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There are 23505 results for: content related to: Enhanced inhibitory neurotransmission in the cerebellar cortex of Atp1a3 -deficient heterozygous mice

  1. You have free access to this content
    Decreased neuronal Na+,K+-ATPase activity in Atp1a3 heterozygous mice increases susceptibility to depression-like endophenotypes by chronic variable stress

    Genes, Brain and Behavior

    Volume 10, Issue 5, July 2011, Pages: 542–550, G. S. Kirshenbaum, K. Saltzman, B. Rose, J. Petersen, B. Vilsen and J. C. Roder

    Version of Record online : 13 APR 2011, DOI: 10.1111/j.1601-183X.2011.00691.x

  2. Regulation of Na+/K+-ATPase by neuron-specific transcription factor Sp4: implication in the tight coupling of energy production, neuronal activity and energy consumption in neurons

    European Journal of Neuroscience

    Volume 39, Issue 4, February 2014, Pages: 566–578, Kaid Johar, Anusha Priya and Margaret T. T. Wong-Riley

    Version of Record online : 12 NOV 2013, DOI: 10.1111/ejn.12415

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    Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly

    Epilepsia

    Volume 56, Issue 3, March 2015, Pages: 422–430, Alex R. Paciorkowski, Sharon S. McDaniel, Laura A. Jansen, Hannah Tully, Emily Tuttle, Dalia H. Ghoneim, Srinivasan Tupal, Sonya A. Gunter, Valeria Vasta, Qing Zhang, Thao Tran, Yi B. Liu, Laurie J. Ozelius, Allison Brashear, Kathleen J. Sweadner, William B. Dobyns and Sihoun Hahn

    Version of Record online : 5 FEB 2015, DOI: 10.1111/epi.12914

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    Differential expression of Na+/K+-ATPase α-subunits in mouse hippocampal interneurones and pyramidal cells

    The Journal of Physiology

    Volume 585, Issue 2, December 2007, Pages: 491–505, Kathryn S. Richards, Kurt Bommert, Gabor Szabo and Richard Miles

    Version of Record online : 6 DEC 2007, DOI: 10.1113/jphysiol.2007.144733

  5. Basal Ganglia Gliosis in a Case of Rapid-Onset Dystonia-Parkinsonism (DYT12) with a Novel Mutation in ATPase 1A3 (ATP1A3)

    Movement Disorders Clinical Practice

    Jacinda B. Sampson, Tamar H. Michaeli, Brenton A. Wright, James E. Goldman, Jean-Paul Vonsattel and Stanley Fahn

    Version of Record online : 19 MAY 2016, DOI: 10.1002/mdc3.12354

  6. The Endless Expansion of the Phenotypic Spectrum of ATP1A3 Mutations: A True Diagnostic Challenge

    Movement Disorders Clinical Practice

    Niccolò E. Mencacci

    Version of Record online : 9 MAY 2016, DOI: 10.1002/mdc3.12358

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    Knock-in mouse model of alternating hemiplegia of childhood: Behavioral and electrophysiologic characterization

    Epilepsia

    Volume 56, Issue 1, January 2015, Pages: 82–93, Arsen S. Hunanyan, Nina A. Fainberg, Molly Linabarger, Eric Arehart, A. Soren Leonard, Syed M. Adil, Ashley R. Helseth, Amanda K. Swearingen, Stacy L. Forbes, Ramona M. Rodriguiz, Theodore Rhodes, Xiaodi Yao, Nadine Kibbi, Daryl W. Hochman, William C. Wetsel, Ute Hochgeschwender and Mohamad A. Mikati

    Version of Record online : 19 DEC 2014, DOI: 10.1111/epi.12878

  8. What happens when the pumps fail? Mutations in ATP1A3 are linked to dystonia

    Clinical Genetics

    Volume 66, Issue 5, November 2004, Pages: 393–395, S Warby

    Version of Record online : 11 OCT 2004, DOI: 10.1111/j.1399-0004.2004.0357a.x

  9. Alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism are allelic disorders due to ATP1A3 gene mutations

    Movement Disorders

    Volume 27, Issue 12, October 2012, Page: 1494, Athanasia Alexoudi and Susanne A. Schneider

    Version of Record online : 18 OCT 2012, DOI: 10.1002/mds.25222

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    ATP1A3 mutations in infants: a new rapid-onset dystonia–Parkinsonism phenotype characterized by motor delay and ataxia

