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One or more keywords matched the following items that are connected to Gomez, Christopher M.
Item TypeName
Concept Calcium Channels
Concept Calcium Channels, P-Type
Concept Calcium Channels, N-Type
Concept Calcium Channels, Q-Type
Concept Calcium Channels, L-Type
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 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 A beta-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome.
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 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 Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits.
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.
Concept Voltage-Gated Sodium Channel Blockers
Search Criteria
  • Voltage
  • Gated
  • Calcium Channels