L H Hwang|E Gilboa - JoVE Visualize

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Cancer Research|June 1, 1995

Efficient gene transfer with adeno-associated virus-based plasmids complexed to cationic liposomes for gene therapy of human prostate cancerJ Vieweg, D Boczkowski, K M Roberson, et al.

The American Journal of Gastroenterology|March 1, 1996

Clinical significance of serum hepatitis C virus titers in patients with chronic type C hepatitisJ H Kao, M Y Lai, P J Chen, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986

Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cellsS F Yu, T von Rüden, P W Kantoff, et al.

Biochemical and Biophysical Research Communications|January 27, 1999

An ELISA for RNA helicase activity: application as an assay of the NS3 helicase of hepatitis C virusC C Hsu, L H Hwang, Y W Huang, et al.

Biochemical and Biophysical Research Communications|September 25, 1995

Improved gene expression by a modified bicistronic retroviral vectorC L Hsieh, B F Chen, C C Wang, et al.

Journal of Medical Virology|January 1, 1995

Unbiased usage of T-cell receptor beta variable region genes in peripheral blood cells of hepatitis C patients: no correlation with superantigen effectC C Wang, L H Hwang, P M Yang, et al.

Acta Biochimica Polonica|August 29, 2000

ATP-binding domain of NTPase/helicase as a target for hepatitis C antiviral therapyP Borowski, O Mueller, A Niebuhr, et al.

Journal of Virology|August 3, 2001

Structure-based mutational analysis of the hepatitis C virus NS3 helicaseC L Tai, W C Pan, S H Liaw, et al.

Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|September 1, 1993

Retroviral gene transfer of epidermal growth factor receptor into HL60 cells results in a partial block of retinoic acid-induced granulocytic differentiationL L Chen, B Gansbacher, E Gilboa, et al.

Human Gene Therapy|August 1, 1993

Transfer of the ADA gene into bone marrow cells and peripheral blood lymphocytes for the treatment of patients affected by ADA-deficient SCIDC Bordignon, F Mavilio, G Ferrari, et al.

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Showing results (111-120 of 143) with videos related to

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Pageof 15

Cancer Research|June 1, 1995

Efficient gene transfer with adeno-associated virus-based plasmids complexed to cationic liposomes for gene therapy of human prostate cancerJ Vieweg, D Boczkowski, K M Roberson, et al.

The American Journal of Gastroenterology|March 1, 1996

Clinical significance of serum hepatitis C virus titers in patients with chronic type C hepatitisJ H Kao, M Y Lai, P J Chen, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986

Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cellsS F Yu, T von Rüden, P W Kantoff, et al.

Biochemical and Biophysical Research Communications|January 27, 1999

An ELISA for RNA helicase activity: application as an assay of the NS3 helicase of hepatitis C virusC C Hsu, L H Hwang, Y W Huang, et al.

Biochemical and Biophysical Research Communications|September 25, 1995

Improved gene expression by a modified bicistronic retroviral vectorC L Hsieh, B F Chen, C C Wang, et al.

Journal of Medical Virology|January 1, 1995

Unbiased usage of T-cell receptor beta variable region genes in peripheral blood cells of hepatitis C patients: no correlation with superantigen effectC C Wang, L H Hwang, P M Yang, et al.

Acta Biochimica Polonica|August 29, 2000

ATP-binding domain of NTPase/helicase as a target for hepatitis C antiviral therapyP Borowski, O Mueller, A Niebuhr, et al.

Journal of Virology|August 3, 2001

Structure-based mutational analysis of the hepatitis C virus NS3 helicaseC L Tai, W C Pan, S H Liaw, et al.

Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|September 1, 1993

Retroviral gene transfer of epidermal growth factor receptor into HL60 cells results in a partial block of retinoic acid-induced granulocytic differentiationL L Chen, B Gansbacher, E Gilboa, et al.

Human Gene Therapy|August 1, 1993

Transfer of the ADA gene into bone marrow cells and peripheral blood lymphocytes for the treatment of patients affected by ADA-deficient SCIDC Bordignon, F Mavilio, G Ferrari, et al.

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