ライフサイエンスコーパス: sensory epithelia

1 ntly expressed in terminally differentiating sensory epithelia.

2 rsor cell differentiation in avian inner ear sensory epithelia.

3 eural gene atonal, is expressed in inner ear sensory epithelia.

4 ere identified which were not within defined sensory epithelia.

5 the supporting cell layer in the vestibular sensory epithelia.

6 re present in normal auditory and vestibular sensory epithelia.

7 blished role for support cells in vertebrate sensory epithelia.

8 mbryos, including posterior otoliths and all sensory epithelia.

9 nd the production of new hair cells in adult sensory epithelia.

10 s in the early otic epithelium and inner ear sensory epithelia.

11 y in space and contain intricately patterned sensory epithelia.

12 fferent physical media and entirely separate sensory epithelia.

13 ly localized in avian and mammalian auditory sensory epithelia.

14 ransition that reliably yields new polarized sensory epithelia.

15 cortical actin belts than those in embryonic sensory epithelia.

16 s of GJC between the auditory and vestibular sensory epithelia.

17 ory structures, including olfactory bulb and sensory epithelia.

18 yte subtypes in normal posthatch chicken ear sensory epithelia.

19 rate-specific Hmx activities to regulate the sensory epithelia.

20 s that regulate the overall formation of the sensory epithelia.

21 ypes of hair cells are present in vestibular sensory epithelia.

22 mal and drug-damaged auditory and vestibular sensory epithelia.

23 tal expression of espin in chicken inner ear sensory epithelia.

24 tected in supporting cells of the vestibular sensory epithelia.

25 ons is replaced during metamorphosis in both sensory epithelia.

26 ndle hair cells in the peripheral regions of sensory epithelia.

27 for both the structure and function of these sensory epithelia.

28 present in both sensory ganglion neurons and sensory epithelia.

29 om nonsensory regions, the hair cells of the sensory epithelia accumulate class III beta-tubulin, whe

30 a cellular mosaic similar to the endogenous sensory epithelia and expansion of the sensory mosaic th

31 lf inhibited DNA synthesis in the vestibular sensory epithelia and failed to potentiate the effects o

32 manipulation of the regenerative program in sensory epithelia and other vertebrate neuroepithelia.

33 icted expression, confined mainly to the pro-sensory epithelia and the neural processes from the coch

34 ouse inner ear - the vestibular and cochlear sensory epithelia and the spiral ganglion - by measuring

35 hd7-deficient mice or whether the vestibular sensory epithelia and their associated innervation and f

36 is localized to the vestibular and cochlear sensory epithelia and to the spiral ganglions.

37 ted DNA synthesis in vestibular and auditory sensory epithelia and was not cytotoxic at the concentra

38 HC proteome with other IE subproteomes from sensory epithelia and whole IE.

39 sable for basal body docking in otic vesicle sensory epithelia and, surprisingly, short cilia form in

40 n the saccular otoliths, two-planar saccular sensory epithelia, and a unique orientation pattern of s

41 However, competence to form sensory epithelia appears to be limited to discrete regi

42 The most common leukocytes in inner ear sensory epithelia are ramified cells of the myeloid line

43 te-positive territory from which most of the sensory epithelia arise.

44 e cell proliferation in adult rat vestibular sensory epithelia, as does the infusion of transforming

45 t several classes of supporting cells in the sensory epithelia, as well as Schwann cells and satellit

46 do not reside in normal or drug-damaged ear sensory epithelia at 1-3 days post insult but are presen

47 neurons may modulate afferent pathways from sensory epithelia at the periphery.

48 t-1 in differentiating inner ear neurons and sensory epithelia cells, perhaps in the specification of

49 Inner ear sensory epithelia contain mechanosensitive hair cells th

50 ession in developing auditory and vestibular sensory epithelia correlates with maturation of hair cel

51 o we investigated the effect of forskolin on sensory epithelia cultured from the ears of mammals.

52 important, the NSCs can incorporate into the sensory epithelia, demonstrating their therapeutic poten

53 epigenetic status of the Atoh1 locus during sensory epithelia development in the mouse.

54 The remaining sensory epithelia display a dense pattern of cProx1 expr

55 9 AChR expression in cochlear and vestibular sensory epithelia during neonatal development.

56 unctional maturation of hair cells in intact sensory epithelia excised from the inner ears of embryon

57 gun-mediated transfection of mouse inner ear sensory epithelia explants shows selective accumulation

58 ting the type I hair cells of the vestibular sensory epithelia form distinct calyceal synapses.

59 he transcriptomes of auditory and vestibular sensory epithelia from early postnatal mice.

60 The label densities of sensory epithelia from experimental preparations of ampu

61 and mechanical methods were used to isolate sensory epithelia from mature chick basilar papillae, an

62 rt the stepwise differentiation of inner ear sensory epithelia from mouse embryonic stem cells (ESCs)

63 It is unclear how to develop these sensory epithelia from pluripotent stem cells, a process

64 Small pieces of sensory epithelia from the chicken utricle were cultured

65 specific miRNAs might influence formation of sensory epithelia from the primitive otic neuroepitheliu

66 Lgr5(+) progenitor cells from the sensory epithelia gave rise to hair cell-like cells, but

67 In isolated sensory epithelia, however, caspase inhibitors did not a

68 faces of sensory and supporting cells in all sensory epithelia in a pattern that correlates with the

69 r to the possibility of repopulating damaged sensory epithelia in humans.

