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Volumn 3, Issue 108, 2010, Pages

ARD1 stabilization of TSC2 suppresses tumorigenesis through the mTOR signaling pathway

(21)  Kuo, Hsu Ping a,b   Lee, Dung Fang a,b   Chen, Chun Te a,b   Liu, Mo a,b   Chou, Chao Kai a,b   Lee, Hong Jen a,b   Du, Yi a,b   Xie, Xiaoming a,c   Wei, Yongkun a   Xia, Weiya a   Weihua, Zhang d   Yang, Jer Yen a,b   Yen, Chia Jui a   Huang, Tzu Hsuan a   Tan, Minjia e   Xing, Gang f   Zhao, Yingming e,f   Lin, Chien Hsing g   Tsai, Shih Feng g   Fidler, Isaiah J b,d   more..


Author keywords

[No Author keywords available]

Indexed keywords

ARREST DEFECTIVE PROTEIN 1; CELL PROTEIN; MAMMALIAN TARGET OF RAPAMYCIN; TUBERIN; UNCLASSIFIED DRUG; ACYLTRANSFERASE; ARD1A PROTEIN, HUMAN; SMALL INTERFERING RNA; TUMOR SUPPRESSOR PROTEIN;

EID: 77951643083     PISSN: 19450877     EISSN: 19379145     Source Type: Journal    
DOI: 10.1126/scisignal.2000590     Document Type: Article
Times cited : (92)

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    • Acknowledgments: We thank D. J. Kwiatkowski, J. Blenis, and K.-L. Guan for providing the cells and constructs; S. Zhang, J. Shi, B. Spohn, J.-F. Lee, Z. Han, H.-W. Yeh, T.-L. Liao, Y.-H. Chang, and K. Dunner Jr., for their technical support; The University of Texas M. D. Anderson Cancer Center MDACC Institutional Core Grant CA16672 High Resolution Electron Microscopy facility for electron microscopy analysis; The University of Texas MDACC DNA Core Facility for fluorescent DNA fragment analysis; and the Department of Scientific Publications at M. D. Anderson for editing this manuscript. This work was partially supported by NIH grants R01 CA109311, CCSG CA16672, and P01 CA099031
    • Acknowledgments: We thank D. J. Kwiatkowski, J. Blenis, and K.-L. Guan for providing the cells and constructs; S. Zhang, J. Shi, B. Spohn, J.-F. Lee, Z. Han, H.-W. Yeh, T.-L. Liao, Y.-H. Chang, and K. Dunner Jr., for their technical support; The University of Texas M. D. Anderson Cancer Center (MDACC) Institutional Core Grant CA16672 High Resolution Electron Microscopy facility for electron microscopy analysis; The University of Texas MDACC DNA Core Facility for fluorescent DNA fragment analysis; and the Department of Scientific Publications at M. D. Anderson for editing this manuscript. This work was partially supported by NIH grants R01 CA109311, CCSG CA16672, and P01 CA099031; M. D. Anderson Specialized Programs of Research Excellence grants (P50 CA116199 for breast Cancer and P50 CA83639 for ovarian cancer), MDACC-China Medical University and Hospital Sister Institution Fund, Patel Memorial Breast Cancer Endowment Fund, and grants from the Kadoorie Charitable Foundations, the National Breast Cancer Foundation, Inc., and Taiwan National Science Council (NSC-96-3111-B) to M.-C. H.; a grant R01 CA126832 to Y. Z.; a predoctoral fellowship from the U. S. Army Breast Cancer Research Program (grant W81XWH-08-1-0397), and the Andrew Sowell-Wade Huggins Scholarship from the University of Texas Graduate School of Biomedical Sciences at Houston to H.-P. K.; a predoctoral fellowship from the U. S. Army Breast Cancer Research Program (grant W81XWH-05-1-0252) and the T. C. Hsu Endowed Memorial Scholarship, Andrew Sowell-Wade Huggins Scholarship and Presidents' Research Scholarship from the University of Texas Graduate School of Biomedical Sciences at Houston to D.-F. L.; a predoctoral fellowship from the U. S. Army Breast Cancer Research Program (grant W81XWH-06-1-0709) to C.-K. C.; and a research assistant scholarship from the University of Texas Graduate School of Biomedical Sciences at Houston to M. L.


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