ライフサイエンスコーパス: ciliary ganglion

1 s of AChRs on autonomic motor neurons in the ciliary ganglion.

2 two kinds of neurons in the embryonic avian ciliary ganglion.

3 xcitatory synaptic transmission in the chick ciliary ganglion.

4 terminals on parasympathetic neurons in the ciliary ganglion.

5 using the calyx-type synapse of the chicken ciliary ganglion.

6 preganglionic parasympathetic outflow to the ciliary ganglion.

7 ing neuronal markers were found in the chick ciliary ganglion.

8 ng the calyx synapse isolated from the chick ciliary ganglion.

9 that regulate neuropeptide phenotype in the ciliary ganglion.

10 ons from the nasociliary nerve traversed the ciliary ganglion; a small number of varicose axons were

11 eural crest and placodal contribution to the ciliary ganglion and associated nerves.

12 as a trophic factor for motor neurons in the ciliary ganglion and spinal cord, leading to its evaluat

13 On the other hand, PSA synthesis in both the ciliary ganglion and the developing tectum appears to be

14 s a parasympathetic response mediated by the ciliary ganglion and we find that in Phox2b heterozygous

15 Misexpressing PSCA before cell death in the ciliary ganglion blocks alpha7-nAChR activation by nicot

16 day (E) 8, before neuronal cell loss in the ciliary ganglion, but increases >100-fold as the number

17 ependence and kinetic properties of stage 40 ciliary ganglion calcium currents were determined using

18 In the chick ciliary ganglion, calyx terminals from preganglionic neu

19 urrounded 80% of ciliary ganglion cells, but ciliary ganglion cell somata were unstained.

20 ctivities, the NPY-LI nerve fibers investing ciliary ganglion cells in the rhesus monkey are most lik

21 Most ciliary ganglion cells were TH-LI, but only a few were D

22 ctive (LI) nerve terminals surrounded 80% of ciliary ganglion cells, but ciliary ganglion cell somata

23 reactivity was detected in nerves contacting ciliary ganglion cells, the NPY-LI input to ciliary neur

24 ) are expressed in the parasympathetic chick ciliary ganglion (CG) and that BDNF-like protein is pres

25 The vertebrate ciliary ganglion (CG) is a relay station in the parasymp

26 AFK immunoreactivity was detected in ciliary ganglion (CG) lysates and neurons, and STI571 ap

27 expression during synapse formation in chick ciliary ganglion (CG) neurons developing in situ.

28 2+)-activated K(+) (K(Ca)) channels in chick ciliary ganglion (CG) neurons developing in vivo and in

29 ng neuronal death were investigated in chick ciliary ganglion (CG) neurons in vitro isolated from emb

30 2+-activated K+ currents (IK[Ca]) in chicken ciliary ganglion (CG) neurons is dependent in part on tr

31 a is not expressed in normal levels in chick ciliary ganglion (CG) neurons prior to synapse formation

32 ivated K+ channels (KCa) in developing chick ciliary ganglion (CG) neurons requires interactions with

33 2+)-activated K(+) channels (K(Ca)) in chick ciliary ganglion (CG) neurons requires interactions with

34 A-currents (IA) of chick ciliary ganglion (CG) neurons were blocked reversibly by

35 To test this hypothesis, ciliary ganglion (CG) neurons were cultured with or with

36 In parasympathetic ciliary ganglion (CG) neurons, activity mimicked by KCl

37 In chick parasympathetic ciliary ganglion (CG) neurons, alpha7-nAChRs are exclude

38 Ciliary ganglion (CG) neurons, like other neuronal popul

39 ptors or perisynaptic alpha7-nAChRs on chick ciliary ganglion (CG) neurons.

40 nd localization in the avian parasympathetic ciliary ganglion (CG) to determine whether these protein

41 This issue can be addressed in the avian ciliary ganglion (CG) which contains two cholinergic pop

42 tic vesicle protein (SVP) genes in the chick ciliary ganglion (CG).

43 Preganglionic motoneurons supplying the ciliary ganglion control lens accommodation and pupil di

44 St. 29, neurons and nonneuronal cells in the ciliary ganglion expressed the neural crest markers HNK-

45 y labeled by introducing tracer into the cat ciliary ganglion generally fell into two morphologic cat

46 In the avian ciliary ganglion, half the neurons are eliminated betwee

47 At cholinergic synapses in the chick ciliary ganglion, however, membrane formations and physi

48 reganglionic and postganglionic cells of the ciliary ganglion in different species of birds and mamma

49 The two populations of the ciliary ganglion innervate different targets: choroid ne

50 that the regulation of neuron number in the ciliary ganglion is a dynamic process involving both cel

51 The chick ciliary ganglion is a neural crest-derived parasympathet

52 to be largely unaffected indicating that the ciliary ganglion is exquisitely sensitive to a reduction

53 calyciform synapse in the embryonic chicken ciliary ganglion is mediated by two classes of nicotinic

54 ur data indicate that the innervation of the ciliary ganglion is more complex than previously thought

55 enesis has been well documented in the avian ciliary ganglion, it has not been clear whether cell dea

56 developmental regulation of PSA synthesis by ciliary ganglion motorneurons is not reflected in the le

57 e pharmacology of acetylcholine release from ciliary ganglion nerve terminals changes during developm

58 In the chick ciliary ganglion, neuronal number is kept constant betwe

59 On chick ciliary ganglion neurons alpha7-containing receptors are

60 identified functional receptors for CNTF on ciliary ganglion neurons and demonstrated the CNTF-speci

61 o protect nerve growth factor (NGF)-deprived ciliary ganglion neurons and hypoxic cortical neurons.

