about
Inhibition of bacterial mutagenesis by Citrus flavonoidsBiological evaluation of proanthocyanidin dimers and related polyphenolsAdenosine-1 active ligands: cirsimarin, a flavone glycoside from Microtea debilis.Antiviral activity of simalikalactone D, a quassinoid from Quassia africana.Interactions of cryptolepine and neocryptolepine with unusual DNA structures.Effect of Pycnogenol® on attention-deficit hyperactivity disorder (ADHD): study protocol for a randomised controlled trial.Antiplasmodial and other constituents from four Indonesian Garcinia spp.NMR determination of pKa values of indoloquinoline alkaloids.A red yeast rice-olive extract supplement reduces biomarkers of oxidative stress, OxLDL and Lp-PLA2, in subjects with metabolic syndrome: a randomised, double-blind, placebo-controlled trialQuantification of xanthohumol, isoxanthohumol, 8-prenylnaringenin, and 6-prenylnaringenin in hop extracts and derived capsules using secondary standards.Kavalactones, a novel class of protein glycation and lipid peroxidation inhibitors.Treatment with Rhus tripartita extract curtails isoproterenol-elicited cardiotoxicity and oxidative stress in rats.Antiplasmodial Activity, Cytotoxicity and Structure-Activity Relationship Study of Cyclopeptide Alkaloids.Legal requirements for the quality of herbal substances and herbal preparations for the manufacturing of herbal medicinal products in the European union.The value of central-African traditional medicine for lead finding: Some case studies.Triterpenoid Saponins from Maesa argentea Leaves.In vitro antiprotozoal activity and cytotoxicity of extracts and isolated constituents from Greenwayodendron suaveolens.In vitro and in vivo investigations on the antitumour activity of Chelidonium majus.Antimicrobial activity of some Clerodendrum species from Egypt.Isolation and Structure Elucidation of Glucosylated Colchicinoids from the Seeds of Gloriosa superba by LC-DAD-SPE-NMR.Schistosomicidal and molluscicidal activities of aminoalkylamino substituted neo- and norneocryptolepine derivatives.In vitro and in vivo antimalarial activity and cytotoxicity of extracts and fractions from the leaves, root-bark and stem-bark of Triclisia gilletii.Antiprotozoal screening and cytotoxicity of extracts and fractions from the leaves, stem bark and root bark of Alstonia congensis.Ethnobotanical survey and antibacterial activity of some plants used in Guinean traditional medicine.In vitro antiprotozoal and cytotoxic activity of 33 ethonopharmacologically selected medicinal plants from Democratic Republic of Congo.The use of chemometrics to study multifunctional indole alkaloids from Psychotria nemorosa (Palicourea comb. nov.). Part II: Indication of peaks related to the inhibition of butyrylcholinesterase and monoamine oxidase-A.Antioxidant and Antiglycating Constituents from Leaves of Ziziphus oxyphylla and Cedrela serrata.Chemical and biological investigation of some Clerodendrum species cultivated in Egypt.Antimalarial efficacy of a quantified extract of Nauclea pobeguinii stem bark in human adult volunteers with diagnosed uncomplicated falciparum malaria. Part 1: a clinical phase IIA trial.Phytochemical and Pharmacological Investigations on Nymphoides indica Leaf Extracts.Phytochemical and biological investigations of Elaeodendron schlechteranum.Screening of Tanzanian medicinal plants against Plasmodium falciparum and human immunodeficiency virus.Selective antileishmania activity of 13,28-epoxy-oleanane and related triterpene saponins from the plant families Myrsinaceae, Primulaceae, Aceraceae and Icacinaceae.Ethnomedical and ethnobotanical investigations on the response capacities of Guinean traditional health practioners in the management of outbreaks of infectious diseases: The case of the Ebola virus epidemic.Antiprotozoal and cytotoxic screening of 45 plant extracts from Democratic Republic of Congo.Antitrypanosomal activity of triterpenoids and sterols from the leaves of Strychnos spinosa and related compounds.The malaria co-infection challenge: An investigation into the antimicrobial activity of selected Guinean medicinal plants.In vitro antiprotozoal and cytotoxic activity of ethnopharmacologically selected guinean plants.Bioguided isolation of pharmacologically active plant components, still a valuable strategy for the finding of new lead compounds?Antileishmanial activity, cytotoxicity and QSAR analysis of synthetic dihydrobenzofuran lignans and related benzofurans.
