Papers associated with cacna1f

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	Trpc1 as the Missing Link Between the Bmp and Ca2+ Signalling Pathways During Neural Specification in Amphibians., Néant I, Leung HC, Webb SE, Miller AL, Miller AL, Moreau M, Leclerc C., Sci Rep. November 5, 2019; 9 (1): 16049.
	Calcium Signaling in Vertebrate Development and Its Role in Disease., Paudel S, Sindelar R, Saha M., Int J Mol Sci. October 30, 2018; 19 (11):
	The role of voltage-gated calcium channels in neurotransmitter phenotype specification: Coexpression and functional analysis in Xenopus laevis., Lewis BB, Miller LE, Herbst WA, Saha MS., J Comp Neurol. August 1, 2014; 522 (11): 2518-31.
	Cloning and characterization of voltage-gated calcium channel alpha1 subunits in Xenopus laevis during development., Lewis BB, Wester MR, Miller LE, Nagarkar MD, Johnson MB, Saha MS., Dev Dyn. November 1, 2009; 238 (11): 2891-902.
	An extracellular Cu2+ binding site in the voltage sensor of BK and Shaker potassium channels., Ma Z, Wong KY, Horrigan FT., J Gen Physiol. May 1, 2008; 131 (5): 483-502.
	Effects of congenital stationary night blindness type 2 mutations R508Q and L1364H on Cav1.4 L-type Ca2+ channel function and expression., Hoda JC, Zaghetto F, Singh A, Koschak A, Striessnig J., J Neurochem. March 1, 2006; 96 (6): 1648-58.
	Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channels., Hoda JC, Zaghetto F, Koschak A, Striessnig J., J Neurosci. January 5, 2005; 25 (1): 252-9.
	Opsin activation as a cause of congenital night blindness., Jin S, Cornwall MC, Oprian DD., Nat Neurosci. July 1, 2003; 6 (7): 731-5.

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