about
Isosilybin B causes androgen receptor degradation in human prostate carcinoma cells via PI3K-Akt-Mdm2-mediated pathwayIdentification of isosilybin a from milk thistle seeds as an agonist of peroxisome proliferator-activated receptor gammaIdentification of hepatoprotective flavonolignans from silymarinCytotoxic epipolythiodioxopiperazine alkaloids from filamentous fungi of the BionectriaceaeDiscovery of Anticancer Agents of Diverse Natural OriginThe most widely recognized mushroom: chemistry of the genus AmanitaEthanolic Echinacea purpurea Extracts Contain a Mixture of Cytokine-Suppressive and Cytokine-Inducing Compounds, Including Some That Originate from Endophytic BacteriaBiochemometrics for Natural Products Research: Comparison of Data Analysis Approaches and Application to Identification of Bioactive CompoundsSpatial and Temporal Profiling of Griseofulvin Production in Xylaria cubensis Using Mass Spectrometry MappingMapping of Sample Collection Data: GIS Tools for the Natural Product ResearcherFreshwater ascomycetes: Minutisphaera (Dothideomycetes) revisited, including one new species from Japan.Dereplicating and Spatial Mapping of Secondary Metabolites from Fungal Cultures in Situ.Isochromenones, isobenzofuranone, and tetrahydronaphthalenes produced by Paraphoma radicina, a fungus isolated from a freshwater habitat.Greensporones: resorcylic acid lactones from an aquatic Halenospora sp.Minutisphaerales (Dothideomycetes, Ascomycota): a new order of freshwater ascomycetes including a new family, Minutisphaeraceae, and two new species from North Carolina, USA.Differential in vitro effects of intravenous versus oral formulations of silibinin on the HCV life cycle and inflammation.Fungal Planet description sheets: 371-399.Acetophenone derivatives from a freshwater fungal isolate of recently described Lindgomyces madisonensis (G416).Safety assessment of mushrooms in dietary supplements by combining analytical data with in silico toxicology evaluation.Cytotoxic and antimicrobial constituents of the bark of Diospyros maritima collected in two geographical locations in Indonesia.Antioxidant activity and total phenolic content of aqueous and methanolic extracts of Jordanian plants: an ICBG project.Thielavin B methyl ester: a cytotoxic benzoate trimer from an unidentified fungus (MSX 55526) from the Order SordarialesEnhanced dereplication of fungal cultures via use of mass defect filtering.Dereplication of macrocyclic trichothecenes from extracts of filamentous fungi through UV and NMR profiles.Physiologically based pharmacokinetic modeling framework for quantitative prediction of an herb-drug interaction.Two flavonolignans from milk thistle (Silybum marianum) inhibit CYP2C9-mediated warfarin metabolism at clinically achievable concentrationsEpigenetic Manipulation of a Filamentous Fungus by the Proteasome-Inhibitor Bortezomib Induces the Production of an Additional Secondary Metabolite.Comparison of Metabolomics Approaches for Evaluating the Variability of Complex Botanical Preparations: Green Tea (Camellia sinensis) as a Case Study.Polyhydroxyanthraquinones as quorum sensing inhibitors from the guttates of Penicillium restrictum and their analysis by desorption electrospray ionization mass spectrometry.Bioactive constituents of the stem bark of Mitrephora glabra.Biosynthesis of Fluorinated Peptaibols Using a Site-Directed Building Block Incorporation Approach.Resorcylic acid lactones with cytotoxic and NF-κB inhibitory activities and their structure-activity relationshipsFingolimod (FTY720): a recently approved multiple sclerosis drug based on a fungal secondary metabolite.Identification of diet-derived constituents as potent inhibitors of intestinal glucuronidation.Angiopreventive efficacy of pure flavonolignans from milk thistle extract against prostate cancer: targeting VEGF-VEGFR signaling.Labeled content of two furanocoumarins in dietary supplements correlates with neither actual content nor CYP3A inhibitory activityMilk thistle and prostate cancer: differential effects of pure flavonolignans from Silybum marianum on antiproliferative end points in human prostate carcinoma cells.Isolation and identification of intestinal CYP3A inhibitors from cranberry (Vaccinium macrocarpon) using human intestinal microsomes.Influence of dietary substances on intestinal drug metabolism and transport.Dendrimer-encapsulated camptothecins: increased solubility, cellular uptake, and cellular retention affords enhanced anticancer activity in vitro.
