sameAs
Internally quenched fluorescent peptide substrates disclose the subsite preferences of human caspases 1, 3, 6, 7 and 8Recent advances in covalent, site-specific protein immobilizationA comparative study of the physicochemical properties of iron isomaltoside 1000 (Monofer), a new intravenous iron preparation and its clinical implicationsSolid-phase glycosylation of peptide templates and on-bead MAS-NMR analysis: perspectives for glycopeptide libraries.Combinatorial library of peptide isosters based on Diels-Alder reactions: identification of novel inhibitors against a recombinant cysteine protease from Leishmania mexicana.'One bead two compound libraries' for detecting chemical and biochemical conversions.Solid-phase library synthesis, screening, and selection of tight-binding reduced peptide bond inhibitors of a recombinant Leishmania mexicana cysteine protease B.Fluorescence-quenched solid phase combinatorial libraries in the characterization of cysteine protease substrate specificity.Glycopeptide and Oligosaccharide Libraries.The substrate specificity of a recombinant cysteine protease from Leishmania mexicana: application of a combinatorial peptide library approach.The Pictet-Spengler reaction in solid-phase combinatorial chemistry.Glycopeptides as oligosaccharide mimics: high affinity sialopeptide ligands for sialoadhesin from combinatorial libraries.MUC1-derived glycopeptide libraries with improved MHC anchors are strong antigens and prime mouse T cells for proliferative responses to lysates of human breast cancer tissue.Efficient solid-phase synthesis of peptide-based phosphine ligands: towards combinatorial libraries of selective transition metal catalysts.Synthesis of aldehyde building blocks protected as acid labile N-Boc N,O-acetals: toward combinatorial solid phase synthesis of novel peptide isosteres.N-Terminal peptide aldehydes as electrophiles in combinatorial solid phase synthesis of novel peptide isosteres.The extracellular polysaccharide of Pichia (Hansenula) holstii NRRL Y-2448: the phosphorylated side chains.Synthetic methods of glycopeptide assembly, and biological analysis of glycopeptide products.Inhibition of cruzipain visualized in a fluorescence quenched solid-phase inhibitor library assay. D-amino acid inhibitors for cruzipain, cathepsin B and cathepsin L.The one-bead two-compound assay for solid phase screening of combinatorial libraries.Solid-phase combinatorial library of norstatine-type isosters by the nitroaldol reaction.Combinatorial library of peptidotriazoles: identification of [1,2,3]-triazole inhibitors against a recombinant Leishmania mexicana cysteine protease.Solid-phase synthesis of pyrroloisoquinolines via the intramolecular N-acyliminium Pictet-Spengler reaction.Solid-phase synthesis of a peptide-based P,S-ligand system designed for generation of combinatorial catalyst libraries.Controlled peptide solvation in portion-mixing libraries of FRET peptides: improved specificity determination for Dengue 2 virus NS2B-NS3 protease and human cathepsin S.Expression and substrate specificity of a recombinant cysteine proteinase B of Leishmania braziliensis.Small-molecule affinity ligands for protein purification: combined computational enrichment and automated in-line screening of an optically encoded library.Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides.Processing of glycans on glycoprotein and glycopeptide antigens in antigen-presenting cellsSubstrate preferences of glutamic-acid-specific endopeptidases assessed by synthetic peptide substrates based on intramolecular fluorescence quenching.Cu-catalyzed azide-alkyne cycloadditionIn vivo imaging of matrix metalloproteinase 12 and matrix metalloproteinase 13 activities in the mouse model of collagen-induced arthritis.Substrate Specificity Profiling of Peptidyl-Lys Metallopeptidase of Armillaria mellea by FRET Based Peptide Library.Specific Electrostatic Molecular Recognition in Water.Susceptibility of glycans to beta-elimination in Fmoc-based O-glycopeptide synthesis.Glycopeptide mimics of mammalian Man9GlcNAc2. Ligand binding to mannan-binding proteins (MBPs).Characterization of the substrate specificity of the major cysteine protease (cruzipain) from Trypanosoma cruzi using a portion-mixing combinatorial library and fluorogenic peptides.Synthesis, characterization and biocompatibility of PEGA resins.Multiple column synthesis of a library of T-cell stimulating Tn-antigenic glycopeptide analogues for the molecular characterization of T-cell-glycan specificity.Solid-phase synthesis of complex and pharmacologically interesting heterocycles.
