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Spectroscopically labeled peptaibiotic analogs: the 4-nitrophenylalanine infrared absorption probe inserted at different positions into trichogin GA IV.Partial thioamide scan on the lipopeptaibiotic trichogin GA IV. Effects on folding and bioactivityReliability of a decision-tree model in predicting occupational lead poisoning in a group of highly exposed workers.Main-chain length control of conformation, membrane activity, and antibiotic properties of lipopeptaibol sequential analogues.New tools for the control of peptide conformation and supramolecular chemistry: crown-carrier, C(alpha)-methyl L-DOPA amino acids.Solution synthesis, conformational analysis, and antimicrobial activity of three alamethicin F50/5 analogs bearing a trifluoroacetyl label.Induced axial chirality in the biphenyl core of the proatropoisomeric, C alpha-tetrasubstituted alpha-amino acid residue Bip in peptides.Conformational properties, membrane interaction, and antibacterial activity of the peptaibiotic chalciporin A: Multitechnique spectroscopic and biophysical investigations on the natural compound and labeled analogs.A topographically and conformationally constrained, spin-labeled, alpha-amino acid: crystallographic characterization in peptides*Linear Configuration of the Spins of a Stable Trinitroxide Radical Based on a Ternary Helical PeptideDistance dependency of exciton coupled circular dichroism using turn and helical peptide spacersPhotoinduced intramolecular covalent bond formation in structurally rigid -Bpa-(spacer)-Met hexapeptidesSpectroscopically labeled peptaibiotics. Synthesis and properties of selected trichogin GA IV analogs bearing a side-chain-monofluorinated aromatic amino acid for (19) F-NMR analysisKinetic studies on the oxidative stabilization effect of red onion skins anthocyanins extract on parsley (Petroselinum crispum) seed oil
P50
Q30583903-CA207F89-EC31-4CDD-B1D8-ADE1ED716BA8Q36281175-93338C1B-3B8C-4FF9-AEAE-BA286647BA21Q39740064-386BA787-D6E3-4257-A61D-D4BF58F22ED9Q44460004-20179E87-B565-4AEF-831E-6B41AF4F37ABQ44781096-6780990A-F85D-4290-B843-3D3F6BAA9CDBQ45881924-1140D075-9895-447B-92F5-C0F1B98F5F19Q46602348-191C7081-5F0E-409F-B743-D4DB14CE0DF5Q47358988-2C6F5194-8CB4-4D78-83FC-7BBF11C94A82Q58440787-6B3EA4C9-3916-463B-A210-54D0498EE5DCQ58440796-79B63202-ABF4-46AC-A805-F24ABBC1E7D9Q72988613-E6E5E8CD-0ADA-4858-8A26-A5B963E1122EQ83740978-44F4788F-F3A4-4445-A84E-2917112EE8FDQ86815164-A031CD60-4E81-4568-9223-B0E253ABBCB0Q89045980-D256741A-19AB-41DC-A051-E533C092F63F
P50
description
researcher
@en
wetenschapper
@nl
name
Simona Oancea
@en
Simona Oancea
@nl
type
label
Simona Oancea
@en
Simona Oancea
@nl
prefLabel
Simona Oancea
@en
Simona Oancea
@nl
P106
P31
P496
0000-0003-3832-6041