WordNet

the 21st letter of the Roman alphabet (同)u
any of various enzymes that move a chemical group from one compound to another compound
an orange-yellow pigment in the bile that forms as a product of hemoglobin; excess amounts in the blood produce the yellow appearance observed in jaundice (同)hematoidin, haematoidin

PrepTutorEJDIC

uraniumの化学記号
上流の,上流階級にふさわしい / (映画が)児童観覧用の

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1. ビリルビン代謝 bilirubin metabolism
2. ビリルビン過剰産生によるジルベール症候群および非抱合型ビリルビン過剰産生 gilbert syndrome and unconjugated hyperbilirubinemia due to bilirubin overproduction
3. 血清ビリルビン定量の臨床的側面 clinical aspects of serum bilirubin determination
4. 肝胆道の異常を有するHIV感染患者の評価 evaluation of the hiv infected patient with hepatobiliary complaints
5. 黄疸または無症候性高ビリルビン血症の分類および原因 classification and causes of jaundice or asymptomatic hyperbilirubinemia

English Journal

Non tumoral hyperserotoninaemia responsive to octreotide due to dual polymorphism in UGT1A1 and UGT1A6.

Maladaki A, Yavropoulou MP, Kotsa K, Tranga T, Ventis S, Yovos JG.SourceDivision of Endocrinology and Metabolism, 1st Internal Medicine Department, AHEPA University Hospital, Aristotle University of Thessaloniki, Greece. ann.malad@hotmail.com
Hormones (Athens, Greece).Hormones (Athens).2012 Jan-Mar;11(1):104-8.
Gilbert's syndrome is a common inherited metabolic disorder, caused by genetic aberration in the enzyme UDP-glucuronosyl-transferase 1A1 that leads to reduced glucuronidation of bilirubin. Recent advances in molecular genetics have frequently reported the concurrence of dual genetic polymorphisms in
PMID 22450351

The relationship between UGT1A4 polymorphism and serum concentration of lamotrigine in patients with epilepsy.

Gulcebi MI, Ozkaynakcı A, Goren MZ, Aker RG, Ozkara C, Onat FY.SourceDepartment of Pharmacology, School of Medicine, University of Marmara, Istanbul, Turkey. mgfarma@gmail.com
Epilepsy research.Epilepsy Res.2011 Jun;95(1-2):1-8. Epub 2011 May 20.
Lamotrigine (LTG) which has a widespread use in epilepsy treatment as an antiepileptic agent is metabolized by UDP-glucuronosyl transferase (UGT) enzymes. In this study, single nucleotide polymorphisms, P24T and L48V, of the UGT1A4 enzyme have been investigated in a Turkish population of patients wi
PMID 21601426

Japanese Journal

Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyl transferase

KOIWAI O
Hum. Mol. Genet. 4, 1183-1186, 1995
NAID 30024453261

A new type of genetic defect of bilirubin UDP-glucuronosyl-transferase gene in a patient with Crigler-Najjar syndrome type I : Abstracts of Papers Presented at the Thirty-Third Annual Meeting of the Japanese Teratology Society Nagoya, Japan, July 21-23, 1993

AONO S.,YAMADA Y.,KEIN H.,SASAOKA Y.,NAKAGAWA T.,YAZAWA T.,MIMURA S.,KOIWAI O.,SATO H.
Congenital anomalies 33(3), 293, 1993-09-30
NAID 110002787331

Comparison of UDP-Glucuronosyl Transferase Activities between Gunn and Wistar Rats which have Genetic Deficiency in Bilirubin and Androsterone Glucuronidation

共立薬科大学研究年報 32, 122-123, 1987-03-25
NAID 110000058948

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Heme Degradation and Jaundice UDP-Glucuronosyl Transferase 1A1: Genetic Music glucuronyl transferase and conjugation of bili | Exam study, Board exam, Pediatrics Glucuronidation of Antiallergic Drug, Tranilast: Identification of Human UDP Glucuronide formation - Metabolic Activation Glucuronosyltransferase; Glucuronyltransferase; UDP Glucuronosyltransferase Schematic representation of bilirubin biliary elimination pathway and | Download