Corpechot C - Search Results

1

Expanding the mutational spectrum of the ABCB4 gene in inherited adult cholestatic liver disorders with four novel pathogenic variants.

Huynh MT, Delaunay JL, Muller L, Corpechot C, Tran CT, Barbu V. Huynh MT, et al. Among authors: corpechot c. Rev Esp Enferm Dig. 2019 Jan;111(1):76-79. doi: 10.17235/reed.2018.5828/2018. Rev Esp Enferm Dig. 2019. PMID: 30449124 Free article.

2

Fetal microchimerism in primary biliary cirrhosis.

Corpechot C, Barbu V, Chazouillères O, Poupon R. Corpechot C, et al. J Hepatol. 2000 Nov;33(5):696-700. doi: 10.1016/s0168-8278(00)80298-6. J Hepatol. 2000. PMID: 11097475

3

Apolipoprotein E polymorphism, a marker of disease severity in primary biliary cirrhosis?

Corpechot C, Benlian P, Barbu V, Chazouillères O, Poupon RE, Poupon R. Corpechot C, et al. J Hepatol. 2001 Sep;35(3):324-8. doi: 10.1016/s0168-8278(01)00137-4. J Hepatol. 2001. PMID: 11592592

4

Hepatocyte growth factor and c-Met inhibition by hepatic cell hypoxia: a potential mechanism for liver regeneration failure in experimental cirrhosis.

Corpechot C, Barbu V, Wendum D, Chignard N, Housset C, Poupon R, Rosmorduc O. Corpechot C, et al. Am J Pathol. 2002 Feb;160(2):613-20. doi: 10.1016/S0002-9440(10)64881-X. Am J Pathol. 2002. PMID: 11839582 Free PMC article.

5

Hypoxia-induced VEGF and collagen I expressions are associated with angiogenesis and fibrogenesis in experimental cirrhosis.

Corpechot C, Barbu V, Wendum D, Kinnman N, Rey C, Poupon R, Housset C, Rosmorduc O. Corpechot C, et al. Hepatology. 2002 May;35(5):1010-21. doi: 10.1053/jhep.2002.32524. Hepatology. 2002. PMID: 11981751

6

Identification of a novel 974C-->G nonsense mutation of the MRP2/ABCC2 gene in a patient with Dubin-Johnson syndrome and analysis of the effects of rifampicin and ursodeoxycholic acid on serum bilirubin and bile acids.

Corpechot C, Ping C, Wendum D, Matsuda F, Barbu V, Poupon R. Corpechot C, et al. Am J Gastroenterol. 2006 Oct;101(10):2427-32. doi: 10.1111/j.1572-0241.2006.00695.x. Epub 2006 Sep 4. Am J Gastroenterol. 2006. PMID: 16952291

7

Genetic factors of susceptibility and of severity in primary biliary cirrhosis.

Poupon R, Ping C, Chrétien Y, Corpechot C, Chazouillères O, Simon T, Heath SC, Matsuda F, Poupon RE, Housset C, Barbu V. Poupon R, et al. Among authors: corpechot c. J Hepatol. 2008 Dec;49(6):1038-45. doi: 10.1016/j.jhep.2008.07.027. Epub 2008 Oct 1. J Hepatol. 2008. PMID: 18930330

8

Genotype-phenotype relationships in the low-phospholipid-associated cholelithiasis syndrome: a study of 156 consecutive patients.

Poupon R, Rosmorduc O, Boëlle PY, Chrétien Y, Corpechot C, Chazouillères O, Housset C, Barbu V. Poupon R, et al. Among authors: corpechot c. Hepatology. 2013 Sep;58(3):1105-10. doi: 10.1002/hep.26424. Epub 2013 Jul 29. Hepatology. 2013. PMID: 23533021

9

Portal myofibroblasts promote vascular remodeling underlying cirrhosis formation through the release of microparticles.

Lemoinne S, Cadoret A, Rautou PE, El Mourabit H, Ratziu V, Corpechot C, Rey C, Bosselut N, Barbu V, Wendum D, Feldmann G, Boulanger C, Henegar C, Housset C, Thabut D. Lemoinne S, et al. Among authors: corpechot c. Hepatology. 2015 Mar;61(3):1041-55. doi: 10.1002/hep.27318. Epub 2015 Jan 22. Hepatology. 2015. PMID: 25043701

10

Intrahepatic Cholestasis Owing to a Novel Heterozygous ABCG8 Mutation and SLC4A2 Polymorphism With Favorable Outcome Under Ursodeoxycholic Acid.

Ciocan D, Voican CS, Barbu V, Corpechot C, Rainteau D, Prevot S, Lebrun A, Perlemuter G. Ciocan D, et al. Among authors: corpechot c. Am J Gastroenterol. 2019 Sep;114(9):1556-1559. doi: 10.14309/ajg.0000000000000328. Am J Gastroenterol. 2019. PMID: 31335361 No abstract available.

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