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Volumn 9, Issue 10, 1998, Pages 1397-1407

Retroviral vector-modified bone marrow stromal cells secrete biologically active factor IX in vitro and transiently deliver therapeutic levels of human factor IX to the plasma of dogs after reinfusion

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBODY; BLOOD CLOTTING FACTOR 9; VIRUS VECTOR; VITAMIN K GROUP;

EID: 17344364147     PISSN: 10430342     EISSN: None     Source Type: Journal    
DOI: 10.1089/hum.1998.9.10-1397     Document Type: Article
Times cited : (36)

References (12)
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  • 3
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    • Phenotypic correction of factor IX deficiency in skin fibroblasts of hemophific dogs
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  • 4
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    • Gene therapy to human diseases: Ex vivo and in vivo studies (Review)
    • BOULIKAS, T. (1996). Gene therapy to human diseases: Ex vivo and in vivo studies (Review). Int. J. Oncol. 9(6), 1239-1251.
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    • Boulikas, T.1
  • 6
    • 0003135354 scopus 로고
    • Clinical manifestations and therapy of inherited coagulation factor deficiencies
    • R.W. Colman, J. Hirsh, V.J. Marder, and E.W. Salzman, eds. (Lippincott, Philadelphia, PA)
    • BRETTLER, D.B., and LEVINE, P.H. (1994). Clinical manifestations and therapy of inherited coagulation factor deficiencies. In Hemostasis and Thrombosis: Basic Principles and Clinical Practice, 3rd Ed. R.W. Colman, J. Hirsh, V.J. Marder, and E.W. Salzman, eds. (Lippincott, Philadelphia, PA) pp. 169-183.
    • (1994) Hemostasis and Thrombosis: Basic Principles and Clinical Practice, 3rd Ed. , pp. 169-183
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  • 7
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    • Gene transfer in the hemophilias: Retrospect and prospect
    • BRINKHOUS, K.M. (1992). Gene transfer in the hemophilias: Retrospect and prospect. Thromb Res 67(3), 329-338.
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    • Brinkhous, K.M.1
  • 9
    • 0028661063 scopus 로고
    • Use of safety-modified retroviruses to introduce chemotherapy resistance sequences into normal hematopoietic cells for chemoprotection during the therapy of ovarian cancer A pilot trial
    • DEISSEROTH, A.B., KAVANAGH, J., and CHAMPLIN, R. (1994). Use of safety-modified retroviruses to introduce chemotherapy resistance sequences into normal hematopoietic cells for chemoprotection during the therapy of ovarian cancer A pilot trial. Hum. Gene Ther. 5, 1507-1522.
    • (1994) Hum. Gene Ther. , vol.5 , pp. 1507-1522
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  • 10
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    • DEISSEROTH, A.B., HOLMES, F., HORTOBAGYI, G., and CHAMPLIN, R. (1996). Use of safety-modified retroviruses to introduce chemotherapy resistance sequences into normal hematopoietic cells for chemoprotection during the therapy of breast cancer: A pilot study. Hum. Gene Ther. 7, 401-416.
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    • The stromal cells as a vehicle for ex vivo gene therapy
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.