Biomedical Engineering Reference
In-Depth Information
27. Hermeziu, B., Sanlaville, D., Girard, M., Leonard, C., Lyonnet, S. and Jacquemin, E.
(2006) Heterozygous bile salt export pump deficiency: a possible genetic predisposition
to transient neonatal cholestasis. J Pediatr Gastroenterol Nutr , 42 , 114-116.
28. Stieger, B., Fattinger, K., Madon, J., Kullak-Ublick, G.A. and Meier, P.J. (2000) Drug-
and estrogen-induced cholestasis through inhibition of the hepatocellular bile salt export
pump (Bsep) of rat liver. Gastroenterology , 118 , 422-430.
29. Eloranta, M.L., Hakli, T., Hiltunen, M., Helisalmi, S., Punnonen, K. and Heinonen, S.
(2003) Association of single nucleotide polymorphisms of the bile salt export pump gene
with intrahepatic cholestasis of pregnancy. Scand J Gastroenterol , 38 , 648-652.
30. De Vree, J.M., Jacquemin, E., Sturm, E., Cresteil, D., Bosma, P.J., Aten, J., Deleuze,
J.F., Desrochers, M., Burdelski, M., Bernard, O. et al. (1998) Mutations in the MDR3
gene cause progressive familial intrahepatic cholestasis. Proc Natl Acad Sci U S A , 95 ,
282-287.
31. Jacquemin, E., De Vree, J.M., Cresteil, D., Sokal, E.M., Sturm, E., Dumont, M., Scheffer,
G.L., Paul, M., Burdelski, M., Bosma, P.J. et al. (2001) The wide spectrum of multidrug
resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood. Gastroen-
terology , 120 , 1448-1458.
32. Rosmorduc, O., Hermelin, B. and Poupon, R. (2001) MDR3 gene defect in adults with
symptomatic intrahepatic and gallbladder cholesterol cholelithiasis. Gastroenterology ,
120 , 1459-1467.
33. Pauli-Magnus, C., Lang, T., Meier, Y., Zodan-Marin, T., Jung, D., Breymann, C., Zim-
mermann, R., Kenngott, S., Beuers, U., Reichel, C. et al. (2004) Sequence analysis of bile
salt export pump (ABCB11) and multidrug resistance P-glycoprotein 3 (ABCB4, MDR3)
in patients with intrahepatic cholestasis of pregnancy. Pharmacogenetics , 14 , 91-102.
34. Kartenbeck, J., Leuschner, U., Mayer, R. and Keppler, D. (1996) Absence of the canalic-
ular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in
Dubin-Johnson syndrome. Hepatology , 23 , 1061-1066.
35. Paulusma, C.C., Kool, M., Bosma, P.J., Scheffer, G.L., ter Borg, F., Scheper, R.J., Tytgat,
G.N., Borst, P., Baas, F. and Oude Elferink, R.P. (1997) A mutation in the human canalic-
ular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome.
Hepatology , 25 , 1539-1542.
36. Tsujii, H., Konig, J., Rost, D., St ockel, B., Leuschner, U. and Keppler, D. (1999) Exon-
intron organization of the human multidrug-resistance protein 2 (MRP2) gene mutated
in Dubin-Johnson syndrome. Gastroenterology , 117 , 653-660.
37. Keitel, V., Kartenbeck, J., Nies, A.T., Spring, H., Brom, M. and Keppler, D. (2000)
Impaired protein maturation of the conjugate export pump multidrug resistance protein
2 as a consequence of a deletion mutation in Dubin-Johnson syndrome. Hepatology , 32 ,
1317-1328.
38. Oelkers, P., Kirby, L.C., Heubi, J.E. and Dawson, P.A. (1997) Primary bile acid malab-
sorption caused by mutations in the ileal sodium-dependent bile acid transporter gene
(SLC10A2). J Clin Invest , 99 , 1880-1887.
39. Ho, R.H., Leake, B.F., Roberts, R.L., Lee, W. and Kim, R.B. (2004) Ethnicity-dependent
polymorphism in Na + -taurocholate cotransporting polypeptide (SLC10A1) reveals a
domain critical for bile acid substrate recognition. J Biol Chem , 279 , 7213-7222.
40. Zollner, G., Fickert, P., Silbert, D., Fuchsbichler, A., Marschall, H.U., Zatloukal, K., Denk,
H. and Trauner, M. (2003) Adaptive changes in hepatobiliary transporter expression in
primary biliary cirrhosis. J Hepatol , 38 , 717-727.
 
Search WWH ::




Custom Search