The identification of FANCD2 DNA binding domains reveals nuclear localization sequences-Reference-Cited by-同舟云学术

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The identification of FANCD2 DNA binding domains reveals nuclear localization sequences

Published:2017-06-28 Issue:14 Volume:45 Page:8341-8357
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Niraj Joshi,Caron Marie-Christine,Drapeau Karine,Bérubé Stéphanie,Guitton-Sert Laure,Coulombe Yan,Couturier Anthony M.,Masson Jean-Yves

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/45/14/8341/22894836/gkx543.pdf

Reference46 articles.

1. Fanconi anaemia and the repair of Watson and Crick DNA crosslinks;Nature,2013

2. How the fanconi anemia pathway guards the genome;Annu. Rev. Genet.,2009

3. Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype;Cancer Discov.,2015

4. Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia;Am. J. Hum. Genet.,2013

5. Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia;Am. J. Hum. Genet.,2013

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2. Multiple cancers escape from multiple MAPK pathway inhibitors and use DNA replication stress signaling to tolerate aberrant cell cycles;Science Signaling;2023-08

3. FANCD2 and RAD51 recombinase directly inhibit DNA2 nuclease at stalled replication forks and FANCD2 acts as a novel RAD51 mediator in strand exchange to promote genome stability;Nucleic Acids Research;2023-08-01

4. Multiple cancer types rapidly escape from multiple MAPK inhibitors to generate mutagenesis-prone subpopulations;2023-03-21

5. Fanconi anemia: current insights regarding epidemiology, cancer, and DNA repair;Human Genetics;2022-05-21

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