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 s, and in the central zone of the horizontal crista.
2 r cells located in the central region of the crista.
3 n-polaritons on the surface of mitochondrial crista.
4 exception of 1 of 14 strains), Streptococcus crista (3 strains), Streptococcus anginosus (1 strain),
5      Sensory dendrites in the hearing organ (crista acustica [CA]) are hypothesized to stretch, there
6                                          The crista acustica is located on a curved triangular surfac
7 th data from a previous study to predict the crista acustica stiffness.
8 organized along the longitudinal axis of the crista acustica, the bushcricket's hearing organ.
9                 Their inner ears contain the crista acustica, which holds tonotopically arranged sens
10 nsible for the effects of L-ARG on the RA of crista afferent fibers.
11 ultrastructural similarities of the goldfish crista afferents to calyx afferents found in amniotes (b
12 ly described in the ear of this species, the crista also contained enlarged afferent terminals that e
13  subset of hair cells in the utricle and the crista ampullaris express BK channels.
14 w type of afferent terminal structure in the crista ampullaris of the goldfish Carassius auratus.
15 ssed in the neurosensorial epithelium of the crista ampullaris of the rat by immunohistochemistry.
16 upula is a gelatinous membrane overlying the crista ampullaris of the semicircular canal, important f
17 iber recordings in the acutely excised mouse crista ampullaris of the semicircular canals.
18 oma underlying the sensory epithelium of the crista ampullaris of the semicircular canals.
19 ent results show that the semicircular canal crista ampullaris of the toadfish, Opsanus tau, is sensi
20 ear sensory epithelium and the stroma of the crista ampullaris of the vestibular labyrinth.
21                               The chinchilla crista ampullaris was studied in 10 samples, each contai
22 epithelia of the macula utricle, sacule, and crista ampullaris, and the membranous vestibular labyrin
23                                       In the crista ampullaris, high levels of BDNF transcripts were
24 iptomic characterization of the cells of the crista ampullaris, sensory structures at the base of the
25 n the hair cells and supporting cells of the crista ampullaris.
26 s in the central and peripheral zones of the crista ampullaris.
27  described above on FFPE sections from human crista ampullaris.
28 Aergic hair cells are present throughout the crista ampullaris.
29 restricted domains of gene expression in the crista and ampulla.
30 for neurosensory formation of the horizontal crista and associated sensory neurons.
31                    The fluid pressure at the crista and crista motion were used to calculate the acou
32 ged the horizontal semicircular canal (HSCC) crista and cupula of toadfish, Opsanus tau, by using a)
33 cus connective tissue shells rising from the crista and extending toward the ampullary roof.
34  play a role in corncob formation between S. crista and Fusobacterium nucleatum, this property was ex
35                             Only the lateral crista and the macula neglecta were initially Fgf10 nega
36 followed by the superior crista, the lateral crista, and the macula utriculi at 12 dpc.
37 es protein complexes involved in maintaining crista architecture and protein import and is thus essen
38       We show that the predictions made with CRISTA are more accurate than other available methodolog
39 rus and ampullae housing the sensory tissue (crista) are intact.
40 upular shell fibers cover the surface of the crista, are roughly parallel, and are associated with a
41 he hair cells, support cells and glia of the crista as well as dark cells and other nonsensory epithe
42 teral crista, saccular macula, and posterior crista, as confirmed by immunolabeling for hair cell ant
43 te loss of the horizontal semicircular canal crista, as well as a fusion of the utricle and saccule e
44  the macula sacculi at stage 20, the lateral crista at stage 22, the basilar papilla and lagena at st
45 hen only supporting cells are present in the crista, BDNF mRNA was undetectable.
46 adhesin genes was cloned, from Streptococcus crista CC5A, and sequenced.
47    Some cells of this group terminate in the crista cerebellaris.
48 hort and stout tibiotarsus, poorly developed crista cnemialis cranialis, short and wide tarsometatars
49 er in the peripheral regions of the ampullar crista compared to the vertex.
50 that contains both tubular and flat lamellar crista components.
51 ent observations, however, have demonstrated crista conduction.
52 average of about 43 prohibitin complexes per crista, covering 1-3% of the crista membrane area.