62 with the period of synapse formation between ciliary ganglion neurons and peripheral eye muscles.

63 a4, and alpha5 subunits are found in chicken ciliary ganglion neurons and some human neuroblastoma ce

64 ced by the same inhibitors in cultured chick ciliary ganglion neurons and suggests that the mediation

65 ing polypeptide (PACAP) are present on chick ciliary ganglion neurons and that receptor occupation in

66 e same calcium and kinase dependence seen in ciliary ganglion neurons and was absent in hippocampal s

67 Since all ciliary ganglion neurons are born prior to St. 29, these

68 2+)-activated K(+) channels (K(Ca)) in chick ciliary ganglion neurons are regulated by target-derived

69 During development, parasympathetic ciliary ganglion neurons arise from the neural crest and

70 and extends to homologous receptors on chick ciliary ganglion neurons as well.

71 NRTN promoted the outgrowth and survival of ciliary ganglion neurons at early embryonic (E) stages (

72 n were measured in acutely dissociated chick ciliary ganglion neurons at embryonic stages 34, 37, and

73 trast, activates CREB and gene expression in ciliary ganglion neurons both in culture and in situ onl

74 n of Ca2+ and K+ channels in embryonic chick ciliary ganglion neurons by somatostatin (Som) and opioi

75 with either TGFbeta1 or beta-neuregulin-1 in ciliary ganglion neurons developing in vitro.

76 functional Ca(2+)-activated K(+) currents in ciliary ganglion neurons developing in vivo is therefore

77 ression of Ca(2+)-activated K(+) currents in ciliary ganglion neurons developing in vivo, indicating

78 ression of Ca(2+)-activated K(+) currents in ciliary ganglion neurons developing in vivo.

79 Nicotine application to dissociated ciliary ganglion neurons diminished subsequent GABAA rec

80 Chick ciliary ganglion neurons express two major nAChR types:

81 amily members at nicotinic synapses on chick ciliary ganglion neurons in culture execute multiple fun

82 e receptors (nAChRs) on the surface of chick ciliary ganglion neurons in culture.

83 ing whole-cell patch-clamp analysis of chick ciliary ganglion neurons in situ, we show that the recep

84 nduces somatostatin-like immunoreactivity in ciliary ganglion neurons in vivo and in vitro, controls

85 localization at postsynaptic sites in avian ciliary ganglion neurons in vivo.

86 tor required for the development of K(Ca) in ciliary ganglion neurons is an isoform of beta-neureguli

87 opic Ca(2+)-activated K(+) currents in chick ciliary ganglion neurons is dependent on an avian orthol

88 On chick ciliary ganglion neurons the receptors are concentrated

89 rodent hippocampal interneurons and on chick ciliary ganglion neurons these alpha7-nAChRs are often c

90 te that target-derived GDNF is necessary for ciliary ganglion neurons to innervate ciliary muscle in

91 Single L-type calcium channels in chick ciliary ganglion neurons were studied at high current re

92 osphatidylinositol linkage (GPIalpha btx) in ciliary ganglion neurons with the retroviral vector RCAS

93 ted component drebrin, as do the clusters on ciliary ganglion neurons, but the clusters on preganglio

94 y a target tissue (iris) extract in cultured ciliary ganglion neurons, indicating that TGFbeta3 is an

95 In chick ciliary ganglion neurons, nicotinic acetylcholine recept

96 nd Ret, but not of GFRalpha2, in innervating ciliary ganglion neurons, the results also suggest that

97 of cell death in trophically deprived chick ciliary ganglion neurons, we hypothesized that early cel

98 -cell patch-clamp recording from dissociated ciliary ganglion neurons, we show that responses from al

99 te with filamentous actin, as do clusters on ciliary ganglion neurons, where the actin represents a s

100 Highest levels have been reported for chick ciliary ganglion neurons, where the postsynaptic recepto

101 stain for lipid raft components as found for ciliary ganglion neurons, where the rafts embed the rece

102 microheterogeneity on chick parasympathetic ciliary ganglion neurons-under one presynaptic terminal,

103 its neurotrophic activity on cultured chick ciliary ganglion neurons.

104 titute target-derived factors for developing ciliary ganglion neurons.

105 rated on somatic spines emanating from chick ciliary ganglion neurons.

106 ng receptors are excluded from such sites on ciliary ganglion neurons.

107 in at least one respect from that seen with ciliary ganglion neurons.

108 ta3, is also expressed in a target tissue of ciliary ganglion neurons.

109 al root ganglion neurons and parasympathetic ciliary ganglion neurons.

110 naptic transmission in the embryonic chicken ciliary ganglion occurs through the activation of two di

111 s a few early differentiating neurons to the ciliary ganglion, oculomotor nerve, and connecting branc

112 ated in the target and trajectory pathway of ciliary ganglion pioneer axons during the period of targ

113 The factors that promote the ciliary ganglion pioneer axons to grow toward their targ

114 dbrain/forebrain junction, precursors to the ciliary ganglion separate from the main migratory stream

115 In the chick ciliary ganglion such receptors generate large synaptic

116 l crest-derived precursors in the developing ciliary ganglion that can differentiate into neurons in

117 We used the avian ciliary ganglion to dissect the relative contributions o

118 d the calyx-type nerve terminal of the chick ciliary ganglion to examine which G-proteins are involve

119 be involved in the development of the avian ciliary ganglion, we identified 6 Gallus genes by their

120 lover of ACh at a model synapse in the chick ciliary ganglion, where ACh activates diffusely distribu

121 m cholinergic parasympathetic neurons in the ciliary ganglion, while trunk neural crest cells normall