4.6 Article

Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Gastroenterology & Hepatology

Compound Heterozygote of a Novel Missense Mutation (p. K402T) and a Double Missense Mutation (p.[G71R;Y486D]) in Type II Crigler-Najjar Syndrome

Yoshihiro Maruo et al.

JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2011)

Article Gastroenterology & Hepatology

Combined effect of regulatory polymorphisms on transcription of UGT1A1 as a cause of Gilbert syndrome

Katsuyuki Matsui et al.

BMC GASTROENTEROLOGY (2010)

Article Multidisciplinary Sciences

Developmental hyperbilirubinemia and CNS toxicity in mice humanized with the UDP glucuronosyltransferase 1 (UGT1) locus

Ryoichi Fujiwara et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Medicine, General & Internal

Die Prävalenz des Gilbert-Syndroms in Deutschland

A. Sieg et al.

DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT (2008)

Article Gastroenterology & Hepatology

Crigler-Najjar syndrome type II caused by a homozygous triple mutation [T-3279G, A(TA)7TAA, and H39D] of UGT1A1

Y Maruo et al.

JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2006)

Article Biochemistry & Molecular Biology

Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia

J Sugatani et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2002)