ライフサイエンスコーパス: cervical ganglion

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

2 cal sympathetic trunk caudal to the superior cervical ganglion.

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

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

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

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

7 in rat sympathetic neurons from the superior cervical ganglion and inhibition of the native calcium c

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

9 n peaks when innervation of the rat superior cervical ganglion and the tail of Xenopus tropicalis tad

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

11 p within sympathetic neurons of the superior cervical ganglion, and have no effect on the excitabilit

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

13 the enteric nervous system and the superior cervical ganglion, and is uniquely dependent on c-ret fu

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

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

16 g innervation of pulley SM from the superior cervical ganglion by projections using norepinephrine.

17 t membrane patches excised from rat superior cervical ganglion cells containing M-channels, it had no

18 nockdown of Spry3 in cultured mouse superior cervical ganglion cells inhibits and promotes, respectiv

19 e' of the M-current recorded in rat superior cervical ganglion cells under whole-cell conditions prec

20 e most rostral population, which we call the cervical ganglion, differentiates several days before tr

21 observed increased axon growth from superior cervical ganglion explants (SCG) towards innervated comp

22 ed by surgical removal of the right superior cervical ganglion in rats.

23 NPY-LI cells were present in the superior cervical ganglion, in which almost all cells were TH- an

24 hiasmatic nucleus clock mediated by superior cervical ganglion innervation of the pineal.

25 ympathetic fibers, arising from the superior cervical ganglion, into the dentate gyrus and CA3 region

26 artially affected; furthermore, the superior cervical ganglion is absent, while more posterior sympat

27 The wild-type superior cervical ganglion is composed of phasic, adapting, and t

28 ion in mouse hippocampal slices and superior cervical ganglion neuron boutons (sites of synaptic NE r

29 st cholinergic transmission between superior cervical ganglion neurones (SCGNs) in culture.

30 ctivity and G protein modulation in superior cervical ganglion neurones (SCGNs).

31 ssion and Ca(V) channel activity in superior cervical ganglion neurons (SCGNs).

32 (2+) channels and Na(+) channels in superior cervical ganglion neurons at similar concentrations.

33 Furthermore, in superior cervical ganglion neurons coinjected with CB1 and CRIP1a

34 Infection of superior cervical ganglion neurons did not affect normal electric

35 btype found in rat intracardiac and superior cervical ganglion neurons exhibits a slow rate of desens

36 ion, we followed the development of superior cervical ganglion neurons explanted from Syt VII-deficie

37 whole-cell currents were absent in superior cervical ganglion neurons from beta2-/-beta4-/- mice and

38 nal neurofilament array of cultured superior cervical ganglion neurons from DLS/LeJ dilute lethal mic

39 ganglion neurons hyperexcitable and superior cervical ganglion neurons hypoexcitable.

40 ion of syntaphilin into presynaptic superior cervical ganglion neurons in culture inhibits synaptic t

41 5 binding sequence into presynaptic superior cervical ganglion neurons in culture reversibly inhibite

42 cholinergic autapses established by superior cervical ganglion neurons in culture show that presynapt

43 duction of SNAP-29 into presynaptic superior cervical ganglion neurons in culture significantly inhib

44 nts were recorded from cultured rat superior cervical ganglion neurons injected intranuclearly with D

45 ted modulation of N-type current in superior cervical ganglion neurons may be important in regulating

46 ectrode reports that nearly 100% of superior cervical ganglion neurons show phasic class 3 firing.

47 eatment suppressed M-current in rat superior cervical ganglion neurons, an effect negated by overexpr

48 death of differentiated PC12 cells, superior cervical ganglion neurons, and hippocampal pyramidal neu

49 with KIF1A in axons of primary rat superior cervical ganglion neurons, and overexpression or disrupt

50 ithin both dorsal root ganglion and superior cervical ganglion neurons, and renders dorsal root gangl

51 synaptic plasticity in transfected superior cervical ganglion neurons, and these regulatory effects

52 uronal cell line (GT1-1 trk) and in superior cervical ganglion neurons, both of which express the tra

53 In cultured superior cervical ganglion neurons, expression of ubiquilin-1 abo

54 In superior cervical ganglion neurons, N-(piperidiny-1-yl)-5-(4-chlo

55 In superior cervical ganglion neurons, we find that the signaling pa

56 blastoma neuro-2A cells and primary superior cervical ganglion neurons, where APP is highly expressed

57 receptors found in PC-12 cells and superior cervical ganglion neurons.

