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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.