10 results for author:"Vignier N." in Literature citations
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| Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice. Fraysse B., Weinberger F., Bardswell S.C., Cuello F., Vignier N., Geertz B., Starbatty J., Kramer E., Coirault C., Eschenhagen T. et al. J. Mol. Cell. Cardiol. 52:1299-1307(2012) · Mapped (6) |
| Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic mice. Vignier N., Schlossarek S., Fraysse B., Mearini G., Kramer E., Pointu H., Mougenot N., Guiard J., Reimer R., Hohenberg H. et al. Circ. Res. 105:239-248(2009) · Mapped (6) |
| Altered myocardial gene expression reveals possible maladaptive processes in heterozygous and homozygous cardiac myosin-binding protein C knockout mice. Eijssen L.M., van den Bosch B.J., Vignier N., Lindsey P.J., van den Burg C.M., Carrier L., Doevendans P.A., van der Vusse G.J., Smeets H.J. Genomics 91:52-60(2008) · Mapped (15) |
| Cardiac myosin-binding protein C is required for complete relaxation in intact myocytes. Pohlmann L., Kroger I., Vignier N., Schlossarek S., Kramer E., Coirault C., Sultan K.R., El-Armouche A., Winegrad S., Eschenhagen T. et al. Circ. Res. 101:928-938(2007) · Mapped (6) |
| Length and protein kinase A modulations of myocytes in cardiac myosin binding protein C-deficient mice. Cazorla O., Szilagyi S., Vignier N., Salazar G., Kramer E., Vassort G., Carrier L., Lacampagne A. Cardiovasc. Res. 69:370-380(2006) · Mapped (6) |
| Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice. Carrier L., Knoll R., Vignier N., Keller D.I., Bausero P., Prudhon B., Isnard R., Ambroisine M.L., Fiszman M., Ross J. Jr. et al. Cardiovasc. Res. 63:293-304(2004) · Mapped (6) |
| Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha2 chain gene. Besse S., Allamand V., Vilquin J.T., Li Z., Poirier C., Vignier N., Hori H., Guenet J.L., Guicheney P. Neuromuscul. Disord. 13:216-222(2003) · Mapped (7) |
| Congenital muscular dystrophy with primary partial laminin alpha-2 chain deficiency: molecular study. He Y., Jones K.J., Vignier N., Morgan G., Chevallay M., Barois A., Estournet-Mathiaud B., Hori H., Mizuta T., Tome F.M.S. et al. Neurology 57:1319-1322(2001) · UniProtKB (1) |
| Structure, genetic localization, and identification of the cardiac and skeletal muscle transcripts of the human integrin alpha7 gene (ITGA7). Vignier N., Moghadaszadeh B., Gary F., Beckmann J., Mayer U., Guicheney P. Biochem. Biophys. Res. Commun. 260:357-364(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) |