Nonsense-mediated mRNA decay and ubiquitin–proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic mice N Vignier, S Schlossarek, B Fraysse, G Mearini, E Krämer, H Pointu, ... Circulation research 105 (3), 239-248, 2009 | 179 | 2009 |
Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice L Carrier, R Knöll, N Vignier, DI Keller, P Bausero, B Prudhon, R Isnard, ... Cardiovascular research 63 (2), 293-304, 2004 | 165 | 2004 |
Length and protein kinase A modulations of myocytes in cardiac myosin binding protein C-deficient mice O Cazorla, S Szilagyi, N Vignier, G Salazar, E Krämer, G Vassort, ... Cardiovascular research 69 (2), 370-380, 2006 | 158 | 2006 |
Cardiac myosin-binding protein C is required for complete relaxation in intact myocytes L Pohlmann, I Kröger, N Vignier, S Schlossarek, E Krämer, C Coirault, ... Circulation research 101 (9), 928-938, 2007 | 154 | 2007 |
Genomic Organization of the KCNQ1 K+ Channel Gene and Identification of C-Terminal Mutations in the Long-QT Syndrome N Neyroud, P Richard, N Vignier, C Donger, I Denjoy, L Demay, ... Circulation research 84 (3), 290-297, 1999 | 148 | 1999 |
Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice B Fraysse, F Weinberger, SC Bardswell, F Cuello, N Vignier, B Geertz, ... Journal of molecular and cellular cardiology 52 (6), 1299-1307, 2012 | 142 | 2012 |
Distinctive serum miRNA profile in mouse models of striated muscular pathologies N Vignier, F Amor, P Fogel, A Duvallet, J Poupiot, S Charrier, M Arock, ... PloS one 8 (2), e55281, 2013 | 109 | 2013 |
ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene M Chatzifrangkeskou, C Le Dour, W Wu, JP Morrow, LC Joseph, ... Human Molecular Genetics 25 (11), 2220-2233, 2016 | 95 | 2016 |
Can cold or heat shock improve skeletal myoblast engraftment in infarcted myocardium? A Maurel, K Azarnoush, L Sabbah, N Vignier, M Le Lorc'h, C Mandet, ... Transplantation 80 (5), 660-665, 2005 | 78 | 2005 |
Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis P Guicheney, N Vignier, A Helbling-Leclerc, M Nissinen, X Zhang, ... Neuromuscular Disorders 7 (3), 180-186, 1997 | 72 | 1997 |
PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy. P Guicheney, N Vignier, X Zhang, Y He, C Cruaud, V Frey, ... Journal of medical genetics 35 (3), 211-217, 1998 | 69 | 1998 |
Rescue of biosynthesis of nicotinamide adenine dinucleotide protects the heart in cardiomyopathy caused by lamin A/C gene mutation N Vignier, M Chatzifrangkeskou, B Morales Rodriguez, M Mericskay, ... Human Molecular Genetics 27 (22), 3870-3880, 2018 | 50 | 2018 |
Partial laminin α2 chain deficiency in a patient with myopathy resembling inclusion body myositis C Di Blasi, M Mora, D Pareyson, L Farina, A Sghirlanzoni, N Vignier, ... Annals of Neurology: Official Journal of the American Neurological …, 2000 | 48 | 2000 |
Striated muscle laminopathies F Azibani, A Muchir, N Vignier, G Bonne, AT Bertrand Seminars in cell & developmental biology 29, 107-115, 2014 | 42 | 2014 |
Congenital muscular dystrophy with primary partial laminin α2 chain deficiency: molecular study Y He, KJ Jones, N Vignier, G Morgan, M Chevallay, A Barois, ... Neurology 57 (7), 1319-1322, 2001 | 42 | 2001 |
Structure, genetic localization, and identification of the cardiac and skeletal muscle transcripts of the human integrin α7 gene (ITGA7) N Vignier, B Moghadaszadeh, F Gary, J Beckmann, U Mayer, ... Biochemical and biophysical research communications 260 (2), 357-364, 1999 | 36 | 1999 |
Cardiac myosin-binding protein C modulates the tuning of the molecular motor in the heart Y Lecarpentier, N Vignier, P Oliviero, A Guellich, L Carrier, C Coirault Biophysical Journal 95 (2), 720-728, 2008 | 35 | 2008 |
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings H Topaloğlu, B Talim, N Vignier, A Helbling-Leclerc, M Yetük, IE Afşin, ... Neuromuscular Disorders 8 (3-4), 169-174, 1998 | 30 | 1998 |
Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy AC Guenantin, I Jebeniani, J Leschik, E Watrin, G Bonne, N Vignier, ... The Journal of clinical investigation 131 (1), 2021 | 29 | 2021 |
Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene S Besse, V Allamand, JT Vilquin, Z Li, C Poirier, N Vignier, H Hori, ... Neuromuscular Disorders 13 (3), 216-222, 2003 | 27 | 2003 |