about
sameAs
The UBIAD1 prenyltransferase links menaquinone-4 [corrected] synthesis to cholesterol metabolic enzymesHydrogen peroxide - production, fate and role in redox signaling of tumor cellsOne pot synthesis of selenocysteine containing peptoid libraries by Ugi multicomponent reactions in water11th German Conference on Chemoinformatics (GCC 2015) : Fulda, Germany. 8-10 November 2015.UBIAD1 mutation alters a mitochondrial prenyltransferase to cause Schnyder corneal dystrophyBiosynthesis and Metabolism of Cyclopropane Rings in Natural CompoundsPhytochemical Profiles and Antimicrobial Activities of Allium cepa Red cv. and A. sativum Subjected to Different Drying Methods: A Comparative MS-Based Metabolomics.Altered protein expression pattern in colon tissue of mice upon supplementation with distinct selenium compounds.Metabolomics reveals biotic and abiotic elicitor effects on the soft coral Sarcophyton ehrenbergi terpenoid content.Methionine and seleno-methionine type peptide and peptoid building blocks synthesized by five-component five-center reactions.No Silver Bullet - Canonical Poly(ADP-Ribose) Polymerases (PARPs) Are No Universal Factors of Abiotic and Biotic Stress Resistance of Arabidopsis thaliana.Rats' urinary metabolomes reveal the potential roles of functional foods and exercise in obesity management.Osmotic stress is accompanied by protein glycation in Arabidopsis thalianaNatural Products from Microalgae with Potential against Alzheimer's Disease: Sulfolipids Are Potent Glutaminyl Cyclase Inhibitors.Passerini Reactions on Biocatalytically Derived Chiral Azetidines.Individual effects of different selenocompounds on the hepatic proteome and energy metabolism of mice.Solution- and Solid-Phase Macrocyclization of Peptides by the Ugi-Smiles Multicomponent Reaction: Synthesis of N-Aryl-Bridged Cyclic Lipopeptides.Combinatorial synthesis, in silico, molecular and biochemical studies of tetrazole-derived organic selenides with increased selectivity against hepatocellular carcinoma.Chilenopeptins A and B, Peptaibols from the Chilean Sepedonium aff. chalcipori KSH 883.Tricyclic Acylphloroglucinols from Hypericum lanceolatum and Regioselective Synthesis of Selancins A and B.Soft Corals Biodiversity in the Egyptian Red Sea: A Comparative MS and NMR Metabolomics Approach of Wild and Aquarium Grown Species.Comparative metabolite profiling and fingerprinting of genus Passiflora leaves using a multiplex approach of UPLC-MS and NMR analyzed by chemometric tools.Prenylated phenyl polyketides and acylphloroglucinols from Hypericum peplidifolium.Ericoside, a new antibacterial biflavonoid from Erica mannii (Ericaceae).A Snapshot of the Plant Glycated Proteome: STRUCTURAL, FUNCTIONAL, AND MECHANISTIC ASPECTS.Versatile antitumor potential of isoxanthohumol: Enhancement of paclitaxel activity in vivo.Metabolite profiling in 18 Saudi date palm fruit cultivars and their antioxidant potential via UPLC-qTOF-MS and multivariate data analyses.Structure and Absolute Configuration of Pseudohygrophorones A(12) and B(12), Alkyl Cyclohexenone Derivatives from Hygrophorus abieticola (Basidiomycetes).Arabidopsis thaliana isoprenyl diphosphate synthases produce the C25 intermediate geranylfarnesyl diphosphate.Phytochemical, antioxidant and antidiabetic evaluation of eight Bauhinia L. species from Egypt using UHPLC-PDA-qTOF-MS and chemometrics.Isolation and anticancer, anthelminthic, and antiviral (HIV) activity of acylphloroglucinols, and regioselective synthesis of empetrifranzinans from Hypericum roeperianum.A study on the biosynthesis of hygrophorone B(12) in the mushroom Hygrophorus abieticola reveals an unexpected labelling pattern in the cyclopentenone moiety.Unraveling the active hypoglycemic agent trigonelline in Balanites aegyptiaca date fruit using metabolite fingerprinting by NMR.Diacetin, a reliable cue and private communication channel in a specialized pollination systemA fluorescence-based bioassay for antibacterials and its application in screening natural product extracts.Protease-inhibiting, molecular modeling and antimicrobial activities of extracts and constituents from Helichrysum foetidum and Helichrysum mechowianum (compositae)Organoselenocyanates and symmetrical diselenides redox modulators: Design, synthesis and biological evaluation.Unequivocal glycyrrhizin isomer determination and comparative in vitro bioactivities of root extracts in four Glycyrrhiza speciesSynthesis of antibacterial 1,3-diyne-linked peptoids from an Ugi-4CR/Glaser coupling approachScreening of synthetic and natural product databases: Identification of novel androgens and antiandrogens.
