The NF1 Tumor Suppressor Critically Regulates TSC2 and mTOR
The NF1 Tumor Suppressor Critically Regulates TSC2 and mTOR
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United States: National Academy of Sciences
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Language
English
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Publisher
United States: National Academy of Sciences
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Contents
Loss-of-function mutations in the NF1 tumor suppressor gene underlie the familial cancer syndrome neurofibromatosis type I (NF1). The NF1-encoded protein, neurofibromin, functions as a Ras-GTPase activating protein (RasGAP). Accordingly, deregulation of Ras is thought to contribute to NF1 development. However, the critical effector pathways involve...
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Full title
The NF1 Tumor Suppressor Critically Regulates TSC2 and mTOR
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TN_cdi_proquest_miscellaneous_17356696
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_17356696
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ISSN
0027-8424
E-ISSN
1091-6490
DOI
10.1073/pnas.0503224102