    Developmental Medicine & Child Neurology

    Volume 54, Issue 11, November 2012, Pages: 1065–1067, ALLISON BRASHEAR, JONATHAN W MINK, DEBORAH F HILL, NIKI BOGGS, W VAUGHN MCCALL, MARK A STACY, BEVERLY SNIVELY, LANEY S LIGHT, KATHLEEN J SWEADNER, LAURIE J OZELIUS and LESLIE MORRISON

    Version of Record online : 28 AUG 2012, DOI: 10.1111/j.1469-8749.2012.04421.x

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    Defective interaction between dual oscillators for respiratory rhythm generation in Na+,K+-ATPase α2 subunit-deficient mice

    The Journal of Physiology

    Volume 584, Issue 1, October 2007, Pages: 271–284, Hiroshi Onimaru, Keiko Ikeda and Kiyoshi Kawakami

    Version of Record online : 28 SEP 2007, DOI: 10.1113/jphysiol.2007.136572

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    Shortening and intracellular Ca2+ in ventricular myocytes and expression of genes encoding cardiac muscle proteins in early onset type 2 diabetic Goto–Kakizaki rats

    Experimental Physiology

    Volume 97, Issue 12, December 2012, Pages: 1281–1291, K. A. Salem, T. E. Adrian, M. A. Qureshi, K. Parekh, M. Oz and F. C. Howarth

    Version of Record online : 12 JUL 2012, DOI: 10.1113/expphysiol.2012.066639

  13. Recognizable facial features in patients with alternating hemiplegia of childhood

    American Journal of Medical Genetics Part A

    Fiorella Gurrieri, Francesco Danilo Tiziano, Giuseppe Zampino and Giovanni Neri

    Version of Record online : 17 JUN 2016, DOI: 10.1002/ajmg.a.37808

  14. Absence of a significant linkage between Na+,K+-ATPase subunit (ATP1A3 and ATP1B3) genotypes and bipolar affective disorder in the old-order Amish

    American Journal of Medical Genetics

    Volume 105, Issue 3, 8 April 2001, Pages: 291–294, R.A. Philibert, D. Cheung, N. Welsh, P. Damschroder-Williams, B. Thiel, E.I. Ginns and Howard K. Gershenfeld

    Version of Record online : 5 APR 2001, DOI: 10.1002/ajmg.1322

  15. Mutations in ATP1A3 cause alternating hemiplegia of childhood

    Clinical Genetics

    Volume 83, Issue 1, January 2013, Pages: 32–33, F Aminkeng

    Version of Record online : 29 OCT 2012, DOI: 10.1111/cge.12031

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    Poster Session

    Movement Disorders

    Volume 31, Issue S2, June 2016, Pages: S1–S697,

    Version of Record online : 19 JUN 2016, DOI: 10.1002/mds.26688

  17. Distribution of Na/K-ATPase alpha 3 isoform, a sodium-potassium P-type pump associated with rapid-onset of dystonia parkinsonism (RDP) in the adult mouse brain

    Journal of Comparative Neurology

    Volume 519, Issue 2, 1 February 2011, Pages: 376–404, Pernille Bøttger, Zuzanna Tracz, Anders Heuck, Poul Nissen, Marina Romero-Ramos and Karin Lykke-Hartmann

    Version of Record online : 16 DEC 2010, DOI: 10.1002/cne.22524

  18. Cognitive impairment in rapid-onset dystonia-parkinsonism

    Movement Disorders

    Volume 29, Issue 3, March 2014, Pages: 344–350, Jared F. Cook, Deborah F. Hill, Beverly M. Snively, Niki Boggs, Cynthia K. Suerken, Ihtsham Haq, Mark Stacy, W. Vaughn McCall, Laurie J. Ozelius, Kathleen J. Sweadner and Allison Brashear

    Version of Record online : 16 JAN 2014, DOI: 10.1002/mds.25790

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    Targeting Na+/K+-translocating adenosine triphosphatase in cancer treatment

    Clinical and Experimental Pharmacology and Physiology

    Volume 42, Issue 5, May 2015, Pages: 427–443, Cameron T. Durlacher, Kevin Chow, Xiao-Wu Chen, Zhi-Xu He, Xueji Zhang, Tianxin Yang and Shu-Feng Zhou

    Version of Record online : 23 APR 2015, DOI: 10.1111/1440-1681.12385

  20. Linkage arrangement of Na,K-ATPase genes in the tetraploid-derived genome of the rainbow trout (Oncorhynchus mykiss)

    Animal Genetics

    Volume 35, Issue 4, August 2004, Pages: 321–325, K. Gharbi, J. W. Semple, M. M. Ferguson, P. M. Schulte and R. G. Danzmann

    Version of Record online : 8 JUN 2004, DOI: 10.1111/j.1365-2052.2004.01152.x