Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 106

1.

A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesis.

Raynaud P, Tate J, Callens C, Cordi S, Vandersmissen P, Carpentier R, Sempoux C, Devuyst O, Pierreux CE, Courtoy P, Dahan K, Delbecque K, Lepreux S, Pontoglio M, Guay-Woodford LM, Lemaigre FP.

Hepatology. 2011 Jun;53(6):1959-66. doi: 10.1002/hep.24292. Epub 2011 May 2.

2.

The onecut transcription factor HNF6 is required for normal development of the biliary tract.

Clotman F, Lannoy VJ, Reber M, Cereghini S, Cassiman D, Jacquemin P, Roskams T, Rousseau GG, Lemaigre FP.

Development. 2002 Apr;129(8):1819-28.

3.

Suppression of C/EBPalpha expression in periportal hepatoblasts may stimulate biliary cell differentiation through increased Hnf6 and Hnf1b expression.

Yamasaki H, Sada A, Iwata T, Niwa T, Tomizawa M, Xanthopoulos KG, Koike T, Shiojiri N.

Development. 2006 Nov;133(21):4233-43. Epub 2006 Oct 4.

4.

A new set of classifications for ductal plate malformations.

Huppert SS.

Hepatology. 2011 Jun;53(6):1795-7. doi: 10.1002/hep.24404. No abstract available.

PMID:
21557279
5.

Hepatic artery malformations associated with a primary defect in intrahepatic bile duct development.

Clotman F, Libbrecht L, Gresh L, Yaniv M, Roskams T, Rousseau GG, Lemaigre FP.

J Hepatol. 2003 Nov;39(5):686-92.

PMID:
14568248
7.

Proliferation-Independent Initiation of Biliary Cysts in Polycystic Liver Diseases.

Beaudry JB, Cordi S, Demarez C, Lepreux S, Pierreux CE, Lemaigre FP.

PLoS One. 2015 Jun 30;10(6):e0132295. doi: 10.1371/journal.pone.0132295. eCollection 2015.

8.

Morphological and immunohistochemical analysis of ductal plate malformation: correlation with fetal liver.

Awasthi A, Das A, Srinivasan R, Joshi K.

Histopathology. 2004 Sep;45(3):260-7.

PMID:
15330804
9.

The homeobox gene Hhex is essential for proper hepatoblast differentiation and bile duct morphogenesis.

Hunter MP, Wilson CM, Jiang X, Cong R, Vasavada H, Kaestner KH, Bogue CW.

Dev Biol. 2007 Aug 15;308(2):355-67. Epub 2007 May 25.

10.

A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD).

Moser M, Matthiesen S, Kirfel J, Schorle H, Bergmann C, Senderek J, Rudnik-Schöneborn S, Zerres K, Buettner R.

Hepatology. 2005 May;41(5):1113-21.

PMID:
15830394
12.

Embryonic ductal plate cells give rise to cholangiocytes, periportal hepatocytes, and adult liver progenitor cells.

Carpentier R, Suñer RE, van Hul N, Kopp JL, Beaudry JB, Cordi S, Antoniou A, Raynaud P, Lepreux S, Jacquemin P, Leclercq IA, Sander M, Lemaigre FP.

Gastroenterology. 2011 Oct;141(4):1432-8, 1438.e1-4. doi: 10.1053/j.gastro.2011.06.049. Epub 2011 Jun 25.

13.

Intrahepatic bile ducts develop according to a new mode of tubulogenesis regulated by the transcription factor SOX9.

Antoniou A, Raynaud P, Cordi S, Zong Y, Tronche F, Stanger BZ, Jacquemin P, Pierreux CE, Clotman F, Lemaigre FP.

Gastroenterology. 2009 Jun;136(7):2325-33. doi: 10.1053/j.gastro.2009.02.051. Epub 2009 Feb 21.

14.
15.

Immunohistochemical detection of polyductin and co-localization with liver progenitor cell markers during normal and abnormal development of the intrahepatic biliary system and in adult hepatobiliary carcinomas.

Dorn L, Menezes LF, Mikuz G, Otto HF, Onuchic LF, Sergi C.

J Cell Mol Med. 2009 Jul;13(7):1279-90. doi: 10.1111/j.1582-4934.2008.00519.x. Epub 2008 Oct 6.

16.

Polycystic kidney rat is a novel animal model of Caroli's disease associated with congenital hepatic fibrosis.

Sanzen T, Harada K, Yasoshima M, Kawamura Y, Ishibashi M, Nakanuma Y.

Am J Pathol. 2001 May;158(5):1605-12.

17.

Imaging features of ductal plate malformations in adults.

Venkatanarasimha N, Thomas R, Armstrong EM, Shirley JF, Fox BM, Jackson SA.

Clin Radiol. 2011 Nov;66(11):1086-93. doi: 10.1016/j.crad.2011.05.008. Epub 2011 Aug 15. Review.

PMID:
21840516
18.

[Cystic diseases of the liver. From embryology to malformations].

Desmet VJ.

Gastroenterol Clin Biol. 2005 Aug-Sep;29(8-9):858-60. Review. French.

19.

Murine autosomal recessive polycystic kidney disease with multiorgan involvement induced by the cpk gene.

Gattone VH 2nd, MacNaughton KA, Kraybill AL.

Anat Rec. 1996 Jul;245(3):488-99.

Items per page

Supplemental Content

Write to the Help Desk