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SuperSAGE analysis of the Nicotiana attenuata transcriptome after fatty acid-amino acid elicitation (FAC): identification of early mediators of insect responsesDifferential regulation of mRNA levels of acyl carrier protein isoforms in ArabidopsisVolatile emission in bracken fern is induced by jasmonates but not by Spodoptera littoralis or Strongylogaster multifasciata herbivoryPhenotypic, genetic and genomic consequences of natural and synthetic polyploidization of Nicotiana attenuata and Nicotiana obtusifoliaPectin methylesterase NaPME1 contributes to the emission of methanol during insect herbivory and to the elicitation of defence responses in Nicotiana attenuata.Rapid modification of the insect elicitor N-linolenoyl-glutamate via a lipoxygenase-mediated mechanism on Nicotiana attenuata leaves.RNAi-mediated silencing of the HD-Zip gene HD20 in Nicotiana attenuata affects benzyl acetone emission from corollas via ABA levels and the expression of metabolic genes.The Nicotiana attenuata GLA1 lipase controls the accumulation of Phytophthora parasitica-induced oxylipins and defensive secondary metabolites.Arabidopsis AtHB7 and AtHB12 evolved divergently to fine tune processes associated with growth and responses to water stressEmpoasca leafhoppers attack wild tobacco plants in a jasmonate-dependent manner and identify jasmonate mutants in natural populations.Perception of insect feeding by plants.Nicotiana attenuata NaHD20 plays a role in leaf ABA accumulation during water stress, benzylacetone emission from flowers, and the timing of bolting and flower transitions.New insights into the early biochemical activation of jasmonic acid biosynthesis in leaves.HSPRO controls early Nicotiana attenuata seedling growth during interaction with the fungus Piriformospora indica.The Nicotiana attenuata LECTIN RECEPTOR KINASE 1 is involved in the perception of insect feeding.Nicotiana attenuata LECTIN RECEPTOR KINASE1 suppresses the insect-mediated inhibition of induced defense responses during Manduca sexta herbivory.JA-Ile signalling in Solanum nigrum is not required for defence responses in nature.Herbivore-associated elicitors: FAC signaling and metabolism.Regulation of jasmonate metabolism and activation of systemic signaling in Solanum nigrum: COI1 and JAR4 play overlapping yet distinct roles.Lipoxygenase-mediated modification of insect elicitors: generating chemical diversity on the leaf wound surface.HAHB4, a sunflower HD-Zip protein, integrates signals from the jasmonic acid and ethylene pathways during wounding and biotic stress responses.A rapid and sensitive method for the simultaneous analysis of aliphatic and polar molecules containing free carboxyl groups in plant extracts by LC-MS/MS.HSPRO acts via SnRK1-mediated signaling in the regulation of Nicotiana attenuata seedling growth promoted by Piriformospora indica.Transduction of wound and herbivory signals in plastids.Lipases and the biosynthesis of free oxylipins in plants.Nicotiana attenuata SIPK, WIPK, NPR1, and fatty acid-amino acid conjugates participate in the induction of jasmonic acid biosynthesis by affecting early enzymatic steps in the pathway.Characterization of cyclopropane fatty-acid synthase from Sterculia foetida.Disruption of the FATB gene in Arabidopsis demonstrates an essential role of saturated fatty acids in plant growth.Metabolic responses to the reduction in palmitate caused by disruption of the FATB gene in Arabidopsis.The use of VIGS technology to study plant-herbivore interactions.Analysis of the aliphatic monomer composition of polyesters associated with Arabidopsis epidermis: occurrence of octadeca-cis-6, cis-9-diene-1,18-dioate as the major component.Jasmonate