ライフサイエンスコーパス: autopolyploid

1 racterize gene segregation in the progeny of autopolyploids.

2 paring diploids and new and well-established autopolyploids.

3 nd expands our knowledge of the evolution of autopolyploids.

4 tant gap in the population genetic theory of autopolyploids.

5 yploids and grew further in more established autopolyploids.

6 pecies, and could also be extended to higher autopolyploids.

7 In contrast to allopolyploids, autopolyploid A. thaliana showed the same photosynthetic

8 enetic diversity, variation and evolution in autopolyploids, a class of polyploids derived from the g

9 equenced the transcriptomes of two synthetic autopolyploid accessions of Arabidopsis (Arabidopsis tha

10 d gene expression have been observed in both autopolyploids and allopolyploids, but the effects of po

11 of protein changes in leaves of Arabidopsis autopolyploids and allotetraploids and their progenitors

12 ignificantly higher in the newly established autopolyploids and grew further in more established auto

13 genome copy number in Arabidopsis synthetic autopolyploids and in a haploid-induced diploid line.

14 describe a maximum-likelihood estimator for autopolyploids, and quantify its statistical performance

15 specifying the degree of double reduction of autopolyploids, are estimated.

16 investigating two-point linkage analysis for autopolyploids, based on the random chromosome pairing m

17 trolled manner, there are limited studies on autopolyploids compared to allopolyploids.

18 ations of Achillea borealis (Asteraceae), an autopolyploid complex consisting of tetraploid and hexap

19 Blueberry (Vaccinium spp.) is an important autopolyploid crop with significant benefits for human h

20 zation and subsequent chromosome doubling or autopolyploids due to chromosome doubling of the same ge

21 ses and whether WGD results from an allo- or autopolyploid event is inconsistent with recent data fro

22 This finding suggests an autopolyploid genome identity of S. spontaneum with a hi

23 We have assembled a high-quality autopolyploid genome of S. spontaneum Np-X (2n = 4x = 40

24 For autopolyploids, however, all homologous chromosomes can

25 In autopolyploids, immediate transcriptional changes were m

26 QTL mapping in autopolyploids is complicated by the possibility of segr

27 as used to illustrate the construction of an autopolyploid map.

28 O recombination interactions and that stable autopolyploid meiosis can emerge by evolution of a "supe

29 eiotic recombination; however, studies using autopolyploid meiotic mutants are scarce.

30 and arise frequently by genome duplication (autopolyploids) or interspecific hybridization (allopoly

31 Modern sugarcane, a highly allo-autopolyploid organism, has a very complex genome.

32 WGDs generally can be classified into autopolyploids (ploidy increase descended from one speci

33 Synthetic autopolyploid represents an ideal system to investigate

34 In autopolyploid Saccharum, 36 significant associations bet

35 We developed a synthetic autopolyploid series in potato (Solanum phureja) that in

36 ranscriptomic variation associated with this autopolyploid series using a potato cDNA microarray cont

37 ical methods for genetic map construction in autopolyploid species with particular reference to the u

38 Naturally occurring autopolyploid species, such as the autotetraploid potato

39 lenges involved with the genetic analyses of autopolyploid species, such as the tetraploid potato, So

40 and breeding of tetraploid potato and other autopolyploid species.

41 erential pairing in these recently generated autopolyploids, suggesting that genetic variation in sta

42 However, linkage analysis in autopolyploids, the kernel of linkage map construction,

43 so simplify CO patterns among chromosomes in autopolyploids, thereby promoting bivalent formation.

44 Autopolyploids, which arise by within-species whole-geno