The organ-specific expression of terpene synthase genes contributes to the terpene hydrocarbon composition of chamomile essential oilsPositive selection driving diversification in plant secondary metabolismPlant tropane alkaloid biosynthesis evolved independently in the Solanaceae and ErythroxylaceaeSuccessful herbivore attack due to metabolic diversion of a plant chemical defenseThe effects of arbuscular mycorrhizal fungi on direct and indirect defense metabolites of Plantago lanceolata LFeeding Experience Affects the Behavioral Response of Polyphagous Gypsy Moth Caterpillars to Herbivore-induced Poplar VolatilesPlant defense and herbivore counter-defense: benzoxazinoids and insect herbivoresConstitutive plant toxins and their role in defense against herbivores and pathogensGlucosinolate hydrolysis in Lepidium sativum--identification of the thiocyanate-forming proteinPlant community diversity influences allocation to direct chemical defence in Plantago lanceolataNon-photochemical quenching capacity in Arabidopsis thaliana affects herbivore behaviourA Latex Metabolite Benefits Plant Fitness under Root Herbivore AttackEvolution in an ancient detoxification pathway is coupled with a transition to herbivory in the drosophilidaeBiosynthesis of the major tetrahydroxystilbenes in spruce, astringin and isorhapontin, proceeds via resveratrol and is enhanced by fungal infectionJasmonic Acid and Ethylene Signaling Pathways Regulate Glucosinolate Levels in Plants During Rhizobacteria-Induced Systemic Resistance Against a Leaf-Chewing HerbivoreThe Bark-Beetle-Associated Fungus, Endoconidiophora polonica, Utilizes the Phenolic Defense Compounds of Its Host as a Carbon SourceArabidopsis thaliana isoprenyl diphosphate synthases produce the C25 intermediate geranylfarnesyl diphosphate.Molecular and biochemical evolution of maize terpene synthase 10, an enzyme of indirect defense.From amino acid to glucosinolate biosynthesis: protein sequence changes in the evolution of methylthioalkylmalate synthase in Arabidopsis.Real-time analysis of alarm pheromone emission by the pea aphid (acyrthosiphon pisum) under predationRestoring a maize root signal that attracts insect-killing nematodes to control a major pest.Methyl jasmonate induces traumatic resin ducts, terpenoid resin biosynthesis, and terpenoid accumulation in developing xylem of Norway spruce stems.Metabolism of poplar salicinoids by the generalist herbivore Lymantria dispar (Lepidoptera).The products of a single maize sesquiterpene synthase form a volatile defense signal that attracts natural enemies of maize herbivores.Exogenous application of methyl jasmonate elicits defenses in Norway spruce (Picea abies) and reduces host colonization by the bark beetle Ips typographus.Microchemical analysis of laser-microdissected stone cells of Norway spruce by cryogenic nuclear magnetic resonance spectroscopy.Cloning and characterization of isoprenyl diphosphate synthases with farnesyl diphosphate and geranylgeranyl diphosphate synthase activity from Norway spruce (Picea abies) and their relation to induced oleoresin formation.Functional identification and differential expression of 1-deoxy-D-xylulose 5-phosphate synthase in induced terpenoid resin formation of Norway spruce (Picea abies).Nonuniform distribution of glucosinolates in Arabidopsis thaliana leaves has important consequences for plant defense.Characterization of a root-specific Arabidopsis terpene synthase responsible for the formation of the volatile monoterpene 1,8-cineole.Peroxisomal ATP-binding cassette transporter COMATOSE and the multifunctional protein abnormal INFLORESCENCE MERISTEM are required for the production of benzoylated metabolites in Arabidopsis seeds.Induced carbon reallocation and compensatory growth as root herbivore tolerance mechanisms.Emission of volatile organic compounds after herbivory from Trifolium pratense (L.) under laboratory and field conditions.Phyllotreta striolata flea beetles use host plant defense compounds to create their own glucosinolate-myrosinase system.Constitutive emission of the aphid alarm pheromone, (E)-β-farnesene, from plants does not serve as a direct defense against aphids.The nonmevalonate pathway supports both monoterpene and sesquiterpene formation in snapdragon flowersIdentification and characterization of CYP79D6v4, a cytochrome P450 enzyme producing aldoximes in black poplar (Populus nigra).Volatile chemicals from leaf litter are associated with invasiveness of a neotropical weed in Asia.Terpene synthases of oregano (Origanum vulgare L.) and their roles in the pathway and regulation of terpene biosynthesis.Subgroup 4 R2R3-MYBs in conifer trees: gene family expansion and contribution to the isoprenoid- and flavonoid-oriented responses.
