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dc.contributor.authorKlai Upsorn Pongrapeepornen_US
dc.contributor.authorWattana Leowattanaen_US
dc.contributor.authorWilairat Nuchpramoolen_US
dc.contributor.authorKwandoa Kerdsaengen_US
dc.contributor.authorPikun Thepsuriyanonen_US
dc.contributor.authorSudcharee Kiartivichen_US
dc.contributor.authorPreyanuj Yamwongen_US
dc.contributor.authorSompong Ong-Ajyoothen_US
dc.contributor.authorAnchalee Amornrattanaen_US
dc.contributor.authorLumpoon Kasemsuken_US
dc.contributor.authorSivadee Laungsuwanen_US
dc.contributor.authorKosit Sribhenen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherAmersham Pharmacia Biotech.en_US
dc.date.accessioned2018-09-07T09:44:22Z-
dc.date.available2018-09-07T09:44:22Z-
dc.date.issued2001-12-01en_US
dc.identifier.citationJournal of the Medical Association of Thailand. Vol.84, No.SUPPL. 3 (2001)en_US
dc.identifier.issn01252208en_US
dc.identifier.other2-s2.0-0035749842en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035749842&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/26649-
dc.description.abstractPrimary hypercholesterolemia includes both monogenic disorders and polygenic conditions. Two well defined monogenic disorders are familial hypercholesterolemia (FH) and familial defective apolipoprotein (apo) B-100 (FDB). Both disorders convey high risk of premature coronary artery disease. FH and FDB are caused by mutations in LDL receptor and apo B-100 genes, respectively. In the present study, mutations in both genes in Thai subjects with primary hyper-cholesterolemia were screened. For apo B-100 gene, a common mutation R3500Q was screened. This mutation was not observed in the patients (n = 45). For LDL receptor gene, mutations in the exons encoding the ligand - binding domain were screened. By PCR-CFLP analysis, 18 abnormal CFLP patterns in exon 4, the hot spot for mutations, were found in patients (n=45). One of the DNA samples with abnormal CFLP patterns was previously identified and reported as a possible disease-causing mutation, namely D151Y. For the other exons, the screening technique was PCR-SSCP. Abnormal SSCP patterns in DNA samples from patients (n=20) were found as follows, two in exon 3, one in exon 5 and another one in exon 6. Further characterization by DNA sequencing and family studies for these abnormal patterns are underway.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0035749842&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleScreening for mutations in exons encoding the ligand-binding domain of the LDL receptor gene using PCR-CFLP and PCR-SSCPen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
Appears in Collections:Scopus 2001-2005

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