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1 en compounds and total phytoestrogens in red clover.
2 ltures of MFRE colonising a flowering plant, clover.
3 a chromosome-scale reference genome for red clover.
4 and bean in apparent competition with CR on clover.
5 ing two distinct HCTs were identified in red clover.
8 breeding approaches is tractable, making red clover a suitable candidate for association studies and
9 th genome sequence comparisons between white clover, a recently evolved allotetraploid, and its diplo
11 roportion of cyanogenic individuals of white clover amongst 200 individuals in each of 32 neighbourin
12 eryngo, lavender, Jerusalem tea, astragalus, clover and acacia), two different honeydew honeys (lime
16 content of isoflavonoids was observed in the clover and chickpea sprouts, which amounted to 1.1 g/100
18 or HCT2 in phaselic acid accumulation in red clover and define a previously undescribed pathway for t
19 stry (e.g. Crotalaria, Stylosanthes, Berseem clover and Desmodium) are most effective in parasitic we
21 with different floral origins (rata, kamahi, clover and manuka) obtained from producers in New Zealan
24 previously developed the green-red FRET pair Clover and mRuby2, which improves responsiveness in intr
27 ex to gain insight into the genesis of white clover and the consequences of allopolyploidization.
29 yr rotation (maize-soybean-small grain + red clover) and a 4-yr rotation (maize-soybean-small grain +
30 lower fitness on broad bean relative to red clover) and fitness benefits when on red clover (higher
31 2-year corn-soybean, 3-year corn-soybean-oat/clover, and 4-year corn-soybean-oat/alfalfa-alfalfa syst
32 2-year corn-soybean, 3-year corn-soybean-oat/clover, and 4-year corn-soybean-oat/alfalfa-alfalfa syst
37 indicate that cyanogenesis evolved in white clover as a product of the interspecific hybridization t
40 Evidence of a direct interaction between Clover-AZIN and antizyme-mRuby2 was observed within cell
44 at intercropping prairie cordgrass with kura clover can enhance biomass yield and reduce fertilizer-d
46 lonies grew heavier near thiacloprid-treated clover compared to controls lacking clover, while coloni
49 ressure to Obviate Lung Injury]) and sepsis (CLOVERS [Crystalloid Liberal or Vasopressors Early Resus
50 d: one planted with a legume (Purple Prairie Clover, Dalea purpureum), one planted with grass (Blue-J
51 ey samples obtained were buckwheat, caraway, clover, dandelion, fireweed, heather, lime tree, lingonb
53 acking clover, while colonies near untreated clover did not differ from colonies in neither of the ot
55 he definitive studies concerning this issue, Clover et al. identified a series of mutants with putati
58 ostmenopausal osteopenia.We used a novel red clover extract (RCE) rich in isoflavone aglycones and pr
61 (flowers + pesticide), untreated organic red clover fields (flowers), or landscapes lacking clover fi
62 onies in 18 landscapes with conventional red clover fields treated with the neonicotinoid thiacloprid
63 ssion activity as they traveled within white clover from their original confined habitats to a global
64 lists with a flowering plant by showing that clover gained both (15) N and (33) P tracers directly fr
66 identifying monofloral blueberry, buckwheat, clover, goldenrod, linden, or other honey with a nested
69 guminous species including red clover, white clover, hairy vetch, mung bean, alfalfa, lentil, snow pe
73 red clover) and fitness benefits when on red clover (higher fitness on red clover relative to broad b
74 degrees C was the same for manuka honey and clover honey doped with 2000 or 10,000mg/kg DHA and for
75 honey was stored at 20 and 27 degrees C and clover honey spiked with compounds of interest were stor
79 rty-seven New Zealand manuka honeys and four clover honeys were analysed for various chemical and phy
81 viduals specialized to either alfalfa or red clover in order to perform both a biometrical analysis a
88 ot reduced in meta-analysis of trials of red clover isoflavone extracts and results were mixed for so
89 n transgenic alfalfa, M. truncatula or white clover, LAP1 induced massive accumulation of anthocyanin
90 ostructural organization of these AFMs into "clover leaf" clusters, consistent with the macrostructur
91 in the antisense strand does not alter the 'clover leaf' bend and sugar puckers that are critical fo
92 the direct one-pot synthesis of "tripartite" clover-leaf shaped nanoparticles which would be difficul
94 over crop species rye, triticale and crimson clover may have potential to enhance P availability as w
97 ic variation and population structure in red clover natural populations from Europe and Asia, and var
