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 ndle hair cells in the peripheral regions of sensory epithelia.
2 for both the structure and function of these sensory epithelia.
3 present in both sensory ganglion neurons and sensory epithelia.
4 rsor cell differentiation in avian inner ear sensory epithelia.
5 eural gene atonal, is expressed in inner ear sensory epithelia.
6 ere identified which were not within defined sensory epithelia.
7  the supporting cell layer in the vestibular sensory epithelia.
8 re present in normal auditory and vestibular sensory epithelia.
9 blished role for support cells in vertebrate sensory epithelia.
10 mbryos, including posterior otoliths and all sensory epithelia.
11 s in the early otic epithelium and inner ear sensory epithelia.
12  pressure rise and repetitive microtrauma to sensory epithelia.
13 ed otic placode, epithelium, neuroblasts and sensory epithelia.
14 ons is replaced during metamorphosis in both sensory epithelia.
15 nd the production of new hair cells in adult sensory epithelia.
16 y in space and contain intricately patterned sensory epithelia.
17 fferent physical media and entirely separate sensory epithelia.
18 ly localized in avian and mammalian auditory sensory epithelia.
19 ransition that reliably yields new polarized sensory epithelia.
20 cortical actin belts than those in embryonic sensory epithelia.
21 s of GJC between the auditory and vestibular sensory epithelia.
22 ory structures, including olfactory bulb and sensory epithelia.
23 yte subtypes in normal posthatch chicken ear sensory epithelia.
24 ntly expressed in terminally differentiating sensory epithelia.
25 rate-specific Hmx activities to regulate the sensory epithelia.
26 s that regulate the overall formation of the sensory epithelia.
27 ypes of hair cells are present in vestibular sensory epithelia.
28 mal and drug-damaged auditory and vestibular sensory epithelia.
29 tal expression of espin in chicken inner ear sensory epithelia.
30 tected in supporting cells of the vestibular sensory epithelia.
31 om nonsensory regions, the hair cells of the sensory epithelia accumulate class III beta-tubulin, whe
32  a cellular mosaic similar to the endogenous sensory epithelia and expansion of the sensory mosaic th
33 lf inhibited DNA synthesis in the vestibular sensory epithelia and failed to potentiate the effects o
34  manipulation of the regenerative program in sensory epithelia and other vertebrate neuroepithelia.
35 icted expression, confined mainly to the pro-sensory epithelia and the neural processes from the coch
36 ouse inner ear - the vestibular and cochlear sensory epithelia and the spiral ganglion - by measuring
37 hd7-deficient mice or whether the vestibular sensory epithelia and their associated innervation and f
38 ence of mechanical differences between those sensory epithelia and their supporting cells prompted us
39  is localized to the vestibular and cochlear sensory epithelia and to the spiral ganglions.
40 ted DNA synthesis in vestibular and auditory sensory epithelia and was not cytotoxic at the concentra
41  HC proteome with other IE subproteomes from sensory epithelia and whole IE.
42 sable for basal body docking in otic vesicle sensory epithelia and, surprisingly, short cilia form in
43 n the saccular otoliths, two-planar saccular sensory epithelia, and a unique orientation pattern of s
44                  However, competence to form sensory epithelia appears to be limited to discrete regi
45      The most common leukocytes in inner ear sensory epithelia are ramified cells of the myeloid line
46 te-positive territory from which most of the sensory epithelia arise.
47  ANKS4B, the scaffold USH1G that operates in sensory epithelia as part of the Usher complex, lacks th
48 e cell proliferation in adult rat vestibular sensory epithelia, as does the infusion of transforming
49 t several classes of supporting cells in the sensory epithelia, as well as Schwann cells and satellit
50  do not reside in normal or drug-damaged ear sensory epithelia at 1-3 days post insult but are presen
51  neurons may modulate afferent pathways from sensory epithelia at the periphery.
52 t-1 in differentiating inner ear neurons and sensory epithelia cells, perhaps in the specification of
53                                The inner ear sensory epithelia contain mechanosensitive hair cells an
54                                    Inner ear sensory epithelia contain mechanosensitive hair cells th
55 ession in developing auditory and vestibular sensory epithelia correlates with maturation of hair cel
56 o we investigated the effect of forskolin on sensory epithelia cultured from the ears of mammals.
57 important, the NSCs can incorporate into the sensory epithelia, demonstrating their therapeutic poten
58  epigenetic status of the Atoh1 locus during sensory epithelia development in the mouse.
59                                The remaining sensory epithelia display a dense pattern of cProx1 expr
60 9 AChR expression in cochlear and vestibular sensory epithelia during neonatal development.
61 unctional maturation of hair cells in intact sensory epithelia excised from the inner ears of embryon
62 gun-mediated transfection of mouse inner ear sensory epithelia explants shows selective accumulation
63 ting the type I hair cells of the vestibular sensory epithelia form distinct calyceal synapses.
64 he transcriptomes of auditory and vestibular sensory epithelia from early postnatal mice.
65                       The label densities of sensory epithelia from experimental preparations of ampu
66  and mechanical methods were used to isolate sensory epithelia from mature chick basilar papillae, an
67 rt the stepwise differentiation of inner ear sensory epithelia from mouse embryonic stem cells (ESCs)
68           It is unclear how to develop these sensory epithelia from pluripotent stem cells, a process
69                              Small pieces of sensory epithelia from the chicken utricle were cultured
70 specific miRNAs might influence formation of sensory epithelia from the primitive otic neuroepitheliu
71    Coordinated hair cell orientations within sensory epithelia further tune stimulus detection at the
72            Lgr5(+) progenitor cells from the sensory epithelia gave rise to hair cell-like cells, but
73                                  In isolated sensory epithelia, however, caspase inhibitors did not a
74 faces of sensory and supporting cells in all sensory epithelia in a pattern that correlates with the
75 r to the possibility of repopulating damaged sensory epithelia in humans.
