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Summary Expression Phenotypes Gene Literature (5) GO Terms (111) Nucleotides (164) Proteins (60) Interactants (28) Wiki
XB-GENEPAGE-996130

Papers associated with atp1a3



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ATP1A3 Disease Spectrum Includes Paroxysmal Weakness and Encephalopathy Not Triggered by Fever., Immanneni C, Calame D, Jiao S, Emrick LT, Holmgren M, Yano ST., Neurol Genet. June 1, 2024; 10 (3): e200150.   


Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity., Lazarov E, Hillebrand M, Schröder S, Ternka K, Hofhuis J, Ohlenbusch A, Barrantes-Freer A, Pardo LA, Fruergaard MU, Nissen P, Brockmann K, Gärtner J, Rosewich H., Neurobiol Dis. September 1, 2020; 143 105012.   


A functional correlate of severity in alternating hemiplegia of childhood., Li M, Jazayeri D, Corry B, McSweeney KM, Heinzen EL, Goldstein DB, Petrou S., Neurobiol Dis. May 1, 2015; 77 88-93.

Developmental expression analysis of Na, K-ATPase α subunits in Xenopus., Rahman MM, Tae HJ, Cho HS, Shin GW, Park BY., Dev Genes Evol. April 1, 2015; 225 (2): 105-11.

Neurological disease mutations compromise a C-terminal ion pathway in the Na(+)/K(+)-ATPase., Poulsen H, Khandelia H, Morth JP, Bublitz M, Mouritsen OG, Egebjerg J, Nissen P., Nature. September 2, 2010; 467 (7311): 99-102.

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