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The PCR products were eluted from the gels, amplified, and subcloned into pCRTM2.1 (Invitrogen). Recombinant plasmids were sequenced by the dideoxy chain termination method, with a Sequenase DNA sequencing kit (United States Biochemical). DNA was also reamplified and purified with QIAquick PCR purification kit (Qiagen) and sequenced with the ABI PRISMTM dye terminator cycle sequencing kit (Perkin-Elmer). The DNA sequences obtained by the two methods were identical.
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-. The properties of a subset of these tumors, were described in (1).
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1842302777
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We thank D. Casacuberta for comments on the manuscript and G. Wahl for his gift of the CAL51 cell line. Supported by NIH grants CA63585 and CA38579. H.Y. is a postdoctoral fellow from the Japan Society for the Promotion of Science.
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