58 and microtubule organization in rat superior cervical ganglion neurons.

59 enzymatically dissociated adult rat superior cervical ganglion neurons.

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

61 n short-term synaptic plasticity in superior cervical ganglion neurons.

62 ated the action potential firing of superior cervical ganglion neurons.

63 atal rat brain and intracardiac and superior cervical ganglion neurons.

64 neurons were investigated using rat superior cervical ganglion neurons.

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

66 erve terminals originating from the superior cervical ganglion occurred throughout the corneal epithe

67 ganglia was studied in the isolated superior cervical ganglion of the rat, using extracellularly reco

68 ned in sympathetic neurons from the superior cervical ganglion of the rat.

69 clock-controlled activities of the superior cervical ganglion, persists in constant darkness, and is

70 ects of activity deprivation in the superior cervical ganglion-pineal circuit of adult rats, which ca

71 to sympathetic neurons of the adult superior cervical ganglion (SCG) after injection into the anterio

72 n species (ROS) occurs in apoptotic superior cervical ganglion (SCG) and cerebellar granule (CG) neur

73 we use the readily accessible mouse superior cervical ganglion (SCG) and submandibular ganglion (SMG)

74 Here we examined ATF3-IR in the superior cervical ganglion (SCG) and the middle and inferior cerv

75 Mature sympathetic neurons in the superior cervical ganglion (SCG) are regulated by target-derived

76 using a similar technique with rat superior cervical ganglion (SCG) as donor tissue and rabbit endot

77 following bilateral axotomy of the superior cervical ganglion (SCG) at short term (1 day, 7 day) and

78 gland and to a lesser extent in the superior cervical ganglion (SCG) but not in other tissues.

79 d histologically as innervating the superior cervical ganglion (SCG) by the presence of Lucifer Yello

80 The mammalian superior cervical ganglion (SCG) contains a complex mixture of ne

81 otomy of sympathetic neurons in the superior cervical ganglion (SCG) dramatically increases levels of

82 receptors on neurons of guinea-pig superior cervical ganglion (SCG) has been carried out using a who

83 The superior cervical ganglion (SCG) is a well-characterized model of

84 TP) of the nicotinic pathway of the superior cervical ganglion (SCG) is remarkably similar to that of

85 Live-cell imaging of rat superior cervical ganglion (SCG) neuronal axons in a chamber syst

86 inhibition has been studied in rat superior cervical ganglion (SCG) neurones in primary culture.

87 dogenous nicotinic receptors in rat superior cervical ganglion (SCG) neurones, using identical soluti

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

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

90 Af), I(As), I(K), and I(SS), in rat superior cervical ganglion (SCG) neurons and demonstrated that I(

91 In both rat superior cervical ganglion (SCG) neurons and mouse hippocampal CA

92 ere heterologously expressed in rat superior cervical ganglion (SCG) neurons by intranuclear microinj

93 abinoid receptors were expressed in superior cervical ganglion (SCG) neurons by microinjection of hCB

94 type 1 (HSV-1) infection of rodent superior cervical ganglion (SCG) neurons disrupts mitochondrial m

95 minal ganglion (TG) and sympathetic superior cervical ganglion (SCG) neurons expressed adrenergic rec

96 ere heterologously expressed in rat superior cervical ganglion (SCG) neurons following intranuclear i

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

98 Dissociated rat superior cervical ganglion (SCG) neurons have been shown to posse

99 bunit was detected on postnatal rat superior cervical ganglion (SCG) neurons in culture and in cryose

100 Superior cervical ganglion (SCG) neurons isolated from Tg.sgk mic

101 Loss of AKAP150 in sympathetic cervical ganglion (SCG) neurons reduces muscarinic suppr

102 at M(1)R inhibition of N-current in superior cervical ganglion (SCG) neurons requires loss of PIP(2)

103 ium (Ca2+) currents in rat neonatal superior cervical ganglion (SCG) neurons using barium (Ba2+) as t

104 a Bgt) were studied on isolated rat superior cervical ganglion (SCG) neurons using whole-cell patch c

105 noradrenaline neurotransmitter from superior cervical ganglion (SCG) neurons, respectively.

