Works matching DE "ALLOPOLYPLOIDY in plant chromosomes"
Results: 194
Phylogenetic relationships of Coronidium, Xerochrysum and several neglected Australian species of "Helichrysum" (Asteraceae: Gnaphalieae).
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- Taxon, 2015, v. 64, n. 1, p. 96, doi. 10.12705/641.5
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Phylogenetic relationships of Coronidium, Xerochrysum and several neglected Australian species of "Helichrysum" (Asteraceae: Gnaphalieae).
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- Taxon, 2015, v. 64, n. 1, p. 96, doi. 10.12705/641.5
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Low-copy nuclear data confirm rampant allopolyploidy in the Cystopteridaceae (Polypodiales).
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- Taxon, 2014, v. 63, n. 5, p. 1026, doi. 10.12705/635.32
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Phylogenetic relationships in Helichrysum (Compositae: Gnaphalieae) and related genera: Incongruence between nuclear and plastid phylogenies, biogeographic and morphological patterns, and implications for generic delimitation.
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- Taxon, 2014, v. 63, n. 3, p. 608, doi. 10.12705/633.8
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Generic status, circumscription, and allopolyploid origin of Faberia (Asteraceae: Cichorieae) as revealed by ITS and chloroplast DNA sequence data.
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- Taxon, 2013, v. 62, n. 6, p. 1235, doi. 10.12705/626.14
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Isolation and characterization of novel Glu- St1 alleles from Pseudoroegneria spicata and Pd. strigosa.
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- Genetica, 2014, v. 142, n. 5, p. 433, doi. 10.1007/s10709-014-9787-0
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Evidence for genetic allopolyploidy in Eutrema edwardsii (Brassicaceae): implications for conservation.
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- Plant Systematics & Evolution, 2018, v. 304, n. 1, p. 133, doi. 10.1007/s00606-017-1447-2
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Nucleotide diversity in the two co-resident genomes of allopolyploid cotton.
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- Plant Systematics & Evolution, 2017, v. 303, n. 8, p. 1021, doi. 10.1007/s00606-017-1411-1
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Time-calibrated phylogenetic trees establish a lag between polyploidisation and diversification in Nicotiana (Solanaceae).
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- Plant Systematics & Evolution, 2017, v. 303, n. 8, p. 1001, doi. 10.1007/s00606-017-1416-9
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Partial interfertility between independently originated populations of the neo-allopolyploid Mimulus peregrinus.
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- Plant Systematics & Evolution, 2017, v. 303, n. 8, p. 1081, doi. 10.1007/s00606-017-1426-7
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Molecular cytogenetic characterization of Triticum timopheevii chromosomes provides new insight on genome evolution of T. zhukovskyi.
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- Plant Systematics & Evolution, 2016, v. 302, n. 8, p. 943, doi. 10.1007/s00606-016-1309-3
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The first karyogram of a Bromeliaceae species: an allopolyploid genome.
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- Plant Systematics & Evolution, 2013, v. 299, n. 6, p. 1135, doi. 10.1007/s00606-013-0784-z
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Genome synteny and evolution of AABB allotetraploids in Hibiscus section Furcaria revealed by interspecific hybridization, ISSR and SSR markers.
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- Plant Systematics & Evolution, 2012, v. 298, n. 7, p. 1257, doi. 10.1007/s00606-012-0632-6
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Allopolyploid speciation of Calypogeia sphagnicola (Jungermanniopsida, Calypogeiaceae) based on isozyme and DNA markers.
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- Plant Systematics & Evolution, 2012, v. 298, n. 3, p. 549, doi. 10.1007/s00606-011-0565-5
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Homeologous Gene Expression in Response to Growing Temperature in a Recent Allopolyploid (Coffea arabica L.).
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- Journal of Heredity, 2012, v. 103, n. 1, p. 36, doi. 10.1093/jhered/esr120
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Adaptation of the Pivotal-Differential Genome Pattern for the Induction of Intergenomic Chromosome Recombination in Hybrids of Synthetic Amphidiploids within Triticeae Tribe.
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- Frontiers in Plant Science, 2017, p. 1, doi. 10.3389/fpls.2017.01300
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Mimulus peregrinus (Phrymaceae): A new British allopolyploid species.
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- PhytoKeys, 2012, n. 14, p. 1, doi. 10.3897/phytokeys.14.3305
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Mysterious meiotic behavior of autopolyploid and allopolyploid maize.
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- Comparative Cytogenetics, 2018, v. 12, n. 2, p. 247, doi. 10.3897/CompCytogen.v12i2.24907
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Identifying parental chromosomes and genomic rearrangements in animal hybrid complexes of species with small genome size using Genomic In Situ Hybridization (GISH).
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- Comparative Cytogenetics, 2012, v. 6, n. 3, p. 287, doi. 10.3897/CompCytogen.v6i3.3543
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Reactions of Nicotiana species to inoculation with monopartite and bipartite begomoviruses.
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- Virology Journal, 2011, v. 8, n. 1, p. 475, doi. 10.1186/1743-422X-8-475
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Digital gene expression analysis of gene expression differences within Brassica diploids and allopolyploids.
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- BMC Plant Biology, 2015, v. 15, n. 1, p. 620, doi. 10.1186/s12870-015-0417-5
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The role of small RNAs in wide hybridisation and allopolyploidisation between Brassica rapa and Brassica nigra.
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- BMC Plant Biology, 2014, v. 14, n. 1, p. 2, doi. 10.1186/s12870-014-0272-9
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Homoeolog expression bias and expression level dominance in resynthesized allopolyploid Brassica napus.
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- BMC Genomics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12864-018-4966-5
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Natural variation in stress response gene activity in the allopolyploid Arabidopsis suecica.
