells monitor the status of the interhomolog recombination complex | Q72988432 | ||
| Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family | Q27930009 | ||
| Synaptonemal complex morphogenesis and sister-chromatid cohesion require Mek1-dependent phosphorylation of a meiotic chromosomal protein | Q27930215 | ||
| Bidirectional resection of DNA double-strand breaks by Mre11 and Exo1 | Q27930407 | ||
| Yeast Pch2 promotes domainal axis organization, timely recombination progression, and arrest of defective recombinosomes during meiosis | Q27931107 | ||
| The HOP1 gene encodes a meiosis-specific component of yeast chromosomes | Q27933061 | ||
| Feedback control of mitosis in budding yeast | Q28131696 | ||
| Caenorhabditis elegans msh-5 is required for both normal and radiation-induced meiotic crossing over but not for completion of meiosis | Q28140164 | ||
| Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis | Q28279936 | ||
| Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project | Q28301622 | ||
| Meiotic DNA double-strand breaks and chromosome asynapsis in mice are monitored by distinct HORMAD2-independent and -dependent mechanisms | Q28585141 | ||
| Functional conservation of Mei4 for meiotic DNA double-strand break formation from yeasts to mice | Q28586489 | ||
| Mouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPase | Q28586590 | ||
| Mouse TRIP13/PCH2 is required for recombination and normal higher-order chromosome structure during meiosis | Q28594413 | ||
| Meiotic homologue alignment and its quality surveillance are controlled by mouse HORMAD1. | Q28594654 | ||
| Homologue engagement controls meiotic DNA break number and distribution | Q28658207 | ||
| Robust crossover assurance and regulated interhomolog access maintain meiotic crossover number | Q28729155 | ||
| ATM controls meiotic double-strand-break formation | Q28742900 | ||
| C. elegans germ cells switch between distinct modes of double-strand break repair during meiotic prophase progression | Q28756805 | ||
| Meiotic recombination, noncoding DNA and genomic organization in Caenorhabditis elegans | Q28769447 | ||
| The mouse Spo11 gene is required for meiotic chromosome synapsis | Q29618404 | ||
| Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis | Q30411151 | ||
| X-chromosome silencing in the germline of C. elegans | Q30412367 | ||
| Crossover distribution and frequency are regulated by him-5 in Caenorhabditis elegans | Q30421573 | ||
| RAD-51-dependent and -independent roles of a Caenorhabditis elegans BRCA2-related protein during DNA double-strand break repair | Q30780655 | ||
| Recombinational landscape and population genomics of Caenorhabditis elegans | Q33417666 | ||
| Pch2 links chromosome axis remodeling at future crossover sites and crossover distribution during yeast meiosis | Q33486503 | ||
| Differential localization and independent acquisition of the H3K9me2 and H3K9me3 chromatin modifications in the Caenorhabditis elegans adult germ line | Q33526991 | ||
| Chromosome axis defects induce a checkpoint-mediated delay and interchromosomal effect on crossing over during Drosophila meiosis | Q33658726 | ||
| Cytoskeletal forces span the nuclear envelope to coordinate meiotic chromosome pairing and synapsis. | Q33674350 | ||
| Crossing over during Caenorhabditis elegans meiosis requires a conserved MutS-based pathway that is partially dispensable in budding yeast | Q33878802 | ||
| RNAi and heterochromatin repress centromeric meiotic recombination | Q33928327 | ||
| A cis-acting locus that promotes crossing over between X chromosomes in Caenorhabditis elegans | Q33962654 | ||
| A bouquet makes ends meet | Q34085740 | ||
| The MRN complex in double-strand break repair and telomere maintenance | Q34127693 | ||
| Multiple functions and dynamic activation of MPK-1 extracellular signal-regulated kinase signaling in Caenorhabditis elegans germline development | Q36416137 | ||
