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1                                              Endophytic A. persicinum (OTU5) and plant pathogenic fun
2             The negative association between endophytic A. persicinum (OTU5) and plant pathogenic fun
3 ve to PGBP-free controls while the extent of endophytic accumulation depended on the colonization mod
4            The rise in relative abundance of endophytic Acremonium persicinum (operational taxonomic
5  mesophyll region of host leaves occurs, but endophytic and epiphytic bacterial growths are not corre
6 ccurring microbial communities contribute to endophytic and epiphytic colonization.
7 ved among bradyrhizobia and plant-associated endophytic and pathogenic bacteria.
8 istorical host-range expansion together with endophytic and pathogenic capabilities are likely to hav
9 accharide derived from exopolysaccharides of endophytic and pathogenic fungi.
10 f also provides a protective environment for endophytic and pathogenic microbes alike.
11  of 135 fungal genomes from 73 saprotrophic, endophytic and pathogenic species, and 62 mycorrhizal sp
12                     Herein, we evaluated the endophytic and rhizosphere microbial communities of two
13  and Dazzle respectively, and much higher in endophytic and tightly bound cells than in epiphytic and
14 ng lifestyles on angiosperms - pathogenic vs endophytic - are able to infect Mp and cause tissue mace
15  from genus Epichloe, which form mutualistic endophytic associations with cool-season grass hosts.
16 discovered root-fungus associations, such as endophytic associations, which offer potential benefits
17 ata indicate that the collection of 58 plant endophytic Bacillus strains represents an important geno
18  tequilana leaves after inoculation of their endophytic bacteria (Enterobacter cloacae).
19 he combination of native pollutant-degrading endophytic bacteria and fast-growing poplar tree systems
20 ly, we found the genomes of rhizospheric and endophytic bacteria associated with S. salsa to be enric
21 diversity, composition, and functionality of endophytic bacteria between ungerminated and germinated
22                         Non-plant pathogenic endophytic bacteria can promote plant growth, improve ni
23            Furthermore, potential beneficial endophytic bacteria contained in their seed microbiomes
24                           In particular, the endophytic bacteria H. seropedicae showed strong epiphyt
25 ur results provide preliminary evidence that endophytic bacteria harbor chemically diverse secondary
26  necessary for this interior colonization in endophytic bacteria have been identified.
27 tential of secondary metabolites produced by endophytic bacteria isolated from Enhydra fluctuans Lour
28                          The genomes of four endophytic bacteria now available should promote discove
29         This study was aimed to isolate leaf endophytic bacteria of Rauvolfia serpentina, investigate
30 information is available on the influence of endophytic bacteria on phytoremediation of widespread en
31 l studies have demonstrated the relevance of endophytic bacteria on the growth and fitness of agricul
32  colonization of plants we demonstrated that endophytic bacteria potentially transfer more nitrogen t
33  present evidence showing nitrogen flow from endophytic bacteria to plants in a process that appears
34      Plants form symbiotic associations with endophytic bacteria within tissues of leaves, stems, and
35 ene transfer into neighboring plant species, endophytic bacteria, and mycorrhizal fungi.
36 y found in plant-associated, nodulating, and endophytic bacteria.
37 her or how plants obtain nitrogen from these endophytic bacteria.
38 as to analyze and compare the composition of endophytic bacterial communities associated with roots a
39 e composition, diversity, and interaction of endophytic bacterial communities in plants struggling fo
40 te the composition and putative functions of endophytic bacterial communities in ungerminated and ger
41       The abundance and composition of their endophytic bacterial communities was determined by quant
42  the main microbial functional groups in the endophytic bacterial community.
