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1 ng accession Bd21 and the delayed-flowering accession Bd1-1 were grown in a variety of environmental conditions to enable
2 O(2) spring and an adjacent control site (ambient [CO(2) ]) were grown in a common environment for one generation, and th
3 K adapted wheat cultivars dating from between 1790 and 2012 were grown in replicated randomised field trials for three ye
9 ped CdTe with varying acceptor density and two undoped CdTe were grown in Cd-rich and Te-rich environments.
13 a drastic reduction of cell growth, not only when the cells were grown in normoxia (21% O(2)) but also remarkably in hypo
14 etected in the DeltarpoZ strain compared with CS when cells were grown in high CO2 but not in ambient air.
15 Ten genotypes from different climates were grown in a common garden under watering treatments repro
16 In order to detect the antibiotic resistant E. coli were grown in the presence of different concentration of ampi
17 xidation, crystals of cationic mixed-valence (MV) complexes were grown in which the organic salts organize into face-to-f
18 Soybean plants of the variety 'MG/BR Conquista' were grown in open top chambers, simulating elevated CO(2) co
21 Six commercial African cassava cultivars were grown in a greenhouse in Erlangen, Germany, and in the f
24 Nine tree species from the boreal-temperate ecotone were grown in natural neighborhoods under ambient and elevate
25 Magallana gigas, an oyster well known for chalk expression, were grown in Bodega Harbor, Bodega Bay, CA.
28 Four summer annuals and a collection of maize hybrids were grown in a common garden experiment conducted at two lev
31 icon substrate, metal-organic framework (MOF) nanoparticles were grown in-situ on the silicon electrode.
32 a common environment for one generation, and then offspring were grown in ambient or elevated [CO(2) ] growth chambers.
34 gare L. cv Optic) mutant (NRH) and its wildtype (WT) parent were grown in tubes of sieved (<250 mum) sandy loam soil unde
35 ing performance and its associated microbiome, maize plants were grown in the greenhouse in soils preceded by either maiz
36 tially reversed when the mtacp1 mtacp2 double mutant plants were grown in a nonphotorespiratory condition (i.e. 1% CO(2)
37 eld, as well as the isotopic ratios of the soils the plants were grown in in the laboratory, indicate that anthropogenic
38 of glyphosate to all plants, and in the second trial plants were grown in either ambient (450 ppm) or elevated CO(2) leve
39 C+) and the mutant mycorrhiza-defective tomato genotype rmc were grown in microcosms in a glasshouse experiment manipulat
40 Askona' F(1), 'Samba' F(1), 'Kazan' F(1) and 'White Satin') were grown in soil fertilized with KI (4 kg I ha(-1)) and Na(
43 rops, corn and soybean differing in iron uptake strategies, were grown in irrigated synthetic soil under semiarid conditi
44 ca sativa and a commercial variety of Diplotaxis tenuifolia were grown in the UK (summer) and subjected to commercial gro
46 r endothelial cells with reduced EGL thickness because they were grown in the absence of fluid shear stress.
48 Genotypes (G) of grafted and non-grafted tomato were grown in different environments (E) in the 2017 and 2018
50 Fourteen wheat (Triticum aestivum) varieties were grown in soil columns packed to three bulk densities rep