P50
Q21261990-6563692E-BC70-4642-9A8A-D689BD1D630CQ24548505-9D57A3C4-D990-492E-8BCF-8D86C8206FABQ24594972-F64A06EF-5098-4DA0-BE0C-27A2E959C3B2Q24626313-4D75D094-A65C-4153-A99E-159B42A3567EQ24647551-BC2DCF3A-1C5D-4C7F-8437-4903D70842A6Q27315824-A7B8D962-A325-4664-A564-20F5F8583DE0Q28069714-A52E5B97-E156-4122-9061-6AA7D4D98DF8Q28218008-B6DF3C36-0A15-45E6-8D3B-87571C5995B6Q28276691-D6EF891D-09D0-4D1C-B7FB-15176BE297AAQ28478333-0A33A883-AFC4-4D24-BB96-E794AD93C1F5Q28484773-FBA11583-39E9-4162-83BE-1D11062C4124Q28552040-981B097D-2747-4D1F-AF77-AA860FDA913AQ28654444-69E3A131-FE7C-48CB-8908-316B32FC177BQ28743922-961738C7-A136-4452-83CB-00149A8A8E24Q28817652-DCDCF90D-A639-46A8-BD42-18690E5DFFF4Q28830653-DDF1BA8A-ED91-4039-AC2F-921BD2CE72C9Q30316006-62DA0FFF-676C-4A79-A45E-781C4C8398EEQ30319049-80B83EAC-EF6C-4DDE-B57B-1E2991747541Q30398165-51F30037-C07C-457E-A4F5-D5D016DE20E3Q30486116-900C435F-976B-4164-8F57-1B06E990D2C4Q30489500-038F6380-26CA-475F-95B1-B210F4AD56B5Q30836305-0DE589AF-47F7-4B96-82F6-B611AB73F258Q31120441-0E869064-D98A-4706-B8FA-712AA6A78922Q33231825-59F95AE0-CFC9-429F-B4A2-139F19CC99F9Q33235356-8FF6BA6C-3221-4A17-8BCA-B893201C556FQ33260313-0D559F10-9D91-482D-9F20-B442FE4998A7Q33290527-8712D371-C045-4FEE-B33D-7D0596D27E8BQ33293698-855B1F38-2B86-45A4-84B9-A4ED7D508894Q33327935-A636D25D-82AC-4D1A-9172-AEEB03DE97DFQ33340283-4DF73ED7-8BE3-4335-AE1E-06C18C15EC0DQ33357142-F5FC6ED2-6483-423F-89C8-55E0A5063CD6Q33358318-3BE4F51A-C92F-4F64-B7BF-AD8929972C12Q33555167-DDD67628-79EB-405D-B09F-13EE4CBB5A26Q33665307-7AB010A9-CB3D-455A-8B66-9CA678F5EC0CQ33752201-7291B35F-B20B-48C8-8D91-2BBA8701B45FQ33756633-D419572B-006E-4046-A205-4AF40CF1F3D7Q33879540-29FA4BFD-3A48-4D66-8220-E6EDE69DA156Q33913904-EA9B1846-2797-48D4-8F3F-F5E3EEF89971Q34112118-EA29D357-1B4F-4729-8498-DFE6E581C153Q34112256-32FBD009-9C1A-4BA4-B407-CA6099B9B878
P50
description
American biochemist
@en
Amerikaans biochemicus
@nl
amerikanischer Biochemiker
@de
biocimiciste american
@lfn
bioquímicu estauxunidense
@ast
usona biokemiisto
@eo
عالم كيمياء حيوية من الولايات المتحدة الأمريكية
@ar
name
Jonathan Gershenzon
@af
Jonathan Gershenzon
@an
Jonathan Gershenzon
@ast
Jonathan Gershenzon
@bar
Jonathan Gershenzon
@br
Jonathan Gershenzon
@ca
Jonathan Gershenzon
@co
Jonathan Gershenzon
@cs
Jonathan Gershenzon
@cy
Jonathan Gershenzon
@da
type
label
Jonathan Gershenzon
@af
Jonathan Gershenzon
@an
Jonathan Gershenzon
@ast
Jonathan Gershenzon
@bar
Jonathan Gershenzon
@br
Jonathan Gershenzon
@ca
Jonathan Gershenzon
@co
Jonathan Gershenzon
@cs
Jonathan Gershenzon
@cy
Jonathan Gershenzon
@da
prefLabel
Jonathan Gershenzon
@af
Jonathan Gershenzon
@an
Jonathan Gershenzon
@ast
Jonathan Gershenzon
@bar
Jonathan Gershenzon
@br
Jonathan Gershenzon
@ca
Jonathan Gershenzon
@co
Jonathan Gershenzon
@cs
Jonathan Gershenzon
@cy
Jonathan Gershenzon
@da
P214
P227
P244
P1053
K-1331-2013
P106
P2038
Jonathan_Gershenzon
P21
P213
0000 0000 3084 6913
P214
P227
1128621657
P244
P31
P3829
P496
0000-0002-1812-1551
P569
1955-01-01T00:00:00Z
P734
P735
P7859
lccn-n87143019