about
Threshold response of stomatal closing ability to leaf abscisic acid concentration during growth.Nutritional composition of minor indigenous fruits: cheapest nutritional source for the rural people of Bangladesh.Foliar abscisic acid content underlies genotypic variation in stomatal responsiveness after growth at high relative air humidity.Benzoxazinoids: Cereal phytochemicals with putative therapeutic and health-protecting properties.Quantification of neonicotinoid insecticide residues in soils from cocoa plantations using a QuEChERS extraction procedure and LC-MS/MS.Benzoxazinoids in Prostate Cancer Patients after a Rye-Intensive Diet: Methods and Initial Results.Comparison of the levels of bioactive benzoxazinoids in different wheat and rye fractions and the transformation of these compounds in homemade foods.Plasma and urine concentrations of bioactive dietary benzoxazinoids and their glucuronidated conjugates in rats fed a rye bread-based diet.Chemical ecology in wheat plant-pest interactions. how the use of modern techniques and a multidisciplinary approach can throw new light on a well-known phenomenon: allelopathy.Quantitative analysis of absorption, metabolism, and excretion of benzoxazinoids in humans after the consumption of high- and low-benzoxazinoid diets with similar contents of cereal dietary fibres: a crossover study.Identification and Quantification of Loline-Type Alkaloids in Endophyte-Infected Grasses by LC-MS/MS.Correlation of Deoxynivalenol Accumulation in Fusarium-Infected Winter and Spring Wheat Cultivars with Secondary Metabolites at Different Growth Stages.Dietary exposure to benzoxazinoids enhances bacteria-induced monokine responses by peripheral blood mononuclear cells.Synthesis and quantitation of six phenolic amides in Amaranthus spp.Fate and availability of glyphosate and AMPA in agricultural soil.Leaching of pesticides through normal-tillage and low-tillage soil--a lysimeter study. I. Isoproturon.Leaching of pesticides through normal-tillage and low-tillage soil--a lysimeter study. II. Glyphosate.First European interlaboratory study of the analysis of benzoxazinone derivatives in plants by liquid chromatography.Bioactive benzoxazinoids in rye bread are absorbed and metabolized in pigs.Transformation products of 2-benzoxazolinone (BOA) in soil.Biotransformation of 2-benzoxazolinone to 2-amino-(3H)-phenoxazin-3-one and 2-acetylamino-(3H)-phenoxazin-3-one in soil.Variation of polyphenols and betaines in aerial parts of young, field-grown Amaranthus genotypes.Transformation kinetics of 6-methoxybenzoxazolin-2-one in soil.Fate of benzoxazinone allelochemicals in soil after incorporation of wheat and rye sprouts.Elucidating the transformation pattern of the cereal allelochemical 6-methoxy-2-benzoxazolinone (MBOA) and the trideuteriomethoxy analogue [D3]-MBOA in soil.Transformation of benzoxazinones and derivatives and microbial activity in the test environment of soil ecotoxicological tests on Poecilus cupreus and Folsomia candida.Biosynthesis and chemical transformation of benzoxazinoids in rye during seed germination and the identification of a rye Bx6-like gene.2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one (DIMBOA) inhibits trichothecene production by Fusarium graminearum through suppression of Tri6 expression.Alterations of the Benzoxazinoid Profiles of Uninjured Maize Seedlings During Freezing, Storage, and Lyophilization.Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of azoxystrobin and its metabolites, azoxystrobin free acid and 2-hydroxybenzonitrile, in greenhouse-grown lettuce.Maize root culture as a model system for studying azoxystrobin biotransformation in plants.Corrigendum to "Biosynthesis and chemical transformation of benzoxazinoids in rye during seed germination and the identification of a rye Bx6-like gene" [Phytochemistry 140 (2017) 95-107].Amaranth (Amaranthus hypochondriacus) as an alternative crop for sustainable food production: Phenolic acids and flavonoids with potential impact on its nutraceutical qualityBenzoxazinoid concentrations show correlation with Fusarium Head Blight resistance in Danish wheat varietiesPhenolic Acids from Wheat Show Different Absorption Profiles in Plasma: A Model Experiment with Catheterized PigsAbsorption and metabolic fate of bioactive dietary benzoxazinoids in humansPhytotoxic Effect, Uptake, and Transformation of Biochanin A in Selected Weed SpeciesMaize synthesized benzoxazinoids affect the host associated microbiomeSorption and degradation of neonicotinoid insecticides in tropical soilsIdentification of Azoxystrobin Glutathione Conjugate Metabolites in Maize Roots by LC-MS
P50
Q33957524-EB5C7683-B3B0-4532-946C-E19F6E51BE79Q34677971-7CC3DAE4-A33A-49CB-BC31-F967DF4A0E87Q37337467-88B866F2-2095-4618-91A6-97250407D65BQ38323876-E34E4290-8054-4051-B94E-F7B205C2FFC8Q38961516-FE0EAF63-F89D-4050-9219-54986B644067Q39309875-C2923D8A-363D-4D3A-9553-F88D1FCA0A57Q39402169-3CB585BB-A70A-427A-BCDE-67E0EFE51A0CQ39527752-D588FBC1-B750-40EF-9201-B3C08A237406Q40350865-3CDDA9E9-70BD-4632-A663-22D77DC9958BQ40373038-5B63C668-69EE-4C1B-91CD-33FCAC005841Q40607921-63C2B330-0805-4FBC-BEB1-424867BF8B99Q40668142-AF8053FB-35CD-4A79-8014-7AE220442588Q41062760-5EFF78C5-14D7-4A0F-B6CE-48FF1C5553F8Q43076271-7EB06FA3-1BA4-4E14-A504-DC92135A4704Q43431606-92EBB0E7-9FEB-4F6D-8496-4768490667A8Q44325776-8C0B4256-5089-4A5D-B081-00761A17A6BAQ44325779-39A8B96C-7AE6-43B0-99D5-189961FB35C2Q45104506-31D48C83-E434-426A-899B-7D5813A4A348Q45416497-6C49506D-2090-40E7-97A0-559E60C8C5FDQ46474426-0E3134A6-5052-494E-B329-5ED661801445Q46670875-65E5C3F5-1765-4A38-A97E-6C332D0E70F2Q46724407-14A018DB-A534-47F6-A114-F594C8D39C62Q46831511-BB8AADCC-000F-444D-8B07-42FBCDF19611Q46944413-55CA0BAE-3B51-4A09-9A92-657724367785Q46944416-772F1282-9A1B-434D-8520-0EA069A4FDDCQ46944420-C0D02441-AC41-4067-97DD-17A81F00D12FQ47830645-9F52BB3E-B21D-40D5-A8F2-8EBAE06A2AF5Q47914000-4335D644-81D4-4E6E-92BA-EB26321B1C78Q48214378-A0ED10F4-709E-4149-87B1-7B750A53A68BQ48315341-841B8D06-8FA2-4300-8865-A338014A6DCCQ49491812-B70F71C1-6270-4E3E-9FF2-19882431EC53Q50084597-57B509E8-B23F-4B73-8762-D7AE77121ABFQ56873349-614A49FD-6715-4284-B289-0C732C692A48Q59462563-42D9004D-B99A-411A-B7F0-5110A6DF6789Q61530911-48B4ED89-0D8B-427E-B096-BC076DF49DF3Q61919171-02AA80DA-4A6E-4EE4-9DCA-17945085B925Q61919180-7C32A81A-E554-4A79-8CAE-93E9F3F61908Q64056196-97F0315C-840C-4952-9DA4-EAE9F29E3251Q88771674-C39B9D90-26CF-44E0-BDA0-E7AD5FF09259Q91714342-9F9DFC40-4CAF-42CD-85A4-425C968AC58E
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Inge S Fomsgaard
@nl
Inge S Fomsgaard
@sl
Inge S. Fomsgaard
@en
Inge S. Fomsgaard
@es
type
label
Inge S Fomsgaard
@nl
Inge S Fomsgaard
@sl
Inge S. Fomsgaard
@en
Inge S. Fomsgaard
@es
prefLabel
Inge S Fomsgaard
@nl
Inge S Fomsgaard
@sl
Inge S. Fomsgaard
@en
Inge S. Fomsgaard
@es
P1053
A-1053-2015
P106
P1153
6602072404
P31
P3829
P496
0000-0003-4987-8511