His scientific interests lie mostly in Biochemistry, Molecular biology, DNA, Transfer RNA and Stereochemistry. His work in the fields of Escherichia coli, Enzyme and Base pair overlaps with other areas such as 8-Hydroxy-2'-deoxyguanosine. His Molecular biology study combines topics from a wide range of disciplines, such as DNA glycosylase, Reactive oxygen species and Mutant, Gene, Transfection.
In his study, Oral administration and Peroxisome is strongly linked to Carcinogen, which falls under the umbrella field of DNA. His studies examine the connections between Transfer RNA and genetics, as well as such issues in Ribosome, with regards to Mitochondrion, Gene targeting, Protein biosynthesis and Aminoacylation. His work carried out in the field of Stereochemistry brings together such families of science as Plasma protein binding, Ribose, Binding site and A-DNA.
His primary scientific interests are in Biochemistry, Transfer RNA, Molecular biology, Stereochemistry and DNA. His is involved in several facets of Biochemistry study, as is seen by his studies on Escherichia coli, Nucleic acid sequence, Enzyme, Guanine and Queuine. The concepts of his Transfer RNA study are interwoven with issues in Residue and Nucleotide.
His Molecular biology research includes elements of DNA glycosylase and Mutation, Gene, Mutant, Oligonucleotide. The various areas that Susumu Nishimura examines in his Stereochemistry study include Amino acid and Topoisomerase. His DNA research integrates issues from Carcinogenesis, Radical and Carcinogen.
Susumu Nishimura mainly focuses on Biochemistry, Molecular biology, Stereochemistry, Gene and Indolocarbazole. His study in Biochemistry concentrates on Enzyme, Transfer RNA, DNA, Escherichia coli and Lyase activity. His Transfer RNA research includes themes of Nucleotide, Guanine and Saccharomyces cerevisiae.
His Molecular biology study integrates concerns from other disciplines, such as Oxidative stress, DNA glycosylase, Reactive oxygen species, Mutant and Complementary DNA. His studies in Stereochemistry integrate themes in fields like Peptide sequence, Group, Plasma protein binding and Binding site. His Indolocarbazole research incorporates themes from Topoisomerase, In vitro, Lethal dose and Chemotherapy.
Susumu Nishimura mainly investigates Biochemistry, Molecular biology, Stereochemistry, Mutant and Transfer RNA. Indolocarbazole, Kinase, Lyase activity, Enzyme and DNA glycosylase are subfields of Biochemistry in which his conducts study. His Molecular biology study incorporates themes from Amino acid, Reactive oxygen species, Selenocysteine and Gene.
His biological study spans a wide range of topics, including DNA damage, DNA and Mutation frequency. His studies deal with areas such as Plasma protein binding and Binding site as well as Stereochemistry. His study in the fields of Queuosine under the domain of Transfer RNA overlaps with other disciplines such as Haloferax volcanii.
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8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G----T and A----C substitutions.
Keith C. Cheng;David S. Cahill;Hiroshi Kasai;Susumu Nishimura.
Journal of Biological Chemistry (1992)
Formation of 8-hydroxyguanine moiety in cellular DNA by agents producing oxygen radicals and evidence for its repair
H. Kasai;P.F. Crain;Y. Kuchino;S. Nishimura.
Molecular switch for signal transduction: structural differences between active and inactive forms of protooncogenic ras proteins
Michael V. Milburn;Liang Tong;Abraham M. deVos;Axel Brünger.
Hydroxylation of deoxyguanosine at the C-8 position by ascorbic acid and other reducing agents
Hiroshi Kasai;Susumu Nishimura.
Nucleic Acids Research (1984)
Misreading of DNA templates containing 8-hydroxydeoxyguanosine at the modified base and at adjacent residues
Y Kuchino;F Mori;H Kasai;H Inoue.
8-oxoguanine (8-hydroxyguanine) DNA glycosylase and its substrate specificity.
J Tchou;H Kasai;S Shibutani;M H Chung.
Proceedings of the National Academy of Sciences of the United States of America (1991)
Three-dimensional structure of an oncogene protein: catalytic domain of human c-H-ras p21.
A. M. De Vos;Liang Tong;M. V. Milburn;P. M. Matias.
The consensus motif for phosphorylation by cyclin D1-Cdk4 is different from that for phosphorylation by cyclin A/E-Cdk2.
M. Kitagawa;H. Higashi;H.-K. Jung;I. Suzuki-Takahashi.
The EMBO Journal (1996)
Codon and amino-acid specificities of a transfer RNA are both converted by a single post-transcriptional modification.
Tomonari Muramatsu;Kazuya Nishikawa;Fumiko Nemoto;Yoshiyuki Kuchino.
Mmh/Ogg1 gene inactivation results in accumulation of 8-hydroxyguanine in mice
Osamu Minowa;Tsuyoshi Arai;Masanori Hirano;Yoshiaki Monden.
Proceedings of the National Academy of Sciences of the United States of America (2000)
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