SOS1 mutations are rare in human malignancies: Implications for Noonan syndrome patients
Year: 2007
Type: article
Study design: Observational Study
Source: Genes Chromosomes and Cancer
DOI: 10.1002/gcc.20527
Authors: Kenneth D. Swanson, Jordan M. Winter, Marcelo Reis, Mohamed Bentires‐Alj, Heidi Greulich, Rupinder Grewal, Ralph H. Hruban, Charles J. Yeo, Yosuf Yassin, Oleg Iartchouk, Kate Montgomery, Susan P. Whitman, Michael A. Caligiuri, Mignon L. Loh, D. Gary Gilliland, A. Thomas Look, Raju Kucherlapati, Scott E. Kern, Matthew Meyerson, Benjamin G. Neel
Institutions: Beth Israel Deaconess Medical Center, Harvard University, Johns Hopkins University, Sidney Kimmel Comprehensive Cancer Center, Broad Institute, Dana-Farber Cancer Institute, Johns Hopkins Medicine, Thomas Jefferson University, The Ohio State University, University of California, San Francisco, Brigham and Women's Hospital
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
Awards: G1722823168, Inhibitor-sensitive and -resistant EGFR mutants from lung cancer and glioblastoma, G2203245522, Ras Pathway Mutations in Human Leukemia, Signal Transduction by Non-transmembrane PTPs, Comparative Genetics of the DiGeorge Syndrome Gene TBX1, New Approaches to the Biology and Treatment of Myelodysplastic Syndromes (MDS), G5267616762, G5296533023, Mouse Models for Human Cancer, SPORE in Gastrointestinal Cancers, Clinical and Laboratory Research Training for Gastrointestinal Surgeons, Cancer Center Support Grant, G970037175
OpenAlex ID: W2006564538