List of works - Nicolas Vignier

AT1 blockade abolishes left ventricular hypertrophy in heterozygous cMyBP-C null mice: role of FHL1.

scientific article published on 18 April 2013

Alteration of performance in a mouse model of Emery-Dreifuss muscular dystrophy caused by A-type lamins gene mutation

scientific article published on 01 July 2019

Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice

scientific article

Cardiac Myosin-binding protein C modulates the tuning of the molecular motor in the heart

scientific article published on 28 March 2008

Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study

scientific article published on 01 October 2001

Distinctive serum miRNA profile in mouse models of striated muscular pathologies

scientific article

ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

scientific article published on 30 April 2016

Effect of genetic background on the cardiac phenotype in a mouse model of Emery-Dreifuss muscular dystrophy

scientific article published on 12 July 2019

Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

article

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.

scientific article published in February 1999

Identification of homozygous and heterozygous dy 2J mice by PCR

scientific article published on 01 January 2000

Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic mice

scientific article

Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositis

scientific article published on 01 June 2000

Rescue of biosynthesis of nicotinamide adenine dinucleotide protects the heart in cardiomyopathy caused by lamin A/C gene mutation

article

Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene

article

Striated muscle laminopathies.

scientific article published on 15 January 2014

Structure, genetic localization, and identification of the cardiac and skeletal muscle transcripts of the human integrin alpha7 gene (ITGA7)

scientific article (publication date: 5 July 1999)

Synthetic scrapie infectivity: interaction between recombinant PrP and scrapie brain-derived RNA.

scientific article

Targeted Mybpc3 Knock-Out Mice with Cardiac Hypertrophy Exhibit Structural Mitral Valve Abnormalities

scientific article

The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies

scientific article published on August 24, 2021

List of works by Nicolas Vignier

AT1 blockade abolishes left ventricular hypertrophy in heterozygous cMyBP-C null mice: role of FHL1.

Alteration of performance in a mouse model of Emery-Dreifuss muscular dystrophy caused by A-type lamins gene mutation

Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice

Cardiac Myosin-binding protein C modulates the tuning of the molecular motor in the heart

Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study

Distinctive serum miRNA profile in mouse models of striated muscular pathologies

ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

Effect of genetic background on the cardiac phenotype in a mouse model of Emery-Dreifuss muscular dystrophy

Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.

Identification of homozygous and heterozygous dy 2J mice by PCR

Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic mice

Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositis

Rescue of biosynthesis of nicotinamide adenine dinucleotide protects the heart in cardiomyopathy caused by lamin A/C gene mutation

Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene

Striated muscle laminopathies.

Structure, genetic localization, and identification of the cardiac and skeletal muscle transcripts of the human integrin alpha7 gene (ITGA7)

Synthetic scrapie infectivity: interaction between recombinant PrP and scrapie brain-derived RNA.

Targeted Mybpc3 Knock-Out Mice with Cardiac Hypertrophy Exhibit Structural Mitral Valve Abnormalities

The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies