ライフサイエンスコーパス: pontine nuclei

1 ranule cell layer and a reduction in size of pontine nuclei.

2 tercalatus, reticularis tegmenti pontis, and pontine nuclei.

3 cerebellum by way of a synaptic link in the pontine nuclei.

4 cephalic and pontine reticular formation and pontine nuclei.

5 ed axonal growth in the deafferented basilar pontine nuclei.

6 t of neuropil in the superior colliculus and pontine nuclei.

7 xternal granule layer and development of the pontine nuclei.

8 of RA, including the inferior olive and the pontine nuclei.

9 h were particularly numerous in the residual pontine nuclei.

10 r cells, cerebellar granule neurons, and the pontine nuclei.

11 Zif268 and Fos-like immunoreactivity in the pontine nuclei.

12 When explants of basilar pontine nuclei, a mossy fiber source, were cultured on g

13 ere observed in the dorsolateral area of the pontine nuclei, adjacent to the lateral lemniscus.

14 lts support a pivotal role for noradrenergic pontine nuclei and alpha(2B) adrenoceptors in the analge

15 ess tau-pathology in motor cortex, striatum, pontine nuclei and cerebellum in PSP-PNLA.

16 Information from spinal cord and pontine nuclei and from outputs descending from the fore

17 formance and prevented neuronal cell loss in pontine nuclei and substantia nigra regions.

18 input to the thalamus, thalamic input to the pontine nuclei, and cerebellar feedback to the thalamus.

19 s tractus solitarius, ventrolateral medulla, pontine nuclei, and inferior olivary nucleus.

20 presses high levels of Nfi proteins, and the pontine nuclei are greatly reduced in mice lacking a fun

21 The pontine nuclei are the main precerebellar nuclei, which

22 intricate network involving the serotonergic pontine nuclei, basal ganglia, limbic system, basal fore

23 homeostasis of excitatory input to the basal pontine nuclei (BPN), a motor control hub with dense COL

24 VGLUT1 and -2 were strongly expressed in the pontine nuclei but could not be detected in LC or seroto

25 bral cortex and CA areas of the hippocampus, pontine nuclei, choroid plexus, and the cerebellum.

26 body, superior colliculus, and dorsolateral pontine nuclei, contralaterally in the IC, and bilateral

27 Coupling discrete stimulation of pontine nuclei controlling vigilance state with analytic

28 Ultimately, we wanted to determine if the pontine nuclei could be a component of the descending au

29 cerebellar interpositus nucleus and lateral pontine nuclei during conditioned inhibition of the eyeb

30 ne inferior colliculus of 10 animals and the pontine nuclei examined under a light microscope to dete

31 Neurons in the interpositus and lateral pontine nuclei exhibited significantly less activity dur

32 such population, the neurons of the basilar pontine nuclei, expresses high levels of Nfi proteins, a

33 ene including tooth buds, thymic epithelium, pontine nuclei, fastigial cerebellar nuclei, and cerebra

34 ent (striatum, substantia nigra, olivary and pontine nuclei, hippocampus, forebrain and thalamus, ant

35 eled fibers were observed in the ipsilateral pontine nuclei in 70% of the animals.

36 the mouse by optogenetically stimulating the pontine nuclei in a cued reaching task.

37 ojection from the inferior colliculus to the pontine nuclei in guinea pig.

38 ojection from the inferior colliculus to the pontine nuclei in guinea pig.

39 , such as the spinal cord, basal ganglia and pontine nuclei in the brainstem, can be involved.

40 nucleus, paralemniscal nucleus, red nucleus, pontine nuclei, inferior colliculus and the parvocellula

41 solateral and medial amygdala, central gray, pontine nuclei, interpeduncular nucleus, substantia nigr

42 ndicates that the development of the basilar pontine nuclei is delayed, with pontine neurons migratin

43 including the hippocampus, dentate nucleus, pontine nuclei, locus coeruleus, and paraventricular nuc

44 cleus, ventral nucleus of lateral lemniscus, pontine nuclei, mesencephalic trigeminal nucleus, extern

45 the cup projects to thalamic, midbrain, and pontine nuclei of the ascending auditory pathway.

46 ferences (peripenduncular, dorsal raphe, and pontine nuclei) or negligible Fos (ventral tegmental are

47 Pontine nuclei (PN) neurons mediate the communication be

48 jor projection arises from the contralateral pontine nuclei (PN) to the GCD.

49 n between the STN and the cerebellum via the pontine nuclei (PN), how the STN modulates the activity

50 by dizocilpine with increases in 1CGU in the pontine nuclei, presubiculum and hippocampus and reducti

51 us, in the thalamus, hypothalamus, amygdala, pontine nuclei, spinal cord, and dorsal root ganglion.

52 cortical amygdala, magnocellular red nuclei, pontine nuclei, superior and lateral vestibular nuclei,

53 lt intake, c-Fos activation increased within pontine nuclei that relay gustatory (caudal medial PB) a

54 s hypoglossi, the subtrigeminal nucleus, the pontine nuclei, the dorsal tegmental nucleus, the locus

55 eus, dorsal raphe nucleus, medial lemniscus, pontine nuclei, vagus nerve, inferior olive, abducens nu

56 Tracer overlap in the pontine nuclei was significantly higher than in the othe

57 put from the medial auditory thalamus to the pontine nuclei, which in turn affects input to the cereb

58 ted by pairing electrical stimulation of the pontine nuclei with an airpuff to the eye.

59 area appeared to have a unique complement of pontine nuclei with which it is connected.