Article
The neurofibromin GAP-related domain rescues endothelial but not neural crest development in Nf1 mice.
The Journal of clinical investigation - 1 Sept 2006
Ismat Fraz A, Xu Junwang, Lu Min Min, Epstein Jonathan A
Abstract excerpt
Neurofibromatosis type I (NF1; also known as von Recklinghausen's disease) is a common autosomal-dominant condition primarily affecting neural crest-derived tissues. The disease gene, NF1, encodes neurofibromin, a protein of over 2,800 amino acids that contains a 216-amino acid domain with Ras-GTPase-activating protein (Ras-GAP) activity. Potential therapies for NF1 currently in development and being tested in...
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