Literature DB >> 9434956

The gene encoding the multispecific organic anion transporter (Cmoat) of the hepatocyte canalicular membrane maps to mouse chromosome 19.

F Lammert1, D E Cohen, B Paigen, M C Carey, D R Beier.   

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Year:  1998        PMID： 9434956     DOI： 10.1007/s003359900689

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  17 in total

1.  Mapping genes in the mouse using single-strand conformation polymorphism analysis of recombinant inbred strains and interspecific crosses.

Authors:  D R Beier; H Dushkin; D J Sussman
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-01       Impact factor: 11.205

2.  A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome.

Authors:  C C Paulusma; M Kool; P J Bosma; G L Scheffer; F ter Borg; R J Scheper; G N Tytgat; P Borst; F Baas; R P Oude Elferink
Journal:  Hepatology       Date:  1997-06       Impact factor: 17.425

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

Authors:  J Kartenbeck; U Leuschner; R Mayer; D Keppler
Journal:  Hepatology       Date:  1996-05       Impact factor: 17.425

Review 4.  A Macintosh program for storage and analysis of experimental genetic mapping data.

Authors:  K F Manly
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

Review 5.  Secretion of organic anions by hepatocytes: involvement of homologues of the multidrug resistance protein.

Authors:  M Müller; H Roelofsen; P L Jansen
Journal:  Semin Liver Dis       Date:  1996-05       Impact factor: 6.115

6.  Control analysis of biliary lipid secretion.

Authors:  A K Groen; R P Elferink; J M Tager
Journal:  J Theor Biol       Date:  1996-10-07       Impact factor: 2.691

7.  Hereditary chronic conjugated hyperbilirubinemia in mutant rats caused by defective hepatic anion transport.

Authors:  P L Jansen; W H Peters; W H Lamers
Journal:  Hepatology       Date:  1985 Jul-Aug       Impact factor: 17.425

8.  Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease.

Authors:  J J Smit; A H Schinkel; R P Oude Elferink; A K Groen; E Wagenaar; L van Deemter; C A Mol; R Ottenhoff; N M van der Lugt; M A van Roon
Journal:  Cell       Date:  1993-11-05       Impact factor: 41.582

9.  Two distinct mechanisms for bilirubin glucuronide transport by rat bile canalicular membrane vesicles. Demonstration of defective ATP-dependent transport in rats (TR-) with inherited conjugated hyperbilirubinemia.

Authors:  T Nishida; Z Gatmaitan; J Roy-Chowdhry; I M Arias
Journal:  J Clin Invest       Date:  1992-11       Impact factor: 14.808

10.  Congenital jaundice in rats with a mutation in a multidrug resistance-associated protein gene.

Authors:  C C Paulusma; P J Bosma; G J Zaman; C T Bakker; M Otter; G L Scheffer; R J Scheper; P Borst; R P Oude Elferink
Journal:  Science       Date:  1996-02-23       Impact factor: 47.728
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  1 in total

Review 1.  Bile acid transporters: structure, function, regulation and pathophysiological implications.

Authors:  Waddah A Alrefai; Ravinder K Gill
Journal:  Pharm Res       Date:  2007-04-03       Impact factor: 4.200
  1 in total

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