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The main auxin biosynthesis pathway in ArabidopsisYucasin is a potent inhibitor of YUCCA, a key enzyme in auxin biosynthesis.Identification of IAA transport inhibitors including compounds affecting cellular PIN trafficking by two chemical screening approaches using maize coleoptile systems.Auxin transport sites are visualized in planta using fluorescent auxin analogs.Alkoxy-auxins are selective inhibitors of auxin transport mediated by PIN, ABCB, and AUX1 transporters.Identification and functional analysis of bifunctional ent-kaurene synthase from the moss Physcomitrella patens.Does the brassinosteroid signal pathway in photomorphogenesis overlap with the gravitropic response caused by auxin?Mitochonic Acid 5 (MA-5), a Derivative of the Plant Hormone Indole-3-Acetic Acid, Improves Survival of Fibroblasts from Patients with Mitochondrial Diseases.Distinct Characteristics of Indole-3-Acetic Acid and Phenylacetic Acid, Two Common Auxins in PlantsIncreased levels of IAA are required for system 2 ethylene synthesis causing fruit softening in peach (Prunus persica L. Batsch).Differential downward stream of auxin synthesized at the tip has a key role in gravitropic curvature via TIR1/AFBs-mediated auxin signaling pathways.Thermospermine suppresses auxin-inducible xylem differentiation in Arabidopsis thaliana.UGT74D1 catalyzes the glucosylation of 2-oxindole-3-acetic acid in the auxin metabolic pathway in Arabidopsis.Development of 4-methoxy-7-nitroindolinyl (MNI)-caged auxins which are extremely stable in planta.Yucasin DF, a potent and persistent inhibitor of auxin biosynthesis in plants.Endogenous diterpenes derived from ent-kaurene, a common gibberellin precursor, regulate protonema differentiation of the moss Physcomitrella patens.Antitumor agents. 228. five new agarofurans, Reissantins A-E, and cytotoxic principles from Reissantia buchananii.Manipulation of intracellular auxin in a single cell by light with esterase-resistant caged auxins.Toyocamycin specifically inhibits auxin signaling mediated by SCFTIR1 pathway.Active core structure of terfestatin A, a new specific inhibitor of auxin signaling.Caged gene-inducer spatially and temporally controls gene expression and plant development in transgenic Arabidopsis plant.Analysis of ent-kaurenoic acid by ultra-performance liquid chromatography-tandem mass spectrometry.Pheophytin a, a low molecular weight compound found in the marine brown alga Sargassum fulvellum, promotes the differentiation of PC12 cells.Molecular evolution of the substrate specificity of ent-kaurene synthases to adapt to gibberellin biosynthesis in land plants.Culcitiolides E-J, six new eremophilane-type sesquiterpene derivatives from Senecio culcitioides.Nisamycin, a new manumycin group antibiotic from Streptomyces sp. K106. I. Taxonomy, fermentation, isolation, physico-chemical and biological properties.PINOID AGC kinases are necessary for phytochrome-mediated enhancement of hypocotyl phototropism in Arabidopsis.Design and synthesis of photolabile caged cytokinin.Asymmetric Auxin Distribution is Not Required to Establish Root Phototropism in Arabidopsis.Auxin activates the plasma membrane H+-ATPase by phosphorylation during hypocotyl elongation in Arabidopsis.Rational design of an auxin antagonist of the SCF(TIR1) auxin receptor complex.Antitumor agents. Part 212. Bucidarasins A-C, three new cytotoxic clerodane diterpenes from Bucida buceras.The Tetrazole Analogue of the Auxin Indole-3-acetic Acid Binds Preferentially to TIR1 and Not AFB5Thermorubin and 2-hydroxyphenyl acetic acid, aldose reductase inhibitorsIsolation of an antioxidant from Penicillium roquefortii IFO 5956Nisamycin, a new manumycin group antibiotic from Streptomyces sp. K106Nisamycin, a new manumycin group antibiotic from Streptomyces sp. K106. II. Structure determination and structure-activity relationshipsIsolation and characterization of gibbestatin B, an inhibitor of gibberellin-induced expression of alpha-amylase, and gibbestatin C from streptomycetaesYokonolide A, a new inhibitor of auxin signal transduction, from Streptomyces diastatochromogenes B59Biotransformation of shiromodiol diacetate, myli-4(15)-en-9-one and myliol by Aspergillus niger
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Ken-ichiro Hayashi
@ast
Ken-ichiro Hayashi
@en
Ken-ichiro Hayashi
@es
Ken-ichiro Hayashi
@nl
Ken-ichiro Hayashi
@sl
type
label
Ken-ichiro Hayashi
@ast
Ken-ichiro Hayashi
@en
Ken-ichiro Hayashi
@es
Ken-ichiro Hayashi
@nl
Ken-ichiro Hayashi
@sl
prefLabel
Ken-ichiro Hayashi
@ast
Ken-ichiro Hayashi
@en
Ken-ichiro Hayashi
@es
Ken-ichiro Hayashi
@nl
Ken-ichiro Hayashi
@sl
P106
P31
P496
0000-0002-9812-2801