http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004532046-A

Outgoing Links

Predicate Object
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2310-12
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-1135
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K48-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2002-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2004-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2004532046-A
titleOfInvention bcl-2 DNAzyme
abstract The present invention specifically provides mRNA transcribed from a member of bcl-2 selected from the group consisting of bcl-2, bcl-xl, bcl-w, bfl-1, brag-1, Mcl-1 and A1. Provide a DNAzyme to cut. The DNAzyme has (a) the nucleotide sequence GGCTAGCTACAACGA (SEQ ID NO: 1), a catalytic domain that cleaves mRNA at any targeted purine: pyrimidine cleavage site, and (b) flanks the 5 'end of the catalytic domain. A binding domain, and (c) another binding domain adjacent to the 3 'end of the catalytic domain, both binding domains of the cleavage site to be catalyzed by the DNAzyme in the mRNA of the bcl-2 gene family. Hybridizes to and complementary to two regions adjacent to purine residues, wherein each binding domain is at least 6 nucleotides in length, and both binding domains are at least 14 nucleotides in total .
priorityDate 2001-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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