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B Kohn

Showing results (261-270 of 515) with videos related to

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Human Gene Therapy|August 20, 2009
Stable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon systemTeiko Sumiyoshi, Nathalia G Holt, Roger P Hollis, et al.
Molecular Therapy. Methods & Clinical Development|March 19, 2021
Gene delivery using AAV8 <i>in vivo</i> for disease stabilization in a bimodal gene therapy approach for the treatment of ADA-deficient SCIDDenise A Carbonaro-Sarracino, Krista Chun, Danielle N Clark, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 27, 2005
Neonatal gene therapy of MPS I mice by intravenous injection of a lentiviral vectorHiroshi Kobayashi, Denise Carbonaro, Karen Pepper, et al.
Gene Therapy|January 1, 1996
Increased levels of spliced RNA account for augmented expression from the MFG retroviral vector in hematopoietic cellsW J Krall, D C Skelton, X J Yu, et al.
The CRISPR Journal|April 20, 2021
Optimizing Integration and Expression of Transgenic Bruton's Tyrosine Kinase for CRISPR-Cas9-Mediated Gene Editing of X-Linked AgammaglobulinemiaDavid H Gray, Isaac Villegas, Joseph Long, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Adrenocortical-pituitary hybrid tumor causing Cushing's syndromeN Hiroi, G P Chrousos, B Kohn, et al.
Biotechniques|June 20, 2003
Time course of bioluminescent signal in orthotopic and heterotopic brain tumors in nude miceJ S Burgos, M Rosol, R A Moats, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2006
Lentiviral vector transduction of a dominant-negative Rev gene into human CD34+ hematopoietic progenitor cells potently inhibits human immunodeficiency virus-1 replicationIngrid Bahner, Teiko Sumiyoshi, Mercy Kagoda, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 24, 2007
Foamy virus vectors expressing anti-HIV transgenes efficiently block HIV-1 replicationJason A Taylor, Lucia Vojtech, Ingrid Bahner, et al.
Experimental Biology and Medicine (Maywood, N.J.)|October 26, 2007
Manipulation of OCT4 levels in human embryonic stem cells results in induction of differential cell typesRyan T Rodriguez, J Matthew Velkey, Carolyn Lutzko, et al.
Pageof 52

Showing results (261-270 of 515) with videos related to

Sort By:
Pageof 52
Human Gene Therapy|August 20, 2009
Stable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon systemTeiko Sumiyoshi, Nathalia G Holt, Roger P Hollis, et al.
Molecular Therapy. Methods & Clinical Development|March 19, 2021
Gene delivery using AAV8 <i>in vivo</i> for disease stabilization in a bimodal gene therapy approach for the treatment of ADA-deficient SCIDDenise A Carbonaro-Sarracino, Krista Chun, Danielle N Clark, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 27, 2005
Neonatal gene therapy of MPS I mice by intravenous injection of a lentiviral vectorHiroshi Kobayashi, Denise Carbonaro, Karen Pepper, et al.
Gene Therapy|January 1, 1996
Increased levels of spliced RNA account for augmented expression from the MFG retroviral vector in hematopoietic cellsW J Krall, D C Skelton, X J Yu, et al.
The CRISPR Journal|April 20, 2021
Optimizing Integration and Expression of Transgenic Bruton's Tyrosine Kinase for CRISPR-Cas9-Mediated Gene Editing of X-Linked AgammaglobulinemiaDavid H Gray, Isaac Villegas, Joseph Long, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Adrenocortical-pituitary hybrid tumor causing Cushing's syndromeN Hiroi, G P Chrousos, B Kohn, et al.
Biotechniques|June 20, 2003
Time course of bioluminescent signal in orthotopic and heterotopic brain tumors in nude miceJ S Burgos, M Rosol, R A Moats, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2006
Lentiviral vector transduction of a dominant-negative Rev gene into human CD34+ hematopoietic progenitor cells potently inhibits human immunodeficiency virus-1 replicationIngrid Bahner, Teiko Sumiyoshi, Mercy Kagoda, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 24, 2007
Foamy virus vectors expressing anti-HIV transgenes efficiently block HIV-1 replicationJason A Taylor, Lucia Vojtech, Ingrid Bahner, et al.
Experimental Biology and Medicine (Maywood, N.J.)|October 26, 2007
Manipulation of OCT4 levels in human embryonic stem cells results in induction of differential cell typesRyan T Rodriguez, J Matthew Velkey, Carolyn Lutzko, et al.
Pageof 52