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Different SUMO paralogues determine the fate of wild-type and mutant CFTRs: biogenesis versus degradation

Molecular biology of the cell, 2019-01, Vol.30 (1), p.4-16

2019

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To Grow or Go: TMEM16A Expression as a Switch between Tumor Growth and Metastasis in SCCHN

Clinical cancer research, 2014-09, Vol.20 (17), p.4673-4688

2014

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SLC26A9 is a constitutively active, CFTR-regulated anion conductance in human bronchial epithelia

The Journal of general physiology, 2009-04, Vol.133 (4), p.421-438

2009

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TMEM16A/ANO1 suppression improves response to antibody‐mediated targeted therapy of EGFR and HER2/ERBB2

Genes chromosomes & cancer, 2017-06, Vol.56 (6), p.460-471

2017

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Rab11b regulates the apical recycling of the cystic fibrosis transmembrane conductance regulator in polarized intestinal epithelial cells

Molecular biology of the cell, 2009-04, Vol.20 (8), p.2337-2350

2009

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Phosphorylation-dependent 14-3-3 protein interactions regulate CFTR biogenesis

Molecular biology of the cell, 2012-03, Vol.23 (6), p.996-1009

2012

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The role of regulated CFTR trafficking in epithelial secretion

American Journal of Physiology: Cell Physiology, 2003-07, Vol.285 (1), p.C1-C18

2003

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The epithelial sodium channel (ENaC) establishes a trafficking vesicle pool responsible for its regulation

PloS one, 2012-09, Vol.7 (9), p.e46593-e46593

2012

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Nasal epithelial cell culture fluorescence recovery after photobleaching predicts cystic fibrosis therapeutic response

ERJ open research, 2022-10, Vol.8 (4)

2022

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Interleukin-17A induces bicarbonate secretion in normal human bronchial epithelial cells

American journal of physiology. Lung cellular and molecular physiology, 2009-02, Vol.296 (2), p.L257-L266

2009

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The CFTR trafficking mutation F508del inhibits the constitutive activity of SLC26A9

American journal of physiology. Lung cellular and molecular physiology, 2017-06, Vol.312 (6), p.L912-L925

2017

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Separating the contributions of SLC26A9 and CFTR to anion secretion in primary human bronchial epithelia

American journal of physiology. Lung cellular and molecular physiology, 2021-12, Vol.321 (6), p.L1147-L1160

2021

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Nucleofection disrupts tight junction fence function to alter membrane polarity of renal epithelial cells

American journal of physiology. Renal physiology, 2010-11, Vol.299 (5), p.F1178-F1184

2010

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SLC26A9 is selected for endoplasmic reticulum associated degradation (ERAD) via Hsp70-dependent targeting of the soluble STAS domain

Biochemical journal, 2021-12, Vol.478 (24), p.4203-4220

2021

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Generation and functional characterization of epithelial cells with stable expression of SLC26A9 Cl- channels

American journal of physiology. Lung cellular and molecular physiology, 2016-04, Vol.310 (7), p.L593-L602

2016

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Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approach

American journal of medical genetics. Part A, 2021-07, Vol.185 (7), p.2046-2055

2021

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PKA Regulates Vacuolar H+-ATPase Localization and Activity via Direct Phosphorylation of the A Subunit in Kidney Cells

The Journal of biological chemistry, 2010-08, Vol.285 (32), p.24676-24685

2010

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A physiologically-motivated model of cystic fibrosis liquid and solute transport dynamics across primary human nasal epithelia

Journal of pharmacokinetics and pharmacodynamics, 2019-10, Vol.46 (5), p.457-472

2019

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Pharmacological rescue of the mutant cystic fibrosis transmembrane conductance regulator (CFTR) detected by use of a novel fluorescence platform

Molecular medicine (Cambridge, Mass.), 2012-04, Vol.18 (4), p.685-696

2012

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Chaperone displacement from mutant cystic fibrosis transmembrane conductance regulator restores its function in human airway epithelia

The FASEB journal, 2008-09, Vol.22 (9), p.3255-3263

2008

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Graphing Wizardry

Science, 2000-09, Vol.289 (5486), p.1894-1894

Bertrand, Carol A.

2000

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Color by Number: Imaging Large Data

Science (American Association for the Advancement of Science), 2001-08, Vol.293 (5533), p.1335-1336

Bertrand, Carol A.

2001

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Measurement of membrane capacitance in epithelial monolayers

Methods in molecular biology (Clifton, N.J.), 2002, Vol.188, p.315

2002

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Nasal epithelial cell culture FRAP predicts cystic fibrosis therapeutic response

ERJ open research, 2022-11, p.382

2022

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An algorithm for detecting internalized, FM 1–43 stained membrane in epithelia demonstrates greater membrane internalization in low density cell clusters vs high density monolayers

The FASEB journal, 2006-03, Vol.20 (4), p.A352-A352

2006

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Different SUMO paralogues determine the fate of wild-type and mutant CFTRs: biogenesis versus degradation

To Grow or Go: TMEM16A Expression as a Switch between Tumor Growth and Metastasis in SCCHN

SLC26A9 is a constitutively active, CFTR-regulated anion conductance in human bronchial epithelia

TMEM16A/ANO1 suppression improves response to antibody‐mediated targeted therapy of EGFR and HER2/ERBB2

Rab11b regulates the apical recycling of the cystic fibrosis transmembrane conductance regulator in polarized intestinal epithelial cells

Phosphorylation-dependent 14-3-3 protein interactions regulate CFTR biogenesis

The role of regulated CFTR trafficking in epithelial secretion

The epithelial sodium channel (ENaC) establishes a trafficking vesicle pool responsible for its regulation

Nasal epithelial cell culture fluorescence recovery after photobleaching predicts cystic fibrosis therapeutic response

Interleukin-17A induces bicarbonate secretion in normal human bronchial epithelial cells

The CFTR trafficking mutation F508del inhibits the constitutive activity of SLC26A9

Separating the contributions of SLC26A9 and CFTR to anion secretion in primary human bronchial epithelia

Nucleofection disrupts tight junction fence function to alter membrane polarity of renal epithelial cells

SLC26A9 is selected for endoplasmic reticulum associated degradation (ERAD) via Hsp70-dependent targeting of the soluble STAS domain

Generation and functional characterization of epithelial cells with stable expression of SLC26A9 Cl- channels

Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approach

PKA Regulates Vacuolar H+-ATPase Localization and Activity via Direct Phosphorylation of the A Subunit in Kidney Cells

A physiologically-motivated model of cystic fibrosis liquid and solute transport dynamics across primary human nasal epithelia

Pharmacological rescue of the mutant cystic fibrosis transmembrane conductance regulator (CFTR) detected by use of a novel fluorescence platform

Chaperone displacement from mutant cystic fibrosis transmembrane conductance regulator restores its function in human airway epithelia

Graphing Wizardry

Color by Number: Imaging Large Data

Measurement of membrane capacitance in epithelial monolayers

Nasal epithelial cell culture FRAP predicts cystic fibrosis therapeutic response

An algorithm for detecting internalized, FM 1–43 stained membrane in epithelia demonstrates greater membrane internalization in low density cell clusters vs high density monolayers

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