Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Anne-Marie Durand"'
Autor:
Jean-Louis Delaunay, Ahmad Elbahnsi, Alix Bruneau, Claire Madry, Anne-Marie Durand-Schneider, Anne Stary, Chantal Housset, Jérémie Gautheron, Isabelle Callebaut, Tounsia Aït-Slimane
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 2, p 1236 (2023)
ABCB4 (ATP-binding cassette subfamily B member 4) is a hepatocanalicular floppase involved in biliary phosphatidylcholine (PC) secretion. Variations in the ABCB4 gene give rise to several biliary diseases, including progressive familial intrahepatic
Externí odkaz:
https://doaj.org/article/b42ed66c7598442a905466f5ef479662
Autor:
Alix Bruneau, Jean-Louis Delaunay, Anne-Marie Durand-Schneider, Virginie Vauthier, Amel Ben Saad, Lynda Aoudjehane, Haquima El Mourabit, Romain Morichon, Thomas Falguières, Jérémie Gautheron, Chantal Housset, Tounsia Aït-Slimane
Publikováno v:
Cells, Vol 11, Iss 4, p 617 (2022)
ABCB4, is an adenosine triphosphate-binding cassette (ABC) transporter localized at the canalicular membrane of hepatocytes, where it mediates phosphatidylcholine secretion into bile. Gene variations of ABCB4 cause different types of liver diseases,
Externí odkaz:
https://doaj.org/article/1d4ade379e9b40148174424e5d1942ed
Autor:
Amel Ben Saad, Virginie Vauthier, Martine Lapalus, Elodie Mareux, Evangéline Bennana, Anne-Marie Durand-Schneider, Alix Bruneau, Jean-Louis Delaunay, Emmanuel Gonzales, Chantal Housset, Tounsia Aït-Slimane, François Guillonneau, Emmanuel Jacquemin, Thomas Falguières
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 13, p 7087 (2021)
ABCB4 (ATP-binding cassette subfamily B member 4) is an ABC transporter expressed at the canalicular membrane of hepatocytes where it ensures phosphatidylcholine secretion into bile. Genetic variations of ABCB4 are associated with several rare choles
Externí odkaz:
https://doaj.org/article/9c3eebb2e6de408fb3ca9dfdcd01dc26
Effect of CFTR correctors on the traffic and the function of intracellularly retained ABCB4 variants
Autor:
Ágota Tóth, Emmanuel Jacquemin, Isabelle Garcin, Jean-Louis Delaunay, Chantal Housset, Florent Di Meo, Angelika Janaszkiewicz, Alix Bruneau, Thomas Falguières, Martine Lapalus, Anne-Marie Durand-Schneider, Tounsia Aït-Slimane, Elodie Mareux, Emmanuel Gonzales, Virginie Vauthier, Amel Ben Saad
Publikováno v:
Liver International
Liver International, Wiley-Blackwell, 2021, 41 (6), pp.1344-1357. ⟨10.1111/liv.14839⟩
Liver International, 2021, 41 (6), pp.1344-1357. ⟨10.1111/liv.14839⟩
Liver International, Wiley-Blackwell, 2021, 41 (6), pp.1344-1357. ⟨10.1111/liv.14839⟩
Liver International, 2021, 41 (6), pp.1344-1357. ⟨10.1111/liv.14839⟩
International audience; Background & aim: ABCB4 is expressed at the canalicular membrane of hepatocytes. This ATP-binding cassette (ABC) transporter is responsible for the secretion of phosphatidylcholine into bile canaliculi. Missense genetic variat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f1d478a09ed70ab74550169e6e80f1e
https://hal.sorbonne-universite.fr/hal-03263358/document
https://hal.sorbonne-universite.fr/hal-03263358/document
Autor:
Thomas Falguières, Chantal Housset, Tounsia Aït-Slimane, Nassima Oumata, Amel Ben Saad, Laurent Meijer, Alix Bruneau, Jonathan Elie, Jean-Louis Delaunay, Virginie Vauthier, Anne-Marie Durand-Schneider
