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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 topically between the anterior and posterior maculae.
8 striolar zones of the utricular and saccular maculae.
9 of epithelial cells surrounding the sensory maculae.
12 nued expression and activation of CaMK-II in maculae and cristae in older embryos suggests continued
14 preferential expression in central zones of maculae and cristae, which are innervated by phasic neur
15 ging in age from 21 to 81 years with healthy maculae and in 9 healthy eyes known to be at high-risk o
16 ely one quarter of older adults with healthy maculae and in more than half of persons with early to i
17 localized at the cell surfaces in junctional maculae and showed the same cell-type specific distribut
19 at Type I hair cells in the avian vestibular maculae are immunoreactive for the extracellular matrix
22 chinchilla cristae ampullaris and utricular maculae at the light and electron microscopy level with
24 sensory patches are not completely separate maculae because they lie within a less densely populated
25 highly expressed and was localized to dense maculae; cadherins were not detected in cell-cell contac
26 secondary procedure compared with eyes whose maculae detached (0.29 logMAR VA [Snellen equivalent, 20
28 phological findings support the concept that maculae dynamically preprocess linear acceleratory infor
29 tibular sensory organs of the inner ear, the maculae, exhibit a line of polarity reversal (LPR) acros
30 aired vestibular function in which utricular maculae fail to develop and the utricular otolith gradua
31 Here we describe the development of sensory maculae in juvenile fish and the morphology of the adult
32 transformed a simple ear with few vestibular maculae into a complex three-dimensional structure consi
33 t an initial loss of hair cells in utricular maculae is followed by significant recovery in the numbe
35 ined with uranyl acetate appeared to contain maculae occludentes rather than zonulae occludentes.
36 X3CR1 protein expression was observed in the maculae of AMD eyes bearing T/M280 compared with the con
37 X3CR1 transcripts were not detectable in the maculae of AMD eyes bearing T/M280; however, transcripts
38 pment also was induced and analyzed in eight maculae of four macaque monkeys with laser parameters pr
39 0; however, transcripts were detected in the maculae of normal eyes bearing T/T280 or T/M280 as well
40 rovascular tissues (FVT) were elicited in 12 maculae of seven squirrel monkeys by laser photocoagulat
43 estricted to only one side of the LPR in the maculae or one of the two sibling HCs in neuromasts.
44 ti-cell model of the normal and pathological maculae recapitulate the three growth patterns, under th
45 normal formation of the otocyst and sensory maculae, specific secretion and localization of extracel
47 pectrum of changes ranging from erythematous maculae to vascular tumors, by the presence of spindle a
48 ut the stroma of the cristae ampullaris, the maculae utricle, and saccule in the human and mouse.
49 of 20 subjects aged 19-29 years with normal maculae were imaged using a research adaptive optics sca
50 halmoscope (cSLO) AF fundus images of normal maculae were obtained from both eyes of 10 middle-aged s
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