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1 utcrossing species, is a highly heterozygous autotetraploid.
2 autotetraploid but robust in the established autotetraploid.
3 WE at individual loci in allotetraploids and autotetraploids.
4 disomic in allotetraploids and tetrasomic in autotetraploids.
5 tic cross between A. thaliana and A. arenosa autotetraploids.
6  polymorphic markers in a full-sib family of autotetraploids.
7  and large structural variants in A. arenosa autotetraploids.
8 le reduction and its genomic distribution in autotetraploids.
9        This contrasts with naturally evolved autotetraploid A. arenosa, where accurate chromosome seg
10 y different trajectory to that described for autotetraploid A. arenosa.
11 wledge gap, we generate a haplotype-resolved autotetraploid alfalfa (Medicago sativa subsp.
12 oad geographic sample of natural diploid and autotetraploid alfalfa (Medicago sativa) lineages with a
13 g, and use this method to reanalyze the same autotetraploid alfalfa data and to conduct a simulation
14  applied to single-dose restriction fragment autotetraploid alfalfa data, and the performance is inve
15 is in the triploid hybrid between an induced autotetraploid and a related diploid provides the basis
16  were overrepresented between an A. thaliana autotetraploid and diploid and between two Arabidopsis s
17 w (~6.8%) between an A. thaliana diploid and autotetraploid and intermediate (~8.3 and 8.2%) in F(1)-
18   Moreover, a subset of genes is affected in autotetraploid and multiple independent allotetraploid l
19 num tuberosum L.), a vegetatively propagated autotetraploid and their impact on the transcriptome.
20 ence, we have generated human and chimpanzee autotetraploids and allotetraploids by fusing induced pl
21 patterns in intraspecific populations of neo-autotetraploids and their diploid progenitors within Gal
22 ssed this question by comparing diploid, neo-autotetraploid, and established autotetraploid Arabidops
23  Using seven independently derived synthetic autotetraploid Arabidopsis accessions and a synthetic le
24 upled with elemental profiling to assess how autotetraploid Arabidopsis arenosa adapted to a multicha
25 diploid, neo-autotetraploid, and established autotetraploid Arabidopsis arenosa using new approaches
26      We assess this in high resolution using autotetraploid Arabidopsis arenosa, which repeatedly ada
27  in diploid meiosis, is defective in the neo-autotetraploid but robust in the established autotetrapl
28 togenetic consequences in colchicine-induced autotetraploids (colchiploids) from different Arabidopsi
29 or the development of novel cultivars in the autotetraploid crop species.
30                                              Autotetraploid cytotypes, among which the donors of resi
31 l haplotype-resolved genomes were assembled: autotetraploid D. fruticosa (929.99 Mb) and diploid D. g
32                                  Although an autotetraploid donor is hypothesized to have contributed
33 how how genetic variation gradually rises in autotetraploids due to increased mutational target size.
34 hat the duplicated segments diverged from an autotetraploid form, places the duplication at about 38
35 crop with limited genomics tools and complex autotetraploid genetics.
36                                              Autotetraploids had 33% larger and 88% more pollen, and
37                        Relative to diploids, autotetraploids had proportionally longer sepals and pet
38 wering time in Campanulastrum americanum, an autotetraploid herb, to determine the potential for adap
39 in common conditions, and then resequence 24 autotetraploid individuals from three populations to per
40 s when assessed in single-species diploid or autotetraploid iPSCs.
41  diploid species but is far less advanced in autotetraploids, largely due to a lack of analytical met
42                                              Autotetraploid leaves contained significantly increased
43 methodology to use dosage data on SNPs in an autotetraploid mapping population.
44 encies as an important feature of an evolved autotetraploid meiosis.
45  of gene segregation and recombination in an autotetraploid meiosis.
