Robert P. P. Fuchs focuses on DNA polymerase, Molecular biology, DNA, Genetics and DNA replication. His DNA polymerase study incorporates themes from DNA polymerase IV, DNA polymerase II, Polymerase and DNA repair. His Molecular biology research is multidisciplinary, incorporating elements of Xeroderma pigmentosum, SOS response, Gene, Nucleic acid thermodynamics and Nucleic acid methods.
His DNA research includes themes of Saccharomyces cerevisiae, Frameshift mutation and Carcinogen. His Genetics course of study focuses on Cell biology and Endodeoxyribonucleases, Homologous recombination, Flap endonuclease and Holliday junction. Robert P. P. Fuchs focuses mostly in the field of DNA replication, narrowing it down to topics relating to DNA damage and, in certain cases, DNA synthesis, Rec A Recombinases, Exonuclease and RNA polymerase III.
His primary areas of investigation include Molecular biology, DNA, DNA polymerase, Genetics and Biochemistry. His Molecular biology research incorporates elements of Plasmid, Mutation, Mutagenesis, Frameshift mutation and Escherichia coli. His DNA study incorporates themes from Stereochemistry, Guanine and Carcinogen.
His DNA polymerase research integrates issues from RNA polymerase III, DNA polymerase II, Polymerase and DNA replication. Primase is closely connected to DNA clamp in his research, which is encompassed under the umbrella topic of DNA polymerase II. His studies in DNA replication integrate themes in fields like SOS response, DNA polymerase delta and Proofreading.
His primary areas of study are DNA polymerase, Molecular biology, DNA, DNA replication and Genetics. His study in DNA polymerase is interdisciplinary in nature, drawing from both DNA clamp, Polymerase and DNA damage. His Molecular biology research is multidisciplinary, incorporating elements of Mutagenesis, Homologous recombination, Frameshift mutation, Fusion protein and DNA repair.
In his study, Guanine is strongly linked to Genome instability, which falls under the umbrella field of Frameshift mutation. His biological study spans a wide range of topics, including Escherichia coli and Cell biology. Robert P. P. Fuchs interconnects Proofreading, DNA polymerase delta and DNA polymerase II in the investigation of issues within DNA replication.
Robert P. P. Fuchs spends much of his time researching DNA polymerase, DNA replication, Genetics, DNA polymerase II and DNA clamp. His study explores the link between DNA polymerase and topics such as Polymerase that cross with problems in DNA damage. The concepts of his Genetics study are interwoven with issues in MUS81 and Cell biology.
The study incorporates disciplines such as DNA polymerase delta and Primase in addition to DNA polymerase II. His DNA research is multidisciplinary, incorporating perspectives in Bacterial protein and Saccharomyces cerevisiae. Many of his studies on Processivity involve topics that are commonly interrelated, such as Molecular biology.
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.
The Y-Family of DNA Polymerases
Haruo Ohmori;Errol C. Friedberg;Robert P.P. Fuchs;Myron F. Goodman.
Molecular Cell (2001)
The dinB Gene Encodes a Novel E. coli DNA Polymerase, DNA Pol IV, Involved in Mutagenesis
Jérôme Wagner;Petr Gruz;Su-Ryang Kim;Masami Yamada.
Molecular Cell (1999)
All three SOS-inducible DNA polymerases (Pol II, Pol IV and Pol V) are involved in induced mutagenesis.
R. Napolitano;R. Janel‐Bintz;J. Wagner;R. P. P. Fuchs.
The EMBO Journal (2000)
Trading places: how do DNA polymerases switch during translesion DNA synthesis?
Errol C. Friedberg;Alan R. Lehmann;Robert P.P. Fuchs.
Molecular Cell (2005)
Human SLX4 is a Holliday junction resolvase subunit that binds multiple DNA repair/recombination endonucleases
Samira Fekairi;Sarah Scaglione;Charly Chahwan;Ewan R. Taylor.
Co-localization in replication foci and interaction of human Y-family members, DNA polymerase polη and REVl protein
Agnès Tissier;Patricia Kannouche;Marie-Pierre Reck;Alan R. Lehmann.
DNA Repair (2004)
How DNA lesions are turned into mutations within cells
Vincent Pages;Robert P. P. Fuchs.
Chemically modified nucleic acids as immunodetectable probes in hybridization experiments.
Paul Tchen;Robert P. P. Fuchs;Evelyne Sage;Marc Leng.
Proceedings of the National Academy of Sciences of the United States of America (1984)
Uncoupling of Leading- and Lagging-Strand DNA Replication During Lesion Bypass in Vivo
Vincent Pagès;Robert P. Fuchs.
Physical studies on deoxyribonucleic acid after covalent binding of a carcinogen.
Robert Fuchs;Michel Daune.
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: