Retrovirus-mediated gene transfer offers the potential for stable long-term expression of transduced genes in host cells subsequent to integration of vector DNA into the host genome. Using a murine amphotropic retrovirus vector containing an interleukin-2 receptor (IL-2R) gene as a reporter and a neomycin phosphotransferase
Copyright © 2010 John Wiley & Sons, Ltd.BackgroundCystic fibrosis (CF) is caused by a defect in cyst...
The potential for gene therapy to be an effective treatment for cystic fibrosis (CF) airway disease ...
Cystic fibrosis (CF) is the most common lethal recessive genetic disease in the Caucasian population...
Retrovirus-mediated gene transfer offers the potential for stable long-term expression of transduced...
Cystic fibrosis (CF) is the most common lethal inherited disease in the Caucasian population with an...
Cystic fibrosis (CF) is the most common lethal inherited disease in the Caucasian population with an...
Cystic fibrosis (CF) is the most common lethal inherited dis-ease in the Caucasian population with a...
Gene therapy of cystic fibrosis (CF) lung disease needs highly efficient delivery and long-lasting c...
Gene therapy of cystic fibrosis (CF) lung disease needs highly efficient delivery and long-lasting c...
Cystic Fibrosis (CF) is the most common, fatal autosomal recessive disorder affecting the Caucasian ...
A gene therapy for cystic fibrosis (CF) lung disease by intralumenal delivery of therapeutic transge...
Cystic fibrosis (CF) lung disease is an ideal candidate for a genetic therapy. It has been shown pre...
Adeno-associated virus (AAV) vectors appear promising for use in gene therapy in cystic fibrosis (CF...
Adeno-associated virus (AAV) vectors appear promising for use in gene therapy in cystic fibrosis (CF...
We have used retrovirus-mediated gene transfer to demonstrate complementation of the cystic fibrosis...
Copyright © 2010 John Wiley & Sons, Ltd.BackgroundCystic fibrosis (CF) is caused by a defect in cyst...
The potential for gene therapy to be an effective treatment for cystic fibrosis (CF) airway disease ...
Cystic fibrosis (CF) is the most common lethal recessive genetic disease in the Caucasian population...
Retrovirus-mediated gene transfer offers the potential for stable long-term expression of transduced...
Cystic fibrosis (CF) is the most common lethal inherited disease in the Caucasian population with an...
Cystic fibrosis (CF) is the most common lethal inherited disease in the Caucasian population with an...
Cystic fibrosis (CF) is the most common lethal inherited dis-ease in the Caucasian population with a...
Gene therapy of cystic fibrosis (CF) lung disease needs highly efficient delivery and long-lasting c...
Gene therapy of cystic fibrosis (CF) lung disease needs highly efficient delivery and long-lasting c...
Cystic Fibrosis (CF) is the most common, fatal autosomal recessive disorder affecting the Caucasian ...
A gene therapy for cystic fibrosis (CF) lung disease by intralumenal delivery of therapeutic transge...
Cystic fibrosis (CF) lung disease is an ideal candidate for a genetic therapy. It has been shown pre...
Adeno-associated virus (AAV) vectors appear promising for use in gene therapy in cystic fibrosis (CF...
Adeno-associated virus (AAV) vectors appear promising for use in gene therapy in cystic fibrosis (CF...
We have used retrovirus-mediated gene transfer to demonstrate complementation of the cystic fibrosis...
Copyright © 2010 John Wiley & Sons, Ltd.BackgroundCystic fibrosis (CF) is caused by a defect in cyst...
The potential for gene therapy to be an effective treatment for cystic fibrosis (CF) airway disease ...
Cystic fibrosis (CF) is the most common lethal recessive genetic disease in the Caucasian population...