43 oplastic water potential is a determinant of endophytic bacterial population size, and water stress,
44 al structure of a PRF from the Gram-negative endophytic bacterium Burkholderia phytofirmans The cryst
45 urkholderia seminalis strain TC3.4.2R3 is an endophytic bacterium isolated from sugarcane roots that
46         In this study, a novel strain PLV of endophytic bacterium Paenibacillus lautus was isolated f
47 aspirillum seropedicae is a diazotrophic and endophytic bacterium that associates with economically i
48             Enterobacter sp. SA187 is a root endophytic bacterium that maintains growth and yield of
49               However, leaf mining, a foliar endophytic behavior that today is exhibited exclusively
50 xophytic (eggs laid on plant surfaces) or to endophytic behavior.(6)(,)(7)(,)(8)(,)(9) This ambiguity
51 s in classical biological control, either as endophytic bodyguards-to protect coffee plants from Hemi
52                                The extent of endophytic colonization by strains is regulated by plant
53 t to assess nitrogen absorbed as a result of endophytic colonization of plants we demonstrated that e
54 a H. seropedicae showed strong epiphytic and endophytic colonization of roots.
55  enzyme family PL1_7 links aggressiveness of endophytic colonization to plant health.
56 ay have been co-opted from genes involved in endophytic colonization.
57 ted humidity-dependent dyshomeostasis of the endophytic commensal bacterial community in the phyllosp
58 e more modular than ectomycorrhizal and root endophytic communities, with arbuscular mycorrhizal fung
59                                          The endophytic community of M. domestica and its wild progen
60                        The complexity of the endophytic community was more connected to growth status
61 e (immediately surrounding the root) and the endophytic compartment (within the root) contribute to p
62                Our rigorous definition of an endophytic compartment microbiome should facilitate cont
63 the hypotheses that the root rhizosphere and endophytic compartment microbiota of plants grown under
64                                              Endophytic compartments from both soils feature overlapp
65 y distinct bulk soils and in rhizosphere and endophytic compartments prepared from roots grown in the
66 tive endophyte bacterial isolate library for endophytic competency.
67 was essential for disease suppression by the endophytic consortium.
68 beneficial associations with associative and endophytic diazotrophic bacteria.
69  antifungal activities against saprotrophic, endophytic, entomopathogenic, and garden-pathogenic fung
70 is a pyrrolopyrazine (PPZ) produced by grass-endophytic Epichloe fungi.
71 he precise studies on evolutionary origin of endophytic Epichloe species, their coevolution with host
72 rough horizontal gene transfer (HGT) from an endophytic Epichloe species.
73                                              Endophytic feeding behaviors, including stem borings and
74 es the diversity and abundance of culturable endophytic fungal communities associated with four plant
75                                  We surveyed endophytic fungal communities in leaves of a single tree
76 oi pv. savastanoi (Psv) on the epiphytic and endophytic fungal communities of olive tree twigs from t
77 , diversity, and beneficial effects of plant endophytic fungal communities.
78                          Muscodor is a novel endophytic fungal genus that produces bioactive volatile
79 larity among different mycorrhizal types and endophytic fungal guilds.
80 al, arbuscular mycorrhizal, and dark septate endophytic fungi also shapes tree-associated microbiomes
81 zymes from phylogenetically distant species, endophytic fungi and plants, which resulted in 2 new-to-
82  of the currently characterized antagonistic endophytic fungi and their effects on nematode behavior
83                                              Endophytic fungi are found within the roots of healthy p
84  are consistent with suggestions that foliar endophytic fungi are hyperdiverse.
85 sition, diversity, and dispersal patterns of endophytic fungi associated with needles of Pinus taeda
86  entangled responses of plant pathogenic and endophytic fungi associated with sorghum when droughted
87                       Colonization by foliar endophytic fungi can affect the expression of host plant
88         Colonization of plants by particular endophytic fungi can provide plants with improved defens
89 In part, this may be caused by the fact that endophytic fungi form a rather heterogeneous group.
90  Production potential of natural pigments by endophytic fungi from grapevines was evaluated.
91                                              Endophytic fungi have been proposed as a prominent alter
92                                              Endophytic fungi have been reported from many plants and
93                             All the isolated endophytic fungi improved tomato plants' shoot growth an
94                      We observed turnover of endophytic fungi in all logs, but beetle-colonized logs
95              The application of enzymes from endophytic fungi in constructing biosensors broadens the
96 ogenic interactions, the high bioactivity of endophytic fungi in the Xylariales, coupled with their a
97 scoparium was co-cultured with each of eight endophytic fungi isolated from naturally occurring D. sc
98 onse in the mutualistic interactions between endophytic fungi isolated from unrelated environments an
