Associated Papers
Clinically observed RASA1 missense mutants exhibit diverse RasGAP protein behaviors.
Paul ME et al.
Biorxiv : the Preprint Server for Biology, 2025
41256670 (PubMed )
Supplement: media-1.pdf
EphrinB2-EphB4-RASA1 Signaling in Human Cerebrovascular Development and Disease.
Zeng X et al.
Trends in Molecular Medicine, 2019
Structure-energy-based predictions and network modelling of RASopathy and cancer missense mutations.
Kiel C et al.
Molecular Systems Biology, 2014
24803665 (PubMed )
Supplement: MSB-10-5-727-s13.xls › energies
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformation.
Revencu N et al.
Human Mutation, 2013
Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations.
Revencu N et al.
Human Mutation, 2008
Select a paper to view details