戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 s no evidence that gametophytes later become hermaphroditic.
2  of the fern Ceratopteris are either male or hermaphroditic.
3  of the fern Ceratopteris are either male or hermaphroditic.
4 stems in plants have evolved many times from hermaphroditic ancestors (including monoecious plants wi
5  Separate sexes have evolved repeatedly from hermaphroditic ancestors in flowering plants, and thus s
6 olved on numerous independent occasions from hermaphroditic ancestors in flowering plants.
7             Evolutionary transitions between hermaphroditic and dioecious reproductive states are fou
8 ous species harbor many old haplotypes while hermaphroditic and dioecious species have little to no n
9 the proportion of female progeny produced by hermaphroditic and female plants will show more extreme
10                       We examined males from hermaphroditic and gonochoristic (male-female copulation
11 ng reproductive status to longevity: In both hermaphroditic and gonochoristic Caenorhabditis, mating
12 e measured morphological differences between hermaphroditic and male morph flowers in P. incarnata an
13 ed currents of three identified neurons from hermaphroditic Aplysia californica Two of these neurons,
14                        Both are simultaneous hermaphroditic broadcast spawners that release egg-sperm
15 on analysis and behavioral observations that hermaphroditic C. briggsae and gonochoristic C. remanei
16 y contrast, we show that in the convergently hermaphroditic Caenorhabditis briggsae, GLD-1 acts to pr
17 specific transcriptional master regulator of hermaphroditic cell identity tra-1, which represses the
18 xpression in disc florets from the ancestral hermaphroditic condition to the derived male state.
19  transition from a separate-sexed state to a hermaphroditic condition.
20 tis elegans come into association with their hermaphroditic counterparts they cease foraging behavior
21 velop into females can be respecified toward hermaphroditic development if submitted to dauer-inducin
22 . virginiana and the homeologous autosome of hermaphroditic diploid species.
23 e or transport of sperm, including the small hermaphroditic duct (site of sperm storage before mating
24                                 Sequentially hermaphroditic fish change sex from male to female (prot
25               Here, using a self-fertilizing hermaphroditic fish species, mangrove rivulus (Kryptoleb
26                             Comparisons with hermaphroditic flatworm transcriptomes show masculinisat
27          The lower rate of male sterility of hermaphroditic flowers appears to be regulated by MYB24.
28 wers in P. incarnata were of similar size to hermaphroditic flowers, and there was little evidence of
29 e morph flowers sired twice as many seeds as hermaphroditic flowers.
30                                    While all hermaphroditic forms revert quickly to gonochorism, prot
31 d reproductive success of the simultaneously hermaphroditic freshwater snail Physa acuta.
32                                     Multiple hermaphroditic genera in Juglandaceae, including walnuts
33 s on germline-less glp-1(e2144) mutants, the hermaphroditic germline of C. elegans provides an excell
34  (cox1), for multiple populations of several hermaphroditic, gynodioecious, and dioecious species in
35                    Most flowering plants are hermaphroditic, having flowers with both male and female
36  fern Ceratopteris richardii (Ceratopteris), hermaphroditic (her) mutants develop as hermaphrodites e
37 ion were previously isolated and include the hermaphroditic (her), the transformer (tra) and feminiza
38 sometimes leading to co-occurring female and hermaphroditic individuals (gynodioecy).
39 , resulting in the coexistence of female and hermaphroditic individuals (gynodioecy).
40  Gynodioecy, the co-occurrence of female and hermaphroditic individuals within a population, is an im
41  species consist primarily or exclusively of hermaphroditic individuals, gonochoristic males occur at
42 odioecious plant species containing male and hermaphroditic individuals.
43                                       In the hermaphroditic leech, T and P mechanosensory neurons res
44 use one of two different mating systems-male/hermaphroditic, like the model organism Caenorhabditis e
45                                       In the hermaphroditic marine-snail, Aplysia californica, synapt
46 derstanding the existence of males; and that hermaphroditic mating is reciprocal.
47 ompetition and love darts-common features of hermaphroditic mating.
48                                          The hermaphroditic mode of reproduction could potentially re
49  their similar morphology, life history, and hermaphroditic mode of reproduction.
