Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects-Reference-Cited by-同舟云学术

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

Published:2008-07-20 Issue:8 Volume:40 Page:963-970
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

McGowan Kelly A,Li Jun Z,Park Christopher Y,Beaudry Veronica,Tabor Holly K,Sabnis Amit J,Zhang Weibin,Fuchs Helmut,de Angelis Martin Hrabé,Myers Richard M,Attardi Laura D,Barsh Gregory S

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.188.pdf

Reference50 articles.

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3. Oliver, E.R., Saunders, T.L., Tarle, S.A. & Glaser, T. Ribosomal protein L24 defect in belly spot and tail (Bst), a mouse Minute. Development 131, 3907–3920 (2004).

4. Draptchinskaia, N. et al. The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nat. Genet. 21, 169–175 (1999).

5. Cmejla, R., Cmejlova, J., Handrkova, H., Petrak, J. & Pospisilova, D. Ribosomal protein S17 gene (RPS17) is mutated in Diamond-Blackfan anemia. Hum. Mutat. 28, 1178–1182 (2007).

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