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P L Zeitlin

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American Journal of Respiratory Cell and Molecular Biology|June 1, 1995
CIC-2: a developmentally dependent chloride channel expressed in the fetal lung and downregulated after birthC B Murray, M M Morales, T R Flotte, et al.
The Journal of Clinical Investigation|December 1, 1991
Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosisA Hamosh, B C Trapnell, P L Zeitlin, et al.
The Journal of Biological Chemistry|February 15, 1993
Expression of the cystic fibrosis transmembrane conductance regulator from a novel adeno-associated virus promoterT R Flotte, S A Afione, R Solow, et al.
JAMA|October 12, 2000
Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general populationX Wang, B Moylan, D A Leopold, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 1998
Analysis of ClC-2 channels as an alternative pathway for chloride conduction in cystic fibrosis airway cellsE M Schwiebert, L P Cid-Soto, D Stafford, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
CFTR protein expression in primary and cultured epitheliaP L Zeitlin, I Crawford, L Lu, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vectorT R Flotte, S A Afione, C Conrad, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1991
Immunocytochemical localization of the cystic fibrosis gene product CFTRI Crawford, P C Maloney, P L Zeitlin, et al.
The Journal of Biological Chemistry|June 5, 1991
Down-regulation of cystic fibrosis gene mRNA transcript levels and induction of the cystic fibrosis chloride secretory phenotype in epithelial cells by phorbol esterB C Trapnell, P L Zeitlin, C S Chu, et al.
Biochemistry|July 18, 1995
A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine selectively activates chloride efflux from human epithelial and mouse fibroblast cell lines expressing the cystic fibrosis transmembrane regulator delta F508 mutationC Guay-Broder, K A Jacobson, S Barnoy, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
American Journal of Respiratory Cell and Molecular Biology|June 1, 1995
CIC-2: a developmentally dependent chloride channel expressed in the fetal lung and downregulated after birthC B Murray, M M Morales, T R Flotte, et al.
The Journal of Clinical Investigation|December 1, 1991
Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosisA Hamosh, B C Trapnell, P L Zeitlin, et al.
The Journal of Biological Chemistry|February 15, 1993
Expression of the cystic fibrosis transmembrane conductance regulator from a novel adeno-associated virus promoterT R Flotte, S A Afione, R Solow, et al.
JAMA|October 12, 2000
Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general populationX Wang, B Moylan, D A Leopold, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 1998
Analysis of ClC-2 channels as an alternative pathway for chloride conduction in cystic fibrosis airway cellsE M Schwiebert, L P Cid-Soto, D Stafford, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
CFTR protein expression in primary and cultured epitheliaP L Zeitlin, I Crawford, L Lu, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vectorT R Flotte, S A Afione, C Conrad, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1991
Immunocytochemical localization of the cystic fibrosis gene product CFTRI Crawford, P C Maloney, P L Zeitlin, et al.
The Journal of Biological Chemistry|June 5, 1991
Down-regulation of cystic fibrosis gene mRNA transcript levels and induction of the cystic fibrosis chloride secretory phenotype in epithelial cells by phorbol esterB C Trapnell, P L Zeitlin, C S Chu, et al.
Biochemistry|July 18, 1995
A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine selectively activates chloride efflux from human epithelial and mouse fibroblast cell lines expressing the cystic fibrosis transmembrane regulator delta F508 mutationC Guay-Broder, K A Jacobson, S Barnoy, et al.
Pageof 5