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Items: 1 to 20 of 83

1.

Chronic hypoxia impairs muscle function in the Drosophila model of Duchenne's muscular dystrophy (DMD).

Mosqueira M, Willmann G, Ruohola-Baker H, Khurana TS.

PLoS One. 2010 Oct 20;5(10):e13450. doi: 10.1371/journal.pone.0013450.

2.

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.

3.

Respiratory Control in the mdx Mouse Model of Duchenne Muscular Dystrophy.

Burns DP, Edge D, O'Malley D, O'Halloran KD.

Adv Exp Med Biol. 2015;860:239-44. doi: 10.1007/978-3-319-18440-1_27.

PMID:
26303487
4.

Evidence of hypoxic tolerance in weak upper airway muscle from young mdx mice.

Burns DP, O'Halloran KD.

Respir Physiol Neurobiol. 2016 Jun;226:68-75. doi: 10.1016/j.resp.2015.12.001. Epub 2015 Dec 9.

PMID:
26691169
5.

Immunoproteasome in animal models of Duchenne muscular dystrophy.

Chen CN, Graber TG, Bratten WM, Ferrington DA, Thompson LV.

J Muscle Res Cell Motil. 2014 Apr;35(2):191-201. doi: 10.1007/s10974-014-9385-x. Epub 2014 Jun 17.

6.

Harnessing the potential of dystrophin-related proteins for ameliorating Duchenne's muscular dystrophy.

Krag TO, Gyrd-Hansen M, Khurana TS.

Acta Physiol Scand. 2001 Mar;171(3):349-58. Review.

PMID:
11412148
7.

Brain function in Duchenne muscular dystrophy.

Anderson JL, Head SI, Rae C, Morley JW.

Brain. 2002 Jan;125(Pt 1):4-13. Review.

PMID:
11834588
8.

Na(+)/Ca(2+) exchange in human myotubes: intracellular calcium rises in response to external sodium depletion are enhanced in DMD.

Deval E, Levitsky DO, Marchand E, Cantereau A, Raymond G, Cognard C.

Neuromuscul Disord. 2002 Oct;12(7-8):665-73.

PMID:
12207936
9.

Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy.

Porter JD, Merriam AP, Leahy P, Gong B, Feuerman J, Cheng G, Khanna S.

Hum Mol Genet. 2004 Feb 1;13(3):257-69. Epub 2003 Dec 17.

PMID:
14681298
10.

Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy.

Kayali R, Ku JM, Khitrov G, Jung ME, Prikhodko O, Bertoni C.

Hum Mol Genet. 2012 Sep 15;21(18):4007-20. doi: 10.1093/hmg/dds223. Epub 2012 Jun 12.

11.

Muscular degeneration in Duchenne's dystrophy may be caused by a mitochondrial defect.

Lucas-Heron B.

Med Hypotheses. 1995 Apr;44(4):298-300.

PMID:
7666833
12.

Human muscle gene expression responses to endurance training provide a novel perspective on Duchenne muscular dystrophy.

Timmons JA, Larsson O, Jansson E, Fischer H, Gustafsson T, Greenhaff PL, Ridden J, Rachman J, Peyrard-Janvid M, Wahlestedt C, Sundberg CJ.

FASEB J. 2005 May;19(7):750-60.

PMID:
15857889
13.

Morpholinos and their peptide conjugates: therapeutic promise and challenge for Duchenne muscular dystrophy.

Moulton HM, Moulton JD.

Biochim Biophys Acta. 2010 Dec;1798(12):2296-303. doi: 10.1016/j.bbamem.2010.02.012. Epub 2010 Feb 17.

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Muscle dysfunction and structural defects of dystrophin-null sapje mutant zebrafish larvae are rescued by ataluren treatment.

Li M, Andersson-Lendahl M, Sejersen T, Arner A.

FASEB J. 2014 Apr;28(4):1593-9. doi: 10.1096/fj.13-240044. Epub 2013 Dec 26.

PMID:
24371125
17.

Microtubules underlie dysfunction in duchenne muscular dystrophy.

Khairallah RJ, Shi G, Sbrana F, Prosser BL, Borroto C, Mazaitis MJ, Hoffman EP, Mahurkar A, Sachs F, Sun Y, Chen YW, Raiteri R, Lederer WJ, Dorsey SG, Ward CW.

Sci Signal. 2012 Aug 7;5(236):ra56. doi: 10.1126/scisignal.2002829.

18.

Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling.

Turk R, Sterrenburg E, de Meijer EJ, van Ommen GJ, den Dunnen JT, 't Hoen PA.

BMC Genomics. 2005 Jul 13;6:98.

19.

Identification of altered gene expression in skeletal muscles from Duchenne muscular dystrophy patients.

Tkatchenko AV, Piétu G, Cros N, Gannoun-Zaki L, Auffray C, Léger JJ, Dechesne CA.

Neuromuscul Disord. 2001 Apr;11(3):269-77.

PMID:
11297942
20.

Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies.

Kornegay JN, Bogan JR, Bogan DJ, Childers MK, Li J, Nghiem P, Detwiler DA, Larsen CA, Grange RW, Bhavaraju-Sanka RK, Tou S, Keene BP, Howard JF Jr, Wang J, Fan Z, Schatzberg SJ, Styner MA, Flanigan KM, Xiao X, Hoffman EP.

Mamm Genome. 2012 Feb;23(1-2):85-108. doi: 10.1007/s00335-011-9382-y. Epub 2012 Jan 5. Review.

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