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Chest|May 11, 2019
A Prospective Cohort Study to Define the Clinical Features and Outcome of Lung Cancers Harboring HER2 Aberration in Japan (HER2-CS STUDY)Kiichiro Ninomiya, Tae Hata, Hiroshige Yoshioka, et al.
Nucleic Acids Research|June 1, 2013
A novel interplay between the Fanconi anemia core complex and ATR-ATRIP kinase during DNA cross-link repairJunya Tomida, Akiko Itaya, Tomoko Shigechi, et al.
Nucleic Acids Research|February 3, 2018
Replication stress induces accumulation of FANCD2 at central region of large fragile genesYusuke Okamoto, Watal M Iwasaki, Kazuto Kugou, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|August 3, 2019
Rapid Acquisition of Alectinib Resistance in ALK-Positive Lung Cancer With High Tumor Mutation BurdenGo Makimoto, Kadoaki Ohashi, Shuta Tomida, et al.
Molecular Cell|June 19, 2012
A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair networkZhijiang Yan, Rong Guo, Manikandan Paramasivam, et al.
The EMBO Journal|March 31, 2007
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathwayChen Ling, Masamichi Ishiai, Abdullah Mahmood Ali, et al.
Journal of Clinical Immunology|May 12, 2017
Common Variable Immunodeficiency Caused by FANC MutationsYujin Sekinaka, Noriko Mitsuiki, Kohsuke Imai, et al.
Cancer Medicine|November 8, 2022
Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2-mutation carriersTomoharu Mori, Yusuke Okamoto, Anfeng Mu, et al.
Cancer Research|December 17, 2005
Multiple repair pathways mediate tolerance to chemotherapeutic cross-linking agents in vertebrate cellsKuniharu Nojima, Helfrid Hochegger, Alihossein Saberi, et al.
Human Mutation|September 13, 2019
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in IndiaFrank X Donovan, Avani Solanki, Minako Mori, et al.
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