Dubin-Johnson-Syndrom

None (1993) Dubin-Johnson and Rotor syndromes: molecular basis and pathogenesis.

WOLF RL et al. (1960) Chronic idiopathic jaundice. A study of two afflicted families.

CALDERON A et al. (1961) Chronic idiopathic jaundice. A case report.

BEKER S et al. (1958) Familial DubinJohnson syndrome.

DUBIN IN et al. (1954) Chronic idiopathic jaundice with unidentified pigment in liver cells; a new clinicopathologic entity with a report of 12 cases.

Kartenbeck J et al. (1996) Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome.

Mayer R et al. (1995) Expression of the MRP gene-encoded conjugate export pump in liver and its selective absence from the canalicular membrane in transport-deficient mutant hepatocytes.

Du JN et al. (1967) Dubin-Johnson syndrome: a family with three affected sisters.

Butt HR et al. (1966) Studies of chronic idiopathic jaundice (Dubin-Johnson syndrome). II. Evaluation of a large family with the trait.

Seligsohn U et al. (1970) Dubin-Johnson syndrome in Israel. II. Association with factor-VII deficiency.

None (1971) Inheritable and congenital hyperbilirubinemia. Models for the study of drug metabolism.

Wolkoff AW et al. (1973) Inheritance of the Dubin-Johnson syndrome.

Swartz HM et al. (1987) Further evidence that the pigment in the Dubin-Johnson syndrome is not melanin.

None (1975) Inheritance of the Dubin-Johnson-Sprinz syndrome.

Nakata F et al. (1979) Dubin-Johnson syndrome in a neonate.

Pacifico L et al. (2010) Mutational analysis of ABCC2 gene in two siblings with neonatal-onset Dubin Johnson syndrome.

Mor-Cohen R et al. (2001) Identification and functional analysis of two novel mutations in the multidrug resistance protein 2 gene in Israeli patients with Dubin-Johnson syndrome.

Toh S et al. (1999) Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome.

Kajihara S et al. (1998) A splice mutation in the human canalicular multispecific organic anion transporter gene causes Dubin-Johnson syndrome.

Wada M et al. (1998) Mutations in the canilicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome.

van Kuijck MA et al. (1997) Assignment of the canalicular multispecific organic anion transporter gene (CMOAT) to human chromosome 10q24 and mouse chromosome 19D2 by fluorescent in situ hybridization.

Ito K et al. (1997) Molecular cloning of canalicular multispecific organic anion transporter defective in EHBR.

Paulusma CC et al. (1996) Congenital jaundice in rats with a mutation in a multidrug resistance-associated protein gene.

Shani M et al. (1970) Dubin-Johnson syndrome in Israel. I. Clinical, laboratory, and genetic aspects of 101 cases.

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