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Items: 1 to 20 of 52

1.

Recurrence of bile salt export pump deficiency after liver transplantation.

Jara P, Hierro L, Martínez-Fernández P, Alvarez-Doforno R, Yánez F, Diaz MC, Camarena C, De la Vega A, Frauca E, Muñoz-Bartolo G, López-Santamaría M, Larrauri J, Alvarez L.

N Engl J Med. 2009 Oct 1;361(14):1359-67. doi: 10.1056/NEJMoa0901075.

2.

Differential effects of progressive familial intrahepatic cholestasis type 1 and benign recurrent intrahepatic cholestasis type 1 mutations on canalicular localization of ATP8B1.

Folmer DE, van der Mark VA, Ho-Mok KS, Oude Elferink RP, Paulusma CC.

Hepatology. 2009 Nov;50(5):1597-605. doi: 10.1002/hep.23158.

PMID:
19731236
3.

Genetic variation in the vascular endothelial growth factor gene is associated with biliary atresia.

Lee HC, Chang TY, Yeung CY, Chan WT, Jiang CB, Chen WF, Chan HW, Liu HF, Lin M, Lee YJ.

J Clin Gastroenterol. 2010 Feb;44(2):135-9. doi: 10.1097/MCG.0b013e3181b152c2.

PMID:
19713864
4.

Neonatal NK cells target the mouse duct epithelium via Nkg2d and drive tissue-specific injury in experimental biliary atresia.

Shivakumar P, Sabla GE, Whitington P, Chougnet CA, Bezerra JA.

J Clin Invest. 2009 Aug;119(8):2281-90.

5.

De novo bile salt transporter antibodies as a possible cause of recurrent graft failure after liver transplantation: a novel mechanism of cholestasis.

Keitel V, Burdelski M, Vojnisek Z, Schmitt L, Häussinger D, Kubitz R.

Hepatology. 2009 Aug;50(2):510-7. doi: 10.1002/hep.23083.

PMID:
19642168
6.

Prognostic value of computerized quantification of liver fibrosis in children with biliary atresia.

Pape L, Olsson K, Petersen C, von Wasilewski R, Melter M.

Liver Transpl. 2009 Aug;15(8):876-82. doi: 10.1002/lt.21711.

7.

Sox17 regulates organ lineage segregation of ventral foregut progenitor cells.

Spence JR, Lange AW, Lin SC, Kaestner KH, Lowy AM, Kim I, Whitsett JA, Wells JM.

Dev Cell. 2009 Jul;17(1):62-74. doi: 10.1016/j.devcel.2009.05.012.

8.

New molecular insights into the mechanisms of cholestasis.

Wagner M, Zollner G, Trauner M.

J Hepatol. 2009 Sep;51(3):565-80. doi: 10.1016/j.jhep.2009.05.012. Epub 2009 May 28. Review.

9.

Prevalence of subclinical vitamin K deficiency in cholestatic liver disease.

Strople J, Lovell G, Heubi J.

J Pediatr Gastroenterol Nutr. 2009 Jul;49(1):78-84. doi: 10.1097/MPG.0b013e31819a61ff.

PMID:
19502999
10.

Allograft steatohepatitis in progressive familial intrahepatic cholestasis type 1 after living donor liver transplantation.

Miyagawa-Hayashino A, Egawa H, Yorifuji T, Hasegawa M, Haga H, Tsuruyama T, Wen MC, Sumazaki R, Manabe T, Uemoto S.

Liver Transpl. 2009 Jun;15(6):610-8. doi: 10.1002/lt.21686.

11.

Single nucleotide polymorphism-mediated translational suppression of endoplasmic reticulum mannosidase I modifies the onset of end-stage liver disease in alpha1-antitrypsin deficiency.

Pan S, Huang L, McPherson J, Muzny D, Rouhani F, Brantly M, Gibbs R, Sifers RN.

Hepatology. 2009 Jul;50(1):275-81. doi: 10.1002/hep.22974.

12.

Impact of age at Kasai operation on its results in late childhood and adolescence: a rational basis for biliary atresia screening.

Serinet MO, Wildhaber BE, Broué P, Lachaux A, Sarles J, Jacquemin E, Gauthier F, Chardot C.

Pediatrics. 2009 May;123(5):1280-6. doi: 10.1542/peds.2008-1949.

PMID:
19403492
13.

The extent of biliary proliferation in liver biopsies from patients with biliary atresia at portoenterostomy is associated with the postoperative prognosis.

Santos JL, Kieling CO, Meurer L, Vieira S, Ferreira CT, Lorentz A, Silveira TR.

J Pediatr Surg. 2009 Apr;44(4):695-701. doi: 10.1016/j.jpedsurg.2008.09.013.

PMID:
19361628
14.

Congenital biliary atresia: liver injury begins at birth.

Makin E, Quaglia A, Kvist N, Petersen BL, Portmann B, Davenport M.

J Pediatr Surg. 2009 Mar;44(3):630-3. doi: 10.1016/j.jpedsurg.2008.10.069.

PMID:
19302872
15.

Defective development of the gall bladder and cystic duct in Lgr4- hypomorphic mice.

Yamashita R, Takegawa Y, Sakumoto M, Nakahara M, Kawazu H, Hoshii T, Araki K, Yokouchi Y, Yamamura K.

Dev Dyn. 2009 Apr;238(4):993-1000. doi: 10.1002/dvdy.21900.

16.

A missense mutation in ABCB4 gene involved in progressive familial intrahepatic cholestasis type 3 leads to a folding defect that can be rescued by low temperature.

Delaunay JL, Durand-Schneider AM, Delautier D, Rada A, Gautherot J, Jacquemin E, Aït-Slimane T, Maurice M.

Hepatology. 2009 Apr;49(4):1218-27. doi: 10.1002/hep.22775.

PMID:
19185004
17.

Epithelial-mesenchymal transition induced by biliary innate immunity contributes to the sclerosing cholangiopathy of biliary atresia.

Harada K, Sato Y, Ikeda H, Isse K, Ozaki S, Enomae M, Ohama K, Katayanagi K, Kurumaya H, Matsui A, Nakanuma Y.

J Pathol. 2009 Apr;217(5):654-64. doi: 10.1002/path.2488.

PMID:
19116990
18.

Missense mutations and single nucleotide polymorphisms in ABCB11 impair bile salt export pump processing and function or disrupt pre-messenger RNA splicing.

Byrne JA, Strautnieks SS, Ihrke G, Pagani F, Knisely AS, Linton KJ, Mieli-Vergani G, Thompson RJ.

Hepatology. 2009 Feb;49(2):553-67. doi: 10.1002/hep.22683.

PMID:
19101985
19.

Cholangiocytes as immune modulators in rotavirus-induced murine biliary atresia.

Barnes BH, Tucker RM, Wehrmann F, Mack DG, Ueno Y, Mack CL.

Liver Int. 2009 Sep;29(8):1253-61. doi: 10.1111/j.1478-3231.2008.01921.x. Epub 2008 Nov 15.

20.

Effect of ursodeoxycholic acid on liver function in children after successful surgery for biliary atresia.

Willot S, Uhlen S, Michaud L, Briand G, Bonnevalle M, Sfeir R, Gottrand F.

Pediatrics. 2008 Dec;122(6):e1236-41. doi: 10.1542/peds.2008-0986. Epub 2008 Nov 24.

PMID:
19029197

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