about
Qualitative and quantitative study of the highly specialized lipid tissues of cetaceans using HR-MAS NMR and classical GC.In vivo characterization of the first acyl-CoA Delta6-desaturase from a member of the plant kingdom, the microalga Ostreococcus tauriFast screening of highly glycosylated plant sphingolipids by tandem mass spectrometry.The bifunctional protein TtFARAT from Tetrahymena thermophila catalyzes the formation of both precursors required to initiate ether lipid biosynthesis.Soil water stress affects both cuticular wax content and cuticle-related gene expression in young saplings of maritime pine (Pinus pinaster Ait)The very-long-chain hydroxy fatty acyl-CoA dehydratase PASTICCINO2 is essential and limiting for plant development.Metabolic engineering of fatty acids for breeding of new oilseed crops: strategies, problems and first results.An ethoxylated surfactant enhances the penetration of the sulfated laminarin through leaf cuticle and stomata, leading to increased induced resistance against grapevine downy mildew.Relief for fish stocks: oceanic fatty acids in transgenic oilseeds.Plant fatty acyl reductases: enzymes generating fatty alcohols for protective layers with potential for industrial applications.Suberin: biosynthesis, regulation, and polymer assembly of a protective extracellular barrier.Plant Surface Lipids and Epidermis Development.Wax esters of different compositions produced via engineering of leaf chloroplast metabolism in Nicotiana benthamiana.Novel fatty acid elongases and their use for the reconstitution of docosahexaenoic acid biosynthesis.Primary Fatty Alcohols Are Major Components of Suberized Root Tissues of Arabidopsis in the Form of Alkyl Hydroxycinnamates.Three Arabidopsis fatty acyl-coenzyme A reductases, FAR1, FAR4, and FAR5, generate primary fatty alcohols associated with suberin deposition.New insight into Phaeodactylum tricornutum fatty acid metabolism. Cloning and functional characterization of plastidial and microsomal delta12-fatty acid desaturases.Overexpression of the epidermis-specific homeodomain-leucine zipper IV transcription factor Outer Cell Layer1 in maize identifies target genes involved in lipid metabolism and cuticle biosynthesis.Identification of amino acids conferring chain length substrate specificities on fatty alcohol-forming reductases FAR5 and FAR8 from Arabidopsis thaliana.Acyl carriers used as substrates by the desaturases and elongases involved in very long-chain polyunsaturated fatty acids biosynthesis reconstituted in yeast.Biosynthesis of very-long-chain polyunsaturated fatty acids in transgenic oilseeds: constraints on their accumulation.Intracellular Distribution of Manganese by the Trans-Golgi Network Transporter NRAMP2 is Critical for Photosynthesis and Cellular Redox Homeostasis.The Arabidopsis cer26 mutant, like the cer2 mutant, is specifically affected in the very long chain fatty acid elongation process.Acyl-lipid thioesterase1-4 from Arabidopsis thaliana form a novel family of fatty acyl-acyl carrier protein thioesterases with divergent expression patterns and substrate specificities.The Glycerol-3-Phosphate Acyltransferase GPAT6 from Tomato Plays a Central Role in Fruit Cutin Biosynthesis.Production of polyunsaturated fatty acids by polyketide synthases in both prokaryotes and eukaryotes.Suberin-associated fatty alcohols in Arabidopsis: distributions in roots and contributions to seed coat barrier properties.Analyses of tomato fruit brightness mutants uncover both cutin-deficient and cutin-abundant mutants and a new hypomorphic allele of GDSL lipase.The VLCFA elongase gene family in Arabidopsis thaliana: phylogenetic analysis, 3D modelling and expression profiling.Biochemical characterization of a chloroplast localized fatty acid reductase from Arabidopsis thalianaReconstitution of plant alkane biosynthesis in yeast demonstrates that Arabidopsis ECERIFERUM1 and ECERIFERUM3 are core