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Times Cited: 760
Times Cited: 760
Times Cited
Times Co-cited
Similarity
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
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Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
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Nomenclature of voltage-gated calcium channels.
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Primary structure of a calcium channel that is highly expressed in the rat cerebellum.
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Different types of calcium channels mediate central synaptic transmission.
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Three types of neuronal calcium channel with different calcium agonist sensitivity.
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Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel.
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A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
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Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
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The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.
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The I-II loop of the Ca2+ channel alpha1 subunit contains an endoplasmic reticulum retention signal antagonized by the beta subunit.
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The alpha2delta subunits of voltage-gated calcium channels form GPI-anchored proteins, a posttranslational modification essential for function.
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RIM proteins tether Ca2+ channels to presynaptic active zones via a direct PDZ-domain interaction.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.