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F Candotti

Showing results (11-20 of 49) with videos related to

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Acta Haematologica|April 15, 1999
Gene therapy for severe combined immunodeficiency caused by adenosine deaminase deficiency: improved retroviral vectors for clinical trialsM Onodera, D M Nelson, Y Sakiyama, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1991
[Bone marrow transplantation in congenital defects of immunity]F Porta, L D Notarangelo, F Candotti, et al.
Blood|August 15, 2000
Lentiviral-mediated gene transfer into human lymphocytes: role of HIV-1 accessory proteinsD Chinnasamy, N Chinnasamy, M J Enriquez, et al.
DNA and Cell Biology|September 1, 1993
Application of molecular analysis to genetic counseling in the Wiskott-Aldrich syndrome (WAS)L D Notarangelo, F Candotti, O Parolini, et al.
Gene Therapy|August 24, 1999
Retrovirus-mediated WASP gene transfer corrects defective actin polymerization in B cell lines from Wiskott-Aldrich syndrome patients carrying 'null' mutationsF Candotti, F Facchetti, L Blanzuoli, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 10, 2000
Lymphoid development and function in X-linked severe combined immunodeficiency mice after stem cell gene therapyM Otsu, S M Anderson, D M Bodine, et al.
Blood|April 15, 1996
Retroviral-mediated gene correction for X-linked severe combined immunodeficiencyF Candotti, J A Johnston, J M Puck, et al.
Gene Therapy|November 3, 1998
Generation of a conditionally neo(r)-containing retroviral producer cell line: effects of neo(r) on retroviral titer and transgene expressionO Wildner, F Candotti, E G Krecko, et al.
Clinical Immunology (Orlando, Fla.)|November 15, 2011
Development of IgA nephropathy-like glomerulonephritis associated with Wiskott-Aldrich syndrome protein deficiencyM Shimizu, N P Nikolov, K Ueno, et al.
Human Gene Therapy|September 15, 2000
Efficient gene transfer to human peripheral blood monocyte-derived dendritic cells using human immunodeficiency virus type 1-based lentiviral vectorsN Chinnasamy, D Chinnasamy, J F Toso, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Acta Haematologica|April 15, 1999
Gene therapy for severe combined immunodeficiency caused by adenosine deaminase deficiency: improved retroviral vectors for clinical trialsM Onodera, D M Nelson, Y Sakiyama, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1991
[Bone marrow transplantation in congenital defects of immunity]F Porta, L D Notarangelo, F Candotti, et al.
Blood|August 15, 2000
Lentiviral-mediated gene transfer into human lymphocytes: role of HIV-1 accessory proteinsD Chinnasamy, N Chinnasamy, M J Enriquez, et al.
DNA and Cell Biology|September 1, 1993
Application of molecular analysis to genetic counseling in the Wiskott-Aldrich syndrome (WAS)L D Notarangelo, F Candotti, O Parolini, et al.
Gene Therapy|August 24, 1999
Retrovirus-mediated WASP gene transfer corrects defective actin polymerization in B cell lines from Wiskott-Aldrich syndrome patients carrying 'null' mutationsF Candotti, F Facchetti, L Blanzuoli, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 10, 2000
Lymphoid development and function in X-linked severe combined immunodeficiency mice after stem cell gene therapyM Otsu, S M Anderson, D M Bodine, et al.
Blood|April 15, 1996
Retroviral-mediated gene correction for X-linked severe combined immunodeficiencyF Candotti, J A Johnston, J M Puck, et al.
Gene Therapy|November 3, 1998
Generation of a conditionally neo(r)-containing retroviral producer cell line: effects of neo(r) on retroviral titer and transgene expressionO Wildner, F Candotti, E G Krecko, et al.
Clinical Immunology (Orlando, Fla.)|November 15, 2011
Development of IgA nephropathy-like glomerulonephritis associated with Wiskott-Aldrich syndrome protein deficiencyM Shimizu, N P Nikolov, K Ueno, et al.
Human Gene Therapy|September 15, 2000
Efficient gene transfer to human peripheral blood monocyte-derived dendritic cells using human immunodeficiency virus type 1-based lentiviral vectorsN Chinnasamy, D Chinnasamy, J F Toso, et al.
Pageof 5