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Nael A McCarty

Showing results (31-40 of 71) with videos related to

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The Journal of Biological Chemistry|May 28, 2013
Two salt bridges differentially contribute to the maintenance of cystic fibrosis transmembrane conductance regulator (CFTR) channel functionGuiying Cui, Cody S Freeman, Taylor Knotts, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
Membrane-resolved epithelial electrophysiology revealed using extracellular electrochemical impedance spectroscopy (EEIS)Athena J Chien, Erica Lull, Guiying Cui, et al.
Biophysical Journal|September 14, 2004
CFTR: a cysteine at position 338 in TM6 senses a positive electrostatic potential in the poreXuehong Liu, Zhi-Ren Zhang, Matthew D Fuller, et al.
Scientific Reports|October 19, 2017
Zebrafish aversive taste co-receptor is expressed in both chemo- and mechanosensory cells and plays a role in lateral line developmentNazia Mojib, Jin Xu, Zinka Bartolek, et al.
The Journal of General Physiology|July 16, 2014
Three charged amino acids in extracellular loop 1 are involved in maintaining the outer pore architecture of CFTRGuiying Cui, Kazi S Rahman, Daniel T Infield, et al.
Frontiers in Physiology|June 24, 2021
Alteration of Membrane Cholesterol Content Plays a Key Role in Regulation of Cystic Fibrosis Transmembrane Conductance Regulator Channel ActivityGuiying Cui, Kirsten A Cottrill, Kerry M Strickland, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|January 14, 2011
Low abundance of sweat duct Cl- channel CFTR in both healthy and cystic fibrosis athletes with exceptionally salty sweat during exerciseMary Beth Brown, Karla K V Haack, Brian P Pollack, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|June 28, 2015
Junctional abnormalities in human airway epithelial cells expressing F508del CFTRSamuel A Molina, Brandon Stauffer, Hannah K Moriarty, et al.
Journal of Proteome Research|October 18, 2019
Early Detection of Cystic Fibrosis Acute Pulmonary Exacerbations by Exhaled Breath Condensate MetabolomicsXiaoling Zang, María Eugenia Monge, David A Gaul, et al.
Methods in Molecular Biology (Clifton, N.J.)|April 20, 2021
Reconstitution of Detergent-Solubilized Membrane Proteins into Proteoliposomes and Nanodiscs for Functional and Structural StudiesKerry M Strickland, Kasahun Neselu, Arshay J Grant, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
The Journal of Biological Chemistry|May 28, 2013
Two salt bridges differentially contribute to the maintenance of cystic fibrosis transmembrane conductance regulator (CFTR) channel functionGuiying Cui, Cody S Freeman, Taylor Knotts, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
Membrane-resolved epithelial electrophysiology revealed using extracellular electrochemical impedance spectroscopy (EEIS)Athena J Chien, Erica Lull, Guiying Cui, et al.
Biophysical Journal|September 14, 2004
CFTR: a cysteine at position 338 in TM6 senses a positive electrostatic potential in the poreXuehong Liu, Zhi-Ren Zhang, Matthew D Fuller, et al.
Scientific Reports|October 19, 2017
Zebrafish aversive taste co-receptor is expressed in both chemo- and mechanosensory cells and plays a role in lateral line developmentNazia Mojib, Jin Xu, Zinka Bartolek, et al.
The Journal of General Physiology|July 16, 2014
Three charged amino acids in extracellular loop 1 are involved in maintaining the outer pore architecture of CFTRGuiying Cui, Kazi S Rahman, Daniel T Infield, et al.
Frontiers in Physiology|June 24, 2021
Alteration of Membrane Cholesterol Content Plays a Key Role in Regulation of Cystic Fibrosis Transmembrane Conductance Regulator Channel ActivityGuiying Cui, Kirsten A Cottrill, Kerry M Strickland, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|January 14, 2011
Low abundance of sweat duct Cl- channel CFTR in both healthy and cystic fibrosis athletes with exceptionally salty sweat during exerciseMary Beth Brown, Karla K V Haack, Brian P Pollack, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|June 28, 2015
Junctional abnormalities in human airway epithelial cells expressing F508del CFTRSamuel A Molina, Brandon Stauffer, Hannah K Moriarty, et al.
Journal of Proteome Research|October 18, 2019
Early Detection of Cystic Fibrosis Acute Pulmonary Exacerbations by Exhaled Breath Condensate MetabolomicsXiaoling Zang, María Eugenia Monge, David A Gaul, et al.
Methods in Molecular Biology (Clifton, N.J.)|April 20, 2021
Reconstitution of Detergent-Solubilized Membrane Proteins into Proteoliposomes and Nanodiscs for Functional and Structural StudiesKerry M Strickland, Kasahun Neselu, Arshay J Grant, et al.
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