These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2. Segall L; Scanzano R; Kaunisto MA; Wessman M; Palotie A; Gargus JJ; Blostein R J Biol Chem; 2004 Oct; 279(42):43692-6. PubMed ID: 15308625 [TBL] [Abstract][Full Text] [Related]
7. Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine. Vanmolkot KR; Kors EE; Turk U; Turkdogan D; Keyser A; Broos LA; Kia SK; van den Heuvel JJ; Black DF; Haan J; Frants RR; Barone V; Ferrari MD; Casari G; Koenderink JB; van den Maagdenberg AM Eur J Hum Genet; 2006 May; 14(5):555-60. PubMed ID: 16538223 [TBL] [Abstract][Full Text] [Related]
8. Alternating Hemiplegia of Childhood mutations have a differential effect on Na(+),K(+)-ATPase activity and ouabain binding. Weigand KM; Messchaert M; Swarts HG; Russel FG; Koenderink JB Biochim Biophys Acta; 2014 Jul; 1842(7):1010-6. PubMed ID: 24631656 [TBL] [Abstract][Full Text] [Related]
9. A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2. Kaunisto MA; Harno H; Vanmolkot KR; Gargus JJ; Sun G; Hämäläinen E; Liukkonen E; Kallela M; van den Maagdenberg AM; Frants RR; Färkkilä M; Palotie A; Wessman M Neurogenetics; 2004 Jun; 5(2):141-6. PubMed ID: 15133718 [TBL] [Abstract][Full Text] [Related]
10. The α2β2 isoform combination dominates the astrocytic Na Stoica A; Larsen BR; Assentoft M; Holm R; Holt LM; Vilhardt F; Vilsen B; Lykke-Hartmann K; Olsen ML; MacAulay N Glia; 2017 Nov; 65(11):1777-1793. PubMed ID: 28787093 [TBL] [Abstract][Full Text] [Related]
11. Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2. Tavraz NN; Friedrich T; Dürr KL; Koenderink JB; Bamberg E; Freilinger T; Dichgans M J Biol Chem; 2008 Nov; 283(45):31097-106. PubMed ID: 18728015 [TBL] [Abstract][Full Text] [Related]
12. Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms. Li Y; Tang W; Kang L; Kong S; Dong Z; Zhao D; Liu R; Yu S J Headache Pain; 2021 Aug; 22(1):92. PubMed ID: 34384358 [TBL] [Abstract][Full Text] [Related]
13. The structure of the Na+,K+-ATPase and mapping of isoform differences and disease-related mutations. Morth JP; Poulsen H; Toustrup-Jensen MS; Schack VR; Egebjerg J; Andersen JP; Vilsen B; Nissen P Philos Trans R Soc Lond B Biol Sci; 2009 Jan; 364(1514):217-27. PubMed ID: 18957371 [TBL] [Abstract][Full Text] [Related]
14. Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine. Tavraz NN; Dürr KL; Koenderink JB; Freilinger T; Bamberg E; Dichgans M; Friedrich T Channels (Austin); 2009; 3(2):82-7. PubMed ID: 19372756 [TBL] [Abstract][Full Text] [Related]
15. Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2. Leo L; Gherardini L; Barone V; De Fusco M; Pietrobon D; Pizzorusso T; Casari G PLoS Genet; 2011 Jun; 7(6):e1002129. PubMed ID: 21731499 [TBL] [Abstract][Full Text] [Related]
16. Functional differences between alpha subunit isoforms of the rat Na,K-ATPase expressed in Xenopus oocytes. Horisberger JD; Kharoubi-Hess S J Physiol; 2002 Mar; 539(Pt 3):669-80. PubMed ID: 11897839 [TBL] [Abstract][Full Text] [Related]
17. New molecular determinants controlling the accessibility of ouabain to its binding site in human Na,K-ATPase alpha isoforms. Crambert G; Schaer D; Roy S; Geering K Mol Pharmacol; 2004 Feb; 65(2):335-41. PubMed ID: 14742675 [TBL] [Abstract][Full Text] [Related]
18. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. De Fusco M; Marconi R; Silvestri L; Atorino L; Rampoldi L; Morgante L; Ballabio A; Aridon P; Casari G Nat Genet; 2003 Feb; 33(2):192-6. PubMed ID: 12539047 [TBL] [Abstract][Full Text] [Related]