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Selectivity of Digitalis Glycosides for Isoforms of Human Na,K-ATPase

The Journal of biological chemistry, 2010-06, Vol.285 (25), p.19582-19592

2010

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Role of FXYD proteins in ion transport

Annual review of physiology, 2006-01, Vol.68 (1), p.431-459

2006

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Stimulation, Inhibition, or Stabilization of Na,K-ATPase Caused by Specific Lipid Interactions at Distinct Sites

The Journal of biological chemistry, 2015-02, Vol.290 (8), p.4829-4842

2015

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FXYD Proteins Stabilize Na,K-ATPase: AMPLIFICATION OF SPECIFIC PHOSPHATIDYLSERINE-PROTEIN INTERACTIONS

The Journal of biological chemistry, 2011-03, Vol.286 (11), p.9699-9712

2011

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Neutralization of the Charge on Asp369 of Na+,K+-ATPase Triggers E1 ↔ E2 Conformational Changes

The Journal of biological chemistry, 2009-11, Vol.284 (45), p.31038-31051

2009

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An Efficient One‐Pot Enzymatic Synthesis of Cardiac Glycosides with Varied Sugar Chain Lengths

Advanced synthesis & catalysis, 2019-07, Vol.361 (13), p.3114-3119

2019

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Hypermagnesuria in Humans Following Acute Intravenous Administration of Digoxin

Nephron (2015), 2018-01, Vol.138 (2), p.113-118

2018

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Stabilization of the α2 Isoform of Na,K-ATPase by Mutations in a Phospholipid Binding Pocket

The Journal of biological chemistry, 2011-12, Vol.286 (50), p.42888-42899

2011

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Revisiting the binding kinetics and inhibitory potency of cardiac glycosides on Na+,K+-ATPase (α1β1): Methodological considerations

Journal of pharmacological and toxicological methods, 2018-11, Vol.94 (Pt 2), p.64-72

2018

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Selective Assembly of Na,K-ATPase α2β2 Heterodimers in the Heart

The Journal of biological chemistry, 2016-10, Vol.291 (44), p.23159-23174

2016

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Neutral Phospholipids Stimulate Na,K-ATPase Activity

The Journal of biological chemistry, 2013-04, Vol.288 (14), p.10073-10081

2013

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Purification of Na+,K+-ATPase Expressed in Pichia pastoris Reveals an Essential Role of Phospholipid-Protein Interactions

The Journal of biological chemistry, 2005-04, Vol.280 (17), p.16610-16618

2005

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Do Src Kinase and Caveolin Interact Directly with Na,K-ATPase?

The Journal of biological chemistry, 2016-05, Vol.291 (22), p.11736-11750

2016

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Specific phospholipid binding to Na,K-ATPase at two distinct sites

Proceedings of the National Academy of Sciences - PNAS, 2017-03, Vol.114 (11), p.2904-2909

2017

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Familial hyperkalemia and hypertension and a hypothesis to explain proximal renal tubular acidosis

Proceedings of the National Academy of Sciences - PNAS, 2019-08, Vol.116 (33), p.16173-16174

2019

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A digoxin derivative that potently reduces intraocular pressure: efficacy and mechanism of action in different animal models

American Journal of Physiology: Cell Physiology, 2024-05, Vol.326 (5), p.C1505-C1519

2024

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Association of Familial Hyperkalemia and Hypertension with Proximal Renal Tubular Acidosis and Epileptic Seizures

Nephron (2015), 2024-03, Vol.148 (3), p.179-184

2024

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Neutral phospholipids stimulate Na,K-ATPase activity: a specific lipid-protein interaction

The Journal of biological chemistry, 2013-04, Vol.288 (14), p.10073-10081

2013

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A missense mutation converts the Na+,K+-ATPase into an ion channel and causes therapy-resistant epilepsy

The Journal of biological chemistry, 2021-12, Vol.297 (6), p.101355-101355, Article 101355

