about
Photoenhanced oxidative DNA cleavage with non-heme iron(II) complexes.DNA and RNA induced enantioselectivity in chemical synthesis.Artificial metalloenzymes for enantioselective catalysis.DNA-based hybrid catalysis.Efficient nuclear DNA cleavage in human cancer cells by synthetic bleomycin mimics.Mechanism of intramolecular photostabilization in self-healing cyanine fluorophores.Targeting Nrf2 in healthy and malignant ovarian epithelial cells: Protection versus promotion.Novel artificial metalloenzymes by in vivo incorporation of metal-binding unnatural amino acids.DNA-Accelerated Catalysis of Carbene-Transfer Reactions by a DNA/Cationic Iron Porphyrin HybridCorrigendum: A simple and versatile design concept for fluorophore derivatives with intramolecular photostabilization.Design of an enantioselective artificial metallo-hydratase enzyme containing an unnatural metal-binding amino acid.Control over enzymatic activity by DNA-directed split enzyme reassembly.Artificial Metalloproteins for Binding and Stabilization of a Semiquinone Radical.Selenoglutaredoxin as a glutathione peroxidase mimic.Corrigendum: A simple and versatile design concept for fluorophore derivatives with intramolecular photostabilization.Multidrug resistance regulators (MDRs) as scaffolds for the design of artificial metalloenzymes.A metal ion regulated artificial metalloenzyme.Responsive DNA G-quadruplex micelles.Characterisation of the interactions between substrate, copper(II) complex and DNA and their role in rate acceleration in DNA-based asymmetric catalysis.Photo-induced oxidation of [Fe(II)(N4Py)CH3CN] and related complexes.DNA cleavage activity of Fe(II)N4Py under photo irradiation in the presence of 1,8-naphthalimide and 9-aminoacridine: unexpected effects of reactive oxygen species scavengers.Protein engineering: The power of four.An Artificial Heme Enzyme for Cyclopropanation Reactions.Importance of Metal-Ion Exchange for the Biological Activity of Coordination Complexes of the Biomimetic Ligand N4Py.Ligand denticity controls enantiomeric preference in DNA-based asymmetric catalysisA designer enzyme for hydrazone and oxime formation featuring an unnatural catalytic aniline residueThe Power of Two: Covalent Coupling of Photostabilizers for Fluorescence ApplicationsAuthor Correction: A simple and versatile design concept for fluorophore derivatives with intramolecular photostabilizationSupramolecular Assembly of Artificial Metalloenzymes Based on the Dimeric Protein LmrR as Promiscuous ScaffoldEnantioselective Artificial Metalloenzymes by Creation of a Novel Active Site at the Protein Dimer InterfaceHierarchical Self-Assembly of a Biomimetic Light-Harvesting Antenna Based on DNA G-QuadruplexesEnhanced selectivity in non-heme iron catalysed oxidation of alkanes with peracids: evidence for involvement of Fe(iv)O speciesLmrR: A Privileged Scaffold for Artificial MetalloenzymesA "Broad Spectrum" Carbene Transferase for Synthesis of Chiral α-Trifluoromethylated OrganoboronsDirected Evolution of a Designer Enzyme Featuring an Unnatural Catalytic Amino AcidAlpha,beta-unsaturated 2-acyl imidazoles as a practical class of dienophiles for the DNA-based catalytic asymmetric Diels-Alder reaction in waterHighly enantioselective DNA-based catalysisProbing the molecular basis of protein function through chemistryModular assembly of novel DNA-based catalystsOrganic co-solvents in aqueous DNA-based asymmetric catalysis
P50
Q33740936-3938A312-8CB5-4652-9E0D-77C6F18F50F2Q36716470-2BBCB389-C310-4520-9308-C46C6E1D5A65Q38194395-CE5E13C5-A57B-443B-8928-2D5219D889C5Q38314618-6F25340A-2009-48F1-9310-7459FE9B561CQ39023922-C1A01681-5F79-46D8-8B56-8A9980C8104FQ39302107-3FEB8772-4B76-4A3C-B7E8-1D9A4181DBB4Q41136568-69D38AEA-BAC8-49A4-9A80-ACB3BC032A45Q41509330-AFE8E0B7-883D-4C98-92DB-62C46B77C818Q41836215-94DDC913-9DCC-41B9-BBAD-9DC6CDB2F3C8Q42343387-1F334092-91C2-4183-920B-4E7C0BAF68F7Q42707737-F291110D-3275-44B0-AD64-E14F04488058Q42860752-EBAEF325-DF96-4CE0-AD42-F9D8038BDD75Q43406491-8931A97E-D926-4FBF-AA9B-088D4A7E6647Q46544398-D175715A-67E4-4A5B-8837-93930C865AB5Q47126173-38380644-5EA7-43AD-93EB-3385FA3D0F35Q48100604-26AF9C15-B518-4E61-A3A2-77428DA57980Q48140354-151A0283-8FC3-4C91-998D-BFBCCD65A053Q49907465-70FFFA14-A2C7-470F-8152-DC8370CE6D4BQ50996638-B993C299-EBE8-45E8-9DD4-08384686641FQ51317705-7C2850AA-1A48-4281-A227-59B23ACFC2E0Q53211888-741C4237-DA98-457F-B0BC-D14190D022A3Q53284280-82197E0E-ADA7-4CC1-8A60-D8FC4D04D30FQ53689020-DA7C4370-89A9-4B2D-82EA-35FDE78DEA72Q55439551-56659DC2-CC28-4C7D-9935-CA47154F42A2Q56743218-53C048F5-3E50-4B39-AC54-3518B058FAF8Q57165472-FAB43560-6957-4B97-A6FD-BBBC1C47FE1DQ58034187-A331ECC1-4166-4680-8FA2-A23AAAE3114EQ61135561-CE1AFC12-0520-4126-BBC0-E189DF76F2B3Q63359762-9816ABF5-20D7-4F0F-8BC9-A791D96BC065Q63359776-264064EE-3628-47D2-97CA-0E84CC663CE8Q63982104-2AB6EA7E-98CD-4CD3-84BA-3141E9779997Q63982231-977F29AF-A379-4A0C-8E48-E061DAC29C81Q64109035-D5D6CF1D-3F17-47E1-9C1E-1EF2AADF98B0Q64234072-4C8848B5-D62A-4F5C-B7DE-75ABC5227539Q64258242-24E1B874-BB1D-498C-9477-0C27C7834C2FQ80764899-F5D994DB-151D-48D8-B78F-CE09C0A096AAQ82422957-457CCD3E-B674-4E3E-A760-B03D810818A0Q82449277-B7CE7C3F-DA38-497C-992F-CCEF8B5B4E0BQ82710866-150190E5-7C0E-4FAA-979C-FB703A8C2EC5Q83136816-EF34952C-FF25-4FD5-8192-E781AC77714A
P50
description
investigador
@es
researcher
@en
name
Gerard Roelfes
@en
Gerard Roelfes
@nl
type
label
Gerard Roelfes
@en
Gerard Roelfes
@nl
prefLabel
Gerard Roelfes
@en
Gerard Roelfes
@nl
P31
P496
0000-0002-0364-9564