[PDF][PDF] Absence of the canalicular isoform of the MRP gene–encoded conjugate export pump from the hepatocytes in Dubin‐Johnson syndrome

Hepatology, 1996 - Wiley Online Library
Abstract The Dubin‐Johnson syndrome is characterized by an inherited defect in the
secretion of amphiphilic anionic conjugates from hepatocytes into the bile. We have recently …

[引用][C] Absence of the canalicular isoform of the MRP gene: Encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome

J KARTENBECK, U LEUSCHNER… - Hepatology …, 1996 - pascal-francis.inist.fr
Absence of the canalicular isoform of the MRP gene : Encoded conjugate export pump from
the hepatocytes in Dubin-Johnson syndrome CNRS Inist Pascal-Francis CNRS Pascal and …

Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome

J Kartenbeck, U Leuschner… - Hepatology …, 1996 - pubmed.ncbi.nlm.nih.gov
The Dubin-Johnson syndrome is characterized by an inherited defect in the secretion of
amphiphilic anionic conjugates from hepatocytes into the bile. We have recently identified …

Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome

J Kartenbeck, U Leuschner, R Mayer, D Keppler - Hepatology, 1996 - Elsevier
The Dubin-Johnson syndrome is characterized by an inherited defect in the secretion of
amphiphilic anionic conjugates from hepatocytes into the bile. We have recently identified …

Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome.

J Kartenbeck, U Leuschner, R Mayer… - Hepatology (Baltimore …, 1996 - europepmc.org
The Dubin-Johnson syndrome is characterized by an inherited defect in the secretion of
amphiphilic anionic conjugates from hepatocytes into the bile. We have recently identified …

Absence of the canalicular isoform of theMRPgene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome

J Kartenbeck, U Leuschner, R Mayer, D Keppler - Hepatology, 1996 - journals.lww.com
Abstract The Dubin-Johnson syndrome is characterized by an inherited defect in the
secretion of amphiphilic anionic conjugates from hepatocytes into the bile. We have recently …

[引用][C] Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome

J KARTENBECK - Hepatology, 1996 - cir.nii.ac.jp
Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from
the hepatocytes in Dubin-Johnson syndrome | CiNii Research CiNii 国立情報学研究所 学術 …

Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome

J Kartenbeck, U Leuschner, R Mayer, D Keppler - Hepatology, 1996 - infona.pl
The Dubin-Johnson syndrome is characterized by an inherited defect in the secretion of
amphiphilic anionic conjugates from hepatocytes into the bile. We have recently identified …

[引用][C] Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome

J KARTENBECK - Hepatology, 1996 - cir.nii.ac.jp
Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from
the hepatocytes in Dubin-Johnson syndrome | CiNii Research CiNii 国立情報学研究所 学術 …

[引用][C] Absence of the canalicular isoform of the MRP gene: Encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome

J KARTENBECK, U LEUSCHNER, R MAYER… - Hepatology, 1996 - Wiley