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Sarcoglycan Complexes

Known as: Complex, Sarcoglycan, sarcoglycan-sarcospan complex location, sarcoglycan complex location 
A protein complex formed of four sarcoglycans plus sarcospan; there are six known sarcoglycans: alpha-, beta-, gamma-, delta-, epsilon- and zeta… 
National Institutes of Health

Related topics

Related topics

2 relations
Sarcoglycans

Broader (1)

dystroglycan complex

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
No muscle involvement in myoclonus‐dystonia caused by ɛ‐sarcoglycan gene mutations
Mutations in the ɛ‐sarcoglycan gene (SGCE) can cause autosomal dominant inherited myoclonus‐dystonia (M‐D). Defects in other… 
2007
2007
Skeletal myosphere-derived progenitor cell transplantation promotes neovascularization in delta-sarcoglycan knockdown cardiomyopathy.
Highly Cited
2002
Highly Cited
2002
Dystroglycan Is Not Required for Localization of Dystrophin, Syntrophin, and Neuronal Nitric-oxide Synthase at the Sarcolemma but Regulates Integrin α7B Expression and Caveolin-3 Distribution*
Dystroglycan is part of the dystrophin-associated protein complex, which joins laminin in the extracellular matrix to dystrophin… 
2001
2001
Localization of sarcoglycan, neuronal nitric oxide synthase, β‐dystroglycan, and dystrophin molecules in normal skeletal myofiber: Triple immunogold labeling electron microscopy
In order to investigate the mode of existence of the sarcoglycan complex, neuronal nitric oxide synthase (nNOS), β‐dystroglycan… 
2000
2000
Disruption of the b-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2
1999
1999
Developmental expression of sarcoglycan gene products in cultured myocytes.
The sarcoglycan complex consists of four membrane-spanning proteins and was shown to be exclusively distributed in striated… 
1999
1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin–glycoprotein complex
Based on the pattern of distribution of the SG proteins in patients with LGMD2C and 2D, and on the observed decreased abundance… 
1998
1998
Animal Model Molecular Pathogenesis of Muscle Degeneration in the d-Sarcoglycan-Deficient Hamster
The BIO14.6 hamster is an extensively used animal model of autosomal recessive cardiomyopathy and muscular dystrophy. Recently, a… 
1996
1996
Expression of a dystrophin-sarcoglycan complex in serum-deprived BC3H1 cells and involvement of alpha-sarcoglycan in substrate attachment.
Dystrophin and alpha- and gamma-sarcoglycans were newly expressed in BC3H1 cells during differentiation induced by serum… 
1996
1996
Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy.
We have identified 12 cases from a group of 45 patients with early onset limb-girdle muscular dystrophy (LGMD), who have a… 
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