http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006183122-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1f9b478edbf085cabed49823c5f856a4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1a89990807c796b76293a8e166e028c2
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-106
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6886
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-47
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filingDate 2003-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e403b493dcacc7c97c8499e81147f85
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03581bd86f4b4d0d37127264d54cce6a
publicationDate 2006-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2006183122-A1
titleOfInvention Fanc gene mutations in cancer
abstract The present invention relates to methods of determining if a patient has cancer or is at increased risk of developing cancer, particularly pancreatic cancer, the method comprising testing a FANC gene for the presence of a cancer-associated coding change, wherein said presence of one or more cancer-associated coding changes is indicative of cancer or an increased risk of cancer in said patient. The invention further relates to methods of treating a patient having cancer, particularly pancreatic cancer, who has one or more cancer-associated coding changes in the FANC genes comprising the step of administering a therapeutically effective amount of a chemotherapeutic cross-linking agent.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016049286-A1
priorityDate 2002-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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