http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2107915-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-00
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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-00
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filingDate 1992-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_558aca2ebe32ca1f2151519f4e45ea8b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_927aa65ec459e7fcd67d48ab30fe4e15
publicationDate 1992-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2107915-A1
titleOfInvention Antisense oligonucleotides to c-kit proto-oncogene and uses thereof
abstract Oligonucleotides are provided having a nucleotide sequence complementary to at least a portion of the mRNA transcript of the human c-kit gene. These "antisense" oligonucleotides are hybridizable to the c-kit mRNA transcript. Such oligonucleotides are useful in selectively inhibiting proliferation of erythroid cells, particularly in disorders characterized by an elevated hematocrit due to overproduction of erythrocytes. The antisense oligomers also have activity agent hematologic neoplastic cells and are therefore suitable as bone marrow purging agents.
priorityDate 1991-05-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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