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 ories of the evolution of host-microorganism symbioses.
2 hway shared by the rhizobial and mycorrhizal symbioses.
3 ce of chemically prolific bacteria living in symbioses.
4 nificance of the biodiversity of mycorrhizal symbioses.
5 emodeled by pathways remaining from previous symbioses.
6 required for the establishment of these two symbioses.
7 al adaptation in arbuscular mycorrhizal (AM) symbioses.
8 There is not one but many ambrosia symbioses.
9 le is known of their function in mutualistic symbioses.
10 cteria are highly adapted to engage in these symbioses.
11 of substrates known to power chemosynthetic symbioses.
12 ralizing host defense responses to establish symbioses.
13 own transport activities in these beneficial symbioses.
14 del system to understand mutually beneficial symbioses.
15 s are required for both bacterial and fungal symbioses.
16 esis of infectious disease and in beneficial symbioses.
17 ranscriptional reprogramming facilitates the symbioses.
18 the molecular foundations of human-bacterial symbioses.
19 mportance of the encoded protein in multiple symbioses.
20 t in stabilizing a wide range of mutualistic symbioses.
21 rapid evolutionary changes in host-pathogen symbioses.
22 e (PHB), in maintaining the Rhizobium-legume symbioses.
23 agement of one of the world's most important symbioses.
24 ole in osmoregulation during legume/rhizobia symbioses.
25 o recruit luminous bacteria into light organ symbioses.
26 d not previously been known to exist in such symbioses.
27 the N2-fixing efficiency of Rhizobium-legume symbioses.
28 agonism-to-mutualism transition in heritable symbioses.
29 ns elusive, but may be linked to mycorrhizal symbioses.
30 more targeted studies in other host-microbe symbioses.
31 renowned for establishing complex microbial symbioses.
32 ng crosskingdom signaling and host-bacterial symbioses.
33 nfection and development of rhizobial and AM symbioses.
34 ntly the best understood of all host-microbe symbioses.
35 nce regulation of nodulation in actinorhizal symbioses.
36 raw material for natural selection in coral symbioses.
37 robial nutrition, and host health in diverse symbioses.
38 ation or decoding of calcium-spiking in both symbioses.
39 te change through the establishment of novel symbioses.
40 onal stage in the evolutionary succession of symbioses.
41 fering with plant carbon allocation and root symbioses.
42 osition is not required for establishment of symbioses.
43 lants and other photosynthetic organisms and symbioses(3,4), but there has yet to be any direct link
47 odel plant for the analysis of plant-microbe symbioses and for addressing questions pertaining to leg
48 view the current state of knowledge of these symbioses and highlight important avenues for future stu
49 ogy, photosynthetic pathway, nitrogen-fixing symbioses and life histories have relied on either expli
50 is a new variant among reported root nodule symbioses and may reflect an unusual nitrogen transfer p
51 ght on the evolution of plant-cyanobacterium symbioses and may suggest a route to establish productiv
52 ese results highlight the powerful role that symbioses and plant defense play in driving tree growth
53 e results to both the evolution of Wolbachia symbioses and proposed applied strategies for the use of
54 tic algae (Symbiodinium spp.) - unless these symbioses are able to adapt to global warming, bleaching
61 in global ecology and biogeochemical cycles, symbioses are poorly characterized in open ocean plankto
62 t novel associations, which suggest that the symbioses are probably more widespread than conventional
65 iple, it has been suggested that mycorrhizal symbioses are the stable derivatives of ancestral antago
73 abitat partitioning among the chemosynthetic symbioses at hydrothermal vents and illustrate the coupl
78 ntified at least five independent origins of symbioses between herbivorous ants and related Rhizobial
81 ommunities on the one hand, and facilitating symbioses between organisms on the other, is only just b
82 f ecosystems, particularly by disrupting the symbioses between reef-building corals and their photosy
85 sis signaling pathway that is shared in both symbioses but also modulate innate immune responses.
86 even in predominantly vertically transmitted symbioses by stabilizing the cooperative association ove
88 servations demonstrating that Epichloe-grass symbioses can modulate grassland ecosystems via both abo
89 nce and conjecture that coral-dinoflagellate symbioses change partnerships in response to changing ex
92 various trophic levels (cyanobacteria, root symbioses, cycad seeds, cycad flour, flying foxes eaten
93 deep-sea hydrothermal vents, chemosynthetic symbioses dominate the biomass, contributing substantial
94 s on host cells and do not produce effective symbioses, emphasizing the importance of understanding t
96 karyotes and encourages exploration of other symbioses for drug discovery and better understanding of
97 mportance to sustainable agriculture are the symbioses formed between more than 80% of terrestrial pl
98 establishment of arbuscular mycorrhizal (AM) symbioses, formed by most flowering plants in associatio
101 ecruited during the evolution of root nodule symbioses from the already existing arbuscular mycorrhiz
102 of the genes required for nodulation and AM symbioses from the two model legumes, Medicago truncatul
105 legume genes required for nodulation and AM symbioses have their putative orthologs in nonlegumes.
