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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 1988-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e08d82899ae0806ec5e8d18c56d7cb24
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publicationDate 1992-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5087559-A
titleOfInvention Method of detecting single base substitutions in nucleic acids
abstract A method for detecting point mutations or base substitutions in a nucleic acid polymer is especially useful for detecting such mutations in the highest melting domain (HMD) of a double-stranded nucleic acid polymer and is particularly suited for use with RNA. The method involves the steps of: (a) preparing a solution containing a double-stranded nucleic acid polymer comprising a duplex of a single-stranded nucleic acid polymer to be analyzed and a complementary portion of a corresponding wild-type nucleic acid polymer; (b) placing an aliquot of the solution of the double-stranded nucleic acid polymer into each of a series of containers having a range of denaturing conditions, said series including at least one container in which the denaturing conditions are such that a mismatched nucleic acid duplex having one or more base-pair mismatches within its HMD would be denatured to single-stranded nucleic acid polymers, but in which a perfectly matched nucleic acid duplex having no base-pair mismatches within its HMD would not be so denatured; and (c) comparing the occurrence of single stranded nucleic acids in each container after incubation with a standard.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9521268-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5633129-A
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Total number of triples: 28.