Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II
about
Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotypeSpectrum of UGT1A1 Variations in Chinese Patients with Crigler-Najjar Syndrome Type IIGenetic variations and haplotype diversity of the UGT1 gene cluster in the Chinese populationUnconjugated Bilirubin exerts Pro-Apoptotic Effect on Platelets via p38-MAPK activationMolecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type IPazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGT1A1 polymorphism.Pharmacogenetics research on chemotherapy resistance in colorectal cancer over the last 20 yearsBilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.Pharmacogenetics of irinotecan: An ethnicity-based prediction of irinotecan adverse events.Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type IIUGT genomic diversity: beyond gene duplication.Pharmacogenomics of human UDP-glucuronosyltransferase enzymes.A GWAS Study on Liver Function Test Using eMERGE Network ParticipantsRole of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia.Association between UGT1A1 Polymorphism and Risk of Laryngeal Squamous Cell Carcinoma.Pharmacogenetics of uridine diphosphoglucuronosyltransferase (UGT) 1A family members and its role in patient response to irinotecan.Pharmacogenomics in colorectal cancer: the first step for individualized-therapyPharmacogenetics of Gilbert's syndrome.Distribution of selected gene polymorphisms of UGT1A1 in a Saudi population.Prediction of deleterious non-synonymous single-nucleotide polymorphisms of human uridine diphosphate glucuronosyltransferase genes.Comprehensive variant screening of the UGT gene familyAn overview of the recent progress in irinotecan pharmacogenetics.Gene replacement therapy for genetic hepatocellular jaundice.UGT1A1 genotype and irinotecan therapy: general review and implementation in routine practice.Truncated UDP-glucuronosyltransferase (UGT) from a Crigler-Najjar syndrome type II patient colocalizes with intact UGT in the endoplasmic reticulum.Inhibitory effect of 5β-pregnane-3α,20β-diol on transcriptional activity and enzyme activity of human bilirubin UDP-glucuronosyltransferase.Structure and function of uridine diphosphate glucuronosyltransferases.Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.Gilbert-Meulengracht's syndrome and pharmacogenetics: is jaundice just the tip of the iceberg?Variations in the UDP-glucuronosyltransferase 1A1 gene for the development of unconjugated hyperbilirubinemia in Taiwanese.Comparative genomics analysis of human sequence variation in the UGT1A gene cluster.Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II.Role of UGT1A1 mutation in fasting hyperbilirubinemia.Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia.Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.
P2860
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P2860
Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II
description
1993 nî lūn-bûn
@nan
1993 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Identification of defect in th ...... rigler-Najjar syndrome type II
@ast
Identification of defect in th ...... rigler-Najjar syndrome type II
@en
Identification of defect in th ...... rigler-Najjar syndrome type II
@nl
type
label
Identification of defect in th ...... rigler-Najjar syndrome type II
@ast
Identification of defect in th ...... rigler-Najjar syndrome type II
@en
Identification of defect in th ...... rigler-Najjar syndrome type II
@nl
prefLabel
Identification of defect in th ...... rigler-Najjar syndrome type II
@ast
Identification of defect in th ...... rigler-Najjar syndrome type II
@en
Identification of defect in th ...... rigler-Najjar syndrome type II
@nl
P2093
P356
P1476
Identification of defect in th ...... rigler-Najjar syndrome type II
@en
P2093
T Nakagawa
P304
P356
10.1006/BBRC.1993.2610
P407
P577
1993-12-30T00:00:00Z