Characteristics of the heme catabolic pathway in mild unconjugated hyperbilirubinemia and their associations with inflammation and disease prevention
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-00933-y.pdf
Reference72 articles.
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3. Barbarino, J. M., Haidar, C. E., Klein, T. E. & Altman, R. B. PharmGKB summary: very important pharmacogene information for UGT1A1. Pharmacogenet. Genomics 24, 177–183 (2014).
4. AlFadhli, S., Al-Jafer, H., Hadi, M., Al-Mutairi, M. & Nizam, R. The Effect of UGT1A1 Promoter Polymorphism in the Development of Hyperbilirubinemia and Cholelithiasis in Hemoglobinopathy Patients. PLoS One 8, e77681 (2013).
5. Strassburg, C. P., Lankisch, T. O., Manns, M. P. & Ehmer, U. Family 1 uridine-5′-diphosphate glucuronosyltransferases (UGT1A): from Gilbert’s syndrome to genetic organization and variability. Arch. Toxicol. 82, 415–433 (2008).
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