P50
Q24304189-0AFB91A4-EAD4-4F2C-BCDE-7D24966F54C1Q26787065-06233481-BAFF-4E5D-852C-A510A60C643DQ28194628-36FEF369-E64D-46D1-888D-E42AF5D5A899Q28550032-F71BD6C3-F330-42AA-8161-AACCA6BA39A9Q28752010-497B9961-47F3-499E-8AEF-77602167EC5CQ29397941-F0FA98AD-4A6F-4825-BF75-C0735C81930DQ30313196-467986BB-A19B-4917-9161-2CE525F5542FQ30313250-09C75D5F-B4DA-414E-875F-4F160F93A5CCQ30313274-5FF21408-A94D-41DB-9928-EADB11A2AC73Q30313327-1E7B124F-1B80-4BD8-B7E3-CB3271B70AEDQ30313407-30B0C430-AE52-4FE2-B78F-6953B97EE3CFQ30313428-92745367-8BE0-4A50-AD5E-55FE588386BEQ30313686-A4390973-97C1-4DB6-B33F-79EC417FB113Q30313757-8BDC65D5-33AD-4FAB-AA9E-19320F30EA00Q30313891-560AC507-215C-40B7-879C-203814B49A06Q30313914-B9CAEEA7-0BAC-4981-91C0-FC087A2BAB79Q30313943-F4EE9FE1-0FBF-4731-BE10-ECECD5067FD1Q30314276-83137262-7B9B-42F8-B56A-9088DD989DBBQ30315486-0DFA0517-24CD-444F-B93A-A9D8B4FC1522Q30315493-3A7CC5A4-6232-4B6A-B004-770C9673A800Q30315551-F3EEB8A1-9465-4F33-AAF5-FC5F1C1BE36CQ30315558-5399368D-7E80-44C7-BD39-46FAADA9F100Q30315562-448ADC1B-A17D-45AC-9F6A-F64571527679Q30315693-F89B2535-D5EF-4DC4-AECB-5CEDB3857775Q30315721-20671596-037B-41E7-99A6-25E6F20FDC59Q30315742-B95AD7D3-914F-401F-9543-E2F1F6567EF2Q30315763-A17E51A8-F70B-498D-97E7-1338607BD872Q30315843-E1971BED-2B44-4BF9-8CB6-0AFAF3F31D4BQ30316006-9CE1B1BF-3179-4765-953C-0D87BEA8BDBEQ30316099-AB72A940-0437-4093-BDD5-3B8CA15EA169Q30316185-363CCA97-50A3-48B6-966A-E904677640F1Q30316208-4F9C985E-6495-461C-96B8-E7F4C7C5A25CQ30316274-9AAC40ED-1356-49AB-869D-E71C4ED27F76Q30316300-70961BAC-1993-4430-AB51-6624CD8FB4D5Q30316401-95CACC05-3540-415E-9722-9B22AE3CEDC3Q30316483-9F15C671-6518-4E39-B701-8C51D44D033DQ30316562-38E9F252-756A-4E69-84D7-5389EDFF0EB5Q30316767-D0029463-C476-4067-974F-78765BF6288DQ30316783-B405B378-C922-4E1A-BC2B-850524215DB6Q30316929-55CE7E19-1F0A-4921-9923-254F118DB52C
P50
description
researcher ORCID ID = 0000-0003-2060-8235
@en
wetenschapper
@nl
name
Ludger A Wessjohann
@ast
Ludger A Wessjohann
@en
Ludger A Wessjohann
@nl
type
label
Ludger A Wessjohann
@ast
Ludger A Wessjohann
@en
Ludger A Wessjohann
@nl
altLabel
Ludger Wessjohann
@en
prefLabel
Ludger A Wessjohann
@ast
Ludger A Wessjohann
@en
Ludger A Wessjohann
@nl
P31
P496
0000-0003-2060-8235