UNVEILING THE MYSTERIES OF INHERITED DISORDERS OF BILIRUBIN GLUCURONIDATION

[1] CHRONIC NONHEMOLYTIC UNCONJUGATED HYPERBILIRUBINEMIA WITH GLUCURONYL TRANSFERASE DEFICIENCY - CLINICAL, BIOCHEMICAL, PHARMACOLOGIC AND GENETIC EVIDENCE FOR HETEROGENEITY [J]. AMERICAN JOURNAL OF MEDICINE, 1969, 47 (03) : 395 - &

[2] CONSTITUTIONAL HEPATIC DYSFUNCTION (GILBERTS SYNDROME) - A NEW DEFINITION BASED ON KINETIC STUDIES WITH UNCONJUGATED RADIOBILIRUBIN [J]. AMERICAN JOURNAL OF MEDICINE, 1970, 49 (03) : 296 - &

[3] BERK PD, 1979, J CLIN INVEST, V48, P2176

[4] BOCK KW, 1973, BIOCHIM BIOPHYS ACTA, V327, P45

[5] A MUTATION IN BILIRUBIN URIDINE 5'-DIPHOSPHATE-GLUCURONOSYLTRANSFERASE ISOFORM-1 CAUSING CRIGLER-NAJJAR SYNDROME TYPE-II [J]. GASTROENTEROLOGY, 1993, 105 (01) : 216 - 220

[6] MECHANISMS OF INHERITED DEFICIENCIES OF MULTIPLE UDP-GLUCURONOSYLTRANSFERASE ISOFORMS IN 2 PATIENTS WITH CRIGLER-NAJJAR SYNDROME, TYPE-I [J]. FASEB JOURNAL, 1992, 6 (10) : 2859 - 2863

[7] SEQUENCE OF EXONS AND THE FLANKING REGIONS OF HUMAN BILIRUBIN-UDP-GLUCURONOSYLTRANSFERASE GENE-COMPLEX AND IDENTIFICATION OF A GENETIC MUTATION IN A PATIENT WITH CRIGLER-NAJJAR SYNDROME, TYPE-I [J]. HEPATOLOGY, 1992, 15 (05) : 941 - 947

[8] Burchell, 1977, PROGR DRUG METABOLIS, V2, P1

[9] THE UDP GLUCURONOSYLTRANSFERASE GENE SUPERFAMILY - SUGGESTED NOMENCLATURE BASED ON EVOLUTIONARY DIVERGENCE [J]. DNA AND CELL BIOLOGY, 1991, 10 (07) : 487 - 494

[10] CARBONE JV, 1957, P SOC EXP BIOL MED, V94, P461

[1] CHRONIC NONHEMOLYTIC UNCONJUGATED HYPERBILIRUBINEMIA WITH GLUCURONYL TRANSFERASE DEFICIENCY - CLINICAL, BIOCHEMICAL, PHARMACOLOGIC AND GENETIC EVIDENCE FOR HETEROGENEITY [J]. AMERICAN JOURNAL OF MEDICINE, 1969, 47 (03) : 395 - &

[2] CONSTITUTIONAL HEPATIC DYSFUNCTION (GILBERTS SYNDROME) - A NEW DEFINITION BASED ON KINETIC STUDIES WITH UNCONJUGATED RADIOBILIRUBIN [J]. AMERICAN JOURNAL OF MEDICINE, 1970, 49 (03) : 296 - &

[3] BERK PD, 1979, J CLIN INVEST, V48, P2176

[4] BOCK KW, 1973, BIOCHIM BIOPHYS ACTA, V327, P45

[5] A MUTATION IN BILIRUBIN URIDINE 5'-DIPHOSPHATE-GLUCURONOSYLTRANSFERASE ISOFORM-1 CAUSING CRIGLER-NAJJAR SYNDROME TYPE-II [J]. GASTROENTEROLOGY, 1993, 105 (01) : 216 - 220

[6] MECHANISMS OF INHERITED DEFICIENCIES OF MULTIPLE UDP-GLUCURONOSYLTRANSFERASE ISOFORMS IN 2 PATIENTS WITH CRIGLER-NAJJAR SYNDROME, TYPE-I [J]. FASEB JOURNAL, 1992, 6 (10) : 2859 - 2863

[7] SEQUENCE OF EXONS AND THE FLANKING REGIONS OF HUMAN BILIRUBIN-UDP-GLUCURONOSYLTRANSFERASE GENE-COMPLEX AND IDENTIFICATION OF A GENETIC MUTATION IN A PATIENT WITH CRIGLER-NAJJAR SYNDROME, TYPE-I [J]. HEPATOLOGY, 1992, 15 (05) : 941 - 947

[8] Burchell, 1977, PROGR DRUG METABOLIS, V2, P1

[9] THE UDP GLUCURONOSYLTRANSFERASE GENE SUPERFAMILY - SUGGESTED NOMENCLATURE BASED ON EVOLUTIONARY DIVERGENCE [J]. DNA AND CELL BIOLOGY, 1991, 10 (07) : 487 - 494

[10] CARBONE JV, 1957, P SOC EXP BIOL MED, V94, P461