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Airway Surface Liquid pH Regulation in Airway Epithelium Current Understandings and Gaps in Knowledge

International journal of molecular sciences, 2021-03, Vol.22 (7), p.3384

2021

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pH-dependence of the Plasmodium falciparum chloroquine resistance transporter is linked to the transport cycle

Nature communications, 2023-07, Vol.14 (1), p.4234-4234, Article 4234

2023

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Putting bicarbonate on the spot: pharmacological insights for CFTR correction in the airway epithelium

Frontiers in pharmacology, 2023-12, Vol.14, p.1293578-1293578

2023

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In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening

Scientific reports, 2017-08, Vol.7 (1), p.7249-15, Article 7249

2017

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A new human NHERF1 mutation decreases renal phosphate transporter NPT2a expression by a PTH-independent mechanism

PloS one, 2012-04, Vol.7 (4), p.e34764-e34764

2012

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Increased expression of ATP12A proton pump in cystic fibrosis airways

JCI insight, 2018-10, Vol.3 (20)

2018

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Airway surface hyperviscosity and defective mucociliary transport by IL-17/TNF-α are corrected by β-adrenergic stimulus

JCI insight, 2022-11, Vol.7 (22)

2022

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A variant of ASIC2 mediates sodium retention in nephrotic syndrome

JCI insight, 2021-08, Vol.6 (15)

2021

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Functional interaction between CFTR and the sodium-phosphate co-transport type 2a in Xenopus laevis oocytes

PloS one, 2012-04, Vol.7 (4), p.e34879-e34879

2012

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Expression of the human erythroid Rh glycoprotein (RhAG) enhances both NH3 and NH4+ transport in HeLa cells

Pflügers Archiv, 2005-06, Vol.450 (3), p.155-167

2005

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Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome

Journal of inherited metabolic disease, 2013-01, Vol.36 (1), p.103-112

2013

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Evidence for Activation of Endogenous Transporters in Xenopus laevis Oocytes Expressing the Plasmodium falciparum Chloroquine Resistance Transporter, PfCRT

The Journal of biological chemistry, 2004-09, Vol.279 (38), p.39438-39446

2004

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Does the Colonic H,K-ATPase also Act as an Na,K-ATPase?

Proceedings of the National Academy of Sciences - PNAS, 1998-05, Vol.95 (11), p.6516-6520

1998

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Analysis of CLCNKB mutations at dimer‐interface, calcium‐binding site, and pore reveals a variety of functional alterations in ClC‐Kb channel leading to Bartter syndrome

Human mutation, 2020-04, Vol.41 (4), p.774-785

2020

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Ammonium Homeostasis and Human Rhesus Glycoproteins

Nephron. Physiology, 2007-01, Vol.105 (1), p.p11-p17

Planelles, Gabrielle

2007

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Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis

Scientific reports, 2019-04, Vol.9 (1), p.6516-6516, Article 6516

2019

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Phosphomimetic substitution at Ser-33 of the chloroquine resistance transporter PfCRT reconstitutes drug responses in Plasmodium falciparum

The Journal of biological chemistry, 2019-08, Vol.294 (34), p.12766-12778

2019

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NHERF1 Mutations and Responsiveness of Renal Parathyroid Hormone

The New England journal of medicine, 2008-09, Vol.359 (11), p.1128-1135

2008

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Iron is a substrate of the Plasmodium falciparum chloroquine resistance transporter PfCRT in Xenopus oocytes

The Journal of biological chemistry, 2017-09, Vol.292 (39), p.16109-16121

2017

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The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation

Human molecular genetics, 2012-03, Vol.21 (6), p.1287-1298

2012

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ANP-stimulated Na + secretion in the collecting duct prevents Na + retention in the renal adaptation to acid load

American journal of physiology. Renal physiology, 2019-08, Vol.317 (2), p.F435-F443

2019

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Chloride transport in the renal proximal tubule

Pflügers Archiv, 2004-09, Vol.448 (6), p.561-570

Planelles, Gabrielle

2004

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PfCHA is a mitochondrial divalent cation/H⁺ antiporter in Plasmodium falciparum

Molecular microbiology, 2010-06, Vol.76 (6), p.1591-1606

2010

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Nephrolithiasis and Osteoporosis Associated with Hypophosphatemia Caused by Mutations in the Type 2a Sodium–Phosphate Cotransporter

The New England journal of medicine, 2002-09, Vol.347 (13), p.983-991

2002

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Airway Surface Liquid pH Regulation in Airway Epithelium Current Understandings and Gaps in Knowledge

pH-dependence of the Plasmodium falciparum chloroquine resistance transporter is linked to the transport cycle

Putting bicarbonate on the spot: pharmacological insights for CFTR correction in the airway epithelium

In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening

A new human NHERF1 mutation decreases renal phosphate transporter NPT2a expression by a PTH-independent mechanism

Increased expression of ATP12A proton pump in cystic fibrosis airways

Airway surface hyperviscosity and defective mucociliary transport by IL-17/TNF-α are corrected by β-adrenergic stimulus

A variant of ASIC2 mediates sodium retention in nephrotic syndrome

Functional interaction between CFTR and the sodium-phosphate co-transport type 2a in Xenopus laevis oocytes

Expression of the human erythroid Rh glycoprotein (RhAG) enhances both NH3 and NH4+ transport in HeLa cells

Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome

Evidence for Activation of Endogenous Transporters in Xenopus laevis Oocytes Expressing the Plasmodium falciparum Chloroquine Resistance Transporter, PfCRT

Does the Colonic H,K-ATPase also Act as an Na,K-ATPase?

Chloride deregulation and GABA depolarization in MTOR related malformations of cortical development

Analysis of CLCNKB mutations at dimer‐interface, calcium‐binding site, and pore reveals a variety of functional alterations in ClC‐Kb channel leading to Bartter syndrome

Ammonium Homeostasis and Human Rhesus Glycoproteins

Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis

Phosphomimetic substitution at Ser-33 of the chloroquine resistance transporter PfCRT reconstitutes drug responses in Plasmodium falciparum

NHERF1 Mutations and Responsiveness of Renal Parathyroid Hormone

Iron is a substrate of the Plasmodium falciparum chloroquine resistance transporter PfCRT in Xenopus oocytes

The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation

ANP-stimulated Na + secretion in the collecting duct prevents Na + retention in the renal adaptation to acid load

Chloride transport in the renal proximal tubule

PfCHA is a mitochondrial divalent cation/H⁺ antiporter in Plasmodium falciparum

Nephrolithiasis and Osteoporosis Associated with Hypophosphatemia Caused by Mutations in the Type 2a Sodium–Phosphate Cotransporter

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