ライフサイエンスコーパス: sympathetic ganglia

1 are reciprocally expressed in rat brain and sympathetic ganglia ().

2 neural crest-derived cells from the gut and sympathetic ganglia.

3 lly along the sympathetic trunk to innervate sympathetic ganglia.

4 All three genes are expressed in peripheral sympathetic ganglia.

5 ations in the ganglionic neurons of bullfrog sympathetic ganglia.

6 vertebral celiac/superior mesenteric (C/SMG) sympathetic ganglia.

7 as formed in the adrenal gland and preaortic sympathetic ganglia.

8 gnate 3.1 kb mRNA is highly enriched in frog sympathetic ganglia.

9 o by nonneuronal cells neighboring embryonic sympathetic ganglia.

10 ion of Lin28B and Let-7a in developing chick sympathetic ganglia.

11 ion potentials was tested in intact bullfrog sympathetic ganglia.

12 by E8 are more than 100-fold higher than in sympathetic ganglia.

13 ic axonal ingrowth from the spinal cord into sympathetic ganglia.

14 of activated Ret in neuroblastoma cells and sympathetic ganglia.

15 with hyperplastic lesions in early postnatal sympathetic ganglia.

16 differentiate into metameric dorsal root and sympathetic ganglia.

17 ession in the brain, the spinal cord and the sympathetic ganglia.

18 Ang II directly activates neurones in sympathetic ganglia.

19 ological role of hand2 in the development of sympathetic ganglia.

20 by N-cadherin, coordinate to sculpt discrete sympathetic ganglia.

21 of elavl3 (HuC) is not reduced in hands off sympathetic ganglia.

22 luding the branchial arches, dorsal root and sympathetic ganglia.

23 catecholaminergic and cholinergic neurons in sympathetic ganglia.

24 ects in condensing cranial sensory and trunk sympathetic ganglia.

25 the trunk of host chick embryos colonise the sympathetic ganglia.

26 +) NCCs to contribute to sensory rather than sympathetic ganglia.

27 ventral horn, in dorsal root ganglia, and in sympathetic ganglia.

28 sed, as was the amount of NT3 present within sympathetic ganglia.

29 ic development, it is strikingly absent from sympathetic ganglia.

30 incident with BMPR-IB mRNA expression in the sympathetic ganglia.

31 cillators regulate synaptic amplification in sympathetic ganglia.

32 analysis of rapidly frozen neurons from frog sympathetic ganglia.

33 ly reconstructed nerve terminals in bullfrog sympathetic ganglia.

34 s studied in preparations of bullfrog lumbar sympathetic ganglia 7-10 and the dorsal aorta.

35 from isolated preparations of paravertebral sympathetic ganglia 9 and 10.

36 unoreactivity (SN-LI) was studied in the rat sympathetic ganglia/adrenal gland, enteric and sensory g

37 rophy in diabetic or age-matched control rat sympathetic ganglia after 7 or 10 months of continuous a

38 opment, sympathetic axons grow from thoracic sympathetic ganglia along rib periosteum to reach the st

39 how that this pathway is conserved, as human sympathetic ganglia also contain SAMs expressing the ana

40 renal medulla, enlargement of the associated sympathetic ganglia and a male reproductive defect.

41 NB develops in sympathetic ganglia and adrenal medulla and is elicited

42 in neuroblastoma (NB), a childhood tumor in sympathetic ganglia and adrenal medulla.

43 lop profound neuroglial hyperplasia of their sympathetic ganglia and adrenal medullae.

44 rom bullfrog (Rana catesbiana) paravertebral sympathetic ganglia and characterized functional propert

45 Sequencing of cDNA from human sympathetic ganglia and colon revealed processed transcr

46 nscription factor is expressed in neurons of sympathetic ganglia and has previously been shown to ind

47 NAD did not develop in diabetic ZDF rat sympathetic ganglia and ileal mesenteric nerves as asses

48 Sympathetic ganglia and innervation of target tissues ap

49 The elk1 gene is expressed in sympathetic ganglia and is also expressed in sciatic ner

50 ent, PSS1 is transiently expressed in lumbar sympathetic ganglia and is detectable at low levels thro

51 adipose tissue (SAT) via its actions both on sympathetic ganglia and on the SAT itself.

