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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
6 n of T-DNA-tagged mutant collections of salt cress, already in progress, will open the door to a new
8 ipt expression changes in germinating garden cress and Arabidopsis (Arabidopsis thaliana) seeds sugge
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
15 e, mouse, chicken, dog, worm, fly, rice, and cress, as well as those for a wide variety of other spec
18 la halophila (Thellungiella salsuginea; salt cress), displays extreme tolerance to high salinity, low
23 tire proteomes: human, mouse, rat, mouse-ear cress, fruit fly, the S. pombe yeast, the E. coli bacter
25 ere studied by following individual roots of cress (Lepidium sativum L.) through reorientation and cl
27 with alpha-linolenic acid (ALA) rich Garden cress oil (GCO) and assess their modulatory effect on li
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
34 veral ethyl methanesulfonate mutants of salt cress that have reduced salinity tolerance, which provid
36 anate-forming protein (TFP) from field-penny cress, Thlaspi arvense (Brassicaceae), is a representati
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