70 r hair cell differentiation in all hair cell sensory epithelia in the chicken.

71 f GJ distribution in auditory and vestibular sensory epithelia in the different vertebrate classes.

72 and establishment of neuronal projections to sensory epithelia in the embryonic inner ear, but their

73 small RNAs in development and maturation of sensory epithelia in the mouse inner ear will be conside

74 n-2) localize to tTJs of the sensory and non-sensory epithelia in the organ of Corti and vestibular e

75 dles when situated in cochlear or vestibular sensory epithelia in vivo.

76 d in both the CNS and PNS as well as in many sensory epithelia including the developing inner ear epi

77 Cells derived from these sensory epithelia, including migrating GnRH neurons and

78 mRNA was first observed in HCs at E16 in all sensory epithelia, increased to its highest levels by P0

79 rant receptor (Or) gene are scattered across sensory epithelia, intermingled with neurons that expres

80 Hair cells differentiate only in sensory epithelia known or proposed to have a lineage re

81 of Atoh1 is sufficient to establish ectopic sensory epithelia, making Atoh1 a good candidate for gen

82 te are known to be present in the vestibular sensory epithelia of a variety of species, the functiona

83 egulated and alpha6 was downregulated in the sensory epithelia of both the auditory and vestibular sy

84 In developing auditory and vestibular sensory epithelia of Brn-3c-/- mice, hair cells are foun

85 he progression of recovery of the vestibular sensory epithelia of guinea pigs after gentamicin-induce

86 llulin becomes mislocalized in the inner ear sensory epithelia of ILDR1 null mice after the first pos

87 single cells from the utricular and cochlear sensory epithelia of newborn mice to circumvent this cha

88 Leukocytes reside in undamaged sensory epithelia of the avian inner ear and increase in

89 ridization within areas corresponding to the sensory epithelia of the cochlea and vestibular systems

90 Genotypically mutant HCs were found in all sensory epithelia of the inner ear at all ages examined.

91 bution and size of gap junctions (GJ) in the sensory epithelia of the inner ear have been examined in

92 et-1 becomes up-regulated in the presumptive sensory epithelia of the inner ear in regions that are d

93 ic of hair cells and supporting cells in the sensory epithelia of the inner ear is regulated by Notch

94 Sensory epithelia of the inner ear require a coordinated

95 Grxcr1 is expressed in sensory epithelia of the inner ear, and its encoded prot

96 hair cells and supporting cells comprise the sensory epithelia of the inner ear.

97 bition to eliminate patterning errors in the sensory epithelia of the inner ear.

98 At E15.5, Six1 is expressed in all sensory epithelia of the inner ear.

99 omal cells underneath the non-immunoreactive sensory epithelia of the macula utricle, sacule, and cri

100 CP) proteins are distributed normally in the sensory epithelia of the mutants, suggesting that PCDH15

101 Wnt1-Cre labeled cells are localized within sensory epithelia of the saccule, utricle and cochlea th

102 antigen occurred in both the nonsensory and sensory epithelia of the sacculus.

103 missing ampullae, structures that house the sensory epithelia of the semicircular canals.

104 us perception is achieved by associating the sensory epithelia of the three mechanoreceptor organs, t

105 ic miR-183 expression in the three remaining sensory epithelia (posterior crista, utricle, and cochle

106 identify genes expressed in the regenerating sensory epithelia (SE) of the chicken inner ear.

107 ototoxic antibiotics were used to damage the sensory epithelia (SE).

108 ion, in many nonmammalian vertebrates, these sensory epithelia show remarkable regenerative potential

109 Afferent innervation of the ear sensory epithelia shows numerous fibers overshooting the

110 division in cultured auditory and vestibular sensory epithelia taken from posthatch chickens.

111 sicles develop into inner ear organoids with sensory epithelia that are innervated by sensory neurons

112 The inner ear contains sensory epithelia that detect head movements, gravity an

113 In the vestibular sensory epithelia, the virus transduced large numbers of

114 ceptor protein and projects an axon from the sensory epithelia to an olfactory bulb glomerulus, which

115 nt study used cultures of isolated inner ear sensory epithelia to identify cellular signals that regu

116 ts of stereocilia, was used to delineate the sensory epithelia, to visualize the distribution of hair

117 It is debatable whether the sensory epithelia underwent progressive segregation or e

118 In the inner ear, cochlear and vestibular sensory epithelia utilize grossly similar cell types to

119 Decreased innervation to vestibular sensory epithelia was detected at E13.5-15, when progres

120 The ability of atoh1a to induce ectopic sensory epithelia was maximal when activated during plac

121 onfocal microscopy of immunostained cochlear sensory epithelia, was coupled with a corresponding func

122 lated tissues, chick auditory and vestibular sensory epithelia, we find that glycolytic enzymes are e