scholarly article | Q13442814 |
P2093 | author name string | Ashwini Oke | |
Jennifer C Fung | |||
Carol M Anderson | |||
Phoebe Yam | |||
Tangna Zhuge | |||
P2860 | cites work | Controlling meiotic recombinational repair - specifying the roles of ZMMs, Sgs1 and Mus81/Mms4 in crossover formation | Q21144863 |
Phosphorylation of the axial element protein Hop1 by Mec1/Tel1 ensures meiotic interhomolog recombination. | Q51962360 | ||
Budding Yeast Sae2 is an In Vivo Target of the Mec1 and Tel1 Checkpoint Kinases During Meiosis. | Q53609546 | ||
Tel1(ATM)-mediated interference suppresses clustered meiotic double-strand-break formation. | Q53659612 | ||
SPO11 is required for sex-body formation, and Spo11 heterozygosity rescues the prophase arrest of Atm-/- spermatocytes. | Q53667783 | ||
Covariation of synaptonemal complex length and mammalian meiotic exchange rates | Q74253817 | ||
A THIRD GROUP OF LINKED GENES IN DROSOPHILA AMPELOPHILA | Q81187298 | ||
ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomes | Q21145047 | ||
Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage | Q24529923 | ||
Distinct DNA-damage-dependent and -independent responses drive the loss of oocytes in recombination-defective mouse mutants | Q24557469 | ||
Differential association of the conserved SUMO ligase Zip3 with meiotic double-strand break sites reveals regional variations in the outcome of meiotic recombination | Q27934547 | ||
Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis | Q27934770 | ||
Pch2 acts through Xrs2 and Tel1/ATM to modulate interhomolog bias and checkpoint function during meiosis | Q27936069 | ||
Interhomolog bias during meiotic recombination: meiotic functions promote a highly differentiated interhomolog-only pathway | Q27936249 | ||
Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis | Q27936900 | ||
High-resolution mapping of meiotic crossovers and non-crossovers in yeast | Q27938210 | ||
Zip3 provides a link between recombination enzymes and synaptonemal complex proteins | Q27939710 | ||
Meiotic crossover control by concerted action of Rad51-Dmc1 in homolog template bias and robust homeostatic regulation | Q27940335 | ||
Differential timing and control of noncrossover and crossover recombination during meiosis | Q28207440 | ||
Mouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPase | Q28586590 | ||
Gradual implementation of the meiotic recombination program via checkpoint pathways controlled by global DSB levels | Q28649852 | ||
Homologue engagement controls meiotic DNA break number and distribution | Q28658207 | ||
ATM controls meiotic double-strand-break formation | Q28742900 | ||
The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination | Q29618523 | ||
Meiotic chromosome synapsis-promoting proteins antagonize the anti-crossover activity of sgs1. | Q30827295 | ||
Mapping meiotic single-strand DNA reveals a new landscape of DNA double-strand breaks in Saccharomyces cerevisiae | Q33310052 | ||
MUS81 generates a subset of MLH1-MLH3-independent crossovers in mammalian meiosis | Q33369076 | ||
Pch2 links chromosome axis remodeling at future crossover sites and crossover distribution during yeast meiosis | Q33486503 | ||
Characterization of meiotic crossovers and gene conversion by whole-genome sequencing in Saccharomyces cerevisiae | Q33510816 | ||
Genetic interference: don't stand so close to me. | Q33867674 | ||
Crossing over during Caenorhabditis elegans meiosis requires a conserved MutS-based pathway that is partially dispensable in budding yeast | Q33878802 | ||
Factors that affect the location and frequency of meiosis-induced double-strand breaks in Saccharomyces cerevisiae. | Q33965142 | ||
Competition between adjacent meiotic recombination hotspots in the yeast Saccharomyces cerevisiae | Q33969559 | ||
Topoisomerase II mediates meiotic crossover interference | Q34026349 | ||
ReCombine: a suite of programs for detection and analysis of meiotic recombination in whole-genome datasets | Q34064311 | ||
RTEL-1 enforces meiotic crossover interference and homeostasis | Q34102182 | ||
The synaptonemal complex shapes the crossover landscape through cooperative assembly, crossover promotion and crossover inhibition during Caenorhabditis elegans meiosis | Q34131609 | ||
Does crossover interference count in Saccharomyces cerevisiae? | Q34567177 | ||
Chromosome-wide regulation of meiotic crossover formation in Caenorhabditis elegans requires properly assembled chromosome axes | Q34569555 | ||
Interference-mediated synaptonemal complex formation with embedded crossover designation | Q34601423 | ||
Distribution of crossing over on mouse synaptonemal complexes using immunofluorescent localization of MLH1 protein. | Q34606677 | ||
