Loss of neurofibromin Ras-GAP activity enhances the formation of cardiac blood islands in murine embryos
Type I neurofibromatosis (NF1) is caused by mutations in the NF1 gene encoding neurofibromin. Neurofibromin exhibits Ras GTPase activating protein (Ras-GAP) activity that is thought to mediate cellular functions relevant to disease phenotypes. Loss of murine Nf1 results in embryonic lethality due to...
Main Authors: | Amanda D Yzaguirre, Arun Padmanabhan, Eric D de Groh, Kurt A Engleka, Jun Li, Nancy A Speck, Jonathan A Epstein |
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Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2015-10-01
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Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/07780 |
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