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Nitric oxide triggers a transient metabolic reprogramming in ArabidopsisBenzoic acid 2-hydroxylase, a soluble oxygenase from tobacco, catalyzes salicylic acid biosynthesisA permeable cuticle is associated with the release of reactive oxygen species and induction of innate immunity.Antisense-mediated depletion of a potato lipoxygenase reduces wound induction of proteinase inhibitors and increases weight gain of insect pestsDiverse functional interactions between nitric oxide and abscisic acid in plant development and responses to stress.Histone H2A.Z and homologues of components of the SWR1 complex are required to control immunity in Arabidopsis.Nitric oxide sensing in plants is mediated by proteolytic control of group VII ERF transcription factors.Oxygen sensing coordinates photomorphogenesis to facilitate seedling survival.Inhibition of Arabidopsis O-acetylserine(thiol)lyase A1 by tyrosine nitration.Pathogen and circadian controlled 1 (PCC1) protein is anchored to the plasma membrane and interacts with subunit 5 of COP9 signalosome in Arabidopsis.Is Salicylic Acid a Translocated Signal of Systemic Acquired Resistance in Tobacco?Involvement of nitric oxide and auxin in signal transduction of copper-induced morphological responses in Arabidopsis seedlings.Induction of Benzoic Acid 2-Hydroxylase in Virus-Inoculated Tobacco.Pathway of Salicylic Acid Biosynthesis in Healthy and Virus-Inoculated Tobacco.Inactivation of PYR/PYL/RCAR ABA receptors by tyrosine nitration may enable rapid inhibition of ABA signaling by nitric oxide in plants.Reversible protein phosphorylation regulates jasmonic acid-dependent and -independent wound signal transduction pathways in Arabidopsis thaliana.Differential distribution of the lipoxygenase pathway enzymes within potato chloroplasts.FYVE1/FREE1 Interacts with the PYL4 ABA Receptor and Mediates its Delivery to the Vacuolar Degradation Pathway.Nitric oxide regulates DELLA content and PIF expression to promote photomorphogenesis in Arabidopsis.The TRANSPLANTA collection of Arabidopsis lines: a resource for functional analysis of transcription factors based on their conditional overexpression.Pathogen and Circadian Controlled 1 (PCC1) regulates polar lipid content, ABA-related responses, and pathogen defence in Arabidopsis thaliana.Nitric Oxide Controls Constitutive Freezing Tolerance in Arabidopsis by Attenuating the Levels of Osmoprotectants, Stress-Related Hormones and Anthocyanins.Nitric oxide responses in Arabidopsis hypocotyls are mediated by diverse phytohormone pathwaysCross-talk between wound signalling pathways determines local versus systemic gene expression in Arabidopsis thalianaHydrogen Peroxide Stimulates Salicylic Acid Biosynthesis in TobaccoAntisense-mediated depletion of potato leaf omega3 fatty acid desaturase lowers linolenic acid content and reduces gene activation in response to woundingRAP2.3 negatively regulates nitric oxide biosynthesis and related responses through a rheostat-like mechanism in ArabidopsisPresent knowledge and controversies, deficiencies, and misconceptions on nitric oxide synthesis, sensing, and signaling in plantsNitric oxide deficiency decreases C-repeat binding factor-dependent and -independent induction of cold acclimation
P50
Q28593229-7AAC0778-AC00-424D-B402-C40B39D38CF3Q33841683-46CA9D72-57A5-4CF3-AFC4-D56216369273Q33987429-9CC016AC-20C3-4FB7-BCA6-72E7B87ED498Q34961491-926926B0-D5E9-4D86-AF43-60DD3177387FQ38174051-7167347A-4C43-4279-A564-030A49ED827EQ38296632-24AC5163-8F0A-466D-8815-B5BF793D50AFQ38552244-E5D03D94-C6AB-4BC1-96E8-03412EC5A6A6Q40931852-4E281323-D7A0-4376-B54F-75CBC82F6004Q41558001-3B41E1A3-C61A-4733-BB64-9E644BFE98D1Q41894165-1986602E-D749-4417-AC6B-D32F6B05B452Q42526133-C70493FD-358E-4D9B-A810-8074C3D614BCQ42871522-54E4C3F8-AF23-44CE-8D25-33FBDA8E5C27Q45730931-79EC326C-C134-40CF-A832-E51AF3E4C034Q45730932-C20785B3-0A23-4570-9FDA-AC5F44E24B86Q46676067-C2F9E99E-7761-4347-AD7A-034D03348BDAQ47780078-A9843E74-7840-4A11-A165-F2635F4DD03BQ48082401-87C814C3-9C1F-4DF8-9EE0-1F9F6A0F7C90Q49031264-BA17F708-0C9D-49D4-AF52-9757BFD3462FQ50277812-AB01BF73-E799-4057-B4EC-E4C5A3156859Q50694047-0D790BA1-8DD2-4086-AE27-6980BB037372Q50853169-4D92BBFD-6324-427C-9CA1-89BD183729E7Q55360308-91FAD685-E871-4554-A04F-98154F7317D8Q58802604-285C5C7C-7D16-44A9-B19E-C50FE50CCB56Q73205242-276A986D-713E-425F-ADA6-DE926EC2578CQ74781769-1E04DBBE-BE41-4288-BDB4-BD681A2089BCQ77773054-770CD231-6AF9-42A7-BD48-ECB8431C490CQ89688926-85B966C7-2DB2-44E8-88B9-346D31EF9BD8Q92025584-E23D41D7-7453-42E2-8CE1-827205DB0688Q92354098-A553EBF5-BF2E-4437-8864-985F5B15ED53
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
José León
@ast
José León
@en
José León
@es
José León
@nl
José León
@sl
type
label
José León
@ast
José León
@en
José León
@es
José León
@nl
José León
@sl
prefLabel
José León
@ast
José León
@en
José León
@es
José León
@nl
José León
@sl
P1053
C-4756-2016
P106
P1153
19934029900
P21
P31
P3829
P496
0000-0002-7332-1572