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The Biochemical Journal
|
December 8, 1998
Cell surface expression and biosynthesis of epithelial Na+ channels
L 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 ATP
A 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 bridge
J F Cotten, M J Welsh
The American Journal of Physiology
|
September 1, 1980
Pathways of ion movement in the canine tracheal epithelium
M J Welsh, J H Widdicombe
Nature Structural Biology
|
March 21, 1998
Cystic fibrosis problem probed by proteolysis
M 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 regulator
J F Cotten, M J Welsh
The Journal of Clinical Investigation
|
April 1, 1992
cAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epithelia
J J Smith, M J Welsh
Science (New York, N.Y.)
|
December 11, 1992
Correction
M 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 epithelia
M P Anderson, M J Welsh
Physiological Reviews
|
January 29, 1999
Structure and function of the CFTR chloride channel
D N Sheppard, M J Welsh
Page
of 33
Search research articles
Search
Showing results (71-80 of 323) with videos related to
Sort By:
Page
of 33
The Biochemical Journal
|
December 8, 1998
Cell surface expression and biosynthesis of epithelial Na+ channels
L 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 ATP
A 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 bridge
J F Cotten, M J Welsh
The American Journal of Physiology
|
September 1, 1980
Pathways of ion movement in the canine tracheal epithelium
M J Welsh, J H Widdicombe
Nature Structural Biology
|
March 21, 1998
Cystic fibrosis problem probed by proteolysis
M 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 regulator
J F Cotten, M J Welsh
The Journal of Clinical Investigation
|
April 1, 1992
cAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epithelia
J J Smith, M J Welsh
Science (New York, N.Y.)
|
December 11, 1992
Correction
M 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 epithelia
M P Anderson, M J Welsh
Physiological Reviews
|
January 29, 1999
Structure and function of the CFTR chloride channel
D N Sheppard, M J Welsh
Page
of 33