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Journal of Cell Science. Supplement
|
January 1, 1993
Dysfunction of CFTR bearing the delta F508 mutation
M J Welsh, G M Denning, L S Ostedgaard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1991
A 45-kDa protein antigenically related to band 3 is selectively expressed in kidney mitochondria
L S Ostedgaard, M L Jennings, L P Karniski, et al.
Cell
|
March 25, 1994
The amino-terminal portion of CFTR forms a regulated Cl- channel
D N Sheppard, L S Ostedgaard, D P Rich, et al.
Biochemistry
|
February 11, 1997
Association of domains within the cystic fibrosis transmembrane conductance regulator
L S Ostedgaard, D P Rich, L G DeBerg, et al.
The Journal of Biological Chemistry
|
October 20, 2000
Cystic fibrosis transmembrane conductance regulator Cl- channels with R domain deletions and translocations show phosphorylation-dependent and -independent activity
O Baldursson, L S Ostedgaard, T Rokhlina, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 3, 2000
A functional R domain from cystic fibrosis transmembrane conductance regulator is predominantly unstructured in solution
L S Ostedgaard, O Baldursson, D W Vermeer, et al.
The Journal of Clinical Investigation
|
January 1, 1992
Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia
G M Denning, L S Ostedgaard, S H Cheng, et al.
The American Journal of Physiology
|
April 1, 1994
Expression of cystic fibrosis transmembrane conductance regulator in a model epithelium
D N Sheppard, M R Carson, L S Ostedgaard, et al.
The Journal of Biological Chemistry
|
May 15, 1992
Cyclic AMP-dependent protein kinase activation of cystic fibrosis transmembrane conductance regulator chloride channels in planar lipid bilayers
B C Tilly, M C Winter, L S Ostedgaard, et al.
Cell
|
April 23, 1993
Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast
J L Teem, H A Berger, L S Ostedgaard, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Journal of Cell Science. Supplement
|
January 1, 1993
Dysfunction of CFTR bearing the delta F508 mutation
M J Welsh, G M Denning, L S Ostedgaard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1991
A 45-kDa protein antigenically related to band 3 is selectively expressed in kidney mitochondria
L S Ostedgaard, M L Jennings, L P Karniski, et al.
Cell
|
March 25, 1994
The amino-terminal portion of CFTR forms a regulated Cl- channel
D N Sheppard, L S Ostedgaard, D P Rich, et al.
Biochemistry
|
February 11, 1997
Association of domains within the cystic fibrosis transmembrane conductance regulator
L S Ostedgaard, D P Rich, L G DeBerg, et al.
The Journal of Biological Chemistry
|
October 20, 2000
Cystic fibrosis transmembrane conductance regulator Cl- channels with R domain deletions and translocations show phosphorylation-dependent and -independent activity
O Baldursson, L S Ostedgaard, T Rokhlina, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 3, 2000
A functional R domain from cystic fibrosis transmembrane conductance regulator is predominantly unstructured in solution
L S Ostedgaard, O Baldursson, D W Vermeer, et al.
The Journal of Clinical Investigation
|
January 1, 1992
Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia
G M Denning, L S Ostedgaard, S H Cheng, et al.
The American Journal of Physiology
|
April 1, 1994
Expression of cystic fibrosis transmembrane conductance regulator in a model epithelium
D N Sheppard, M R Carson, L S Ostedgaard, et al.
The Journal of Biological Chemistry
|
May 15, 1992
Cyclic AMP-dependent protein kinase activation of cystic fibrosis transmembrane conductance regulator chloride channels in planar lipid bilayers
B C Tilly, M C Winter, L S Ostedgaard, et al.
Cell
|
April 23, 1993
Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast
J L Teem, H A Berger, L S Ostedgaard, et al.
Page
of 3