99                                              Endophytic fungi live asymptomatically within plants.
100             These results suggest that these endophytic fungi might be a considerable boost to sustai
101           Simple ecological traits of foliar endophytic fungi observed in culture can translate to sy
102                                          The endophytic fungi of woody plants may be diverse as often
103 l terrestrial plants are colonized by foliar endophytic fungi that can affect plant growth and physio
104               A new study sheds light on why endophytic fungi that live inside Yew trees also make th
105 Every plant species examined to date harbors endophytic fungi within its asymptomatic aerial tissues,
106 r pest management include the application of endophytic fungi, such as Trichoderma harzianum, that ac
107 ing,(4) our study reveals the sensitivity of endophytic fungi, their reservoirs of biodiversity, and
108 our species-rich communities of asymptomatic endophytic fungi.
109 l approach to mine the chemical diversity of endophytic fungi.
110  at the C8' and C9' positions, isolated from endophytic fungus Colletotrichum sp. SC1355 and Tetrapte
111 es A-E, isolated from a culture broth of the endophytic fungus Curvularia geniculata, is described.
112                    Here, cocultivation of an endophytic fungus Epicoccum dendrobii with the model fun
113 ucted by physical adsorption of the isolated endophytic fungus Eupenicillium shearii FREI-39 esterase
114 he mechanism of action of Muscodor albus, an endophytic fungus known for its volatile antimicrobial a
115  produced by an indeterminate species of the endophytic fungus Nodulisporium.
116 om the fermentation broth of an unidentified endophytic fungus obtained from the bark of Ficus microc
117 S-based metabolomic analysis of the Hawaiian endophytic fungus Paraphaeosphaeria neglecta FT462 led t
118 ay of spiro compounds, and an extract of the endophytic fungus Penicillum namyslowski, containing gri
119                                     The root endophytic fungus Piriformospora indica enhances plant a
120 ) by lipid extracts from the beneficial root endophytic fungus Serendipita indica and compare them to
121                                              Endophytic fungus Serendipita indica can bolster plant g
122 a high-affinity sulfate transporter from the endophytic fungus Serendipita indica.
123 discovered a novel compound isolated from an endophytic fungus that inhibits fungal sphingolipid synt
124 ogen-fixing symbiont, the plants harbored an endophytic fungus that produced elemental Se.
125 at, under phosphate-limiting conditions, the endophytic fungus, Colletotrichum tofieldiae, provides g
126 ults on our earlier reported Taxol-producing endophytic fungus, Fusarium solani from the standpoint o
127 dial pigmentation and development in a plant endophytic fungus, Pestalotiopsis fici.
128 cing of Calcarisporium arbuscula, a mushroom-endophytic fungus, revealed 68 core genes that are invol
129 nt membrane architecture favoring epithelial endophytic growth into the dermis and accelerating invas
130    This is especially true for Rafflesia, an endophytic holoparasite that produces the largest flower
131  unrecorded diversity of Trichoderma species endophytic in both wild and cultivated Coffea, and mycop
132  genera characterized as rhizospheric and/or endophytic independent of the application of urea, reten
133 M32-eGFP that binds to the chitosan exposing endophytic infection structures of Puccinia graminis f.
134 viding strong evidence of the ability of the endophytic inoculated trees to effectively remove TCE fr
135 Arabidopsis and SA187 in the free-living and endophytic interaction states.
136                                              Endophytic isolates RSLB3 and RSLB18 exhibited most pote
137 n was detected between these populations and endophytic isolates were pathogenic to potato and behave
138 anins significantly enhance the abundance of endophytic lactic acid bacteria within plant leaves.
139 ons that expanded outwards from the duct and endophytic lesions that grew inwards to the ductal lumen
140      Complex renal tumors, such as hilar and endophytic lesions, have also been performed robotically
141  of insect pathogenesis while maintaining an endophytic lifestyle and provide examples of genes that
142  Genome analysis revealed a link between its endophytic lifestyle and the expansion of its repertoire
143 is known pertaining to the interplay between endophytic microbes which release phytohormones and stim
144 itation may degrade and obtain nitrogen from endophytic microbes.
