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Volumn 18, Issue SUPPL.4, 2012, Pages 13-17

Gene therapy for haemophilia B

Author keywords

AAV; Clinical trial; Gene therapy; Haemophilia B

Indexed keywords

ALANINE AMINOTRANSFERASE; BLOOD CLOTTING FACTOR 9; PARVOVIRUS VECTOR; PREDNISOLONE; RECOMBINANT BLOOD CLOTTING FACTOR 9;

EID: 84862882940     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2012.02823.x     Document Type: Article
Times cited : (20)

References (9)
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  • 3
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    • Xiao, X.1    Li, J.2    Samulski, R.J.3
  • 5
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    • AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
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    • Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response
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    • Manno, C.S.1    Pierce, G.F.2    Arruda, V.R.3
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    • Self-complementary adeno-associated virus vectors containing a novel liver-specific human factor IX expression cassette enable highly efficient transduction of murine and nonhuman primate liver
    • Nathwani AC, Gray JT, Ng CY et al. Self-complementary adeno-associated virus vectors containing a novel liver-specific human factor IX expression cassette enable highly efficient transduction of murine and nonhuman primate liver. Blood 2006; 107: 2653-61.
    • (2006) Blood , vol.107 , pp. 2653-2661
    • Nathwani, A.C.1    Gray, J.T.2    Ng, C.Y.3
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    • Long-term safety and efficacy following systemic administration of a self-complementary AAV vector encoding human FIX pseudotyped with serotype 5 and 8 capsid proteins
    • Nathwani AC, Rosales C, McIntosh J et al. Long-term safety and efficacy following systemic administration of a self-complementary AAV vector encoding human FIX pseudotyped with serotype 5 and 8 capsid proteins. Mol Ther 2011; 19: 876-85.
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    • Adenovirus-associated virus vector-mediated gene transfer in hemophilia B
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.