ライフサイエンスコーパス: hermaphroditism

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1 r results for the maintenance of dioecy over hermaphroditism.

2 nate evolution of behavioral dimorphism with hermaphroditism.

3 omosome in gonadal tissue has been linked to hermaphroditism.

4 lization during the evolution of dioecy from hermaphroditism.

5 xual reproduction, particularly simultaneous hermaphroditism.

6 idisation and transitions between dioecy and hermaphroditism.

7 hy gld-1 is repeatedly recruited to regulate hermaphroditism.

8 hypotheses about the genetic architecture of hermaphroditism.

9 have a breeding system intermediate between hermaphroditism and complete separation of the sexes (di

10 Atrazine (> or =0.1 ppb) induced hermaphroditism and demasculinized the larynges of expos

11 ion may be divided into two main categories: hermaphroditism and dioecy (Botany)/gonochorism (Zoology

12 edicted by models for the transition between hermaphroditism and dioecy.

13 s Mercurialis, transitions between combined (hermaphroditism) and separate sexes (dioecy or androdioe

14 ty before gestational day 11, hydrocephalus, hermaphroditism, and cystic ovaries.

15 n in the fog-2 locus, thereby reestablishing hermaphroditism as the primary means of reproduction for

16 n males and females, while the facts of true hermaphroditism can be viewed as remnants of temperature

17 those most consistent with the simultaneous hermaphroditism can predominate only when a substantial

18 Furthermore, the condition of true hermaphroditism does not fit into a simple genotype/phen

19 been shaped by natural selection, perhaps as hermaphroditism evolved.

20 have arisen during evolution of self-fertile hermaphroditism from an ancestral female/male species.

21 briggsae independently evolved self-fertile hermaphroditism from gonochoristic ancestors.

22 Compared to hermaphroditism, gynodioecy generally reduces effective

23 stic spatial simulations we demonstrate that hermaphroditism has an even greater advantage when local

24 s in the evolution of this animal group: (i) Hermaphroditism has evolved independently in C. elegans

25 r focusses on self-incompatible simultaneous hermaphroditism in animals.

26 l, in the repeated evolution of self-fertile hermaphroditism in Caenorhabditis nematodes.

27 Thus, the evolution of hermaphroditism in Caenorhabditis probably required two

28 , it is not fully understood what determines hermaphroditism in the domesticated subspecies and male

29 , it is not fully understood what determines hermaphroditism in the domesticated subspecies and male

30 des further support for the observation that hermaphroditism is associated with sedentary species, su

31 It proposes that such hermaphroditism is not stable in sufficiently heterogene

32 he evolution of separate sexes (dioecy) from hermaphroditism is one of the major evolutionary transit

33 ations, suggesting a possible reason for why hermaphroditism is rare among evolved animal species.

34 Hermaphroditism is rare and phylogenically in decline am

35 ring, but no hermaphrodites, suggesting that hermaphroditism is recessive to femaleness.

36 Hermaphroditism leads to reduced sexual selection and ca

37 Overall, our results show that sequential hermaphroditism may affect Ne differently over varying t

38 le competition associated with the origin of hermaphroditism may have permitted the global spread of

39 it descended from a male/female species, so hermaphroditism provides a model for the origin of novel

40 cific pathways can drive the transition from hermaphroditism to dioecy.

41 models for the evolutionary transition from hermaphroditism to monoecy, multiple sex determining gen

42 are consistent with convergent evolution of hermaphroditism, which is marked by considerable develop

43 increases or decreases N(en) as compared to hermaphroditism with the same selfing rate of hermaphrod

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