http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9970056-B2

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filingDate 2015-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_68575d8b916e0805640dcb29bddd170d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_09e477a0c4f37564bd67114d75b9c59e
publicationDate 2018-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9970056-B2
titleOfInvention Methods and kits for diagnosing, prognosing and monitoring parkinson's disease
abstract Network-based meta-analysis of four independent microarray studies identified the hepatocyte nuclear factor (HNF4A), a transcription factor associated with gluconeogenesis and diabetes, as a central regulatory hub gene upregulated in blood of PD patients. In parallel, the polypyrimidine tract binding protein 1 (PTBP1), involved in the stabilization and mRNA translation of insulin, was identified as the most downregulated gene. Using both markers, PD patients were classified with 90% sensitivity and 80% specificity. Longitudinal performance analysis demonstrated that relative abundance of HNF4A and PTBP1 mRNAs significantly decreased and increased, respectively, in PD patients during 3 years follow up period. The inverse regulation of HNF4A and PTBP1 provides a molecular rationale for the altered insulin signaling observed in PD patients. The longitudinally dynamic biomarkers identified in this study may be useful for monitoring disease-modifying therapies for PD.
priorityDate 2015-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 1559.