Research field (5):
Molecular biology
, Medical biochemistry
, Pathobiochemistry
, Environmental effects of radiation
, Environmental effects of chemicals
2018 - 2021 Establishment of a bio-assay for DNA homologous recombination ability using breast cancer cells to catalog responsible genetic alterations
2017 - 2020 DNA double strand break repair factors mutated in a new syndrome with microcephaly
2016 - 2019 Mitochondrial DNA deletions as a bioindicator of radiation exposure in papillary thyroid carcinoma
2016 - 2018 Establishment of a system to measure DNA repair activity using circulating tumor cells: the key to predict sensitivity to PARP inhibitors
2015 - 2017 Analysis of a new genetic disorder caused by the deficiency in radiation-induced DNA double-strand break repair
2012 - 2015 Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia
2009 - 2010 Screening for novel factors involved in nucleotide excision repair
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Papers (44):
Paula J. van der Meer, George Yakoub, Yuka Nakazawa, Tomoo Ogi, Martijn Luijsterburg. Clearance of DNA damage-arrested RNAPII is selectively impaired in Cockayne syndrome cells. 2024
Nakazawa Y, Oka Y, Matsunaga T, Ogi T. Transcription-coupled repair -mechanisms of action, regulation, and associated human disorders. FEBS Letters. 2024
Chikako Senju*, Yuka Nakazawa*, Taichi Oso*, Mayuko Shimada, Kana Kato, Michiko Matsuse, Mariko Tsujimoto, Taro Masaki, Yasushi Miyazaki, Satoshi Fukushima, et al. Deep intronic founder mutations identified in the ERCC4/XPF gene are potential therapeutic targets for a high-frequency form of xeroderma pigmentosum. PNAS (Proceedings of the National Academy of Sciences of the United States of America). 2023. 120. 27. e2217423120
Yasukazu Daigaku, Thomas Etheridge, Yuka Nakazawa, Tomoo Ogi, Antony Carr. Maintenance of unperturbed DNA replication by ubiquitylation of the replication sliding clamp. GENES & GENETIC SYSTEMS. 2016. 91. 6. 324-324
N. Jia, Y. Nakazawa, C. Guo, M. Shimada, M. Sethi, Y. Takahashi, H. Ueda, Y. Nagayama, T. Ogi. Click-iT DNA damage and repair assay. Assay and Drug Development Technologies. 2015. 13. 186-187
Nakazawa Yuka, Ogi Tomoo, Guo Chaowan, Shimada Mayuko, Jia Nan. P-011 XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency(Poster Sessions). 2015. 44. 98-98
Coordinated ubiquitination of RPB1-K1268 and UVSSA-K414 promotes transcription-coupled nucleotide excision repair
(日本放射線影響学会第64回大会 2021)
Alterations in the RNA polymerase IIo ubiquitination cause TC-NER defect and Cockayne syndrome-like premature aging phenotype in mice
(International Symposium on XP and other Nucleotide Excision Repair Disorders 2019)