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alpha-Sarcoglycan

Known as: Adhalin, Dystrophin-Associated glycoprotein, 50-kDa, alpha Sarcoglycan 
National Institutes of Health

Related topics

Related topics

2 relations
SGCA gene

Broader (1)

Sarcoglycans

Papers overview

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2018
2018
Sarcoglycan Alpha Mitigates Neuromuscular Junction Decline in Aged Mice by Stabilizing LRP4
During aging, acetylcholine receptor (AChR) clusters become fragmented and denervated at the neuromuscular junction (NMJ… 
Highly Cited
2009
Highly Cited
2009
Overexpression of Galgt2 reduces dystrophic pathology in the skeletal muscles of alpha sarcoglycan-deficient mice.
Recent studies have shown that a number of genes that are not mutated in various forms of muscular dystrophy may serve as… 
Highly Cited
1999
Highly Cited
1999
Ecto-ATPase Activity of α-Sarcoglycan (Adhalin)*
α-Sarcoglycan is a component of the sarcoglycan complex of dystrophin-associated proteins. Mutations of any of the sarcoglycan… 
Highly Cited
1998
Highly Cited
1998
Human ϵ‐sarcoglycan is highly related to α‐sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene 1
Highly Cited
1997
Highly Cited
1997
ε-Sarcoglycan, a Broadly Expressed Homologue of the Gene Mutated in Limb-Girdle Muscular Dystrophy 2D*
The sarcoglycans are transmembrane components of the dystrophin-glycoprotein complex, which links the cytoskeleton to the… 
Highly Cited
1997
Highly Cited
1997
DNA‐fragmentation and expression of apoptosis‐related proteins in muscular dystrophies
Although numerous sarcolemmal protein defects in muscular dystrophies have been identified, the mechanisms linking these defects… 
Highly Cited
1996
Highly Cited
1996
In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genes.
Adenoviral vectors have been shown to effect efficient somatic gene transfer in skeletal muscle and thus offer potential for the… 
Highly Cited
1995
Highly Cited
1995
Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
Marked deficiency of muscle adhalin, a 50 kDa sarcolemmal dystrophin-associated glycoprotein1–3, has been reported in severe… 
Highly Cited
1995
Highly Cited
1995
Laminin β2 chain and adhalin deficiency in the skeletal muscle of Walker‐Warburg syndrome (cerebroocular dysplasia‐muscular dystrophy)
Muscular dystrophy may be caused by disturbances in a number of muscle proteins that appear to be part of a chain of interacting… 
Highly Cited
1994
Highly Cited
1994
Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.
Mutations in the dystrophin gene cause the X chromosome-linked, recessive Duchenne and Becker muscular dystrophies. Dystrophin, a… 
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