Jacquemin E - Search Results

1

Functional rescue of an ABCB11 mutant by ivacaftor: A new targeted pharmacotherapy approach in bile salt export pump deficiency.

Mareux E, Lapalus M, Amzal R, Almes M, Aït-Slimane T, Delaunay JL, Adnot P, Collado-Hilly M, Davit-Spraul A, Falguières T, Callebaut I, Gonzales E, Jacquemin E. Mareux E, et al. Among authors: jacquemin e. Liver Int. 2020 Aug;40(8):1917-1925. doi: 10.1111/liv.14518. Epub 2020 Jun 8. Liver Int. 2020. PMID: 32433800

2

Progressive familial intrahepatic cholestasis. Genetic basis and treatment.

Jacquemin E. Jacquemin E. Clin Liver Dis. 2000 Nov;4(4):753-63. doi: 10.1016/s1089-3261(05)70139-2. Clin Liver Dis. 2000. PMID: 11232355 Review.

3

Role of multidrug resistance 3 deficiency in pediatric and adult liver disease: one gene for three diseases.

Jacquemin E. Jacquemin E. Semin Liver Dis. 2001 Nov;21(4):551-62. doi: 10.1055/s-2001-19033. Semin Liver Dis. 2001. PMID: 11745043

4

Genetic cholestatic liver diseases: the example of progressive familial intrahepatic cholestasis and related disorders.

Baussan C, Cresteil D, Gonzales E, Raynaud N, Dumont M, Bernard O, Hadchouel M, Jacquemin E. Baussan C, et al. Among authors: jacquemin e. Acta Gastroenterol Belg. 2004 Apr-Jun;67(2):179-83. Acta Gastroenterol Belg. 2004. PMID: 15285575 Review. No abstract available.

5

Heterozygous bile salt export pump deficiency: a possible genetic predisposition to transient neonatal cholestasis.

Hermeziu B, Sanlaville D, Girard M, Léonard C, Lyonnet S, Jacquemin E. Hermeziu B, et al. Among authors: jacquemin e. J Pediatr Gastroenterol Nutr. 2006 Jan;42(1):114-6. doi: 10.1097/01.mpg.0000184429.34001.68. J Pediatr Gastroenterol Nutr. 2006. PMID: 16385265 No abstract available.

6

Rat hepatocytes express functional P2X receptors.

Gonzales E, Prigent S, Abou-Lovergne A, Boucherie S, Tordjmann T, Jacquemin E, Combettes L. Gonzales E, et al. Among authors: jacquemin e. FEBS Lett. 2007 Jul 10;581(17):3260-6. doi: 10.1016/j.febslet.2007.06.016. Epub 2007 Jun 19. FEBS Lett. 2007. PMID: 17597621 Free article.

7

CFC1 gene involvement in biliary atresia with polysplenia syndrome.

Davit-Spraul A, Baussan C, Hermeziu B, Bernard O, Jacquemin E. Davit-Spraul A, et al. Among authors: jacquemin e. J Pediatr Gastroenterol Nutr. 2008 Jan;46(1):111-2. doi: 10.1097/01.mpg.0000304465.60788.f4. J Pediatr Gastroenterol Nutr. 2008. PMID: 18162845

8

Progressive familial intrahepatic cholestasis.

Davit-Spraul A, Gonzales E, Baussan C, Jacquemin E. Davit-Spraul A, et al. Among authors: jacquemin e. Orphanet J Rare Dis. 2009 Jan 8;4:1. doi: 10.1186/1750-1172-4-1. Orphanet J Rare Dis. 2009. PMID: 19133130 Free PMC article. Review.

9

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. Delaunay JL, et al. Among authors: jacquemin e. Hepatology. 2009 Apr;49(4):1218-27. doi: 10.1002/hep.22775. Hepatology. 2009. PMID: 19185004

10

Liver diseases related to MDR3 (ABCB4) gene deficiency.

Gonzales E, Davit-Spraul A, Baussan C, Buffet C, Maurice M, Jacquemin E. Gonzales E, et al. Among authors: jacquemin e. Front Biosci (Landmark Ed). 2009 Jan 1;14(11):4242-56. doi: 10.2741/3526. Front Biosci (Landmark Ed). 2009. PMID: 19273348 Free article. Review.

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