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

Heterozygous mice deficient in Atp1a3 exhibit motor deficits by chronic restraint stress

(2014) Hiroki Sugimoto et al.   BEHAVIOURAL BRAIN RESEARCH

Impairment of kindling development in phospholipase Cγ1 heterozygous mice

(2014) Xiao Ping He et al.   EPILEPSIA

Distinct neurological disorders with ATP1A3 mutations

(2014) Erin L Heinzen et al.   LANCET NEUROLOGY

Genotype-phenotype correlations in alternating hemiplegia of childhood

(2014) M. Sasaki et al.   NEUROLOGY

The expanding clinical and genetic spectrum of ATP1A3-related disorders

(2014) H. Rosewich et al.   NEUROLOGY

ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients

(2014) Xiaoling Yang et al.   PLoS One

GABA actions and ionic plasticity in epilepsy

(2013) Kai Kaila et al.   CURRENT OPINION IN NEUROBIOLOGY

Seizure predisposition after perinatal hypoxia: Effects of subsequent age and of an epilepsy predisposing gene mutation

(2013) A. Soren Leonard et al.   EPILEPSIA

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

(2013) Keiko Ikeda et al.   JOURNAL OF PHYSIOLOGY-LONDON

Decreased expression of proteins involved in energy metabolism in the hippocampal granular layer of rats submitted to the pilocarpine epilepsy model

(2013) Bruno Araujo et al.   NEUROSCIENCE LETTERS

Alternating Hemiplegia of Childhood-Related Neural and Behavioural Phenotypes in Na+,K+-ATPase α3 Missense Mutant Mice

(2013) Greer S. Kirshenbaum et al.   PLoS One

Intra-hippocampal injection of lipopolysaccharide inhibits kindled seizures and retards kindling rate in adult rats

(2013) Amin Ahmadi et al.   EXPERIMENTAL BRAIN RESEARCH

Genetic suppression of agrin reduces mania-like behavior in Na+, K+-ATPaseα3 mutant mice

(2012) G. S. Kirshenbaum et al.   GENES BRAIN AND BEHAVIOR

Enhanced Neuronal Excitability in Adult Rat Brainstem Causes Widespread Repetitive Brainstem Depolarizations with Cardiovascular Consequences

(2012) Frank Richter et al.   JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM

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

Brain regions and genes affecting limb-clasping responses

(2011) R. Lalonde et al.   BRAIN RESEARCH REVIEWS

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

The neural substrates of rapid-onset Dystonia-Parkinsonism

(2011) D Paola Calderon et al.   NATURE NEUROSCIENCE

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

Lesions of the rat perirhinal cortex spare the acquisition of a complex configural visual discrimination yet impair object recognition.

(2010) John P. Aggleton et al.   BEHAVIORAL NEUROSCIENCE

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

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

Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults

(2010) Eleni Panagiotakaki et al.   BRAIN

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

Neural Correlates of Novel Object and Novel Location Recognition Behavior in the Mouse Anterior Cingulate Cortex

(2009) Aldis P. Weible et al.   JOURNAL OF NEUROPHYSIOLOGY

Tests to assess motor phenotype in mice: a user's guide

(2009) Simon P. Brooks et al.   NATURE REVIEWS NEUROSCIENCE

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

Abnormal motor function and dopamine neurotransmission in DYT1 ΔGAG transgenic mice

(2008) Yu Zhao et al.   EXPERIMENTAL NEUROLOGY