http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004018711-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_048f1afe2ab1cf8d53aeba1c0e224189
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_69df0c0b3d3d93288e5c810e2eb6797e
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2003-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_88d5479a303d5563e3d9858d03de9ffc
publicationDate 2004-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2004018711-A2
titleOfInvention Diagnostic test
abstract The present invention relates to the prognosis of patients suffering from cervical intraepithelial neoplasia (CIN). Accordingly, the invention provides methods for diagnosing the susceptibility of such a patient to persistence or progression of the CIN. In particular, the invention provides a method of diagnosing susceptibility to persistence or progression of cervical intraepithelial neoplasia (CIN) in an individual suffering therefrom; the method comprising: d) providing a sample of dyskaryotic cells from said individual and a sample of non-dyskaryotic cells from said individual; b) detecting an allelic deletion in one or more genes selected from FHIT, PR, DLEC 1 and TRIM 29 by comparing the FHIT, PR, DLEC 1 and/or TRIM 29 polynucleotides or proteins present in the samples of step a) derived, respectively, from the non-dyskaryotic and dyskaryotic sample, wherein detection of an allelic deletion between the non-dyskaryotic and dyskaryotic samples is correlated with a susceptibility to persistence or progression of CIN.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016046635-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2014098135-A1
priorityDate 2002-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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