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1 , human) and Arabidopsis thaliana (AT, thale cress).
2 SION 1 (TOC1) in Arabidopsis thaliana (thale cress).
3 e gene exchange between Arabidopsis and salt cress.
4 usion protein of Arabidopsis thaliana (thale cress) 4-coumaroyl-CoA ligase (At4CL1) and Vitis vinifer
5             Efficient transformation of salt cress allows for simple gene exchange between Arabidopsi
6 n of T-DNA-tagged mutant collections of salt cress, already in progress, will open the door to a new
7                                         Salt cress, although salt and cold tolerant, is not exception
8 ipt expression changes in germinating garden cress and Arabidopsis (Arabidopsis thaliana) seeds sugge
9 uorescence and EM studies on root cells from cress and maize.
10 ntly lower intron densities in yeasts, thale cress and mice.
11  hydroxycinnamoyl transferase (HCT) in thale cress (Arabidopsis thaliana) and alfalfa (Medicago sativ
12 eat (Triticum aestivum cv Augusta) and thale cress (Arabidopsis thaliana), whereas the pattern of exp
13                              Stomata of salt cress are distributed on the leaf surface at higher dens
14                               Leaves of salt cress are more succulent-like, have a second layer of pa
15 e, mouse, chicken, dog, worm, fly, rice, and cress, as well as those for a wide variety of other spec
16         In miniaturized biotests with garden cress, (-)-beflubutamid showed at least 1000x higher her
17                                Roots of salt cress develop both an extra endodermis and cortex cell l
18 la halophila (Thellungiella salsuginea; salt cress), displays extreme tolerance to high salinity, low
19            Several enterovirus genotypes and CRESS DNA genomes were associated with ICD relative to h
20 of all viral reads, followed by 9 to 17% for CRESS DNA virus sequences.
21 s circular Rep-encoding single-stranded DNA (CRESS DNA) viral genomes, were identified.
22                             Analysis of salt cress expressed sequence tags provides evidence for the
23 tire proteomes: human, mouse, rat, mouse-ear cress, fruit fly, the S. pombe yeast, the E. coli bacter
24                                         Salt cress is an extremophile native to harsh environments an
25 ere studied by following individual roots of cress (Lepidium sativum L.) through reorientation and cl
26 ation occur during the germination of garden cress (Lepidium sativum).
27  with alpha-linolenic acid (ALA) rich Garden cress oil (GCO) and assess their modulatory effect on li
28 a noticeably higher level in unstressed salt cress plants and are induced rapidly under stress.
29 mine ITCs in broccoli, white cabbage, garden cress, radish, horseradish and papaya.
30                       Hybridizations of salt cress RNA targets to an Arabidopsis whole-genome oligonu
31 ay datasets, one from an experiment of thale cress seedlings and the other from an experiment of maiz
32 ffected differently shoot and root length of cress seedlings in germination tests highlighting its co
33                                       Garden cress seeds were undergone for different processing meth
34 veral ethyl methanesulfonate mutants of salt cress that have reduced salinity tolerance, which provid
35                                         Salt cress (Thellungiella halophila) is a small winter annual
36 anate-forming protein (TFP) from field-penny cress, Thlaspi arvense (Brassicaceae), is a representati

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