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The NF1 Tumor Suppressor Critically Regulates TSC2 and mTOR

The NF1 Tumor Suppressor Critically Regulates TSC2 and mTOR

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_17356696

The NF1 Tumor Suppressor Critically Regulates TSC2 and mTOR

About this item

Full title

The NF1 Tumor Suppressor Critically Regulates TSC2 and mTOR

Publisher

United States: National Academy of Sciences

Journal title

Proceedings of the National Academy of Sciences - PNAS, 2005-06, Vol.102 (24), p.8573-8578

Language

English

Formats

Publication information

Publisher

United States: National Academy of Sciences

More information

Scope and Contents

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...

Alternative Titles

Full title

The NF1 Tumor Suppressor Critically Regulates TSC2 and mTOR

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_17356696

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_17356696

Other Identifiers

ISSN

0027-8424

E-ISSN

1091-6490

DOI

10.1073/pnas.0503224102

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