| Chiasma formation: chromatin/axis interplay and the role(s) of the synaptonemal complex | Q36429060 | ||
| H3K23me2 is a new heterochromatic mark in Caenorhabditis elegans | Q36676559 | ||
| Cytological analysis of meiosis in Caenorhabditis elegans | Q36816851 | ||
| Numerical constraints and feedback control of double-strand breaks in mouse meiosis | Q36832176 | ||
| Crossovers trigger a remodeling of meiotic chromosome axis composition that is linked to two-step loss of sister chromatid cohesion | Q36942440 | ||
| Impaired resection of meiotic double-strand breaks channels repair to nonhomologous end joining in Caenorhabditis elegans | Q36978345 | ||
| Transposons in C. elegans | Q37006254 | ||
| The axial element protein HTP-3 promotes cohesin loading and meiotic axis assembly in C. elegans to implement the meiotic program of chromosome segregation | Q37287574 | ||
| A yeast two-hybrid screen for SYP-3 interactors identifies SYP-4, a component required for synaptonemal complex assembly and chiasma formation in Caenorhabditis elegans meiosis | Q37343724 | ||
| mre11S--a yeast mutation that blocks double-strand-break processing and permits nonhomologous synapsis in meiosis | Q37367245 | ||
| Crossover heterogeneity in the absence of hotspots in Caenorhabditis elegans | Q37412741 | ||
| Identification of chromosome sequence motifs that mediate meiotic pairing and synapsis in C. elegans | Q37727084 | ||
| Initiation of meiotic recombination: how and where? Conservation and specificities among eukaryotes | Q38139495 | ||
| Meiotic recombination in mammals: localization and regulation | Q38153644 | ||
| Endonucleolytic processing of covalent protein-linked DNA double-strand breaks | Q38322004 | ||
| Meiotic segregation, synapsis, and recombination checkpoint functions require physical interaction between the chromosomal proteins Red1p and Hop1p | Q39455264 | ||
| HTP-1-dependent constraints coordinate homolog pairing and synapsis and promote chiasma formation during C. elegans meiosis | Q39705513 | ||
| HTP-1 coordinates synaptonemal complex assembly with homolog alignment during meiosis in C. elegans | Q39705533 | ||
| A Caenorhabditis elegans cohesion protein with functions in meiotic chromosome pairing and disjunction | Q40424054 | ||
| The synaptonemal complex shapes the crossover landscape through cooperative assembly, crossover promotion and crossover inhibition during Caenorhabditis elegans meiosis | Q34131609 | ||
| Partner choice during meiosis is regulated by Hop1-promoted dimerization of Mek1. | Q34148240 | ||
| Divergent kleisin subunits of cohesin specify mechanisms to tether and release meiotic chromosomes. | Q34241406 | ||
| SLX-1 is required for maintaining genomic integrity and promoting meiotic noncrossovers in the Caenorhabditis elegans germline | Q34395310 | ||
| A conserved checkpoint monitors meiotic chromosome synapsis in Caenorhabditis elegans | Q34474546 | ||
| Comparative analysis of metazoan chromatin organization | Q34486035 | ||
| Broad chromosomal domains of histone modification patterns in C. elegans | Q34548272 | ||
| Nondisjunction Mutants of the Nematode CAENORHABDITIS ELEGANS. | Q34605661 | ||
| xnd-1 regulates the global recombination landscape in Caenorhabditis elegans. | Q34610168 | ||
| Transposons but not retrotransposons are located preferentially in regions of high recombination rate in Caenorhabditis elegans | Q34610956 | ||
| Caenorhabditis elegans chromosome arms are anchored to the nuclear membrane via discontinuous association with LEM-2 | Q34613778 | ||
| Recombinogenic effects of suppressors of position-effect variegation in Drosophila | Q34614362 | ||
| Roles for Caenorhabditis elegans rad-51 in meiosis and in resistance to ionizing radiation during development | Q34614445 | ||
| The chromosome axis controls meiotic events through a hierarchical assembly of HORMA domain proteins | Q34625506 | ||
