ライフサイエンスコーパス: calyces

1 t in processes originating from the necks of calyces.

2 er processes, intramacular nerve fibers, and calyces.

3 rom afferent nerve fibers and basal parts of calyces.

4 both slow and rapid forms of endocytosis at calyces.

5 dy, including a giant neuron innervating the calyces.

6 c insects its mushroom bodies possess robust calyces.

7 eruli that characterize insect mushroom body calyces.

8 ntennal lobes and attenuation or loss of the calyces.

9 te as those of mushroom bodies equipped with calyces.

10 f the two Kenyon cell populations of the two calyces.

11 of the pedunculus and the basal ring of the calyces.

12 d the organization of their terminals in the calyces.

13 ink many regions of the protocerebrum to the calyces.

14 s represent zones of afferent endings in the calyces.

15 control), agave DF (ADF) or ADF with jamaica calyces (ADF-JC).

16 The expression of h-alpha-synA53Tin calyces also inhibited vesicle replenishment to the read

17 Recordings from dissociated calyces and afferent endings revealed large K+ conductan

18 pectively), lobulated kidneys with prominent calyces and diabetes mellitus (diagnosed at ages 33 and

19 transitional epithelium that lines the renal calyces and pelvis, ureters, and bladder.

20 responsible of the intense red color of the calyces, and have potential as natural colorants for foo

21 tency (jitter) was increased in VCN neurons, calyces, and MNTB neurons of -/- mice compared with +/+

22 the lateral protocerebrum, the mushroom body calyces, and the lobula complex.

23 s from adjacent Kenyon cell dendrites in the calyces are adjacent in the lobes even after their polar

24 and intrinsic neurons (Kenyon cells) in the calyces are arranged according to polar coordinates.

25 se to MACs and synapses and hypothesize that calyces are composed of multiple activity modules, each

26 orescent tracer injections revealed that the calyces are exclusively supplied by visual neurons from

27 alin, though the overall architecture of the calyces are very different.

28 cies that generally lack antennal lobes, the calyces are vestigial or absent.

29 ushroom bodies, the primary input region, or calyces, are predominantly supplied by olfactory project

30 Feedback pathways to the calyces arise from satellite neuropils adjacent to the m

31 stibular periphery, staining was observed in calyces around type I hair cells, at the synaptic pole o

32 gonia, featuring highly inflated, five-lobed calyces, as a newly identified species of the derived, d

33 SV release in postnatal day (P) 16-19 mouse calyces, as their release properties resemble mature cal

34 ded whole-cell responses from hair cells and calyces at room temperature and body temperature.

35 plies sparse immunoreactive processes to the calyces' basal ring, collar, and lip.

36 Inhibition of GABAergic signaling in the MB calyces, but not in the lobes, impairs patterning discri

37 senting one of three concentric zones of the calyces, called the lip, collar, and basal ring.

38 A region immediately beneath the calyces, called the neck, is invaded by these neurons as

39 ches that were presynaptic to type II cells, calyces, calyceal processes, and other nerve fibers in t

40 n of nicotine induced inward currents in the calyces capable of generating action potentials that ove

41 t mushroom bodies possesses a pair of simple calyces comprising two populations of Kenyon cells, the

42 tional and structural data showed that young calyces could form within 2 d, well before the onset of

43 rinary tract, namely the ureter, pelvis, and calyces, could be depicted with radiography.

44 We show that rat vestibular calyces express an unusual mix of voltage-gated Na and K

45 Calyces express presynaptic glycine receptors whose acti

46 y 11 (P11), and before the onset of hearing, calyces expressed high levels of ionotropic GABA(A) rece

47 alization and distention of the nondependent calyces for definitive renal access with an 18-gauge 5-F

48 ergic feedback neurons from the lobes to the calyces for nonelemental learning.

49 The ATP-independent endocytosis occurred at calyces from postnatal days 8-15, suggesting its existen

50 patches excised from the nonsynaptic face of calyces, GABA and glycine evoked single-channel currents

51 Results showed that calyces had 1) vesiculated, spine-like processes that in

52 time of the receptor potential and (2) some calyces had nonquantal transmission with little synaptic

53 s even after their polar arrangements in the calyces have been transformed to rectilinear arrangement

54 ch in fructans and insoluble DF, and jamaica calyces (Hibiscus sabdariffa), which is rich in DF and p

55 esses invades all zones of the mushroom body calyces in Periplaneta.

