Showing results (91-100 of 112) with videos related to
Sort By:
Pageof 12
Cell|November 16, 1990
Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosisS H Cheng, R J Gregory, J Marshall, et al.Science (New York, N.Y.)|July 12, 1991
Demonstration that CFTR is a chloride channel by alteration of its anion selectivityM P Anderson, R J Gregory, S Thompson, et al.Journal of Virology|April 10, 1999
Novel role for E4 region genes in protection of adenovirus vectors from lysis by cytotoxic T lymphocytesJ M Kaplan, D Armentano, A Scaria, et al.Journal of Virology|July 10, 1999
E4ORF3 requirement for achieving long-term transgene expression from the cytomegalovirus promoter in adenovirus vectorsD Armentano, M P Smith, C C Sookdeo, et al.The Journal of Biological Chemistry|April 15, 1994
External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanismH F Cantiello, A G Prat, I L Reisin, et al.Cancer Gene Therapy|March 1, 1996
Adenovirus-mediated p53 gene transfer inhibits growth of human tumor cells expressing mutant p53 proteinM P Harris, S Sutjipto, K N Wills, et al.Human Gene Therapy|October 1, 1995
Characterization of an adenovirus gene transfer vector containing an E4 deletionD Armentano, C C Sookdeo, K M Hehir, et al.Journal of Virology|March 1, 1997
Effect of the E4 region on the persistence of transgene expression from adenovirus vectorsD Armentano, J Zabner, C Sacks, et al.The Journal of Clinical Investigation|October 1, 1991
Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channelH A Berger, M P Anderson, R J Gregory, et al.Molecular and Cellular Biology|August 1, 1991
Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2R J Gregory, D P Rich, S H Cheng, et al.Pageof 12