| An asymmetric chromosome pair undergoes synaptic adjustment and crossover redistribution during Caenorhabditis elegans meiosis: implications for sex chromosome evolution | Q34714921 | ||
| Budding yeast ATM/ATR control meiotic double-strand break (DSB) levels by down-regulating Rec114, an essential component of the DSB-machinery. | Q34795521 | ||
| The C. elegans DSB-2 protein reveals a regulatory network that controls competence for meiotic DSB formation and promotes crossover assurance. | Q34945606 | ||
| Meiotic checkpoints and the interchromosomal effect on crossing over in Drosophila females | Q35079067 | ||
| Nuclear reorganization and homologous chromosome pairing during meiotic prophase require C. elegans chk-2. | Q35079512 | ||
| Pairing centers recruit a Polo-like kinase to orchestrate meiotic chromosome dynamics in C. elegans | Q35128564 | ||
| Synapsis and chiasma formation in Caenorhabditis elegans require HIM-3, a meiotic chromosome core component that functions in chromosome segregation | Q35205580 | ||
| Spo11 and the Formation of DNA Double-Strand Breaks in Meiosis | Q35212439 | ||
| HIM-8 binds to the X chromosome pairing center and mediates chromosome-specific meiotic synapsis | Q35619440 | ||
| Chromosome sites play dual roles to establish homologous synapsis during meiosis in C. elegans | Q35619465 | ||
| Dynein-dependent processive chromosome motions promote homologous pairing in C. elegans meiosis | Q35666304 | ||
| A role for Caenorhabditis elegans chromatin-associated protein HIM-17 in the proliferation vs. meiotic entry decision | Q35757732 | ||
| Synapsis-dependent and -independent mechanisms stabilize homolog pairing during meiotic prophase in C. elegans | Q35804006 | ||
| COSA-1 reveals robust homeostasis and separable licensing and reinforcement steps governing meiotic crossovers | Q35919527 | ||
| SYP-3 restricts synaptonemal complex assembly to bridge paired chromosome axes during meiosis in Caenorhabditis elegans | Q35945636 | ||
| Mek1 kinase is regulated to suppress double-strand break repair between sister chromatids during budding yeast meiosis | Q35950096 | ||
| Direct Visualization Reveals Kinetics of Meiotic Chromosome Synapsis | Q36048178 | ||
| The Chromosome Axis Mediates Feedback Control of CHK-2 to Ensure Crossover Formation in C. elegans | Q36218780 | ||
| A conserved function for a Caenorhabditis elegans Com1/Sae2/CtIP protein homolog in meiotic recombination | Q36274716 | ||
| Meiotic crossover number and distribution are regulated by a dosage compensation protein that resembles a condensin subunit | Q36367233 | ||
| P921 | main subject | Caenorhabditis elegans | Q91703 |
| P304 | page(s) | 106-116 | |
| P577 | publication date | 2016-03-21 | |
| P1433 | published in | Seminars in Cell & Developmental Biology | Q14330411 |
| P1476 | title | Meiotic recombination and the crossover assurance checkpoint in Caenorhabditis elegans | |
| P478 | volume | 54 |
| Q64114668 | A DNA repair protein and histone methyltransferase interact to promote genome stability in the Caenorhabditis elegans germ line |
| Q46110383 | A Surveillance System Ensures Crossover Formation in C. elegans. |
| Q52361832 | A compartmentalized signaling network mediates crossover control in meiosis. |
| Q92749685 | Engineering meiotic recombination pathways in rice |
| Q33725749 | Functional characterization of the meiosis-specific DNA double-strand break inducing factor SPO-11 from C. elegans. |
| Q46301631 | Genome Architecture and Evolution of a Unichromosomal Asexual Nematode |
| Q92077899 | Leagues of their own: sexually dimorphic features of meiotic prophase I |
| Q55221543 | The conserved LEM-3/Ankle1 nuclease is involved in the combinatorial regulation of meiotic recombination repair and chromosome segregation in Caenorhabditis elegans. |
| Q42741313 | To Break or Not To Break: Sex Chromosome Hemizygosity During Meiosis in Caenorhabditis |
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