Maruo Y - Search Results

1

Role of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia.

Fujiwara R, Maruo Y, Chen S, Tukey RH. Fujiwara R, et al. Among authors: maruo y. Toxicol Appl Pharmacol. 2015 Nov 15;289(1):124-32. doi: 10.1016/j.taap.2015.08.018. Epub 2015 Sep 2. Toxicol Appl Pharmacol. 2015. PMID: 26342858 Free PMC article. Review.

2

Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.

Maruo Y, Morioka Y, Fujito H, Nakahara S, Yanagi T, Matsui K, Mori A, Sato H, Tukey RH, Takeuchi Y. Maruo Y, et al. J Pediatr. 2014 Jul;165(1):36-41.e1. doi: 10.1016/j.jpeds.2014.01.060. Epub 2014 Mar 17. J Pediatr. 2014. PMID: 24650397 Free PMC article.

3

Intestinal UDP-Glucuronosyltransferase 1A1 and Protection against Irinotecan-Induced Toxicity in a Novel UDP-Glucuronosyltransferase 1A1 Tissue-Specific Humanized Mouse Model.

Mennillo E, Yang X, Weber AA, Maruo Y, Verreault M, Barbier O, Chen S, Tukey RH. Mennillo E, et al. Among authors: maruo y. Drug Metab Dispos. 2022 Jan;50(1):33-42. doi: 10.1124/dmd.121.000644. Epub 2021 Oct 25. Drug Metab Dispos. 2022. PMID: 34697081 Free PMC article.

4

Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.

Maruo Y, Nishizawa K, Sato H, Sawa H, Shimada M. Maruo Y, et al. Pediatrics. 2000 Nov;106(5):E59. doi: 10.1542/peds.106.5.e59. Pediatrics. 2000. PMID: 11061796

5

Effect of common exon variant (p.P364L) on drug glucuronidation by the human UDP-glucuronosyltransferase 1 family.

Mimura Y, Maruo Y, Ohta Y, Sato H, Takeuchi Y. Mimura Y, et al. Among authors: maruo y. Basic Clin Pharmacol Toxicol. 2011 Dec;109(6):486-93. doi: 10.1111/j.1742-7843.2011.00754.x. Epub 2011 Aug 18. Basic Clin Pharmacol Toxicol. 2011. PMID: 21726413 Free article.

6

Bilirubin Uridine Diphosphate-glucuronosyltransferase Polymorphism as a Risk Factor for Prolonged Hyperbilirubinemia in Japanese Preterm Infants.

Yanagi T, Nakahara S, Maruo Y. Yanagi T, et al. Among authors: maruo y. J Pediatr. 2017 Nov;190:159-162.e1. doi: 10.1016/j.jpeds.2017.07.014. Epub 2017 Sep 6. J Pediatr. 2017. PMID: 28888563

7

[UDP-glucuronosyltransferase].

Maruo Y, Sato H. Maruo Y, et al. Nihon Eiseigaku Zasshi. 2002 Jan;56(4):629-33. Nihon Eiseigaku Zasshi. 2002. PMID: 11868392 Review. Japanese.

8

Polymorphism of UDP-glucuronosyltransferase and drug metabolism.

Maruo Y, Iwai M, Mori A, Sato H, Takeuchi Y. Maruo Y, et al. Curr Drug Metab. 2005 Apr;6(2):91-9. doi: 10.2174/1389200053586064. Curr Drug Metab. 2005. PMID: 15853761 Review.

9

Inhibitory effect of 5β-pregnane-3α,20β-diol on transcriptional activity and enzyme activity of human bilirubin UDP-glucuronosyltransferase.

Ota Y, Maruo Y, Matsui K, Mimura Y, Sato H, Takeuchi Y. Ota Y, et al. Among authors: maruo y. Pediatr Res. 2011 Nov;70(5):453-7. doi: 10.1203/PDR.0b013e31822f242e. Pediatr Res. 2011. PMID: 21796020

10

Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism.

Maruo Y, Nishizawa K, Sato H, Doida Y, Shimada M. Maruo Y, et al. Pediatrics. 1999 Jun;103(6 Pt 1):1224-7. doi: 10.1542/peds.103.6.1224. Pediatrics. 1999. PMID: 10353933

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