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W H Colledge

Showing results (81-90 of 90) with videos related to

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The EMBO Journal|July 16, 1997
Complementation of null CF mice with a human CFTR YAC transgeneA L Manson, A E Trezise, L J MacVinish, et al.
Gene Therapy|September 26, 2001
Mucus altering agents as adjuncts for nonviral gene transfer to airway epitheliumS Ferrari, C Kitson, R Farley, et al.
The Journal of Physiology|March 15, 1997
Chloride secretion in the trachea of null cystic fibrosis mice: the effects of transfection with pTrial10-CFTR2L J MacVinish, D R Gill, S C Hyde, et al.
Molecular and Cellular Biology|February 18, 2004
Null mutation of the Lmo4 gene or a combined null mutation of the Lmo1/Lmo3 genes causes perinatal lethality, and Lmo4 controls neural tube development in miceE Tse, A J H Smith, S Hunt, et al.
Nature|March 15, 2000
Eomesodermin is required for mouse trophoblast development and mesoderm formationA P Russ, S Wattler, W H Colledge, et al.
Gene Therapy|January 13, 1998
A second dose of a CFTR cDNA-liposome complex is as effective as the first dose in restoring cAMP-dependent chloride secretion to null CF mice tracheaC A Goddard, R Ratcliff, J R Anderson, et al.
Cancer Research|April 16, 1998
Thymic lymphomas in mice with a truncating mutation in Brca2L S Friedman, F C Thistlethwaite, K J Patel, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2004
Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY(3-36)B G Challis, A P Coll, G S H Yeo, et al.
Gene Therapy|March 1, 1997
A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosisD R Gill, K W Southern, K A Mofford, et al.
Gene Therapy|August 2, 2000
Repeat administration of DNA/liposomes to the nasal epithelium of patients with cystic fibrosisS C Hyde, K W Southern, U Gileadi, et al.
Pageof 9

Showing results (81-90 of 90) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
The EMBO Journal|July 16, 1997
Complementation of null CF mice with a human CFTR YAC transgeneA L Manson, A E Trezise, L J MacVinish, et al.
Gene Therapy|September 26, 2001
Mucus altering agents as adjuncts for nonviral gene transfer to airway epitheliumS Ferrari, C Kitson, R Farley, et al.
The Journal of Physiology|March 15, 1997
Chloride secretion in the trachea of null cystic fibrosis mice: the effects of transfection with pTrial10-CFTR2L J MacVinish, D R Gill, S C Hyde, et al.
Molecular and Cellular Biology|February 18, 2004
Null mutation of the Lmo4 gene or a combined null mutation of the Lmo1/Lmo3 genes causes perinatal lethality, and Lmo4 controls neural tube development in miceE Tse, A J H Smith, S Hunt, et al.
Nature|March 15, 2000
Eomesodermin is required for mouse trophoblast development and mesoderm formationA P Russ, S Wattler, W H Colledge, et al.
Gene Therapy|January 13, 1998
A second dose of a CFTR cDNA-liposome complex is as effective as the first dose in restoring cAMP-dependent chloride secretion to null CF mice tracheaC A Goddard, R Ratcliff, J R Anderson, et al.
Cancer Research|April 16, 1998
Thymic lymphomas in mice with a truncating mutation in Brca2L S Friedman, F C Thistlethwaite, K J Patel, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2004
Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY(3-36)B G Challis, A P Coll, G S H Yeo, et al.
Gene Therapy|March 1, 1997
A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosisD R Gill, K W Southern, K A Mofford, et al.
Gene Therapy|August 2, 2000
Repeat administration of DNA/liposomes to the nasal epithelium of patients with cystic fibrosisS C Hyde, K W Southern, U Gileadi, et al.
Pageof 9