Evidence for a specific uptake system for iron phytosiderophores in roots of grasses.
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Biosynthesis of Phytosiderophores : In Vitro Biosynthesis of 2'-Deoxymugineic Acid from l-Methionine and NicotianamineCloning two genes for nicotianamine aminotransferase, a critical enzyme in iron acquisition (Strategy II) in graminaceous plantsThe Response of the Root Apex in Plant Adaptation to Iron Heterogeneity in SoilSiderophores in environmental research: roles and applicationsIron stress-induced changes in root epidermal cell fate are regulated independently from physiological responses to low iron availability(52)Fe translocation in barley as monitored by a positron-emitting tracer imaging system (PETIS): evidence for the direct translocation of Fe from roots to young leaves via phloem.Early iron-deficiency-induced transcriptional changes in Arabidopsis roots as revealed by microarray analyses.Integrating microarray analysis and the soybean genome to understand the soybeans iron deficiency response.Alternative functions of Arabidopsis Yellow Stripe-Like3: from metal translocation to pathogen defense.Dealing with iron metabolism in rice: from breeding for stress tolerance to biofortificationMapping and Characterization of the fefe Gene That Controls Iron Uptake in Melon (Cucumis melo L.).ClpC1, an ATP-dependent Clp protease in plastids, is involved in iron homeostasis in Arabidopsis leaves.Bacillus licheniformis SA03 Confers Increased Saline-Alkaline Tolerance in Chrysanthemum Plants by Induction of Abscisic Acid Accumulation.Nicotianamine chelates both FeIII and FeII. Implications for metal transport in plantsAhNRAMP1 iron transporter is involved in iron acquisition in peanut.ZmYS1 functions as a proton-coupled symporter for phytosiderophore- and nicotianamine-chelated metals.Genetic improvement of iron content and stress adaptation in plants using ferritin gene.A putative role for amino acid permeases in sink-source communication of barley tissues uncovered by RNA-seq.Enhanced tolerance of rice to low iron availability in alkaline soils using barley nicotianamine aminotransferase genes.Recent insights into iron homeostasis and their application in graminaceous crops.Genome-wide identification, classification and expression profiling of nicotianamine synthase (NAS) gene family in maize.Three-dimensional distribution of vessels, passage cells and lateral roots along the root axis of winter wheat (Triticum aestivum)2'-Deoxymugineic acid promotes growth of rice (Oryza sativa L.) by orchestrating iron and nitrate uptake processes under high pH conditionsMetabolome analysis of Arabidopsis thaliana roots identifies a key metabolic pathway for iron acquisition.Brachypodium distachyon as a new model system for understanding iron homeostasis in grasses: phylogenetic and expression analysis of Yellow Stripe-Like (YSL) transporters.Transgenic petunia with the iron(III)-phytosiderophore transporter gene acquires tolerance to iron deficiency in alkaline environments.Salicylic acid modulates arsenic toxicity by reducing its root to shoot translocation in rice (Oryza sativa L.).Genome-wide analysis of overlapping genes regulated by iron deficiency and phosphate starvation reveals new interactions in Arabidopsis roots.The Organization of Controller Motifs Leading to Robust Plant Iron HomeostasisOsYSL16 plays a role in the allocation of ironIron homeostasis in Arabidopsis thaliana: transcriptomic analyses reveal novel FIT-regulated genes, iron deficiency marker genes and functional gene networks.Characterization of the cytokinin-responsive transcriptome in riceThe transcription factor IDEF1 regulates the response to and tolerance of iron deficiency in plantsA new transgenic rice line exhibiting enhanced ferric iron reduction and phytosiderophore production confers tolerance to low iron availability in calcareous soilNitric Oxide Alleviated Arsenic Toxicity by Modulation of Antioxidants and Thiol Metabolism in Rice (Oryza sativa L.).Rice genes involved in phytosiderophore biosynthesis are synchronously regulated during the early stages of iron deficiency in roots.Jasmonate signaling is activated in the very early stages of iron deficiency responses in rice rootsOsYSL18 is a rice iron(III)-deoxymugineic acid transporter specifically expressed in reproductive organs and phloem of lamina joints.The iron-regulated transporter, MbNRAMP1, isolated from Malus baccata is involved in Fe, Mn and Cd trafficking.Cadmium transport and tolerance in rice: perspectives for reducing grain cadmium accumulation.
P2860
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P2860
Evidence for a specific uptake system for iron phytosiderophores in roots of grasses.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年学术文章
@wuu
1986年学术文章
@zh
1986年学术文章
@zh-cn
1986年学术文章
@zh-hans
1986年学术文章
@zh-my
1986年学术文章
@zh-sg
1986年學術文章
@yue
1986年學術文章
@zh-hant
name
Evidence for a specific uptake system for iron phytosiderophores in roots of grasses.
@en
Evidence for a specific uptake system for iron phytosiderophores in roots of grasses.
@nl
type
label
Evidence for a specific uptake system for iron phytosiderophores in roots of grasses.
@en
Evidence for a specific uptake system for iron phytosiderophores in roots of grasses.
@nl
prefLabel
Evidence for a specific uptake system for iron phytosiderophores in roots of grasses.
@en
Evidence for a specific uptake system for iron phytosiderophores in roots of grasses.
@nl
P356
P1433
P1476
Evidence for a specific uptake system for iron phytosiderophores in roots of grasses.
@en
P2093
Marschner H
P2860
P304
P356
10.1104/PP.80.1.175
P407
P577
1986-01-01T00:00:00Z