106 wal-induced apoptosis of intact rat superior cervical ganglion (SCG) neurons, we observe the redistri

107 tion of Gbeta gamma subunits in rat superior cervical ganglion (SCG) neurons.

108 oupled pathways in acutely isolated superior cervical ganglion (SCG) neurons.

109 rylation in primary cultures of rat superior cervical ganglion (SCG) neurons.

110 g of NPY in primary cultures of rat superior cervical ganglion (SCG) neurons.

111 urvival and neuritogenesis of mouse superior cervical ganglion (SCG) neurons.

112 onsible for the M current (I(M)) in superior cervical ganglion (SCG) neurons.

113 thetic system, we have analyzed the superior cervical ganglion (SCG) of embryonic and postnatal mice

114 In the isolated superior cervical ganglion (SCG) of the rat (superfused with Lock

115 on was investigated in the isolated superior cervical ganglion (SCG) of the rat.

116 inic pathway of transmission in the superior cervical ganglion (SCG) of the rat.

117 controlling discharge properties of superior cervical ganglion (SCG) sympathetic neurons and the mech

118 s and various forms of Homer in rat superior cervical ganglion (SCG) sympathetic neurons by intranucl

119 angiotensin suppression of I(M) in superior cervical ganglion (SCG) sympathetic neurons involves AKA

120 tory and neurotrophic activities on superior cervical ganglion (SCG) sympathetic neurons with pharmac

121 subpopulation of neurons in the rat superior cervical ganglion (SCG) was found to lack immunostaining

122 tides in sympathetic neurons of the superior cervical ganglion (SCG) was investigated.

123 neuronal cells harvested from mice superior cervical ganglion (SCG) were cultured on two dimensional

124 ed sympathetic neurons from the rat superior cervical ganglion (SCG), a native neuronal system with a

125 ported to parent cell bodies in the superior cervical ganglion (SCG), and subsequently released into

126 ine hydroxylase was observed in the superior cervical ganglion (SCG), as well as in the pontine nucle

127 SR4; also known as Hs.mrgX1) in rat superior cervical ganglion (SCG), dorsal root ganglion (DRG), and

128 Following removal of the superior cervical ganglion (SCG), large molecular weight (MW) NGF

129 In the superior cervical ganglion (SCG), naturally occurring neuronal de

130 In the superior cervical ganglion (SCG), particularly in Wld(s) mice, ma

131 nerve, L5 dorsal root ganglion, and superior cervical ganglion (SCG), respectively, in rats with EDN.

132 in rat sympathetic neurons from the superior cervical ganglion (SCG), the mGluR2/G protein coupling p

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

134 mammalian sympathetic ganglion, the superior cervical ganglion (SCG).

135 es and sympathetic neurons from the superior cervical ganglion (SCG).

136 ld increase in neuron number in the superior cervical ganglion (SCG).

137 nnels in neurones cultured from rat superior cervical ganglion (SCG).

138 nnels in neurones cultured from rat superior cervical ganglion (SCG).

139 us (PRV) injections into either the superior cervical ganglion, stellate ganglion, celiac ganglion, o

140 In superior cervical ganglion sympathetic neurons, muscarinic M(1),

141 , and Cdk6, in primary cultured rat superior cervical ganglion sympathetic neurons.

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

143 set of sympathetic neurons from the superior cervical ganglion to a preferred intermediate target, th

144 and in the acutely isolated intact superior cervical ganglion using whole cell patch electrode recor

145 the sympathetic nervous system, the superior cervical ganglion was characterized in transgenic mice o

146 dary EPSPs recorded from the intact superior cervical ganglion were modelled as virtual synapses in c

147 t performed surgical removal of the superior cervical ganglion, which supplies sympathetic fibers to