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Summary Expression Phenotypes Gene Literature (11) GO Terms (10) Nucleotides (243) Proteins (51) Interactants (118) Wiki

Papers associated with atp1a2

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Developmental gene expression patterns in the brain and liver of Xenopus tropicalis during metamorphosis climax., Yaoita Y, Nakajima K., Genes Cells. December 1, 2018; 23 (12): 998-1008.              

A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms., Sampedro Castañeda M, Zanoteli E, Scalco RS, Scaramuzzi V, Marques Caldas V, Conti Reed U, da Silva AMS, O'Callaghan B, Phadke R, Bugiardini E, Sud R, McCall S, Hanna MG, Poulsen H, Männikkö R, Matthews E., Brain. January 1, 2018; 141 (12): 3308-3318.        

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.

Functional analysis of human Na(+)/K(+)-ATPase familial or sporadic hemiplegic migraine mutations expressed in Xenopus oocytes., Spiller S, Friedrich T., World J Biol Chem. May 26, 2014; 5 (2): 240-53.

Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsy., Pisano T, Spiller S, Mei D, Guerrini R, Cianchetti C, Friedrich T, Pruna D., Cephalalgia. December 1, 2013; 33 (16): 1302-10.

Hyperpolarization-activated inward leakage currents caused by deletion or mutation of carboxy-terminal tyrosines of the Na+/K+-ATPase {alpha} subunit., Meier S, Tavraz NN, Dürr KL, Friedrich T., J Gen Physiol. February 1, 2010; 135 (2): 115-34.                

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). March 1, 2009; 3 (2): 82-7.

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. November 7, 2008; 283 (45): 31097-106.

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine., Todt U, Dichgans M, Jurkat-Rott K, Heinze A, Zifarelli G, Koenderink JB, Goebel I, Zumbroich V, Stiller A, Ramirez A, Friedrich T, Göbel H, Kubisch C., Hum Mutat. October 1, 2005; 26 (4): 315-21.

Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation., Koenderink JB, Zifarelli G, Qiu LY, Schwarz W, De Pont JJ, Bamberg E, Friedrich T., Biochim Biophys Acta. May 15, 2005; 1669 (1): 61-8.

Asymmetries in H+/K+-ATPase and cell membrane potentials comprise a very early step in left-right patterning., Levin M, Thorlin T, Robinson KR, Nogi T, Mercola M., Cell. October 4, 2002; 111 (1): 77-89.              

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