Fibrillin-1 is the major structural component of the 10 nm-diameter microfibrils that confer key physical and mechanical properties to virtually every tissue, alone and together with elastin in the elastic fibers. Mutations in fibrillin-1 cause pleiotropic manifestations in Marfan syndrome (MFS), including dissecting thoracic aortic aneurysms, myocardial dysfunction, progressive bone loss, disproportionate skeletal growth, and the dislocation of the crystalline lens. The characterization of these MFS manifestations in mice, that replicate the human phenotype, have revealed that the underlying mechanisms are distinct and organ-specific. This brief review summarizes relevant findings supporting this conclusion
Mutations in the gene for fibrillin-1 cause Marfan syndrome (MFS), a common hereditary disorder of c...
International audienceThe Marfan syndrome (MFS) is a prominent member of heritable disorders of conn...
Fibrillin-1 is the major backbone of extracellular matrix microfibrils throughout many tissues. Gene...
The Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder with a prevalence of 2...
Fibrillin-1 is a ubiquitous extracellular matrix molecule that sequesters latent growth factor compl...
<div><p>Fibrillin-1 is a ubiquitous extracellular matrix molecule that sequesters latent growth fact...
Marfan syndrome (MFS), a relatively common autosomal dominant hereditary disorder of connective tiss...
Fibrillin-1 is a major glycoprotein component of 10-12 nm microfibrils, consisting predominantly of ...
Mutations in fibrillin-1 result in Marfan syndrome, which affects the cardiovascular, skeletal and o...
Fibrillin-1 is a 350 kDa calcium-binding protein which assembles to form 10-12 nm microfibrils in th...
Marfan syndrome (MFS) is a systemic disorder of connective tissue caused by pathogenic variants in t...
The Marfan syndrome (MFS) is a connective tissue disorder inherited as an autosomal dominant trait a...
Fibrillin-1 is the major component of the 10-12 nm diameter extracellular matrix microfibrils. The m...
International audienceMicrofibrils are macromolecular complexes associated with elastin to form elas...
National audienceMicrofibrils contain a variety of proteins, the most prominent of which are the two...
Mutations in the gene for fibrillin-1 cause Marfan syndrome (MFS), a common hereditary disorder of c...
International audienceThe Marfan syndrome (MFS) is a prominent member of heritable disorders of conn...
Fibrillin-1 is the major backbone of extracellular matrix microfibrils throughout many tissues. Gene...
The Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder with a prevalence of 2...
Fibrillin-1 is a ubiquitous extracellular matrix molecule that sequesters latent growth factor compl...
<div><p>Fibrillin-1 is a ubiquitous extracellular matrix molecule that sequesters latent growth fact...
Marfan syndrome (MFS), a relatively common autosomal dominant hereditary disorder of connective tiss...
Fibrillin-1 is a major glycoprotein component of 10-12 nm microfibrils, consisting predominantly of ...
Mutations in fibrillin-1 result in Marfan syndrome, which affects the cardiovascular, skeletal and o...
Fibrillin-1 is a 350 kDa calcium-binding protein which assembles to form 10-12 nm microfibrils in th...
Marfan syndrome (MFS) is a systemic disorder of connective tissue caused by pathogenic variants in t...
The Marfan syndrome (MFS) is a connective tissue disorder inherited as an autosomal dominant trait a...
Fibrillin-1 is the major component of the 10-12 nm diameter extracellular matrix microfibrils. The m...
International audienceMicrofibrils are macromolecular complexes associated with elastin to form elas...
National audienceMicrofibrils contain a variety of proteins, the most prominent of which are the two...
Mutations in the gene for fibrillin-1 cause Marfan syndrome (MFS), a common hereditary disorder of c...
International audienceThe Marfan syndrome (MFS) is a prominent member of heritable disorders of conn...
Fibrillin-1 is the major backbone of extracellular matrix microfibrils throughout many tissues. Gene...