Contribution of KCNJ10 Gene Polymorphisms in Childhood Epilepsy

Genetic association of KCNJ10 rs1130183 with seizure susceptibility and computational analysis of deleterious non-synonymous SNPs of KCNJ10 gene

(2014) Nagaraja M. Phani et al.   GENE

KCNJ10 Mutations Display Differential Sensitivity to Heteromerisation with KCNJ16

(2013) Sophie Parrock et al.   NEPHRON PHYSIOLOGY

Expressional analysis of the astrocytic Kir4.1 channel in a pilocarpine–induced temporal lobe epilepsy model

(2013) Yuki Nagao et al.   Frontiers in Cellular Neuroscience

Genetic contribution to common epilepsies

(2011) Sanjay M Sisodiya et al.   CURRENT OPINION IN NEUROLOGY

Evidence that compromised K+ spatial buffering contributes to the epileptogenic effect of mutations in the human kir4.1 gene (KCNJ10)

(2011) Nadia Nabil Haj-Yasein et al.   GLIA

Epilepsy: Five New Things

(2011) L. A. Rudzinski et al.   NEUROLOGY

KCNJ10 potassium ion channel single nucleotide polymorphism in pediatric patients with idiopathic generalized epilepsy

(2011) Alper Ibrahim Dai et al.   NEUROLOGY PSYCHIATRY AND BRAIN RESEARCH

Potassium channel activity and glutamate uptake are impaired in astrocytes of seizure-susceptible DBA/2 mice

(2010) Mikhail Inyushin et al.   EPILEPSIA

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

Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy

(2009) Kjell Heuser et al.   EPILEPSY RESEARCH

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, andKCNJ10Mutations

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

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