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Items: 1 to 20 of 1066

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Decreased myocardial nNOS, increased iNOS and abnormal ECGs in mouse models of Duchenne muscular dystrophy.

Bia BL, Cassidy PJ, Young ME, Rafael JA, Leighton B, Davies KE, Radda GK, Clarke K.

J Mol Cell Cardiol. 1999 Oct;31(10):1857-62.

PMID:
10525423
5.

Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the dystrophin associated protein complex in skeletal muscle.

Wells KE, Torelli S, Lu Q, Brown SC, Partridge T, Muntoni F, Wells DJ.

Neuromuscul Disord. 2003 Jan;13(1):21-31.

PMID:
12467729
6.

Defects in neuromuscular junction structure in dystrophic muscle are corrected by expression of a NOS transgene in dystrophin-deficient muscles, but not in muscles lacking alpha- and beta1-syntrophins.

Shiao T, Fond A, Deng B, Wehling-Henricks M, Adams ME, Froehner SC, Tidball JG.

Hum Mol Genet. 2004 Sep 1;13(17):1873-84. Epub 2004 Jul 6.

PMID:
15238508
7.

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. Epub 2003 Mar 28.

PMID:
12670877
8.

Downstream utrophin enhancer is required for expression of utrophin in skeletal muscle.

Tanihata J, Suzuki N, Miyagoe-Suzuki Y, Imaizumi K, Takeda S.

J Gene Med. 2008 Jun;10(6):702-13. doi: 10.1002/jgm.1190.

PMID:
18338831
9.

CAPON expression in skeletal muscle is regulated by position, repair, NOS activity, and dystrophy.

Ségalat L, Grisoni K, Archer J, Vargas C, Bertrand A, Anderson JE.

Exp Cell Res. 2005 Jan 15;302(2):170-9.

PMID:
15561099
10.

A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice.

Wehling M, Spencer MJ, Tidball JG.

J Cell Biol. 2001 Oct 1;155(1):123-31.

11.

Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin.

Rooney JE, Welser JV, Dechert MA, Flintoff-Dye NL, Kaufman SJ, Burkin DJ.

J Cell Sci. 2006 Jun 1;119(Pt 11):2185-95. Epub 2006 May 9.

12.

Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy.

Guo C, Willem M, Werner A, Raivich G, Emerson M, Neyses L, Mayer U.

Hum Mol Genet. 2006 Mar 15;15(6):989-98. Epub 2006 Feb 13.

PMID:
16476707
13.

Muscular nitric oxide synthase (muNOS) and utrophin.

Chaubourt E, Voisin V, Fossier P, Baux G, Israël M, De La Porte S.

J Physiol Paris. 2002 Jan-Mar;96(1-2):43-52.

PMID:
11755782
14.

Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice.

Rafael JA, Tinsley JM, Potter AC, Deconinck AE, Davies KE.

Nat Genet. 1998 May;19(1):79-82.

PMID:
9590295
15.

Stimulation of calcineurin signaling attenuates the dystrophic pathology in mdx mice.

Chakkalakal JV, Harrison MA, Carbonetto S, Chin E, Michel RN, Jasmin BJ.

Hum Mol Genet. 2004 Feb 15;13(4):379-88. Epub 2003 Dec 17.

PMID:
14681302
16.

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.

17.

A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration.

Weir AP, Morgan JE, Davies KE.

Neuromuscul Disord. 2004 Jan;14(1):19-23.

PMID:
14659408
18.

Dystrophin and utrophin: genetic analyses of their role in skeletal muscle.

Rafael JA, Brown SC.

Microsc Res Tech. 2000 Feb 1-15;48(3-4):155-66. Review.

PMID:
10679963
19.

Dystrophin and utrophin influence fiber type composition and post-synaptic membrane structure.

Rafael JA, Townsend ER, Squire SE, Potter AC, Chamberlain JS, Davies KE.

Hum Mol Genet. 2000 May 22;9(9):1357-67.

PMID:
10814717
20.

Talin, vinculin and nestin expression in orofacial muscles of dystrophin deficient mdx mice.

Spassov A, Gredes T, Pavlovic D, Gedrange T, Lehmann C, Lucke S, Kunert-Keil C.

Arch Immunol Ther Exp (Warsz). 2012 Apr;60(2):137-43. doi: 10.1007/s00005-012-0167-0. Epub 2012 Feb 4.

PMID:
22307364

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