Kathryn W. Peters

University of Pittsburgh — United States

Medicine · Health Sciences

21h-index1.9kcitations30works0.02yr avg
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Research Topics

Cystic Fibrosis Research Advances(14), Ion Transport and Channel Regulation(11), Ion channel regulation and function(9), Neonatal Respiratory Health Research(5), Cellular transport and secretion(4)

Publications30 total

Cystic Fibrosis Transmembrane Conductance Regulator Folding Mutations Reveal Differences in Corrector Efficacy Linked to Increases in Immature Cystic Fibrosis Transmembrane Conductance Regulator Expression
Frontiers in Physiology·2021· 3 citedOpen Access
Co-Translational Folding of the First Transmembrane Domain of ABC-Transporter CFTR is Supported by Assembly with the First Cytosolic Domain
Journal of Molecular Biology·2021· 50 citedOpen Access
Co-translational folding of the first transmembrane domain of ABC-transporter CFTR is supported by assembly with the first cytosolic domain
2020· 2 citedOpen Access
From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutations
UNC Libraries·2020Open Access
Comparative analyses of long non-coding RNA profiles in vivo in cystic fibrosis lung airway and parenchyma tissues
Respiratory Research·2019· 8 citedOpen Access
From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutations
Molecular Biology of the Cell·2016· 583 citedOpen Access
miR-16 rescues F508del-CFTR function in native cystic fibrosis epithelial cells
Gene Therapy·2015· 23 citedOpen Access
Small heat shock proteins target mutant cystic fibrosis transmembrane conductance regulator for degradation via a small ubiquitin-like modifier–dependent pathway
Molecular Biology of the Cell·2012· 82 cited
Pharmacological Rescue of the Mutant Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Detected by Use of a Novel Fluorescence Platform
Molecular Medicine·2012· 50 citedOpen Access
Phosphorylation-dependent 14-3-3 protein interactions regulate CFTR biogenesis
Molecular Biology of the Cell·2012· 63 citedOpen Access
CFTR Folding Consortium: Methods Available for Studies of CFTR Folding and Correction
Methods in molecular biology·2011· 35 cited
AS160 Modulates Aldosterone-stimulated Epithelial Sodium Channel Forward Trafficking
Molecular Biology of the Cell·2010· 47 citedOpen Access
The Rab‐GAP, AS160, participates in the regulation of apical membrane epithelial sodium channel (ENaC) density and recycling
The FASEB Journal·2010
Regulation of CFTR Trafficking by Its R Domain
Journal of Biological Chemistry·2008· 21 citedOpen Access
An Obligatory Heterodimer of 14-3-3β and 14-3-3ϵ Is Required for Aldosterone Regulation of the Epithelial Sodium Channel
Journal of Biological Chemistry·2008· 69 citedOpen Access
The Epithelial Sodium Channel (ENaC) Traffics to Apical Membrane in Lipid Rafts in Mouse Cortical Collecting Duct Cells
Journal of Biological Chemistry·2007· 67 citedOpen Access
Electrogenic bicarbonate secretion by prairie dog gallbladder
American Journal of Physiology-Gastrointestinal and Liver Physiology·2007· 21 cited
Airway Surface Liquid Volume Regulates ENaC by Altering the Serine Protease-Protease Inhibitor Balance
Journal of Biological Chemistry·2006· 107 citedOpen Access
Identification and membrane localization of electrogenic sodium bicarbonate cotransporters in Calu-3 cells
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease·2006· 28 cited
14-3-3 Isoforms Are Induced by Aldosterone and Participate in Its Regulation of Epithelial Sodium Channels
Journal of Biological Chemistry·2006· 77 citedOpen Access
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Frequent Co-authors

Raymond A. Frizzell(27), Michael Butterworth(9), John P. Johnson(6), Robert S. Edinger(5), Juanjuan Qi(5), Simon C. Watkins(5), Xiubin Liang(5), Harvey B. Pollard(4), Gergely L. Lukács(4), William B. Guggino(3), William E. Balch(3), William R. Skach(3), Eric J. Sorscher(3), Jeffrey L. Brodsky(3), Ineke Braakman(3), Guido Veit(2), Radu G. Avramescu(2), Annette Chiang(2), Scott A. Houck(2), Jeong S. Hong(2)