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Items: 1 to 20 of 733

1.

The role of ABC transporters' gene polymorphism in the etiology of intrahepatic cholestasis of pregnancy.

Piątek K, Kurzawińska G, Magiełda J, Drews K, Barlik M, Malewski Z, Ożarowski M, Maciejewska M, Seremak-Mrozikiewicz A.

Ginekol Pol. 2018;89(7):393-397. doi: 10.5603/GP.a2018.0067.

2.

Alterations in Intestinal Microbiota Lead to Production of Interleukin 17 by Intrahepatic γδ T-Cell Receptor-Positive Cells and Pathogenesis of Cholestatic Liver Disease.

Tedesco D, Thapa M, Chin CY, Ge Y, Gong M, Li J, Gumber S, Speck P, Elrod EJ, Burd EM, Kitchens WH, Magliocca JF, Adams AB, Weiss DS, Mohamadzadeh M, Grakoui A.

Gastroenterology. 2018 Jun;154(8):2178-2193. doi: 10.1053/j.gastro.2018.02.019. Epub 2018 Feb 15.

PMID:
29454797
3.

Liver transplantation for decompensated liver cirrhosis caused by progressive familial intrahepatic cholestasis type 3: A case report.

Xiang D, He J, Wang H, Xiong F, Cheng H, Ai J, Shan R, Wan R, Zhang L, Shi J.

Medicine (Baltimore). 2017 Dec;96(50):e9158. doi: 10.1097/MD.0000000000009158.

4.

Mechanisms of canalicular transporter endocytosis in the cholestatic rat liver.

Miszczuk GS, Barosso IR, Larocca MC, Marrone J, Marinelli RA, Boaglio AC, Sánchez Pozzi EJ, Roma MG, Crocenzi FA.

Biochim Biophys Acta. 2018 Apr;1864(4 Pt A):1072-1085. doi: 10.1016/j.bbadis.2018.01.015. Epub 2018 Jan 31.

PMID:
29355600
5.

ATP-Binding Cassette Transporter A Subfamily 8 Is a Sinusoidal Efflux Transporter for Cholesterol and Taurocholate in Mouse and Human Liver.

Sasaki K, Tachikawa M, Uchida Y, Hirano S, Kadowaki F, Watanabe M, Ohtsuki S, Terasaki T.

Mol Pharm. 2018 Feb 5;15(2):343-355. doi: 10.1021/acs.molpharmaceut.7b00679. Epub 2018 Jan 24.

PMID:
29300488
6.

Resveratrol modifies biliary secretion of cholephilic compounds in sham-operated and cholestatic rats.

Dolezelova E, Prasnicka A, Cermanova J, Carazo A, Hyrsova L, Hroch M, Mokry J, Adamcova M, Mrkvicova A, Pavek P, Micuda S.

World J Gastroenterol. 2017 Nov 21;23(43):7678-7692. doi: 10.3748/wjg.v23.i43.7678.

7.
8.

Glucocorticoids Cause Gender-Dependent Reversal of Hepatic Fibrosis in the MDR2-Knockout Mouse Model.

Petrescu AD, Grant S, Frampton G, Kain J, Hadidi K, Williams E, McMillin M, DeMorrow S.

Int J Mol Sci. 2017 Nov 10;18(11). pii: E2389. doi: 10.3390/ijms18112389.

9.

Zebrafish abcb11b mutant reveals strategies to restore bile excretion impaired by bile salt export pump deficiency.

Ellis JL, Bove KE, Schuetz EG, Leino D, Valencia CA, Schuetz JD, Miethke A, Yin C.

Hepatology. 2018 Apr;67(4):1531-1545. doi: 10.1002/hep.29632. Epub 2018 Feb 23.

PMID:
29091294
10.

Activation of insulin-like growth factor 1 receptor participates downstream of GPR30 in estradiol-17β-D-glucuronide-induced cholestasis in rats.

Barosso IR, Miszczuk GS, Ciriaci N, Andermatten RB, Maidagan PM, Razori V, Taborda DR, Roma MG, Crocenzi FA, Sánchez Pozzi EJ.

Arch Toxicol. 2018 Feb;92(2):729-744. doi: 10.1007/s00204-017-2098-3. Epub 2017 Oct 31.

PMID:
29090346
11.

Adenovirus-mediated human aquaporin-1 expression in hepatocytes improves lipopolysaccharide-induced cholestasis.

Marrone J, Danielli M, Gaspari CI, Marinelli RA.

IUBMB Life. 2017 Dec;69(12):978-984. doi: 10.1002/iub.1689. Epub 2017 Oct 31.

PMID:
29087027
12.

Post-transplant Recurrent Bile Salt Export Pump Disease: A Form of Antibody-mediated Graft Dysfunction and Utilization of C4d.

Patel KR, Harpavat S, Finegold M, Eldin K, Hicks J, Firan M, Keitel V, Kubitz R, Wu H.

