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

1 V, eliminating over 90% of latent virus from superior cervical ganglia.

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

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

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

5 sympathetic postganglionic neurons from the superior cervical ganglia.

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

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

8 radrenergic innervation originating from the superior cervical ganglia.

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

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

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

12 ies on cultured rat sympathetic neurons from superior cervical ganglia (and also insect neurons) have

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

33 Superior cervical ganglia of postnatal mice with a targe

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

35 hannel activity of neurons isolated from the superior cervical ganglia of young (12 weeks), middle-ag

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

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

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

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

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

41 rmed microgels, to culture individual murine superior cervical ganglia (SCG) neurons or epithelial ce

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

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

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

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

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

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

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

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

50 NA sequencing traced this defect back to the superior cervical ganglia (SCG), which responded to card

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

52 5 (E15) and postnatal day 1 (P1) sympathetic superior cervical ganglia (SCG).

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

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

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

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

57 14.8% +/- 3.5% of SPN (C8-T3) innervating superior cervical ganglia were activated.

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

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