Delta-viniferin, a resveratrol dehydrodimer: one of the major stilbenes synthesized by stressed grapevine leaves.
about
Wine polyphenols: potential agents in neuroprotectionAnthocyanins and Human Health: An In Vitro Investigative ApproachTranscriptomic and Metabolomic Networks in the Grape Berry Illustrate That it Takes More Than Flavonoids to Fight Against Ultraviolet RadiationMALDI mass spectrometry imaging for the simultaneous location of resveratrol, pterostilbene and viniferins on grapevine leavesIn vivo localization at the cellular level of stilbene fluorescence induced by Plasmopara viticola in grapevine leavesIsolation and purification of two antioxidant isomers of resveratrol dimer from the wine grape by counter-current chromatography.Identification of putative stage-specific grapevine berry biomarkers and omics data integration into networks.Genome-wide analysis of the grapevine stilbene synthase multigenic family: genomic organization and expression profiles upon biotic and abiotic stresses.Reference gene validation for quantitative RT-PCR during biotic and abiotic stresses in Vitis viniferaResveratrol is a peroxidase-mediated inactivator of COX-1 but not COX-2: a mechanistic approach to the design of COX-1 selective agents.Study of Grape Polyphenols by Liquid Chromatography-High-Resolution Mass Spectrometry (UHPLC/QTOF) and Suspect Screening AnalysisThiamine modulates metabolism of the phenylpropanoid pathway leading to enhanced resistance to Plasmopara viticola in grapevineA review (research and patents) on jasmonic acid and its derivatives.Multiomics in grape berry skin revealed specific induction of the stilbene synthetic pathway by ultraviolet-C irradiation.Jasmonates are induced by the PAMP flg22 but not the cell death-inducing elicitor Harpin in Vitis rupestris.Molecular analysis of the early interaction between the grapevine flower and Botrytis cinerea reveals that prompt activation of specific host pathways leads to fungus quiescence.Bioactive oligostilbenoids from Shorea maxwelliana King and their chemotaxonomic significance.Vaticanol B, a resveratrol tetramer, regulates endoplasmic reticulum stress and inflammation.Muscadinia rotundifolia 'Noble' defense response to Plasmopara viticola inoculation by inducing phytohormone-mediated stilbene accumulation.Characterization of triterpenoid profiles and triterpene synthase expression in the leaves of eight Vitis vinifera cultivars grown in the Upper Rhine Valley.Phenolic Compounds and Bioactivity of Healthy and Infected Grapevine Leaf Extracts from Red Varieties Merlot and Vranac (Vitis vinifera L.).Soybean and casein hydrolysates induce grapevine immune responses and resistance against Plasmopara viticola.Metabolic constituents of grapevine and grape-derived products.Stilbene production in cell cultures of Vitis vinifera L. cvs Red Globe and Michele Palieri elicited by methyl jasmonate.Enantioselective intramolecular C-H insertion reactions of donor-donor metal carbenoids.The R2R3-MYB transcription factors MYB14 and MYB15 regulate stilbene biosynthesis in Vitis vinifera.Ultraviolet induction of antifungal activity in plants.Investigation of monomeric and oligomeric wine stilbenoids in red wines by ultra-high-performance liquid chromatography/electrospray ionization quadrupole time-of-flight mass spectrometry.Synthesis of Benzodihydrofurans by Asymmetric C-H Insertion Reactions of Donor/Donor Rhodium Carbenes.Study of leaf metabolome modifications induced by UV-C radiations in representative Vitis, Cissus and Cannabis species by LC-MS based metabolomics and antioxidant assays.Insights on the stilbenes in Raboso Piave grape (Vitis vinifera L.) as a consequence of postharvest vs on-vine dehydration.Grapevine Botryosphaeria dieback