100 we assess the effects of the ncsgRNA of red clover necrotic mosaic virus (RCNMV), called SR1f, in in
103 spot virus (CLSV; genus Aureusvirus) and red clover necrotic mosaic virus (RCNMV; genus Dianthovirus)
104 ar mutations introduced into the related Red clover necrotic mosaic virus capsid protein gene failed
105 tivator (TA) located within the RNA-2 of Red clover necrotic mosaic virus folds into a simple hairpin
107 cts with antibodies directed against the red clover necrotic mosaic virus movement protein (RCNMV MP)
110 rum, but supplementation of leptosperin into clover or artificial honeys generated the MM1 fluorescen
111 Based on these data, we estimate that white clover originated ~15,000 to 28,000 years ago during the
112 otein from Dianthus caryophyllus (carnation, clover pink) is induced in response to ethylene producti
115 parallel evolution by sampling 110,019 white clover plants from 6169 populations in 160 cities global
116 family in date palm, spinach, maize, and red clover plants with a high allergenicity score that might
120 Sequence comparisons among the three red clover PPO clones indicated they are 87% to 90% identica
121 model system to further characterize the red clover PPO enzymes and PPO-mediated inhibition of postha
124 s in leaf extracts of alfalfa expressing red clover PPO1 was dramatically reduced in the presence of
128 trace element/isotopic data (for manuka and clover, Q(2)=0.65), while the other chemical parameters
129 r all four honeys, Q(2)=0.52; for manuka and clover, Q(2)=0.76) and the trace element/isotopic data (
130 eriment, we examined the relative fitness on clover race (CR) and alfalfa race (AR) pea aphids on bro
131 animals were fed two forage-based diets: red clover (RC) and grass silage (GS), in a crossover-design
132 ts when on red clover (higher fitness on red clover relative to broad bean), whether or not in appare
133 to use the legume crops pea, alfalfa and red clover, respectively, were analysed, and a total of 67 r
135 dynamics and symbiont infectibility of white clover root hairs but that CLOSs alone are not sufficien
136 nosarum bv. trifolii on development of white clover root hairs, and the role of these bioactive glyco
138 onally, ryegrass also showed enrichment when clover roots received the gas, provided there was direct
139 otifViz, for three motif discovery programs, Clover, Rover and Motifish, covering most available flav
140 iation, appears to have contributed to white clover's ecological success as a globally distributed we
141 ure of these polymorphisms may reflect white clover's evolutionary origin as an allotetraploid derive
143 bean sequence, a 3-year corn-soybean-oat/red clover sequence, and 4-year corn-soybean-oat/alfalfa-alf
144 rusion and its trajectory was modulated in a clover-shaped pattern perpendicularly to the protrusion.
147 per, we observed the jumping behavior of the clover springtail Sminthurus viridis (Linnaeus, 1758) an
156 xonomic similarities were confirmed for both clover taxa examined, especially in terms of the most ab
158 od (implemented as a computer program called Clover) to dopamine-responsive promoters, sequences flan
159 h sepsis-induced hypotension included in the CLOVERS trial, 622 (39.8%) received lactated Ringer's so
160 In this prospective cohort study of the CLOVERS trial, peripheral administration of vasopressors
161 oid Liberal vs Early Vasopressors in Sepsis (CLOVERS) trial conducted in 60 US hospitals from March 2
164 ns were made with a protein extract from red clover (Trifolium pratense L.) before adding a synthetic
167 ed populations of the forage legume crop red clover (Trifolium pratense L.) that were recurrently sel
168 sweetclover (Melilotus officinalis L.), red clover (Trifolium pratense L.), and birdsfoot trefoil (L
172 Rice, tomato (Solanum lycopersicum) and red clover (Trifolium pratense) were exposed to iAs, monomet
173 soybean (Glycine max), pea (Pisum sativum), clover (Trifolium pratense), and common bean (Phaseolus
175 We tested these predictions by letting white clover (Trifolium repens) invade ryegrass (Lolium perenn
178 excelsa), kamahi (Weinmannia racemosa), and clover (Trifolium spp.) honeys did not exhibit unique fl
180 PRG; n = 20) or perennial ryegrass and white clover (WCPRG; n = 19) swards, was characterised using 1
181 -treated clover compared to controls lacking clover, while colonies near untreated clover did not dif
182 from other leguminous species including red clover, white clover, hairy vetch, mung bean, alfalfa, l
185 uckwheat, cloudberry-bog, lingonberry, sweet clover, willowherb and multifloral honeys) were investig
186 ADAM22 shows that it is a compact four-leaf clover with the metalloproteinase-like domain held in th