Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

Sandra Strautnieks, Laura N. Bull, Alexander S. Knisely et al. · Nature Genetics · 1998 · 993 citations

Hepatology, Biliary Tract, Natural Sciences +11

The Sister of P-glycoprotein Represents the Canalicular Bile Salt Export Pump of Mammalian Liver

Thomas Gerloff, Bruno Stieger, Bruno Hagenbuch et al. · Journal of Biological Chemistry · 1998 · 935 citations · Full text

Glycobiology, Molecular Biology, Canalicular Rat Liver +21

A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

Laura N. Bull, Michiel J. T. van Eijk, Ludmila Pawlikowska et al. · Nature Genetics · 1998 · 735 citations

Biology, P-type Atpase, Cellular Enzymology +7

The physical chemistry of cholesterol solubility in bile. Relationship to gallstone formation and dissolution in man.

Martin C. Carey, Donald Small · Journal of Clinical Investigation · 1978 · 696 citations · Full text

Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis

Peter L. M. Jansen, Sandra Strautnieks, Emmanuel Jacquemin et al. · Gastroenterology · 1999 · 434 citations · Full text

Hepatology, Biliary Tract, Liver Physiology +5