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Human Hypertension Caused by Mutations in WNK Kinases

Science (American Association for the Advancement of Science), 2001-08, Vol.293 (5532), p.1107-1112

2001

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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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The Expanding Spectrum of G Protein Diseases

The New England journal of medicine, 1999-04, Vol.340 (13), p.1012-1020

1999

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G-protein diseases furnish a model for the turn-on switch

Nature (London), 1998-07, Vol.394 (6688), p.35-38

1998

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Complex drug-drug-disease interactions between amiodarone, warfarin, and the thyroid gland

Medicine (Baltimore), 2004-03, Vol.83 (2), p.107-113

2004

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Hairy cell leukemia presenting as multiple discrete hepatic lesions

World journal of gastroenterology : WJG, 2009-09, Vol.15 (35), p.4453-4456

2009

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Distinct pathways for the involvement of WNK4 in the signaling of hypertonicity and EGF

The FEBS journal, 2008-04, Vol.275 (8), p.1631-1642

2008

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Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21

Nature genetics, 1997-06, Vol.16 (2), p.202-205

1997

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

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

2024

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Conditional Activation Defect of a Human Gsα Mutant

Proceedings of the National Academy of Sciences - PNAS, 1997-05, Vol.94 (11), p.5656-5661

1997

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Cyclosporine metabolic side effects: association with the WNK4 system

European journal of clinical investigation, 2011-10, Vol.41 (10), p.1113-1120

2011

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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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Pseudohypoaldosteronism Type II: Marked Sensitivity to Thiazides, Hypercalciuria, Normomagnesemia, and Low Bone Mineral Density

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3248-3254

2002

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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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Pseudohypoaldosteronism type II: Marked sensitivity to thiazides, hypercalciuria, normomagnesemia, and low bone mineral density

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3248-3254

2002

Volltextzugriff (PDF)

Renal Mg handling, FXYD 2 and the central role of the Na,K‐ ATP ase

Physiological reports, 2018-09, Vol.6 (17)

2018

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Familial Hyperkalemia and Hypertension (FHHt) and KLHL3: Description of a Family with a New Recessive Mutation (S553L) Compared to a Family with a Dominant Mutation, Q309R, with Analysis of Urinary Sodium Chloride Cotransporter

Nephron (2015), 2017-01, Vol.137 (1), p.77-84

2017

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Selective Assembly of Na,K-ATPase α2β2 Heterodimers in the Heart: DISTINCT FUNCTIONAL PROPERTIES AND ISOFORM-SELECTIVE INHIBITORS

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

2016

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Effect of age and affection status on blood pressure, serum potassium and stature in familial hyperkalaemia and hypertension

Nephrology, dialysis, transplantation, 2011-05, Vol.26 (5), p.1547-1553

2011

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Hypercalciuria in Familial Hyperkalemia and Hypertension with KLHL3 Mutations

Nephron (2015), 2015-01, Vol.130 (1), p.59-65

2015

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Hypercalciuria in Familial Hyperkalemia and Hypertension Accompanies Hyperkalemia and Precedes Hypertension: Description of a Large Family with the Q565E WNK4 Mutation

The journal of clinical endocrinology and metabolism, 2004-08, Vol.89 (8), p.4025-4030

2004

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Increased urinary Na-Cl cotransporter protein in familial hyperkalaemia and hypertension

Nephrology, dialysis, transplantation, 2008-02, Vol.23 (2), p.492-496

2008

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Familial Hyperkalemia and Hypertension: Pathogenetic Insights Based on Lithium Clearance

The journal of clinical endocrinology and metabolism, 2009-08, Vol.94 (8), p.3010-3016

2009

Volltextzugriff (PDF)

Cyclosporine metabolic side effects: association with the WNK4 system: CYCLOSPORINE SIDE EFFECTS AND WNK4

European journal of clinical investigation, 2011-10, Vol.41 (10), p.1113-1120

2011

Volltextzugriff (PDF)

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Human Hypertension Caused by Mutations in WNK Kinases

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

The Expanding Spectrum of G Protein Diseases

G-protein diseases furnish a model for the turn-on switch

Complex drug-drug-disease interactions between amiodarone, warfarin, and the thyroid gland

Hairy cell leukemia presenting as multiple discrete hepatic lesions

Distinct pathways for the involvement of WNK4 in the signaling of hypertonicity and EGF

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21

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

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

Conditional Activation Defect of a Human Gsα Mutant

Cyclosporine metabolic side effects: association with the WNK4 system

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

Pseudohypoaldosteronism Type II: Marked Sensitivity to Thiazides, Hypercalciuria, Normomagnesemia, and Low Bone Mineral Density

Hypermagnesuria in Humans Following Acute Intravenous Administration of Digoxin

Pseudohypoaldosteronism type II: Marked sensitivity to thiazides, hypercalciuria, normomagnesemia, and low bone mineral density

Renal Mg handling, FXYD 2 and the central role of the Na,K‐ ATP ase

Familial Hyperkalemia and Hypertension (FHHt) and KLHL3: Description of a Family with a New Recessive Mutation (S553L) Compared to a Family with a Dominant Mutation, Q309R, with Analysis of Urinary Sodium Chloride Cotransporter

Selective Assembly of Na,K-ATPase α2β2 Heterodimers in the Heart: DISTINCT FUNCTIONAL PROPERTIES AND ISOFORM-SELECTIVE INHIBITORS

Effect of age and affection status on blood pressure, serum potassium and stature in familial hyperkalaemia and hypertension

Hypercalciuria in Familial Hyperkalemia and Hypertension with KLHL3 Mutations

Hypercalciuria in Familial Hyperkalemia and Hypertension Accompanies Hyperkalemia and Precedes Hypertension: Description of a Large Family with the Q565E WNK4 Mutation

Increased urinary Na-Cl cotransporter protein in familial hyperkalaemia and hypertension

Familial Hyperkalemia and Hypertension: Pathogenetic Insights Based on Lithium Clearance

Cyclosporine metabolic side effects: association with the WNK4 system: CYCLOSPORINE SIDE EFFECTS AND WNK4

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