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The following pages link to Quantitative analysis of the oxidative DNA lesion, 2,2-diamino-4-(2-deoxy-beta-D-erythro-pentofuranosyl)amino]-5(2H)-oxazolone (oxazolone), in vitro and in vivo by isotope dilution-capillary HPLC-ESI-MS/MS (Q35130551):
Displaying 41 items.
- Reconciliation of chemical, enzymatic, spectroscopic and computational data to assign the absolute configuration of the DNA base lesion spiroiminodihydantoin (Q30692305) (← links)
- Characterization of 2′-deoxyguanosine oxidation products observed in the Fenton-like system Cu(ii)/H2O2/reductant in nucleoside and oligodeoxynucleotide contexts (Q33561899) (← links)
- Mechanisms of free radical-induced damage to DNA. (Q34030395) (← links)
- Comparison of transition metal-mediated oxidation reactions of guanine in nucleoside and single-stranded oligodeoxynucleotide contexts (Q34812595) (← links)
- Spirodi(iminohydantoin) products from oxidation of 2'-deoxyguanosine in the presence of NH4Cl in nucleoside and oligodeoxynucleotide contexts (Q34992472) (← links)
- 5-Carboxamido-5-formamido-2-iminohydantoin, in Addition to 8-oxo-7,8-Dihydroguanine, Is the Major Product of the Iron-Fenton or X-ray Radiation-Induced Oxidation of Guanine under Aerobic Reducing Conditions in Nucleoside and DNA Contexts (Q35871453) (← links)
- Type I and Type II Photosensitized Oxidation Reactions: Guidelines and Mechanistic Pathways. (Q36248440) (← links)
- Quantitation of DNA adducts by stable isotope dilution mass spectrometry (Q36390390) (← links)
- In situ analysis of 8-oxo-7,8-dihydro-2'-deoxyguanosine oxidation reveals sequence- and agent-specific damage spectra (Q36415837) (← links)
- Comparative analysis of four oxidized guanine lesions from reactions of DNA with peroxynitrite, singlet oxygen, and γ-radiation (Q36627024) (← links)
- pH-Dependent Equilibrium between 5-Guanidinohydantoin and Iminoallantoin Affects Nucleotide Insertion Opposite the DNA Lesion (Q36714153) (← links)
- Guanine oxidation product 5-carboxamido-5-formamido-2-iminohydantoin induces mutations when bypassed by DNA polymerases and is a substrate for base excision repair (Q36728705) (← links)
- Mass spectrometry of structurally modified DNA. (Q36979806) (← links)
- Genotoxicity of nano/microparticles in in vitro micronuclei, in vivo comet and mutation assay systems (Q37350056) (← links)
- Analysis of 8-oxo-7,8-dihydro-2'-deoxyguanosine by ultra high pressure liquid chromatography-heat assisted electrospray ionization-tandem mass spectrometry (Q37376032) (← links)
- Sources of extracellular, oxidatively-modified DNA lesions: implications for their measurement in urine (Q37407483) (← links)
- An overview of chemical processes that damage cellular DNA: spontaneous hydrolysis, alkylation, and reactions with radicals (Q37598234) (← links)
- Mapping structurally defined guanine oxidation products along DNA duplexes: influence of local sequence context and endogenous cytosine methylation (Q37701731) (← links)
- DNA damage spectra induced by photosensitization (Q37928944) (← links)
- DNA damage by reactive species: Mechanisms, mutation and repair. (Q38023114) (← links)
- DNA base damage by reactive oxygen species, oxidizing agents, and UV radiation. (Q38078916) (← links)
- (31) P NMR Evidence for Peroxide Intermediates in Lipid Emulsion Photooxidations: Phosphine Substituent Effects in Trapping. (Q38672354) (← links)
- Excessive Reactive Oxygen Species and Exotic DNA Lesions as an Exploitable Liability (Q38943129) (← links)
- Formation and processing of DNA damage substrates for the hNEIL enzymes (Q39018239) (← links)
- Rates of chemical cleavage of DNA and RNA oligomers containing guanine oxidation products (Q39020441) (← links)
- Formation and repair of oxidatively generated damage in cellular DNA. (Q39037391) (← links)
- Generation, repair and replication of guanine oxidation products (Q41195935) (← links)
- G-quadruplex folds of the human telomere sequence alter the site reactivity and reaction pathway of guanine oxidation compared to duplex DNA. (Q41788288) (← links)
- Structural context effects in the oxidation of 8-oxo-7,8-dihydro-2'-deoxyguanosine to hydantoin products: electrostatics, base stacking, and base pairing (Q41814086) (← links)
- DNA sequence context as a determinant of the quantity and chemistry of guanine oxidation produced by hydroxyl radicals and one-electron oxidants (Q41932407) (← links)
- Chlorella virus pyrimidine dimer glycosylase and Escherichia coli endonucleases IV and V have incision activity on 2,2,4-triamino-5(2H)-oxazolone (Q42175969) (← links)
- Microfluidic array for simultaneous detection of DNA oxidation and DNA-adduct damage. (Q42388013) (← links)
- Effects of stability of base pairs containing an oxazolone on DNA elongation (Q43075936) (← links)
- 8-Oxo-7,8-dihydro-2'-deoxyguanosine and abasic site tandem lesions are oxidation prone yielding hydantoin products that strongly destabilize duplex DNA. (Q46303021) (← links)
- Self-Cyclizing Antioxidants to Prevent DNA Damage Caused by Hydroxyl Radical. (Q46320803) (← links)
- Establishment of an in vivo simulating co-culture assay platform for genotoxicity of multi-walled carbon nanotubes. (Q49997339) (← links)
- Chemoprevention against arsenic-induced mutagenic DNA breakage and apoptotic liver damage in rat via antioxidant and SOD1 upregulation by green tea (Camellia sinensis) which recovers broken DNA resulted from arsenic-H2O2 related in vitro oxidant str (Q50445043) (← links)
- Mapping Three Guanine Oxidation Products along DNA Following Exposure to Three Types of Reactive Oxygen Species. (Q52558780) (← links)
- Conformational stabilities of iminoallantoin and its base pairs in DNA: implications for mutagenicity. (Q54163647) (← links)
- Oxidation Chemistry of DNA and p53 Tumor Suppressor Gene (Q64110005) (← links)
- Human NEIL3 Gene Expression Regulated by Epigenetic-Like Oxidative DNA Modification (Q93044129) (← links)