Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 The genetic basis of Gilbert's syndrome.

Literature DB >> 8596313

The genetic basis of Gilbert's syndrome.

H Sato¹, Y Adachi, O Koiwai.

Abstract

Entities: Disease

Mesh：

Substances：

Year: 1996 PMID： 8596313 DOI： 10.1016/s0140-6736(96)91266-0

Source DB: PubMed Journal: Lancet ISSN： 0140-6736 Impact factor: 79.321

Keyword Cloud
Cited

× No keyword cloud information.

23 in total

Review 1. Glucuronidation in humans. Pharmacogenetic and developmental aspects.

Authors: S N de Wildt; G L Kearns; J S Leeder; J N van den Anker
Journal: Clin Pharmacokinet Date: 1999-06 Impact factor: 6.447

2. Gilbert's syndrome: High frequency of the (TA)7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene.

Authors: Shabana Farheen; Sanghamitra Sengupta; Amal Santra; Suparna Pal; Gopal Krishna Dhali; Meenakshi Chakravorty; Partha P Majumder; Abhijit Chowdhury
Journal: World J Gastroenterol Date: 2006-04-14 Impact factor: 5.742

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

Authors: Yoshihiro Maruo; Yoriko Morioka; Hiroshi Fujito; Sayuri Nakahara; Takahide Yanagi; Katsuyuki Matsui; Asami Mori; Hiroshi Sato; Robert H Tukey; Yoshihiro Takeuchi
Journal: J Pediatr Date: 2014-03-17 Impact factor: 4.406

4. Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients.

Authors: Akitaka Nomura; Yoshihiro Maruo; Takashi Taga; Yoshihiro Takeuchi
Journal: Pediatr Res Date: 2016-04-08 Impact factor: 3.756

The genetic basis of Gilbert's syndrome.

Review 1. Glucuronidation in humans. Pharmacogenetic and developmental aspects.

2. Gilbert's syndrome: High frequency of the (TA)7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene.

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

4. Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients.

5. Molecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type I.

Review 6. Pharmacogenetics: a tool for individualizing antineoplastic therapy.

7. Polymorphisms of uridine-diphosphoglucuronosyltransferase 1A7 gene in Taiwan Chinese.

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

Review 9. Gene replacement therapy for genetic hepatocellular jaundice.

10. Induction of human UGT1A1 by a complex of dexamethasone-GR dependent on proximal site and independent of PBREM.