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The neurofibromin GAP-related domain rescues endothelial but not neural crest development in Nf1(–/–) mice

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–GTPas...

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Detalhes bibliográficos
Main Authors: Ismat, Fraz A., Xu, Junwang, Lu, Min Min, Epstein, Jonathan A.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2006
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1533876/
https://ncbi.nlm.nih.gov/pubmed/16906226
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI28341
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