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Page 1
Veratridine Induces Vasorelaxation in Mouse Cecocolic Mesenteric Arteries.
Park J, Sahyoun C, Frangieh J, Réthoré L, Proux C, Grimaud L, Vessières E, Bourreau J, Mattei C, Henrion D, Marionneau C, Fajloun Z, Legendre C, Legros C. Park J, et al. Among authors: marionneau c. Toxins (Basel). 2024 Dec 10;16(12):533. doi: 10.3390/toxins16120533. Toxins (Basel). 2024. PMID: 39728791 Free PMC article.
Functional Epicardial Conduction Disturbances Due to a SCN5A Variant Associated With Brugada Syndrome.
Renard E, Walton RD, Benoist D, Brette F, Bru-Mercier G, Chaigne S, Charron S, Constantin M, Douard M, Dubes V, Guillot B, Hof T, Magat J, Martinez ME, Michel C, Pallares-Lupon N, Pasdois P, Récalde A, Vaillant F, Sacher F, Labrousse L, Rogier J, Kyndt F, Baudic M, Schott JJ, Barc J, Probst V, Sarlandie M, Marionneau C, Ashton JL, Hocini M, Haïssaguerre M, Bernus O. Renard E, et al. Among authors: marionneau c. JACC Clin Electrophysiol. 2023 Aug;9(8 Pt 1):1248-1261. doi: 10.1016/j.jacep.2023.03.009. Epub 2023 May 24. JACC Clin Electrophysiol. 2023. PMID: 37227351 Free PMC article.
FHF2 phosphorylation and regulation of native myocardial Na V 1.5 channels.
Lesage A, Lorenzini M, Burel S, Sarlandie M, Bibault F, Maloney D, Silva JR, Reid Townsend R, Nerbonne JM, Marionneau C. Lesage A, et al. Among authors: marionneau c. bioRxiv [Preprint]. 2023 Feb 3:2023.01.31.526475. doi: 10.1101/2023.01.31.526475. bioRxiv. 2023. Update in: J Gen Physiol. 2023 Sep 4;155(9):e202213293. doi: 10.1085/jgp.202213293 PMID: 36778222 Free PMC article. Updated. Preprint.
Proteomic and functional mapping of cardiac NaV1.5 channel phosphorylation sites.
Lorenzini M, Burel S, Lesage A, Wagner E, Charrière C, Chevillard PM, Evrard B, Maloney D, Ruff KM, Pappu RV, Wagner S, Nerbonne JM, Silva JR, Townsend RR, Maier LS, Marionneau C. Lorenzini M, et al. Among authors: marionneau c. J Gen Physiol. 2021 Feb 1;153(2):e202012646. doi: 10.1085/jgp.202012646. J Gen Physiol. 2021. PMID: 33410863 Free PMC article.
Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction.
Al Sayed ZR, Canac R, Cimarosti B, Bonnard C, Gourraud JB, Hamamy H, Kayserili H, Girardeau A, Jouni M, Jacob N, Gaignerie A, Chariau C, David L, Forest V, Marionneau C, Charpentier F, Loussouarn G, Lamirault G, Reversade B, Zibara K, Lemarchand P, Gaborit N. Al Sayed ZR, et al. Among authors: marionneau c. Cardiovasc Res. 2021 Jul 27;117(9):2092-2107. doi: 10.1093/cvr/cvaa259. Cardiovasc Res. 2021. PMID: 32898233 Free article.
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.
Belbachir N, Portero V, Al Sayed ZR, Gourraud JB, Dilasser F, Jesel L, Guo H, Wu H, Gaborit N, Guilluy C, Girardeau A, Bonnaud S, Simonet F, Karakachoff M, Pattier S, Scott C, Burel S, Marionneau C, Chariau C, Gaignerie A, David L, Genin E, Deleuze JF, Dina C, Sauzeau V, Loirand G, Baró I, Schott JJ, Probst V, Wu JC, Redon R, Charpentier F, Le Scouarnec S. Belbachir N, et al. Among authors: marionneau c. Eur Heart J. 2019 Oct 1;40(37):3081-3094. doi: 10.1093/eurheartj/ehz308. Eur Heart J. 2019. PMID: 31114854 Free PMC article.
42 results