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Page 1
Anti-viral strategies.
Chuah MK, VandenDriessche T, Morgan RA. Chuah MK, et al. Mol Cell Biol Hum Dis Ser. 1995;5:175-94. doi: 10.1007/978-94-011-0547-7_10. Mol Cell Biol Hum Dis Ser. 1995. PMID: 9532567 Review. No abstract available.
Gene therapy for hemophilia: hopes and hurdles.
Chuah MK, Collen D, VandenDriessche T. Chuah MK, et al. Crit Rev Oncol Hematol. 1998 Sep;28(3):153-71. doi: 10.1016/s1040-8428(98)00022-5. Crit Rev Oncol Hematol. 1998. PMID: 9793744 Review. No abstract available.
Gene therapy for hemophilia.
Chuah MK, Collen D, VandenDriessche T. Chuah MK, et al. J Gene Med. 2001 Jan-Feb;3(1):3-20. doi: 10.1002/1521-2254(200101/02)3:1<3::AID-JGM167>3.0.CO;2-H. J Gene Med. 2001. PMID: 11269333 Review.
Viral vector-mediated gene therapy for hemophilia.
VandenDriessche T, Collen D, Chuah MK. VandenDriessche T, et al. Among authors: chuah mk. Curr Gene Ther. 2001 Sep;1(3):301-15. doi: 10.2174/1566523013348508. Curr Gene Ther. 2001. PMID: 12109144 Review.
Clinical gene transfer studies for hemophilia A.
Chuah MK, Collen D, VandenDriessche T. Chuah MK, et al. Semin Thromb Hemost. 2004 Apr;30(2):249-56. doi: 10.1055/s-2004-825638. Semin Thromb Hemost. 2004. PMID: 15118936 Review.
A murine model for induction of long-term immunologic tolerance to factor VIII does not require persistent detectable levels of plasma factor VIII and involves contributions from Foxp3+ T regulatory cells.
Matsui H, Shibata M, Brown B, Labelle A, Hegadorn C, Andrews C, Chuah M, VandenDriessche T, Miao CH, Hough C, Lillicrap D. Matsui H, et al. Among authors: chuah m. Blood. 2009 Jul 16;114(3):677-85. doi: 10.1182/blood-2009-03-202267. Epub 2009 May 20. Blood. 2009. PMID: 19458355 Free PMC article.
204 results