Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese
- 1 May 2005
- journal article
- review article
- Published by Springer Science and Business Media LLC in Journal of Biomedical Science
- Vol. 12 (3), 445-450
- https://doi.org/10.1007/s11373-005-3863-5
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Polymorphisms of uridine-diphosphoglucuronosyltransferase 1A7 gene in Taiwan ChineseWorld Journal of Gastroenterology, 2005
- Risk Factors for Severe Hyperbilirubinemia in NeonatesPediatric Research, 2004
- High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1)Pharmacogenetics, 2004
- Polymorphisms of OATP-C (SLC21A6) and OAT3 (SLC22A8) genes: Consequences for pravastatin pharmacokineticsClinical Pharmacology & Therapeutics, 2003
- The Human Organic Anion Transport Protein SLC21A6 Is Not Sufficient for Bilirubin TransportPublished by Elsevier BV ,2003
- Genetic Polymorphisms of the UDP‐Glucuronosyltransferase 1A7 Gene and Irinotecan Toxicity in Japanese Cancer PatientsJapanese Journal of Cancer Research, 2002
- Polymorphisms in OATP-CPublished by Elsevier BV ,2001
- Hepatic Uptake of Bilirubin and Its Conjugates by the Human Organic Anion Transporter SLC21A6Journal of Biological Chemistry, 2001
- Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infantsAmerican Journal of Hematology, 1996
- Association between Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Jaundice: Interaction with Multiple Risk FactorsInternational Journal of Epidemiology, 1992