http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2360745-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fdaa64756184e715af6cb25ebc318917
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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-71
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-71
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-04
filingDate 2000-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ed72e68a09b54a7f31d0aa5f4ad67eb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee6f464602bdacdbbd37976ede7d1b57
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5c5c04f7028c8990a1638ad584546a6
publicationDate 2000-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2360745-A1
titleOfInvention Screening assay for antagonists of fgfr-mediated malignant cell transformation and tumor formation
abstract In vitro and in vivo screening assays for antagonists of fibroblast growth factor receptor (FGFR)-mediated malignant cell transformation are provided using stable cell lines genetically engineered to express a recombinant wild type or constitutively active mutant FGFR selected from FGFR1, FGFR2 and FGFR3, the malignant potential of said cell lines being modulated by said FG FR.
priorityDate 1999-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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