about
High resolution crystal structure of domain I of the Saccharomyces cerevisiae homing endonuclease PI-SceI.High-resolution structures ofThermus thermophilusenoyl-acyl carrier protein reductase in the apo form, in complex with NAD+and in complex with NAD+and triclosanIn vivo genome editing as a potential treatment strategy for inherited retinal dystrophiesNovel missense mutation in the EDA gene in a family affected by oligodontia.Photocross-linking of the homing endonuclease PI-SceI to its recognition sequence.Controlling the enzymatic activity of a restriction enzyme by light.Type II restriction endonucleases--a historical perspective and moreTALE-PvuII fusion proteins--novel tools for gene targeting.Generation of novel nucleases with extended specificity by rational and combinatorial strategies.Redesigning the single-chain variant of the restriction endonuclease PvuII by circular permutation.Photocaged variants of the MunI and PvuII restriction enzymes.The Flavobacterium okeanokoites adenine-N6-specific DNA-methyltransferase M.FokI is a tandem enzyme of two independent domains with very different kinetic properties.Site- and strand-specific nicking of DNA by fusion proteins derived from MutH and I-SceI or TALE repeatsCreating highly specific nucleases by fusion of active restriction endonucleases and catalytically inactive homing endonucleases.Type II restriction endonucleases - a historical perspective and more.A novel zinc-finger nuclease platform with a sequence-specific cleavage module.Tracking of single quantum dot labeled EcoRV sliding along DNA manipulated by double optical tweezers.Editorial: Alfred Pingoud (1945-2015).Identification of conserved features of LAGLIDADG homing endonucleases.Peculiarities of the interaction of the restriction endonuclease BspD6I with DNA containing its recognition site.STED nanoscopy combined with optical tweezers reveals protein dynamics on densely covered DNA.[Genome Editing Tools and their Application in Experimental Ophthalmology].Synthesis and DNA cleavage activity of Bis-3-chloropiperidines as alkylating agents.EcoRV-T94V: a mutant restriction endonuclease with an altered substrate specificity towards modified oligodeoxynucleotides.A procedure for renaturation and purification of the extracellular Serratia marcescens nuclease from genetically engineered Escherichia coli.On the Divalent Metal Ion Dependence of DNA Cleavage by Restriction Endonucleases of the EcoRI FamilyThe Mechanism of DNA Cleavage by the Type II. Restriction Enzyme EcoRV: Asp36 Is Not Directly Involved in DNA Cleavage but Serves to Couple Indirect. Readout to CatalysisDetermination of the DNA bend angle induced by the restriction endonuclease EcoRV in the presence of Mg2+The production and characterization of artificial heterodimers of the restriction endonuclease EcoRV[Analysis of binding and cleavage of DNA by the gene conversion PI-SCEI endonuclease using site-directed mutagenesis]A similar active site for non-specific and specific endonucleasesA sliding restriction enzyme pausesDevelopment of a Reporter System to Explore MMEJ in the Context of Replacing Large Genomic Fragments
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Wolfgang Wende
@ast
Wolfgang Wende
@de
Wolfgang Wende
@en
Wolfgang Wende
@es
Wolfgang Wende
@nl
type
label
Wolfgang Wende
@ast
Wolfgang Wende
@de
Wolfgang Wende
@en
Wolfgang Wende
@es
Wolfgang Wende
@nl
prefLabel
Wolfgang Wende
@ast
Wolfgang Wende
@de
Wolfgang Wende
@en
Wolfgang Wende
@es
Wolfgang Wende
@nl
P106
P31
P496
0000-0001-6577-9535