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M J Welsh

Showing results (291-300 of 323) with videos related to

Pageof 33
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Science (New York, N.Y.)|July 12, 1991
Demonstration that CFTR is a chloride channel by alteration of its anion selectivityM P Anderson, R J Gregory, S Thompson, et al.
Molecular Endocrinology (Baltimore, Md.)|December 1, 1994
The hsp56 immunophilin component of untransformed steroid receptor complexes is localized both to microtubules in the cytoplasm and to the same nonrandom regions within the nucleus as the steroid receptorM J Czar, J K Owens-Grillo, A W Yem, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 12, 2000
The osmolyte xylitol reduces the salt concentration of airway surface liquid and may enhance bacterial killingJ Zabner, M P Seiler, J L Launspach, et al.
American Journal of Respiratory Cell and Molecular Biology|May 5, 1999
Activity of abundant antimicrobials of the human airwayS M Travis, B A Conway, J Zabner, et al.
Human Gene Therapy|February 1, 1994
Cystic fibrosis gene therapy using an adenovirus vector: in vivo safety and efficacy in nasal epitheliumM J Welsh, A E Smith, J Zabner, et al.
The Journal of Clinical Investigation|June 1, 1995
Adenoviral-mediated gene transfer to fetal pulmonary epithelia in vitro and in vivoP B McCray, K Armstrong, J Zabner, et al.
The American Journal of Physiology|April 1, 1995
Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpressionS H Cheng, S L Fang, J Zabner, et al.
Cell|December 15, 1995
Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channelP M Snyder, M P Price, F J McDonald, et al.
The Journal of Biological Chemistry|May 9, 2001
HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27)R Benndorf, X Sun, R R Gilmont, et al.
The Journal of Clinical Investigation|October 1, 1995
A mouse model for the delta F508 allele of cystic fibrosisB G Zeiher, E Eichwald, J Zabner, et al.
Pageof 33

Showing results (291-300 of 323) with videos related to

Sort By:
Pageof 33
Science (New York, N.Y.)|July 12, 1991
Demonstration that CFTR is a chloride channel by alteration of its anion selectivityM P Anderson, R J Gregory, S Thompson, et al.
Molecular Endocrinology (Baltimore, Md.)|December 1, 1994
The hsp56 immunophilin component of untransformed steroid receptor complexes is localized both to microtubules in the cytoplasm and to the same nonrandom regions within the nucleus as the steroid receptorM J Czar, J K Owens-Grillo, A W Yem, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 12, 2000
The osmolyte xylitol reduces the salt concentration of airway surface liquid and may enhance bacterial killingJ Zabner, M P Seiler, J L Launspach, et al.
American Journal of Respiratory Cell and Molecular Biology|May 5, 1999
Activity of abundant antimicrobials of the human airwayS M Travis, B A Conway, J Zabner, et al.
Human Gene Therapy|February 1, 1994
Cystic fibrosis gene therapy using an adenovirus vector: in vivo safety and efficacy in nasal epitheliumM J Welsh, A E Smith, J Zabner, et al.
The Journal of Clinical Investigation|June 1, 1995
Adenoviral-mediated gene transfer to fetal pulmonary epithelia in vitro and in vivoP B McCray, K Armstrong, J Zabner, et al.
The American Journal of Physiology|April 1, 1995
Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpressionS H Cheng, S L Fang, J Zabner, et al.
Cell|December 15, 1995
Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channelP M Snyder, M P Price, F J McDonald, et al.
The Journal of Biological Chemistry|May 9, 2001
HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27)R Benndorf, X Sun, R R Gilmont, et al.
The Journal of Clinical Investigation|October 1, 1995
A mouse model for the delta F508 allele of cystic fibrosisB G Zeiher, E Eichwald, J Zabner, et al.
Pageof 33