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Year | Number of Results |
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2013 | 1 |
2015 | 1 |
2016 | 1 |
2025 | 0 |
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Multilineage transduction of resident lung cells in vivo by AAV2/8 for α1-antitrypsin gene therapy.
Mol Ther Methods Clin Dev. 2016 Jun 29;3:16042. doi: 10.1038/mtm.2016.42. eCollection 2016.
Mol Ther Methods Clin Dev. 2016.
PMID: 27408904
Free PMC article.
Lentiviral delivery of RNAi for in vivo lineage-specific modulation of gene expression in mouse lung macrophages.
Wilson AA, Kwok LW, Porter EL, Payne JG, McElroy GS, Ohle SJ, Greenhill SR, Blahna MT, Yamamoto K, Jean JC, Mizgerd JP, Kotton DN.
Wilson AA, et al.
Mol Ther. 2013 Apr;21(4):825-33. doi: 10.1038/mt.2013.19. Epub 2013 Feb 12.
Mol Ther. 2013.
PMID: 23403494
Free PMC article.
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Emergence of a stage-dependent human liver disease signature with directed differentiation of alpha-1 antitrypsin-deficient iPS cells.
Wilson AA, Ying L, Liesa M, Segeritz CP, Mills JA, Shen SS, Jean J, Lonza GC, Liberti DC, Lang AH, Nazaire J, Gower AC, Müeller FJ, Mehta P, Ordóñez A, Lomas DA, Vallier L, Murphy GJ, Mostoslavsky G, Spira A, Shirihai OS, Ramirez MI, Gadue P, Kotton DN.
Wilson AA, et al.
Stem Cell Reports. 2015 May 12;4(5):873-85. doi: 10.1016/j.stemcr.2015.02.021. Epub 2015 Apr 2.
Stem Cell Reports. 2015.
PMID: 25843048
Free PMC article.
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