Papers associated with brain (and cacna1a)

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	A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.
	Functional assessment of the "two-hit" model for neurodevelopmental defects in Drosophila and X. laevis., Pizzo L., PLoS Genet. April 5, 2021; 17 (4): e1009112.
	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):
	A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx., Bahamonde MI., PLoS One. January 1, 2015; 10 (12): e0146035.
	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.
	Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)., Figueroa KP., PLoS One. March 29, 2011; 6 (3): e17811.
	Cloning and characterization of voltage-gated calcium channel alpha1 subunits in Xenopus laevis during development., Lewis BB., Dev Dyn. November 1, 2009; 238 (11): 2891-902.
	The P/Q-type voltage-dependent calcium channel as pharmacological target in spinocerebellar ataxia type 6: gabapentin and pregabalin may be of therapeutic benefit., Gazulla J., Med Hypotheses. January 1, 2007; 68 (1): 131-6.
	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.
	Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia., Imbrici P., Brain. December 1, 2004; 127 (Pt 12): 2682-92.
	Ca2+ and phosphatidylinositol 4,5-bisphosphate stabilize a Gbeta gamma-sensitive state of Ca V2 Ca 2+ channels., Rousset M., J Biol Chem. April 9, 2004; 279 (15): 14619-30.
	Human neuronal stargazin-like proteins, gamma2, gamma3 and gamma4; an investigation of their specific localization in human brain and their influence on CaV2.1 voltage-dependent calcium channels expressed in Xenopus oocytes., Moss FJ., BMC Neurosci. September 23, 2003; 4 23.
	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.
	The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes., Restituito S., J Neurosci. September 1, 2000; 20 (17): 6394-403.

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