P50
Q24309684-63F8155D-B7AF-4A3D-8DD0-E85BE496E948Q24567657-FCEA77DC-D34C-4D59-B429-23FA6547F265Q24600492-AA96D737-5B24-4C3C-9C5C-7953A83F1AE9Q24620027-1C39FF6F-21DD-4BB6-BB91-F36D90EE30B0Q28068341-6B59E077-3026-4E4E-AB1D-11889112CF78Q28275354-DB67B8F5-1BFD-4C7E-935C-44050E0BD0A6Q28546956-92B74494-E623-4005-A4E9-566E2C579F45Q28818007-A46DF1BF-DC77-4CC9-B468-E8E33C7586D6Q28834246-0461765C-B64A-4144-9F59-EB43952E3447Q30491535-159DB0AD-D7DD-47DC-8038-C8B9C2AAF264Q30633177-0BF996D3-F8FF-4D85-A0C9-ADC7A4C8432FQ30664541-CB868179-AA92-4483-A4E2-C9DB1D0DCADCQ30821820-8B92121B-1A2F-4F33-8C42-4355A2495DABQ30840705-703F3010-FC1F-4D79-8BE5-05DEA3A8FF8FQ30990421-15C63CA1-BEA5-431F-856E-0990F04C49D3Q30997889-3718E1F8-B188-49BF-B15C-BF682FC530BFQ31041030-49565F26-76A0-45CD-9C56-318BBB573EAAQ31060182-3779FF89-3825-4AB9-87A3-D7DD13E188BFQ31171627-6CDCD2FD-542E-4061-A3F5-0584E86AC33FQ33205131-BE8229AE-733D-4DAB-A6BD-6FA826B1DB0DQ33298775-19DBC0FB-6BF0-402A-867E-CB4A1BAFB2E5Q33454403-073E8A43-7691-4242-B2C0-F8EA6DBD9051Q33611257-09EEC2DB-C615-4F88-ADB6-3BDF2CB1A6DAQ33637247-CB2C02D4-8BB4-4B7F-ACE2-757FE4725E7FQ33702513-A61D8B95-7304-47E3-9D79-D6801B4C7C87Q33714834-8AE11AC5-F916-41C3-B7F9-59596589A939Q33771618-CB318AE5-478E-4390-A7AF-EA4B3CECC8C0Q33793287-FF769CE9-F440-4FDB-B0C7-994DAC0B5546Q33815668-61C76FB3-D03E-452A-A500-178E4531831AQ33822014-91425051-240E-4EF3-9321-69BFC99EC582Q33836344-DB317B50-9C2E-4B05-BE37-441E75EA5EA1Q33879712-8BFBE3C1-2212-48E1-AA42-484EF8E6B8B6Q34174973-3BAEFB1A-CC90-46C7-8746-F62090D17FE4Q34185989-97B8464B-5305-4F9C-98B8-1BB556F1107DQ34238619-D890D3F1-9E40-45F3-800B-A4257B5E3BABQ34269870-038CC47D-2F15-47C2-8F9C-7881E878CEABQ34419539-71044CC5-BB18-44BF-ADF5-71A38F390557Q34504635-DA63EB64-022F-445E-B7F3-0F78965D445DQ34553835-FB8BAB75-F180-412D-B0FD-B872C9A093D2Q34592802-5DC2BE7C-B12B-4E83-93B1-9EEC42C4F79B
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Nicholas H Oberlies
@nl
Nicholas H Oberlies
@sl
Nicholas H. Oberlies
@en
Nicholas H. Oberlies
@es
type
label
Nicholas H Oberlies
@nl
Nicholas H Oberlies
@sl
Nicholas H. Oberlies
@en
Nicholas H. Oberlies
@es
prefLabel
Nicholas H Oberlies
@nl
Nicholas H Oberlies
@sl
Nicholas H. Oberlies
@en
Nicholas H. Oberlies
@es
P106
P1153
6602133808
P21
P2798
P31
P3835
nicholas-oberlies
P496
0000-0002-0354-8464