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1 that represent the transverse motions of the tectorial and basilar membranes within the organ of Cort
2 ar motion and endolymphatic flow between the tectorial membrane (TM) and reticular lamina (RL), is co
3  stationary osseous spiral lamina (OSL), the tectorial membrane (TM) attaches to the limbus above the
4                                          The tectorial membrane (TM) clearly plays a mechanical role
5 m was to determine whether detachment of the tectorial membrane (TM) from the organ of Corti in Tecta
6                                          The tectorial membrane (TM) has a significantly larger stiff
7       However, genetic studies targeting the tectorial membrane (TM) have demonstrated both sharper a
8  were used to measure shear impedance of the tectorial membrane (TM) in two dimensions.
9                   The solid component of the tectorial membrane (TM) is a porous matrix made up of th
10                                          The tectorial membrane (TM) is an acellular structure of the
11                                          The tectorial membrane (TM) is an extracellular matrix that
12                                          The tectorial membrane (TM) is widely believed to play an im
13                                          The tectorial membrane (TM) of the mammalian cochlea is a co
14 relation and the pore radius of the isolated tectorial membrane (TM) of the mouse were determined.
15  altering the mechanical load applied by the tectorial membrane (TM) on the outer hair cell HB.
16 ent studies suggest that wave motions of the tectorial membrane (TM) play a critical role in determin
17                                          The tectorial membrane (TM) plays a key role in this process
18 e spatial extent and propagation velocity of tectorial membrane (TM) travelling waves and that these
19                            The motion of the tectorial membrane (TM) with respect to the reticular la
20            In the Otoa(EGFP/EGFP) mouse, the tectorial membrane (TM), a ribbon-like strip of ECM that
21 nchoring of their tallest stereocilia in the tectorial membrane (TM), an acellular structure overlyin
22                                          The tectorial membrane (TM), an aECM in the cochlea mediatin
23 that mutations of the genes expressed in the tectorial membrane (TM), an extracellular matrix located
24 is a modular, non-collagenous protein of the tectorial membrane (TM), an extracellular matrix of the
25 creted glycoproteins that are present in the tectorial membrane (TM), an extracellular structure over
26 , and DC shift on the basilar membrane (BM), tectorial membrane (TM), and OHC potentials are predicte
27 uency selectivity and wave properties of the tectorial membrane (TM).
28 the BM and another extracellular matrix, the tectorial membrane (TM).
29  the tips of the tallest stereocilia and the tectorial membrane (TM).
30 non-syndromic hearing loss, and suggest that tectorial membrane abnormalities may be one aetiology of
31                           These mutants have tectorial membrane abnormalities, including a prominent
32 rom a minimum in the radial impedance of the tectorial membrane and its limbal attachment.
33  the development of the limbal domain of the tectorial membrane and its medial anchorage to the spira
34 silar membrane, the radial vibrations of the tectorial membrane and reticular lamina were tuned.
35  structures that deflect the OHC bundle, the tectorial membrane and reticular lamina, to the transver
36 imulate the outer hair cell stereocilia, the tectorial membrane and reticular lamina, were sharply tu
37 ations, except in the narrow gap between the tectorial membrane and reticular lamina, where lubricati
38 ted to a reduction in the acting mass of the tectorial membrane and reveal a new function for this st
39                            Specifically, the tectorial membrane and the Deiters cell are mechanically
40  quantified the mechanical properties of the tectorial membrane and the Deiters cell in situ.
41 and their surrounding structures such as the tectorial membrane and the Deiters cell is critical to r
42 interactions between the organ of Corti, the tectorial membrane and the subtectorial fluid, and/or el
43 th (especially of the inner hair cells), the tectorial membrane appeared to be more resistant to post
44 stic trachea as well as the extension of the tectorial membrane are not correlated to the tonotopy.
45 , tip links are only sensitive to BAPTA, and tectorial membrane attachment crowns are removed by subt
46 nks appear around the base of the bundle and tectorial membrane attachment crowns are seen at the ste
47 s: tip links, horizontal top connectors, and tectorial membrane attachment crowns.
48                  The radial stiffness of the tectorial membrane attachment was found to be a crucial
49  that Kolliker's organ is involved in normal tectorial membrane collagen fibril development and matur
50                                          The tectorial membrane contains radially organized collagen
51                                   Hence, the tectorial membrane contributes to control of hearing sen
52 gap size between the IHC stereocilia and the tectorial membrane determine the characteristic frequenc
53                 Combined with the changes in tectorial membrane dimensions from base to apex, the rad
54                                  Because the tectorial membrane directly overlies the inner hair cell
55                                          The tectorial membrane extracellular matrix in the cochlea c
56                   have provided insight into tectorial membrane formation, demonstrating proteolytic
57 al workings of the organ of Corti and of the tectorial membrane have resisted exploration.
58 tically isolated a second major role for the tectorial membrane in hearing: it enables the motion of
59 s with electron-lucent cytoplasm; and 4) the tectorial membrane in the BWC papilla was narrow, coveri
60 r noncollagenous components of the mammalian tectorial membrane in the inner ear.
