Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype-Reference-Cited by-同舟云学术

Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype

Published:2007-08-19 Issue:9 Volume:39 Page:1120-1126
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Brems Hilde,Chmara Magdalena,Sahbatou Mourad,Denayer Ellen,Taniguchi Koji,Kato Reiko,Somers Riet,Messiaen Ludwine,De Schepper Sofie,Fryns Jean-Pierre,Cools Jan,Marynen Peter,Thomas Gilles,Yoshimura Akihiko,Legius Eric

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng2113.pdf

Reference26 articles.

1. Bundschu, K., Walter, U. & Schuh, K. The VASP-Spred-Sprouty domain puzzle. J. Biol. Chem. 281, 36477–36481 (2006).

2. Wakioka, T. et al. Spred is a Sprouty-related suppressor of Ras signalling. Nature 412, 647–651 (2001).

3. Shannon, K. & Bollag, G. Sending out an SOS. Nat. Genet. 39, 8–9 (2007).

4. Bentires-Alj, M., Kontaridis, M.I. & Neel, B.G. Stops along the RAS pathway in human genetic disease. Nat. Med. 12, 283–285 (2006).

5. Legius, E., Marchuk, D.A., Collins, F.S. & Glover, T.W. Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis. Nat. Genet. 3, 122–126 (1993).

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