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P G Middleton

Showing results (51-60 of 63) with videos related to

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The American Journal of Physiology|February 1, 1995
Bioelectric characteristics of exon 10 insertional cystic fibrosis mouse: comparison with humansS N Smith, D M Steel, P G Middleton, et al.
Nature Medicine|January 1, 1995
Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosisN J Caplen, E W Alton, P G Middleton, et al.
American Journal of Respiratory Cell and Molecular Biology|December 31, 1998
The in vivo effects of milrinone on the airways of cystic fibrosis mice and human subjectsS N Smith, P G Middleton, S Chadwick, et al.
Nature Genetics|October 1, 1993
Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant miceE W Alton, P G Middleton, N J Caplen, et al.
Thorax|March 26, 2009
Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosisC Goubau, M Wilschanski, V Skalická, et al.
Gene Therapy|November 3, 1998
The effects of jet nebulisation on cationic liposome-mediated gene transfer in vitroM Stern, F Sorgi, C Hughes, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
New clinical diagnostic procedures for cystic fibrosis in EuropeK De Boeck, N Derichs, I Fajac, et al.
Leukemia|September 10, 2005
A single nucleotide polymorphism in the coding region of ABL and its effects on sensitivity to imatinibL C Crossman, T O'Hare, T Lange, et al.
British Journal of Haematology|September 21, 2000
A comparison of molecular and enzyme-based assays for the detection of thiopurine methyltransferase mutationsS A Coulthard, C Rabello, J Robson, et al.
Gene Therapy|December 1, 1996
Laboratory and clinical studies in support of cystic fibrosis gene therapy using pCMV-CFTR-DOTAPG McLachlan, L P Ho, H Davidson-Smith, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
The American Journal of Physiology|February 1, 1995
Bioelectric characteristics of exon 10 insertional cystic fibrosis mouse: comparison with humansS N Smith, D M Steel, P G Middleton, et al.
Nature Medicine|January 1, 1995
Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosisN J Caplen, E W Alton, P G Middleton, et al.
American Journal of Respiratory Cell and Molecular Biology|December 31, 1998
The in vivo effects of milrinone on the airways of cystic fibrosis mice and human subjectsS N Smith, P G Middleton, S Chadwick, et al.
Nature Genetics|October 1, 1993
Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant miceE W Alton, P G Middleton, N J Caplen, et al.
Thorax|March 26, 2009
Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosisC Goubau, M Wilschanski, V Skalická, et al.
Gene Therapy|November 3, 1998
The effects of jet nebulisation on cationic liposome-mediated gene transfer in vitroM Stern, F Sorgi, C Hughes, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
New clinical diagnostic procedures for cystic fibrosis in EuropeK De Boeck, N Derichs, I Fajac, et al.
Leukemia|September 10, 2005
A single nucleotide polymorphism in the coding region of ABL and its effects on sensitivity to imatinibL C Crossman, T O'Hare, T Lange, et al.
British Journal of Haematology|September 21, 2000
A comparison of molecular and enzyme-based assays for the detection of thiopurine methyltransferase mutationsS A Coulthard, C Rabello, J Robson, et al.
Gene Therapy|December 1, 1996
Laboratory and clinical studies in support of cystic fibrosis gene therapy using pCMV-CFTR-DOTAPG McLachlan, L P Ho, H Davidson-Smith, et al.
Pageof 7