about
Azathioprine and UVA light generate mutagenic oxidative DNA damageTriplet formation of 4-thiothymidine and its photosensitization to oxygen studied by time-resolved thermal lensing technique.Thiothymidine combined with UVA as a potential novel therapy for bladder cancer.Thiothymidine plus low-dose UVA kills hyperproliferative human skin cells independently of their human papilloma virus status.Ambiguous coding is required for the lethal interaction between methylated DNA bases and DNA mismatch repair.UVA photoactivation of DNA containing halogenated thiopyrimidines induces cytotoxic DNA lesions.Topical 4-thiothymidine is a viable photosensitiser for the photodynamic therapy of skin malignancies.Reactive oxygen-mediated damage to a human DNA replication and repair protein.Novel DNA lesions generated by the interaction between therapeutic thiopurines and UVA light.4-Thio-5-bromo-2'-deoxyuridine: chemical synthesis and therapeutic potential of UVA-induced DNA damage.The effect of S-substitution at the O6-guanine site on the structure and dynamics of a DNA oligomer containing a G:T mismatch.Unambiguous structural elucidation of base-modified purine nucleosides using NMR.Spotlight on medicinal chemistry education.Acid Dissociation Equilibrium and Singlet Molecular Oxygen Quantum Yield of Acetylated 6,8-Dithioguanosine in Aqueous Buffer Solution.NMR studies on 4-thio-5-furan-modified and 4-thio-5-thiophene-modified nucleosides.Base analog and neighboring base effects on substrate specificity of recombinant human G:T mismatch-specific thymine DNA-glycosylase.Site-specific 15N-labelling of oligonucleotides for NMR: the trp operator and its interaction with the trp repressor.The cytotoxicity of DNA carboxymethylation and methylation by the model carboxymethylating agent azaserine in human cellsCharacteristics of the excited triplet states of thiolated guanosine derivatives and singlet oxygen generationDNA mismatch binding and incision at modified guanine bases by extracts of mammalian cells: implications for tolerance to DNA methylation damageReactive DNA. 2. Thioguanine used as a peg site for direct and specific introduction of biologically useful functional groupsNMR and UV studies of 4-thio-2'-deoxyuridine and its derivativesSystematic assignment of NMR spectra of 5-substituted-4-thiopyrimidine nucleosides
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Yao-Zhong Xu
@ast
Yao-Zhong Xu
@en
Yao-Zhong Xu
@es
Yao-Zhong Xu
@nl
Yao-Zhong Xu
@sl
type
label
Yao-Zhong Xu
@ast
Yao-Zhong Xu
@en
Yao-Zhong Xu
@es
Yao-Zhong Xu
@nl
Yao-Zhong Xu
@sl
prefLabel
Yao-Zhong Xu
@ast
Yao-Zhong Xu
@en
Yao-Zhong Xu
@es
Yao-Zhong Xu
@nl
Yao-Zhong Xu
@sl
P106
P31
P496
0000-0002-5713-8030