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Gomez, Christopher M.

One or more keywords matched the following items that are connected to Gomez, Christopher M.

Item Type	Name
Concept	Calcium Channels
Concept	Calcium Channels, P-Type
Concept	Calcium Signaling
Concept	Calcium Channels, N-Type
Concept	Large-Conductance Calcium-Activated Potassium Channel alpha Subunits
Concept	Calcium Channels, Q-Type
Concept	Calcium
Concept	Calcium-Binding Proteins
Concept	Calcium Channels, L-Type
Academic Article	Slow-channel transgenic mice: a model of postsynaptic organellar degeneration at the neuromuscular junction.
Academic Article	Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndrome.
Academic Article	Focal caspase activation underlies the endplate myopathy in slow-channel syndrome.
Academic Article	Activation of apoptotic pathways at muscle fiber synapses is circumscribed and reversible in a slow-channel syndrome model.
Academic Article	Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome.
Academic Article	Skeletal muscle IP3R1 receptors amplify physiological and pathological synaptic calcium signals.
Academic Article	Stable respiratory activity requires both P/Q-type and N-type voltage-gated calcium channels.
Academic Article	Spinocerebellar ataxia type 6.
Academic Article	Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6.
Academic Article	WDR81 is necessary for purkinje and photoreceptor cell survival.
Academic Article	Dominant-negative suppression of Cav2.1 currents by alpha(1)2.1 truncations requires the conserved interaction domain for beta subunits.
Academic Article	Molecular pathogenesis of spinocerebellar ataxia type 6.
Academic Article	Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
Academic Article	The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes.
Academic Article	C-termini of P/Q-type Ca2+ channel alpha1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity.
Academic Article	Novel beta subunit mutation causes a slow-channel syndrome by enhancing activation and decreasing the rate of agonist dissociation.
Academic Article	Impaired eye movements in presymptomatic spinocerebellar ataxia type 6.
Academic Article	Revelations from a bicistronic calcium channel gene.
Academic Article	Polyglutamine aggregates in SCA6 Purkinje cells: a tail of two toxicities.
Academic Article	Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.
Academic Article	Inositol-1,4,5-triphosphate receptors mediate activity-induced synaptic Ca2+ signals in muscle fibers and Ca2+ overload in slow-channel syndrome.
Academic Article	Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits.
Academic Article	Macroscopic properties of spontaneous mutations in slow-channel syndrome: correlation by domain and disease severity.
Academic Article	DnaJ-1 and karyopherin a3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6.
Academic Article	An miRNA-mediated therapy for SCA6 blocks IRES-driven translation of the CACNA1A second cistron.
Academic Article	Evaluation of parkinsonism and striatal dopamine transporter loss in patients with spinocerebellar ataxia type 6.
Academic Article	Erratum to: Spinocerebellar Ataxia Type 6: Molecular Mechanisms and Calcium Channel Genetics.
Academic Article	Targeting the CACNA1A IRES as a Treatment for Spinocerebellar Ataxia Type 6.
Academic Article	Spinocerebellar [corrected] Ataxia Type 6: Molecular Mechanisms and Calcium Channel Genetics.
Academic Article	a1ACT Is Essential for Survival and Early Cerebellar Programming in a Critical Neonatal Window.
Academic Article	Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia.
Concept	S100 Calcium Binding Protein G

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Calcium