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laminin A

Known as: alpha1 laminin, laminin alpha1 
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
Alport disease is caused by mutations in genes encoding the alpha3, alpha4, or alpha5 chains of type IV collagen, which form the… 
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Highly Cited
2006
Highly Cited
2006
Absence of laminin alpha2 chain leads to a severe form of congenital muscular dystrophy (MDC1A) associated with peripheral… 
Highly Cited
2005
Highly Cited
2005
Laminins are important for basement membrane structure and function. The laminin alpha2 chain is a major component of muscle… 
Highly Cited
2005
Highly Cited
2005
Laminins are heterotrimeric glycoproteins of the basement membranes. Laminin 1 (α1, β1, γ1) is the major laminin expressed during… 
Highly Cited
2004
Highly Cited
2004
BACKGROUND Airway remodeling is a key feature of persistent asthma and includes alterations in the extracellular matrix protein… 
Highly Cited
2002
Highly Cited
2002
Protein levels, mRNA expression, and localization of laminin alpha1 and alpha2 chains in development and in adult mice were… 
Highly Cited
2002
Highly Cited
2002
Laminin alpha/beta/gamma heterotrimers are the major noncollagenous components of all basement membranes. To date, five alpha… 
2000
2000
In addition to being the specialized site for transmission of force from the muscle to the tendon, the myotendinous junction (MTJ… 
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Highly Cited
1999
Highly Cited
1999
The terminal colon is aganglionic in mice lacking endothelin-3 or its receptor, endothelin B. To analyze the effects of… 
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1999
1999
The dy/dy mouse is an animal model for human merosin-negative congenital muscular dystrophy (CMD), which has been reported to…