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J Bijman

Showing results (41-50 of 52) with videos related to

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The American Journal of Physiology|March 1, 1993
Low-conductance chloride channels in IEC-6 and CF nasal cells expressing CFTRJ Bijman, W Dalemans, M Kansen, et al.
The Journal of Biological Chemistry|November 3, 1995
Isotype-specific activation of cystic fibrosis transmembrane conductance regulator-chloride channels by cGMP-dependent protein kinase IIP J French, J Bijman, M Edixhoven, et al.
Hepatology (Baltimore, Md.)|February 1, 1997
Cystic fibrosis transmembrane conductance regulator mediates the cyclic adenosine monophosphate-induced fluid secretion but not the inhibition of resorption in mouse gallbladder epitheliumR H Peters, J H van Doorninck, P J French, et al.
The American Journal of Physiology|December 1, 1996
CFTR expression and mucin secretion in cultured mouse gallbladder epithelial cellsR H Peters, P J French, J H van Doorninck, et al.
Biochemical and Biophysical Research Communications|February 14, 1991
Cultured epithelial cells from patients with cystic fibrosis have an increased expression of the 14 kDa Ca2(+)-binding protein CFAJ Keulemans, V Van Heyningen, B J Scholte, et al.
Biochemical and Biophysical Research Communications|August 31, 1992
Nucleotide-activated chloride channels in lysosomal membranesB C Tilly, G M Mancini, J Bijman, et al.
The Journal of Clinical Investigation|September 15, 1996
A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivoP J French, J H van Doorninck, R H Peters, et al.
Gastroenterology|July 13, 2000
Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study ConsortiumI Bronsveld, F Mekus, J Bijman, et al.
Biochimica Et Biophysica Acta|June 9, 1992
Regulation of chloride transport in cultured normal and cystic fibrosis keratinocytesM Kansen, J Keulemans, A T Hoogeveen, et al.
The Journal of Clinical Investigation|December 26, 2001
Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblingsI Bronsveld, F Mekus, J Bijman, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
The American Journal of Physiology|March 1, 1993
Low-conductance chloride channels in IEC-6 and CF nasal cells expressing CFTRJ Bijman, W Dalemans, M Kansen, et al.
The Journal of Biological Chemistry|November 3, 1995
Isotype-specific activation of cystic fibrosis transmembrane conductance regulator-chloride channels by cGMP-dependent protein kinase IIP J French, J Bijman, M Edixhoven, et al.
Hepatology (Baltimore, Md.)|February 1, 1997
Cystic fibrosis transmembrane conductance regulator mediates the cyclic adenosine monophosphate-induced fluid secretion but not the inhibition of resorption in mouse gallbladder epitheliumR H Peters, J H van Doorninck, P J French, et al.
The American Journal of Physiology|December 1, 1996
CFTR expression and mucin secretion in cultured mouse gallbladder epithelial cellsR H Peters, P J French, J H van Doorninck, et al.
Biochemical and Biophysical Research Communications|February 14, 1991
Cultured epithelial cells from patients with cystic fibrosis have an increased expression of the 14 kDa Ca2(+)-binding protein CFAJ Keulemans, V Van Heyningen, B J Scholte, et al.
Biochemical and Biophysical Research Communications|August 31, 1992
Nucleotide-activated chloride channels in lysosomal membranesB C Tilly, G M Mancini, J Bijman, et al.
The Journal of Clinical Investigation|September 15, 1996
A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivoP J French, J H van Doorninck, R H Peters, et al.
Gastroenterology|July 13, 2000
Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study ConsortiumI Bronsveld, F Mekus, J Bijman, et al.
Biochimica Et Biophysica Acta|June 9, 1992
Regulation of chloride transport in cultured normal and cystic fibrosis keratinocytesM Kansen, J Keulemans, A T Hoogeveen, et al.
The Journal of Clinical Investigation|December 26, 2001
Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblingsI Bronsveld, F Mekus, J Bijman, et al.
Pageof 6