Papers associated with sensory system (and kcnj10)

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	Developmental gene expression patterns in the brain and liver of Xenopus tropicalis during metamorphosis climax., Yaoita Y., Genes Cells. December 1, 2018; 23 (12): 998-1008.
	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.
	A novel method for inducing nerve growth via modulation of host resting potential: gap junction-mediated and serotonergic signaling mechanisms., Blackiston DJ., Neurotherapeutics. January 1, 2015; 12 (1): 170-84.
	Generation and validation of a zebrafish model of EAST (epilepsy, ataxia, sensorineural deafness and tubulopathy) syndrome., Mahmood F., Dis Model Mech. May 1, 2013; 6 (3): 652-60.
	KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16., Parrock S., Nephron Physiol. January 1, 2013; 123 (3-4): 7-14.
	Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations., Bockenhauer D., N Engl J Med. May 7, 2009; 360 (19): 1960-70.
	Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome., Yang T., Am J Hum Genet. May 1, 2009; 84 (5): 651-7.
	Protein kinase C dependent inhibition of the heteromeric Kir4.1-Kir5.1 channel., Rojas A., Biochim Biophys Acta. September 1, 2007; 1768 (9): 2030-42.

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