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SSPN protein, human

Known as: SPN1, SPN2, Kirsten-Ras-Associated Protein 
Sarcospan (1304 aa, 144 kD) is a cell adhesion process protein that is encoded by the human SSPN gene and has roles in muscle contraction and cell… Expand
National Institutes of Health

Related topics

Related topics

10 relations

Broader (3)

Carrier ProteinsMembrane ProteinsNeoplasm Proteins
Cell-Matrix JunctionIntegral Membrane ProteinsLigand BindingMuscle Contraction
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
Dystrophin complex functions as a scaffold for signalling proteins.
  • B. Constantin
  • Biochimica et biophysica acta
  • 2014
    • Corpus ID: 39220723
Dystrophin is a 427kDa sub-membrane cytoskeletal protein, associated with the inner surface membrane and incorporated in a large… Expand
Highly Cited
2009
Highly Cited
2009
Crystal Structure of the Nuclear Export Receptor CRM1 in Complex with Snurportin1 and RanGTP
Nuclear Import/Export Receptor Nuclear transport receptors constantly shuttle cargo between the nucleus and the cytoplasm through… Expand
2008
2008
Effects of terlipressin on the aquaretic system: evidence of antidiuretic effects.
The vasopressin analog terlipressin is believed to cause vasoconstriction selectively by V1 receptor stimulation. However, a… Expand
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Highly Cited
2006
Highly Cited
2006
Spirochaeta coccoides sp. nov., a Novel Coccoid Spirochete from the Hindgut of the Termite Neotermes castaneus
ABSTRACT A novel spirochete strain, SPN1, was isolated from the hindgut contents of the termite Neotermes castaneus. The highest… Expand
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Highly Cited
2001
Highly Cited
2001
Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex.
Cardiomyopathy is a multifactorial disease, and the dystrophin-glycoprotein complex has been implicated in the pathogenesis of… Expand
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Highly Cited
2000
Highly Cited
2000
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.
Limb-girdle muscular dystrophy type 2E (LGMD 2E) is caused by mutations in the beta-sarcoglycan gene, which is expressed in… Expand
Highly Cited
2000
Highly Cited
2000
Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy.
The sarcoglycan complex is composed of four membrane-spanning dystrophin-associated proteins (DAPs) and is essential for skeletal… Expand
Highly Cited
1999
Highly Cited
1999
Disruption of the Sarcoglycan–Sarcospan Complex in Vascular Smooth Muscle A Novel Mechanism for Cardiomyopathy and Muscular Dystrophy
To investigate mechanisms in the pathogenesis of cardiomyopathy associated with mutations of the dystrophin-glycoprotein complex… Expand
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Highly Cited
1999
Highly Cited
1999
Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.
beta-Sarcoglycan, one of the subunits of the sarcoglycan complex, is a transmembranous glycoprotein which associates with… Expand
Highly Cited
1999
Highly Cited
1999
Biochemical Characterization of the Epithelial Dystroglycan Complex*
Dystroglycan is a widely expressed extracellular matrix receptor that plays a critical role in basement membrane formation… Expand
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