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

 
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