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Current Opinion in Molecular Therapeutics|March 16, 2001
Gene therapy for leukocyte adhesion deficiencyT R Bauer, D D HicksteinHuman Gene Therapy|February 10, 1997
Transduction of human hematopoietic cells and cell lines using a retroviral vector containing a modified murine CD4 reporter geneT R Bauer, D D HicksteinBlood|September 15, 1995
Improved transfer of the leukocyte integrin CD18 subunit into hematopoietic cell lines by using retroviral vectors having a gibbon ape leukemia virus envelopeT R Bauer, A D Miller, D D HicksteinHuman Gene Therapy|June 1, 1994
Expression from leukocyte integrin promoters in retroviral vectorsT R Bauer, W R Osborne, W W Kwok, et al.Blood Cells, Molecules & Diseases|April 25, 2000
The ETS family member Tel antagonizes the Fli-1 phenotype in hematopoietic cellsB A Kwiatkowski, A G Zielinska-Kwiatkowska, T R Bauer, et al.Blood|March 21, 1998
Retroviral-mediated gene transfer of the leukocyte integrin CD18 into peripheral blood CD34+ cells derived from a patient with leukocyte adhesion deficiency type 1T R Bauer, B R Schwartz, W C Liles, et al.Biochemical and Biophysical Research Communications|June 30, 1993
A point mutation associated with leukocyte adhesion deficiency type 1 of moderate severityA L Back, M Kerkering, D Baker, et al.The Journal of Biological Chemistry|July 4, 1998
The ets family member Tel binds to the Fli-1 oncoprotein and inhibits its transcriptional activityB A Kwiatkowski, L S Bastian, T R Bauer, et al.Gene Therapy|February 19, 2010
Lentiviral vectors incorporating a human elongation factor 1alpha promoter for the treatment of canine leukocyte adhesion deficiencyE J R Nelson, L M Tuschong, M J Hunter, et al.Gene Therapy|March 29, 2008
Potential genotoxicity from integration sites in CLAD dogs treated successfully with gammaretroviral vector-mediated gene therapyM Hai, R L Adler, T R Bauer, et al.Pageof 5