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L S Ostedgaard

Showing results (1-10 of 25) with videos related to

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The Journal of Biological Chemistry|December 25, 1992
Partial purification of the cystic fibrosis transmembrane conductance regulatorL S Ostedgaard, M J Welsh
Molecular Medicine Today|July 1, 1996
Understanding how cystic fibrosis mutations cause a loss of Cl- channel functionD N Sheppard, L S Ostedgaard
Nature Structural Biology|March 21, 1998
Cystic fibrosis problem probed by proteolysisM 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-CFTRL 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 domainL 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 epitheliumL S Ostedgaard, D M Shasby, M J Welsh
Nature|January 1, 1999
Structural biology. The ABC of a versatile engineM 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 epitheliaG 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 regulatorJ 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 sufficiencyD N Sheppard, L S Ostedgaard, M C Winter, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
The Journal of Biological Chemistry|December 25, 1992
Partial purification of the cystic fibrosis transmembrane conductance regulatorL S Ostedgaard, M J Welsh
Molecular Medicine Today|July 1, 1996
Understanding how cystic fibrosis mutations cause a loss of Cl- channel functionD N Sheppard, L S Ostedgaard
Nature Structural Biology|March 21, 1998
Cystic fibrosis problem probed by proteolysisM 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-CFTRL 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 domainL 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 epitheliumL S Ostedgaard, D M Shasby, M J Welsh
Nature|January 1, 1999
Structural biology. The ABC of a versatile engineM 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 epitheliaG 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 regulatorJ 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 sufficiencyD N Sheppard, L S Ostedgaard, M C Winter, et al.
Pageof 3