J Pediatr Gastroenterol Nutr. 2017 Oct;65(4):364-369. doi: 10.1097/MPG.0000000000001653.

PMID:
28945205
13.

Hepatic Tmem30a Deficiency Causes Intrahepatic Cholestasis by Impairing Expression and Localization of Bile Salt Transporters.

Liu L, Zhang L, Zhang L, Yang F, Zhu X, Lu Z, Yang Y, Lu H, Feng L, Wang Z, Chen H, Yan S, Wang L, Ju Z, Jin H, Zhu X.

Am J Pathol. 2017 Dec;187(12):2775-2787. doi: 10.1016/j.ajpath.2017.08.011. Epub 2017 Sep 15. Erratum in: Am J Pathol. 2018 Aug;188(8):1934.

PMID:
28919113
14.

p53-mediated regulation of bile acid disposition attenuates cholic acid-induced cholestasis in mice.

Chen P, Li D, Chen Y, Sun J, Fu K, Guan L, Zhang H, Jiang Y, Li X, Zeng X, Chen X, Huang M, Bi H.

Br J Pharmacol. 2017 Dec;174(23):4345-4361. doi: 10.1111/bph.14035. Epub 2017 Oct 22.

PMID:
28910492
15.

Partial external biliary diversion in bile salt export pump deficiency: Association between outcome and mutation.

Ellinger P, Stindt J, Dröge C, Sattler K, Stross C, Kluge S, Herebian D, Smits SHJ, Burdelski M, Schulz-Jürgensen S, Ballauff A, Schulte Am Esch J, Mayatepek E, Häussinger D, Kubitz R, Schmitt L.

World J Gastroenterol. 2017 Aug 7;23(29):5295-5303. doi: 10.3748/wjg.v23.i29.5295.

16.

Cholestasis After Pediatric Liver Transplantation-Recurrence of a Progressive Familial Intrahepatic Cholestasis Phenotype as a Rare Differential Diagnosis: A Case Report.

Prusinskas B, Kathemann S, Pilic D, Hegen B, Küster P, Keitel V, Häussinger D, Büscher R, Baba HA, Hoyer PF, Lainka E.

Transplant Proc. 2017 Sep;49(7):1628-1633. doi: 10.1016/j.transproceed.2017.06.011.

PMID:
28838453
17.

Molecular Mechanism of Taurocholate Transport by the Bile Salt Export Pump, an ABC Transporter Associated with Intrahepatic Cholestasis.

Sohail MI, Schmid D, Wlcek K, Spork M, Szakács G, Trauner M, Stockner T, Chiba P.

Mol Pharmacol. 2017 Oct;92(4):401-413. doi: 10.1124/mol.117.108688. Epub 2017 Aug 7.

PMID:
28784620
18.

Sequencing of FIC1, BSEP and MDR3 in a large cohort of patients with cholestasis revealed a high number of different genetic variants.

Dröge C, Bonus M, Baumann U, Klindt C, Lainka E, Kathemann S, Brinkert F, Grabhorn E, Pfister ED, Wenning D, Fichtner A, Gotthardt DN, Weiss KH, McKiernan P, Puri RD, Verma IC, Kluge S, Gohlke H, Schmitt L, Kubitz R, Häussinger D, Keitel V.

J Hepatol. 2017 Dec;67(6):1253-1264. doi: 10.1016/j.jhep.2017.07.004. Epub 2017 Jul 19.

PMID:
28733223
19.

Biliary bile acids in hepatobiliary injury - What is the link?

Fickert P, Wagner M.

J Hepatol. 2017 Sep;67(3):619-631. doi: 10.1016/j.jhep.2017.04.026. Epub 2017 Jul 14. Review.

PMID:
28712691
20.

Reconstruction of the mouse extrahepatic biliary tree using primary human extrahepatic cholangiocyte organoids.

Sampaziotis F, Justin AW, Tysoe OC, Sawiak S, Godfrey EM, Upponi SS, Gieseck RL 3rd, de Brito MC, Berntsen NL, Gómez-Vázquez MJ, Ortmann D, Yiangou L, Ross A, Bargehr J, Bertero A, Zonneveld MCF, Pedersen MT, Pawlowski M, Valestrand L, Madrigal P, Georgakopoulos N, Pirmadjid N, Skeldon GM, Casey J, Shu W, Materek PM, Snijders KE, Brown SE, Rimland CA, Simonic I, Davies SE, Jensen KB, Zilbauer M, Gelson WTH, Alexander GJ, Sinha S, Hannan NRF, Wynn TA, Karlsen TH, Melum E, Markaki AE, Saeb-Parsy K, Vallier L.

Nat Med. 2017 Aug;23(8):954-963. doi: 10.1038/nm.4360. Epub 2017 Jul 3.

PMID:
28671689

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