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B R Grubb

Showing results (51-60 of 56) with videos related to

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Molecular Cell|August 21, 2001
The CF salt controversy: in vivo observations and therapeutic approachesR Tarran, B R Grubb, D Parsons, et al.
Cell|January 6, 1999
Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways diseaseH Matsui, B R Grubb, R Tarran, et al.
Gene Therapy|January 24, 2014
Restoring ciliary function to differentiated primary ciliary dyskinesia cells with a lentiviral vectorL E Ostrowski, W Yin, M Patel, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 22, 2001
Cloning and functional characterization of two murine uridine nucleotide receptors reveal a potential target for correcting ion transport deficiency in cystic fibrosis gallbladderE R Lazarowski, L G Rochelle, W K O'Neal, et al.
Nature|October 27, 1994
Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humansB R Grubb, R J Pickles, H Ye, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 17, 1999
Salt restriction induces pseudohypoaldosteronism type 1 in mice expressing low levels of the beta-subunit of the amiloride-sensitive epithelial sodium channelS Pradervand, P M Barker, Q Wang, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Molecular Cell|August 21, 2001
The CF salt controversy: in vivo observations and therapeutic approachesR Tarran, B R Grubb, D Parsons, et al.
Cell|January 6, 1999
Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways diseaseH Matsui, B R Grubb, R Tarran, et al.
Gene Therapy|January 24, 2014
Restoring ciliary function to differentiated primary ciliary dyskinesia cells with a lentiviral vectorL E Ostrowski, W Yin, M Patel, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 22, 2001
Cloning and functional characterization of two murine uridine nucleotide receptors reveal a potential target for correcting ion transport deficiency in cystic fibrosis gallbladderE R Lazarowski, L G Rochelle, W K O'Neal, et al.
Nature|October 27, 1994
Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humansB R Grubb, R J Pickles, H Ye, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 17, 1999
Salt restriction induces pseudohypoaldosteronism type 1 in mice expressing low levels of the beta-subunit of the amiloride-sensitive epithelial sodium channelS Pradervand, P M Barker, Q Wang, et al.
Pageof 6