http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101018960-B1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-186
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-573
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-576
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-573
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-569
filingDate 2009-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2011-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101018960-B1
titleOfInvention Analytical Methods for Significant Liver Fibrosis Diagnosis
abstract The present invention provides the information necessary for the diagnosis of significant liver fibrosis, the concentration of gamma-glutamyl transferase, the concentration of matrix metalloproteinase 2, the metalloproteinase from the patient's sample. Provides an analytical method for diagnosing significant liver fibrosis by measuring the concentration of tissue inhibitor 1, α2-macroglobulin, and haptoglobin in a newly designed scoring system, i. do.n n n According to the present invention, gamma-glutamyl transferase, matrix metalloproteinase 2, tissue inhibitors of metalloproteinase 1, α2-macroglobulin, and haptoggle as serum markers for the diagnosis of significant liver fibrosis Robin was found to be a significant variable, and the scoring system devised using it can be used to diagnose significant liver fibrosis with good diagnostic accuracy. Therefore, the analysis method according to the present invention can be usefully used to diagnose significant hepatic fibrosis in patients with chronic liver disease, including hepatitis B viral liver disease or hepatitis C viral liver disease.n n n n Liver fibrosis
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102346672-B1
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priorityDate 2009-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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