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1 xceptionally low Ca(2+) concentration of the endolymph.
2 ar epithelial cells that secretes HCO3- into endolymph.
3 the saccule was merely derived from cochlear endolymph.
4 hlea that maintains the ionic composition of endolymph.
5 cium for crystallization in the calcium-poor endolymph.
6 se of the drastic reduction in the volume of endolymph.
7 in maintaining the ionic composition of the endolymph.
8 n the recycling of potassium to the cochlear endolymph.
9 efractive index greater than the surrounding endolymph.
10 ir bundles above the low level found in bulk endolymph.
11 ation of 70 microM similar to that in turtle endolymph.
12 pproximately the concentration found in frog endolymph.
13 at isk mediates potassium secretion into the endolymph.
14 leration due to insufficient displacement of endolymph.
16 canal using known physical properties of the endolymph and perilymph in three diverse conditions: sur
17 aging-based techniques for quantification of endolymph and perilymph may be useful for improved clini
18 ally distinct extracellular cochlear fluids, endolymph and perilymph, are separated by tight junction
20 ochlear duct are thought to compartmentalize endolymph and provide structural support for the auditor
21 , both patient groups demonstrated increased endolymph and reduced perilymph, a disorder termed endol
23 mitochondria-rich cells, in contact with the endolymph, and associated with clathrin-coated pits wher
24 upporting cells in K(+ )recycling within the endolymph, and its apical turn location may explain the
25 a, where it is involved in the generation of endolymph, and on the basolateral membrane in the distal
26 ith the positive electrical potential of the endolymph, but roles of other anion channels in the inne
30 The effects of perfusion of 50 microM Ca2+ endolymph depended on the BAPTA concentration of the ele
34 at the midline, while in mutant adults, the endolymph-filled lumen of the semicircular canals is sev
35 be investigated using the morphology of the endolymph-filled semicircular ducts of the inner ear, wh
36 ntrast, the PN cupula is probably coupled to endolymph flow by viscous forces, in which case its disp
37 ocation of the PN, which allows it to sample endolymph flow from both vertical semicircular canals.
38 sts EphB2 may regulate ionic homeostasis and endolymph fluid production through macromolecular associ
39 o inner ear sensory organs, dysplasia of the endolymph fluid space, and abnormally formed otoconia (e
40 y longitudinally characterizes variations in endolymph fluid volume and correlations with hearing cha
43 epends upon regulation of its luminal fluid, endolymph, for normal transduction of linear acceleratio
47 We emphasize that the unique, dual role of endolymph in the delivery of both ionic current and flui
48 disorder associated with an accumulation of endolymph in the membranous labyrinth in the inner ear.
56 on and volume of the inner ear luminal fluid endolymph is essential for normal hearing and balance.
62 the apical surface was bathed in artificial endolymph, many hair bundles exhibited spontaneous oscil
63 lus the unique ionic microenvironment of the endolymph near its epithelium likely contribute to the s
64 tly by external factors such as innervation, endolymph, normal mechanical stimulation, or an intact o
65 enovirus with the Math1 gene insert into the endolymph of the mature guinea pig cochlea results in Ma
66 o mechanisms by infusing substances into the endolymph or perilymph of the chinchilla's cochlea and t
67 ain proper endolymph pH, implicate ATP6B1 in endolymph pH homeostasis and in normal auditory function
68 r active proton secretion to maintain proper endolymph pH, implicate ATP6B1 in endolymph pH homeostas
69 essed in and controls the development of the endolymph-producing cells of the inner ear: the strial m
72 n of several genes thought to play a role in endolymph production is downregulated, including the sod
74 y NHE9 in hair bundles, exploits the high-K+ endolymph, responds only to pH imbalance across the bund
77 the extracellular Ca2+ concentration in the endolymph surrounding the hair bundles is < 100 microM,
78 Lorentz force mechanism acting on vestibular endolymph that acts to stimulate semicircular canals.
79 blast exposure revealed dynamic increases in endolymph that involved hair cell mechanoelectrical tran
89 ransition of mammal ancestors would decrease endolymph viscosity, negatively affecting semicircular d
91 lin-deficient mice when generation of normal endolymph was inhibited by a concomitant deletion of the