Bilirubin metabolism: Applied physiology

[1]  P. Jansen,et al.  Bilirubin Metabolism and its Disorders , 2006 .

[2]  S. Onishi,et al.  Kinetic study of the photochemical changes of (ZZ)-bilirubin IXa bound to human serum albumin Demonstration of (EZ)-bilirubin IXa as an intermediate in photochemical changes from (ZZ)-bilirubin IXa to (EZ)-cyclobilirubin IXa , 2005 .

[3]  A. Kappas,et al.  Chemoprevention of severe neonatal hyperbilirubinemia. , 2004, Seminars in perinatology.

[4]  P. Horn,et al.  Serum bilirubin levels in the U.S. Population: Gender effect and inverse correlation with colorectal cancer , 2004, Hepatology.

[5]  C. Scriver,et al.  The Metabolic and Molecular Bases of Inherited Disease, 8th Edition 2001 , 2001, Journal of Inherited Metabolic Disease.

[6]  P. Borst,et al.  Mammalian ABC transporters in health and disease. , 2002, Annual review of biochemistry.

[7]  P. Bosma,et al.  Jaundice and disorders of bilirubin metabolism , 1998 .

[8]  P. Bosma,et al.  Reduced bilirubin UDP-glucuronosyltransferase expression in Gilbert syndrome is caused by a sequence abnormality in the promoter region , 1996 .

[9]  D Lindhout,et al.  The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. , 1995, The New England journal of medicine.

[10]  P. Bosma,et al.  Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase. , 1994, The Journal of clinical investigation.

[11]  J. Seppen,et al.  DISCRIMINATION BETWEEN CRIGLER-NAJJAR TYPE-I AND TYPE-II BY EXPRESSION OF MUTANT BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE , 1994 .

[12]  P. Bosma,et al.  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 , 1992, Hepatology.

[13]  J. Ritter,et al.  A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini. , 1992, The Journal of biological chemistry.

[14]  B. Ponder,et al.  Principles and practice of medical genetics (2nd edn) edited by A.E.H. Emery and D.L. Rimoin Churchill Livingstone, 1990. £195.00 (xxi + 938 pages, Vol. 1; xxii + 2079 pages, Vol. 2) ISBN O 443 03583 0 , 1991 .

[15]  S. Onishi,et al.  Kinetic study of the photochemical changes of (ZZ)-bilirubin IX alpha bound to human serum albumin. Demonstration of (EZ)-bilirubin IX alpha as an intermediate in photochemical changes from (ZZ)-bilirubin IX alpha to (EZ)-cyclobilirubin IX alpha. , 1985, The Biochemical journal.

[16]  F. Iber Hepatology: A Textbook of Liver Disease , 1983 .

[17]  J. J. Lauff,et al.  Quantitative liquid-chromatographic estimation of bilirubin species in pathological serum. , 1983, Clinical chemistry.

[18]  B. Fleshler,et al.  The Liver: Biology and Pathobiology , 1983 .

[19]  R. Bonnett,et al.  Structure of bilirubin , 1976, Nature.

[20]  A. Wolkoff,et al.  Rotor's syndrome. A distinct inheritable pathophysiologic entity. , 1976, The American journal of medicine.

[21]  J. Walker-Smith,et al.  CHRONIC NONHAEMOLYTIC UNCONJUGATED HYPERBILIRUBINAEMIA , 1973, Australian paediatric journal.

[22]  G. H. Lathe DISORDERS OF BILIRUBIN METABOLISM. , 1965, Clinical chemistry.