ライフサイエンスコーパス: utricular

1 broadband inertial accelerometer, processing utricular acceleration signals to control the activity o

2 define the central projections of the gerbil utricular afferents by injecting horseradish peroxidase

3 to investigate the projections of individual utricular afferents by injecting HRP intracellularly int

4 Individual utricular afferents collateralize extensively, projectin

5 We found that utricular afferents in the gerbil projected to all divis

6 transcriptomes for 301 single cells from the utricular and cochlear sensory epithelia of newborn mice

7 perch were found, including expansion of the utricular and lagenar otoliths, close proximity between

8 Thresholds were similar for utricular and saccular afferents, as well as for lateral

9 sal across the striola is absent in both the utricular and saccular maculae.

10 r shows regions of homology to the zebrafish utricular and saccular maculae.

11 tely innervate the peristriolar zones of the utricular and saccular maculae.

12 The central projections of the utricular and saccular nerve in macaques were examined u

13 the ventral DON and TON receive principally utricular and semicircular canal afferents.

14 entral DON, and ventral MgON) receive mainly utricular and semicircular canal inputs, suggesting vest

15 When we cultured utricular epithelia from chickens, we found that cellula

16 to the cultures significantly inhibited the utricular epithelial cell proliferation.

17 The cultured utricular epithelial cells expressed exclusively epithel

18 , immunostainings revealed that the cultured utricular epithelial cells expressed FGF and IGF-1 recep

19 wth factors on the proliferation of pure rat utricular epithelial cells in culture.

20 actor (EGF), stimulated proliferation of the utricular epithelial cells.

21 eripheral epithelial cells, was confirmed in utricular epithelial sheet cultures.

22 Utricular epithelial sheets were separated and partially

23 Utricular fibers coursed through ventral parts of the ce

24 In the tangential nucleus, utricular fibers formed a few large axosomatic terminals

25 In addition, utricular fibers projected to regions in the vestibular

26 Although utricular hair cells differ in their rates and extent of

27 Furthermore, we show that utricular hair cells from STAT1-deficient mice are resis

28 We expressed the mutant myosin-1c in utricular hair cells of transgenic mice, delivered an AD

29 cells expressed FGF and IGF-1 receptors, and utricular hair cells produced FGF-2 in vivo.

30 In perforated-patch recordings from rat utricular hair cells, immature hair cells [younger than

31 orting cells in extrastriolar regions of the utricular macula and in the canal ampullae, with weaker

32 of the posterior crista, whereas the reduced utricular macula demonstrates weak miR-183 expression an

33 igated in the human vestibular endorgan, the utricular macula, using postmortem specimens from indivi

34 nt from supporting cell gap junctions of the utricular macula.

35 cells in the basilar papilla but not in the utricular macula.

36 y were restricted to a region in or near the utricular macula.

37 fferents in the medial part of the adult rat utricular macula.

38 nd biotinylated dextran amine (BDA) into the utricular macula; and 2) to investigate the projections

39 ted in the chinchilla cristae ampullaris and utricular maculae at the light and electron microscopy l

40 ads to impaired vestibular function in which utricular maculae fail to develop and the utricular otol

41 showed that an initial loss of hair cells in utricular maculae is followed by significant recovery in

42 known to be required for development of the utricular maculae, is expressed downstream of hmx2 and h

43 In contrast, the utricular nerve projects more rostrally into areas of kn

44 nciple brainstem areas of termination of the utricular nerve were the lateral/dorsal medial vestibula

45 rojections of primary afferent fibers in the utricular nerve, which convey linear head acceleration s

46 rainstem area innervated by the whole of the utricular nerve.

47 e was injected directly into the saccular or utricular neuroepithelium of fascicularis (Macaca fascic

48 intracellularly into functionally identified utricular neurons.

49 uroepithelium and occasional malformation of utricular otoconia.

50 Other than the utricular otolith deficiency, all structures in the ear

51 ch utricular maculae fail to develop and the utricular otolith gradually fuses with the saccular otol

52 ifically perturbs formation of the anterior (utricular) otolith in the developing ear.

53 llifer-group sciaenid, both the saccular and utricular otoliths are enlarged relative to those in oth

54 Roughly half of such chimeras formed utricular otoliths normally, indicating that the transpl

55 h there is extensive overlap of saccular and utricular projections, saccular inputs to the lateral po

56 Here we show that the adult utricular sensory epithelium contains cells that display

57 that an elastic force opposes growth of the utricular sensory epithelium during development, confine

58 mulation and/or aminoglycoside damage in the utricular sensory epithelium of the adult rat.

59 which +/+ cells formed support cells in the utricular sensory epithelium were rescued.

60 s of capillaries located in the normal human utricular stroma showed vascular endothelial cells with

61 term cultures showed that only a few mitotic utricular supporting cells became calretinin positive.

62 ion also facilitated conversion of postnatal utricular supporting cells into hair cells.

63 ssion is weak and restricted to saccular and utricular supporting cells.

64 In addition, small utricular terminals contacted numerous dendrites and a f

65 apping and other methods to demonstrate that utricular type II vestibular hair cells undergo turnover

66 is a small organ lying in the ventrolateral utricular wall between the posterior crista (PC) and the

67 , and, in some cases, a small portion of the utricular wall.

68 semicircular canals and to the ampullary and utricular walls.