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Results by year

Year	Number of Results
1984	2
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1996	32
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2005	51
2006	63
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2009	80
2010	89
2011	103
2012	98
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2014	5
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1,288 results

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Results by year

Page 1

Intestine of dystrophic mice presents enhanced contractile resistance to stretching despite morphological impairment.

Alves GA, Silva LR, Rosa EF, Aboulafia J, Freymüller-Haapalainen E, Souccar C, Nouailhetas VL. Alves GA, et al. Am J Physiol Gastrointest Liver Physiol. 2014 Feb;306(3):G191-9. doi: 10.1152/ajpgi.00314.2013. Epub 2013 Nov 27. Am J Physiol Gastrointest Liver Physiol. 2014. PMID: 24284964 Free article.

Inhibition of Coxsackievirus-associated dystrophin cleavage prevents cardiomyopathy.

Lim BK, Peter AK, Xiong D, Narezkina A, Yung A, Dalton ND, Hwang KK, Yajima T, Chen J, Knowlton KU. Lim BK, et al. J Clin Invest. 2013 Dec;123(12):5146-51. doi: 10.1172/JCI66271. Epub 2013 Nov 8. J Clin Invest. 2013. PMID: 24200690 Free PMC article.

Revertant fibers in the mdx murine model of Duchenne muscular dystrophy: an age- and muscle-related reappraisal.

Pigozzo SR, Da Re L, Romualdi C, Mazzara PG, Galletta E, Fletcher S, Wilton SD, Vitiello L. Pigozzo SR, et al. PLoS One. 2013 Aug 28;8(8):e72147. doi: 10.1371/journal.pone.0072147. eCollection 2013. PLoS One. 2013. PMID: 24015212 Free PMC article.

Mechanical and morphological aspects of the calcaneal tendon of mdx mice at 21 days of age.

Nakagaki WR, Tomiosso TC, Pimentel ER, Camilli JA. Nakagaki WR, et al. Anat Rec (Hoboken). 2013 Oct;296(10):1546-51. doi: 10.1002/ar.22759. Epub 2013 Aug 12. Anat Rec (Hoboken). 2013. PMID: 23934706 Free article.

Subcellular localization of dystrophin isoforms in cardiomyocytes and phenotypic analysis of dystrophin-deficient mice reveal cardiac myopathy is predominantly caused by a deficiency in full-length dystrophin.

Masubuchi N, Shidoh Y, Kondo S, Takatoh J, Hanaoka K. Masubuchi N, et al. Exp Anim. 2013;62(3):211-7. doi: 10.1538/expanim.62.211. Exp Anim. 2013. PMID: 23903056 Free PMC article.

A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy.

de Brouwer AP, Nabuurs SB, Verhaart IE, Oudakker AR, Hordijk R, Yntema HG, Hordijk-Hos JM, Voesenek K, de Vries BB, van Essen T, Chen W, Hu H, Chelly J, den Dunnen JT, Kalscheuer VM, Aartsma-Rus AM, Hamel BC, van Bokhoven H, Kleefstra T. de Brouwer AP, et al. Eur J Hum Genet. 2014 Apr;22(4):480-5. doi: 10.1038/ejhg.2013.169. Epub 2013 Jul 31. Eur J Hum Genet. 2014. PMID: 23900271 Free PMC article.

Micro-dystrophin and follistatin co-delivery restores muscle function in aged DMD model.

Rodino-Klapac LR, Janssen PM, Shontz KM, Canan B, Montgomery CL, Griffin D, Heller K, Schmelzer L, Handy C, Clark KR, Sahenk Z, Mendell JR, Kaspar BK. Rodino-Klapac LR, et al. Hum Mol Genet. 2013 Dec 15;22(24):4929-37. doi: 10.1093/hmg/ddt342. Epub 2013 Jul 17. Hum Mol Genet. 2013. PMID: 23863459 Free PMC article.

The proton pump inhibitor lansoprazole improves the skeletal phenotype in dystrophin deficient mdx mice.

Sali A, Many GM, Gordish-Dressman H, van der Meulen JH, Phadke A, Spurney CF, Cnaan A, Hoffman EP, Nagaraju K. Sali A, et al. PLoS One. 2013 Jul 2;8(7):e66617. doi: 10.1371/journal.pone.0066617. Print 2013. PLoS One. 2013. PMID: 23843959 Free PMC article.

Isobaric Tagging-Based Quantification for Proteomic Analysis: A Comparative Study of Spared and Affected Muscles from mdx Mice at the Early Phase of Dystrophy.

Matsumura CY, Menezes de Oliveira B, Durbeej M, Marques MJ. Matsumura CY, et al. PLoS One. 2013 Jun 18;8(6):e65831. doi: 10.1371/journal.pone.0065831. Print 2013. PLoS One. 2013. PMID: 23823696 Free PMC article.

Magnetic resonance spectroscopy and molecular studies in ornithine transcarbamylase deficiency novel mutation c.802A>G in exon 8 (p.Met268Val).

Jamroz E, Paprocka J, Sokół M, Popowska E, Ciara E. Jamroz E, et al. Neurol Neurochir Pol. 2013 May-Jun;47(3):283-9. doi: 10.5114/ninp.2013.35488. Neurol Neurochir Pol. 2013. PMID: 23821427