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Gene Therapy|February 22, 2002
Efficacy of recombinant adenovirus as vector for allergen gene therapy in a mouse model of type I allergyS Sudowe, E Montermann, J Steitz, et al.Cancer Gene Therapy|March 17, 1999
Induction of tumor antigen-specific immunity using plasmid DNA immunization in miceT Tüting, A Gambotto, A DeLeo, et al.Clinical and Experimental Dermatology|October 4, 2005
Absence of CD26 expression on skin-homing CLA+ CD4+ T lymphocytes in peripheral blood is a highly sensitive marker for early diagnosis and therapeutic monitoring of patients with Sézary syndromeM Sokolowska-Wojdylo, J Wenzel, E Gaffal, et al.Gene Therapy|March 1, 2000
Efficient transduction of mature CD83+ dendritic cells using recombinant adenovirus suppressed T cell stimulatory capacityH Jonuleit, T Tüting, J Steitz, et al.Cancer Gene Therapy|March 17, 1999
Induction of antitumor immunity by direct intratumoral injection of a recombinant adenovirus vector expressing interleukin-12A Gambotto, T Tüting, D L McVey, et al.Gene Therapy|February 15, 2001
Immunogenicity of enhanced green fluorescent protein (EGFP) in BALB/c mice: identification of an H2-Kd-restricted CTL epitopeA Gambotto, G Dworacki, V Cicinnati, et al.The Journal of Gene Medicine|February 7, 2001
Dendritic cell-based genetic immunization in mice with a recombinant adenovirus encoding murine TRP2 induces effective anti-melanoma immunityT Tüting, J Steitz, J Brück, et al.Gene Therapy|May 31, 2003
Transcriptional targeting of dendritic cells for gene therapy using the promoter of the cytoskeletal protein fascinR Ross, S Sudowe, J Beisner, et al.The British Journal of Dermatology|February 25, 2005
Circulating clonal CLA(+) and CD4(+) T cells in Sezary syndrome express the skin-homing chemokine receptors CCR4 and CCR10 as well as the lymph node-homing chemokine receptor CCR7M Sokolowska-Wojdylo, J Wenzel, E Gaffal, et al.Gene Therapy|February 12, 1998
Interferon-alpha gene therapy for cancer: retroviral transduction of fibroblasts and particle-mediated transfection of tumor cells are both effective strategies for gene delivery in murine tumor modelsT Tüting, A Gambotto, J Baar, et al.Pageof 5