2021

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Ouabain-induced Internalization and Lysosomal Degradation of the Na+/K+-ATPase

The Journal of biological chemistry, 2014-01, Vol.289 (2), p.1049-1059

2014

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Cardiac glycosides induced toxicity in human cells expressing α1-, α2-, or α3-isoforms of Na-K-ATPase

American Journal of Physiology: Cell Physiology, 2015-07, Vol.309 (2), p.C126-C135

2015

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Renal Mg handling, FXYD2 and the central role of the Na,K‐ATPase

Physiological reports, 2018-09, Vol.6 (17), p.e13843-n/a

2018

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Structure and mechanism of Na,K-ATPase: functional sites and their interactions

Annual review of physiology, 2003-01, Vol.65 (1), p.817-849

2003

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Digoxin derivatives with selectivity for the α2β3 isoform of Na,K-ATPase potently reduce intraocular pressure

Proceedings of the National Academy of Sciences - PNAS, 2015-11, Vol.112 (44), p.13723-13728

2015

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Molecular Mechanisms and Kinetic Effects of FXYD1 and Phosphomimetic Mutants on Purified Human Na,K-ATPase

The Journal of biological chemistry, 2015-11, Vol.290 (48), p.28746-28759

2015

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Selectivity of Digitalis Glycosides for Isoforms of Human Na,K-ATPase

Role of FXYD proteins in ion transport

Stimulation, Inhibition, or Stabilization of Na,K-ATPase Caused by Specific Lipid Interactions at Distinct Sites

FXYD Proteins Stabilize Na,K-ATPase: AMPLIFICATION OF SPECIFIC PHOSPHATIDYLSERINE-PROTEIN INTERACTIONS

Neutralization of the Charge on Asp369 of Na+,K+-ATPase Triggers E1 ↔ E2 Conformational Changes

An Efficient One‐Pot Enzymatic Synthesis of Cardiac Glycosides with Varied Sugar Chain Lengths

Hypermagnesuria in Humans Following Acute Intravenous Administration of Digoxin

Stabilization of the α2 Isoform of Na,K-ATPase by Mutations in a Phospholipid Binding Pocket

Revisiting the binding kinetics and inhibitory potency of cardiac glycosides on Na+,K+-ATPase (α1β1): Methodological considerations

Selective Assembly of Na,K-ATPase α2β2 Heterodimers in the Heart

Neutral Phospholipids Stimulate Na,K-ATPase Activity

Purification of Na+,K+-ATPase Expressed in Pichia pastoris Reveals an Essential Role of Phospholipid-Protein Interactions

Do Src Kinase and Caveolin Interact Directly with Na,K-ATPase?

Specific phospholipid binding to Na,K-ATPase at two distinct sites

Familial hyperkalemia and hypertension and a hypothesis to explain proximal renal tubular acidosis

A digoxin derivative that potently reduces intraocular pressure: efficacy and mechanism of action in different animal models

Association of Familial Hyperkalemia and Hypertension with Proximal Renal Tubular Acidosis and Epileptic Seizures

Neutral phospholipids stimulate Na,K-ATPase activity: a specific lipid-protein interaction

A missense mutation converts the Na+,K+-ATPase into an ion channel and causes therapy-resistant epilepsy

Ouabain-induced Internalization and Lysosomal Degradation of the Na+/K+-ATPase

Cardiac glycosides induced toxicity in human cells expressing α1-, α2-, or α3-isoforms of Na-K-ATPase

Renal Mg handling, FXYD2 and the central role of the Na,K‐ATPase

Structure and mechanism of Na,K-ATPase: functional sites and their interactions

Digoxin derivatives with selectivity for the α2β3 isoform of Na,K-ATPase potently reduce intraocular pressure

Molecular Mechanisms and Kinetic Effects of FXYD1 and Phosphomimetic Mutants on Purified Human Na,K-ATPase

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