ライフサイエンスコーパス: crista

1 s, and in the central zone of the horizontal crista.

2 r cells located in the central region of the crista.

3 exception of 1 of 14 strains), Streptococcus crista (3 strains), Streptococcus anginosus (1 strain),

4 nsible for the effects of L-ARG on the RA of crista afferent fibers.

5 ultrastructural similarities of the goldfish crista afferents to calyx afferents found in amniotes (b

6 ly described in the ear of this species, the crista also contained enlarged afferent terminals that e

7 subset of hair cells in the utricle and the crista ampullaris express BK channels.

8 w type of afferent terminal structure in the crista ampullaris of the goldfish Carassius auratus.

9 ssed in the neurosensorial epithelium of the crista ampullaris of the rat by immunohistochemistry.

10 oma underlying the sensory epithelium of the crista ampullaris of the semicircular canals.

11 ent results show that the semicircular canal crista ampullaris of the toadfish, Opsanus tau, is sensi

12 ear sensory epithelium and the stroma of the crista ampullaris of the vestibular labyrinth.

13 The chinchilla crista ampullaris was studied in 10 samples, each contai

14 epithelia of the macula utricle, sacule, and crista ampullaris, and the membranous vestibular labyrin

15 In the crista ampullaris, high levels of BDNF transcripts were

16 described above on FFPE sections from human crista ampullaris.

17 Aergic hair cells are present throughout the crista ampullaris.

18 s in the central and peripheral zones of the crista ampullaris.

19 for neurosensory formation of the horizontal crista and associated sensory neurons.

20 ged the horizontal semicircular canal (HSCC) crista and cupula of toadfish, Opsanus tau, by using a)

21 cus connective tissue shells rising from the crista and extending toward the ampullary roof.

22 play a role in corncob formation between S. crista and Fusobacterium nucleatum, this property was ex

23 Only the lateral crista and the macula neglecta were initially Fgf10 nega

24 followed by the superior crista, the lateral crista, and the macula utriculi at 12 dpc.

25 es protein complexes involved in maintaining crista architecture and protein import and is thus essen

26 We show that the predictions made with CRISTA are more accurate than other available methodolog

27 upular shell fibers cover the surface of the crista, are roughly parallel, and are associated with a

28 teral crista, saccular macula, and posterior crista, as confirmed by immunolabeling for hair cell ant

29 te loss of the horizontal semicircular canal crista, as well as a fusion of the utricle and saccule e

30 the macula sacculi at stage 20, the lateral crista at stage 22, the basilar papilla and lagena at st

31 hen only supporting cells are present in the crista, BDNF mRNA was undetectable.

32 adhesin genes was cloned, from Streptococcus crista CC5A, and sequenced.

33 Some cells of this group terminate in the crista cerebellaris.

34 er in the peripheral regions of the ampullar crista compared to the vertex.

35 that contains both tubular and flat lamellar crista components.

36 ent observations, however, have demonstrated crista conduction.

37 Here, we introduce CRISTA (CRISPR Target Assessment), a novel algorithm wit

38 mild headtossing associated with a posterior crista defect.

39 D afferents innervating the turtle posterior crista during electrical stimulation of efferent neurons

40 n afferents innervating the turtle posterior crista during electrical stimulation of vestibular effer

41 trometers and Telescopes for the Atmosphere (CRISTA) during shuttle mission STS-66 have provided meas

42 onic inhibitory effect on the RA of afferent crista fibers in cephalopod statocysts.

43 GMP on the resting activity (RA) of afferent crista fibers were studied in isolated preparations of t

44 AP) on the resting activity (RA) of afferent crista fibers were studied in isolated statocysts of the

45 RG) on the resting activity (RA) of afferent crista fibers were studied in isolated statocysts of the

46 r the gain of a third semicircular canal and crista in gnathostomes, but also for the separation of t

47 nd show that it is essential for maintaining crista integrity and mitochondrial function.

48 ct sites and plays a key role in maintaining crista integrity.

49 Consistent with the proposal that the crista is concentrically organized, the intermediate and

50 l outer membrane permeabilization (MOMP) and crista junction opening (CJO) were caspase independent a

51 Additionally, the crista junction opening diameter was reduced to 50% sugg

52 Crista junctions (CJs) are tubular invaginations of the

53 Chd3 complexes with multiple proteins at the crista junctions and contact sites and plays a key role

54 omplex that is required for the formation of crista junctions and contact sites between inner and out

55 Crista structure was polarized in that crista junctions, circular openings of the inner membran

56 me c release but only a subtle alteration of crista junctions, which involved the disassembly of Opa1

57 ge 23 that correspond to the future superior crista, lateral crista, saccular macula, and posterior c

58 often appear to be wrapped around cristae or crista-like inner membrane invaginations.