76 r hair cell differentiation in all hair cell sensory epithelia in the chicken.
77 f GJ distribution in auditory and vestibular sensory epithelia in the different vertebrate classes.
78 and establishment of neuronal projections to sensory epithelia in the embryonic inner ear, but their
79  small RNAs in development and maturation of sensory epithelia in the mouse inner ear will be conside
80 n-2) localize to tTJs of the sensory and non-sensory epithelia in the organ of Corti and vestibular e
81 elivery of Yap5SA in the postnatal inner ear sensory epithelia in vivo drives cell cycle reentry afte
82 dles when situated in cochlear or vestibular sensory epithelia in vivo.
83 d in both the CNS and PNS as well as in many sensory epithelia including the developing inner ear epi
84                     Cells derived from these sensory epithelia, including migrating GnRH neurons and
85 mRNA was first observed in HCs at E16 in all sensory epithelia, increased to its highest levels by P0
86 rant receptor (Or) gene are scattered across sensory epithelia, intermingled with neurons that expres
87             Hair cells differentiate only in sensory epithelia known or proposed to have a lineage re
88  of Atoh1 is sufficient to establish ectopic sensory epithelia, making Atoh1 a good candidate for gen
89 te are known to be present in the vestibular sensory epithelia of a variety of species, the functiona
90 egulated and alpha6 was downregulated in the sensory epithelia of both the auditory and vestibular sy
91        In developing auditory and vestibular sensory epithelia of Brn-3c-/- mice, hair cells are foun
92 he progression of recovery of the vestibular sensory epithelia of guinea pigs after gentamicin-induce
93 llulin becomes mislocalized in the inner ear sensory epithelia of ILDR1 null mice after the first pos
94 ce of Tmc protein reliance in the vestibular sensory epithelia of mammals to the maculae of zebrafish
95 single cells from the utricular and cochlear sensory epithelia of newborn mice to circumvent this cha
96               Leukocytes reside in undamaged sensory epithelia of the avian inner ear and increase in
97 ridization within areas corresponding to the sensory epithelia of the cochlea and vestibular systems
98   Genotypically mutant HCs were found in all sensory epithelia of the inner ear at all ages examined.
99 bution and size of gap junctions (GJ) in the sensory epithelia of the inner ear have been examined in
100 et-1 becomes up-regulated in the presumptive sensory epithelia of the inner ear in regions that are d
101 ic of hair cells and supporting cells in the sensory epithelia of the inner ear is regulated by Notch
102                                              Sensory epithelia of the inner ear require a coordinated
103                       Grxcr1 is expressed in sensory epithelia of the inner ear, and its encoded prot
104  together with supporting cells comprise the sensory epithelia of the inner ear.
105 hair cells and supporting cells comprise the sensory epithelia of the inner ear.
106 bition to eliminate patterning errors in the sensory epithelia of the inner ear.
107           At E15.5, Six1 is expressed in all sensory epithelia of the inner ear.
108 omal cells underneath the non-immunoreactive sensory epithelia of the macula utricle, sacule, and cri
109 CP) proteins are distributed normally in the sensory epithelia of the mutants, suggesting that PCDH15
110  Wnt1-Cre labeled cells are localized within sensory epithelia of the saccule, utricle and cochlea th
111  antigen occurred in both the nonsensory and sensory epithelia of the sacculus.
112  missing ampullae, structures that house the sensory epithelia of the semicircular canals.
113 us perception is achieved by associating the sensory epithelia of the three mechanoreceptor organs, t
114 ic miR-183 expression in the three remaining sensory epithelia (posterior crista, utricle, and cochle
115 munostaining of hair cells in the vestibular sensory epithelia revealed that organ-specific alteratio
116 identify genes expressed in the regenerating sensory epithelia (SE) of the chicken inner ear.
117 ototoxic antibiotics were used to damage the sensory epithelia (SE).
118 ion, in many nonmammalian vertebrates, these sensory epithelia show remarkable regenerative potential
119              Afferent innervation of the ear sensory epithelia shows numerous fibers overshooting the
120                             In the inner ear sensory epithelia, stereociliary hair bundles atop senso
121 division in cultured auditory and vestibular sensory epithelia taken from posthatch chickens.
122 sicles develop into inner ear organoids with sensory epithelia that are innervated by sensory neurons
123                       The inner ear contains sensory epithelia that detect head movements, gravity an
124                            In the vestibular sensory epithelia, the virus transduced large numbers of
125 ceptor protein and projects an axon from the sensory epithelia to an olfactory bulb glomerulus, which
126 nt study used cultures of isolated inner ear sensory epithelia to identify cellular signals that regu
127 ts of stereocilia, was used to delineate the sensory epithelia, to visualize the distribution of hair
128                  It is debatable whether the sensory epithelia underwent progressive segregation or e
129    In the inner ear, cochlear and vestibular sensory epithelia utilize grossly similar cell types to
130          Decreased innervation to vestibular sensory epithelia was detected at E13.5-15, when progres
131      The ability of atoh1a to induce ectopic sensory epithelia was maximal when activated during plac
132 onfocal microscopy of immunostained cochlear sensory epithelia, was coupled with a corresponding func
133 lated tissues, chick auditory and vestibular sensory epithelia, we find that glycolytic enzymes are e
134 ignificantly smaller auditory and vestibular sensory epithelia, while conditional overexpression of a
135 highly specialized regions of the vestibular sensory epithelia with specific functions in detecting h

 
Page Top