| 摘要 |
Compounds of the form O-(x-L)n, where O is an oligonucleoside having at least a plurality of N3'->P5' thiophosphoramidate (NPS) internucleoside linkages, a conjugated lipid moiety L, and at least one G-rich sequence motif as described, are effective to morphologically alter and reduce adhesion of cancer cells.
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