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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2012 | 1 |
2013 | 2 |
2014 | 1 |
2015 | 3 |
2016 | 1 |
2024 | 0 |
Search Results
6 results
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Page 1
The potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophy.
FEBS J. 2013 Sep;280(17):4210-29. doi: 10.1111/febs.12295. Epub 2013 May 13.
FEBS J. 2013.
PMID: 23601082
Free PMC article.
Review.
Eplerenone for early cardiomyopathy in Duchenne muscular dystrophy: a randomised, double-blind, placebo-controlled trial.
Raman SV, Hor KN, Mazur W, Halnon NJ, Kissel JT, He X, Tran T, Smart S, McCarthy B, Taylor MD, Jefferies JL, Rafael-Fortney JA, Lowe J, Roble SL, Cripe LH.
Raman SV, et al.
Lancet Neurol. 2015 Feb;14(2):153-61. doi: 10.1016/S1474-4422(14)70318-7. Epub 2014 Dec 30.
Lancet Neurol. 2015.
PMID: 25554404
Free PMC article.
Clinical Trial.
Item in Clipboard
The E3 ubiquitin ligase TRIM32 regulates myoblast proliferation by controlling turnover of NDRG2.
Mokhonova EI, Avliyakulov NK, Kramerova I, Kudryashova E, Haykinson MJ, Spencer MJ.
Mokhonova EI, et al.
Hum Mol Genet. 2015 May 15;24(10):2873-83. doi: 10.1093/hmg/ddv049. Epub 2015 Feb 20.
Hum Mol Genet. 2015.
PMID: 25701873
Free PMC article.
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Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations.
Rudnik-Schöneborn S, Senderek J, Jen JC, Houge G, Seeman P, Puchmajerová A, Graul-Neumann L, Seidel U, Korinthenberg R, Kirschner J, Seeger J, Ryan MM, Muntoni F, Steinlin M, Sztriha L, Colomer J, Hübner C, Brockmann K, Van Maldergem L, Schiff M, Holzinger A, Barth P, Reardon W, Yourshaw M, Nelson SF, Eggermann T, Zerres K.
Rudnik-Schöneborn S, et al.
Neurology. 2013 Jan 29;80(5):438-46. doi: 10.1212/WNL.0b013e31827f0f66. Epub 2013 Jan 2.
Neurology. 2013.
PMID: 23284067
Free PMC article.
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Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.
Wan J, Yourshaw M, Mamsa H, Rudnik-Schöneborn S, Menezes MP, Hong JE, Leong DW, Senderek J, Salman MS, Chitayat D, Seeman P, von Moers A, Graul-Neumann L, Kornberg AJ, Castro-Gago M, Sobrido MJ, Sanefuji M, Shieh PB, Salamon N, Kim RC, Vinters HV, Chen Z, Zerres K, Ryan MM, Nelson SF, Jen JC.
Wan J, et al.
Nat Genet. 2012 Apr 29;44(6):704-8. doi: 10.1038/ng.2254.
Nat Genet. 2012.
PMID: 22544365
Free PMC article.
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Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders.
Brown R, Lee H, Eskin A, Kichaev G, Lohmueller KE, Reversade B, Nelson SF, Pasaniuc B.
Brown R, et al.
Eur J Hum Genet. 2016 Jan;24(1):113-9. doi: 10.1038/ejhg.2015.68. Epub 2015 Apr 22.
Eur J Hum Genet. 2016.
PMID: 25898925
Free PMC article.
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