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Bicarbonate transport in cell physiology and disease

Biochemical journal, 2009-01, Vol.417 (2), p.423-439

2009

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Molecular phenotype of SLC4A11 missense mutants: Setting the stage for personalized medicine in corneal dystrophies

Human mutation, 2018-05, Vol.39 (5), p.676-690

2018

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Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context

Biochimica et biophysica acta, 2016-07, Vol.1858 (7), p.1507-1532

2016

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Ophthalmic Nonsteroidal Anti-Inflammatory Drugs as a Therapy for Corneal Dystrophies Caused by SLC4A11 Mutation

Investigative ophthalmology & visual science, 2018-08, Vol.59 (10), p.4258-4267

2018

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Bicarbonate transporters in corals point towards a key step in the evolution of cnidarian calcification

Scientific reports, 2015-06, Vol.5 (1), p.9983-9983, Article 9983

2015

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Sensors and regulators of intracellular pH

Nature reviews. Molecular cell biology, 2010-01, Vol.11 (1), p.50

2010

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Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies

Scientific reports, 2019-07, Vol.9 (1), p.9681-15, Article 9681

2019

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Corneal Dystrophy-Causing SLC4A11 Mutants: Suitability for Folding-Correction Therapy

Human mutation, 2014-09, Vol.35 (9), p.1082-1091

2014

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Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases

Human molecular genetics, 2013-11, Vol.22 (22), p.4579-4590

2013

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Carbonic anhydrase II binds to and increases the activity of the epithelial sodium-proton exchanger, NHE3

American journal of physiology. Renal physiology, 2015-08, Vol.309 (4), p.F383-F392

2015

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Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies

American Journal of Physiology: Cell Physiology, 2016-11, Vol.311 (5), p.C735-C748

2016

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Carbonic Anhydrase Inhibitors. Design of Selective, Membrane-Impermeant Inhibitors Targeting the Human Tumor-Associated Isozyme IX

Journal of medicinal chemistry, 2004-04, Vol.47 (9), p.2337-2347

2004

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High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4A11

Investigative ophthalmology & visual science, 2015-12, Vol.56 (13), p.7739-7753

2015

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Altered gene expression in slc4a11 -/- mouse cornea highlights SLC4A11 roles

Scientific reports, 2021-10, Vol.11 (1), p.20885-20885, Article 20885

2021

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Human red blood cell uptake and sequestration of arsenite and selenite: Evidence of seleno-bis(S-glutathionyl) arsinium ion formation in human cells

Biochemical pharmacology, 2020-10, Vol.180 (C), p.114141, Article 114141

2020

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Cytosolic H+ microdomain developed around AE1 during AE1‐mediated Cl−/HCO3− exchange

The Journal of physiology, 2011-04, Vol.589 (7), p.1551-1569

2011

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Three-Dimensional Model for the Human Cl−/HCO3− Exchanger, AE1, by Homology to the E. coli ClC Protein

Journal of molecular biology, 2013-07, Vol.425 (14), p.2591-2608

2013

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Topology of transmembrane proteins by scanning cysteine accessibility mutagenesis methodology

Methods (San Diego, Calif.), 2007-04, Vol.41 (4), p.439-450

2007

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Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)

Nature genetics, 2006-07, Vol.38 (7), p.755-757

2006

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Large conformational dynamics in Band 3 protein: Significance for erythrocyte senescence signalling

Biochimica et biophysica acta. Biomembranes, 2021-10, Vol.1863 (10), p.183678-183678, Article 183678

2021

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Bicarbonate transport in health and disease

IUBMB life, 2014-09, Vol.66 (9), p.596-615

2014

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Red Fluorescent Protein pH Biosensor to Detect Concentrative Nucleoside Transport

The Journal of biological chemistry, 2009-07, Vol.284 (31), p.20499-20511

2009

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Bicarbonate homeostasis in excitable tissues: role of AE3 Cl-/HCO3- exchanger and carbonic anhydrase XIV interaction

American Journal of Physiology: Cell Physiology, 2009-11, Vol.297 (5), p.C1091-C1102

2009

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Molecular mechanism for the red blood cell senescence clock

IUBMB life, 2018-01, Vol.70 (1), p.32-40

2018

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Novel Topology in C-terminal Region of the Human Plasma Membrane Anion Exchanger, AE1

The Journal of biological chemistry, 2003-01, Vol.278 (5), p.3112-3120

2003

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Bicarbonate transport in cell physiology and disease

Molecular phenotype of SLC4A11 missense mutants: Setting the stage for personalized medicine in corneal dystrophies

Band 3, the human red cell chloride/bicarbonate anion exchanger (AE1, SLC4A1), in a structural context

Ophthalmic Nonsteroidal Anti-Inflammatory Drugs as a Therapy for Corneal Dystrophies Caused by SLC4A11 Mutation

Bicarbonate transporters in corals point towards a key step in the evolution of cnidarian calcification

Sensors and regulators of intracellular pH

Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies

Corneal Dystrophy-Causing SLC4A11 Mutants: Suitability for Folding-Correction Therapy

Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases

Carbonic anhydrase II binds to and increases the activity of the epithelial sodium-proton exchanger, NHE3

Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies

Carbonic Anhydrase Inhibitors. Design of Selective, Membrane-Impermeant Inhibitors Targeting the Human Tumor-Associated Isozyme IX

High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4A11

Altered gene expression in slc4a11 -/- mouse cornea highlights SLC4A11 roles

Human red blood cell uptake and sequestration of arsenite and selenite: Evidence of seleno-bis(S-glutathionyl) arsinium ion formation in human cells

Cytosolic H+ microdomain developed around AE1 during AE1‐mediated Cl−/HCO3− exchange

Three-Dimensional Model for the Human Cl−/HCO3− Exchanger, AE1, by Homology to the E. coli ClC Protein

Topology of transmembrane proteins by scanning cysteine accessibility mutagenesis methodology

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)

Large conformational dynamics in Band 3 protein: Significance for erythrocyte senescence signalling

Bicarbonate transport in health and disease

Red Fluorescent Protein pH Biosensor to Detect Concentrative Nucleoside Transport

Bicarbonate homeostasis in excitable tissues: role of AE3 Cl-/HCO3- exchanger and carbonic anhydrase XIV interaction

Molecular mechanism for the red blood cell senescence clock

Novel Topology in C-terminal Region of the Human Plasma Membrane Anion Exchanger, AE1

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