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 ions (detected by maculae of the utricle and saccule).
2 ular hair cells in the striola region of the saccule.
3  ERalpha, and aromatase in the forebrain and saccule.
4 in the auditory thresholds recorded from the saccule.
5 nd extra-striolar regions of the utricle and saccule.
6 ed loss of vestibular hair cells only in the saccule.
7 structures such as the cochlea, utricle, and saccule.
8 mitotically blocked cultures of the bullfrog saccule.
9 n that of sensory epithelium from utricle or saccule.
10  approximately threefold larger than in frog saccule.
11  in higher frequency organs such as the frog saccule.
12 r epithelial type I and type II cells within saccules.
13 eries and veins, bronchioles, and developing saccules.
14 e otic capsule and terminates lateral to the saccules.
15 with compensatory hyperinflation of immature saccules.
16  apparatus, such as the formation of dilated saccules.
17 in-duct strictures and grapelike clusters of saccules.
18  in DKO lung blood vessels, bronchioles, and saccules.
19 ently have reduced dopaminergic input to the saccule [19].
20 processes low-frequency vibrations using the saccule, an inner ear organ previously thought to serve
21 Hair bundle defects are also observed in the saccule and ampullae of Ptprq(-/-) mice.
22                  Defects in the shape of the saccule and cochlea were variable in Otx1-/- mice and we
23 x2 were co-expressed, in regions such as the saccule and cochlea.
24 ver, Gbx2 promotes ventral fates such as the saccule and cochlear duct, possibly by restricting Otx2
25 sterior semicircular canals, and a malformed saccule and cochlear duct.
26 sed dissociated hair cells from the bullfrog saccule and high-speed video imaging to characterize thi
27        Unlike most vertebrates that have the saccule and lagena as two separate pouches ventral to th
28 indbrain exclusively receives input from the saccule and projects to the auditory midbrain, the torus
29 t reduction in the number of otoconia in the saccule and the utricle, were consistently observed in t
30 owing to a depletion of sensory cells in the saccule and utricle, and a complete loss of the horizont
31 nse lateral and ventral projections from the saccule and utricle, and medial and dorsal projections f
32                 However, the origin of these saccules and the function of the cytoplasmic droplet hav
33 agenar otoliths, close proximity between the saccules and the utricles, deeply grooved sulci on the s
34  Neonatal transgenic mice exhibited enlarged saccules and thickened primary septa.
35 crista, the lateral crista, the utricle, the saccule, and both the basilar papilla and lagenar macula
36 shapen and smaller ear with a fused utricle, saccule, and cochlea and absent horizontal canal, aberra
37 ntion was focused on the developing utricle, saccule, and cochlea.
38  of hair cells differentiate in the utricle, saccule, and cochlear base but sensory epithelium format
39 nd sac, in distinct areas of the utricle and saccule, and in the external sulcus region within the co
40 rom the three otolithic organs (the utricle, saccule, and lagena) project to the intermediate DON in
41 ithin the three macular organs, the utricle, saccule, and lagena, consistent with the reported distin
42 show that Pax2-/- ears often lack a distinct saccule, and the endolymphatic duct and common crus are
43                Surprisingly, in all mutants, saccules are produced from lung cysts at the proper deve
44                    Female midshipman use the saccule as the primary end organ for hearing to detect a
45        Here, we show that dopamine decreases saccule auditory sensitivity via a D2-like receptor.
46 ting hundreds of thousands of pigment-filled saccules (chromatophores) in the skin, which are control
47 ing the mature semicircular canals, utricle, saccule, cochlear duct, endolymphatic duct and sac, and
48 labeling of the main auditory end organ, the saccule, combined with tyrosine hydroxylase immunofluore
49                  SEM also showed recovery in saccules comparable to that in utricles.
50 l specification when the nascent utricle and saccule constitute a continuous prosensory domain.
51             We show that DA terminals in the saccule contain vesicles but transmitter release appears
52 projections indicate that activity along the saccule could be modulated by a single efferent.
53 he three mechanoreceptor organs, the utricle/saccule, cristae, and cochlea, with distinct types of ac
54                                              Saccule D2a receptor expression is reduced in the summer
55 cceleration) and otolith organs (utricle and saccule; detecting linear acceleration, vibration, and h
56 ista, as well as a fusion of the utricle and saccule endolymphatic spaces into a common utriculosaccu
57 ystem provide a release of inhibition in the saccule, enhancing peripheral encoding of social-acousti
58 ha(7) was expressed in conducting airway and saccule epithelial cells.
59 brane of vestibular hair cells from the frog saccule extrudes H+ via an Na+-dependent mechanism, bund
60 ing in Dreher mutants, where the utricle and saccule fail to segregate, labels a continuous field of
61 derivatives, including the cochlear duct and saccule, fail to form, and dorsal otic derivatives, incl
62 mal compartments to generate mature alveolar saccules for efficient gas exchange.
