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Nicolas Vignier
Nicolas Vignier
Institut de Myologie
Adresse e-mail validée de upmc.fr
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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
1792009
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
1652004
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
1582006
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
1542007
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
1481999
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
1422012
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
1092013
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
952016
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
782005
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
721997
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
691998
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
502018
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
482000
Striated muscle laminopathies
F Azibani, A Muchir, N Vignier, G Bonne, AT Bertrand
Seminars in cell & developmental biology 29, 107-115, 2014
422014
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
422001
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
361999
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
352008
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
301998
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
292021
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
272003
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