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Therapeutic factor VIII levels and negligible toxicity in mouse and dog models of hemophilia A following gene therapy with high-capacity adenoviral vectors.
Blood. 2003 Mar 1;101(5):1734-43. doi: 10.1182/blood-2002-03-0823. Epub 2002 Oct 24.
Blood. 2003.
PMID: 12406898
Free article.
Efficacy and safety of adeno-associated viral vectors based on serotype 8 and 9 vs. lentiviral vectors for hemophilia B gene therapy.
Vandendriessche T, Thorrez L, Acosta-Sanchez A, Petrus I, Wang L, Ma L, DE Waele L, Iwasaki Y, Gillijns V, Wilson JM, Collen D, Chuah MK.
Vandendriessche T, et al. Among authors: gillijns v.
J Thromb Haemost. 2007 Jan;5(1):16-24. doi: 10.1111/j.1538-7836.2006.02220.x. Epub 2006 Sep 26.
J Thromb Haemost. 2007.
PMID: 17002653
Free article.
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Phenotypic correction of von Willebrand disease type 3 blood-derived endothelial cells with lentiviral vectors expressing von Willebrand factor.
De Meyer SF, Vanhoorelbeke K, Chuah MK, Pareyn I, Gillijns V, Hebbel RP, Collen D, Deckmyn H, VandenDriessche T.
De Meyer SF, et al. Among authors: gillijns v.
Blood. 2006 Jun 15;107(12):4728-36. doi: 10.1182/blood-2005-09-3605. Epub 2006 Feb 14.
Blood. 2006.
PMID: 16478886
Free PMC article.
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