339 related articles for article (PubMed ID: 16710609)
1. Role of dystrophin and utrophin for assembly and function of the dystrophin glycoprotein complex in non-muscle tissue.
Haenggi T; Fritschy JM
Cell Mol Life Sci; 2006 Jul; 63(14):1614-31. PubMed ID: 16710609
[TBL] [Abstract][Full Text] [Related]
2. Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex.
Crosbie RH; Lebakken CS; Holt KH; Venzke DP; Straub V; Lee JC; Grady RM; Chamberlain JS; Sanes JR; Campbell KP
J Cell Biol; 1999 Apr; 145(1):153-65. PubMed ID: 10189375
[TBL] [Abstract][Full Text] [Related]
3. Sarcospan reduces dystrophic pathology: stabilization of the utrophin-glycoprotein complex.
Peter AK; Marshall JL; Crosbie RH
J Cell Biol; 2008 Nov; 183(3):419-27. PubMed ID: 18981229
[TBL] [Abstract][Full Text] [Related]
4. Characterization of the intermolecular associations of the dystrophin-associated glycoprotein complex in retinal Müller glial cells.
Claudepierre T; Dalloz C; Mornet D; Matsumura K; Sahel J; Rendon A
J Cell Sci; 2000 Oct; 113 Pt 19():3409-17. PubMed ID: 10984432
[TBL] [Abstract][Full Text] [Related]
5. Constitutive properties, not molecular adaptations, mediate extraocular muscle sparing in dystrophic mdx mice.
Porter JD; Merriam AP; Khanna S; Andrade FH; Richmonds CR; Leahy P; Cheng G; Karathanasis P; Zhou X; Kusner LL; Adams ME; Willem M; Mayer U; Kaminski HJ
FASEB J; 2003 May; 17(8):893-5. PubMed ID: 12670877
[TBL] [Abstract][Full Text] [Related]
6. Loss of sarcospan exacerbates pathology in mdx mice, but does not affect utrophin amelioration of disease.
Gibbs EM; McCourt JL; Shin KM; Hammond KG; Marshall JL; Crosbie RH
Hum Mol Genet; 2021 Apr; 30(3-4):149-159. PubMed ID: 33432327
[TBL] [Abstract][Full Text] [Related]
7. The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCs) in the choroid plexus and microvasculature of the brain.
Haenggi T; Soontornmalai A; Schaub MC; Fritschy JM
Neuroscience; 2004; 129(2):403-13. PubMed ID: 15501597
[TBL] [Abstract][Full Text] [Related]
8. Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex.
Grady RM; Zhou H; Cunningham JM; Henry MD; Campbell KP; Sanes JR
Neuron; 2000 Feb; 25(2):279-93. PubMed ID: 10719885
[TBL] [Abstract][Full Text] [Related]
9. Sub-physiological sarcoglycan expression contributes to compensatory muscle protection in mdx mice.
Li D; Long C; Yue Y; Duan D
Hum Mol Genet; 2009 Apr; 18(7):1209-20. PubMed ID: 19131360
[TBL] [Abstract][Full Text] [Related]
10. Differential distribution of the members of the dystrophin glycoprotein complex in mouse retina: effect of the mdx(3Cv) mutation.
Dalloz C; Claudepierre T; Rodius F; Mornet D; Sahel J; Rendon A
Mol Cell Neurosci; 2001 May; 17(5):908-20. PubMed ID: 11358487
[TBL] [Abstract][Full Text] [Related]
11. Regulation of the cardiac sodium channel Nav1.5 by utrophin in dystrophin-deficient mice.
Albesa M; Ogrodnik J; Rougier JS; Abriel H
Cardiovasc Res; 2011 Feb; 89(2):320-8. PubMed ID: 20952415
[TBL] [Abstract][Full Text] [Related]
12. Talin, vinculin and DRP (utrophin) concentrations are increased at mdx myotendinous junctions following onset of necrosis.
Law DJ; Allen DL; Tidball JG
J Cell Sci; 1994 Jun; 107 ( Pt 6)():1477-83. PubMed ID: 7962191
[TBL] [Abstract][Full Text] [Related]
13. 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; 2012 Oct; 21(20):4378-93. PubMed ID: 22798625
[TBL] [Abstract][Full Text] [Related]
14. Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and α7 integrin.
Marshall JL; Oh J; Chou E; Lee JA; Holmberg J; Burkin DJ; Crosbie-Watson RH
Hum Mol Genet; 2015 Apr; 24(7):2011-22. PubMed ID: 25504048
[TBL] [Abstract][Full Text] [Related]
15. Xanthine oxidase is hyper-active in Duchenne muscular dystrophy.
Lindsay A; McCourt PM; Karachunski P; Lowe DA; Ervasti JM
Free Radic Biol Med; 2018 Dec; 129():364-371. PubMed ID: 30312761
[TBL] [Abstract][Full Text] [Related]
16. The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma.
Lapidos KA; Kakkar R; McNally EM
Circ Res; 2004 Apr; 94(8):1023-31. PubMed ID: 15117830
[TBL] [Abstract][Full Text] [Related]
17. Protein-Anchoring Therapy of Biglycan for Mdx Mouse Model of Duchenne Muscular Dystrophy.
Ito M; Ehara Y; Li J; Inada K; Ohno K
Hum Gene Ther; 2017 May; 28(5):428-436. PubMed ID: 27485975
[TBL] [Abstract][Full Text] [Related]
18. Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice.
Burkin DJ; Wallace GQ; Nicol KJ; Kaufman DJ; Kaufman SJ
J Cell Biol; 2001 Mar; 152(6):1207-18. PubMed ID: 11257121
[TBL] [Abstract][Full Text] [Related]
19. Cerebellar synaptic defects and abnormal motor behavior in mice lacking alpha- and beta-dystrobrevin.
Grady RM; Wozniak DF; Ohlemiller KK; Sanes JR
J Neurosci; 2006 Mar; 26(11):2841-51. PubMed ID: 16540561
[TBL] [Abstract][Full Text] [Related]
20. Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies.
Grady RM; Grange RW; Lau KS; Maimone MM; Nichol MC; Stull JT; Sanes JR
Nat Cell Biol; 1999 Aug; 1(4):215-20. PubMed ID: 10559919
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
