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 |