53                           Here, we introduce CRISTA (CRISPR Target Assessment), a novel algorithm wit
54 mild headtossing associated with a posterior crista defect.
55 rain mitochondria are larger and have higher crista density and increased physical interactions betwe
56 D afferents innervating the turtle posterior crista during electrical stimulation of efferent neurons
57 n afferents innervating the turtle posterior crista during electrical stimulation of vestibular effer
58 trometers and Telescopes for the Atmosphere (CRISTA) during shuttle mission STS-66 have provided meas
59 megamitochondria (MGs), and nanotunnels] and crista dynamics.
60 d 2) The geometric effect of a mitochondrial crista enhances the transmembrane-electrostatically loca
61 onic inhibitory effect on the RA of afferent crista fibers in cephalopod statocysts.
62 GMP on the resting activity (RA) of afferent crista fibers were studied in isolated preparations of t
63 AP) on the resting activity (RA) of afferent crista fibers were studied in isolated statocysts of the
64 RG) on the resting activity (RA) of afferent crista fibers were studied in isolated statocysts of the
65 RNA-seq could be important for understanding crista function and the markers identified in this study
66 r the gain of a third semicircular canal and crista in gnathostomes, but also for the separation of t
67 nd show that it is essential for maintaining crista integrity and mitochondrial function.
68 ct sites and plays a key role in maintaining crista integrity.
69        Consistent with the proposal that the crista is concentrically organized, the intermediate and
70 l outer membrane permeabilization (MOMP) and crista junction opening (CJO) were caspase independent a
71                            Additionally, the crista junction opening diameter was reduced to 50% sugg
72                                              Crista junctions (CJs) are tubular invaginations of the
73 Chd3 complexes with multiple proteins at the crista junctions and contact sites and plays a key role
74 omplex that is required for the formation of crista junctions and contact sites between inner and out
75 e discovered the polarization of cristae and crista junctions in mitochondria tethered to the SSC in
76 detailed distribution of its subunits around crista junctions is unclear because such small length sc
77                         MICOS is enriched at crista junctions, but the detailed distribution of its s
78       Crista structure was polarized in that crista junctions, circular openings of the inner membran
79 s a key role in establishing and maintaining crista junctions, tubular or slit-like structures that c
80 me c release but only a subtle alteration of crista junctions, which involved the disassembly of Opa1
81 al inner membrane, is localized primarily at crista junctions.
82 a, suggesting an ordered distribution of the crista junctions.
83 , suggesting that Mic60 surrounds individual crista junctions.
84 ge 23 that correspond to the future superior crista, lateral crista, saccular macula, and posterior c
85 often appear to be wrapped around cristae or crista-like inner membrane invaginations.
86  orientations, but the lateral canal sensory crista looks like the "hemicrista" of some amphibians an
87 n complexes per crista, covering 1-3% of the crista membrane area.
88 ory complexes segregate into curved and flat crista membrane domains, respectively.
89         In addition to its canonical role in crista membrane structure, MIC60 regulates mitochondrial
90 s lateral organization and morphology of the crista membrane.
91 ular cristae or loss of cristae, and reduced crista membrane.
92 lation complex machinery most notably on the crista membranes.
93  proteins mitofilin and OPA1, which regulate crista morphology, and the outer membrane protein Sam50,
94         The fluid pressure at the crista and crista motion were used to calculate the acoustic impeda
95 lateral utricular wall between the posterior crista (PC) and the utriculosaccular foramen.
96 nction experiments, we show that FGFs in the crista promote canal development by upregulating Bmp2.
97 sis requires a subtle form of Opa1-dependent crista remodeling that is induced by BH3-only proteins a
98            The remarkable longevity of these crista residents was not shared by all mitochondrial pro
99 spond to the future superior crista, lateral crista, saccular macula, and posterior crista, as confir
100  easily identified and were present in every crista sampled.
101                         The magnitude of the crista stiffness was similar to basilar membrane stiffne
102 ling plays a substantial role in determining crista stiffness.
