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1 on redistribution and/or polar transport of indoleacetic acid.
3 he effect of Ca on the polar movement of [3H]indoleacetic acid ([3H]IAA) in gravistimulated roots was
5 rescued by gibberellin, brassinosteroid, or indoleacetic acid application and is not attributable to
6 ic compounds such as N-acetylserotonin and 3-indoleacetic acid are produced during the alcoholic ferm
7 mone, SCF(TIR1) targets members of the auxin/indoleacetic acid (Aux/IAA) family of transcriptional re
8 ein ligase that targets members of the auxin/indoleacetic acid (Aux/IAA) family of transcriptional re
10 sport Inhibitor Response (TIR1) with auxin/3-indoleacetic acid (Aux/IAAs) proteins, further supportin
11 of ipdC, a plant inducible gene involved in indoleacetic acid biosynthesis in Erwinia herbicola, amo
12 stant in seedlings treated with auxin (30 mM indoleacetic acid for 2 and 24 h; 100 nm indoleacetic ac
13 mM indoleacetic acid for 2 and 24 h; 100 nm indoleacetic acid for 2 h); however, permeability is dim
14 ategies were employed to examine the role of indoleacetic acid (IAA) in regulating floral organ absci
16 ensity of lateral roots and reduced the free indoleacetic acid (IAA) levels in the root and [3H]IAA t
17 ence of anionic peroxidase overexpression on indoleacetic acid (IAA) metabolism was also examined.
18 . cv Victory) were treated unilaterally with indoleacetic acid (IAA) or gibberellic acid (GA3) with o
20 The plant growth hormone auxin typified by indoleacetic acid (IAA) transcriptionally activates earl
21 se two tissues as affected by gravistimulus, indoleacetic acid (IAA), gibberellic acid (GA3), and fus
22 We examined the changes in the levels of indoleacetic acid (IAA), IAA esters, and a 22-kilodalton
25 are also targets of AGL15, and we found that INDOLEACETIC ACID-INDUCED PROTEIN30 is involved in promo
26 xpression was affected by the plant hormones indoleacetic acid, jasmonic acid, salicylic acid, and gi
27 s (5-hydroxytryptophan, N-acetylserotonin, 3-indoleacetic acid, l-tryptophan ethyl ester) in commerci