61 in a cross section of the organ of Corti and tectorial membrane in the mammalian cochlea, and quantif
62 ctorin (Tecta) is a major constituent of the tectorial membrane in the mammalian cochlea.
63                                          The tectorial membrane is an extracellular structure of the
64 ated in Tecta(C1509G/C1509G) mice, where the tectorial membrane is detached from OHC stereocilia, arg
65 micromechanics of the organ of Corti and the tectorial membrane is then analyzed by our new method.
66 band, when the hair bundle was loaded with a tectorial membrane mass.
67 a imprint pattern at the undersurface of the tectorial membrane may provide a way to detect possible
68 ngs are as follows: The reticular lamina and tectorial membrane move in unison with essentially no sq
69 l and Deiters cells and was deposited in the tectorial membrane of the cochlea between postnatal days
70                   Electron microscopy of the tectorial membrane of these mice revealed loss of organi
71 ably form higher order structures with other tectorial membrane proteins such as alpha-tectorin and b
72     Inertial loading of a hair bundle by the tectorial membrane reduces the bundle's reactive load, a
73 ts are consistent with the hypothesis that a tectorial membrane resonance introduces the correct phas
74  the hemicochlea, we are able to show that a tectorial membrane stiffness gradient exists along the c
75       Unlike the natural situation where the tectorial membrane stimulates hair-cell stereocilia even
76                            We found that the tectorial membrane sustains traveling wave propagation.
77 pared with basilar membrane traveling waves, tectorial membrane traveling waves have larger dynamic r
78 uted to decreases in spread of excitation of tectorial membrane traveling waves.
79 in the hair cell epithelium is distinct from tectorial membrane tuning.
80 ort, to our knowledge, the first measures of tectorial membrane vibration within the unopened cochlea
81 ere we show that the spread of excitation of tectorial membrane waves is similar in humans and mice,
82 lear physics, which are the stiffness of the tectorial membrane with respect to the hair bundle and t
83 ene mutation for alpha-tectorin indicate the tectorial membrane's key role in the mechanoelectrical t
84 abnormalities do not seriously influence the tectorial membrane's known role in ensuring that cochlea
85  mice with the Y1870C mutation in Tecta, the tectorial membrane's matrix structure is disrupted, and
86 e inner ear, direct experimental data on the tectorial membrane's physical properties are limited, an
87  of the outer hair cells are imbedded in the tectorial membrane, a sheet of extracellular matrix that
88 rin (encoded by Tecta) is a component of the tectorial membrane, an extracellular matrix of the cochl
89  beta-tectorin reveal multiple roles for the tectorial membrane, an extracellular matrix unique to th
90         Loud sounds depleted Ca(2+) from the tectorial membrane, and Ca(2+) manipulations had large e
91 ts, such as the viscoelastic response of the tectorial membrane, and the cochlear input impedance.
92 ir bundles are not attached to the overlying tectorial membrane, are a notable exception.
93             NGAL was highly expressed in the tectorial membrane, cochlear neurons, and organ of Corti
94 ticular lamina greatly surpasses that of the tectorial membrane, giving rise to shear that deflects t
95 sory structure close to the stereocilia, the tectorial membrane, had much higher Ca(2+) than the surr
96 otion were hundreds of times larger than the tectorial membrane, reticular lamina (RL), and pillar ce
97  also exhibited obvious abnormalities in the tectorial membrane, supporting cells, and Reissner's mem
98 ilar membrane, the reticular lamina, and the tectorial membrane.
99 hearing between the reticular lamina and the tectorial membrane.
100 als for precise collagen organisation in the tectorial membrane.
101 id-filled space between reticular lamina and tectorial membrane.
102 affects interactions of stereocilia with the tectorial membrane.
103 mechanical link of outer hair cells with the tectorial membrane.
104 lia to maintain stable interactions with the tectorial membrane.
105 s similar in dead mice and in mice lacking a tectorial membrane.
106 chanical coupling of outer hair cells to the tectorial membrane.
107 ir cell stereocilia by mirroring them on the tectorial membrane.
108 to produce fast lateral displacements of the tectorial membrane.
109 nd influences the physical properties of the tectorial membrane.
110 d graded mechanical properties of guinea pig tectorial membrane.
111 and sensory epithelium, and deformity of the tectorial membrane.
112 lear partition upon tip-link destruction and tectorial-membrane removal, suggesting that these struct
113 real cochlea, the motions of the basilar and tectorial membranes are fundamentally different during i
114   In cochlear sections of Ceacam16(-/-) mice tectorial membranes were significantly more often stretc
115  of Corti sandwiched between the basilar and tectorial membranes, contains the outer hair cells that
116 r matrices, including otoconial, cupular and tectorial membranes, in Oc90 null mice, likely due to an
117 chlear resonance, presumably the basilar and tectorial membranes, move together in phase during the o
118 mited, and only a few direct measurements on tectorial micromechanics are available.
119  functional component of the cupula, but not tectorial or otoconial membranes.

 
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