103 he dual roles of MIC60 in both mitochondrial crista structure and motility position it as a crucial p
104 el cytoskeletal framework, and indicate that crista structure can be specialized for particular funct
105                            Disruption of the crista structure has been implicated in a variety of car
106                                              Crista structure was polarized in that crista junctions,
107 itochondria, as well as the breakdown of the crista structure, whereas the number and ultrastructure
108 he inner mitochondrial membranes to maintain crista structure.
109 and fuse inner membranes as well as maintain crista structures and propose a model for how the mitoch
110 dynamics, specifically in the maintenance of crista structures.
111 3 patients), other atrial scar (3 patients), crista terminalis (3 patients), and right atrioventricul
112 ardias and to define their relation with the crista terminalis (CT).
113 ena cave isthmus (IS) and either side of the crista terminalis (CT).
114 pulmonary veins (n=5), left atrium (n=2), or crista terminalis (n=3).
115 thin the SAN, failing to directly excite the crista terminalis and intraatrial septum.
116        It has been shown previously that the crista terminalis and its continuation as the eustachian
117                      In six animals, zone 1 (crista terminalis and limbus) was ablated first, followe
118 ation distal to major branching sites of the crista terminalis and pectinate bundles, culminating in
119 ink-to-source effect at branch points of the crista terminalis and pectinate muscles is important in
120 atrium, especially in the trabeculae and the crista terminalis of the right atrial appendage.
121 eight of 35 focal ATs were located along the crista terminalis or tricuspid annulus.
122 hs could arise from a region parallel to the crista terminalis that is significantly larger (26.1 +/-
123 n three right atrial locations: (1) from the crista terminalis to the tricuspid annulus; (2) from the
124 the 3-D shift in caudal activation along the crista terminalis was more pronounced after RFA than dur
125 ral annulus, fossa ovalis, eustachian ridge, crista terminalis, and superior vena cava); or arm 3, st
126 trial node, from the initiation point to the crista terminalis, found that the action potential condu
127  usually due to foci in the pulmonary veins, crista terminalis, or left atrium.
128 s of specialized myofiber tracts such as the crista terminalis, pectinate muscles, and the Bachman bu
129 r muscle bundles of the atria, including the crista terminalis, pectinate muscles, limbus of the foss
130 ary vein (PV) in 3 patients, mitral annulus, crista terminalis, tricuspid annulus, and right-sided PV
131  of the right atrium and superior vena cava, crista terminalis, tricuspid valve isthmus, coronary sin
132 ck or double potentials in the region of the crista terminalis.
133  showed normal activation occurring near the crista terminalis.
134 ent had foci in both the pulmonary veins and crista terminalis.
135 l differences in the APD at junctions of the crista terminalis/pectinate muscle, pulmonary veins/left
136 id annulus; (2) from the fossa ovalis to the crista terminalis; and (3) from the inferior vena cava t
137 trial flutter have found linear block at the crista terminalis; this was thought to predispose the pa
138 al genesis zone adjacent to each prospective crista that corresponds to the Bone morphogenetic protei
139 cterized by high or multiple breaks over the crista, the ECG showed changes that depended on the init
140 at 11.5 dpc and was followed by the superior crista, the lateral crista, and the macula utriculi at 1
141 ing to the regions within which the anterior crista, the lateral crista, the utricle, the saccule, an
142 ole-tissue preparation of the rat vestibular crista, the sensory organ of the semicircular canals tha
143 ithin which the anterior crista, the lateral crista, the utricle, the saccule, and both the basilar p
144 oton concentration at a curved mitochondrial crista tip can be significantly higher than that at the
145 rostatically localized proton density to the crista tip where the ATP synthase can readily utilize th
146 three remaining sensory epithelia (posterior crista, utricle, and cochlea) that closely corresponds t
147 In the wild-type, the high-curvature edge of crista vesicles was densely populated with ATP synthase
148 ;Otx2(+/)- mutants revealed that the lateral crista was absent.
149                                The posterior crista was the first organ to appear at 11.5 dpc and was
150 d in near-normal hair cells of the posterior crista, whereas the reduced utricular macula demonstrate
151 erve afferents close to the turtle posterior crista while efferent fibers were electrically stimulate
152 mall caudal patch within which the posterior crista will develop, and a larger anterior patch.

 
Page Top