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Large retrotransposon derivatives: abundant, conserved but nonautonomous retroelements of barley and related genomesEnvelope-class retrovirus-like elements are widespread, transcribed and spliced, and insertionally polymorphic in plantsIntroduction on Using the FastPCR Software and the Related Java Web Tools for PCR and Oligonucleotide Assembly and AnalysisIn Silico PCR Tools for a Fast Primer, Probe, and Advanced SearchingA high-density cytogenetic map of the Aegilops tauschii genome incorporating retrotransposons and defense-related genes: insights into cereal chromosome structure and function.iPBS: a universal method for DNA fingerprinting and retrotransposon isolation.Transposable elements in a marginal plant population: temporal fluctuations provide new insights into genome evolution of wild diploid wheatFastPCR software for PCR, in silico PCR, and oligonucleotide assembly and analysis.Diversity of long terminal repeat retrotransposon genome distribution in natural populations of the wild diploid wheat Aegilops speltoides.Analysis of plant diversity with retrotransposon-based molecular markers.Genome evolution of wild barley (Hordeum spontaneum) by BARE-1 retrotransposon dynamics in response to sharp microclimatic divergence.Novel alleles of the VERNALIZATION1 genes in wheat are associated with modulation of DNA curvature and flexibility in the promoter region.Design and validation of an STR hexaplex assay for DNA profiling of grapevine cultivars.FastPCR: An in silico tool for fast primer and probe design and advanced sequence analysis.Cassandra retrotransposons carry independently transcribed 5S RNAGeneration of SNP markers for short straw in oat (Avena sativa L.).Discovery, evaluation and distribution of haplotypes and new alleles of the Photoperiod-A1 gene in wheat.Assessment of genetic diversity in Nordic timothy (Phleum pratense L.).Variability, recombination, and mosaic evolution of the barley BARE-1 retrotransposon.Transposon-based tagging: IRAP, REMAP, and iPBS.Genetic variability in sunflower (Helianthus annuus L.) and in the Helianthus genus as assessed by retrotransposon-based molecular markers.Retrotransposon BARE-1: expression of encoded proteins and formation of virus-like particles in barley cellsThe Tvv1 retrotransposon family is conserved between plant genomes separated by over 100 million years.Comparison of the utility of barley retrotransposon families for genetic analysis by molecular marker techniques.Allelic variation at the VERNALIZATION-A1, VRN-B1, VRN-B3, and PHOTOPERIOD-A1 genes in cultivars of Triticum durum Desf.Copy-number variation of housekeeping gene rpl13a in rat strains selected for nervous system excitability.Genetic diversity of cultivated flax (Linum usitatissimum L.) germplasm assessed by retrotransposon-based markers.Development of IRAP- and REMAP-derived SCAR markers for marker-assisted selection of the stripe rust resistance gene Yr15 derived from wild emmer wheat.TRIM retrotransposons occur in apple and are polymorphic between varieties but not sports.Retrotransposon-Based Genetic Diversity Assessment in Wild Emmer Wheat (Triticum turgidum ssp. dicoccoides)Allelic Diversity of Acetyl Coenzyme A Carboxylase / Genes Implicated in Nuclear-Cytoplasmic Conflict in the Wild and Domesticated Pea ( sp.)Natural History of a Satellite DNA Family: From the Ancestral Genome Component to Species-Specific Sequences, Concerted and Non-Concerted EvolutionIRAP and REMAP: two new retrotransposon-based DNA fingerprinting techniquesActive retrotransposons are a common feature of grass genomesRetrotransposons and genomic stability in populations of the young allopolyploid species Spartina anglica C.E. Hubbard (Poaceae)Reme1, a Copia retrotransposon in melon, is transcriptionally induced by UV lightIRAP and REMAP for retrotransposon-based genotyping and fingerprintingMapping of major spot-type and net-type net-blotch resistance genes in the Ethiopian barley line CI 9819A major gene for grain cadmium accumulation in oat (Avena sativa L.).A doubled haploid rye linkage map with a QTL affecting α-amylase activity
P50
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