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Items: 14

1.

Induction of immune tolerance to FIX following muscular AAV gene transfer is AAV-dose/FIX-level dependent.

Kelly ME, Zhuo J, Bharadwaj AS, Chao H.

Mol Ther. 2009 May;17(5):857-63. doi: 10.1038/mt.2009.25. Epub 2009 Feb 24.

2.
3.

RNA repair for haemophilia A.

Chao H, Walsh CE.

Expert Rev Mol Med. 2006 Jan 10;8(1):1-8. Review.

PMID:
16401355
4.

AAV vectors for hemophilia B gene therapy.

Chao H, Walsh CE.

Mt Sinai J Med. 2004 Oct;71(5):305-13. Review.

PMID:
15543431
5.

Phenotype correction of hemophilia A mice by spliceosome-mediated RNA trans-splicing.

Chao H, Mansfield SG, Bartel RC, Hiriyanna S, Mitchell LG, Garcia-Blanco MA, Walsh CE.

Nat Med. 2003 Aug;9(8):1015-9. Epub 2003 Jul 6.

PMID:
12847523
6.

Hemophilia gene therapy: novel rAAV vectors and RNA repair strategy.

Chao H, Walsh CE.

Curr Opin Mol Ther. 2002 Oct;4(5):499-504. Review.

PMID:
12435052
7.

Expression of human factor VIII by splicing between dimerized AAV vectors.

Chao H, Sun L, Bruce A, Xiao X, Walsh CE.

Mol Ther. 2002 Jun;5(6):716-22.

8.

Parvovirus-mediated gene transfer for the haemophilias.

Walsh CE, Chao H.

Haemophilia. 2002 Mar;8 Suppl 2:60-7. Review.

PMID:
11966856
9.
10.

Induction of tolerance to human factor VIII in mice.

Chao H, Walsh CE.

Blood. 2001 May 15;97(10):3311-2.

11.

Several log increase in therapeutic transgene delivery by distinct adeno-associated viral serotype vectors.

Chao H, Liu Y, Rabinowitz J, Li C, Samulski RJ, Walsh CE.

Mol Ther. 2000 Dec;2(6):619-23.

12.

Sustained expression of human factor VIII in mice using a parvovirus-based vector.

Chao H, Mao L, Bruce AT, Walsh CE.

Blood. 2000 Mar 1;95(5):1594-9.

13.

Endogenous canine FIX antigen exists in Chapel Hill strain hemophilia B canine.

Chao H, Walsh CE.

Thromb Haemost. 1999 Oct;82(4):1378. No abstract available.

PMID:
10544943
14.

Persistent expression of canine factor IX in hemophilia B canines.

Chao H, Samulski R, Bellinger D, Monahan P, Nichols T, Walsh C.

Gene Ther. 1999 Oct;6(10):1695-704.

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