Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome–associated Sos1 mutation-Reference-Cited by-同舟云学术

Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome–associated Sos1 mutation

Published:2010-12-01 Issue:12 Volume:120 Page:4353-4365
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Chen Peng-Chieh,Wakimoto Hiroko,Conner David,Araki Toshiyuki,Yuan Tao,Roberts Amy,Seidman Christine E.,Bronson Roderick,Neel Benjamin G.,Seidman Jonathan G.,Kucherlapati Raju

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference64 articles.

1. The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation

2. Noonan syndrome

3. Malignant Diseases in Noonan Syndrome and Related Disorders

4. Duchenne Muscular Dystrophy and Concomitant Metastatic Alveolar Rhabdomyosarcoma

5. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

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