P50
Q24532133-9BA15784-754A-48FA-9D73-C8C2044FEF0BQ28067254-E39DF937-117F-46E5-A5AA-62BEEF42D851Q28307966-591D9BDF-8CE1-4345-B33E-03AF326054A3Q30710488-F6A905FD-DC4A-4716-AA12-0054A40AA4C0Q30713686-7EF7ACBA-4B86-45C5-A7D6-C406F88C460BQ30832292-FE9AA2DD-9E6A-42CF-B78F-520C9ED582D8Q30835088-4B735D79-0F4F-4294-8129-86A7C3795706Q30854464-F8C08976-FA18-47EF-8C48-21948F84086DQ30858335-041F899D-F4FC-42C7-B230-E618E3FB922FQ31037396-61EF57F7-AF7D-4B65-87BB-0D665067818BQ31040130-1E5250D5-0C35-45A8-8592-27F15B4903E7Q31125606-D5A9824B-1186-4313-A233-8931DC12EE53Q31144055-BA10577E-EFB7-4C10-9840-81DE86102138Q31165361-E3AF40B0-D470-4714-85EF-8EFEEF555054Q31810454-C33C83A5-33CA-46EA-B01A-0EF0861C966AQ31810461-A83197CD-8EFE-435A-ADAB-D171010BCE89Q32031907-7BDF1F5F-A0A4-44FD-99EE-B8EFACE0744CQ32052996-B6197A08-4FF1-4C5D-9AAB-1101B730BAAAQ32061568-42CC1969-3BE1-4261-99A4-FA25779C6133Q33184660-26703616-4DB7-4942-B89E-F37CEBC43380Q33186307-732AB988-1214-472F-BE99-AC00908885E2Q33202737-08A26411-AC06-47AC-A21A-E63EAA40F490Q33218514-4D25EBB1-6BC0-4E69-AC22-6C17113372DCQ33268395-995B8FE4-6125-48F8-A2BF-AF8866EF8F19Q33287393-DFFD1728-12DA-408B-8EE1-84659EA7AADFQ33353163-578A1148-6FF7-44F0-BEC9-85999F79B9B4Q33543228-FED13317-FD95-46A7-BE75-D887776C3781Q33958790-A1288DDB-01C7-4DFC-9D66-5D843A21D98DQ34074716-E768DDA8-7434-4C5B-AFCE-0A780228BDA1Q34416179-F54CF049-AAAB-482C-A074-4304A775F975Q34807878-B1A7DB78-4FB8-437F-A089-ADCE6CA1EFD5Q35103645-258CEB3E-D44B-402E-ABD3-B2DB6DB17220Q35595628-12ECE974-7CE9-4362-867B-8CBEA018BD80Q35987973-09884914-4EAB-4E80-BE2F-46A350D4402CQ36723683-ED9DF6E7-60D4-4D78-8F04-B27107F674DFQ36843663-DBDB8B9B-2811-4C50-AFB0-8C9A770E4148Q36862577-A6E8E48F-933A-4CD5-BA34-27C72D6587E4Q36871015-C48D698E-F36D-44BA-94BC-5716782CD784Q36872179-2D3F144C-2144-4FE9-9426-18040D0DEAC7Q37628579-9ADAB8B1-2DB5-4DD3-8890-AE28B03E289B
P50
description
Danish biochemist
@en
Dänischer Chemiker
@de
dansk kjemiker
@nb
scheikundige
@nl
հետազոտող
@hy
name
Morten Meldal
@nl
Morten P. Meldal
@ast
Morten P. Meldal
@da
Morten P. Meldal
@de
Morten P. Meldal
@en
Morten P. Meldal
@es
Morten P. Meldal
@nb
Morten P. Meldal
@sl
type
label
Morten Meldal
@nl
Morten P. Meldal
@ast
Morten P. Meldal
@da
Morten P. Meldal
@de
Morten P. Meldal
@en
Morten P. Meldal
@es
Morten P. Meldal
@nb
Morten P. Meldal
@sl
altLabel
Morten Meldal
@ast
Morten Meldal
@de
Morten Meldal
@en
Morten Meldal
@es
Morten Meldal
@sl
prefLabel
Morten Meldal
@nl
Morten P. Meldal
@ast
Morten P. Meldal
@da
Morten P. Meldal
@de
Morten P. Meldal
@en
Morten P. Meldal
@es
Morten P. Meldal
@nb
Morten P. Meldal
@sl
P106
P1053
B-7626-2016
P1153
7006752933
P21
P27
P31
P3829
P496
0000-0001-6114-9018
P569
1954-01-01T00:00:00Z