The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel

Variable loss of Kir4.1 channel function in SeSAME syndrome mutations

(2010) Xiaofang Tang et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Random mutagenesis screening indicates the absence of a separate H+-sensor in the pH-sensitive Kir channels

(2010) Jennifer J. Paynter et al.   Channels

Molecular Mechanisms of EAST/SeSAME Syndrome Mutations in Kir4.1 (KCNJ10)

(2010) Monica Sala-Rabanal et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Implication of Kir4.1 Channel in Excess Potassium Clearance: An In Vivo Study on Anesthetized Glial-Conditional Kir4.1 Knock-Out Mice

(2010) O. Chever et al.   JOURNAL OF NEUROSCIENCE

Molecular Basis of Decreased Kir4.1 Function in SeSAME/EAST Syndrome

(2010) D. M. Williams et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

2009 Homer W. Smith Award: Minerals in Motion: From New Ion Transporters to New Concepts

(2010) R. J. M. Bindels   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function

(2010) M. Reichold et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Novel Ca receptor signaling pathways for control of renal ion transport

(2009) Chunfa Huang et al.   CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION

Functional Analysis of the Kv1.1 N255D Mutation Associated with Autosomal Dominant Hypomagnesemia

(2009) Jenny van der Wijst et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

A missense mutation in the Kv1.1 voltage-gated potassium channel–encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia

(2009) Bob Glaudemans et al.   JOURNAL OF CLINICAL INVESTIGATION

HNF1B Mutations Associate with Hypomagnesemia and Renal Magnesium Wasting

(2009) S. Adalat et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

New molecular players facilitating Mg2+ reabsorption in the distal convoluted tubule

(2009) Bob Glaudemans et al.   KIDNEY INTERNATIONAL

The EAST Syndrome andKCNJ10Mutations

(2009)   NEW ENGLAND JOURNAL OF MEDICINE

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, andKCNJ10Mutations

(2009) Detlef Bockenhauer et al.   NEW ENGLAND JOURNAL OF MEDICINE

Potassium Ion Movement in the Inner Ear: Insights from Genetic Disease and Mouse Models

(2009) Anselm A. Zdebik et al.   PHYSIOLOGY

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

(2009) U. I. Scholl et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The acidic motif of WNK4 is crucial for its interaction with the K channel ROMK

(2008) Meena Murthy et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Regulation of magnesium reabsorption in DCT

(2008) Qi Xi et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

Mechanisms of Disease: the kidney-specific chloride channels ClCKA and ClCKB, the Barttin subunit, and their clinical relevance

(2007) Bernhard K Krämer et al.   Nature clinical practice. Nephrology