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Guidelines for genome-wide association studiesMeiotic transmission of an in vitro-assembled autonomous maize minichromosomeWho's driving the centromere?A meiotic tapas menuFANCM limits meiotic crossoversPLOS Genetics Data Sharing Policy: In Pursuit of Functional UtilityA Decad(e) of Reasons to Contribute to a PLOS Community-Run JournalThe cotton centromere contains a Ty3-gypsy-like LTR retroelementFluorescent Arabidopsis tetrads: a visual assay for quickly developing large crossover and crossover interference data sets.Synergid cell death in Arabidopsis is triggered following direct interaction with the pollen tube.The role of AtMUS81 in interference-insensitive crossovers in A. thalianaThe cyclin-A CYCA1;2/TAM is required for the meiosis I to meiosis II transition and cooperates with OSD1 for the prophase to first meiotic division transition.Arabidopsis RAD51, RAD51C and XRCC3 proteins form a complex and facilitate RAD51 localization on chromosomes for meiotic recombination.Fluorescence-tagged transgenic lines reveal genetic defects in pollen growth--application to the eIF3 complex.Genetic interference: don't stand so close to me.Detection of genomic variations and DNA polymorphisms and impact on analysis of meiotic recombination and genetic mapping.Epigenetic remodeling of meiotic crossover frequency in Arabidopsis thaliana DNA methyltransferase mutants.Deep genome-wide measurement of meiotic gene conversion using tetrad analysis in Arabidopsis thalianaDoes crossover interference count in Saccharomyces cerevisiae?Crossover interference on nucleolus organizing region-bearing chromosomes in Arabidopsis.Crossover interference in ArabidopsisUsing Arabidopsis to understand centromere function: progress and prospects.Juxtaposition of heterozygous and homozygous regions causes reciprocal crossover remodelling via interference during Arabidopsis meiosisPollen tetrad-based visual assay for meiotic recombination in Arabidopsis.Assaying genome-wide recombination and centromere functions with Arabidopsis tetrads.The rapidly evolving field of plant centromeres.Analysis of the Relationships between DNA Double-Strand Breaks, Synaptonemal Complex and Crossovers Using the Atfas1-4 Mutant.Formation of interference-sensitive meiotic cross-overs requires sufficient DNA leading-strand elongationArabidopsis PCH2 Mediates Meiotic Chromosome Remodeling and Maturation of Crossovers.Arabidopsis Cell Division Cycle 20.1 Is Required for Normal Meiotic Spindle Assembly and Chromosome Segregation.Recombination Rate Heterogeneity within Arabidopsis Disease Resistance GenesPlant genetics: when not to interfere.The DNA replication factor RFC1 is required for interference-sensitive meiotic crossovers in Arabidopsis thaliana.The RNA polymerase I transactivator upstream binding factor requires its dimerization domain and high-mobility-group (HMG) box 1 to bend, wrap, and positively supercoil enhancer DNA.Arabidopsis meiotic crossover hot spots overlap with H2A.Z nucleosomes at gene promotersVisual markers for detecting gene conversion directly in the gametes of Arabidopsis thaliana.The RNA polymerase I transcription factor UBF is a sequence-tolerant HMG-box protein that can recognize structured nucleic acidsMeiotic recombination gets stressed out: CO frequency is plastic under pressure.A positive but complex association between meiotic double-strand break hotspots and open chromatin in Saccharomyces cerevisiae.Bringing PLOS Genetics Editors to Preprint Servers.
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P50
description
hulumtues
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researcher
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հետազոտող
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name
Gregory P Copenhaver
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Gregory P Copenhaver
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Gregory P. Copenhaver
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Gregory P. Copenhaver
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Gregory P Copenhaver
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Gregory P Copenhaver
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Gregory P. Copenhaver
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Gregory P. Copenhaver
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GP Copenhaver Gregory Copenhaver, Greg Copenhaver, Greg P. Copenhaver, G Copenhaver
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Gregory P Copenhaver
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Gregory P Copenhaver
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Gregory P. Copenhaver
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Gregory P. Copenhaver
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P1053
A-7549-2014
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P1153
7004315338
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Gcopenhaver1
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0000-0002-7962-3862