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SSPN protein, human
Known as:
SPN1
, SPN2
, Kirsten-Ras-Associated Protein
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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…
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National Institutes of Health
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Related topics
Related topics
10 relations
Broader (3)
Carrier Proteins
Membrane Proteins
Neoplasm Proteins
Cell-Matrix Junction
Integral Membrane Proteins
Ligand Binding
Muscle 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
Highly Cited
2009
Highly Cited
2009
Crystal Structure of the Nuclear Export Receptor CRM1 in Complex with Snurportin1 and RanGTP
T. Monecke
,
T. Güttler
,
P. Neumann
,
A. Dickmanns
,
D. Görlich
,
R. Ficner
Science
2009
Corpus ID: 21116091
Nuclear Import/Export Receptor Nuclear transport receptors constantly shuttle cargo between the nucleus and the cytoplasm through…
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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
S. Dröge
,
J. Fröhlich
,
R. Radek
,
H. König
Applied and Environmental Microbiology
2006
Corpus ID: 18835672
ABSTRACT A novel spirochete strain, SPN1, was isolated from the hindgut contents of the termite Neotermes castaneus. The highest…
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Highly Cited
2001
Highly Cited
2001
Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex.
R. Cohn
,
M. Durbeej
,
S. Moore
,
R. Coral-Vázquez
,
S. Prouty
,
K. Campbell
The Journal of clinical investigation
2001
Corpus ID: 2625909
Cardiomyopathy is a multifactorial disease, and the dystrophin-glycoprotein complex has been implicated in the pathogenesis of…
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Highly Cited
2000
Highly Cited
2000
Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy.
M. Yoshida
,
H. Hama
,
+7 authors
E. Ozawa
Human molecular genetics
2000
Corpus ID: 7326826
The sarcoglycan complex is composed of four membrane-spanning dystrophin-associated proteins (DAPs) and is essential for skeletal…
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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.
M. Durbeej
,
R. Cohn
,
+5 authors
K. Campbell
Molecular cell
2000
Corpus ID: 2251523
Highly Cited
1999
Highly Cited
1999
Disruption of the Sarcoglycan–Sarcospan Complex in Vascular Smooth Muscle A Novel Mechanism for Cardiomyopathy and Muscular Dystrophy
R. Coral-Vázquez
,
R. Cohn
,
+9 authors
K. Campbell
Cell
1999
Corpus ID: 376759
Highly Cited
1999
Highly Cited
1999
Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.
K. Araishi
,
T. Sasaoka
,
+6 authors
E. Ozawa
Human molecular genetics
1999
Corpus ID: 24018275
beta-Sarcoglycan, one of the subunits of the sarcoglycan complex, is a transmembranous glycoprotein which associates with…
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Highly Cited
1999
Highly Cited
1999
Biochemical Characterization of the Epithelial Dystroglycan Complex*
M. Durbeej
,
K. Campbell
The Journal of Biological Chemistry
1999
Corpus ID: 7292644
Dystroglycan is a widely expressed extracellular matrix receptor that plays a critical role in basement membrane formation…
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1996
1996
Coamplification in tumors of KRAS2, type 2 inositol 1,4,5 triphosphate receptor gene, and a novel human gene, KRAG.
J. Heighway
,
D. Betticher
,
P. Hoban
,
H. Altermatt
,
R. Cowen
Genomics
1996
Corpus ID: 20425798
Analysis of a region of DNA, coamplified in tumors with KRAS2, resulted in the identification of the human homologue of the mouse…
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