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1 oid, free-living, amoeboid cells that divide asexually.
2 r organisms that reproduce both sexually and asexually.
3 parasites and that bdelloid rotifers evolved asexually.
4 ng whether seeds can be produced sexually or asexually.
5 c exchanges scattered among regions evolving asexually.
7 l of hybrids, F(1) individuals can reproduce asexually and form long-lived, potentially immortal hybr
8 ine that T.b. gambiense is evolving strictly asexually and is derived from a single progenitor, which
10 ial ascidian Botryllus schlosseri propagates asexually and sexually, presumably from pools of stem ce
11 ae (e.g., Acanthamoeba, Naegleria) reproduce asexually and therefore, according to popular doctrine,
12 ts: mammals or birds, in which they multiply asexually, and mosquitoes with sexual multiplication.
13 sms capable of reproducing both sexually and asexually are expected to mate more frequently when stre
14 rrhizal (AM) fungi (Glomeromycota) reproduce asexually, are multinucleate, and have high genetic vari
17 Our findings suggest that bdelloids evolve asexually but exchange DNA horizontally both within and
23 morphologically indistinguishable from their asexually committed counterparts, defining their charact
24 cycle that begins with invasion by a single, asexually committed merozoite and ends, 48 hours later,
25 colony synchronously dies every week as the asexually derived generation of buds reaches functional
26 cess coincides temporally with the growth of asexually derived primary buds, that harbor a small numb
30 ompensated by their proficiency to reproduce asexually in a wider range of environmental conditions.
31 ucing species to sometimes produce offspring asexually - is known from a wide range of ordinarily sex
32 rile hermaphrodite that may be propagated by asexually produced spores or that may reproduce sexually
33 evere developmental defects were observed in asexually propagating tissues, reflecting a pathologic s
34 proteins, is essential for the commitment of asexually replicating forms to sexual development in Pla
38 The Giardia life cycle alternates between an asexually replicating vegetative form and an infectious
39 ental evidence that senescence occurs in the asexually reproducing marine oligochaete Paranais litora
40 , we consider a simple model of evolution in asexually reproducing populations which considers adapta
41 d on the basis of their activity against the asexually reproducing red blood cell stages of the paras
42 ariety of different types of organisms, from asexually reproducing single-cell organisms to chromosom
44 results apply to a general class of haploid, asexually reproducing, spatially structured populations.
45 ce a substantial fraction of their offspring asexually, so long as the number of sites under selectio
46 frequency with which offspring are produced asexually, through self-fertilization and through sexual
49 ude that the ability of females to reproduce asexually without males reduces selection constraints on
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