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The role of voltage-gated calcium channels in neurotransmitter phenotype specification: Coexpression and functional analysis in Xenopus laevis. , Lewis BB ., J Comp Neurol. August 1, 2014; 522 (11): 2518-31.
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.
Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine. , Tavraz NN., Channels (Austin). January 1, 2009; 3 (2): 82-7.
Functional architecture of the inner pore of a voltage-gated Ca2+ channel. , Zhen XG., J Gen Physiol. September 1, 2005; 126 (3): 193-204.
Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects. , Müllner C., J Biol Chem. December 10, 2004; 279 (50): 51844-50.
Alternative splicing of a beta4 subunit proline-rich motif regulates voltage-dependent gating and toxin block of Cav2.1 Ca2+ channels. , Helton TD., J Neurosci. November 1, 2002; 22 (21): 9331-9.