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The Spirodela polyrhiza genome reveals insights into its neotenous reduction fast growth and aquatic lifestyleDynamics of a novel centromeric histone variant CenH3 reveals the evolutionary ancestral timing of centromere biogenesis.A Ty3/gypsy retrotransposon-like sequence localizes to the centromeric regions of cereal chromosomes.Tissue-specific genome instability in synthetic interspecific hybrids of Pennisetum purpureum (Napier grass) and Pennisetum glaucum (pearl millet) is caused by micronucleation.'Who's who' in two different flower types of Calluna vulgaris (Ericaceae): morphological and molecular analyses of flower organ identity.Shrinking genomes? Evidence from genome size variation in Crepis (Compositae).Division of the nucleolus and its release of CDC14 during anaphase of meiosis I depends on separase, SPO12, and SLK19.Selfish supernumerary chromosome reveals its origin as a mosaic of host genome and organellar sequences.DNA methylation mediated control of gene expression is critical for development of crown gall tumorsFlow karyotyping and sorting of Vicia faba chromosomes.B chromosomes of Aegilops speltoides are enriched in organelle genome-derived sequences.Measuring Meiotic Crossovers via Multi-Locus Genotyping of Single Pollen Grains in Barley.Arabidopsis MZT1 homologs GIP1 and GIP2 are essential for centromere architecture.Chromatin organization and cytological features of carnivorous Genlisea species with large genome size differences.Point mutation impairs centromeric CENH3 loading and induces haploid plantsAnalysis of transposable elements and organellar DNA in male and female genomes of a species with a huge Y chromosome reveals distinct Y centromeres.Holocentromeres in Rhynchospora are associated with genome-wide centromere-specific repeat arrays interspersed among euchromatin.Differentiation induction of mouse embryonic stem cells into sinus node-like cells by suramin.Copy number variation in transcriptionally active regions of sexual and apomictic Boechera demonstrates independently derived apomictic lineages.Chromosome painting in Drosophila.Replication of ribosomal DNA in Arabidopsis occurs both inside and outside the nucleolus during S phase progression.Cytogenetic comparison of heteromorphic and homomorphic sex chromosomes in Coccinia (Cucurbitaceae) points to sex chromosome turnover.Decondensation of chromosomal 45S rDNA sites in Lolium and Festuca genotypes does not result in karyotype instability.Centromere and telomere sequence alterations reflect the rapid genome evolution within the carnivorous plant genus Genlisea.The conserved chimeric transcript UPGRADE2 is associated with unreduced pollen formation and is exclusively found in apomictic Boechera species.Arabidopsis SET DOMAIN GROUP2 is required for H3K4 trimethylation and is crucial for both sporophyte and gametophyte development.Interspecific hybrids of Hordeum marinum ssp. marinum x H. bulbosum are mitotically stable and reveal no gross alterations in chromatin properties.Chromosome arrangement and nuclear architecture but not centromeric sequences are conserved between Arabidopsis thaliana and Arabidopsis lyrata.Altered expression of Aurora kinases in Arabidopsis results in aneu- and polyploidization.Knockdown of CENH3 in Arabidopsis reduces mitotic divisions and causes sterility by disturbed meiotic chromosome segregation.The P. patens chromosome-scale assembly reveals moss genome structure and evolution.The chromosomal distribution of histone methylation marks in gymnosperms differs from that of angiosperms.Evidence for the sexual origin of heterokaryosis in arbuscular mycorrhizal fungi.Plantago lagopus B Chromosome Is Enriched in 5S rDNA-Derived Satellite DNA.Holokinetic centromeres and efficient telomere healing enable rapid karyotype evolution.Vacuolar processing enzyme 4 contributes to maternal control of grain size in barley by executing programmed cell death in the pericarp.Grain yield and quality responses of wheat expressing a barley sucrose transporter to combined climate change factors.How do Alliaceae stabilize their chromosome ends in the absence of TTTAGGG sequences?Loading of Arabidopsis centromeric histone CENH3 occurs mainly during G2 and requires the presence of the histone fold domain.MGO3 and GIP1 act synergistically for the maintenance of centromeric cohesion.
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onderzoeker
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researcher
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հետազոտող
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name
Joerg Fuchs
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Joerg Fuchs
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Joerg Fuchs
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Joerg Fuchs
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Joerg Fuchs
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type
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Joerg Fuchs
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Joerg Fuchs
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Joerg Fuchs
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Joerg Fuchs
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Joerg Fuchs
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prefLabel
Joerg Fuchs
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Joerg Fuchs
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Joerg Fuchs
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Joerg Fuchs
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Joerg Fuchs
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P214
P106
P214
P31
P496
0000-0003-4171-5371
P734
P7859
viaf-47491188