Identification of a Defect in the UGT1A1 Gene Promoter and Its Association with Hyperbilirubinemia-Reference-Cited by-同舟云学术

Identification of a Defect in the UGT1A1 Gene Promoter and Its Association with Hyperbilirubinemia

Published:2002-03 Issue:2 Volume:292 Page:492-497
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Sugatani Junko,Yamakawa Kasumi,Yoshinari Kouich,Machida Takashi,Takagi Hitoshi,Mori Masatomo,Kakizaki Satoru,Sueyoshi Tatsuya,Negishi Masahiko,Miwa Masao

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference24 articles.

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3. The UDP glycosyltransferase gene superfamily: Recommended nomenclature update based on evolutionary divergence;Mackenzie;Pharmacogenetics,1997

4. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome;Bosma;N. Engl. J. Med.,1995

5. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome;Monaghan;Lancet,1996

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