fungi have specific aggressiveness factor repertory involved in wood decay and stilbene metabolization.Changes in grape polyphenols (V. vinifera L.) as a consequence of post-harvest withering by high-resolution mass spectrometry: Raboso Piave versus Corvina.Biomimetic Synthesis of Resveratrol Trimers Catalyzed by Horseradish Peroxidase.Potassium Hexacyanoferrate (III)-Catalyzed Dimerization of Hydroxystilbene: Biomimetic Synthesis of Indane Stilbene Dimers.Identification of Lipid Markers of Plasmopara viticola Infection in Grapevine Using a Non-targeted Metabolomic Approach.Field-Based Metabolomics of Vitis vinifera L. Stems Provides New Insights for Genotype Discrimination and Polyphenol Metabolism Structuring.A High-Throughput UHPLC-QqQ-MS Method for Polyphenol Profiling in Rosé WinesBreeding for grapevine downy mildew resistance: a review of “omics” approachesResveratrol-Related Dehydrodimers: Laccase-Mediated Biomimetic Synthesis and Antiproliferative Activity
P2860
Q21284967-4B371A24-89BC-4E7D-8621-D145C617F99FQ24804969-A00E69D0-3746-4256-83DD-6702F37F418EQ28080131-2813A1F7-F128-4873-A0B6-128414115070Q28244459-2C006A5D-8229-4CD7-BFA3-6DD58C81FC1DQ30519494-CC89BF8F-37D7-4AF1-97EB-33AD062655D5Q31088179-4E248E47-B2C1-4BD1-8C55-6031DB64C453Q33688002-DD987504-A312-43EB-96A2-75639F2A9069Q34366243-81E56600-29C0-4DA8-A80F-28832F814DEDQ34395853-28EFADA2-05DC-4795-8B5D-A121A4AC6047Q34546310-BBBA02DB-E570-4F7A-956B-1FDFA2D46F9EQ35103158-B0937A24-34A6-4086-ABFC-1C5148228E41Q36689911-21AD32D9-F32C-4EB3-9662-2B16071B06AAQ38182501-24986F5E-C93C-4728-98B0-CE3D585DA58FQ38465878-1C3199CD-7F64-4066-BBF0-7A226653B990Q38803465-24804F2E-0AB6-452D-AFC8-48ACB833FB0DQ38940438-9F630D06-CCC8-4CDD-A881-435E227C7704Q39266165-CD6AC0F8-70DE-4408-AB90-45130329DF91Q40138036-2A34738C-4348-4295-B9C4-9563381FFA9AQ40156834-6F0CA5EF-031F-4964-BB6C-78B01BEB1727Q40790358-9D29E199-A4F6-4761-9B50-0C6CA1F53D92Q41108485-1AD564E1-013D-406F-801C-498D52274443Q41558753-3183E060-32EE-4AA2-B004-C57CB47D9CB0Q41808445-D573AED7-22B5-47F2-B8EA-F249E3D017C8Q42919743-6E4BFE9B-DCD1-4EA9-9F77-1058E3EB0EA7Q42998996-39E70F04-532F-44EE-B925-E2EE8A034EEAQ43436192-9225A50F-1689-4216-992D-C7EA57927D90Q44392467-2EC3FE56-3918-4C20-B1EB-24C8DD254217Q45130585-71F6681F-6BF7-4FFE-BF53-75F189DC3202Q45955161-1D676AE4-2147-4AC3-8FD3-6917A77BB9D8Q46841976-63D6A570-A785-407E-8E15-EB36FD30AB03Q48340061-B859937F-6674-46B5-B79F-647552BEEECFQ48376101-F70A90D6-B89A-44F8-B45E-DC4D514E8761Q50231857-EE1DDB76-8A12-456B-99A7-6A980E383C49Q50641393-CA14D996-866C-4C7E-9B84-308400C85DDEQ51596571-3465F597-04E1-4BA7-B79D-5717D86BF44CQ52606140-6DB8EBF7-8A05-474C-8A4A-DC111D3FC84AQ55425878-C958726C-EFE0-4388-8BDB-F49FD5555BAEQ56454120-B869E3E1-5A57-4E00-94A2-C5C253BA5A36Q58866870-C1802E44-BDA0-4CCF-A5BC-CCF15D4FD93FQ59237368-B4F0ED24-6A41-421A-9612-6BA626426274
P2860
Delta-viniferin, a resveratrol dehydrodimer: one of the major stilbenes synthesized by stressed grapevine leaves.
description
2003 nî lūn-bûn
@nan
2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@ast
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@en
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@nl
type
label
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@ast
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@en
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@nl
prefLabel
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@ast
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@en
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@nl
P2093
P356
P1476
Delta-viniferin, a resveratrol ...... by stressed grapevine leaves.
@en
P2093
Camille Perret
Julien Bernard Jean-Denis
Katia Gindro
Olivier Viret
Raffaele Tabacchi
Roger Pezet
P304
P356
10.1021/JF030227O
P407
P577
2003-08-01T00:00:00Z