46 rate the rise of S. tuberosum as a model for autotetraploid meiotic recombination research and highli
47 four lineage pairs of diploids and synthetic autotetraploids of the aquatic plant Spirodela polyrhiza
48 the two parental subgenomes might suggest an autotetraploid origin of horseradish and watercress geno
49 . sylvestris is tetrasomic, confirming their autotetraploid origin.
50 eral aspects of these genealogies support an autotetraploid origin.
51 of preferential pairing in second-generation autotetraploid Pacific oysters from gametic frequencies.
52 renosa, a well characterized natural diploid-autotetraploid plant species, to address these questions
53                             We identify wild autotetraploid plants from Ecuador that are morphologica
54                                              Autotetraploid plants obtained greater fitness enhanceme
55 egation of alleles at genetic marker loci in autotetraploid populations and a novel likelihood-based
56 dopsis arenosa (in 23 diploid and 42 natural autotetraploid populations), we measure the effects of W
57 mental data based on 83 previously sequenced autotetraploid potato cultivars.
58  experimental studies on highly heterozygous autotetraploid potato have shown that available methods
59 arkers scored on 228 full-sib individuals of autotetraploid potato is used to illustrate the utility
60 occurring autopolyploid species, such as the autotetraploid potato Solanum tuberosum, face a variety
61 uencing, and for diploid Ipomoea trifida and autotetraploid potato utilizing contigs assembled from I
62 opies in both organelles in early-generation autotetraploids primarily through multiplication of DNA
63 reflect reduced efficacy of selection in the autotetraploid relative to its diploid relative.
64 ual organs increased by a remarkable 213% in autotetraploids relative to diploids, but that surplus w
65 atment of axillary buds resulted in a set of autotetraploid S. viminalis var. Energo genotypes (polyp
66 an be adapted to study population history in autotetraploids simply by interpreting the timescale in
67  survey in potato, a vegetatively propagated autotetraploid species (2n = 4x = 48).
68 resents a method for QTL interval mapping in autotetraploid species for a full-sib family derived by
69                          Linkage analysis in autotetraploid species has been an historical challenge
70 netic architecture of quantitative traits in autotetraploid species is a methodologically challenging
71 bles QTL mapping analysis to be conducted in autotetraploid species under a rigorous tetrasomic inher
72 d on defined meiotic parameters for allo- or autotetraploid species with a gametophytic S-Z SI system
73   Cultivated potato is a clonally propagated autotetraploid species with a highly heterogeneous genom
74             We develop coalescent models for autotetraploid species with tetrasomic inheritance.
75 ng Rho pairwise distances (F(ST) adapted for autotetraploid species) and analysis of molecular varian
76 o construct high-density linkage maps in any autotetraploid species, and could also be extended to hi
77  for the construction of a linkage map in an autotetraploid species, using either codominant or domin
78 apping in outbred segregating populations of autotetraploid species.
79  of Arabidopsis arenosa, a naturally diploid-autotetraploid species.
80 utility of the method in map construction in autotetraploid species.
81 iversity and population genetic structure in autotetraploid species.
82 even Dipterocarpoideae species including two autotetraploid species.
83 h likely indicates meiotic adaptation to the autotetraploid state.
84 ether with a broad distribution and niche of autotetraploids suggests load accumulation has not yet l
85                     As a clonally propagated autotetraploid that undergoes limited meiosis, dysfuncti
86 cts of genome doubling on gene regulation in autotetraploids, the combination of two divergent genome
87                                           In autotetraploids, the enlargement of organelles, cells an
88 seudoplatanus L.), an economically important autotetraploid tree species.
89 tween Col-0, a diploid, and either a natural autotetraploid (Wa-1) or an induced tetraploid of Col-0.
90 ere not possible until a reference genome of autotetraploid wild type sugarcane specie, Saccharum spo
91 lly, is represented by cultivated potato, an autotetraploid with highly heterozygous genomes.
92 ated that tetraploid blueberry behaves as an autotetraploid with tetrasomic inheritance.
93 efense genes in two outcrossing species, the autotetraploid Zea perennis and its most closely related