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Molecular Cancer Therapeutics
|
October 14, 2003
Transduction of green fluorescent protein increased oxidative stress and enhanced sensitivity to cytotoxic drugs in neuroblastoma cell lines
Hiroaki Goto, Bo Yang, Denise Petersen, et al.
Human Gene Therapy
|
December 9, 2004
Factors influencing the titer and infectivity of lentiviral vectors
Aaron C Logan, Sarah J Nightingale, Dennis L Haas, et al.
American Journal of Respiratory Cell and Molecular Biology
|
November 22, 2002
Marrow-derived cells as vehicles for delivery of gene therapy to pulmonary epithelium
Joanna E Grove, Carolyn Lutzko, Josef Priller, et al.
Pediatrics
|
October 4, 2005
Successful hematopoietic stem cell transplantation for Niemann-Pick disease type B
Ami J Shah, Neena Kapoor, Gay M Crooks, et al.
Orphanet Journal of Rare Diseases
|
December 20, 2015
Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency
Hirsh D Komarow, Robert Sokolic, Michael S Hershfield, et al.
Gene Therapy
|
September 8, 2018
Superior lentiviral vectors designed for BSL-0 environment abolish vector mobilization
Peirong Hu, Yanmin Bi, Hong Ma, et al.
Human Gene Therapy
|
August 20, 2009
Stable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon system
Teiko 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 SCID
Denise 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 vector
Hiroshi Kobayashi, Denise Carbonaro, Karen Pepper, 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 replication
Ingrid Bahner, Teiko Sumiyoshi, Mercy Kagoda, et al.
Page
of 28
Search research articles
Search
Showing results (81-90 of 273) with videos related to
Sort By:
Page
of 28
Molecular Cancer Therapeutics
|
October 14, 2003
Transduction of green fluorescent protein increased oxidative stress and enhanced sensitivity to cytotoxic drugs in neuroblastoma cell lines
Hiroaki Goto, Bo Yang, Denise Petersen, et al.
Human Gene Therapy
|
December 9, 2004
Factors influencing the titer and infectivity of lentiviral vectors
Aaron C Logan, Sarah J Nightingale, Dennis L Haas, et al.
American Journal of Respiratory Cell and Molecular Biology
|
November 22, 2002
Marrow-derived cells as vehicles for delivery of gene therapy to pulmonary epithelium
Joanna E Grove, Carolyn Lutzko, Josef Priller, et al.
Pediatrics
|
October 4, 2005
Successful hematopoietic stem cell transplantation for Niemann-Pick disease type B
Ami J Shah, Neena Kapoor, Gay M Crooks, et al.
Orphanet Journal of Rare Diseases
|
December 20, 2015
Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency
Hirsh D Komarow, Robert Sokolic, Michael S Hershfield, et al.
Gene Therapy
|
September 8, 2018
Superior lentiviral vectors designed for BSL-0 environment abolish vector mobilization
Peirong Hu, Yanmin Bi, Hong Ma, et al.
Human Gene Therapy
|
August 20, 2009
Stable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon system
Teiko 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 SCID
Denise 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 vector
Hiroshi Kobayashi, Denise Carbonaro, Karen Pepper, 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 replication
Ingrid Bahner, Teiko Sumiyoshi, Mercy Kagoda, et al.
Page
of 28