Citations for
1DMD, SSPN, UTRN
Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice.
Marshall JL, Chou E, Oh J, Kwok A, Burkin DJ, Crosbie-Watson RH.
Hum Mol Genet 21(20):4378-93. Epub 2012 Jul 13. 2012
2AKT1, SSPN, UTRN
Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration.
Marshall JL, Holmberg J, Chou E, Ocampo AC, Oh J, Lee J, Peter AK, Martin PT, Crosbie-Watson RH.
J Cell Biol 197(7):1009-27. doi: 10.1083/jcb.201110032. 2012
3SSPN
Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration.
Marshall JL, Holmberg J, Chou E, Ocampo AC, Oh J, Lee J, Peter AK, Martin PT, Crosbie-Watson RH.
J Cell Biol 197(7):1009-27. doi: 10.1083/jcb.201110032. 2012
4CYC1, SSPN, SUPT6H
Spn1 regulates the recruitment of Spt6 and the Swi/Snf complex during transcriptional activation by RNA polymerase II.
Zhang L, Fletcher AG, Cheung V, Winston F, Stargell LA.
Mol Cell Biol 28(4):1393-403. Epub 2007 Dec 17.PMID: 18086892 2008
5SSPN, UTRN
Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex.
Peter AK, Marshall JL, Crosbie RH.
J Cell Biol 183(3):419-27. doi: 10.1083/jcb.200808027. 2008
6SSPN
Reduced expression of sarcospan in muscles of Fukuyama congenital muscular dystrophy.
Wakayama Y, Inoue M, Kojima H, Yamashita S, Shibuya S, Jimi T, Hara H, Matsuzaki Y, Oniki H, Kanagawa M, Kobayashi K, Toda T.
Histol Histopathol 23(12):1425-38. 2008
7SSPN
Gene expression in mouse brain following chronic hypoxia: role of sarcospan in glial cell death.
Zhou D, Wang J, Zapala MA, Xue J, Schork NJ, Haddad GG.
Physiol Genomics 32(3):370-9. Epub 2007 Dec 4. 2008
8SSPN
Analysis of human sarcospan as a candidate gene for CFEOM1.
O'Brien KF, Engle EC, Kunkel LM.
BMC Genet 2:3. Epub 2001 Feb 6. 2001
9SSPN
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.
Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, Collin H, Dovico SA, Stolle CA, Fardeau M, Tome FM, Campbell KP.
Hum Mol Genet 9(13):2019-27. 2000
10SGCA, SGCD, SSPN
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy.
Coral-Vazquez R, et al.
Cell 98(4):465-74. 1999
11SSPN
Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex.
Crosbie RH, Heighway J, Venzke DP, Lee JC, Campbell KP.
J Biol Chem 272(50):31221-4. 1997
12ITPR2, SSPN, KRAS
Coamplification in tumors of KRAS2, type 2 inositol 1,4,5 triphosphate receptor gene, and a novel human gene, KRAG.
Heighway J, et al.
Genomics 35 : 207-214. 1996