BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

325 related articles for article (PubMed ID: 26323479)

  • 1. α-synuclein assemblies sequester neuronal α3-Na+/K+-ATPase and impair Na+ gradient.
    Shrivastava AN; Redeker V; Fritz N; Pieri L; Almeida LG; Spolidoro M; Liebmann T; Bousset L; Renner M; Léna C; Aperia A; Melki R; Triller A
    EMBO J; 2015 Oct; 34(19):2408-23. PubMed ID: 26323479
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clustering of Tau fibrils impairs the synaptic composition of α3-Na
    Shrivastava AN; Redeker V; Pieri L; Bousset L; Renner M; Madiona K; Mailhes-Hamon C; Coens A; Buée L; Hantraye P; Triller A; Melki R
    EMBO J; 2019 Feb; 38(3):. PubMed ID: 30630857
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 2020 Sep; 143():105012. PubMed ID: 32653672
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cell biology and dynamics of Neuronal Na
    Shrivastava AN; Triller A; Melki R
    Neuropharmacology; 2020 Jun; 169():107461. PubMed ID: 30550795
    [TBL] [Abstract][Full Text] [Related]  

  • 5. α-Synuclein oligomers pump it up!
    Kahle PJ; Sugeno N; Skodras A
    EMBO J; 2015 Oct; 34(19):2385-7. PubMed ID: 26373315
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
    de Carvalho Aguiar P; Sweadner KJ; Penniston JT; Zaremba J; Liu L; Caton M; Linazasoro G; Borg M; Tijssen MA; Bressman SB; Dobyns WB; Brashear A; Ozelius LJ
    Neuron; 2004 Jul; 43(2):169-75. PubMed ID: 15260953
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neurological disease mutations of α3 Na
    Holm R; Toustrup-Jensen MS; Einholm AP; Schack VR; Andersen JP; Vilsen B
    Biochim Biophys Acta; 2016 Nov; 1857(11):1807-1828. PubMed ID: 27577505
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cognitive deficits caused by a disease-mutation in the α3 Na(+)/K(+)-ATPase isoform.
    Holm TH; Isaksen TJ; Glerup S; Heuck A; Bøttger P; Füchtbauer EM; Nedergaard S; Nyengaard JR; Andreasen M; Nissen P; Lykke-Hartmann K
    Sci Rep; 2016 Aug; 6():31972. PubMed ID: 27549929
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition.
    Arystarkhova E; Haq IU; Luebbert T; Mochel F; Saunders-Pullman R; Bressman SB; Feschenko P; Salazar C; Cook JF; Demarest S; Brashear A; Ozelius LJ; Sweadner KJ
    Neurobiol Dis; 2019 Dec; 132():104577. PubMed ID: 31425744
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase α3 missense mutant mice.
    Kirshenbaum GS; Dawson N; Mullins JG; Johnston TH; Drinkhill MJ; Edwards IJ; Fox SH; Pratt JA; Brotchie JM; Roder JC; Clapcote SJ
    PLoS One; 2013; 8(3):e60141. PubMed ID: 23527305
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Insights into the Pathology of the α3 Na(+)/K(+)-ATPase Ion Pump in Neurological Disorders; Lessons from Animal Models.
    Holm TH; Lykke-Hartmann K
    Front Physiol; 2016; 7():209. PubMed ID: 27378932
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism.
    Blanco-Arias P; Einholm AP; Mamsa H; Concheiro C; Gutiérrez-de-Terán H; Romero J; Toustrup-Jensen MS; Carracedo A; Jen JC; Vilsen B; Sobrido MJ
    Hum Mol Genet; 2009 Jul; 18(13):2370-7. PubMed ID: 19351654
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuronal modeling of alternating hemiplegia of childhood reveals transcriptional compensation and replicates a trigger-induced phenotype.
    Snow JP; Westlake G; Klofas LK; Jeon S; Armstrong LC; Swoboda KJ; George AL; Ess KC
    Neurobiol Dis; 2020 Jul; 141():104881. PubMed ID: 32348881
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 2015 May; 77():88-93. PubMed ID: 25681536
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The rapid-onset dystonia parkinsonism mutation D923N of the Na+, K+-ATPase alpha3 isoform disrupts Na+ interaction at the third Na+ site.
    Einholm AP; Toustrup-Jensen MS; Holm R; Andersen JP; Vilsen B
    J Biol Chem; 2010 Aug; 285(34):26245-54. PubMed ID: 20576601
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood.
    Kirshenbaum GS; Dachtler J; Roder JC; Clapcote SJ
    Neurogenetics; 2016 Jan; 17(1):57-63. PubMed ID: 26463346
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Relationship between intracellular Na+ concentration and reduced Na+ affinity in Na+,K+-ATPase mutants causing neurological disease.
    Toustrup-Jensen MS; Einholm AP; Schack VR; Nielsen HN; Holm R; Sobrido MJ; Andersen JP; Clausen T; Vilsen B
    J Biol Chem; 2014 Feb; 289(6):3186-97. PubMed ID: 24356962
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Zebrafish as a novel model to assess Na+/K(+)-ATPase-related neurological disorders.
    Doğanli C; Oxvig C; Lykke-Hartmann K
    Neurosci Biobehav Rev; 2013 Dec; 37(10 Pt 2):2774-87. PubMed ID: 24091024
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Paying the price at the pump: dystonia from mutations in a Na+/K+ -ATPase.
    Cannon SC
    Neuron; 2004 Jul; 43(2):153-4. PubMed ID: 15260948
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.