Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors-Reference-Cited by-同舟云学术

Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors

Published:1999-01 Issue:1 Volume:5 Page:64-70
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Snyder Richard O.,Miao Carol,Meuse Leonard,Tubb Julie,Donahue Brian A.,Lin Hui-Feng,Stafford Darrel W.,Patel Salil,Thompson Arthur R.,Nichols Timothy,Read Marjorie S.,Bellinger Dwight A.,Brinkhous Kenneth M.,Kay Mark A.

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm0199_64.pdf

Reference31 articles.

1. Lin, H.-F., Maeda, N., Smithies, O., Straight, D.L. & Stafford, D.W. A Coagulation Factor IX-Deficient Mouse Model for Human Hemophilia B. Blood 90, 3962– 3966 (1997).

2. Bi, L. et al. Targeted disruption of the mouse factor VIII gene produces a model of haemophilia A. Nature Gen. 10, ( 1995).

3. Wang, L. et al. A factor IX-deficient mouse model for hemophilia B gene therapy. Med. Sci. 94, 11563–11566 (1997).

4. Kundu, R.K. et al. Targeted Inactivation of the Coagulation Factor IX Gene Causes Hemophilia B. in Mice. Blood 92, 68– 174 (1998).

5. Nichols, T.C. et al. The roles of von Willebrand factor and factor VIII in arterial thrombosis: studies in canine von Willebrand disease and hemophilia A. Blood 81, 2644–2651 ( 1993).

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