56 ke structures characterize the mushroom body calyces in the brains of certain species of insects; we

57 nsgenically or dialyzed in the short term in calyces, inhibited two of the most common forms of endoc

58 Afferent terminals segment the calyces into discrete zones, I, II, III, and IIIA, which

59 ted release time course found in posthearing calyces is not known.

60 dilatation of the ureter, renal pelvis, and calyces might be seen.

61 We report the presence in calyces of an atypical arrangement of subcellular organe

62 naptic afferents, which grow rapidly to form calyces of Held and to establish mono-innervation betwee

63 These data indicate that calyces of Held follow a noncanonical program to establi

64 Here we confirm that RRPs at calyces of Held from 14 to 21 day old mice have a fixed

65 axonal endings of bushy cells at MNTB cells (calyces of Held), and MNTB neurons of Kcna1-null (-/-) m

66 Interestingly, the parent cell bodies of the calyces of Held, the globular bushy cells of the cochlea

67 as their release properties resemble mature calyces of Held.

68 rminating in large synaptic endings known as calyces of Held.

69 In addition, the calyces of Hymenoptera receive substantial direct input

70 that are comparable to those observed in the calyces of insect mushroom bodies and which characterize

71 ganization of afferent neurons supplying the calyces of the cockroach Periplaneta americana.

72 We describe visual inputs to the calyces of the mushroom bodies of the honeybee Apis mell

73 nnections between the antennal lobes and the calyces of the mushroom bodies.

74 eral protocerebrum and, collaterally, to the calyces of the mushroom body.

75 rve fibers and their large afferent endings (calyces) on type I hair cells branch.

76 Convergence of developing calyces onto postsynaptic targets, indicative of competi

77 When calyces or ciliary neurons were labeled en mass with neu

78 We found that essentially all vesicles in calyces participated in recycling, challenging the small

79 tional plan of the insect mushroom body into calyces, peduncle, and lobes is maintained, as is the ar

80 ry beta4 Na(+) channel subunit into immature calyces (postnatal day 5-6) induced an increase in I(NaR

81 In immature hair cells and calyces (postnatal days (P)1-P4), tuning sharpened at ea

82 to be higher olfactory centers because their calyces receive abundant collaterals of projection neuro

83 synaptically released glutamate at immature calyces, resulting in significant desensitization.

84 postnatal ages (15-17 d after birth) LES rat calyces showed prolonged spike latencies, indicative of

85 uilana alone, or in combination with jamaica calyces, shows promising potential as a bioactive ingred

86 rain possesses a mushroom body equipped with calyces supplied by olfactory projection neurons.

87 Kenyon cells providing dendrites to the calyces supply a pedunculus and lobes divided into subdi

88 d NL, whereas trkB is expressed in the nerve calyces surrounding NM neurons and in the ventral, but n

89 The afferent calyces that innervate type I hair cell, and the basolat

90 ques to record currents in large presynaptic calyces that midbrain neurons form on ciliary neurons.

91 orm large cup-shaped postsynaptic terminals (calyces) that envelope the basolateral surfaces of type

92 ilar at P13 in the parent-cell bodies of the calyces, the bushy cells of the cochlear nucleus.

93 No other sensory inputs reach the calyces, thereby showing a complete switch of calyx moda

94 polar arrangements of their dendrites in the calyces to laminar arrangements of their terminals in th

95 -to-one signal transmission from presynaptic calyces to postsynaptic MNTB neurons and induced extra p

96 -to-one signal transmission from presynaptic calyces to postsynaptic MNTB neurons.

97 Axons from the annular zones of both calyces together provide a sleeve of axons that ensheath

98 sive asynchronous release in Cplx1-deficient calyces triggered aberrant action potentials in their ta

99 er-order cognitive processing (mushroom body calyces) versus peripheral sensory processing (optic and

100 Endocytosis at dynamin 1 KO calyces was the same as in wild type after weak stimuli,

101 predominantly at single active zones in rat calyces, we found that single active zones contained 5-2

102 ic diameter of greater than 3 cm and dilated calyces, we lean more towards surgical intervention.

103 While normal calyces were able to fire APs without failures at impres

104 iteria were developed to classify cells when calyces were not present, as in cultures and neonatal or

105 gth of dendrites in the collar region of the calyces were strongly correlated with worker age, but wh

106 ures at impressive rates of up to 1 kHz, LES calyces were unable to do so.

107 pally after infusion of its dried sepals and calyces, which are usually discarded.

108 In contrast, labeling the calyces with a water-soluble dye by diffusion through th

109 ain sensory input regions are large, doubled calyces with modality-specific, distinct sensory neuropi