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A new class of cancer-associated PTEN mutations defined by membrane translocation defects

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Year: 2014
Type: article
Source: Oncogene
DOI: 10.1038/onc.2014.293
Authors: H-N Nguyen, J-M Yang Jr, M Rahdar, M Keniry, K F Swaney, R Parsons, B H Park, H Sesaki, P N Devreotes, M Iijima
Institutions: Johns Hopkins University, Johns Hopkins Medicine, Icahn School of Medicine at Mount Sinai, Sidney Kimmel Comprehensive Cancer Center
Language: English

Topic: PI3K/AKT/mTOR signaling in cancer
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green

Funders: National Cancer Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke
Awards: G1162449006, G1596605663, G1796279050, Mitochondrial Fusion and Division, Biochemistry, Cellular and Molecular Biology Program, PTEN Tumor Suppressor and Signal Transduction, Signaling Networks in Chemotaxis and Cytokinesis, G617783802, G638208998, G6454624259, Temporal and Spatial Signaling in Chemotaxis, Lipid Signaling in Chemotaxis, Introducing Mitochondrial Stasis in Neurons, Mutual Regulation of PTEN and P-REX2a in Normal and Cancer Cells, G-Protein Linked Signaling Pathways in Chemotaxis, G861814160
OpenAlex ID: W2128328834
FWCI: 1.503
Cites: 34
Cited by: 38
Related to: 10
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