Lista de obras -

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

artículo científico publicado en 2013

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

artículo científico publicado en 2019

Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice

artículo científico publicado en 2004

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

artículo científico publicado en 2008

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

artículo científico publicado en 2001

Distinctive serum miRNA profile in mouse models of striated muscular pathologies

artículo científico publicado en 2013

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

artículo científico publicado en 2016

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

artículo científico publicado en 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.

artículo científico publicado en 1999

Identification of homozygous and heterozygous dy 2J mice by PCR

artículo científico publicado en 2000

Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings ⬇️

artículo científico publicado el 1 de mayo de 1998

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

artículo científico publicado en 2009

PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy ⬇️

artículo científico publicado el 1 de marzo de 1998

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

artículo científico publicado en 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.

artículo científico publicado en 2014

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

artículo científico publicado en 1999

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico

Lista de obras de

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

Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings ⬇️

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

PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy ⬇️

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