P50
Q28283692-5B367CFD-FB41-4F34-9D2B-36FAEED2E26DQ28369768-5DED3B3F-2064-430A-A149-8AD7201455AFQ29354117-434946A9-964F-4CB1-A7B2-77C87DA36F17Q30673314-F4ADA268-C489-4E05-969A-194368332084Q30776140-32360D0B-3A68-4FA5-99CD-99A065C852F0Q30843197-7E8744BD-8F45-4C05-92E3-F2B23F47F914Q33456384-49859DEF-E413-4230-97B7-E20B1269F397Q33490188-E9E197B9-560E-4B2C-BF15-F08496D9FE8FQ33868751-BD68CB30-9FE7-404E-9AA5-024DC6747BD0Q34152010-35EFE429-6ABB-445D-9FB1-F6D0AE131477Q34663811-B802CDEF-0E02-4F94-9EF3-410F3AC4AA53Q36127291-FC02A26A-0FB2-4648-89C3-28A7DC488407Q36269003-0BE64EBA-308C-4895-99F6-B752FB2C85A1Q37389084-6997FBF7-9ECC-43EC-BDBF-CDD245A6449CQ38529124-C29B31FB-565B-403A-8C2A-981CD29A7249Q38741318-4F8957EF-6E1B-4AF4-827C-A92094AB6887Q38742903-053596F0-FF96-4286-9C7C-D23DD25D6544Q38815237-9B35E1C4-185E-4504-84FD-EE43B6DFBCACQ38858089-729957A6-E216-41AC-8CBD-FA76E6C74F2DQ38955477-521C17D7-C423-47D9-A1C6-82D7BA3FC464Q38984212-3BEE7D05-72CF-44A7-A763-FF412B4BB57DQ39121983-1CB64A75-90B4-4A2A-9060-EF30ABFFF8EAQ39161741-6A5B9A6E-9CC6-49C6-A3FE-5E857525DA05Q39202874-7C9FE22E-2E88-4C15-BB5B-CA798C93D0F9Q39384431-5BF603FA-47ED-4D9C-8037-B75477F37614Q39501891-FF79CED4-A152-4DCF-8F07-174659C16377Q39536150-EABBB67D-D287-4237-B94A-547348CDB20BQ39567963-54E7407C-F720-41CE-AA77-2F53256BE906Q39685697-09BA41B6-6A76-49D9-ACF3-7810693245EBQ39695630-6A0E9F2D-443D-4B41-9063-9B0E9E06C147Q39718395-190D9304-11F5-4648-BCF5-7B5FA7831C61Q39817085-03F84B0F-905B-4F0D-B638-8F849FBA0CB7Q39874991-07C2D8A6-083B-4614-BDBF-15561702D4C0Q39980091-A87B4F91-021E-498F-9CFF-ABF49AE06A15Q40037536-806C6F49-00EC-472D-8A56-B0ABE5A75F0AQ40106023-6EE40798-89D5-4ED1-ABCC-204C3A9C5D7FQ40165117-C65548CE-E87F-446B-93C1-D88CFC1D56A2Q40193470-ADAE5FD2-A83E-42AE-BFED-753E1A8EA462Q40408244-A8A17FA0-161C-48F5-8BFC-A2838EBDC176Q40470382-936603D2-2100-4A42-AAE5-3CBCA1D5F88B
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Luc Pieters
@ast
Luc Pieters
@en
Luc Pieters
@es
Luc Pieters
@sl
type
label
Luc Pieters
@ast
Luc Pieters
@en
Luc Pieters
@es
Luc Pieters
@sl
prefLabel
Luc Pieters
@ast
Luc Pieters
@en
Luc Pieters
@es
Luc Pieters
@sl
P1053
P-5820-2016
P106
P21
P2798
P31
P3829
P496
0000-0002-8288-4254