ライフサイエンスコーパス: dioecious

1 criformis, with a ZW system conserved across dioecious and androdioecious populations and that hermap

2 flowers and leaves, and between the sexes of dioecious and gynodioecious species.

3 sexual flowers has evolved numerous times in dioecious and monoecious plant taxa.

4 data for dozens of genera that contain both dioecious and nondioecious species.

5 7 males, females and hermaphrodites from one dioecious and one androdioecious population.

6 isolation of distinctive X and Y alleles in dioecious and trioecious species of Vasconcellea demonst

7 In most dioecious angiosperm species, flowers are initially perf

8 among 10 local populations of Silene alba, a dioecious angiosperm.

9 Sex differences in dioecious animals are pervasive and result from gene exp

10 otandrous hermaphrodite) and the introduced (dioecious) bivalves.

11 Bayesian model for analyzing diallel data on dioecious diploid inbred strains that cleanly decomposes

12 For a dioecious diploid population subdivided into an arbitrar

13 xpression in Schistosoma mansoni, a derived, dioecious flatworm.

14 tion in both male and female roles whereas a dioecious/gonochorist population consists of distinct ma

15 Nitellopsis obtusa (starry stonewort) is a dioecious green alga native to Europe and Asia that has

16 utstanding features of schistosomes is their dioecious lifestyle and the pairing-dependent differenti

17 We found a bimodal distribution, whereby dioecious lineages exhibited higher diversification in c

18 l and evolved populations and found that the dioecious lineages underwent more extinction than androd

19 arding the relative diversification rates of dioecious lineages vs their nondioecious counterparts, d

20 , as frequently happens within clumps of the dioecious liverwort Marchantia inflexa.

21 marker to reject this model: sex in diploid dioecious M. annua is determined at a single locus with

22 s of wild strawberry--one almost exclusively dioecious (males and females), Fragaria chiloensis, and

23 Dioecious members of the genus Thalictrum (meadow-rue),

24 lonally propagating males from lineages in a dioecious metapopulation of the European annual plant Me

25 reproduction in Ocotea tenera (Lauraceae), a dioecious neotropical tree common in lower montane fores

26 tion in crosses and unrelated samples of the dioecious octoploid strawberry Fragaria chiloensis in or

27 re cloned, sequenced and analyzed from three dioecious, one trioecious and one monoecious species of

28 demographic and selection models, including dioecious or monoecious populations, autosomal or sex ch

29 Among dioecious organisms, there is strong evidence for sex di

30 surprisingly given its potential ubiquity in dioecious organisms.

31 us clade) or in Kryptolebias brasiliensis (a dioecious outgroup).

32 s challenge, we established genetic cross of dioecious plant Rumex acetosa and generated RNA-Seq data

33 investigate sex chromosome evolution in the dioecious plant Rumex hastatulus, in which X and Y chrom

34 t of newly generated deletion mutants in the dioecious plant Silene latifolia and refined the locatio

35 protein is linked to the X chromosome in the dioecious plant Silene latifolia, and that it has a dege

36 nant genic markers in genetic mapping of the dioecious plant Silene latifolia, together with comparat

37 Females of dioecious plant species typically invest more in reprodu

38 White campion (Silene latifolia) is a dioecious plant that emits 1,2-dimethoxybenzene (veratro

39 the Caucasian persimmon, Diospyros lotus, a dioecious plant with heterogametic males (XY).

40 Silene latifolia is a dioecious plant with heteromorphic sex chromosomes.

41 S. latifolia is a dioecious plant with morphologically distinct sex chromo

42 f sex chromosome evolution that is common to dioecious plants and animals.

43 d in distinct individuals (dioecy), and most dioecious plants do not have cytologically different (he

44 s and birds, but not for plants, although 48 dioecious plants have already been reported.

45 olia, using Silene dioica, a closely related dioecious plants whose XY sex chromosome system is inher

46 defining feature of gonochorous animals and dioecious plants, but the evolution of SD from an initia

47 odestly diverged SDR may be typical of other dioecious plants.

48 ngly, with a larger sex-linked region in the dioecious population compared with the androdioecious po

49 gests that the hermaphrodite form arose in a dioecious population from a recessive mutation that allo

50 n-genetic model of phenotypic evolution in a dioecious population that incorporates previously neglec

51 rodites should have a twofold advantage over dioecious population when reproduction is limited by mat

52 In a dioecious population, the analogous reduction does not o

53 all genes in the X-linked region in the wild dioecious population, with nucleotide diversity pi syn =

54 single multiallelic locus in a monoecious or dioecious population; in the latter case, the locus may

55 to one Y haplotype (MSY3) found only in wild dioecious populations from the north Pacific region of C

56 hich uses moment-type estimators, applies to dioecious populations in which females and males have id

57 nary analysis of social traits in finite and dioecious populations, where interactions can occur with

58 usual 3-locus system of sex determination in dioecious populations.

59 ubspecies and male or female flowers in wild dioecious relatives (Vitis vinifera ssp.

60 ubspecies and male or female flowers in wild dioecious relatives (Vitis vinifera ssp. sylvestris).

61 onary transitions between hermaphroditic and dioecious reproductive states are found in many groups o

62 Amborella, a monotypic, vessel-less dioecious shrub from New Caledonia, was clearly identifi

63 a suggest that, in both D. glomerata and its dioecious sister species D. cannabina, sex is determined

64 Populations of heterostylous and dioecious species have a small number of mating groups (

65 many old haplotypes while hermaphroditic and dioecious species have little to no nucleotide diversity

66 f several hermaphroditic, gynodioecious, and dioecious species in the genus Silene.

67 Dioecious species may be especially vulnerable to climat

68 The genes governing sex determination in dioecious species remain unknown, but theory predicts th

69 distribution of plant species, particularly dioecious species that show a spatial segregation of the

70 plant lineages, sometimes in closely related dioecious species, and often within the past few million

71 perfectly sex-linked marker was found in the dioecious species, but all markers associated with sex m

72 about the levels of inbreeding depression in dioecious species, obviously because it is difficult to

73 s a powerful hypothesis for the evolution of dioecious species.

74 ved in autosomal and sex-linked genes in the dioecious species.

75 ts compared with co-occurring male plants of dioecious species.

76 s, would be pollinated by A. tuberculatus, a dioecious species.

77 an agriculturally and economically important dioecious tree in the basal dicot family Lauraceae used

78 AULA, was cloned to assess its function in a dioecious tree species.

79 c systems underlying floral development in a dioecious tree, and to provide tools for the manipulatio

80 of MADS box transcription factors, from the dioecious tree, black cottonwood (Populus trichocarpa).

81 s woody structure, perennial life cycle, and dioecious, two-whorled flowers.

82 The sex chromosomes of dioecious white campion, Silene latifolia (Caryophyllace

83 te pollen and seed dispersal patterns of the dioecious wind-pollinated tree, Araucaria angustifolia.

84 Less than 4% of plant species are dioecious (with individuals of separate sexes), and many

85 hism in the plant Silene latifolia, which is dioecious (with separate male and female individuals) an

86 The majority of nematodes are gonochoristic (dioecious) with distinct male and female sexes, but the

87 The genus Populus consists of dioecious woody species with largely unknown genetic mec