1. |
[J]. Scand J Gastroenterol, 2004; 241(Suppl)∶ 60.
|
2. |
van BergeHenegouwen GP, Venneman NG, Portincasa P, et al. Relevance of hereditary defects in lipid transport proteins for the pathogenesis of cholesterol gallstone disease.
|
3. |
Trauner M, Boyer JL. Bile salt transporters: molecular characterization, function, and regulation [J]. Physiol Rev, 2003; 83(2)∶633.
|
4. |
Hoda F, Green RM. Hepatic canalicular membrane transport of bile salt in C57L/J and AKR/J mice: implications for cholesterol gallstone formation [J]. J Membr Biol, 2003; 196(1)∶9.
|
5. |
Huang L, Zhao A, Lew JL, et al. Farnesoid X receptor activates transcription of the phospholipid pump MDR3 [J]. J Biol Chem, 2003; 278(51)∶51085.
|
6. |
Meier PJ, Stieger B. Bile salt transporters [J]. Annu Rev Physiol, 2002; 64(2)∶635.
|
7. |
Plass JR, Mol O, Heegsma J, et al. A progressive familial intrahepatic cholestasis type 2 mutation causes an unstable, temperaturesensitive bile salt export pump [J]. J Hepatol, 2004; 40(1)∶24.
|
8. |
Fickert P, Fuchsbichler A, Wagner M, et al. Regurgitation of bile acids from leaky bile ducts causes sclerosing cholangitis in Mdr2 (Abcb4) knockout mice [J]. Gastroenterology, 2004; 127(1)∶261.
|
9. |
Shoda J, Oda K, Suzuki H, et al. Etiologic significance of defects in cholesterol, phospholipid, and bile acid metabolism in the liver of patients with intrahepatic calculi [J]. Hepatology, 2001; 33(5)∶1194.
|
10. |
Smit JJ, Schinkel AH, Oude Elferink RP, et al. Homozygous disruption of the murine mdr2 Pglycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease [J]. Cell, 1993; 75(3)∶451.
|
11. |
劉君, 龍厚勇, 明晗昕, 等. 肝細胞MDR1基因表達與膽囊膽固醇結石相關性研究 [J]. 中國普外基礎與臨床雜志, 2005; 12(4)∶346.
|