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Volumn 303, Issue 5659, 2004, Pages 844-848

In Vivo Activation of the p53 Pathway by Small-Molecule Antagonists of MDM2

Author keywords

[No Author keywords available]

Indexed keywords

CRYSTAL STRUCTURE; GROWTH KINETICS; ONCOLOGY; TUMORS;

EID: 10744221485     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.1092472     Document Type: Article
Times cited : (4062)

References (31)
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    • note
    • Cells with mutant pS3 accumulate high levels of transcriptionally inactive protein as a result of their inability to up-regulate MDM2 transcription.
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    • unpublished data
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    • note
    • Materials and methods are available as supporting material on Science Online.
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    • note
    • 50 for two mutant p53 lines (SW480 and MDA-MB-43S) and that for three wild-type p53 lines (HCT116, RKO, and SJSA-1). The compounds reported here showed selectivity in the 11 to 18 range.
  • 29
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    • note
    • A deletion construct of human p53 (p53C312) covering the N-terminal binding site and the central DNA binding domain (residues 1 to 312) but lacking the C-terminal tetramerization domain was used for Biacore binding studies.
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    • note
    • We thank C. Tovar, G. Kaplan, K. Dillon, A. Specian, A. Schutt, C.-M. Liu, B. Felix, Q. Xiang, R. Margolis, W. Qing, K. Frank, H. Butscher, and F. Hesse for providing reagents and experimental help; and D. Emerson, D. Fry, S.-S. So, J. Tilley, J. Roberts, D. Presky, H.-J. Mueller, G. Ju, D. Walker, L. Babiss, and D. Heimbrook for discussions. Coordinates are available from the Protein Data Bank with accession code 1RV1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.