perception regulates jasmonate biosynthesis and JA-Ile metabolism: the case of COI1 in Nicotiana attenuata.The fou2 gain-of-function allele and the wild-type allele of Two Pore Channel 1 contribute to different extents or by different mechanisms to defense gene expression in Arabidopsis.Revealing complexity and specificity in the activation of lipase-mediated oxylipin biosynthesis: a specific role of the Nicotiana attenuata GLA1 lipase in the activation of jasmonic acid biosynthesis in leaves and roots.Olive fruits infested with olive fly larvae respond with an ethylene burst and the emission of specific volatiles.C12 derivatives of the hydroperoxide lyase pathway are produced by product recycling through lipoxygenase-2 in Nicotiana attenuata leaves.HAHB10, a sunflower HD-Zip II transcription factor, participates in the induction of flowering and in the control of phytohormone-mediated responses to biotic stress.Fragile X founder effects in ArgentinaThe lipid polyester composition of Arabidopsis thaliana and Brassica napus seedsA gain-of-function allele of TPC1 activates oxylipin biogenesis after leaf wounding in Arabidopsis
P50
Q21262001-E2D3E589-765D-4EBF-BC3E-5D580ED7987FQ28345013-C51EFAB3-A20F-43A1-AC1C-775CF1D29EBFQ28710578-D7655087-4347-449D-8391-FC4258139B46Q28754338-5C215E91-5043-4743-B257-466133D6DD5DQ30489065-8D7C1543-A873-43C4-8893-E6E8BE258BA3Q33652962-1A926A1C-4263-4AFC-BADA-D6977D627AC8Q34252828-37A05E56-5E1A-4445-AD07-C4BD62F4D679Q34309713-E7F28B7A-DF8D-4AC9-9B7B-F50F71E21063Q35177592-50D0F0EB-AF41-46DC-AEF6-738F20384004Q36066402-2AEAC104-A741-4315-AE15-1F3325ED38C2Q38041577-A29137CA-4AE1-4F67-A65F-53692EC37948Q39416317-2C9F278C-C011-4CCC-AE8C-57881F3C0F52Q40900371-ECD64501-886E-4124-8140-D24EC76FDF24Q42012016-E20BAB8E-0DB1-407E-A7CF-510E9F28A932Q42015174-66F04ACD-EB0B-4819-AD6C-B90BF980E07BQ42015877-83629AE4-C44D-40A4-9FB3-C0D7DC94F2FFQ42016040-2969BC92-F52E-4A53-A685-E8B3E5517BB1Q42018086-F7CCC072-E65F-4AFF-8EFF-954454D23354Q42018274-13C0D847-D0C1-4922-B852-5F2BA4CCE40CQ42018744-DCE6D7CF-F887-46C8-97D8-3F49DC34DA24Q42028482-373D7FDD-FDF3-47F1-9A6E-37A3461F678DQ42156682-83B922D3-7178-4AE2-B5B4-C9D55B4B5061Q42283532-9BF210AD-B953-4D3E-AC93-3D8B97D32BB2Q42481107-DF347959-1CF1-494A-8B69-F06475F04A7FQ42729909-7F0A8F79-252E-4C84-A2B2-4C0D415F6215Q43246237-35949B90-6BB7-4057-BECB-95CF18D74F4AQ44299965-EA4B923A-7F90-409B-9333-5AF98EDBEF53Q44387565-7F3BBC49-E51E-46CF-BEF0-A45F7E2EC128Q44987624-E405A22B-642A-4B00-B969-BDA8EAEA62FDQ45160114-A4823187-24AB-4D14-B823-43E153DF0276Q45177812-2836B2AE-2C05-4704-8D1A-03E8F32C6E2FQ46535846-1D301243-427E-43B0-BA8A-80774CBA4E39Q46915262-A77E1040-E061-4008-A337-A10E30868E4DQ48058382-5D2E3E8E-6F20-4F0C-BD12-3247E47F4A4AQ51369652-6F173CA3-3876-4278-9C0A-D8773D804537Q51597660-403B37C6-E02C-4458-B5C2-953C6698C5B4Q51896958-2EEF7B9E-F312-411A-921F-3841AE9E2395Q77464432-B699A3D7-8491-4694-A06C-21DFE5638BD3Q79284885-33863773-7926-4CB7-9D5B-D6BC59067092Q79663064-C9B58721-2A82-45BB-B334-90D9A09306E5
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
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հետազոտող
@hy
name
Gustavo Bonaventure
@ast
Gustavo Bonaventure
@en
Gustavo Bonaventure
@es
Gustavo Bonaventure
@fr
Gustavo Bonaventure
@nl
Gustavo Bonaventure
@sl
type
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Gustavo Bonaventure
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Gustavo Bonaventure
@en
Gustavo Bonaventure
@es
Gustavo Bonaventure
@fr
Gustavo Bonaventure
@nl
Gustavo Bonaventure
@sl
prefLabel
Gustavo Bonaventure
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Gustavo Bonaventure
@en
Gustavo Bonaventure
@es
Gustavo Bonaventure
@fr
Gustavo Bonaventure
@nl
Gustavo Bonaventure
@sl
P106
P21
P31
P496
0000-0001-6120-3897