ライフサイエンスコーパス: superior cervical ganglion

1 maintenance of long-term potentiation in the superior cervical ganglion.

2 the cervical sympathetic trunk caudal to the superior cervical ganglion.

3 gulated by a clock mechanism mediated by the superior cervical ganglion.

4 Here we show that superior cervical ganglion 10 (SCG10), an axonal JNK sub

5 Finally, our data identified superior cervical ganglion-10 (SCG10) as an interacting

6 a-actin [ACTB], thymosin beta-10 [TB10], and superior cervical ganglion-10 [SCG10]).

7 Increasing superior cervical ganglion activity by activating Gq-cou

8 luR cDNA in rat sympathetic neurons from the superior cervical ganglion and inhibition of the native

9 ctivated by sympathetic innervation from the superior cervical ganglion and show that these processes

10 production peaks when innervation of the rat superior cervical ganglion and the tail of Xenopus tropi

11 etrograde tracer) were injected into the rat superior cervical ganglion and, over 16-48 hours, were t

12 tage-clamp within sympathetic neurons of the superior cervical ganglion, and have no effect on the ex

13 d neurons from the rat dorsal root ganglion, superior cervical ganglion, and hippocampus.

14 o most of the enteric nervous system and the superior cervical ganglion, and is uniquely dependent on

15 Analysis of mutant embryos shows that the superior cervical ganglion anlage is present at E10.5, b

16 he postganglionic sympathetic axons from the superior cervical ganglion at E15.5.

17 ther reduce sympathetic neuron number in the superior cervical ganglion at E17.5 but does alter axon

18 indicating innervation of pulley SM from the superior cervical ganglion by projections using norepine

19 inside-out membrane patches excised from rat superior cervical ganglion cells containing M-channels,

20 sion or knockdown of Spry3 in cultured mouse superior cervical ganglion cells inhibits and promotes,

21 ndown rate' of the M-current recorded in rat superior cervical ganglion cells under whole-cell condit

22 ture, we observed increased axon growth from superior cervical ganglion explants (SCG) towards innerv

23 s destroyed by surgical removal of the right superior cervical ganglion in rats.

24 NPY-LI cells were present in the superior cervical ganglion, in which almost all cells we

25 a suprachiasmatic nucleus clock mediated by superior cervical ganglion innervation of the pineal.

26 ipheral sympathetic fibers, arising from the superior cervical ganglion, into the dentate gyrus and C

27 re only partially affected; furthermore, the superior cervical ganglion is absent, while more posteri

28 The wild-type superior cervical ganglion is composed of phasic, adapti

29 e expression in mouse hippocampal slices and superior cervical ganglion neuron boutons (sites of syna

30 ion of fast cholinergic transmission between superior cervical ganglion neurones (SCGNs) in culture.

31 channel activity and G protein modulation in superior cervical ganglion neurones (SCGNs).

32 c transmission and Ca(V) channel activity in superior cervical ganglion neurons (SCGNs).

33 N-type Ca(2+) channels and Na(+) channels in superior cervical ganglion neurons at similar concentrat

34 Furthermore, in superior cervical ganglion neurons coinjected with CB1 a

35 Infection of superior cervical ganglion neurons did not affect normal

36 -nAChR subtype found in rat intracardiac and superior cervical ganglion neurons exhibits a slow rate

37 te extension, we followed the development of superior cervical ganglion neurons explanted from Syt VI

38 activated whole-cell currents were absent in superior cervical ganglion neurons from beta2-/-beta4-/-

39 n the axonal neurofilament array of cultured superior cervical ganglion neurons from DLS/LeJ dilute l

40 sal root ganglion neurons hyperexcitable and superior cervical ganglion neurons hypoexcitable.

41 introduction of syntaphilin into presynaptic superior cervical ganglion neurons in culture inhibits s

42 he SNAP-25 binding sequence into presynaptic superior cervical ganglion neurons in culture reversibly

43 ments in cholinergic autapses established by superior cervical ganglion neurons in culture show that

44 Introduction of SNAP-29 into presynaptic superior cervical ganglion neurons in culture significan

45 ium currents were recorded from cultured rat superior cervical ganglion neurons injected intranuclear

46 tor-mediated modulation of N-type current in superior cervical ganglion neurons may be important in r

47 m microelectrode reports that nearly 100% of superior cervical ganglion neurons show phasic class 3 f

48 ibitor treatment suppressed M-current in rat superior cervical ganglion neurons, an effect negated by

49 ) caused death of differentiated PC12 cells, superior cervical ganglion neurons, and hippocampal pyra

50 ansported with KIF1A in axons of primary rat superior cervical ganglion neurons, and overexpression o

51 ivation within both dorsal root ganglion and superior cervical ganglion neurons, and renders dorsal r

52 hort term synaptic plasticity in transfected superior cervical ganglion neurons, and these regulatory

53 erived neuronal cell line (GT1-1 trk) and in superior cervical ganglion neurons, both of which expres

54 In cultured superior cervical ganglion neurons, expression of ubiqui

55 In superior cervical ganglion neurons, N-(piperidiny-1-yl)-

56 Using these inhibitors in mouse superior cervical ganglion neurons, we find predominantl

57 In superior cervical ganglion neurons, we find that the sig

58 in neuroblastoma neuro-2A cells and primary superior cervical ganglion neurons, where APP is highly

59 to native receptors found in PC-12 cells and superior cervical ganglion neurons.

