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Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat model.
Delwarde C, Toquet C, Aumond P, Kayvanjoo AH, Foucal A, Le Vely B, Baudic M, Lauzier B, Blandin S, Véziers J, Paul-Gilloteaux P, Lecointe S, Baron E, Massaiu I, Poggio P, Rémy S, Anegon I, Le Marec H, Monassier L, Schott JJ, Mass E, Barc J, Le Tourneau T, Merot J, Capoulade R. Delwarde C, et al. Among authors: le marec h. Cardiovasc Res. 2023 May 2;119(3):759-771. doi: 10.1093/cvr/cvac136. Cardiovasc Res. 2023. PMID: 36001550
[Hereditary cardiac arrhythmia].
Le Marec H, Schott JJ. Le Marec H, et al. Arch Mal Coeur Vaiss. 1997 Apr;90 Spec No 1:57-66. Arch Mal Coeur Vaiss. 1997. PMID: 9238458 Review. French.
[Congenital long QT syndromes].
Le Marec H, Schott JJ. Le Marec H, et al. Arch Mal Coeur Vaiss. 1997 Jun;90 Spec No 3:25-35. Arch Mal Coeur Vaiss. 1997. PMID: 9295920 French.
Adult KCNE1-knockout mice exhibit a mild cardiac cellular phenotype.
Charpentier F, Merot J, Riochet D, Le Marec H, Escande D. Charpentier F, et al. Among authors: le marec h. Biochem Biophys Res Commun. 1998 Oct 29;251(3):806-10. doi: 10.1006/bbrc.1998.9554. Biochem Biophys Res Commun. 1998. PMID: 9790991
[Genetics and cardiac arrhythmias].
Probst V, Kyndt F, Allouis M, Schott JJ, Le Marec H. Probst V, et al. Among authors: le marec h. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1054-62. Arch Mal Coeur Vaiss. 2003. PMID: 14694781 Review. French.
14-3-3 is a regulator of the cardiac voltage-gated sodium channel Nav1.5.
Allouis M, Le Bouffant F, Wilders R, Péroz D, Schott JJ, Noireaud J, Le Marec H, Mérot J, Escande D, Baró I. Allouis M, et al. Among authors: le bouffant f, le marec h. Circ Res. 2006 Jun 23;98(12):1538-46. doi: 10.1161/01.RES.0000229244.97497.2c. Epub 2006 May 25. Circ Res. 2006. PMID: 16728661
Mutations in the gene encoding filamin A as a cause for familial cardiac valvular dystrophy.
Kyndt F, Gueffet JP, Probst V, Jaafar P, Legendre A, Le Bouffant F, Toquet C, Roy E, McGregor L, Lynch SA, Newbury-Ecob R, Tran V, Young I, Trochu JN, Le Marec H, Schott JJ. Kyndt F, et al. Among authors: le bouffant f, le marec h. Circulation. 2007 Jan 2;115(1):40-9. doi: 10.1161/CIRCULATIONAHA.106.622621. Epub 2006 Dec 26. Circulation. 2007. PMID: 17190868
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.
Probst V, Wilde AA, Barc J, Sacher F, Babuty D, Mabo P, Mansourati J, Le Scouarnec S, Kyndt F, Le Caignec C, Guicheney P, Gouas L, Albuisson J, Meregalli PG, Le Marec H, Tan HL, Schott JJ. Probst V, et al. Among authors: le scouarnec s, le marec h, le caignec c. Circ Cardiovasc Genet. 2009 Dec;2(6):552-7. doi: 10.1161/CIRCGENETICS.109.853374. Epub 2009 Sep 29. Circ Cardiovasc Genet. 2009. PMID: 20031634
144 results