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Human Gene Therapy|January 1, 1990
In vivo expression and survival of gene-modified T lymphocytes in rhesus monkeysK W Culver, R A Morgan, W R Osborne, et al.Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|August 13, 2002
A novel approach using transcomplementing adenoviral vectors for gene therapy of adrenocortical cancerG W Wolkersdörfer, S R Bornstein, J N Higginbotham, et al.Annals of Surgery|October 1, 1993
The development of gene therapy for the treatment of cancerS A Rosenberg, W F Anderson, M Blaese, et al.Blood|February 7, 1998
Successful peripheral T-lymphocyte-directed gene transfer for a patient with severe combined immune deficiency caused by adenosine deaminase deficiencyM Onodera, T Ariga, N Kawamura, et al.Immunity|December 1, 1996
Signaling via IL-2 and IL-4 in JAK3-deficient severe combined immunodeficiency lymphocytes: JAK3-dependent and independent pathwaysS A Oakes, F Candotti, J A Johnston, et al.Nature Medicine|December 13, 1997
Therapy of malignant brain tumors by intratumoral implantation of retroviral vector-producing cellsZ Ram, K W Culver, E M Oshiro, et al.Blood|November 14, 1997
Structural and functional basis for JAK3-deficient severe combined immunodeficiencyF Candotti, S A Oakes, J A Johnston, et al.Nature Medicine|July 14, 1998
Peripheral expansion of pre-existing mature T cells is an important means of CD4+ T-cell regeneration HIV-infected adultsR E Walker, C S Carter, L Muul, et al.Science (New York, N.Y.)|October 20, 1995
T lymphocyte-directed gene therapy for ADA- SCID: initial trial results after 4 yearsR M Blaese, K W Culver, A D Miller, et al.Nature Medicine|July 14, 1998
T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+ cells in ADA-deficient SCID neonatesD B Kohn, M S Hershfield, D Carbonaro, et al.Pageof 18