Apoptotic effects of platelet factor VIII on megakaryopoiesis: implications for a modified human FVIII for platelet-based gene therapy

Author:

Greene T. K.1,Lyde R. B.2,Bailey S. C.1,Lambert M. P.13,Zhai L.1,Sabatino D. E.13,Camire R. M.13,Arruda V. R.13,Poncz M.13

Affiliation:

1. Division of Hematology; The Children's Hospital of Philadelphia; Philadelphia PA USA

2. Division of Pharmacology; School of Medicine; University of Pennsylvania; Philadelphia PA USA

3. Division of Pediatrics; School of Medicine; University of Pennsylvania; Philadelphia PA USA

Funder

National Institute of Health

Fred Hutchinson Cancer Research Center

Publisher

Wiley

Subject

Hematology

Reference37 articles.

1. Advances toward gene therapy for hemophilia at the millennium;Kaufman;Hum Gene Ther,1999

2. Department of Health and Human Services: National Heart LaBRS Pilot study of hemophilia treatment in the US National Heart, Lung and Blood Resources Studies Vol. 3 1972

3. A multicenter study of recombinant factor VIII (recombinate): safety, efficacy, and inhibitor risk in previously untreated patients with hemophilia A. The Recombinate Study Group;Bray;Blood,1994

4. Recombinant factor VIII for the treatment of previously untreated patients with hemophilia A. Safety, efficacy, and development of inhibitors. Kogenate Previously Untreated Patient Study Group;Lusher;N Engl J Med,1993

5. Rational design of a fully active, long-acting PEGylated factor VIII for hemophilia A treatment;Mei;Blood,2010

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