components of a very-long-chain alkane synthesis complexOverexpression of Arabidopsis ECERIFERUM1 promotes wax very-long-chain alkane biosynthesis and influences plant response to biotic and abiotic stressesA MYB transcription factor regulates very-long-chain fatty acid biosynthesis for activation of the hypersensitive cell death response in ArabidopsisA stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in ArabidopsisBiochemical characterization of 3-ketoacyl-acyl carrier protein synthase II from leek epidermisAntifungal compounds from idioblast cells isolated from avocado fruitsEvidence that oleoyl-CoA and ATP-dependent elongations coexist in rapeseed (Brassica napus L.).Rapid nanoscale quantitative analysis of plant sphingolipid long-chain bases by GC-MSECERIFERUM2-LIKE proteins have unique biochemical and physiological functions in very-long-chain fatty acid elongationCharacterization and heterologous expression of three DGATs from oil palm (Elaeis guineensis) mesocarp in Saccharomyces cerevisiae
P50
Q33874109-A18AF7CD-1117-484F-921B-8F029F3A39C8Q33985785-55C58D00-1D10-4872-9614-0FAD10D4F5ABQ34033441-81885865-210A-427E-83E2-FA8612845870Q34070361-50A7B97E-ADD4-4926-BA7D-E76837FA65A0Q34788246-D63FBFAB-DC84-415B-9B64-BB0F3F56E88EQ34830246-DB87DEC2-6633-4918-9750-6F013F8E917AQ35206554-BD8CC9D7-C30D-4103-B827-5D10C3F85AD0Q35802920-34B7B5A1-7704-413B-9FF3-A754245D85C3Q36062814-8223F60C-9DA7-464F-BDEF-A2580BD6531DQ38026213-58873851-ADD7-4E11-BC06-61D7D2879F1FQ38287585-EE762854-CA05-4FB4-B0A3-B5B9A7168A97Q38792254-A97033D8-4A62-4780-92C0-F355F4A2964CQ39157814-C4F07A94-1E39-4E3A-8C48-9736DBF1B59FQ40491604-FB4A0241-E492-4712-91DB-8D70FF6122BBQ40657281-23FFB874-B205-4AB1-99F7-B58E591F3A71Q42473305-3CC59084-2614-48F5-AF74-E6106F3E0068Q42597083-28D2775C-8260-44D9-95CD-60AB437D1027Q42666862-DFFC1245-3601-45E8-8B1A-78CD7F706983Q42946472-B1737301-7B17-4783-8304-6C4B8C5FCD55Q44497605-2B593760-AB74-4768-A0CA-B74BBBC61FBEQ45065724-5E21287A-499B-4EC6-BC3B-5E026F891C02Q46253267-C2198F15-F67E-45B0-BCF8-202BF8A95D75Q46506767-9B6170F8-A570-4792-82FB-6276D2658D04Q46973318-5E6DB898-B967-4740-94BC-FC889D55A479Q48226678-02584FE6-3E22-41F4-A035-CB9ECFF1085AQ49165921-EEE08EC0-F77E-4D2C-8C56-870FECC689AFQ54244210-C8596585-CDEC-4668-A5B6-CE62DCFB3DD9Q54414120-259C801D-FEC5-495F-8C12-6AEA96EBD9D2Q54533789-D71E9D7E-6B85-47CC-865B-CAD15101D163Q56031083-C03A8440-8170-431D-9B6A-6AD2D2FD9EC6Q57246485-BC50F6A8-F8F6-431B-AE01-83230ED168CEQ57246486-F09C8573-E322-4DA7-946D-8B988C6AD8C9Q63975750-868CA900-5605-45FE-81B0-CCAD3AE3FB07Q64103512-3E367116-9BA1-4820-9974-C52BEB0EAA0DQ73424787-7904F97A-A436-4544-9692-CCF2FED43B42Q73935564-1F4992BA-EB83-4809-99C7-748937A1AA4CQ78003343-9B56E237-36D7-421A-8E83-0B5A2922118FQ84108267-254010CD-D011-4496-BEA2-01AE1AAFF5BDQ86548632-315E5E5B-0764-46E5-AD6E-FC50F0FECA82Q90179697-7F8666EE-E01D-4330-A1BB-4F12E105BE91
P50
description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Frédéric Domergue
@ast
Frédéric Domergue
@en
Frédéric Domergue
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Frédéric Domergue
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Frédéric Domergue
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type
label
Frédéric Domergue
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Frédéric Domergue
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Frédéric Domergue
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Frédéric Domergue
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Frédéric Domergue
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FredDo
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prefLabel
Frédéric Domergue
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Frédéric Domergue
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Frédéric Domergue
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Frédéric Domergue
@nl
Frédéric Domergue
@sl
P106
P1153
55892860400
P21
P31
P496
0000-0002-0183-7000