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XB-ANAT-3344
Papers associated with hand (and cav2)
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Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia., Stendel C., Int J Mol Sci. May 27, 2020; 21 (11): |
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Molecular characterization and functional expression of the Apis mellifera voltage-dependent Ca2+ channels., Cens T., Insect Biochem Mol Biol. March 1, 2015; 58 12-27. |
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The inhibition of functional expression of calcium channels by prion protein demonstrates competition with α2δ for GPI-anchoring pathways., Alvarez-Laviada A., Biochem J. March 1, 2014; 458 (2): 365-74. |
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Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2., Graves TD., Neurobiol Dis. October 1, 2008; 32 (1): 10-5. |
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Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2., Jeng CJ., Am J Physiol Cell Physiol. April 1, 2006; 290 (4): C1209-20. |
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