Enhanced inhibitory neurotransmission in the cerebellar cortex ofAtp1a3-deficient heterozygous mice

Clinical spectrum of disease associated with ATP1A3 mutations

(2012) Laurie J Ozelius   LANCET NEUROLOGY

Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study

(2012) Hendrik Rosewich et al.   LANCET NEUROLOGY

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

(2012) Erin L Heinzen et al.   NATURE GENETICS

Alternative Approaches to Modeling Hereditary Dystonias

(2012) Rachel Fremont et al.   Neurotherapeutics

Climbing fiber synapse elimination in cerebellar Purkinje cells

(2011) Masahiko Watanabe et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Decreased neuronal Na+,K+-ATPase activity inAtp1a3heterozygous mice increases susceptibility to depression-like endophenotypes by chronic variable stress

(2011) G. S. Kirshenbaum et al.   GENES BRAIN AND BEHAVIOR

Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis

(2011) Julie Phukan et al.   LANCET NEUROLOGY

The neural substrates of rapid-onset Dystonia-Parkinsonism

(2011) D Paola Calderon et al.   NATURE NEUROSCIENCE

The functional neuroanatomy of dystonia

(2011) Vladimir K. Neychev et al.   NEUROBIOLOGY OF DISEASE

Mania-like behavior induced by genetic dysfunction of the neuron-specific Na+,K+-ATPase  3 sodium pump

(2011) G. S. Kirshenbaum et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism

(2010) Mark P. DeAndrade et al.   BEHAVIOURAL BRAIN RESEARCH

Glutamate transporter EAAT4 in Purkinje cells controls intersynaptic diffusion of climbing fiber transmitter mediating inhibition of GABA release from interneurons

(2010) Shin’Ichiro Satake et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

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

(2010) Pernille Bøttger et al.   JOURNAL OF COMPARATIVE NEUROLOGY

Hereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimaging

(2010) Martin Niethammer et al.   NEUROBIOLOGY OF DISEASE

Cerebellar molecular layer interneurons – computational properties and roles in learning

(2010) Henrik Jörntell et al.   TRENDS IN NEUROSCIENCES

A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism

(2009) P. Blanco-Arias et al.   HUMAN MOLECULAR GENETICS

Mutation I810N in the  3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS

(2009) S. J. Clapcote et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The basal ganglia and cerebellum interact in the expression of dystonic movement

(2008) V. K. Neychev et al.   BRAIN