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Items: 1 to 20 of 403

1.

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 1;18(7):1209-20. doi: 10.1093/hmg/ddp015. Epub 2009 Jan 8.

2.

Microutrophin delivery through rAAV6 increases lifespan and improves muscle function in dystrophic dystrophin/utrophin-deficient mice.

Odom GL, Gregorevic P, Allen JM, Finn E, Chamberlain JS.

Mol Ther. 2008 Sep;16(9):1539-45. doi: 10.1038/mt.2008.149. Epub 2008 Jul 29.

4.

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 19;152(6):1207-18.

5.

Loss of dystrophin and β-sarcoglycan significantly exacerbates the phenotype of laminin α2 chain-deficient animals.

Gawlik KI, Holmberg J, Durbeej M.

Am J Pathol. 2014 Mar;184(3):740-52. doi: 10.1016/j.ajpath.2013.11.017. Epub 2014 Jan 4.

PMID:
24393714
6.

Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex.

Hack AA, Lam MY, Cordier L, Shoturma DI, Ly CT, Hadhazy MA, Hadhazy MR, Sweeney HL, McNally EM.

J Cell Sci. 2000 Jul;113 ( Pt 14):2535-44.

7.

Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy.

Church JE, Trieu J, Chee A, Naim T, Gehrig SM, Lamon S, Angelini C, Russell AP, Lynch GS.

Exp Physiol. 2014 Apr;99(4):675-87. doi: 10.1113/expphysiol.2013.077255. Epub 2014 Jan 17.

8.

Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.

Crosbie RH, Barresi R, Campbell KP.

FASEB J. 2002 Nov;16(13):1786-91.

PMID:
12409321
9.

Age-related changes in dystrophin-glycoprotein complex and in utrophin are not correlated with intrinsic laryngeal muscles protection in mdx mice.

Ferretti R, Pertille A, Santo Neto H, Marques MJ.

Muscle Nerve. 2011 Dec;44(6):978-80. doi: 10.1002/mus.22235.

PMID:
22102469
10.

Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice.

Judge LM, Arnett AL, Banks GB, Chamberlain JS.

Hum Mol Genet. 2011 Dec 15;20(24):4978-90. doi: 10.1093/hmg/ddr433. Epub 2011 Sep 23.

11.

Muscle structure influences utrophin expression in mdx mice.

Banks GB, Combs AC, Odom GL, Bloch RJ, Chamberlain JS.

PLoS Genet. 2014 Jun 12;10(6):e1004431. doi: 10.1371/journal.pgen.1004431. eCollection 2014 Jun.

12.

Distinct pathophysiological mechanisms of cardiomyopathy in hearts lacking dystrophin or the sarcoglycan complex.

Townsend D, Yasuda S, McNally E, Metzger JM.

FASEB J. 2011 Sep;25(9):3106-14. doi: 10.1096/fj.10-178913. Epub 2011 Jun 10.

13.

Independent variability of microtubule perturbations associated with dystrophinopathy.

Belanto JJ, Olthoff JT, Mader TL, Chamberlain CM, Nelson DM, McCourt PM, Talsness DM, Gundersen GG, Lowe DA, Ervasti JM.

Hum Mol Genet. 2016 Nov 15;25(22):4951-4961. doi: 10.1093/hmg/ddw318.

14.

Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice.

Nguyen HH, Jayasinha V, Xia B, Hoyte K, Martin PT.

Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5616-21.

15.

Altered biomechanical properties of carotid arteries in two mouse models of muscular dystrophy.

Dye WW, Gleason RL, Wilson E, Humphrey JD.

J Appl Physiol (1985). 2007 Aug;103(2):664-72. Epub 2007 May 24.

16.

Analysis of gene expression differences between utrophin/dystrophin-deficient vs mdx skeletal muscles reveals a specific upregulation of slow muscle genes in limb muscles.

Baker PE, Kearney JA, Gong B, Merriam AP, Kuhn DE, Porter JD, Rafael-Fortney JA.

Neurogenetics. 2006 May;7(2):81-91. Epub 2006 Mar 9.

PMID:
16525850
17.

Nitrosative stress elicited by nNOSµ delocalization inhibits muscle force in dystrophin-null mice.

Li D, Yue Y, Lai Y, Hakim CH, Duan D.

J Pathol. 2011 Jan;223(1):88-98. doi: 10.1002/path.2799. Epub 2010 Oct 28.

18.

epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex.

Straub V, Ettinger AJ, Durbeej M, Venzke DP, Cutshall S, Sanes JR, Campbell KP.

J Biol Chem. 1999 Sep 24;274(39):27989-96.

19.

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. Review.

PMID:
16710609
20.

Extraocular muscle is spared despite the absence of an intact sarcoglycan complex in gamma- or delta-sarcoglycan-deficient mice.

Porter JD, Merriam AP, Hack AA, Andrade FH, McNally EM.

Neuromuscul Disord. 2001 Mar;11(2):197-207.

PMID:
11257478

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