ライフサイエンスコーパス: maculae

1 is absent in both the utricular and saccular maculae.

2 e cristae, type II HCs predominate in monkey maculae.

3 logy to the zebrafish utricular and saccular maculae.

4 ngement of three canals and several separate maculae.

5 ablation of all hair cells from the saccular maculae.

6 e presumed to represent saccular and lagenar maculae.

7 giography for comparison with the pathologic maculae.

8 topically between the anterior and posterior maculae.

9 striolar zones of the utricular and saccular maculae.

10 of epithelial cells surrounding the sensory maculae.

11 Maculae (4-mm diameter) from donor eyes free of ocular d

12 Otoliths and otoconia form over sensory maculae and are attached to the otolithic membrane, a ge

13 nued expression and activation of CaMK-II in maculae and cristae in older embryos suggests continued

14 nd, in some, development of sensory patches (maculae and cristae).

15 preferential expression in central zones of maculae and cristae, which are innervated by phasic neur

16 ging in age from 21 to 81 years with healthy maculae and in 9 healthy eyes known to be at high-risk o

17 ely one quarter of older adults with healthy maculae and in more than half of persons with early to i

18 localized at the cell surfaces in junctional maculae and showed the same cell-type specific distribut

19 he striola and extrastriola in otolith organ maculae, and the central and peripheral zones in semicir

20 mate their density in different areas of the maculae, and to perform hair cell counts.

21 at Type I hair cells in the avian vestibular maculae are immunoreactive for the extracellular matrix

22 uity response to medical therapy and thicker maculae at 6 months.

23 hich had borderline worse vision and thicker maculae at baseline, showed larger CST reductions after

24 d abdominal aortic endothelia in the form of maculae at cell-cell appositions.

25 chinchilla cristae ampullaris and utricular maculae at the light and electron microscopy level with

26 aring T/T280 or T/M280 as well as in the AMD maculae bearing T/T280.

27 sensory patches are not completely separate maculae because they lie within a less densely populated

28 highly expressed and was localized to dense maculae; cadherins were not detected in cell-cell contac

29 secondary procedure compared with eyes whose maculae detached (0.29 logMAR VA [Snellen equivalent, 20

30 n may maintain positional information in the maculae during sensory regeneration.

31 phological findings support the concept that maculae dynamically preprocess linear acceleratory infor

32 tibular sensory organs of the inner ear, the maculae, exhibit a line of polarity reversal (LPR) acros

33 aired vestibular function in which utricular maculae fail to develop and the utricular otolith gradua

34 Human donor maculae from controls (n = 99), early AMD (n = 35), or c

35 Here we describe the development of sensory maculae in juvenile fish and the morphology of the adult

36 transformed a simple ear with few vestibular maculae into a complex three-dimensional structure consi

37 t an initial loss of hair cells in utricular maculae is followed by significant recovery in the numbe

38 organization of hair cells in the vestibular maculae is unique because these sensory organs contain t

39 be required for development of the utricular maculae, is expressed downstream of hmx2 and hmx3.

40 mean difference, -3.1 letters) and a thicker maculae (mean difference, +26 mum) at baseline than thos

41 ined with uranyl acetate appeared to contain maculae occludentes rather than zonulae occludentes.

42 We imaged 135 maculae of 89 pediatric patients using the standard Spec

43 X3CR1 protein expression was observed in the maculae of AMD eyes bearing T/M280 compared with the con

44 X3CR1 transcripts were not detectable in the maculae of AMD eyes bearing T/M280; however, transcripts

45 pment also was induced and analyzed in eight maculae of four macaque monkeys with laser parameters pr

46 0; however, transcripts were detected in the maculae of normal eyes bearing T/T280 or T/M280 as well

47 rovascular tissues (FVT) were elicited in 12 maculae of seven squirrel monkeys by laser photocoagulat

48 The vestibular maculae of the inner ear contain sensory receptor hair c

49 In addition, the maculae of the utricle and saccule were partially fused.

50 ut for linear head translations (detected by maculae of the utricle and saccule).

51 Cryosections were cut from the maculae of unfixed human donor eyes with AMD or from age

52 stibular sensory epithelia of mammals to the maculae of zebrafish.

53 estricted to only one side of the LPR in the maculae or one of the two sibling HCs in neuromasts.

54 ti-cell model of the normal and pathological maculae recapitulate the three growth patterns, under th

55 ical coherence tomography (OCT) scans of the maculae revealed a characteristic change in the photorec

56 normal formation of the otocyst and sensory maculae, specific secretion and localization of extracel

57 In vestibular maculae, staining gradients are: striolar > extrastriola

58 pectrum of changes ranging from erythematous maculae to vascular tumors, by the presence of spindle a

59 ut the stroma of the cristae ampullaris, the maculae utricle, and saccule in the human and mouse.

60 stinct hair and supporting cell types in the maculae versus cristae.

61 In the maculae, we identify two subtypes of hair cells that sha

62 Normal and pathologic maculae were imaged in vivo using still and video HMM le

63 of 20 subjects aged 19-29 years with normal maculae were imaged using a research adaptive optics sca

64 halmoscope (cSLO) AF fundus images of normal maculae were obtained from both eyes of 10 middle-aged s

65 generated within the striola regions of the maculae, were absent, indicating that NOTCH1 is critical

66 phrenia were associated with thinner overall maculae, while controlling for confounding factors (b =

67 nisms in hair cells on opposite sides of the maculae, with EMX2-mediated repression of Stk32a determi