63 ut completely prevented loss of ANF, SGN and saccule hair cells.
64                         Only the utricle and saccule have an extremely dense matrix, the otoconial co
65  position is the function of the utricle and saccule in mammals.
66 cristae ampullaris, the maculae utricle, and saccule in the human and mouse.
67 he dorsal medulla shows that fibers from the saccule in the inner ear and from the anterior lateral l
68 ere, we demonstrate an auditory role for the saccule in the tokay gecko (Gekko gecko).
69 ts alveolar formation, resulting in enlarged saccules in Sftpc-Cre/Nkx2.1-Cre; Wlsloxp/loxp mutants.
70 one side of the LPR in the mature utricle or saccule, indicating that this boundary is first establis
71  remodeling and expansion of the distal lung saccules into primitive alveoli.
72                                          The saccule is a vestibular sensory organ that depends upon
73  that the ancestral auditory function of the saccule is likely preserved at least in the lepidosauria
74 om all three of the inner ear endorgans (the saccule, lagena, and utricle) synapse directly on the ip
75 ll proliferation in all inner ear epithelia (saccule, lagena, utricle).
76 ed as a 95-kDa glycoprotein in sunfish whole-saccule lysate and in homogenates of microdissected sacc
77 tained from afferents innervating the middle saccule may reflect curvature of the sensory epithelium
78 ing model) only showed hair cell loss in the saccule of aged males, but both sexes exhibit age-relate
79 conia are biominerals within the utricle and saccule of the inner ear that are critical for the perce
80 omozygous mice is limited to the utricle and saccule of the inner ear, which completely lack otoconia
81 in het mutants is limited to the utricle and saccule of the inner ear, which completely lack otoliths
82 ated with intracellular membranes, including saccules of Golgi and cytoplasmic tubulovesicles.
83 y localized to tubulovesicles that resembled saccules of SER, and less frequently localized to isolat
84 s showing S-LI were prominently localized to saccules of smooth endoplasmic reticulum and mitochondri
85 chT-immunoreactive tubulovesicles resembling saccules of smooth endoplasmic reticulum were often seen
86                Septation of the gas-exchange saccules of the morphologically immature mouse lung requ
87 n the bluegill sunfish (Lepomis macrochirus) saccule, one of the otolithic organs in the inner ear.
88    RARalphaVP16 lungs did not expand to form saccules or morphologically identifiable type I cells.
89 eficient in Rdh10 exhibit failure of utricle-saccule separation, otoconial formation and zonal patter
90 erebellum similar to that of the utricle and saccule suggest that the primary role of the lagena in t
91        Afferents innervating the utricle and saccule terminated generally in the lateral regions of a
92                           In the utricle and saccule the hair cells are arranged in an orderly array
93 n in the central vocal-acoustic networks and saccule, the auditory division of the inner ear.
94  the hindbrain auditory efferent nucleus and saccule, the main hearing endorgan of the inner ear.
95 s in the dopaminergic efferent system in the saccule, their primary organ of hearing.
96  structures such as the cochlea, utricle, or saccule throughout late IE development.
97  Grh1 containing vesicles and tubules into a saccule to generate a mature Acb1 containing compartment
98 ped and used a preparation of isolated mouse saccule to measure transepithelial currents from the ext
99 re localized within sensory epithelia of the saccule, utricle and cochlea throughout development and
100 urons (SGN) and vestibular hair cells in the saccule, utricle and semicircular canals.
101  expression patterns of Cx26 and Cx30 in the saccule, utricle, and ampulla by immunolabeling.
102 r, including the auditory ganglion, cochlea, saccule, utricle, and semicircular canals.
103 aratus, including three semicircular canals, saccule, utricle, and their associated sensory organs, d
104  bundles in different regions of the lagena, saccule, utricle, macula neglecta, and cristae was chara
105 s well as onto the base of hair cells in the saccule via nerve VIII.
106 ious studies suggested that endolymph in the saccule was merely derived from cochlear endolymph.
107 imental preparations of ampulla, utricle and saccule were found to be significantly higher than those
108 s and reduced innervation to the utricle and saccule were observed.
109  In addition, the maculae of the utricle and saccule were partially fused.
110              Otolithic endorgans such as the saccule were thought to be strictly vestibular in amniot
111 ects of adaptation in hair cells of the frog saccule, where adaptation time constants are tens of mil
112  formation of the proximal cochlear duct and saccule, which requires less Shh signaling, is achieved
113 grees, which corresponds to the angle of the saccule with respect to the fish's midline.
114             It also revealed hypo reflective saccules with hyperreflective borders located in the inn
115 r a mechanism to actively form and segregate saccules within the cytoplasmic droplet to promote sperm
116 essential for formation and sequestration of saccules within the cytoplasmic droplet.

 
Page Top