Papers associated with sensory system (and gjb2)

Limit to papers also referencing gene:
Show all sensory system papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest

Sort Oldest To Newest

	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.
	RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D., BMC Res Notes. November 18, 2015; 8 691.
	The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity., Mhaske PV., Am J Physiol Cell Physiol. June 15, 2013; 304 (12): C1150-8.
	Zebrafish cx30.3: identification and characterization of a gap junction gene highly expressed in the skin., Tao L., Dev Dyn. October 1, 2010; 239 (10): 2627-36.
	Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome., Sánchez HA., J Gen Physiol. July 1, 2010; 136 (1): 47-62.
	An atlas of differential gene expression during early Xenopus embryogenesis., Pollet N., Mech Dev. March 1, 2005; 122 (3): 365-439.
	Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss., Meşe G., Hum Genet. August 1, 2004; 115 (3): 191-9.
	Molecular cloning and characterization of a new member of the gap junction gene family, connexin-31., Hoh JH., J Biol Chem. April 5, 1991; 266 (10): 6524-31.

???pagination.result.page??? 1