about
ELONGATED UPPERMOST INTERNODE encodes a cytochrome P450 monooxygenase that epoxidizes gibberellins in a novel deactivation reaction in riceBrassinosteroid-6-oxidases from Arabidopsis and tomato catalyze multiple C-6 oxidations in brassinosteroid biosynthesisThe Arabidopsis DIMINUTO/DWARF1 gene encodes a protein involved in steroid synthesisLATERAL BRANCHING OXIDOREDUCTASE acts in the final stages of strigolactone biosynthesis in ArabidopsisCarlactone is converted to carlactonoic acid by MAX1 in Arabidopsis and its methyl ester can directly interact with AtD14 in vitroThe tomato DWARF enzyme catalyses C-6 oxidation in brassinosteroid biosynthesis.CYP714B1 and CYP714B2 encode gibberellin 13-oxidases that reduce gibberellin activity in rice.RNA-Seq using bulked recombinant inbred line populations uncovers the importance of brassinosteroid for seed longevity after priming treatmentsConfirming stereochemical structures of strigolactones produced by rice and tobacco.BRASSINOSTEROID UPREGULATED1, encoding a helix-loop-helix protein, is a novel gene involved in brassinosteroid signaling and controls bending of the lamina joint in rice.Regulation of transcript levels of the Arabidopsis cytochrome p450 genes involved in brassinosteroid biosynthesis.Isolation and characterization of a rice dwarf mutant with a defect in brassinosteroid biosynthesis.Cloning the tomato curl3 gene highlights the putative dual role of the leucine-rich repeat receptor kinase tBRI1/SR160 in plant steroid hormone and peptide hormone signaling.Brassinosteroid deficiency due to truncated steroid 5alpha-reductase causes dwarfism in the lk mutant of pea.Nitrogen and phosphorus fertilization negatively affects strigolactone production and exudation in sorghum.The last reaction producing brassinolide is catalyzed by cytochrome P-450s, CYP85A3 in tomato and CYP85A2 in Arabidopsis.Patterns of Dwarf expression and brassinosteroid accumulation in tomato reveal the importance of brassinosteroid synthesis during fruit development.Occurrence of brassinosteroids in non-flowering land plants, liverwort, moss, lycophyte and fern.Functional analysis of Arabidopsis CYP714A1 and CYP714A2 reveals that they are distinct gibberellin modification enzymes.Characterization of two brassinosteroid C-6 oxidase genes in pea.Roles of brassinosteroids and related mRNAs in pea seed growth and germination.Blue light-promoted rice leaf bending and unrolling are due to up-regulated brassinosteroid biosynthesis genes accompanied by accumulation of castasterone.Conversion of carlactone to carlactonoic acid is a conserved function of MAX1 homologs in strigolactone biosynthesis.Dwarfism and cytochrome P450-mediated C-6 oxidation of plant steroid hormones.Overexpression of the vascular brassinosteroid receptor BRL3 confers drought resistance without penalizing plant growthProgesterone: its occurrence in plants and involvement in plant growthThe hormonal regulation of de-etiolationShoot-derived signals other than auxin are involved in systemic regulation of strigolactone production in rootsDifference in Striga-susceptibility is reflected in strigolactone secretion profile, but not in compatibility and host preference in arbuscular mycorrhizal symbiosis in two maize cultivarsAvenaol, a germination stimulant for root parasitic plants from Avena strigosaWhich are the major players, canonical or non-canonical strigolactones?Genome Sequence of Striga asiatica Provides Insight into the Evolution of Plant ParasitismRegulation of biosynthesis, perception, and functions of strigolactones for promoting arbuscular mycorrhizal symbiosis and managing root parasitic weedsStructure- and stereospecific transport of strigolactones from roots to shootsLotuslactone, a non-canonical strigolactone from Lotus japonicus
P50
Q24540186-124D647A-BA53-467D-8E08-F13C9C1E0280Q28366681-6FB9C0FD-AAB1-4E03-B45B-75959BD2D119Q28369061-272F16E9-EC37-4827-84F0-805397215C0CQ28828653-9E5BD7E7-FF6E-43F0-AA7E-C2B967F3D469Q34752787-BD533A14-1836-45FF-8985-EDA71F56CCDDQ35014597-D05BC056-1457-4540-B8DD-3BA938383CBDQ36583217-40F33EB4-5A7A-4FA7-BE83-A6AAC574A4D7Q41387394-B1F08F78-A58E-4493-BBB3-621A1FAE887CQ42812647-5852F81D-0B6C-4738-9623-07A3E9A440D5Q43300265-45E2E3CE-FF3D-44D3-BC61-809162C5F6B5Q44134008-A14F727F-84BB-481C-B779-A66DBB0E1D5EQ44213628-9B3ADEC0-D810-4FC0-8D3B-EB115E095AF4Q44240482-D38A0AD8-3598-47EF-8D3D-D30844F1B696Q45001682-3A20C4B6-FF84-4AC8-9895-6E23082710E1Q45255011-C2DA1702-99C1-495E-A966-28B7A7F9D635Q45264853-AB946EE9-CCF1-411E-AA3C-35B393557B90Q46419596-3F24D828-F6D1-4904-977C-4EE9A3CBE171Q46436655-440ECFF0-C9B2-4E80-B2E4-31887052A709Q46972899-B0832A63-3F0D-4F02-9CD6-B55066189A67Q48081288-9385474C-AE23-45B4-A2BE-2E403E8EF42DQ48081290-9440D923-9C6D-41F7-9281-ACC2E7E75917Q50426850-1816C65E-DA6C-4C7D-970D-A2221E87FF8FQ52685889-8BA8C169-C969-4F5C-B96D-EE5861A3F575Q53590820-9636B2E2-298D-43E2-855B-8A268963D399Q58586587-F9641344-27DD-409A-8E2F-FB38096DDE84Q80355452-30B973C1-4F46-434E-8A85-CEB3CAECCBA3Q80537798-46481017-5B62-4425-BD8C-0EF89B003552Q86039668-411C6FCD-DDC7-49DA-B6B1-A48DB2035B13Q86894163-8FC95D47-9C60-4AE0-B10E-B81686868F40Q87757818-842DA647-F9F1-49CD-94E6-FF6DE1960AE0Q88010917-86383B2A-17A7-4538-84C4-8472C04416A5Q90114437-3C575EC5-1239-4B5B-AC8C-E23E90B0A488Q92184410-4D08A1A3-C83A-4CB4-B657-A97BE673DAD5Q92581076-87DB4BB7-421E-4182-A805-F4B326FEA8E3Q93140291-98E12B31-8D1F-4802-99AC-808F887DC285
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Takahito Nomura
@ast
Takahito Nomura
@en
Takahito Nomura
@es
Takahito Nomura
@nl
Takahito Nomura
@sl
type
label
Takahito Nomura
@ast
Takahito Nomura
@en
Takahito Nomura
@es
Takahito Nomura
@nl
Takahito Nomura
@sl
prefLabel
Takahito Nomura
@ast
Takahito Nomura
@en
Takahito Nomura
@es
Takahito Nomura
@nl
Takahito Nomura
@sl
P106
P1153
7403421895
P21
P31
P496
0000-0002-3655-3243
P569
2000-01-01T00:00:00Z