ATPase Na+/K+ transporting subunit alpha 3 ; Homo sapiens






25 Article(s)
Download
PMID
Title
Journal
Pub. Date
#Total Relationship(s)
1 1312709 A dinucleotide repeat polymorphism in the human Na+,K+ ATPase, alpha subunit (ATP1A3) gene. Nucleic Acids Res 1992 Mar 11 1
2 9646882 Evidence for an allelic association between bipolar disorder and a Na+, K+ adenosine triphosphatase alpha subunit gene (ATP1A3). Biol Psychiatry 1998 Jul 1 1
3 16087159 Cardiopulmonary bypass reduces atrial Na+-K+-ATPase expression in children. Biochem Biophys Res Commun 2005 Sep 30 1
4 18675996 [123I]-FP-CIT and [99mTc]-HMPAO single photon emission computed tomography in a new sporadic case of rapid-onset dystonia-parkinsonism. J Neurol Sci 2008 Oct 15 1
5 19351654 A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism. Hum Mol Genet 2009 Jul 1 2
6 20590807 Dystonia-plus syndromes. Eur J Neurol 2010 Jul 1
7 21072501 Risk for antipsychotic-induced extrapyramidal symptoms: influence of family history and genetic susceptibility. Psychopharmacology (Berl) 2011 Apr 1
8 23409136 Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients. PLoS One 2013 1
9 24431296 Genotype-phenotype correlations in alternating hemiplegia of childhood. Neurology 2014 Feb 11 1
10 25433904 Altered glutamate protein co-expression network topology linked to spine loss in the auditory cortex of schizophrenia. Biol Psychiatry 2015 Jun 1 1
11 25439493 Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes. Pediatr Neurol 2014 Dec 1
12 26417536 Intermediate Phenotypes of ATP1A3 Mutations: Phenotype-Genotype Correlations. Tremor Other Hyperkinet Mov (N Y) 2015 1
13 27146299 Treatment with Oral ATP decreases alternating hemiplegia of childhood with de novo ATP1A3 Mutation. Orphanet J Rare Dis 2016 May 4 2
14 28465228 Knockout of sodium pump α3 subunit gene (Atp1a3<sup>-/-</sup>) results in perinatal seizure and defective respiratory rhythm generation. Brain Res 2017 Jul 1 3
15 28969699 A randomized, controlled, double-blind, crossover trial of triheptanoin in alternating hemiplegia of childhood. Orphanet J Rare Dis 2017 Oct 2 2
16 29801903 Targeted gene capture sequencing in diagnosis of dystonia patients. J Neurol Sci 2018 Jul 15 1
17 29895895 Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia. Mol Psychiatry 2020 Apr 1
18 30441791 Impact of Drinking Water Quality on the Development of Enteroviral Diseases in Korea. Int J Environ Res Public Health 2018 Nov 14 2
19 30838301 Failure of Sequential Pallidal and Motor Thalamus DBS for Rapid-Onset Dystonia-Parkinsonism (DYT12). Mov Disord Clin Pract 2018 Jul-Aug 1
20 31218164 Heart rate variability in a patient with alternating hemiplegia. Intractable Rare Dis Res 2019 May 1
21 31746080 Gamabufotalin induces a negative feedback loop connecting ATP1A3 expression and the AQP4 pathway to promote temozolomide sensitivity in glioblastoma cells by targeting the amino acid Thr794. Cell Prolif 2020 Jan 17
22 32684846 Comprehensive analysis of the expression of sodium/potassium-ATPase α subunits and prognosis of ovarian serous cystadenocarcinoma. Cancer Cell Int 2020 4
23 33082768 Effect of Flunarizine on Alternating Hemiplegia of Childhood in a Patient with the p.E815K Mutation in ATP1A3: A Case Report. Case Rep Neurol 2020 Sep-Dec 1
24 34459253 <i>ATP1A3</i>-Encoded Sodium-Potassium ATPase Subunit Alpha 3 D801N Variant Is Associated With Shortened QT Interval and Predisposition to Ventricular Fibrillation Preceded by Bradycardia. J Am Heart Assoc 2021 Sep 7 5
25 34549350 Prioritizing de novo autism risk variants with calibrated gene- and variant-scoring models. Hum Genet 2021 Sep 22 2