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Genetic and biochemical analysis of base excision repair complexes participating in radiation-induced ROS damage repair.
Radiat. Prot. Dosim. 143, 284-288 (2010)
This work is part of the joint research project 'radiation-induced DNA damage' of the KVSF, a BMBF Initiative (maintenance of radiation biology expertise in Germany). The focus of the research is the mechanism of DNA repair, specifically damage repair aspects arising from radiation-induced reactive oxygen species production. The authors will systematically look at potential accessory proteins associated with primarily base excision repair using molecular and biochemical methods. The authors hope to gain knowledge on the initial response mechanisms to varying sources and doses of radiation. By using a highly sensitive marker system, it is intended to achieve a greater resolution of responses induced at lower doses. The work is of relevance for different human diseases caused by defects in DNA repair, e.g. spontaneous and radiation-related cancer. Beyond this, the risk of low radiation doses, for example, in the workplace is of relevance for radiation protection policy and decision-making thereof.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
dna-polymerase-beta; flap
Language
english
Publication Year
2010
HGF-reported in Year
2010
ISSN (print) / ISBN
0144-8420
e-ISSN
1742-3406
Journal
Radiation Protection Dosimetry
Quellenangaben
Volume: 143,
Issue: 2-4,
Pages: 284-288
Publisher
Oxford University Press
Publishing Place
Oxford
Reviewing status
Peer reviewed
Institute(s)
Translational Metabolic Oncology (IDC-TMO)
Institute of Molecular Radiation Biology (IMS)
Institute of Molecular Radiation Biology (IMS)
POF-Topic(s)
30203 - Molecular Targets and Therapies
Research field(s)
Radiation Sciences
PSP Element(s)
G-501000-001
G-500400-001
G-500400-001
PubMed ID
21109544
Scopus ID
79952321731
Erfassungsdatum
2010-12-31