13 results for author:"Neyroud N." in Literature citations
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| Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 alpha-subunits. Clatot J., Ziyadeh-Isleem A., Maugenre S., Denjoy I., Liu H., Dilanian G., Hatem S.N., Deschenes I., Coulombe A., Guicheney P. et al. Cardiovasc. Res. 96:53-63(2012) · Mapped (14) |
| MOG1: a new susceptibility gene for Brugada syndrome. Kattygnarath D., Maugenre S., Neyroud N., Balse E., Ichai C., Denjoy I., Dilanian G., Martins R.P., Fressart V., Berthet M. et al. Circ Cardiovasc Genet 4:261-268(2011) · Mapped (1) |
| Kv4 potassium channels form a tripartite complex with the anchoring protein SAP97 and CaMKII in cardiac myocytes. El-Haou S., Balse E., Neyroud N., Dilanian G., Gavillet B., Abriel H., Coulombe A., Jeromin A., Hatem S.N. |
| The anchoring protein SAP97 retains Kv1.5 channels in the plasma membrane of cardiac myocytes. Abi-Char J., El-Haou S., Balse E., Neyroud N., Vranckx R., Coulombe A., Hatem S.N. Am. J. Physiol. Heart Circ. Physiol. 294:H1851-61(2008) · Mapped (7) |
| Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy. Duboscq-Bidot L., Xu P., Charron P., Neyroud N., Dilanian G., Millaire A., Bors V., Komajda M., Villard E. Cardiovasc. Res. 77:118-125(2008) · Mapped (2) |
| Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk. Chouabe C., Neyroud N., Richard P., Denjoy I., Hainque B., Romey G., Drici M.-D., Guicheney P., Barhanin J. Cardiovasc. Res. 45:971-980(2000) · UniProtKB (1) |
| Congenital long QT syndrome. The value of genetics in prognostic evaluation. Denjoy I., Lupoglazoff J.M., Donger C., Berthet M., Richard P., Neyroud N., Villain E., Lucet V., Coumel P., Guicheney P. Arch. Mal. Coeur Vaiss. 92:557-563(1999) · UniProtKB (1) |
| Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias. Mohammad-Panah R., Demolombe S., Neyroud N., Guicheney P., Kyndt F., van den Hoff M., Baro I., Escande D. Am. J. Hum. Genet. 64:1015-1023(1999) · UniProtKB (1) |
| Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome. Neyroud N., Richard P., Vignier N., Donger C., Denjoy I., Demay L., Shkolnikova M., Pesce R., Chevalier P., Hainque B. et al. Circ. Res. 84:290-297(1999) · UniProtKB (1) |
| Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome. Neyroud N., Denjoy I., Donger C., Gary F., Villain E., Leenhardt A., Benali K., Schwartz K., Coumel P., Guicheney P. Eur. J. Hum. Genet. 6:129-133(1998) · UniProtKB (1) |
| KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome. Donger C., Denjoy I., Berthet M., Neyroud N., Cruaud C., Bennaceur M., Chivoret G., Schwartz K., Coumel P., Guicheney P. Circulation 96:2778-2781(1997) · UniProtKB (1) |
| Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias. Chouabe C., Neyroud N., Guicheney P., Lazdunski M., Romey G., Barhanin J. |
| A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Neyroud N., Tesson F., Denjoy I., Leibovici M., Donger C., Barhanin J., Faure S., Gary F., Coumel P., Petit C. et al. Nat. Genet. 15:186-189(1997) |