569 results on '"Takatsuto, Suguru"'
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52. Light and brassinosteroid signals are integrated via a dark-induced small G protein in etiolated seedling growth
53. Brassinosteroid levels increase drastically prior to morphogenesis of tracheary elements
54. Rice CYP734As function as multisubstrate and multifunctional enzymes in brassinosteroid catabolism
55. Auxin stimulates DWARF4 expression and brassinosteroid biosynthesis in Arabidopsis
56. Light Activates Brassinosteroid Biosynthesis to Promote Hook Opening and Petiole Development in Arabidopsis thaliana
57. A critical role of sterols in embryonic patterning and meristem programming revealed by the fackel mutants of Arabidopsis thaliana
58. A putative role for the tomato genes dumpy and curl-3 in brassinosteroid biosynthesis and response (1)
59. Arabidopsis det2 is defective in the conversion of (24 R)-24-methylcholest-4-En-3-One to (24 R)-24-Methyl-5[alpha]-cholestan-3-one in brassinosteroid biosynthesis (1)
60. Involvement of C-22-Hydroxylated Brassinosteroids in Auxin-Induced Lamina Joint Bending in Rice
61. The AtGenExpress hormone and chemical treatment data set: experimental design, data evaluation, model data analysis and data access
62. The Arabidopsis dwf7/ste1 mutant is defective in the [[DELTA].sup.7] sterol C-5 desaturation step leading to brassinosteroid biosynthesis
63. BEN1, a gene encoding a dihydroflavonol 4-reductase (DFR)-like protein, regulates the levels of brassinosteroids in Arabidopsis thaliana
64. Co-Regulation of Brassinosteroid Biosynthesis-Related Genes During Xylem Cell Differentiation
65. The rice SPINDLY gene functions as a negative regulator of gibberellin signaling by controlling the suppressive function of the DELLA protein, SLR1, and modulating brassinosteroid synthesis
66. Arabidopsis CYP90B1 catalyses the early C-22 hydroxylation of C27, C28 and C29 sterols
67. Biosynthesis of brassinolide from teasterone via typhasterol and castasterone in cultured cells of Catharanthus roseus
68. Biosynthesis of brassinolide from castasterone in cultured cells of Catharanthus roseus
69. BAS1 and SOB7 act redundantly to modulate Arabidopsis photomorphogenesis via unique brassinosteroid inactivation mechanisms
70. CYP90C1 and CYP90D1 are involved in different steps in the brassinosteroid biosynthesis pathway in Arabidopsis thaliana
71. A mammalian steroid action inhibitor spironolactone retards plant growth by inhibition of brassinosteroid action and induces light-induced gene expression in the dark
72. Cytochrome P450-catalyzed brassinosteroid pathway activation through synthesis of castasterone and brassinolide in Phaseolus vulgaris
73. A link between sterol biosynthesis, the cell wall, and cellulose in Arabidopsis
74. A dwarf mutant strain of Pharbitis nil, Uzukobito (kobito), has defective brassinosteroid biosynthesis
75. Brassinosteroid functions in a broad range of disease resistance in tobacco and rice
76. Loss-of-function of a rice brassinosteroid biosynthetic enzyme, C-6 oxidase, prevents the organized arrangement and polar elongation of cells in the leaves and stem
77. A novel brassinosteroid signaling component DWF12
78. Overexpression of DWARF4 in the brassinosteroid biosynthetic pathway results in increased vegetative growth and seed yield in Arabidopsis
79. Lesions in the sterol Δ7 reductase gene of Arabidopsis cause dwarfism due to a block in brassinosteroid biosynthesis
80. The sax1 mutation defines a new locus involved in the brassinosteroid biosynthesis pathway in Arabidopsis thaliana
81. Transcription of the Arabidopsis CPD gene, encoding a steroidogenic cytochrome P450, is negatively controlled by brassinosteroids
82. Biosynthesis of cholestanol in higher plants
83. Capability for and Problems of Practical Uses of Brassinosteroids
84. Microanalysis of Naturally Occurring Brassinosteroids
85. Selective Interaction of Triazole Derivatives with DWF4, a Cytochrome P450 Monooxygenase of the Brassinosteroid Biosynthetic Pathway, Correlates with Brassinosteroid Deficiency in Planta
86. Obtusifoliol 14α-Demethylase (CYP51) Antisense Arabidopsis Shows Slow Growth and Long Life
87. Accumulation of 6-deoxocathasterone and 6-deoxocastasterone in Arabidopsis, pea and tomato is suggestive of common rate-limiting steps in brassinosteroid biosynthesis
88. Light and Brassinosteroid Signals Are Integrated via a Dark-Induced Small G Protein in Etiolated Seedling Growth
89. Roots and shoots of tomato produce 6-deoxo-28-norcathasterone, 6-deoxo-28-nortyphasterol and 6-deoxo-28-norcastasterone, possible precursors of 28-norcastasterone
90. Synthesis and biological activity of 26-norbrassinolide, 26-norcastasterone and 26-nor-6-deoxocastasterone
91. Synthesis of 6-oxy functionalized campest-4-en-3-ones: efficient hydroperoxidation at C-6 of campest-5-en-3-one with molecular oxygen and silica gel
92. 28-Norcastasterone is biosynthesized from castasterone
93. Biosynthesis of brassinosteroids in cultured cells of Catharanthus roseus
94. 2,3,5-Tri- epi-brassinolide: preparation and biological activity in rice lamina inclination test
95. Loose Plant Architecture1(LPA1) determines lamina joint bending by suppressing auxin signalling that interacts with C-22-hydroxylated and 6-deoxo brassinosteroids in rice
96. The Regulation of DWARF4 Expression Is Likely a Critical Mechanism in Maintaining the Homeostasis of Bioactive Brassinosteroids in Arabidopsis1
97. CYP72B1 Inactivates Brassinosteroid Hormones: An Intersection between Photomorphogenesis and Plant Steroid Signal Transduction1
98. A Putative Role for the Tomato Genes DUMPY and CURL-3 in Brassinosteroid Biosynthesis and Response1
99. Castasterone is a likely end product of brassinosteroid biosynthetic pathway in rice
100. A Case Study of the Perception of Science and Technology in Lower Secondary School Class : Introduction of a Teaching Device that Converts Vibrations into Electricity
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