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Title
Assessment of SLX4 Mutations in Hereditary Breast Cancers
Authors
Keywords
Breast cancer, Genetic causes of cancer, Mutation detection, Point mutation, Cultured fibroblasts, Mutation, DNA repair, Fibroblasts
Journal
PLoS One
Volume 8, Issue 6, Pages e66961
Publisher
Public Library of Science (PLoS)
Online
2013-06-27
DOI
10.1371/journal.pone.0066961
References
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Related references
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- (2011) Rosa Landwehr et al. BREAST CANCER RESEARCH AND TREATMENT
- Ubiquitylation and the Fanconi anemia pathway
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- SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype
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- Mammalian BTBD12/SLX4 Assembles A Holliday Junction Resolvase and Is Required for DNA Repair
- (2009) Jennifer M. Svendsen et al. CELL
- Human SLX4 Is a Holliday Junction Resolvase Subunit that Binds Multiple DNA Repair/Recombination Endonucleases
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- Coordination of Structure-Specific Nucleases by Human SLX4/BTBD12 Is Required for DNA Repair
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- The Fanconi Anemia Pathway Promotes Replication-Dependent DNA Interstrand Cross-Link Repair
- (2009) P. Knipscheer et al. SCIENCE
- Genetic Predisposition to Breast Cancer: Past, Present, and Future
- (2008) Clare Turnbull et al. Annual Review of Genomics and Human Genetics
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