60 xtension and microtubule organization in rat superior cervical ganglion neurons.

61 plasm of enzymatically dissociated adult rat superior cervical ganglion neurons.

62 onduction properties of the M-channel in rat superior cervical ganglion neurons.

63 ary cultures of Nmnat2 compound heterozygote superior cervical ganglion neurons.

64 effects on short-term synaptic plasticity in superior cervical ganglion neurons.

65 s in neonatal rat brain and intracardiac and superior cervical ganglion neurons.

66 nd attenuated the action potential firing of superior cervical ganglion neurons.

67 pathetic neurons were investigated using rat superior cervical ganglion neurons.

68 inhibition of N-type Ca(2+) channels in rat superior cervical ganglion neurons.

69 thetic) nerve terminals originating from the superior cervical ganglion occurred throughout the corne

70 pathetic ganglia was studied in the isolated superior cervical ganglion of the rat, using extracellul

71 was examined in sympathetic neurons from the superior cervical ganglion of the rat.

72 y central clock-controlled activities of the superior cervical ganglion, persists in constant darknes

73 vivo effects of activity deprivation in the superior cervical ganglion-pineal circuit of adult rats,

74 nsported to sympathetic neurons of the adult superior cervical ganglion (SCG) after injection into th

75 ive oxygen species (ROS) occurs in apoptotic superior cervical ganglion (SCG) and cerebellar granule

76 s study, we use the readily accessible mouse superior cervical ganglion (SCG) and submandibular gangl

77 Here we examined ATF3-IR in the superior cervical ganglion (SCG) and the middle and infe

78 Mature sympathetic neurons in the superior cervical ganglion (SCG) are regulated by target

79 By using a similar technique with rat superior cervical ganglion (SCG) as donor tissue and rab

80 r targets following bilateral axotomy of the superior cervical ganglion (SCG) at short term (1 day, 7

81 adrenal gland and to a lesser extent in the superior cervical ganglion (SCG) but not in other tissue

82 identified histologically as innervating the superior cervical ganglion (SCG) by the presence of Luci

83 The mammalian superior cervical ganglion (SCG) contains a complex mixt

84 ample, axotomy of sympathetic neurons in the superior cervical ganglion (SCG) dramatically increases

85 on of P2X receptors on neurons of guinea-pig superior cervical ganglion (SCG) has been carried out us

86 ck, namely, the nodose ganglion (NG) and the superior cervical ganglion (SCG) in a cohort of C57BL/6J

87 The superior cervical ganglion (SCG) is a well-characterized

88 iation (LTP) of the nicotinic pathway of the superior cervical ganglion (SCG) is remarkably similar t

89 Live-cell imaging of rat superior cervical ganglion (SCG) neuronal axons in a cha

90 M-current inhibition has been studied in rat superior cervical ganglion (SCG) neurones in primary cul

91 s, and endogenous nicotinic receptors in rat superior cervical ganglion (SCG) neurones, using identic

92 ensitive afterhyperpolarization (AHP) in rat superior cervical ganglion (SCG) neurones.

93 rents, I(Af), I(As), I(K), and I(SS), in rat superior cervical ganglion (SCG) neurons and demonstrate

94 rents, I(Af), I(As), I(K), and I(SS), in rat superior cervical ganglion (SCG) neurons and demonstrate

95 In both rat superior cervical ganglion (SCG) neurons and mouse hippo

96 hannels were heterologously expressed in rat superior cervical ganglion (SCG) neurons by intranuclear

97 CB1 cannabinoid receptors were expressed in superior cervical ganglion (SCG) neurons by microinjecti

98 lex virus type 1 (HSV-1) infection of rodent superior cervical ganglion (SCG) neurons disrupts mitoch

99 ory trigeminal ganglion (TG) and sympathetic superior cervical ganglion (SCG) neurons expressed adren

100 amma 2) were heterologously expressed in rat superior cervical ganglion (SCG) neurons following intra

101 We cultured superior cervical ganglion (SCG) neurons from adult male

102 Dissociated rat superior cervical ganglion (SCG) neurons have been shown

103 alpha4 subunit was detected on postnatal rat superior cervical ganglion (SCG) neurons in culture and

104 Superior cervical ganglion (SCG) neurons isolated from T

105 iously that M(1)R inhibition of N-current in superior cervical ganglion (SCG) neurons requires loss o

106 Exposure of rat primary superior cervical ganglion (SCG) neurons to A1EVs increa

107 tary calcium (Ca2+) currents in rat neonatal superior cervical ganglion (SCG) neurons using barium (B

108 xin (alpha Bgt) were studied on isolated rat superior cervical ganglion (SCG) neurons using whole-cel

109 lease of noradrenaline neurotransmitter from superior cervical ganglion (SCG) neurons, respectively.