52 3+ neurons that populate the dorsal root and sympathetic ganglia and several ectopic sites, including

53 NGF and NT3 were measured in sympathetic ganglia and skin (a major target of sympathe

54 1B subunit of the N channel are expressed in sympathetic ganglia and that alternative splicing within

55 cal ganglion is absent, while more posterior sympathetic ganglia and the adrenal medulla are unaffect

56 p NAD in nerve terminals in the prevertebral sympathetic ganglia and the distal portions of noradrene

57 Exon-containing alpha(1B) mRNA dominated in sympathetic ganglia and was present in approximately 50%

58 s found throughout dorsal root, cranial, and sympathetic ganglia and within kidney glomeruli.

59 H2S is endogenously generated in peripheral sympathetic ganglia and, if so, its effect on synaptic t

60 t is destined to form the neural core of the sympathetic ganglia, and (2) the CXCR4 ligand, SDF-1, is

61 trunk neural crest forms the more posterior sympathetic ganglia, and also contributes to the foregut

62 The development of other parasympathetic and sympathetic ganglia appears to be largely unaffected ind

63 her or not subsets of neurons within complex sympathetic ganglia are predetermined to innervate selec

64 Sympathetic ganglia are primarily composed of noradrener

65 Discrete sympathetic ganglia arise as a consequence of intermixin

66 he segmental pattern of neural-crest-derived sympathetic ganglia arises as a direct result of signals

67 c neurons that comprise a chain of vertebral sympathetic ganglia, arises developmentally is incomplet

68 BMPR-IB mRNA was expressed in the primordial sympathetic ganglia at stage 17, soon after the first ex

69 BMPR-IA mRNA was first expressed in the sympathetic ganglia at stage 18.

70 of mouse cervical and thoracic paravertebral sympathetic ganglia at stages throughout embryonic and p

71 ts encoding dHAND and eHAND are expressed in sympathetic ganglia beginning at Hamburger and Hamilton

72 cotinic transmission was studied in bullfrog sympathetic ganglia by recording synaptic currents from

73 l and neuronal progenitor cells in postnatal sympathetic ganglia, by using mouse superior cervical ga

74 The results support the hypothesis that sympathetic ganglia can produce a 2.4-fold amplification

75 In all these sympathetic ganglia, clusters of small diameter (< 10 mi

76 efore, we assayed beta43' in dissociated rat sympathetic ganglia cultures, which contain nAchR-positi

77 phalic neural crest cells that is TH+ in the sympathetic ganglia decreases with time, while the propo

78 ecially complex given the vertebral chain of sympathetic ganglia derive secondarily from the dorsal m

79 Prevertebral sympathetic ganglia develop markedly enlarged argyrophil

80 In contrast, blood flow in dorsal root and sympathetic ganglia did not vary with changes in pressur

81 The synaptic organization of paravertebral sympathetic ganglia enables them to relay activity from

82 SN-LI in nerve fibers and somata of various sympathetic ganglia, enteric plexus and adrenal medulla

83 c neurons of the superior cervical and other sympathetic ganglia exhibited low-to-moderate levels of

84 wed that the spatiotemporal pattern of chick sympathetic ganglia formation is a two-phase process.

85 ratory behaviors that lead to alterations in sympathetic ganglia formation using a recently developed

86 Motor, sensory, and sympathetic ganglia from 1-, 2-, and 4-month-old P0-GGFb

87 neural crest-derived cells from the gut and sympathetic ganglia had initiated neuronal differentiati

88 The hypertrophy of sympathetic ganglia in the transgenic mice was correlate

89 athetically innervated peripheral organs, in sympathetic ganglia, in adrenal glands, and in brains.

