Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes-Reference-Cited by-同舟云学术

Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes

Published:2011-12-11 Issue:1 Volume:44 Page:53-57
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Graubert Timothy A,Shen Dong,Ding Li,Okeyo-Owuor Theresa,Lunn Cara L,Shao Jin,Krysiak Kilannin,Harris Christopher C,Koboldt Daniel C,Larson David E,McLellan Michael D,Dooling David J,Abbott Rachel M,Fulton Robert S,Schmidt Heather,Kalicki-Veizer Joelle,O'Laughlin Michelle,Grillot Marcus,Baty Jack,Heath Sharon,Frater John L,Nasim Talat,Link Daniel C,Tomasson Michael H,Westervelt Peter,DiPersio John F,Mardis Elaine R,Ley Timothy J,Wilson Richard K,Walter Matthew J

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.1031.pdf

Reference47 articles.

1. Webb, C.J. & Wise, J.A. The splicing factor U2AF small subunit is functionally conserved between fission yeast and humans. Mol. Cell. Biol. 24, 4229–4240 (2004).

2. Wu, S., Romfo, C.M., Nilsen, T.W. & Green, M.R. Functional recognition of the 3′ splice site AG by the splicing factor U2AF35. Nature 402, 832–835 (1999).

3. Welch, J.S. et al. Use of whole-genome sequencing to diagnose a cryptic fusion oncogene. J. Am. Med. Assoc. 305, 1577–1584 (2011).

4. Mardis, E.R. et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N. Engl. J. Med. 361, 1058–1066 (2009).

5. Link, D.C. et al. Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML. J. Am. Med. Assoc. 305, 1568–1576 (2011).

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