110 F withdrawal-induced apoptosis of intact rat superior cervical ganglion (SCG) neurons, we observe the

111 sequestration of Gbeta gamma subunits in rat superior cervical ganglion (SCG) neurons.

112 protein-coupled pathways in acutely isolated superior cervical ganglion (SCG) neurons.

113 t phosphorylation in primary cultures of rat superior cervical ganglion (SCG) neurons.

114 processing of NPY in primary cultures of rat superior cervical ganglion (SCG) neurons.

115 SCs, on survival and neuritogenesis of mouse superior cervical ganglion (SCG) neurons.

116 nels responsible for the M current (I(M)) in superior cervical ganglion (SCG) neurons.

117 the sympathetic system, we have analyzed the superior cervical ganglion (SCG) of embryonic and postna

118 In the isolated superior cervical ganglion (SCG) of the rat (superfused

119 ransmission was investigated in the isolated superior cervical ganglion (SCG) of the rat.

120 the nicotinic pathway of transmission in the superior cervical ganglion (SCG) of the rat.

121 rrent in controlling discharge properties of superior cervical ganglion (SCG) sympathetic neurons and

122 ing mGluRs and various forms of Homer in rat superior cervical ganglion (SCG) sympathetic neurons by

123 ergic and angiotensin suppression of I(M) in superior cervical ganglion (SCG) sympathetic neurons inv

124 nt regulatory and neurotrophic activities on superior cervical ganglion (SCG) sympathetic neurons wit

125 A subpopulation of neurons in the rat superior cervical ganglion (SCG) was found to lack immun

126 PACAP peptides in sympathetic neurons of the superior cervical ganglion (SCG) was investigated.

127 , primary neuronal cells harvested from mice superior cervical ganglion (SCG) were cultured on two di

128 in isolated sympathetic neurons from the rat superior cervical ganglion (SCG), a native neuronal syst

129 ely transported to parent cell bodies in the superior cervical ganglion (SCG), and subsequently relea

130 ith tyrosine hydroxylase was observed in the superior cervical ganglion (SCG), as well as in the pont

131 NSR4 (hSNSR4; also known as Hs.mrgX1) in rat superior cervical ganglion (SCG), dorsal root ganglion (

132 Following removal of the superior cervical ganglion (SCG), large molecular weight

133 In the superior cervical ganglion (SCG), naturally occurring ne

134 In the superior cervical ganglion (SCG), particularly in Wld(s)

135 sciatic nerve, L5 dorsal root ganglion, and superior cervical ganglion (SCG), respectively, in rats

136 d mGluR2 in rat sympathetic neurons from the superior cervical ganglion (SCG), the mGluR2/G protein c

137 tidergic system in cultured neurons from the superior cervical ganglion (SCG).

138 ses in a mammalian sympathetic ganglion, the superior cervical ganglion (SCG).

139 ac myocytes and sympathetic neurons from the superior cervical ganglion (SCG).

140 a. 2.5-fold increase in neuron number in the superior cervical ganglion (SCG).

141 a(2+) channels in neurones cultured from rat superior cervical ganglion (SCG).

142 Ca2+ channels in neurones cultured from rat superior cervical ganglion (SCG).

143 CBD enhanced native M-current in mouse superior cervical ganglion starting at concentrations of

144 abies virus (PRV) injections into either the superior cervical ganglion, stellate ganglion, celiac ga

145 In superior cervical ganglion sympathetic neurons, muscarin

146 dk3, Cdk4, and Cdk6, in primary cultured rat superior cervical ganglion sympathetic neurons.

147 s Ca(2+) (I(Ca)) and M-type K(+) currents in superior cervical ganglion sympathetic neurons.

148 n culture, in the absence of nerves from the superior cervical ganglion, these PSG-derived TH neurons

149 of a subset of sympathetic neurons from the superior cervical ganglion to a preferred intermediate t

150 l culture and in the acutely isolated intact superior cervical ganglion using whole cell patch electr

151 (NGF) on the sympathetic nervous system, the superior cervical ganglion was characterized in transgen

152 and secondary EPSPs recorded from the intact superior cervical ganglion were modelled as virtual syna

153 We first performed surgical removal of the superior cervical ganglion, which supplies sympathetic f