Pages that link to "Q42481415"
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The following pages link to 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 (Q42481415):
Displaying 50 items.
- Insights into the Pathology of the α3 Na( )/K( )-ATPase Ion Pump in Neurological Disorders; Lessons from Animal Models (Q26744625) (← links)
- Insights into the Pathology of the α2-Na( )/K( )-ATPase in Neurological Disorders; Lessons from Animal Models. (Q26747517) (← links)
- Managing Brain Extracellular K( ) during Neuronal Activity: The Physiological Role of the Na( )/K( )-ATPase Subunit Isoforms (Q26752671) (← links)
- Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly (Q27312451) (← links)
- Cognitive deficits caused by a disease-mutation in the α3 Na( )/K( )-ATPase isoform (Q27315555) (← links)
- Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na ,K -ATPase α3 missense mutant mice (Q27331805) (← links)
- In Vivo Modelling of ATP1A3 G316S-Induced Ataxia in C. elegans Using CRISPR/Cas9-Mediated Homologous Recombination Reveals Dominant Loss of Function Defects (Q28554951) (← links)
- Na, K-ATPase α3 is a death target of Alzheimer patient amyloid-β assembly. (Q28572007) (← links)
- 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 (Q33598310) (← links)
- Rapid-onset dystonia-parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropathologic and neuroanatomical study of four siblings (Q33764538) (← links)
- The Structure and Function of the Na,K-ATPase Isoforms in Health and Disease (Q33766129) (← links)
- Distinct neurological disorders with ATP1A3 mutations (Q34546995) (← links)
- Proteome-wide characterization of signalling interactions in the hippocampal CA4/DG subfield of patients with Alzheimer's disease (Q35713134) (← links)
- Spontaneously Fluctuating Motor Cortex Excitability in Alternating Hemiplegia of Childhood: A Transcranial Magnetic Stimulation Study (Q35964886) (← links)
- A case of rapid-onset dystonia-parkinsonism accompanied by pyramidal tract impairment (Q36190197) (← links)
- Aberrant Purkinje cell activity is the cause of dystonia in a shRNA-based mouse model of Rapid Onset Dystonia-Parkinsonism (Q36269315) (← links)
- Importance of the Voltage Dependence of Cardiac Na/K ATPase Isozymes (Q36275520) (← links)
- Regulation of Na( )/K( )-ATPase by nuclear respiratory factor 1: implication in the tight coupling of neuronal activity, energy generation, and energy consumption (Q36418825) (← links)
- A specific and essential role for Na,K-ATPase α3 in neurons co-expressing α1 and α3. (Q36562113) (← links)
- α3Na /K -ATPase deficiency causes brain ventricle dilation and abrupt embryonic motility in zebrafish (Q36724908) (← links)
- A novel de novo mutation in ATP1A3 and childhood-onset schizophrenia (Q37212874) (← links)
- Cognitive impairment in rapid-onset dystonia-parkinsonism (Q37649763) (← links)
- Na( ),K ( )-ATPase as a docking station: protein-protein complexes of the Na( ),K ( )-ATPase (Q38018498) (← links)
- The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond (Q38275252) (← links)
- Isolated and combined dystonia syndromes - an update on new genes and their phenotypes (Q38341164) (← links)
- Motor function domains in alternating hemiplegia of childhood. (Q38764359) (← links)
- Diagnosis and Treatment of Alternating Hemiplegia of Childhood (Q39197876) (← links)
- Corneal afferents differentially target thalamic- and parabrachial-projecting neurons in spinal trigeminal nucleus caudalis (Q39702463) (← links)
- A randomized, controlled, double-blind, crossover trial of triheptanoin in alternating hemiplegia of childhood (Q42284665) (← links)
- Enhanced inhibitory neurotransmission in the cerebellar cortex of Atp1a3-deficient heterozygous mice. (Q42438187) (← links)
- Glutamate transporter activity promotes enhanced Na /K -ATPase-mediated extracellular K management during neuronal activity. (Q42493779) (← links)
- Descending projections from the rostral ventromedial medulla (RVM) to trigeminal and spinal dorsal horns are morphologically and neurochemically distinct (Q42556730) (← links)
- Characterization of cognitive deficits in mice with an alternating hemiplegia-linked mutation (Q43160338) (← links)
- Atp1a3-deficient heterozygous mice show lower rank in the hierarchy and altered social behavior. (Q47645347) (← links)
- Knock-in mouse model of alternating hemiplegia of childhood: behavioral and electrophysiologic characterization. (Q48149416) (← links)
- Genetic suppression of agrin reduces mania-like behavior in Na , K -ATPase α3 mutant mice. (Q48558233) (← links)
- Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 Mutations. (Q49349821) (← links)
- Differential contributions of Ca2 -activated K channels and Na /K -ATPases to the generation of the slow afterhyperpolarization in CA1 pyramidal cells. (Q50068593) (← links)
- Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study (Q50792593) (← links)
- Circadian Disruptions in the Myshkin Mouse Model of Mania Are Independent of Deficits in Suprachiasmatic Molecular Clock Function (Q50901148) (← links)
- Novel pregnancy-triggered episodes of CAPOS syndrome. (Q52843415) (← links)
- Na⁺, K⁺-ATPase Signaling and Bipolar Disorder (Q58796804) (← links)
- Chemical genetic identification of GAK substrates reveals its role in regulating Na/K-ATPase (Q60924151) (← links)
- Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related disease (Q63952205) (← links)
- Influence of Endogenous Cardiac Glycosides, Digoxin, and Marinobufagenin in the Physiology of Epithelial Cells (Q89849213) (← links)
- Review of animal models of bipolar disorder that alter ion regulation (Q90109125) (← links)
- A Transgenic Mouse Model to Selectively Identify α3 Na,K-ATPase Expressing Cells in the Nervous System (Q90380709) (← links)
- Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3 (Q90732197) (← links)
- Deletion of calcineurin from GFAP-expressing astrocytes impairs excitability of cerebellar and hippocampal neurons through astroglial Na /K ATPase (Q90794970) (← links)
- Alternating Hemiplegia of Childhood: Understanding the Genotype-Phenotype Relationship of ATP1A3 Variations (Q91839992) (← links)