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-13 (2019)
Scientific Reports
Scientific Reports
Adenosine triphosphate binding cassette transporter, subfamily B member 4 (ABCB4) is the transporter of phosphatidylcholine at the canalicular membrane of hepatocytes. ABCB4 deficiency, due to genetic variations, is responsible for progressive famili
Autor:
Jean-Louis Delaunay, Isabelle Callebaut, Tounsia Aït-Slimane, Alix Bruneau, Chantal Housset, Brice Hoffmann, Emmanuel Jacquemin, Anne-Marie Durand-Schneider, Michèle Maurice, Véronique Barbu
Publikováno v:
Hepatology (Baltimore, Md.). 65(2)
ABCB4 (MDR3) is an ATP-binding cassette (ABC) transporter expressed at the canalicular membrane of hepatocytes where it mediates phosphatidylcholine (PC) secretion. Variations in the ABCB4 gene are responsible for several biliary diseases, including
Autor:
Matthieu Prot, Sandra Grès, Yves Chrétien, Michèle Maurice, Jean-Sébastien Saulnier-Blache, Odile Colard, Jocelyne Magré, Mona Nemani, Haquima El Mourabit, Jacqueline Capeau, Anne-Marie Durand-Schneider, Emilie Boutet, Eliane Khallouf, Claude Wolf
Publikováno v:
Biochimie. 91:796-803
Berardinelli-Seip congenital lipodystrophy (BSCL) is a rare recessive disease characterized by near absence of adipose tissue and severe insulin resistance. In most cases, BSCL is due to loss-of-function mutations in the genes encoding either seipin
Autor:
Danièle Delautier, Emmanuel Jacquemin, Jean-Louis Delaunay, Alegna Rada, Michèle Maurice, Anne-Marie Durand-Schneider, Julien Gautherot, Tounsia Aït-Slimane
Publikováno v:
Hepatology. 49:1218-1227
Progressive familial intrahepatic cholestasis type 3 (PFIC3) is a rare liver disease characterized by early onset of cholestasis that leads to cirrhosis and liver failure before adulthood. PFIC3 may be improved by chronic administration of ursodeoxyc
Autor:
Anne Davit-Spraul, Claire Dossier, Chantal Housset, Jean-Louis Delaunay, Julien Gautherot, Tounsia Aït-Slimane, Thomas Falguières, Michèle Maurice, Emmanuel Jacquemin, Anne-Marie Durand-Schneider
Publikováno v:
Hepatology
Hepatology, 2015, 63 (5), pp.1620-1631. ⟨10.1002/hep.28300⟩
Hepatology, Wiley-Blackwell, 2015, 63 (5), pp.1620-1631. ⟨10.1002/hep.28300⟩
Hepatology, 2015, 63 (5), pp.1620-1631. ⟨10.1002/hep.28300⟩
Hepatology, Wiley-Blackwell, 2015, 63 (5), pp.1620-1631. ⟨10.1002/hep.28300⟩
International audience; Progressive familial intrahepatic cholestasis type 3 is caused by biallelic variations of ABCB4, most often (≥70%) missense. In this study, we examined the effects of 12 missense variations identified in progressive familial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7230be2093dec065409832e6d0208a8c
https://hal.sorbonne-universite.fr/hal-01258764/file/Delaunay_2015_A_functional.pdf
https://hal.sorbonne-universite.fr/hal-01258764/file/Delaunay_2015_A_functional.pdf
Autor:
Marie-Thérèse Drouet, Michel Arborio, Michèle Maurice, Marie-Pascale Frenkiel, Jean Gruenberg, Anne-Marie Durand-Schneider, Marie Flamand, Isabelle Le Blanc, Sophie Alcon-LePoder, Pascal Roux
Publikováno v:
Journal of Virology. 79:11403-11411
The flavivirus nonstructural protein NS1 is expressed as three discrete species in infected mammalian cells: an intracellular, membrane-associated form essential for viral replication, a cell surface-associated form that may be involved in signal tra