90 on of ERbeta in the nuclei of neurons in the sympathetic ganglia, increase in tyrosine hydroxylase in

91 However, the number of neurons in DRG and sympathetic ganglia increases continuously at least up t

92 rat superior mesenteric or superior cervical sympathetic ganglia indicating that apoptotic neuronal c

93 Individual DRG and sympathetic ganglia initially contain few neurons.

94 ations suggest that increased NGF content in sympathetic ganglia innervating the diabetic alimentary

95 LTP of sympathetic ganglia is 5-HT(3) receptor-dependent and ha

96 Sympathetic ganglia lacking protein tyrosine phosphatase

97 clude an increase in nerve, dorsal root, and sympathetic ganglia lipid hydroperoxides and conjugated

98 ylase in both nerve terminals in the SAT and sympathetic ganglia neurons and an increase of beta3-adr

99 y expressed in dorsal root ganglia (DRG) and sympathetic ganglia neurons, have recently been identifi

100 s when heterologously expressed in adult rat sympathetic ganglia neurons.

101 Neuron number is normal in sympathetic ganglia of adult p75NTR-/- mice.

102 synaptic origin of neuritic dystrophy in the sympathetic ganglia of aged and diabetic human subjects.

103 y AP-2beta is predominantly expressed in the sympathetic ganglia of developing mouse embryos, support

104 the rate of neuroblast proliferation in the sympathetic ganglia of mice lacking the GFRalpha3 subuni

105 in several developing and adult sensory and sympathetic ganglia of the peripheral nervous system.

106 We plated dissociated cells from neonatal sympathetic ganglia on immobilized anti-CD9 antibodies o

107 ing, nor for the formation of dorsal root or sympathetic ganglia, or the adrenal medulla.

108 signals in the gut and in the region of the sympathetic ganglia play a role in the choice of cell fa

109 c potentiation and long-term potentiation in sympathetic ganglia, probably by activation of presynapt

110 the rat model to findings in diabetic human sympathetic ganglia provide promise for the development

111 s and MYCN overexpression in embryonic mouse sympathetic ganglia results in NB-like tumors.

112 mRNA were detected in both superior cervical sympathetic ganglia (SCG) and dorsal root ganglia (DRG)

113 ngly, Nrp/Sema signaling is not required for sympathetic ganglia segmentation.

114 uctures as the dorsal root ganglia (DRG) and sympathetic ganglia (SG), which form in a metameric patt

115 ent during NC cell aggregation into discrete sympathetic ganglia (SG).

116 rete structures, the dorsal root ganglia and sympathetic ganglia (SGs), are unknown.

117 eover, BMP-4 ligand mRNA was detected in the sympathetic ganglia starting at stage 18.

118 EAG genes were found to be expressed in rat sympathetic ganglia, suggesting an important functional

119 ation of both paravertebral and prevertebral sympathetic ganglia targets in vivo independently of its

120 preganglionic sympathetic neurons and their sympathetic ganglia targets.

121 arily from the dorsal migration of 'primary' sympathetic ganglia that are initially located several h

122 of connectivity between the spinal cord and sympathetic ganglia through retrograde control of synaps

123 expression in superior cervical and stellate sympathetic ganglia tissue.

124 n Fz3(-/-) ganglia are able to extend out of sympathetic ganglia toward distal targets, but fail to f

125 Alphaherpesvirus reactivation from thoracic sympathetic ganglia (TSG) and transaxonal spread to targ

126 ne transporter in rat peripheral sensory and sympathetic ganglia was investigated using polymerase ch

127 Neurite outgrowth from sympathetic ganglia was significantly greater at post-li

128 ts of adenosine on long-term potentiation of sympathetic ganglia was studied in the isolated superior

129 current (IM) of single neurons isolated from sympathetic ganglia were studied.

130 c autonomic neuropathy in mouse prevertebral sympathetic ganglia, were increased 14.8-fold and 17.2-f

131 pes, including gut enteroendocrine cells and sympathetic ganglia, where it may play a role in the mai

132 estigators first characterized the enzyme in sympathetic ganglia wherein dopamine-producing cells lin

133 ute to NC derivatives, with the exception of sympathetic ganglia, which appeared to be 'filled' by th

134 The actions of estrogen on sympathetic ganglia, which are key players in the browni

135 st cells fails to express dHAND or TH in the sympathetic ganglia, while a further subset initiates bu

136 sympathetic outgrowth, we co-cultured adult sympathetic ganglia with peri-infarct explants.

137 ilure of neurotransmission through abdominal sympathetic ganglia, with retention of neuronal viabilit