Bilirubin genetics for the nongeneticist: Hereditary defects of neonatal bilirubin conjugation

[1] Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese [J]. JOURNAL OF HUMAN GENETICS, 1999, 44 (01) : 22 - 25

[2] CHRONIC UNCONJUGATED HYPERBILIRUBINEMIA WITHOUT OVERT SIGNS OF HEMOLYSIS IN ADOLESCENTS AND ADULTS [J]. JOURNAL OF CLINICAL INVESTIGATION, 1962, 41 (12) : 2233 - &

[3] Gilbert syndrome accelerates development of neonatal jaundice [J]. JOURNAL OF PEDIATRICS, 1998, 132 (04) : 656 - 660

[4] BENSINGER TA, 1973, P SOC EXP BIOL MED, V144, P417, DOI 10.3181/00379727-144-37603

[5] BERGMAN DA, 1994, PEDIATRICS, V94, P558

[6] DETECTION OF GILBERTS SYNDROME IN PATIENTS WITH HEMOLYSIS - METHOD USING RADIOACTIVE CHROMIUM [J]. ANNALS OF INTERNAL MEDICINE, 1972, 77 (04) : 527 - +

[7] Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter:: A balanced polymorphism for regulation of bilirubin metabolism? [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) : 8170 - 8174

[8] THE GENETIC-BASIS OF THE REDUCED EXPRESSION OF BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE-1 IN GILBERTS-SYNDROME [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (18) : 1171 - 1175

[9] Molecular genetic basis of Gilbert's syndrome [J]. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1999, 14 (10) : 960 - 966

[10] Human hepatocyte transplantation: Gene therapy and more? [J]. PEDIATRICS, 1998, 102 (03) : 647 - 648

[1] Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese [J]. JOURNAL OF HUMAN GENETICS, 1999, 44 (01) : 22 - 25

[2] CHRONIC UNCONJUGATED HYPERBILIRUBINEMIA WITHOUT OVERT SIGNS OF HEMOLYSIS IN ADOLESCENTS AND ADULTS [J]. JOURNAL OF CLINICAL INVESTIGATION, 1962, 41 (12) : 2233 - &

[3] Gilbert syndrome accelerates development of neonatal jaundice [J]. JOURNAL OF PEDIATRICS, 1998, 132 (04) : 656 - 660

[4] BENSINGER TA, 1973, P SOC EXP BIOL MED, V144, P417, DOI 10.3181/00379727-144-37603

[5] BERGMAN DA, 1994, PEDIATRICS, V94, P558

[6] DETECTION OF GILBERTS SYNDROME IN PATIENTS WITH HEMOLYSIS - METHOD USING RADIOACTIVE CHROMIUM [J]. ANNALS OF INTERNAL MEDICINE, 1972, 77 (04) : 527 - +

[7] Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter:: A balanced polymorphism for regulation of bilirubin metabolism? [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) : 8170 - 8174

[8] THE GENETIC-BASIS OF THE REDUCED EXPRESSION OF BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE-1 IN GILBERTS-SYNDROME [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (18) : 1171 - 1175

[9] Molecular genetic basis of Gilbert's syndrome [J]. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1999, 14 (10) : 960 - 966

[10] Human hepatocyte transplantation: Gene therapy and more? [J]. PEDIATRICS, 1998, 102 (03) : 647 - 648