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

1 ia, but was absent in sympathetic neurons of superior cervical ganglia.

2 ntly reduces developmental cell death in the superior cervical ganglia.

3 during naturally occurring cell death in the superior cervical ganglia.

4 sympathetic postganglionic neurons from the superior cervical ganglia.

5 anches of the facial nerve and resecting the superior cervical ganglia.

6 wo to three times greater in dorsal root and superior cervical ganglia.

7 radrenergic innervation originating from the superior cervical ganglia.

8 central structures, and projections from the superior cervical ganglia; activation of this pathway re

9 Bax-deficient superior cervical ganglia and facial nuclei possessed in

10 Curiously, neurons of the superior cervical ganglia and the gut were largely unaff

11 ostnatal sympathetic ganglia, by using mouse superior cervical ganglia as a model system.

12 cholinergic fibers likely originate from the superior cervical ganglia because unilateral ganglionect

13 ed a neural growth-associated protein SCG10 (superior cervical ganglia clone 10) gene.

14 t a novel interaction between JLP and SCG10 (superior cervical ganglia clone 10), which is a microtub

15 nd pancreas, were targeted together with the superior cervical ganglia (control).

16 The visceral efferents of the superior cervical ganglia did not contain 5-HT1D immunor

17 nt levels of cellular proliferation in mouse superior cervical ganglia during the first 18 days after

18 ral sympathetic fibers, originating from the superior cervical ganglia, grow into the cholinergically

19 llular physiological measurements of control superior cervical ganglia identified two distinct types

20 rents was severely reduced in the neurons of superior cervical ganglia in -/- mice with five physiolo

21 of noradrenergic sympathetic fibers from the superior cervical ganglia into hippocampus.

22 doubling of neuron number in trigeminal and superior cervical ganglia, many components of the sensor

23 SCG10 (superior cervical ganglia neural-specific 10 protein) is

24 The microtubule-destabilizing protein SCG10 (superior cervical ganglia, neural specific 10) was found

25 to be determined; however, infection of rat superior cervical ganglia neurons in vitro indicates tha

26 e calcium channels in mammalian Purkinje and superior cervical ganglia neurons with similar IC50 valu

27 Neurons cultured from superior cervical ganglia of B(-)/B(-) mice between embr

28 d with sympathetic neurons isolated from the superior cervical ganglia of newborn rats.

29 Before perfusion, the superior cervical ganglia of one monkey had been injecte

30 In contrast, the peripheral neurons of the superior cervical ganglia of PKR(-/-) x RL(-/-) mice sho

31 Superior cervical ganglia of postnatal mice with a targe

32 Comparable changes failed to develop in the superior cervical ganglia of the NOD mouse or in the SMG

33 bryonic rat trigeminal, dorsal root, nodose, superior cervical ganglia or retina with a variety of na

34 alternative splice variant expression in rat superior cervical ganglia revealed multiple variant isof

35 Fourteen days later, NGF levels in the superior cervical ganglia (SCG) and its targets, the hea

36 mporal expression of BMP5, -6, and -7 in rat superior cervical ganglia (SCG) is consistent with their

37 In patch-clamp studies, nodose, coeliac and superior cervical ganglia (SCG) neurones from wild-type

38 Neurons isolated from the superior cervical ganglia (SCG) of embryonic rodents and

39 ur types of G(q/11)-coupled receptors in rat superior cervical ganglia (SCG) sympathetic neurons.

40 We have used the response of the superior cervical ganglia (SCG) to axotomy to investigat

41 of mud genes was analyzed in developing rat superior cervical ganglia (SCG) undergoing programmed ce

42 de from rat sympathetic neurones in isolated superior cervical ganglia (SCG), coeliac ganglia (CG), a

43 incipally from the neurons of trigeminal and superior cervical ganglia (SCG), respectively.

44 nAChRs in several rat autonomic ganglia: the superior cervical ganglia (SCG), sensory nodose ganglia,

45 ition of neuronal nicotinic receptors in rat superior cervical ganglia (SCG), their single-channel pr

46 or), in control and diabetic rat SMG, CG and superior cervical ganglia (SCG).

47 5 (E15) and postnatal day 1 (P1) sympathetic superior cervical ganglia (SCG).

48 ic ganglia (CG/SMG) but not in paravertebral superior cervical ganglia (SCG).

49 n sympathetic neurons cultured from traf6+/+ superior cervical ganglia (SCGs), there was an increase

50 of preganglionic neurons that innervate the superior cervical ganglia (SCGs).

51 ed in sympathetic neurons, isolated from rat superior cervical ganglia, using whole-cell voltage clam

52 14.8% +/- 3.5% of SPN (C8-T3) innervating superior cervical ganglia were activated.

53 n a nearly total loss of SN-LI fibers in the superior cervical ganglia, whereas immunoreactivity in t

54 Pretreatment of rat isolated superior cervical ganglia with oxyhemoglobin (25-100 mic