106 equencing show great promise for studying EM symbioses; however, metatranscriptomic studies have been
107 known to play a role in marine invertebrate symbioses; (iii) the potential use of hydrogen as an ene
108 genus that forms nitrogen-fixing root-nodule symbioses in a wide range of woody Angiosperms, is accom
109 ermine the consequences of these facultative symbioses in Acyrthosiphon pisum (the pea aphid) for vul
110 ltiple gains of actinorhizal nitrogen-fixing symbioses in angiosperms may have been associated with i
115 mechanisms and consequences of multipartite symbioses, including consortia in which multiple organis
116 cies' physiological functions in mutualistic symbioses increased the range of suboptimal environmenta
120 ties, especially to certain insect-bacterium symbioses involving likewise host peptides for manipulat
121 ical component in the establishment of these symbioses is nuclear-localized calcium (Ca(2+)) oscillat
123 logical importance, but evolution of farming symbioses is thought to be restricted to three terrestri
124 ns, whether in shared ecosystems or intimate symbioses, is fundamentally altering our understanding o
125 model legume used widely for studies of root symbioses, it is apparent that the phosphate transporter
129 st-microbe interaction; for example, several symbioses like the squid-vibrio light organ association
132 Knowledge of intraspecific variation in symbioses may aid in understanding the ecology of widesp
134 molecular insights into mammalian-microbial symbioses may be revealed amid the complexity of the int
135 iversity of microcystins suggest that lichen symbioses may have been an important environment for div
140 In contrast, the nitrogen-fixing root nodule symbioses of plants with bacteria evolved more recently,
142 To establish compatible rhizobial-legume symbioses, plant roots support bacterial infection via h
147 hylogenetic relationships of insect-bacteria symbioses provides the opportunity to assess the effects
148 ion of host cell responses in both AM and RN symbioses, reflecting common mechanisms for plant cell r
152 iscovery of nitrogen-fixing Rhizobium-legume symbioses, researchers have dreamed of transferring this
153 es in the environment of the Campeche Knolls symbioses revealed that these are present at high concen
159 ological settings and invertebrate-bacterial symbioses similar to those of both western Pacific and A
160 carbon, nitrogen, and sulfur cycles) and via symbioses since many novel organisms exhibit restricted
163 these microarray data with those from other symbioses, such as germ-free/conventionalized mice and z
166 ates the range from mutualistic to parasitic symbioses that plants form with diverse organisms, as we
168 ion is thought to be favored in antagonistic symbioses (the "Red Queen effect"), but disfavored in ce
171 xamines a model system for the study of such symbioses, the light organ association between the bobta
175 opmental trajectory of horizontally acquired symbioses through the study of the binary squid-vibrio m
176 epends on the ability of reef-building coral symbioses to adapt or acclimatize to warmer temperatures
178 foundly influence the response of reef coral symbioses to major environmental perturbations but may u
180 rative analyses on 106 unique host-bacterial symbioses to test for correlations between symbiont func
181 teemed with organisms that coordinate their symbioses using chemical signals traversing between the
182 e and distinct from previously characterized symbioses, where multiple microbial partners have associ
183 s is best understood in beneficial bacterial symbioses, where partner fidelity facilitates loss of ge
184 s ammonium is contributed by legume-rhizobia symbioses, which are initiated by the infection of legum
185 rk architecture of below-ground plant-fungus symbioses, which are ubiquitous to terrestrial ecosystem
186 al survival in the world's warmest reefs are symbioses with a newly discovered alga,Symbiodinium ther
188 pteran suborder Auchenorrhyncha show complex symbioses with at least two obligate bacterial symbionts
189 any insect groups depend on ancient obligate symbioses with bacteria that undergo long-term genomic d
190 a: Mollusca) are a family of clams that form symbioses with chemosynthetic gamma-proteobacteria.
191 egative bacterium that forms nitrogen-fixing symbioses with compatible leguminous plants via intracel
193 ome bacterial metabolites may be specific to symbioses with eukaryotes and encourages exploration of
196 e family of caridean shrimp, largely live in symbioses with marine invertebrates of different phyla.
197 inherent to these regions in part thanks to symbioses with microorganisms, and yet these microbial s
200 alacturonide or flg22 treatment and the root symbioses with nitrogen-fixing rhizobia and arbuscular m
201 Leguminous plants can enter into root nodule symbioses with nitrogen-fixing soil bacteria known as rh
204 s, and as such, these arthropods have formed symbioses with nutrient-supplementing microbes that faci
212 rbuscular mycorrhizal (AM) fungi, which form symbioses with the roots of the most important crop spec
213 ungi (AMF) have formed intimate, mutualistic symbioses with the vast majority of land plants and are
214 ngi (order Glomales), which form mycorrhizal symbioses with two out of three of all plant species, ar
215 cter clade of Alphaproteobacteria that forms symbioses with unicellular eukaryotic phytoplankton, suc
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。