50 oward male function is a general response of hermaphroditic modular organisms to impaired prospects f
51                                       In the hermaphroditic mollusc Aplysia, after learning that food
52 osperm mating system of heterodichogamy, two hermaphroditic morphs temporally alternate between male
53 , the coexistence of functionally female and hermaphroditic morphs within plant populations, often ha
54  selection system from the distantly related hermaphroditic moss, Physcomitrium patens, we generated
55                      One was associated with hermaphroditic mutants.
56                                    Using the hermaphroditic nematode Caenorhabditis elegans, we here
57 al effects of males evolved independently in hermaphroditic nematodes.
58 This cost is eliminated by the production of hermaphroditic offspring in the self-fertilizing nematod
59 rmaphrodite crosses produced almost entirely hermaphroditic offspring.
60                                              Hermaphroditic (perfect) flowers were a key trait in gra
61 he model is described using the example of a hermaphroditic plant population.
62 tibility between two closely related diploid hermaphroditic plant species.
63 r model focuses on fertility selection in an hermaphroditic plant.
64 of progeny sex ratios produced by female and hermaphroditic plants in small and large populations of
65          Sex-allocation theory developed for hermaphroditic plants predicts that impaired phenotype o
66 sex ratios showed that progeny sex ratios of hermaphroditic plants were strongly influenced by popula
67 rimary sexual, attraction, mating system) in hermaphroditic plants.
68 ther situations; and the 'mating systems' of hermaphroditic populations, inbreeding, outcrossing or i
69 olved many times from ancestral functionally hermaphroditic populations, often recently.
70 ditis, and may reduce the number of males in hermaphroditic populations; neither males nor females of
71                                 For example, hermaphroditic reproduction evolved independently many t
72  contribute to a better understanding of the hermaphroditic reproduction process in the cold Southeas
73    As a first step towards understanding the hermaphroditic reproductive biology of L. stagnalis, we
74  moth species known only from O'ahu, visited hermaphroditic Schiedea kaalae and S. hookeri and remove
75            Several species of simultaneously hermaphroditic seabasses living on coral reefs mate by a
76 avoidance, the magnitude of which depends on hermaphroditic selfing rates and the strength of inbreed
77 y response to the frequency of unisexuals in hermaphroditic sex allocation, and they verify the quant
78                              In sequentially hermaphroditic (sex-changing) fish, the sex ratio is typ
79 ave male and female sexes), but self-fertile hermaphroditic species are not uncommon, and parthenogen
80 sts, P. brevipalpis strongly preferred these hermaphroditic species over two subdioecious species cap
81 P3) and AGAMOUS (AG) from T. dioicum and the hermaphroditic species T. thalictroides.
82 sity should be greater in gynodioecious than hermaphroditic species.
83 asmic diversity in gynodioecious relative to hermaphroditic species.
84 t the nematode phylum, and is not limited to hermaphroditic species.
85 ual and sexual protogynous (i.e. sequential) hermaphroditic stages.
86 61 ESTs from two developmental stages of the hermaphroditic strain of S. mediterranea; this collectio
87                                       In the hermaphroditic strain of this species, Smed-nanos mRNA i
88      Two strains of S. mediterranea exist: a hermaphroditic strain that reproduces sexually and an as
89 have repeatedly reverted to cosexuality, and hermaphroditic strains of fruit crops such as papaya and
90 ploying 3-deoxy- and 3-C-branched glycals as hermaphroditic substrates is revealed.
91 aptive significance of self-fertilization in hermaphroditic taxa, and both scenarios have been invoke
92 ificance of selfing apparently varies across hermaphroditic taxa.
93 inguish two types of systems: 'sex systems', hermaphroditic versus male/female and other situations;
94 ique because it is the only self-fertilizing hermaphroditic vertebrate, known to date.
95  one reason fish are the only simultaneously hermaphroditic vertebrates.
96              The majority of angiosperms are hermaphroditic with total fitness comprised of both male
97  gonochoric with DUI, one gonochoric and one hermaphroditic without DUI) and of the related gonochori
98 ate the expression of X-linked genes only in hermaphroditic worms.