59 orientations, but the lateral canal sensory crista looks like the "hemicrista" of some amphibians an

60 In addition to its canonical role in crista membrane structure, MIC60 regulates mitochondrial

61 s lateral organization and morphology of the crista membrane.

62 ular cristae or loss of cristae, and reduced crista membrane.

63 lation complex machinery most notably on the crista membranes.

64 proteins mitofilin and OPA1, which regulate crista morphology, and the outer membrane protein Sam50,

65 lateral utricular wall between the posterior crista (PC) and the utriculosaccular foramen.

66 nction experiments, we show that FGFs in the crista promote canal development by upregulating Bmp2.

67 sis requires a subtle form of Opa1-dependent crista remodeling that is induced by BH3-only proteins a

68 spond to the future superior crista, lateral crista, saccular macula, and posterior crista, as confir

69 easily identified and were present in every crista sampled.

70 he dual roles of MIC60 in both mitochondrial crista structure and motility position it as a crucial p

71 el cytoskeletal framework, and indicate that crista structure can be specialized for particular funct

72 Disruption of the crista structure has been implicated in a variety of car

73 Crista structure was polarized in that crista junctions,

74 he inner mitochondrial membranes to maintain crista structure.

75 and fuse inner membranes as well as maintain crista structures and propose a model for how the mitoch

76 dynamics, specifically in the maintenance of crista structures.

77 3 patients), other atrial scar (3 patients), crista terminalis (3 patients), and right atrioventricul

78 ardias and to define their relation with the crista terminalis (CT).

79 ena cave isthmus (IS) and either side of the crista terminalis (CT).

80 pulmonary veins (n=5), left atrium (n=2), or crista terminalis (n=3).

81 thin the SAN, failing to directly excite the crista terminalis and intraatrial septum.

82 It has been shown previously that the crista terminalis and its continuation as the eustachian

83 In six animals, zone 1 (crista terminalis and limbus) was ablated first, followe

84 ation distal to major branching sites of the crista terminalis and pectinate bundles, culminating in

85 ink-to-source effect at branch points of the crista terminalis and pectinate muscles is important in

86 atrium, especially in the trabeculae and the crista terminalis of the right atrial appendage.

87 eight of 35 focal ATs were located along the crista terminalis or tricuspid annulus.

88 hs could arise from a region parallel to the crista terminalis that is significantly larger (26.1 +/-

89 n three right atrial locations: (1) from the crista terminalis to the tricuspid annulus; (2) from the

90 the 3-D shift in caudal activation along the crista terminalis was more pronounced after RFA than dur

91 ral annulus, fossa ovalis, eustachian ridge, crista terminalis, and superior vena cava); or arm 3, st

92 trial node, from the initiation point to the crista terminalis, found that the action potential condu

93 usually due to foci in the pulmonary veins, crista terminalis, or left atrium.

94 s of specialized myofiber tracts such as the crista terminalis, pectinate muscles, and the Bachman bu

95 r muscle bundles of the atria, including the crista terminalis, pectinate muscles, limbus of the foss

96 ary vein (PV) in 3 patients, mitral annulus, crista terminalis, tricuspid annulus, and right-sided PV

97 of the right atrium and superior vena cava, crista terminalis, tricuspid valve isthmus, coronary sin

98 showed normal activation occurring near the crista terminalis.

99 ent had foci in both the pulmonary veins and crista terminalis.

100 ck or double potentials in the region of the crista terminalis.

101 l differences in the APD at junctions of the crista terminalis/pectinate muscle, pulmonary veins/left

102 id annulus; (2) from the fossa ovalis to the crista terminalis; and (3) from the inferior vena cava t

103 trial flutter have found linear block at the crista terminalis; this was thought to predispose the pa

104 al genesis zone adjacent to each prospective crista that corresponds to the Bone morphogenetic protei

105 cterized by high or multiple breaks over the crista, the ECG showed changes that depended on the init

106 at 11.5 dpc and was followed by the superior crista, the lateral crista, and the macula utriculi at 1

107 ing to the regions within which the anterior crista, the lateral crista, the utricle, the saccule, an

108 ole-tissue preparation of the rat vestibular crista, the sensory organ of the semicircular canals tha

109 ithin which the anterior crista, the lateral crista, the utricle, the saccule, and both the basilar p

110 three remaining sensory epithelia (posterior crista, utricle, and cochlea) that closely corresponds t

111 In the wild-type, the high-curvature edge of crista vesicles was densely populated with ATP synthase

112 ;Otx2(+/)- mutants revealed that the lateral crista was absent.

113 The posterior crista was the first organ to appear at 11.5 dpc and was

114 d in near-normal hair cells of the posterior crista, whereas the reduced utricular macula demonstrate

115 erve afferents close to the turtle posterior crista while efferent fibers were electrically stimulate

116 mall caudal patch within which the posterior crista will develop, and a larger anterior patch.