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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

Papers overview

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Review
2014
Review
2014
  • 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
Nuclear Import/Export Receptor Nuclear transport receptors constantly shuttle cargo between the nucleus and the cytoplasm through… Expand
2008
2008
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
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
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
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
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
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
beta-Sarcoglycan, one of the subunits of the sarcoglycan complex, is a transmembranous glycoprotein which associates with… Expand
Highly Cited
1999
Highly Cited
1999
Dystroglycan is a widely expressed extracellular matrix receptor that plays a critical role in basement membrane formation… Expand
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