ライフサイエンスコーパス: flocculus

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1 e Purkinje cell synapses from the cerebellar flocculus.

2 vermal lobules VI-X, the paraflocculus, and flocculus.

3 R) antagonist RU38486 into the ipsi-lesional flocculus also abolished CIE in MVN neurons.

4 bular abnormalities reported with unilateral flocculus and anterior tonsil infarction.

5 als was asymmetric-favoring the ipsilesional flocculus and contralesional vestibular brainstem.

6 localized within parasagittal regions of the flocculus and nodulus.

7 In both visual conditions, flocculus and paraflocculus Purkinje cell labeling was a

8 ly result from dysfunction in the cerebellar flocculus and paraflocculus.

9 ly in the uvula, with fewer afferents in the flocculus and paraflocculus.

10 genu of the facial nerve, to the cerebellar flocculus and ventral paraflocculus was demonstrated.

11 These results demonstrate that, unlike the flocculus and ventral paraflocculus which target a parti

12 sex (relative expansion of total cerebellum, flocculus, and Crus II-lobule VIIIB volumes in males) an

13 In the flocculus, associative plasticity in vitro and in vivo i

14 activity of Purkinje cells in the cerebellar flocculus, but consolidated memories appear to be stored

15 accurately reflecting the size of the neural flocculus, but might also reflect the importance of the

16 l, inferior colliculus, locus coeruleus, and flocculus compared to morphine-dependent animals treated

17 cessing delay for error signals to reach the flocculus during oculomotor learning.

18 but might also reflect the importance of the flocculus for all modes of locomotion in birds.

19 We investigated the role of the cerebellar flocculus in mediating the adaptive changes that occur i

20 ty (94% to the uvula/nodulus and 100% to the flocculus) innervates the peripheral zones of each of th

21 r represents a functional unit in the pigeon flocculus insofar as the CSA of all PCs in the stripe pa

22 flight, some authors have suggested that the flocculus is enlarged in flying species.

23 A primary role of the flocculus is to integrate sensory information about head

24 ojecting to the cerebellar uvula/nodulus and flocculus lobules in the gerbil.

25 efore conclude that the relative size of the flocculus of endocranial casts is an unreliable predicto

26 No projections appeared in the flocculus or paraflocculus.

27 Both the caudal fastigial nucleus and the flocculus/paraflocculus are necessary for the normal smo

28 clei labeled with PRV after infection of the flocculus/paraflocculus, or nodulus/uvula, included the

29 daptation in normal animals was found in the flocculus/paraflocculus, the dorsal cap of the inferior

30 climbing fiber projection to the cerebellar flocculus, PO neurons control limb and digit movements v

31 ted adjacent to, but are not included among, flocculus-projecting supragenual neurons.

32 The pigeon flocculus receives visual-optokinetic information and is

33 Neurons directly inhibited by flocculus stimulation had significantly greater horizont

34 onvergence than did neurons not inhibited by flocculus stimulation.

35 d, in some cases, inhibition from cerebellar flocculus stimulation.

36 ate to the ZII stripes in folium IXcd of the flocculus, such that an optokinetic zone spans a ZII+/-

37 Glycinergic and glutamatergic flocculus target neurons (FTNs) with somata densely surr

38 stsynaptic targets of Purkinje cells, termed flocculus target neurons (FTNs), are thought to be a cri

39 lus and weak projections were present in the flocculus, ventral paraflocculus, bilateral fastigial nu

40 parse, the projections of the utricle to the flocculus/ventral paraflocculus suggest a potential conv

41 Purkinje cell inhibition from the cerebellar flocculus/ventral paraflocculus, exhibit properties that

42 o direct otolith organ-related inputs to the flocculus were observed.

43 red from the relative size of the cerebellar flocculus, which in life protrudes from the lateral surf

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