The expanding menagerie: animal models of hemophilia A
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2010.04053.x/fullpdf
Reference16 articles.
1. Protein replacement therapy and gene transfer in canine models of hemophilia A, hemophilia B, von willebrand disease, and factor VII deficiency;Nichols;ILAR J,2009
2. WAG-F8m1Ycb rats harboring a factor VIII gene mutation provide a new animal model for hemophilia A;Booth;J Thromb Haemost,2010
3. Spontaneous coagulopathy in inbred WAG/RijYcb rats;Booth;Comp Med,2010
4. Clinical and molecular characterization of a re-established line of sheep exhibiting hemophilia A;Porada;J Thromb Haemost,2010
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1. Long-term follow-up of liver-directed, adeno-associated vector-mediated gene therapy in the canine model of hemophilia A;Blood;2022-12-22
2. Application of in-vitro-cultured primary hepatocytes to evaluate species translatability and AAV transduction mechanisms of action;Molecular Therapy - Methods & Clinical Development;2022-09
3. A Foundational Study for Normal F8-Containing Mouse Models for the miRNA Regulation of Hemophilia A: Identification and Analysis of Mouse miRNAs that Downregulate the Murine F8 Gene;International Journal of Molecular Sciences;2020-08-06
4. CRISPR/Cas9-mediated knockin of human factor IX into swine factor IX locus effectively alleviates bleeding in hemophilia B pigs;Haematologica;2020-01-23
5. Clinical Pathology of the Rat;The Laboratory Rat;2020
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