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Trpc1 as the Missing Link Between the Bmp and Ca2+ Signalling Pathways During Neural Specification in Amphibians. , Néant I ., Sci Rep. November 5, 2019; 9 (1): 16049.
Lef1 regulates caveolin expression and caveolin dependent endocytosis, a process necessary for Wnt5a/Ror2 signaling during Xenopus gastrulation. , Puzik K., Sci Rep. October 30, 2019; 9 (1): 15645.
Insights into electrosensory organ development, physiology and evolution from a lateral line-enriched transcriptome. , Modrell MS., Elife. March 27, 2017; 6
The alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform. , Dichmann DS ., Cell Rep. February 3, 2015; 10 (4): 527-36.
Sterol carrier protein 2 regulates proximal tubule size in the Xenopus pronephric kidney by modulating lipid rafts. , Cerqueira DM., Dev Biol. October 1, 2014; 394 (1): 54-64.
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.
Molecular cloning and characterization of a hamster Cav1.3 Ca2+ channel variant with a long carboxyl terminus. , Kang HW., Biochim Biophys Acta. June 1, 2011; 1808 (6): 1629-38.
Cardiac L-type calcium channel ( Cav1.2) associates with gamma subunits. , Yang L., FASEB J. March 1, 2011; 25 (3): 928-36.
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.
Database of queryable gene expression patterns for Xenopus. , Gilchrist MJ ., Dev Dyn. June 1, 2009; 238 (6): 1379-88.
Identification of novel ciliogenesis factors using a new in vivo model for mucociliary epithelial development. , Hayes JM., Dev Biol. December 1, 2007; 312 (1): 115-30.
Novel molecular mechanism involving alpha1D ( Cav1.3) L-type calcium channel in autoimmune-associated sinus bradycardia. , Qu Y., Circulation. June 14, 2005; 111 (23): 3034-41.
Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations. , Splawski I., Proc Natl Acad Sci U S A. June 7, 2005; 102 (23): 8089-96; discussion 8086-8.