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- W2036716410 endingPage "19" @default.
- W2036716410 startingPage "11" @default.
- W2036716410 abstract "The capacity to maintain genomic integrity is shared by all living organisms. Multiple pathways are distinguished that safeguard genomic stability, most of which have originated in primitive life forms. In human individuals, defects in these pathways are typically associated with cancer proneness. The Fanconi anemia pathway, one of these pathways, has evolved relatively late during evolution and exists - in its fully developed form - only in vertebrates. This pathway, in which thus far 13 distinct proteins have been shown to participate, appears essential for error-free DNA replication. Inactivating mutations in the corresponding genes underlie the recessive disease Fanconi anemia (FA). In the last decade the genetic basis of this disorder has been uncovered by a variety of approaches, including complementation cloning, genetic linkage analysis and protein association studies. Here we review these approaches, introduce the encoded proteins, and discuss their possible role in ensuring genomic integrity." @default.
- W2036716410 created "2016-06-24" @default.
- W2036716410 creator A5030281855 @default.
- W2036716410 creator A5048187845 @default.
- W2036716410 date "2009-07-01" @default.
- W2036716410 modified "2023-10-18" @default.
- W2036716410 title "The genetic and molecular basis of Fanconi anemia" @default.
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