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KCNJ10 gene

Known as: KCNJ10, Kir4.1, POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 10 
National Institutes of Health

Related topics

Related topics

4 relations
KCNJ10 protein, humanKCNJ12 geneKCNJ14 genepotassium inwardly-rectifying channel, subfamily J, member 10

Papers overview

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2018
2018
Novel Homozygous KCNJ10 Mutation in a Patient with Non-syndromic Early-Onset Cerebellar Ataxia
Mutations in KCNJ10, which encodes the inwardly rectifying potassium channel Kir4.1, a primary regulator of membrane excitability… 
2016
2016
Founder mutation in KCNJ10 in Pakistani patients with EAST syndrome
EAST syndrome is an autosomal recessive disorder caused by loss‐of‐function mutations in the gene KCNJ10. Among the 14 pathogenic… 
2016
2016
Reticulon 4 A / Nogo-A influences the distribution of Kir 4 . 1 but is not essential for potassium conductance in retinal Müller glia Running title : Nogo-A-Kir 4 . 1 interaction in Müller glia
In the adult retina, we have previously shown that Nogo-A was highly expressed in Müller glia. However, the role of Nogo-A in the… 
2015
2015
Contribution of KCNJ10 Gene Polymorphisms in Childhood Epilepsy
The purpose of this study was to investigate the possible association between childhood epilepsy and KCNJ10 gene polymorphisms… 
2014
2014
Kcnj10 is a major type of K+ channel in mouse corneal epithelial cells and plays a role in initiating EGFR signaling.
We used primary mouse corneal epithelial cells (pMCE) to examine the role of Kcnj10 in determining membrane K(+) conductance and… 
2014
2014
KIR4.1 Antibodies as Biomarkers in Multiple Sclerosis
Multiple sclerosis (MS) is an autoimmune disease caused by the infiltration of autoreactive lymphocytes into the central nervous… 
2013
2013
Enhanced accumulation of Kir4.1 protein, but not mRNA, in a murine model of cuprizone-induced demyelination
2012
2012
KCNJ10 gene mutation in an 8-year-old boy with seizures
2009
2009
Mutations of KCNJ 10 Together with Mutations of SLC 26 A 4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Syndrome
Mutations in SLC26A4 cause nonsyndromic hearing loss associated with an enlarged vestibular aqueduct (EVA, also known as DFNB4… 
Highly Cited
2005
Highly Cited
2005
Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy
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