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A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy.
Hum Mol Genet. 2006 May 15;15(10):1610-22. doi: 10.1093/hmg/ddl082. Epub 2006 Apr 4.
Hum Mol Genet. 2006.
PMID: 16595609
Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy.
Kimura E, Han JJ, Li S, Fall B, Ra J, Haraguchi M, Tapscott SJ, Chamberlain JS.
Kimura E, et al.
Hum Mol Genet. 2008 Aug 15;17(16):2507-17. doi: 10.1093/hmg/ddn151. Epub 2008 May 29.
Hum Mol Genet. 2008.
PMID: 18511457
Free PMC article.
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Dystrophin delivery to muscles of mdx mice using lentiviral vectors leads to myogenic progenitor targeting and stable gene expression.
Kimura E, Li S, Gregorevic P, Fall BM, Chamberlain JS.
Kimura E, et al. Among authors: fall bm.
Mol Ther. 2010 Jan;18(1):206-13. doi: 10.1038/mt.2009.253. Epub 2009 Nov 3.
Mol Ther. 2010.
PMID: 19888194
Free PMC article.
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Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophin.
Li S, Kimura E, Fall BM, Reyes M, Angello JC, Welikson R, Hauschka SD, Chamberlain JS.
Li S, et al. Among authors: fall bm.
Gene Ther. 2005 Jul;12(14):1099-108. doi: 10.1038/sj.gt.3302505.
Gene Ther. 2005.
PMID: 15759015
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Urinary Podocyte Loss Is Increased in Patients with Fabry Disease and Correlates with Clinical Severity of Fabry Nephropathy.
Fall B, Scott CR, Mauer M, Shankland S, Pippin J, Jefferson JA, Wallace E, Warnock D, Najafian B.
Fall B, et al.
PLoS One. 2016 Dec 16;11(12):e0168346. doi: 10.1371/journal.pone.0168346. eCollection 2016.
PLoS One. 2016.
PMID: 27992580
Free PMC article.
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