Regulation of genome stability by TEL1 and MEC1, yeast homologs of the mammalian ATM and ATR genes | Q34615334 | ||
The Mus81/Mms4 Endonuclease Acts Independently of Double-Holliday Junction Resolution to Promote a Distinct Subset of Crossovers During Meiosis in Budding Yeast | Q34617616 | ||
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 | ||
High throughput sequencing reveals alterations in the recombination signatures with diminishing Spo11 activity | Q35034403 | ||
Meiotic crossover patterns: obligatory crossover, interference and homeostasis in a single process. | Q35158050 | ||
Spo11 and the Formation of DNA Double-Strand Breaks in Meiosis | Q35212439 | ||
Drosophila ATM and ATR have distinct activities in the regulation of meiotic DNA damage and repair | Q35503860 | ||
Meiotic double-strand breaks occur once per pair of (sister) chromatids and, via Mec1/ATR and Tel1/ATM, once per quartet of chromatids | Q35647513 | ||
Patterns of recombination and MLH1 foci density along mouse chromosomes: modeling effects of interference and obligate chiasma. | Q35911013 | ||
COSA-1 reveals robust homeostasis and separable licensing and reinforcement steps governing meiotic crossovers | Q35919527 | ||
BLM ortholog, Sgs1, prevents aberrant crossing-over by suppressing formation of multichromatid joint molecules | Q36082370 | ||
Distinct functions of MLH3 at recombination hot spots in the mouse. | Q36571740 | ||
Numerical constraints and feedback control of double-strand breaks in mouse meiosis | Q36832176 | ||
ZMM proteins during meiosis: crossover artists at work | Q36900922 | ||
Positive regulation of meiotic DNA double-strand break formation by activation of the DNA damage checkpoint kinase Mec1(ATR). | Q37058652 | ||
Three distinct modes of Mec1/ATR and Tel1/ATM activation illustrate differential checkpoint targeting during budding yeast early meiosis | Q37122881 | ||
ATR/Mec1 prevents lethal meiotic recombination initiation on partially replicated chromosomes in budding yeast. | Q37208603 | ||
Choreography of recombination proteins during the DNA damage response | Q37310881 | ||
Tying synaptonemal complex initiation to the formation and programmed repair of DNA double-strand breaks | Q37358029 | ||
Crossover patterning by the beam-film model: analysis and implications | Q37533767 | ||
Chromosome spreading and immunofluorescence methods in Saccharomyes cerevisiae | Q37580787 | ||
Homeostatic regulation of meiotic DSB formation by ATM/ATR. | Q38239320 | ||
Self-organization of meiotic recombination initiation: general principles and molecular pathways | Q38271059 | ||
Genome-wide redistribution of meiotic double-strand breaks in Saccharomyces cerevisiae | Q38306251 | ||
Sequence non-specific double-strand breaks and interhomolog interactions prior to double-strand break formation at a meiotic recombination hot spot in yeast | Q40789703 | ||
Meiotic chromosome structures constrain and respond to designation of crossover sites | Q41945337 | ||
Condensins regulate meiotic DNA break distribution, thus crossover frequency, by controlling chromosome structure | Q41948641 | ||
Direct and indirect control of the initiation of meiotic recombination by DNA damage checkpoint mechanisms in budding yeast | Q41971919 | ||
A hierarchical combination of factors shapes the genome-wide topography of yeast meiotic recombination initiation | Q42079090 | ||
Effects of Saccharomyces cerevisiae mec1, tel1, and mre11 mutations on spontaneous and methylmethane sulfonate-induced genome instability | Q43089586 | ||
Global analysis of the meiotic crossover landscape. | Q43196392 | ||
Sae2p phosphorylation is crucial for cooperation with Mre11p for resection of DNA double-strand break ends during meiotic recombination in Saccharomyces cerevisiae | Q46452895 | ||
The Sgs1 Helicase Regulates Chromosome Synapsis and Meiotic Crossing Over | Q47388021 | ||
Imposition of crossover interference through the nonrandom distribution of synapsis initiation complexes | Q47910491 | ||
TEL1, a gene involved in controlling telomere length in S. cerevisiae, is homologous to the human ataxia telangiectasia gene | Q48070727 | ||
Atm deficiency results in severe meiotic disruption as early as leptonema of prophase I. | Q48932881 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 8 | |
P304 | page(s) | e1005478 | |
P577 | publication date | 2015-08-25 | |
P1433 | published in | PLOS Genetics | Q1893441 |
P1476 | title | Reduced Crossover Interference and Increased ZMM-Independent Recombination in the Absence of Tel1/ATM. | |
P478 | volume | 11 |
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