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Tweaking the catalytic efficiency of the CFTR ion channel

The Journal of general physiology, 2023-05, Vol.155 (5), p.1

McCarty, Nael A

2023

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The "new normal": Adapting doctoral trainee career preparation for broad career paths in science

PloS one, 2017-05, Vol.12 (5), p.e0177035-e0177035

2017

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Murine and human CFTR exhibit different sensitivities to CFTR potentiators

American journal of physiology. Lung cellular and molecular physiology, 2015-10, Vol.309 (7), p.L687-L699

2015

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Modeling the conformational changes underlying channel opening in CFTR

PloS one, 2013-09, Vol.8 (9), p.e74574-e74574

2013

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Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis

PLoS genetics, 2014-07, Vol.10 (7), p.e1004376-e1004376

2014

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Comparing ATPase activity of ATP-binding cassette subfamily C member 4, lamprey CFTR, and human CFTR using an antimony-phosphomolybdate assay

Frontiers in pharmacology, 2024-02, Vol.15, p.1363456-1363456

2024

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Junctional abnormalities in human airway epithelial cells expressing F508del CFTR

American journal of physiology. Lung cellular and molecular physiology, 2015-09, Vol.309 (5), p.L475-L487

2015

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Positioning of extracellular loop 1 affects pore gating of the cystic fibrosis transmembrane conductance regulator

American journal of physiology. Lung cellular and molecular physiology, 2016-03, Vol.310 (5), p.L403-L414

2016

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Breathe-Your immune system is counting on it

The Journal of experimental medicine, 2021-04, Vol.218 (4)

McCarty, Nael A

2021

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Flagellum-deficient Pseudomonas aeruginosa is more virulent than non-motile but flagellated mutants in a cystic fibrosis mouse model

Microbiology spectrum, 2024-10, Vol.12 (10), p.e0132524

2024

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Alteration of Membrane Cholesterol Content Plays a Key Role in Regulation of Cystic Fibrosis Transmembrane Conductance Regulator Channel Activity

Frontiers in physiology, 2021-06, Vol.12, p.652513-652513

2021

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Correction: The "new normal": Adapting doctoral trainee career preparation for broad career paths in science

PloS one, 2017-07, Vol.12 (7), p.e0181294-e0181294

2017

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Inflammation and ER Stress Downregulate BDH2 Expression and Dysregulate Intracellular Iron in Macrophages

Journal of Immunology Research, 2014-01, Vol.2014 (2014), p.1-16

2014

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Three charged amino acids in extracellular loop 1 are involved in maintaining the outer pore architecture of CFTR

The Journal of general physiology, 2014-08, Vol.144 (2), p.159-179

2014

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Sphingomyelinase decreases transepithelial anion secretion in airway epithelial cells in part by inhibiting CFTR‐mediated apical conductance

Physiological reports, 2021-08, Vol.9 (15), p.e14928-n/a

2021

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A transistor model for the cystic fibrosis transmembrane conductance regulator

Biophysical reports, 2023-06, Vol.3 (2), p.100108-100108, Article 100108

2023

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Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm

Biophysical reports, 2022-12, Vol.2 (4), p.100083-100083, Article 100083

2022

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Mechanistic analysis and significance of sphingomyelinase‐mediated decreases in transepithelial CFTR currents in nHBEs

Physiological reports, 2021-09, Vol.9 (17), p.e15023-n/a

2021

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Pyoverdine, the Major Siderophore in Pseudomonas aeruginosa, Evades NGAL Recognition

Interdisciplinary Perspectives on Infectious Diseases, 2012, Vol.2012 (2012), p.241-250

2012

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Evolutionary and functional divergence between the cystic fibrosis transmembrane conductance regulator and related ATP-binding cassette transporters

Proceedings of the National Academy of Sciences - PNAS, 2008-12, Vol.105 (48), p.18865-18870

2008

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The molecular evolution of function in the CFTR chloride channel

The Journal of general physiology, 2021-12, Vol.153 (12), p.1

2021

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Isolation and Characterization of a High Affinity Peptide Inhibitor of ClC-2 Chloride Channels

The Journal of biological chemistry, 2009-09, Vol.284 (38), p.26051-26062

2009

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Relating the disease mutation spectrum to the evolution of the cystic fibrosis transmembrane conductance regulator (CFTR)

PloS one, 2012-08, Vol.7 (8), p.e42336

2012

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Doctoral Trainee Preferences for Career Development Resources: The Influence of Peer and Other Supportive Social Capital

International journal of doctoral studies, 2019, Vol.14, p.675-702

2019

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Electrophysiological Approaches for the Study of Ion Channel Function

Methods in molecular biology (Clifton, N.J.), 2021-01, Vol.2302, p.49

2021

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Tweaking the catalytic efficiency of the CFTR ion channel

The "new normal": Adapting doctoral trainee career preparation for broad career paths in science

Murine and human CFTR exhibit different sensitivities to CFTR potentiators

Modeling the conformational changes underlying channel opening in CFTR

Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis

Comparing ATPase activity of ATP-binding cassette subfamily C member 4, lamprey CFTR, and human CFTR using an antimony-phosphomolybdate assay

Junctional abnormalities in human airway epithelial cells expressing F508del CFTR

Positioning of extracellular loop 1 affects pore gating of the cystic fibrosis transmembrane conductance regulator

Breathe-Your immune system is counting on it

Flagellum-deficient Pseudomonas aeruginosa is more virulent than non-motile but flagellated mutants in a cystic fibrosis mouse model

Alteration of Membrane Cholesterol Content Plays a Key Role in Regulation of Cystic Fibrosis Transmembrane Conductance Regulator Channel Activity

Correction: The "new normal": Adapting doctoral trainee career preparation for broad career paths in science

Inflammation and ER Stress Downregulate BDH2 Expression and Dysregulate Intracellular Iron in Macrophages

Three charged amino acids in extracellular loop 1 are involved in maintaining the outer pore architecture of CFTR

Sphingomyelinase decreases transepithelial anion secretion in airway epithelial cells in part by inhibiting CFTR‐mediated apical conductance

A transistor model for the cystic fibrosis transmembrane conductance regulator

Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm

Mechanistic analysis and significance of sphingomyelinase‐mediated decreases in transepithelial CFTR currents in nHBEs

Pyoverdine, the Major Siderophore in Pseudomonas aeruginosa, Evades NGAL Recognition

Evolutionary and functional divergence between the cystic fibrosis transmembrane conductance regulator and related ATP-binding cassette transporters

The molecular evolution of function in the CFTR chloride channel

Isolation and Characterization of a High Affinity Peptide Inhibitor of ClC-2 Chloride Channels

Relating the disease mutation spectrum to the evolution of the cystic fibrosis transmembrane conductance regulator (CFTR)

Doctoral Trainee Preferences for Career Development Resources: The Influence of Peer and Other Supportive Social Capital

Electrophysiological Approaches for the Study of Ion Channel Function

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