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D N Sheppard

Showing results (11-20 of 32) with videos related to

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Neuroscience|December 1, 1992
Transient outward currents in cochlear ganglion neurons of the chick embryoD N Sheppard, M A Valverde, J Represa, et al.
The Journal of Physiology|April 15, 2000
Two mechanisms of genistein inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in murine cell lineK A Lansdell, Z Cai, J F Kidd, et al.
The Journal of Physiology|February 1, 1991
Two types of potassium currents seen in isolated Necturus enterocytes with the single-electrode voltage-clamp techniqueM A Valverde, D N Sheppard, F Giraldez, et al.
The Journal of Physiology|February 1, 1991
Potassium currents of isolated Necturus enterocytes: a whole-cell patch-clamp studyD N Sheppard, M A Valverde, F Giraldez, et al.
The Journal of Biological Chemistry|June 21, 1996
Contribution of proline residues in the membrane-spanning domains of cystic fibrosis transmembrane conductance regulator to chloride channel functionD N Sheppard, S M Travis, H Ishihara, et al.
The Journal of Biological Chemistry|October 11, 1996
Function of Xenopus cystic fibrosis transmembrane conductance regulator (CFTR) Cl channels and use of human-Xenopus chimeras to investigate the pore properties of CFTRM P Price, H Ishihara, D N Sheppard, et al.
The Journal of Physiology|September 1, 1989
Characterization of a phosphorylation-activated Cl-selective channel in isolated Necturus enterocytesF Giraldez, K J Murray, F V Sepúlveda, et al.
Biophysical Journal|May 1, 1994
Effect of ATP concentration on CFTR Cl- channels: a kinetic analysis of channel regulationM C Winter, D N Sheppard, M R Carson, et al.
The American Journal of Physiology|July 1, 1992
Chloride channels in the apical membrane of normal and cystic fibrosis airway and intestinal epitheliaM P Anderson, D N Sheppard, H A Berger, 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 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Neuroscience|December 1, 1992
Transient outward currents in cochlear ganglion neurons of the chick embryoD N Sheppard, M A Valverde, J Represa, et al.
The Journal of Physiology|April 15, 2000
Two mechanisms of genistein inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in murine cell lineK A Lansdell, Z Cai, J F Kidd, et al.
The Journal of Physiology|February 1, 1991
Two types of potassium currents seen in isolated Necturus enterocytes with the single-electrode voltage-clamp techniqueM A Valverde, D N Sheppard, F Giraldez, et al.
The Journal of Physiology|February 1, 1991
Potassium currents of isolated Necturus enterocytes: a whole-cell patch-clamp studyD N Sheppard, M A Valverde, F Giraldez, et al.
The Journal of Biological Chemistry|June 21, 1996
Contribution of proline residues in the membrane-spanning domains of cystic fibrosis transmembrane conductance regulator to chloride channel functionD N Sheppard, S M Travis, H Ishihara, et al.
The Journal of Biological Chemistry|October 11, 1996
Function of Xenopus cystic fibrosis transmembrane conductance regulator (CFTR) Cl channels and use of human-Xenopus chimeras to investigate the pore properties of CFTRM P Price, H Ishihara, D N Sheppard, et al.
The Journal of Physiology|September 1, 1989
Characterization of a phosphorylation-activated Cl-selective channel in isolated Necturus enterocytesF Giraldez, K J Murray, F V Sepúlveda, et al.
Biophysical Journal|May 1, 1994
Effect of ATP concentration on CFTR Cl- channels: a kinetic analysis of channel regulationM C Winter, D N Sheppard, M R Carson, et al.
The American Journal of Physiology|July 1, 1992
Chloride channels in the apical membrane of normal and cystic fibrosis airway and intestinal epitheliaM P Anderson, D N Sheppard, H A Berger, 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 4