Add to ORKGDysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystroph
Alpha-dystroglycan (a-DG) is a cell-surface glycoprotein that acts as a receptor for both extracellu...
We recently described a novel congenital muscular dystrophy (CMD) syndrome characterized by mental r...
Laminopathies, a broad class of diseases that primarily impact mechanically active tissues such as c...
Laminin-211 deficiency leads to the most common form of congenital muscular dystrophy in childhood, ...
Dystrophin is associated with several novel sarcolemmal proteins, including a laminin-binding extrac...
Congenital muscular dystrophy with laminin α2 chain-deficiency (MDC1A) is one of the most severe for...
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most severe for...
Laminin-deficient congenital muscular dystrophy 1A (MDC1A) is the second most prevalent congenital ...
BACKGROUND: Skeletal muscle disorders associated with mutations of lamin A/C gene include autosomal ...
Integrin dysregulation as a possible driver of matrix remodeling in Laminin-deficient congenital mus...
Background: Skeletal muscle disorders associated with mutations of lamin A/C gene include autosomal ...
Laminins are large heterotrimers composed of the α, β and γ subunits with distinct tissue-specific a...
A-type lamin mutations are associated with degenerative disorders causing dilated cardiomyopathy, Ch...
Laminin-211 deficiency leads to the most common form of congenital muscular dystrophy in childhood, ...
International audienceLaminin α2 deficient congenital muscular dystrophy, caused by mutations in the...
Alpha-dystroglycan (a-DG) is a cell-surface glycoprotein that acts as a receptor for both extracellu...
We recently described a novel congenital muscular dystrophy (CMD) syndrome characterized by mental r...
Laminopathies, a broad class of diseases that primarily impact mechanically active tissues such as c...
Laminin-211 deficiency leads to the most common form of congenital muscular dystrophy in childhood, ...
Dystrophin is associated with several novel sarcolemmal proteins, including a laminin-binding extrac...
Congenital muscular dystrophy with laminin α2 chain-deficiency (MDC1A) is one of the most severe for...
Congenital muscular dystrophy with laminin α2 chain deficiency (MDC1A) is one of the most severe for...
Laminin-deficient congenital muscular dystrophy 1A (MDC1A) is the second most prevalent congenital ...
BACKGROUND: Skeletal muscle disorders associated with mutations of lamin A/C gene include autosomal ...
Integrin dysregulation as a possible driver of matrix remodeling in Laminin-deficient congenital mus...
Background: Skeletal muscle disorders associated with mutations of lamin A/C gene include autosomal ...
Laminins are large heterotrimers composed of the α, β and γ subunits with distinct tissue-specific a...
A-type lamin mutations are associated with degenerative disorders causing dilated cardiomyopathy, Ch...
Laminin-211 deficiency leads to the most common form of congenital muscular dystrophy in childhood, ...
International audienceLaminin α2 deficient congenital muscular dystrophy, caused by mutations in the...
Alpha-dystroglycan (a-DG) is a cell-surface glycoprotein that acts as a receptor for both extracellu...
We recently described a novel congenital muscular dystrophy (CMD) syndrome characterized by mental r...
Laminopathies, a broad class of diseases that primarily impact mechanically active tissues such as c...