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- BMC Genomics, 2017, v. 18, n. 1, p. 1, doi. 10.1186/s12864-017-4067-x
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HyLiTE: accurate and flexible analysis of gene expression in hybrid and allopolyploid species.
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- BMC Bioinformatics, 2015, v. 16, n. 1, p. 216, doi. 10.1186/s12859-014-0433-8
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Towards the new normal: Transcriptomic convergence and genomic legacy of the two subgenomes of an allopolyploid weed (Capsella bursa-pastoris).
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- PLoS Genetics, 2019, v. 15, n. 5, p. 1, doi. 10.1371/journal.pgen.1008131
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Parental legacy, demography, and admixture influenced the evolution of the two subgenomes of the tetraploid Capsella bursa-pastoris (Brassicaceae).
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- PLoS Genetics, 2019, v. 15, n. 2, p. 1, doi. 10.1371/journal.pgen.1007949
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Plant Genetics: Joining forces - asexual genome merger creates new allopolyploid species.
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- Nature Reviews Genetics, 2014, v. 15, n. 8, p. 515, doi. 10.1038/nrg3782
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Genomic and epigenetic insights into the molecular bases of heterosis.
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- Nature Reviews Genetics, 2013, v. 14, n. 7, p. 471, doi. 10.1038/nrg3503
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Comparative linkage mapping of diploid, tetraploid, and hexaploid Avena species suggests extensive chromosome rearrangement in ancestral diploids.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48639-7
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Cis–trans controls and regulatory novelty accompanying allopolyploidization.
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- New Phytologist, 2019, v. 221, n. 4, p. 1691, doi. 10.1111/nph.15515
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Functional trait divergence and trait plasticity confer polyploid advantage in heterogeneous environments.
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- New Phytologist, 2019, v. 221, n. 4, p. 2286, doi. 10.1111/nph.15508
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Parental transposable element loads influence their dynamics in young Nicotiana hybrids and allotetraploids.
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- New Phytologist, 2019, v. 221, n. 3, p. 1619, doi. 10.1111/nph.15484
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Meiotic chromosome stability of a newly formed allohexaploid wheat is facilitated by selection under abiotic stress as a spandrel.
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- New Phytologist, 2018, v. 220, n. 1, p. 262, doi. 10.1111/nph.15267
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Homoeologous exchanges cause extensive dosage-dependent gene expression changes in an allopolyploid crop.
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- New Phytologist, 2018, v. 217, n. 1, p. 367, doi. 10.1111/nph.14836
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The poor lonesome A subgenome of Brassica napus var. Darmor ( AACC) may not survive without its mate.
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- New Phytologist, 2017, v. 213, n. 4, p. 1886, doi. 10.1111/nph.14147
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Patterns of abiotic niche shifts in allopolyploids relative to their progenitors.
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- New Phytologist, 2016, v. 212, n. 3, p. 708, doi. 10.1111/nph.14069
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Hybridization and hybrid speciation under global change.
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- New Phytologist, 2016, v. 211, n. 4, p. 1170, doi. 10.1111/nph.14004
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On the relative abundance of autopolyploids and allopolyploids.
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- New Phytologist, 2016, v. 210, n. 2, p. 391, doi. 10.1111/nph.13698
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Altered expression of TaRSL4 gene by genome interplay shapes root hair length in allopolyploid wheat.
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- New Phytologist, 2016, v. 209, n. 2, p. 721, doi. 10.1111/nph.13615
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Multiple origins and chromosomal novelty in the allotetraploid Tragopogon castellanus (Asteraceae).
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- New Phytologist, 2015, v. 206, n. 3, p. 1172, doi. 10.1111/nph.13227
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Independent allopolyploidization events preceded speciation in the temperate and tropical woody bamboos.
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- New Phytologist, 2014, v. 204, n. 1, p. 66, doi. 10.1111/nph.12988
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When fathers are instant losers: homogenization of rDNA loci in recently formed Cardamine × schulzii trigenomic allopolyploid.
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- New Phytologist, 2014, v. 203, n. 4, p. 1096, doi. 10.1111/nph.12873
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Contrasting evolutionary trajectories of multiple retrotransposons following independent allopolyploidy in wild wheats.
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- New Phytologist, 2014, v. 202, n. 3, p. 975, doi. 10.1111/nph.12731
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Radiation of the Nod-independent Aeschynomene relies on multiple allopolyploid speciation events.
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- New Phytologist, 2014, v. 201, n. 4, p. 1457, doi. 10.1111/nph.12594
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Contribution of subgenomes to the transcriptome and their intertwined regulation in the allopolyploid Coffea arabica grown at contrasted temperatures.
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- New Phytologist, 2013, v. 200, n. 1, p. 251, doi. 10.1111/nph.12371
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Allopolyploidy has a moderate impact on restructuring at three contrasting transposable element insertion sites in resynthesized Brassica napus allotetraploids.
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- New Phytologist, 2013, v. 198, n. 2, p. 593, doi. 10.1111/nph.12156
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Prevalence of gene expression additivity in genetically stable wheat allohexaploids.
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- New Phytologist, 2013, v. 197, n. 3, p. 730, doi. 10.1111/nph.12108
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Comparative proteomics of the recently and recurrently formed natural allopolyploid Tragopogon mirus (Asteraceae) and its parents.
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- New Phytologist, 2012, v. 196, n. 1, p. 292, doi. 10.1111/j.1469-8137.2012.04251.x
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Dysfunction of mitotic cell division at shoot apices triggered severe growth abortion in interspecific hybrids between tetraploid wheat and Aegilops tauschii.
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- New Phytologist, 2012, v. 194, n. 4, p. 1143, doi. 10.1111/j.1469-8137.2012.04125.x
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