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1 e Purkinje cell synapses from the cerebellar flocculus.
2  vermal lobules VI-X, the paraflocculus, and flocculus.
3  not altered in the dysplastic paraflocculus/flocculus.
4 l bone, which encapsulates the paraflocculus/flocculus.
5 R) antagonist RU38486 into the ipsi-lesional flocculus also abolished CIE in MVN neurons.
6 bular abnormalities reported with unilateral flocculus and anterior tonsil infarction.
7 als was asymmetric-favoring the ipsilesional flocculus and contralesional vestibular brainstem.
8 localized within parasagittal regions of the flocculus and nodulus.
9                   In both visual conditions, flocculus and paraflocculus Purkinje cell labeling was a
10 ly result from dysfunction in the cerebellar flocculus and paraflocculus.
11 ly in the uvula, with fewer afferents in the flocculus and paraflocculus.
12  genu of the facial nerve, to the cerebellar flocculus and ventral paraflocculus was demonstrated.
13   These results demonstrate that, unlike the flocculus and ventral paraflocculus which target a parti
14 sex (relative expansion of total cerebellum, flocculus, and Crus II-lobule VIIIB volumes in males) an
15                                       In the flocculus, associative plasticity in vitro and in vivo i
16 activity of Purkinje cells in the cerebellar flocculus, but consolidated memories appear to be stored
17 accurately reflecting the size of the neural flocculus, but might also reflect the importance of the
18 us temporal bone autonomous to paraflocculus/flocculus cell populations.
19 l, inferior colliculus, locus coeruleus, and flocculus compared to morphine-dependent animals treated
20 cessing delay for error signals to reach the flocculus during oculomotor learning.
21                  In mice, this paraflocculus/flocculus dysplasia is associated with haploinsufficienc
22 but might also reflect the importance of the flocculus for all modes of locomotion in birds.
23   We investigated the role of the cerebellar flocculus in mediating the adaptive changes that occur i
24 lo-cerebellar lobules, the paraflocculus and flocculus, in mouse models and humans with 22q11.2 delet
25 ty (94% to the uvula/nodulus and 100% to the flocculus) innervates the peripheral zones of each of th
26 r represents a functional unit in the pigeon flocculus insofar as the CSA of all PCs in the stripe pa
27 flight, some authors have suggested that the flocculus is enlarged in flying species.
28                        A primary role of the flocculus is to integrate sensory information about head
29 ojecting to the cerebellar uvula/nodulus and flocculus lobules in the gerbil.
30 asuring and manipulating MLI activity in the flocculus of both sexes of mice before and after vestibu
31 efore conclude that the relative size of the flocculus of endocranial casts is an unreliable predicto
32               No projections appeared in the flocculus or paraflocculus.
33    Both the caudal fastigial nucleus and the flocculus/paraflocculus are necessary for the normal smo
34 clei labeled with PRV after infection of the flocculus/paraflocculus, or nodulus/uvula, included the
35 daptation in normal animals was found in the flocculus/paraflocculus, the dorsal cap of the inferior
36  climbing fiber projection to the cerebellar flocculus, PO neurons control limb and digit movements v
37 ted adjacent to, but are not included among, flocculus-projecting supragenual neurons.
38                                   The pigeon flocculus receives visual-optokinetic information and is
39                Neurons directly inhibited by flocculus stimulation had significantly greater horizont
40 onvergence than did neurons not inhibited by flocculus stimulation.
41 d, in some cases, inhibition from cerebellar flocculus stimulation.
42 ate to the ZII stripes in folium IXcd of the flocculus, such that an optokinetic zone spans a ZII+/-
43                Glycinergic and glutamatergic flocculus target neurons (FTNs) with somata densely surr
44 stsynaptic targets of Purkinje cells, termed flocculus target neurons (FTNs), are thought to be a cri
45 lus and weak projections were present in the flocculus, ventral paraflocculus, bilateral fastigial nu
46 parse, the projections of the utricle to the flocculus/ventral paraflocculus suggest a potential conv
47 Purkinje cell inhibition from the cerebellar flocculus/ventral paraflocculus, exhibit properties that
48 o direct otolith organ-related inputs to the flocculus were observed.
49 red from the relative size of the cerebellar flocculus, which in life protrudes from the lateral surf