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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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