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filingDate 2000-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-01-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0becbee7971744cbc930289073934921
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9824ed00d5bcf26bfaf71be4bc627005
publicationDate 2007-01-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7157436-B2
titleOfInvention Therapeutically useful synthetic oligonucleotides
abstract The present invention provides a composition and method comprising a 2–20 base 3′-OH, 5′-OH synthetic oligonucleotide (sequence) selected from the group consisting of (G x T y ) n , (T y G x ) n , a(G x T y ) n , a(T y G x ) n , (G x T y ) n b, (T y G x ) n b, a(G x T y ) n b, a(T y G x ) n b, wherein x and y is an integer between 1 and 7, n is an integer between 1 and 12, a and b are one or more As, Cs, Gs or Ts and wherein the sequence induces a response selected from the group consisting of induction of cell cycle arrest, inhibition of proliferation, activation of caspases and induction of apoptosis in cancer cells and production of cytokines by immune system cells.
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