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Mitochondrial diabetes and deafness: Possible dysfunction of strial marginal cells of the inner ear
(2011)
Objective: Some patients with the syndrome of mitochondrial diabetes and deafness (MIDD) have a m.3243A>G mutation of the MTTL1 gene encoding transfer ribonucleic acid for the amino acid leucine (tRNALeu(UUR)). One of our ...
Cellular localization of TWIK-1, a two-pore-domain potassium channel in the rodent inner ear
(Elsevier, 2003)
K+ channels in the inner ear regulate the secretion and homeostasis of K+, i.e. the flux of K+ ions required to ensure good mechanosensory transduction. We studied the expression and cellular localization of TWIK-1 and ...