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Year | Number of Results |
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2009 | 2 |
2010 | 1 |
2015 | 1 |
2025 | 0 |
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Progress with Recombinant Adeno-Associated Virus Vectors for Gene Therapy of Alpha-1 Antitrypsin Deficiency.
Hum Gene Ther Methods. 2015 Jun;26(3):77-81. doi: 10.1089/hgtb.2015.086.
Hum Gene Ther Methods. 2015.
PMID: 26067712
Free PMC article.
Review.
Sustained transgene expression despite T lymphocyte responses in a clinical trial of rAAV1-AAT gene therapy.
Brantly ML, Chulay JD, Wang L, Mueller C, Humphries M, Spencer LT, Rouhani F, Conlon TJ, Calcedo R, Betts MR, Spencer C, Byrne BJ, Wilson JM, Flotte TR.
Brantly ML, et al.
Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16363-8. doi: 10.1073/pnas.0904514106. Epub 2009 Aug 12.
Proc Natl Acad Sci U S A. 2009.
PMID: 19706466
Free PMC article.
Clinical Trial.
Item in Clipboard
In vitro and in vivo functional characterization of gutless recombinant SV40-derived CFTR vectors.
Mueller C, Strayer MS, Sirninger J, Braag S, Branco F, Louboutin JP, Flotte TR, Strayer DS.
Mueller C, et al.
Gene Ther. 2010 Feb;17(2):227-37. doi: 10.1038/gt.2009.137. Epub 2009 Nov 5.
Gene Ther. 2010.
PMID: 19890354
Free PMC article.
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