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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

33 Infection of superior cervical ganglion neurons did not affect normal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 In cultured superior cervical ganglion neurons, expression of ubiqui

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

99 Superior cervical ganglion (SCG) neurons isolated from T

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

138 In superior cervical ganglion sympathetic neurons, muscarin

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

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

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

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

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

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

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