145  and plant lineage on the composition of the endophytic microbiome of 11 Malus species, representing
146 munity-wide Bayesian model revealed that the endophytic microbiome of domesticated apple is an admixt
147 earch highlights the importance of exploring endophytic microbiomes of medicinal plants to uncover th
148                                 In addition, endophytic microbiota and the manifold interactions betw
149                           In conclusion, the endophytic microbiota in the rhizosphere of A. glutinosa
150 iversity of ectomycorrhizal (ECM) fungi, the endophytic microbiota in the rhizosphere, and the coloni
151                                              Endophytic microorganisms exist within the living tissue
152 ines, this specimen provides evidence of how endophytic mining behavior may have originated.
153 rrhiza-forming Glomeromycotina and fine-root endophytic Mucoromycotina fungi, both of which coevolved
154                The molecular determinants of endophytic multihost compatibility are largely unknown.
155           Consequently, we characterized the endophytic mycobiome in the taproots of three carrot gen
156 icating that it has greater control over its endophytic mycobiome, which could potentially play a rol
157                           Similarly, neither endophytic Mycosphaerella nor endophytic Rhizosphaera is
158  the performance of the radius, exophytic or endophytic, nearness to collecting system or sinus, ante
159 y of and interactions between pathogenic and endophytic of this fungus are unknown.
160 ential fungal responses leading to either an endophytic or a pathogenic lifestyle during colonization
161 R), comprises three exons, two with apparent endophytic origin and the third containing a large fragm
162 s (OTUs) such as Mycena, and mycorrhizal and endophytic OTUs were characteristic of the south-facing
163 s through plant tissue concealment.(2)(,)(3) Endophytic oviposition behavior is currently common in m
164                                              Endophytic oviposition behavior, the insertion of eggs i
165  expressed in fossil plant stems and leaves, endophytic ovipositional behavior is presumed to have em
166 sions that progressed to malignancy, 12 were endophytic (P = .02).
167 at benign tumors converted from exophytic to endophytic papillomas before progressing to carcinomas.
168 ent the highly modified genome of the iconic endophytic parasite Sapria himalayana Griff.
169                                          The endophytic parasites Rafflesiaceae are placed in the div
170 parasitoid wasps are descendants of a single endophytic parasitoid ancestor that lived around 247 mya
171 ed genes expressed both in the parasitic and endophytic phases of Pc lifecycle.
172 fy genes expressed in both the parasitic and endophytic phases of the Pc lifecycle; these include pro
173 orin (MACPF)-domain protein, harbour altered endophytic phyllosphere microbiota and display leaf-tiss
174 ntrol the level and nurture the diversity of endophytic phyllosphere microbiota for survival and heal
175 oots (rhizospheric) or within plant tissues (endophytic), play an active role in modulating ethylene
176   The evolutionary history of pathogenic and endophytic populations was reconstructed and gene flow b
177                                              Endophytic populations were genetically and genotypicall
178 ntaminated media (400 mg kg(-1) Zn) with the endophytic Pseudomonas brassicacearum and rhizospheric R
179     The most common features on MRI were: 1) endophytic RB lesion (50%); 2) subretinal haemorrhage (3
180 from the more common and easily recognizable endophytic RCH.
181 larly, neither endophytic Mycosphaerella nor endophytic Rhizosphaera isolates were most closely relat
182                   Our results highlight that endophytic root microbiomes harbor a wealth of as yet un
183 s where it arrested biotrophic growth of the endophytic S. reilianum.
184 ify the abundance of the most representative endophytic species in large naturally occurring populati
185             Here we track the movement of an endophytic strain of Streptomyces bacteria throughout a
186 y, a considerable number of the 143 isolated endophytic strains displayed plant growth-promoting trai
187          An effective medium for cultivating endophytic Streptomyces albus strain E56 was selected us
188 Epichloe spp. are naturally occurring fungal endophytic symbionts of many cool-season grasses.
189 ty of microbial interactions associated with endophytic systems.
190 enting the earliest indication of a general, endophytic type of feeding damage and dating from the Mi
191              In common, both associative and endophytic types of colonization can result in beneficia

 
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