18 results for author:"Escande D." in Literature citations
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| Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model. Leoni A.L., Gavillet B., Rougier J.S., Marionneau C., Probst V., Le Scouarnec S., Schott J.J., Demolombe S., Bruneval P., Huang C.L. et al. PLoS ONE 5:e9298-e9298(2010) · Mapped (20) |
| Genetically determined differences in sodium current characteristics modulate conduction disease severity in mice with cardiac sodium channelopathy. Remme C.A., Scicluna B.P., Verkerk A.O., Amin A.S., van Brunschot S., Beekman L., Deneer V.H., Chevalier C., Oyama F., Miyazaki H. et al. Circ. Res. 104:1283-1292(2009) · Mapped (6) |
| Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. Watanabe H., Koopmann T.T., Le Scouarnec S., Yang T., Ingram C.R., Schott J.J., Demolombe S., Probst V., Anselme F., Escande D. et al. J. Clin. Invest. 118:2260-2268(2008) · UniProtKB (1) · Mapped (3) |
| Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes. Mohler P.J., Le Scouarnec S., Denjoy I., Lowe J.S., Guicheney P., Caron L., Driskell I.M., Schott J.J., Norris K., Leenhardt A. et al. Circulation 115:432-441(2007) · Mapped (11) |
| 14-3-3 is a regulator of the cardiac voltage-gated sodium channel Nav1.5. Allouis M., Le Bouffant F., Wilders R., Peroz D., Schott J.J., Noireaud J., Le Marec H., Merot J., Escande D., Baro I. Circ. Res. 98:1538-1546(2006) · Mapped (22) |
| Bradycardia and slowing of the atrioventricular conduction in mice lacking CaV3.1/alpha1G T-type calcium channels. Mangoni M.E., Traboulsie A., Leoni A.L., Couette B., Marger L., Le Quang K., Kupfer E., Cohen-Solal A., Vilar J., Shin H.S. et al. Circ. Res. 98:1422-1430(2006) · Mapped (17) |
| Impaired impulse propagation in Scn5a-knockout mice: combined contribution of excitability, connexin expression, and tissue architecture in relation to aging. van Veen T.A., Stein M., Royer A., Le Quang K., Charpentier F., Colledge W.H., Huang C.L., Wilders R., Grace A.A., Escande D. et al. Circulation 112:1927-1935(2005) · Mapped (7) |
| Mouse model of SCN5A-linked hereditary Lenegre's disease: age-related conduction slowing and myocardial fibrosis. Royer A., van Veen T.A., Le Bouter S., Marionneau C., Griol-Charhbili V., Leoni A.L., Steenman M., van Rijen H.V., Demolombe S., Goddard C.A. et al. Circulation 111:1738-1746(2005) · Mapped (9) |
| Mutation in the KCNQ1 gene leading to the short QT-interval syndrome. Bellocq C., van Ginneken A.C.G., Bezzina C.R., Alders M., Escande D., Mannens M.M.A.M., Baro I., Wilde A.A.M. Circulation 109:2394-2397(2004) · UniProtKB (1) |
| Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death. Mohler P.J., Schott J.-J., Gramolini A.O., Dilly K.W., Guatimosim S., duBell W.H., Song L.-S., Haurogne K., Kyndt F., Ali M.E. et al. |
| Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients. Smits J.P.P., Eckardt L., Probst V., Bezzina C.R., Schott J.-J., Remme C.A., Haverkamp W., Breithardt G., Escande D., Schulze-Bahr E. et al. J. Am. Coll. Cardiol. 40:350-356(2002) · UniProtKB (1) · Mapped (13) |
| Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family. Kyndt F., Probst V., Potet F., Demolombe S., Chevallier J.-C., Baro I., Moisan J.-P., Boisseau P., Schott J.-J., Escande D. et al. Circulation 104:3081-3086(2001) · UniProtKB (1) · Mapped (13) |
| Divergent expression of delayed rectifier K(+) channel subunits during mouse heart development. Franco D., Demolombe S., Kupershmidt S., Dumaine R., Dominguez J.N., Roden D., Antzelevitch C., Escande D., Moorman A.F. Cardiovasc. Res. 52:65-75(2001) · Mapped (16) |
| Mice disrupted for the KvLQT1 potassium channel regulator IsK gene accumulate mature T cells. Chabannes D., Barhanin J., Escande D. Cell. Immunol. 209:1-9(2001) · Mapped (2) |
| Differential expression of KvLQT1 and its regulator IsK in mouse epithelia. Demolombe S., Franco D., de Boer P., Kuperschmidt S., Roden D., Pereon Y., Jarry A., Moorman A.F., Escande D. Am. J. Physiol., Cell Physiol. 280:C359-72(2001) · Mapped (41) |
| Cardiac conduction defects associate with mutations in SCN5A. Schott J.-J., Alshinawi C., Kyndt F., Probst V., Hoorntje T.M., Hulsbeek M., Wilde A.A.M., Escande D., Mannens M.M.A.M., Le Marec H. Nat. Genet. 23:20-21(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) |
| Adult KCNE1-knockout mice exhibit a mild cardiac cellular phenotype. Charpentier F., Merot J., Riochet D., Le Marec H., Escande D. Biochem. Biophys. Res. Commun. 251:806-810(1998) · Mapped (2) |