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1 species, plasticity was not associated with growth form.
2 asonal drought alters the response of either growth form.
3 in mating system, life-history strategy and growth form.
4 mation of biofilms, a sessile, multicellular growth form.
5 roorganisms have developed a unique ramified growth form.
6 ts such as seed dispersal syndrome and plant growth form.
7 or nitrogen differentiate into a filamentous growth form.
8 fferentiate into a filamentous, pseudohyphal growth form.
9 fferentiate into a filamentous, pseudohyphal growth form.
10 leading to a rich variety of polycrystalline growth forms.
11 ted into almost every climate, with manifold growth forms.
12 2) were isolated from species with different growth forms.
13 he strong relationship between seed mass and growth form across present-day species and with the avai
16 osissima and M. claussenii differed in their growth form and exhibited contrasting strategies of wate
17 ve advantage over native SAPs as a result of growth form and greater light-use efficiency that promot
19 g phylogenetic relatedness, climatic ranges, growth form and mycorrhizal associations, we quantified
20 habitats and are minimally affected by plant growth form and phylogenetic ancestry, suggesting that t
21 heory are consistent with this evidence that growth form and seed size evolve in a coordinated manner
25 : (i) constancy in the relative abundance of growth forms and maintained dominance by long-lived, slo
26 s maintained across Koppen climate zones and growth forms and strongest in the wet tropics and within
27 role of epistasis in determining biological growth, form, and shape and for the resolution of develo
29 oapplications; when both plant community and growth form are known, this study allows the isolation o
33 belowground strategy and performance across growth forms, but it will be critical to incorporate pla
35 isual manipulations known to alter axial eye growth: form deprivation by translucent occluders, spher
36 s plants suggest that their physiologies and growth forms differed substantially from most types of m
37 d residues are deleted no longer supports T7 growth, forms dimers, or interacts with either T7 DNA po
38 differences in the relative response between growth forms does not support the hypothesis that elevat
39 ies, photosynthetic pathway (C3 vs. C4 ), or growth form (drought-deciduous shrub vs. evergreen shrub
40 rbs to supercentennial trees, to examine how growth form, habitat, and phylogenetic relationships str
41 s leukemia cells accumulate mutations during growth, forming heterogeneous cell populations that are
42 ntium aciphyllum / Polytrichum strictum) and growth form (hummock / bank) are the major determinants
43 esponses of eight species, representing four growth forms: (i) graminoids (Carex bigellowii and Eriop
45 ogenetic switch from budding yeast to hyphal growth form in response to a variety of stimuli and grow
53 gs are consistent across stress types, plant growth forms, life histories, origins (invasive vs. nati
54 s a wide range of diversity in floral color, growth form, mating system and tolerance to environmenta
56 techniques to assess how transitions between growth forms occur in the moss Physcomitrella patens.
57 Pseudohyphal differentiation, a filamentous growth form of the budding yeast Saccharomyces cerevisia
60 plant species, each representing a different growth form or functional type, is changing the fundamen
61 kely that it is a result of a change in tree growth form or that it is predominantly caused by CO(2)
63 itch between yeast, pseudohyphal, and hyphal growth forms (polymorphism) is one of the most investiga
64 een unicellular yeast cells and filamentous, growth forms), secreted aspartyl proteases and phospholi
67 consistently associated with divergences in growth form than with divergences in any other variable.
68 re more often associated with divergences in growth form than with divergences in dispersal syndrome
69 hich results in a semiclonal or clonal shrub growth form that appears to be ubiquitous in global dese
70 ons between budding, pseudohyphal and hyphal growth forms that promote the virulence of this pathogen
72 pathogen Candida albicans switches from one growth form to another; at the same time, insights are b
73 ements are rarely coupled empirically across growth forms to identify whether belowground strategies
74 nse caveolin-1 exhibit anchorage-independent growth, form tumors in immunodeficient mice and show hyp
75 se in flowering activity may persist in some growth forms until checked by nutrient limitation or by
77 out after fire and/or have graminoid or herb growth forms were particularly affected by postfire weat
78 e the potential relationships of climate and growth form with total ray and axial parenchyma fraction
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