戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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.
15 s of the reticular lamina separate K(+)-rich endolymph and Na(+)-rich perilymph.
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
19  imbalance between the two inner ear fluids, endolymph and perilymph.
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
22 ents involved in generation of the K(+)-rich endolymph and the endocochlear potential.
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
27                                              Endolymph collapse in the lte/nkcc1 mutant shows distinc
28 ia lining the scala media, thus defining the endolymph compartment.
29                 The results demonstrate that endolymph containing high K+, 50 microns Ca2+ and low Mg
30   The effects of perfusion of 50 microM Ca2+ endolymph depended on the BAPTA concentration of the ele
31 dating zebrafish as a model for the study of endolymph disorders.
32 f indentation and at low frequencies compels endolymph displacement along the canal.
33 , its displacement should be proportional to endolymph displacement.
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
41 occurring ionic currents in the labyrinthine endolymph fluid.
42 um in the local regulation of the [Na(+)] of endolymph for maintenance of our sense of balance.
43 epends upon regulation of its luminal fluid, endolymph, for normal transduction of linear acceleratio
44                   In mammals, disruptions to endolymph homeostasis can result in either collapse or d
45 phatic sac (ES) and duct (ED), which mediate endolymph homeostasis.
46 behavioral dysfunction and signs of abnormal endolymph homeostasis.
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.
49              Previous studies suggested that endolymph in the saccule was merely derived from cochlea
50 temporal bones have found an accumulation of endolymph in the scala media of the cochlea.
51 us oscillations driven by undulations in the endolymph in which they are immersed.
52  permit cations to flow from the surrounding endolymph into the cells.
53 proteins, as well as tight regulation of the endolymph ionic environment.
54                                          The endolymph is an extracellular fluid with an atypical com
55 ionic homeostasis of the mammalian inner ear endolymph is essential for HC function.
56 on and volume of the inner ear luminal fluid endolymph is essential for normal hearing and balance.
57                  In the mammalian inner ear, endolymph is produced and resorbed by a complex series o
58                                              Endolymph is the specialised extracellular fluid present
59  (56 +/- 11 microM), a value similar to bulk endolymph levels.
60 cells, which enwrap JO neuronal dendrites in endolymph-like compartments.
61  amenable model to investigate generation of endolymph-like extracellular compartments.
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
70                    EphB2 is expressed in the endolymph-producing dark cells in the inner ear epitheli
71 a role in the development and/or function of endolymph-producing epithelia.
72 n of several genes thought to play a role in endolymph production is downregulated, including the sod
73 e they are involved in NaCl reabsorption and endolymph production, respectively.
74 y NHE9 in hair bundles, exploits the high-K+ endolymph, responds only to pH imbalance across the bund
75 hasized the prominent role of K+ channels in endolymph secretion and mechanical transduction.
76  the inner ear consistent with a decrease in endolymph secretion.
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
80 ), is associated with abnormal production of endolymph, the fluid bathing sensory hair cells.
81 rin) is necessary for normal reabsorption of endolymph, the fluid bathing the inner ear.
82                                In artificial endolymph, the stiffness gradient for the transversal co
83 y pathway for K(+) that is secreted into the endolymph, thus playing a critical role in hearing.
84                                   Individual endolymph-to-perilymph (E/P) ratio variance over time wa
85 strated good repeatability for measuring the endolymph-to-perilymph ratio.
86 se or vestibular schwannoma and measured the endolymph-to-perilymph ratio.
87             Our data indicate that increased endolymph-to-perilymph ratios correlated with the degree
88 e its displacement should be proportional to endolymph velocity.
89 ransition of mammal ancestors would decrease endolymph viscosity, negatively affecting semicircular d
90                                Perilymph and endolymph volumes were quantified using a semi-automatic
91 lin-deficient mice when generation of normal endolymph was inhibited by a concomitant deletion of the
92 ons Ca2+, a concentration similar to that in endolymph, which bathes the hair bundles in vivo.