Mammal-restricted elements predispose human RET to folding impairment by HSCR mutations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Structural Biology
Link
http://www.nature.com/articles/nsmb.1808.pdf
Reference39 articles.
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2. Veiga-Fernandes, H. et al. Tyrosine kinase receptor RET is a key regulator of Peyer's patch organogenesis. Nature 446, 547–551 (2007).
3. Edery, P. et al. Mutations of the RET proto-oncogene in Hirschsprung's disease. Nature 367, 378–380 (1994).
4. Skinner, M.A., Safford, S.D., Reeves, J.G., Jackson, M.E. & Freemerman, A.J. Renal aplasia in humans is associated with RET mutations. Am. J. Hum. Genet. 82, 344–351 (2008).
5. Parkash, V. et al. The structure of the glial cell line-derived neurotrophic factor-coreceptor complex: insights into RET signalling and heparin binding. J. Biol. Chem. 283, 35164–35172 (2008).
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