Aït-Slimane T - Search Results

1

Inhibition of receptor-interacting protein kinase 1 improves experimental non-alcoholic fatty liver disease.

Majdi A, Aoudjehane L, Ratziu V, Islam T, Afonso MB, Conti F, Mestiri T, Lagouge M, Foufelle F, Ballenghien F, Ledent T, Moldes M, Cadoret A, Fouassier L, Delaunay JL, Aït-Slimane T, Courtois G, Fève B, Scatton O, Prip-Buus C, Rodrigues CMP, Housset C, Gautheron J. Majdi A, et al. Among authors: ait slimane t. J Hepatol. 2020 Apr;72(4):627-635. doi: 10.1016/j.jhep.2019.11.008. Epub 2019 Nov 21. J Hepatol. 2020. PMID: 31760070

2

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. Hepatology. 2009 Apr;49(4):1218-27. doi: 10.1002/hep.22775. Hepatology. 2009. PMID: 19185004

3

Effects of cellular, chemical, and pharmacological chaperones on the rescue of a trafficking-defective mutant of the ATP-binding cassette transporter proteins ABCB1/ABCB4.

Gautherot J, Durand-Schneider AM, Delautier D, Delaunay JL, Rada A, Gabillet J, Housset C, Maurice M, Aït-Slimane T. Gautherot J, et al. J Biol Chem. 2012 Feb 10;287(7):5070-8. doi: 10.1074/jbc.M111.275438. Epub 2011 Dec 19. J Biol Chem. 2012. PMID: 22184139 Free PMC article.

4

Oligomerization is required for normal endocytosis/transcytosis of a GPI-anchored protein in polarized hepatic cells.

Galmes R, Delaunay JL, Maurice M, Aït-Slimane T. Galmes R, et al. J Cell Sci. 2013 Aug 1;126(Pt 15):3409-16. doi: 10.1242/jcs.126250. Epub 2013 Jun 7. J Cell Sci. 2013. PMID: 23750006

5

Phosphorylation of ABCB4 impacts its function: insights from disease-causing mutations.

Gautherot J, Delautier D, Maubert MA, Aït-Slimane T, Bolbach G, Delaunay JL, Durand-Schneider AM, Firrincieli D, Barbu V, Chignard N, Housset C, Maurice M, Falguières T. Gautherot J, et al. Hepatology. 2014 Aug;60(2):610-21. doi: 10.1002/hep.27170. Epub 2014 May 19. Hepatology. 2014. PMID: 24723470

6

ABCB4: Insights from pathobiology into therapy.

Falguières T, Aït-Slimane T, Housset C, Maurice M. Falguières T, et al. Clin Res Hepatol Gastroenterol. 2014 Oct;38(5):557-63. doi: 10.1016/j.clinre.2014.03.001. Epub 2014 Jun 19. Clin Res Hepatol Gastroenterol. 2014. PMID: 24953525 Review.

7

A functional classification of ABCB4 variations causing progressive familial intrahepatic cholestasis type 3.

Delaunay JL, Durand-Schneider AM, Dossier C, Falguières T, Gautherot J, Davit-Spraul A, Aït-Slimane T, Housset C, Jacquemin E, Maurice M. Delaunay JL, et al. Hepatology. 2016 May;63(5):1620-31. doi: 10.1002/hep.28300. Epub 2015 Dec 23. Hepatology. 2016. PMID: 26474921

8

A PDZ-Like Motif in the Biliary Transporter ABCB4 Interacts with the Scaffold Protein EBP50 and Regulates ABCB4 Cell Surface Expression.

Venot Q, Delaunay JL, Fouassier L, Delautier D, Falguières T, Housset C, Maurice M, Aït-Slimane T. Venot Q, et al. PLoS One. 2016 Jan 20;11(1):e0146962. doi: 10.1371/journal.pone.0146962. eCollection 2016. PLoS One. 2016. PMID: 26789121 Free PMC article.

9

Functional defect of variants in the adenosine triphosphate-binding sites of ABCB4 and their rescue by the cystic fibrosis transmembrane conductance regulator potentiator, ivacaftor (VX-770).

Delaunay JL, Bruneau A, Hoffmann B, Durand-Schneider AM, Barbu V, Jacquemin E, Maurice M, Housset C, Callebaut I, Aït-Slimane T. Delaunay JL, et al. Hepatology. 2017 Feb;65(2):560-570. doi: 10.1002/hep.28929. Epub 2016 Dec 24. Hepatology. 2017. PMID: 28012258

10

Comparison of in silico prediction and experimental assessment of ABCB4 variants identified in patients with biliary diseases.

Khabou B, Durand-Schneider AM, Delaunay JL, Aït-Slimane T, Barbu V, Fakhfakh F, Housset C, Maurice M. Khabou B, et al. Among authors: ait slimane t. Int J Biochem Cell Biol. 2017 Aug;89:101-109. doi: 10.1016/j.biocel.2017.05.028. Epub 2017 Jun 3. Int J Biochem Cell Biol. 2017. PMID: 28587926

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