Samuel H. Wilson spends much of his time researching Base excision repair, DNA polymerase, Nucleotide excision repair, Molecular biology and AP site. In his works, Samuel H. Wilson performs multidisciplinary study on DNA polymerase and DNA polymerase delta. His biological study spans a wide range of topics, including DNA polymerase beta, DNA glycosylase and Oligonucleotide.
His research in Molecular biology intersects with topics in Polymerase, DNA and DNA synthesis. His AP site research focuses on AP endonuclease in particular. The concepts of his AP endonuclease study are interwoven with issues in DNA- lyase, DNA ligase and Class II AP Endonuclease.
His primary areas of investigation include DNA polymerase, Molecular biology, Base excision repair, Biochemistry and DNA. His DNA polymerase study incorporates themes from Polymerase and Stereochemistry. His Polymerase research is multidisciplinary, incorporating elements of Biophysics, Base pair and Nucleic acid.
Samuel H. Wilson interconnects Promoter, Response element, Poly ADP ribose polymerase and Transcription in the investigation of issues within Molecular biology. His study in Base excision repair is interdisciplinary in nature, drawing from both Lyase activity, Nucleotide excision repair, DNA glycosylase and AP site. His DNA research includes elements of Lyase, Nucleotide and Mutagenesis.
Samuel H. Wilson focuses on Base excision repair, DNA, DNA repair, DNA polymerase and Molecular biology. His studies in Base excision repair integrate themes in fields like Nucleotide excision repair and AP site. DNA is a subfield of Biochemistry that Samuel H. Wilson investigates.
In the field of DNA repair, his study on DNA glycosylase and DNA- lyase overlaps with subjects such as Base and Lesion. Samuel H. Wilson undertakes multidisciplinary studies into DNA polymerase and Protein–DNA interaction in his work. His Molecular biology study frequently links to adjacent areas such as Polymerase.
His primary scientific interests are in Base excision repair, DNA, DNA repair, DNA polymerase and Stereochemistry. Samuel H. Wilson performs multidisciplinary study in Base excision repair and XRCC1 in his work. Samuel H. Wilson integrates many fields, such as XRCC1 and engineering, in his works.
His AP endonuclease study deals with the bigger picture of DNA glycosylase. His DNA polymerase research incorporates themes from Cytosine, 5-Methylcytosine, DNA methylation and Polymerase. Samuel H. Wilson combines subjects such as Lyase activity, Lyase, Nucleotide and DNA synthesis with his study of Histone.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Mammalian Abasic Site Base Excision Repair: IDENTIFICATION OF THE REACTION SEQUENCE AND RATE-DETERMINING STEPS *
Deepak K. Srivastava;Brian J. Vande Berg;Rajendra Prasad;James T. Molina.
Journal of Biological Chemistry (1998)
A role for p53 in base excision repair.
Jianmin Zhou;Jinwoo Ahn;Samuel H. Wilson;Carol Prives.
The EMBO Journal (2001)
Different DNA polymerases are involved in the short- and long-patch base excision repair in mammalian cells.
Paola Fortini;Barbara Pascucci;Eleonora Parlanti;Robert W. Sobol.
Biochemistry (1998)
Role of DNA polymerase beta in the excision step of long patch mammalian base excision repair.
Grigory L. Dianov;Rajendra Prasad;Samuel H. Wilson;Vilhelm A. Bohr.
Journal of Biological Chemistry (1999)
FEN1 stimulation of DNA polymerase beta mediates an excision step in mammalian long patch base excision repair.
Rajendra Prasad;Grigory L. Dianov;Vilhelm A. Bohr;Samuel H. Wilson.
Journal of Biological Chemistry (2000)
DNA Polymerase β-mediated Long Patch Base Excision Repair POLY(ADP-RIBOSE) POLYMERASE-1 STIMULATES STRAND DISPLACEMENT DNA SYNTHESIS
Rajendra Prasad;Olga I. Lavrik;Soon-Jong Kim;Padmini Kedar.
Journal of Biological Chemistry (2001)
Photoaffinity labeling of mouse fibroblast enzymes by a base excision repair intermediate. Evidence for the role of poly(ADP-ribose) polymerase-1 in DNA repair.
Olga I. Lavrik;Olga I. Lavrik;Rajendra Prasad;Robert W. Sobol;Julie K. Horton.
Journal of Biological Chemistry (2001)
DNA structure and aspartate 276 influence nucleotide binding to human DNA polymerase beta. Implication for the identity of the rate-limiting conformational change.
Brian J. Vande Berg;William A. Beard;Samuel H. Wilson.
Journal of Biological Chemistry (2001)
Protection against Methylation-induced Cytotoxicity by DNA Polymerase β-Dependent Long Patch Base Excision Repair
Julie K. Horton;Rajendra Prasad;Esther Hou;Samuel H. Wilson.
Journal of Biological Chemistry (2000)
Base Excision Repair Intermediates Induce p53-independent Cytotoxic and Genotoxic Responses
Robert W. Sobol;Maria Kartalou;Karen H. Almeida;Donna F. Joyce.
Journal of Biological Chemistry (2003)
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