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M J Welsh

Showing results (71-80 of 323) with videos related to

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The Biochemical Journal|December 8, 1998
Cell surface expression and biosynthesis of epithelial Na+ channelsL S Prince, M J Welsh
The Journal of Biological Chemistry|July 13, 2000
Differences between cystic fibrosis transmembrane conductance regulator and HisP in the interaction with the adenine ring of ATPA L Berger, M J Welsh
The Journal of Biological Chemistry|February 20, 1999
Cystic fibrosis-associated mutations at arginine 347 alter the pore architecture of CFTR. Evidence for disruption of a salt bridgeJ F Cotten, M J Welsh
The American Journal of Physiology|September 1, 1980
Pathways of ion movement in the canine tracheal epitheliumM J Welsh, J H Widdicombe
Nature Structural Biology|March 21, 1998
Cystic fibrosis problem probed by proteolysisM J Welsh, L S Ostedgaard
The Journal of Biological Chemistry|November 5, 1997
Covalent modification of the regulatory domain irreversibly stimulates cystic fibrosis transmembrane conductance regulatorJ F Cotten, M J Welsh
The Journal of Clinical Investigation|April 1, 1992
cAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epitheliaJ J Smith, M J Welsh
Science (New York, N.Y.)|December 11, 1992
CorrectionM J Welsh, M P Anderson
Proceedings of the National Academy of Sciences of the United States of America|July 15, 1991
Calcium and cAMP activate different chloride channels in the apical membrane of normal and cystic fibrosis epitheliaM P Anderson, M J Welsh
Physiological Reviews|January 29, 1999
Structure and function of the CFTR chloride channelD N Sheppard, M J Welsh
Pageof 33

Showing results (71-80 of 323) with videos related to

Sort By:
Pageof 33
The Biochemical Journal|December 8, 1998
Cell surface expression and biosynthesis of epithelial Na+ channelsL S Prince, M J Welsh
The Journal of Biological Chemistry|July 13, 2000
Differences between cystic fibrosis transmembrane conductance regulator and HisP in the interaction with the adenine ring of ATPA L Berger, M J Welsh
The Journal of Biological Chemistry|February 20, 1999
Cystic fibrosis-associated mutations at arginine 347 alter the pore architecture of CFTR. Evidence for disruption of a salt bridgeJ F Cotten, M J Welsh
The American Journal of Physiology|September 1, 1980
Pathways of ion movement in the canine tracheal epitheliumM J Welsh, J H Widdicombe
Nature Structural Biology|March 21, 1998
Cystic fibrosis problem probed by proteolysisM J Welsh, L S Ostedgaard
The Journal of Biological Chemistry|November 5, 1997
Covalent modification of the regulatory domain irreversibly stimulates cystic fibrosis transmembrane conductance regulatorJ F Cotten, M J Welsh
The Journal of Clinical Investigation|April 1, 1992
cAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epitheliaJ J Smith, M J Welsh
Science (New York, N.Y.)|December 11, 1992
CorrectionM J Welsh, M P Anderson
Proceedings of the National Academy of Sciences of the United States of America|July 15, 1991
Calcium and cAMP activate different chloride channels in the apical membrane of normal and cystic fibrosis epitheliaM P Anderson, M J Welsh
Physiological Reviews|January 29, 1999
Structure and function of the CFTR chloride channelD N Sheppard, M J Welsh
Pageof 33