Related references
Note: Only part of the references are listed.Selective and stable base pairing by alkynylated nucleosides featuring a spatially-separated recognition interface
Hidenori Okamura et al.
NUCLEIC ACIDS RESEARCH (2022)
Multiple-turnover single nucleotide primer extension reactions to detect 8-oxo-2′-deoxyguanosine in DNA
Yoshiya Kikukawa et al.
CHEMICAL COMMUNICATIONS (2022)
Oxidative-stress-driven mutagenesis in the small intestine of the gpt delta mouse induced by oral administration of potassium bromate
Yasunobu Aoki et al.
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS (2020)
Hachimoji DNA and RNA: A genetic system with eight building blocks
Shuichi Hoshika et al.
SCIENCE (2019)
Sequencing the Mouse Genome for the Oxidatively Modified Base 8-Oxo-7,8-dihydroguanine by OG-Seq
Yun Ding et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2017)
Sequencing of DNA Lesions Facilitated by Site-Specific Excision via Base Excision Repair DNA Glycosylases Yielding Ligatable Gaps
Jan Riedl et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2016)
In-Gene Quantification of O6-Methylguanine with Elongated Nucleoside Analogues on Gold Nanoprobes
Ioannis A. Trantakis et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2016)
The use of an artificial nucleotide for polymerase-based recognition of carcinogenic O6-alkylguanine DNA adducts
Laura A. Wyss et al.
NUCLEIC ACIDS RESEARCH (2016)
2′-O-Methyl- and 2′-O-propargyl-5-methylisocytidine: synthesis, properties and impact on the isoCd-dG and the isoCd-isoGd base pairing in nucleic acids with parallel and antiparallel strand orientation
Sunit K. Jana et al.
ORGANIC & BIOMOLECULAR CHEMISTRY (2016)
Mutations induced by 8-hydroxyguanine (8-oxo-7,8-dihydroguanine), a representative oxidized base, in mammalian cells
Tetsuya Suzuki et al.
GENES AND ENVIRONMENT (2016)
Discrimination Between 8-Oxo-2′-Deoxyguanosine and 2′-Deoxyguanosine in DNA by the Single Nucleotide Primer Extension Reaction with Adap Triphosphate
Yosuke Taniguchi et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2015)
Identification of DNA lesions using a third base pair for amplification and nanopore sequencing
Jan Riedl et al.
NATURE COMMUNICATIONS (2015)
Specific Incorporation of an Artificial Nucleotide Opposite a Mutagenic DNA Adduct by a DNA Polymerase
Laura A. Wyss et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2015)
Adenosine-1,3-diazaphenoxazine Derivative for Selective Base Pair Formation with 8-Oxo-2′-deoxyguanosine in DNA
Yosuke Taniguchi et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)
2′-Deoxy-1-methylpseudocytidine, a stable analog of 2′-deoxy-5-methylisocytidine
Hyo-Joong Kim et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2009)
Feasibility of conducting human studies to address bromate risks
KP Cantor
TOXICOLOGY (2006)
Biomarkers of oxidative damage in human disease
I Dalle-Donne et al.
CLINICAL CHEMISTRY (2006)
Mitochondria take center stage in aging and neurodegeneration
MF Beal
ANNALS OF NEUROLOGY (2005)
The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system
AM Sismour et al.
NUCLEIC ACIDS RESEARCH (2005)
Unique tautomeric properties of isoguanine
JR Blas et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2004)
Urinary 8-OHdG: a marker of oxidative stress to DNA and a risk factor for cancer, atherosclerosis and diabetics
LL Wu et al.
CLINICA CHIMICA ACTA (2004)
Oxidative DNA damage: mechanisms, mutation, and disease
MS Cooke et al.
FASEB JOURNAL (2003)
First principles calculations of the pK(a) values and tautomers of isoguanine and xanthine
KN Rogstad et al.
CHEMICAL RESEARCH IN TOXICOLOGY (2003)
Thermodynamic stability of base pairs, between 2-hydroxyadenine and incoming nucleotides as a determinant of nucleotide incorporation specificity during replication
J Kawakami et al.
NUCLEIC ACIDS RESEARCH (2001)
Share Paper
