Aidan J. Doherty focuses on DNA repair, DNA ligase, DNA, Genetics and Biochemistry. His work in the fields of Non-homologous end joining overlaps with other areas such as Ovarian cancer. Aidan J. Doherty has included themes like dnaN, Molecular biology, Replication protein A and DNA repair protein XRCC4 in his DNA ligase study.
His research brings together the fields of Cell biology and Genetics. His Biochemistry research includes themes of DNA polymerase delta and DNA clamp. His research in DNA damage intersects with topics in Polymerase and Primase.
His primary areas of study are DNA, Genetics, Cell biology, DNA repair and DNA ligase. His study ties his expertise on Mutagenesis together with the subject of DNA. His studies in Genetics integrate themes in fields like Protein structure, Computational biology and Primase.
His work deals with themes such as RNA, Transcription, Gene and DNA End-Joining Repair, which intersect with Cell biology. His DNA repair research focuses on Replication protein A and how it relates to Deinococcus radiodurans. His DNA ligase research is multidisciplinary, relying on both Molecular biology, LIG4 and DNA repair protein XRCC4.
Aidan J. Doherty mainly focuses on Cell biology, DNA replication, DNA, Primase and Polymerase. He interconnects DNA damage, RNA, Transcription, Gene and Heterochromatin in the investigation of issues within Cell biology. His DNA damage research integrates issues from Mutation and Homologous recombination.
His study on DNA is covered under Biochemistry. His Primase research is multidisciplinary, incorporating perspectives in Genetics, Genome, Molecular biology, Gene duplication and Computational biology. He has researched Polymerase in several fields, including Gene expression, Recombinant DNA, Nucleotide excision repair, DNA repair and DNA polymerase.
Aidan J. Doherty mostly deals with Primase, Polymerase, DNA replication, Genetics and Genome. The Primase study combines topics in areas such as DNA damage, Genome instability, Helicase, Molecular biology and Histone. His study in DNA damage is interdisciplinary in nature, drawing from both Mutation and DNA synthesis.
His DNA replication research is within the category of DNA. His DNA course of study focuses on Gene and Cell biology. His biological study spans a wide range of topics, including Gene duplication, Plasma protein binding, Computational biology and SUPERFAMILY.
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A pathway of double-strand break rejoining dependent upon ATM, Artemis, and proteins locating to gamma-H2AX foci.
Enriqueta Riballo;Martin Kühne;Nicole Rief;Aidan Doherty.
Molecular Cell (2004)
EMSY Links the BRCA2 Pathway to Sporadic Breast and Ovarian Cancer
Luke Hughes-Davies;David Huntsman;Margarida Ruas;Francois Fuks.
Cell (2003)
Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient
Riballo E;Critchlow Se;Teo Sh;Doherty Aj.
Current Biology (1999)
Identification of a DNA Nonhomologous End-Joining Complex in Bacteria
Geoffrey R. Weller;Boris Kysela;Rajat Roy;Louise M. Tonkin.
Science (2002)
Mycobacterial Ku and Ligase Proteins Constitute a Two-Component NHEJ Repair Machine
Marina Della;Phillip L. Palmbos;Hui Min Tseng;Louise M. Tonkin;Louise M. Tonkin.
Science (2004)
A heterotrimeric PCNA in the hyperthermophilic archaeon Sulfolobus solfataricus.
Isabelle Dionne;Ravi K Nookala;Stephen P Jackson;Aidan J Doherty.
Molecular Cell (2003)
Crystal Structure of Human 53BP1 Brct Domains Bound to P53 Tumour Suppressor
Dean J. Derbyshire;Balaku P. Basu;Louise C. Serpell;Woo S. Joo.
The EMBO Journal (2002)
PrimPol Bypasses UV Photoproducts during Eukaryotic Chromosomal DNA Replication
Julie Bianchi;Sean G. Rudd;Stanislaw K. Jozwiakowski;Laura J. Bailey.
Molecular Cell (2013)
Making ends meet: repairing breaks in bacterial DNA by non-homologous end-joining.
Richard Bowater;Aidan J Doherty.
PLOS Genetics (2006)
Potential role for 53BP1 in DNA end-joining repair through direct interaction with DNA.
Kuniyoshi Iwabuchi;Balaka Piku Basu;Boris Kysela;Takayuki Kurihara.
Journal of Biological Chemistry (2003)
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