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Journal of Thrombosis and Haemostasis : JTH
|
July 23, 2003
Gene therapy for the hemophilias
T VandenDriessche, D Collen, M K L Chuah
Journal of Thrombosis and Haemostasis : JTH
|
April 27, 2007
Gene therapy, bioengineered clotting factors and novel technologies for hemophilia treatment
G F Pierce, D Lillicrap, S W Pipe, et al.
Cancer Immunology, Immunotherapy : CII
|
July 1, 1996
Introduction of the interferon gamma gene into mouse T lymphoma cells with low MHC class I-expression results in selective induction of H-2Dk and concomitant enhanced metastasis
A B Geldhof, T VandenDriessche, G Opdenakker, et al.
Human Gene Therapy
|
March 21, 1998
Bone marrow stromal cells as targets for gene therapy of hemophilia A
M K Chuah, H Brems, V Vanslembrouck, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
November 30, 2013
Percutaneous occlusion of post-myocardial infarction ventricular septum rupture
F Risseeuw, I Diebels, T Vandendriessche, et al.
Human Gene Therapy
|
December 1, 1994
Inhibition of human immunodeficiency virus type-1 by retroviral vectors expressing antisense-TAR
M K Chuah, T VandenDriessche, H K Chang, et al.
Clinical & Experimental Metastasis
|
January 1, 1994
Tumorigenicity of mouse T lymphoma cells is controlled by the level of major histocompatibility complex class I H-2Kk antigens
T VandenDriessche, M Bakkus, D Toussaint-Demylle, et al.
Genes, Chromosomes & Cancer
|
November 1, 1989
Suggestive evidence that genes controlling invasion and metastasis of T-cell lymphomas are located on mouse chromosome 3
L Verschaeve, H Verschueren, T VandenDriessche, et al.
Journal of Virology
|
July 1, 1995
Inhibition of clinical human immunodeficiency virus (HIV) type 1 isolates in primary CD4+ T lymphocytes by retroviral vectors expressing anti-HIV genes
T VandenDriessche, M K Chuah, L Chiang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1999
Long-term expression of human coagulation factor VIII and correction of hemophilia A after in vivo retroviral gene transfer in factor VIII-deficient mice
T VandenDriessche, V Vanslembrouck, I Goovaerts, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 34) with videos related to
Sort By:
Page
of 4
Journal of Thrombosis and Haemostasis : JTH
|
July 23, 2003
Gene therapy for the hemophilias
T VandenDriessche, D Collen, M K L Chuah
Journal of Thrombosis and Haemostasis : JTH
|
April 27, 2007
Gene therapy, bioengineered clotting factors and novel technologies for hemophilia treatment
G F Pierce, D Lillicrap, S W Pipe, et al.
Cancer Immunology, Immunotherapy : CII
|
July 1, 1996
Introduction of the interferon gamma gene into mouse T lymphoma cells with low MHC class I-expression results in selective induction of H-2Dk and concomitant enhanced metastasis
A B Geldhof, T VandenDriessche, G Opdenakker, et al.
Human Gene Therapy
|
March 21, 1998
Bone marrow stromal cells as targets for gene therapy of hemophilia A
M K Chuah, H Brems, V Vanslembrouck, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
November 30, 2013
Percutaneous occlusion of post-myocardial infarction ventricular septum rupture
F Risseeuw, I Diebels, T Vandendriessche, et al.
Human Gene Therapy
|
December 1, 1994
Inhibition of human immunodeficiency virus type-1 by retroviral vectors expressing antisense-TAR
M K Chuah, T VandenDriessche, H K Chang, et al.
Clinical & Experimental Metastasis
|
January 1, 1994
Tumorigenicity of mouse T lymphoma cells is controlled by the level of major histocompatibility complex class I H-2Kk antigens
T VandenDriessche, M Bakkus, D Toussaint-Demylle, et al.
Genes, Chromosomes & Cancer
|
November 1, 1989
Suggestive evidence that genes controlling invasion and metastasis of T-cell lymphomas are located on mouse chromosome 3
L Verschaeve, H Verschueren, T VandenDriessche, et al.
Journal of Virology
|
July 1, 1995
Inhibition of clinical human immunodeficiency virus (HIV) type 1 isolates in primary CD4+ T lymphocytes by retroviral vectors expressing anti-HIV genes
T VandenDriessche, M K Chuah, L Chiang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1999
Long-term expression of human coagulation factor VIII and correction of hemophilia A after in vivo retroviral gene transfer in factor VIII-deficient mice
T VandenDriessche, V Vanslembrouck, I Goovaerts, et al.
Page
of 4