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Molecular Microbiology|June 9, 2000
Oligomerization of the chromatin-structuring protein H-NSC P Smyth, T Lundbäck, D Renzoni, et al.Nature|October 2, 1986
A family of related ATP-binding subunits coupled to many distinct biological processes in bacteriaC F Higgins, I D Hiles, G P Salmond, 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.The Journal of Clinical Investigation|October 1, 1994
Tamoxifen blocks chloride channels. A possible mechanism for cataract formationJ J Zhang, T J Jacob, M A Valverde, 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.Human Molecular Genetics|April 18, 2000
Heterozygous MDR3 missense mutation associated with intrahepatic cholestasis of pregnancy: evidence for a defect in protein traffickingP H Dixon, N Weerasekera, K J Linton, 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 21