A phenylalanine codon deletion at the UGT1 gene complex locus of a Crigler-Najjar Type I patient generates a pH-sensitive bilirubin UDP- glucuronosyltransferase

Journal of Biological Chemistry

Volumn 268, Issue 31, 1993, Pages 23573-23579

  Ritter, J K ^a   Yeatman, M T ^a   Kaiser, C ^a   Gridelli, B ^a   Owens, I S ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; DNA; GLUCURONOSYLTRANSFERASE; ISOENZYME; PHENYLALANINE;

AMINO ACID SEQUENCE; AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; CODON; CONTROLLED STUDY; CRIGLER NAJJAR SYNDROME; ENZYME ACTIVITY; EXON; GENE DELETION; GENE LOCUS; GLUCURONIDATION; HUMAN; HUMAN CELL; HYDROPHOBICITY; IONIC STRENGTH; LIVER MICROSOME; NONHUMAN; PH; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ALLELES; AMINO ACID SEQUENCE; ANIMAL; BASE SEQUENCE; CODON; COMPARATIVE STUDY; CRIGLER-NAJJAR SYNDROME; DNA PRIMERS; FEMALE; GLUCURONOSYLTRANSFERASE; HUMAN; HYDROGEN-ION CONCENTRATION; MALE; MICROSOMES, LIVER; MOLECULAR SEQUENCE DATA; PHENYLALANINE; RATS; SEQUENCE ALIGNMENT; SEQUENCE DELETION; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 0027370170     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)