Add to ORKGIntegrin dysregulation as a possible driver of matrix remodeling in Laminin-deficient congenital muscular dystrophy (MDC1A
Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder, and one of the most frequently...
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...
Merosin Deficient Congenital Muscular Dystrophy Type 1A (MDC1A) is the most common form of Congenita...
AbstractTransgenically introduced laminin (LN) α1 chain prevents muscular dystrophy in LNα2 chain de...
Transgenically introduced laminin (LN) α1 chain prevents muscular dystrophy in LNα2 chain deficient ...
Laminin-deficient congenital muscular dystrophy 1A (MDC1A) is the second most prevalent congenital ...
Merosin deficient congenital muscular dystrophy type 1A (MDC1A) is caused by the loss of laminin-211...
Mutations in the gene encoding laminin α2 chain, an extracellular matrix protein mainly expressed in...
Laminin-211 is a major constituent of the skeletal muscle basement membrane, exerting its biological...
Laminins are large heterotrimers composed of the α, β and γ subunits with distinct tissue-specific a...
Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient musc...
Laminin α2 chain mutations cause congenital muscular dystrophy with dysmyelination neuropathy (MDC1A...
The extracellular matrix provides a solid scaffold and signals to cells through extracellular matrix...
Congenital muscular dystrophy with laminin α2 chain-deficiency (MDC1A) is one of the most severe for...
Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder, and one of the most frequently...
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...
Merosin Deficient Congenital Muscular Dystrophy Type 1A (MDC1A) is the most common form of Congenita...
AbstractTransgenically introduced laminin (LN) α1 chain prevents muscular dystrophy in LNα2 chain de...
Transgenically introduced laminin (LN) α1 chain prevents muscular dystrophy in LNα2 chain deficient ...
Laminin-deficient congenital muscular dystrophy 1A (MDC1A) is the second most prevalent congenital ...
Merosin deficient congenital muscular dystrophy type 1A (MDC1A) is caused by the loss of laminin-211...
Mutations in the gene encoding laminin α2 chain, an extracellular matrix protein mainly expressed in...
Laminin-211 is a major constituent of the skeletal muscle basement membrane, exerting its biological...
Laminins are large heterotrimers composed of the α, β and γ subunits with distinct tissue-specific a...
Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient musc...
Laminin α2 chain mutations cause congenital muscular dystrophy with dysmyelination neuropathy (MDC1A...
The extracellular matrix provides a solid scaffold and signals to cells through extracellular matrix...
Congenital muscular dystrophy with laminin α2 chain-deficiency (MDC1A) is one of the most severe for...
Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder, and one of the most frequently...
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...