LAMA2 gene

Known as: LAMININ 2, HEAVY CHAIN, MEROSIN, LAMA2 
 
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Posttranslational modification of alpha-dystroglycan (α-DG) by the like-acetylglucosaminyltransferase (LARGE) is required for it… (More)
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Highly Cited
2010
Highly Cited
2010
Alpha-dystroglycan (alpha-DG) is a cell-surface glycoprotein that acts as a receptor for both extracellular matrix proteins… (More)
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Highly Cited
2003
Highly Cited
2003
The congenital muscular dystrophies (CMD) are a heterogeneous group of autosomal recessive disorders. A new pathomechanism has… (More)
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Highly Cited
2003
Highly Cited
2003
Targeted deletion of focal adhesion kinase (fak) in the developing dorsal forebrain resulted in local disruptions of the cortical… (More)
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Highly Cited
2001
Highly Cited
2001
The limb girdle and congenital muscular dystrophies (LGMD and CMD) are characterized by skeletal muscle weakness and dystrophic… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Juvenile hemangiomas are common, benign tumors, distinctive for their perinatal presentation, rapid growth during the… (More)
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Highly Cited
1997
Highly Cited
1997
Using the gene targeting technique, we have generated a new mouse model of congenital muscular dystrophy (CMD), a null mutant for… (More)
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Highly Cited
1996
Highly Cited
1996
Astrocytomas often show high rates of local invasion that lead to local recurrence of the disease. Histologically, the most… (More)
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Highly Cited
1995
Highly Cited
1995
Congenital muscular dystrophies (CMDs), are heterogeneous autosomal recessive disorders. Their severe manifestations consist of… (More)
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Highly Cited
1992
Highly Cited
1992
Development of the human embryo depends on the ability of first trimester cytotrophoblastic stem cells to differentiate and… (More)
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