The wide spectrum of multidrug resistance 3 deficiency: From neonatal cholestasis to cirrhosis of adulthood von Jacquemin, Emmanuel, De Vree, J. Marleen L., Cresteil, Danièle, Sokal, Etienne M., Sturm, Ekkehard, Dumont, Micheline, Scheffer, George L., Paul, Marianne, Burdelski, Martin, Bosma, Piter J., Bernard, Olivier, Hadchouel, Michelle, Oude Elferink, Ronald P.J.

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Correction of liver disease by hepatocyte transplantation in a mouse model of progressive familial intrahepatic cholestasis von De Vree, J.Marleen L., Ottenhoff, Roel, Bosma, Piter J., Smith, Alexander J., Aten, Jan, Oude Elferink, Ronald P.J.

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FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyte von Eppens, Elaine F., van Mil, Saskia W.C., de Vree, J.Marleen L., Mok, Kam S., Juijn, Jenneke A., Oude Elferink, Ronald P.J., Berger, Ruud, Houwen, Roderick H.J., Klomp, Leo W.J.

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Dietary cholesterol does not normalize low plasma cholesterol levels but induces hyperbilirubinemia and hypercholanemia in Mdr2 P-glycoprotein-deficient mice von Voshol, Peter J, Koopen, Nynke R, de Vree, J.Marleen L, Havinga, Rick, Princen, Hans M.G, Oude Elferink, Ronald P.J, Groen, Albert K, Kuipers, Folkert

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