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The Journal of Biological Chemistry
|
December 25, 1992
Partial purification of the cystic fibrosis transmembrane conductance regulator
L S Ostedgaard, M J Welsh
Molecular Medicine Today
|
July 1, 1996
Understanding how cystic fibrosis mutations cause a loss of Cl- channel function
D N Sheppard, L S Ostedgaard
Nature Structural Biology
|
March 21, 1998
Cystic fibrosis problem probed by proteolysis
M J Welsh, L S Ostedgaard
Journal of Cell Science
|
June 11, 1999
Processing of CFTR bearing the P574H mutation differs from wild-type and deltaF508-CFTR
L S Ostedgaard, B Zeiher, M J Welsh
The Journal of Biological Chemistry
|
March 13, 2001
Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by its R domain
L S Ostedgaard, O Baldursson, M J Welsh
The American Journal of Physiology
|
July 1, 1992
Staphylococcus aureus alpha-toxin permeabilizes the basolateral membrane of a Cl(-)-secreting epithelium
L S Ostedgaard, D M Shasby, M J Welsh
Nature
|
January 1, 1999
Structural biology. The ABC of a versatile engine
M J Welsh, A D Robertson, L S Ostedgaard
The Journal of Cell Biology
|
August 1, 1992
Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia
G M Denning, L S Ostedgaard, M J Welsh
The Journal of Biological Chemistry
|
August 30, 1996
Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator
J F Cotten, L S Ostedgaard, M R Carson, et al.
The EMBO Journal
|
March 1, 1995
Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency
D N Sheppard, L S Ostedgaard, M C Winter, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
The Journal of Biological Chemistry
|
December 25, 1992
Partial purification of the cystic fibrosis transmembrane conductance regulator
L S Ostedgaard, M J Welsh
Molecular Medicine Today
|
July 1, 1996
Understanding how cystic fibrosis mutations cause a loss of Cl- channel function
D N Sheppard, L S Ostedgaard
Nature Structural Biology
|
March 21, 1998
Cystic fibrosis problem probed by proteolysis
M J Welsh, L S Ostedgaard
Journal of Cell Science
|
June 11, 1999
Processing of CFTR bearing the P574H mutation differs from wild-type and deltaF508-CFTR
L S Ostedgaard, B Zeiher, M J Welsh
The Journal of Biological Chemistry
|
March 13, 2001
Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by its R domain
L S Ostedgaard, O Baldursson, M J Welsh
The American Journal of Physiology
|
July 1, 1992
Staphylococcus aureus alpha-toxin permeabilizes the basolateral membrane of a Cl(-)-secreting epithelium
L S Ostedgaard, D M Shasby, M J Welsh
Nature
|
January 1, 1999
Structural biology. The ABC of a versatile engine
M J Welsh, A D Robertson, L S Ostedgaard
The Journal of Cell Biology
|
August 1, 1992
Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia
G M Denning, L S Ostedgaard, M J Welsh
The Journal of Biological Chemistry
|
August 30, 1996
Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator
J F Cotten, L S Ostedgaard, M R Carson, et al.
The EMBO Journal
|
March 1, 1995
Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency
D N Sheppard, L S Ostedgaard, M C Winter, et al.
Page
of 3