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1 wn along the anterior aspect of the cerebral peduncle).
2 nitiation and elongation within the cerebral peduncle.
3 a mass in the left cerebellar hemisphere and peduncle.
4 f the LC adjacent to the superior cerebellar peduncle.
5 tput MVP2 neuron innervated by KCs in the MB peduncle.
6 et of Kenyon cells in the core region of the peduncle.
7 rior thalamic radiation, and middle cerebral peduncle.
8 projections to the hypothalamus and cerebral peduncle.
9 aversed by fibers of the superior cerebellar peduncle.
10 teral transection of the inferior cerebellar peduncle.
11 ss of oligodendroglial cells in the cerebral peduncle.
12 ections and ascending fibers of the cerebral peduncle.
13 cells were activated from both striatum and peduncle.
14 e turgor were almost 1 MPa lower than in the peduncle.
15 rates to a position adjacent to the cerebral peduncle.
16 nd migrates to a position above the cerebral peduncle.
17 the right superior and the middle cerebellar peduncles.
18 ed the microstructure of superior cerebellar peduncles.
19 into the SN and partially into the cerebral peduncles.
20 in, i.e., the cerebral and medial cerebellar peduncles.
21 internal and external capsules, and cerebral peduncles.
22 corticospinal tract and superior cerebellar peduncles.
23 perintensities along the superior cerebellar peduncles.
24 corticospinal tract and superior cerebellar peduncles.
25 al fibers, lateral lemniscus, and cerebellar peduncles.
26 ucleus (0.25% increase, P = .01), cerebellar peduncle (0.19% increase, P = .001), and colliculi (0.21
31 rimental situations were examined: the lower peduncle and foot (PF) were injured or removed, a second
33 we tracked connections between the cerebral peduncle and left hemispheric masks of the superior fron
36 T2 signal intensity in the middle cerebellar peduncles and adjacent cerebellar white matter are thoug
38 abnormalities within the superior cerebellar peduncles and midbrain were observed more often in patie
39 o-pontine fibers travel through the cerebral peduncles and reach the cerebellum by way of a synaptic
41 an of the insect mushroom body into calyces, peduncle, and lobes is maintained, as is the arrangement
42 r volume in the pyramids and left cerebellar peduncle, and smaller grey matter volume and cortical th
43 the external capsule, the RLIC, the cerebral peduncle, and the superior corona radiata than did the H
44 blades, the basis pontis, middle cerebellar peduncles, and cerebellar white matter, and elevated suc
50 brain, thalamus, dentate nucleus, cerebellar peduncles, cerebellar vermis and lobules V and VI, and c
51 ritical buckling length Lerof flower stalks (peduncles) collected from isogenic garlic (Allium sativu
52 s, substantia nigra, red nucleus, cerebellar peduncle, colliculi, dentate nucleus, and globus pallidu
53 ying hormone solutions by injection into the peduncle compared to direct application to the intact gr
54 /-) brain: the anterior commissure, cerebral peduncle (corticospinal tract), corpus callosum, fornix,
56 assessment of middle and superior cerebellar peduncle damage contributes to the explanation of cerebe
57 ty measures of middle or superior cerebellar peduncle damage enabled better differentiation between c
58 , namely, the middle and superior cerebellar peduncles, descending motor tracts (containing the corti
59 or functioning, only the superior cerebellar peduncles exhibited an association with the elevated RNA
63 alyses of the data indicate that L and Lerof peduncles harvested from both populations have Weibull f
66 ed by electrical stimulation of the cerebral peduncle in the presence of the glutamate receptor antag
67 observed staining in the superior cerebellar peduncle in the rostal pons, in the corticopontocerebell
68 ectivity strength of the superior cerebellar peduncles in both premutation groups (partial r(2) = 0.2
69 ngiosis was present in the middle cerebellar peduncles in seven of the eight cases in which those tis
70 s lower in the bilateral superior cerebellar peduncles, in the bilateral fornices, white matter regio
71 lfactory tract in the anterior and posterior peduncle indicated that the region is less orderly in mi
72 and that the factor of safety of field grown peduncles is 73% higher than that of glasshouse grown pl
73 fferent axons within the superior cerebellar peduncles is a critical underlying pathophysiological co
74 at the factor of safety for glasshouse grown peduncles is very near unity (i.e. S=1.03), and that the
75 to-spinal tract (CPST) and middle cerebellar peduncle (MCP) dimensions was correlated with holoprosen
77 d for DN-to-pons and DN-to-middle cerebellar peduncle (MCP) ratios by subtracting the SI ratio at the
78 d for DN-to-pons and DN-to-middle cerebellar peduncle (MCP) ratios in a region-of-interest-based anal
79 nal intensity ratio, DN-to-middle cerebellar peduncle (MCP) signal intensity ratio and relative perce
80 us (GP) in relation to the middle cerebellar peduncle (MCP), pons, and thalamus after repeated admini
81 within NAWM including: the middle cerebellar peduncles (MCP), the inferior longitudinal fasciculi (IL
82 ypoplasia with elongated superior cerebellar peduncles (mild "molar tooth sign"), typical cranio-faci
83 10), colliculi (n = 10), superior cerebellar peduncle (n = 7), caudate nucleus (n = 4), whole thalamu
84 The same lesions were also observed in the peduncle of developing flowers, extending to the whole f
86 d the region of the axon tract, the cerebral peduncle, overlying the basilar pons for cellular struct
87 arked abnormalities in the middle cerebellar peduncles (P<0.001), in cingulum bundles (P=0.002), and
88 r fronto-occipital fasciculus, left cerebral peduncle, posterior thalamic radiation, and middle cereb
90 the corpus callosum and superior cerebellar peduncles revealed a high correlation with motor functio
92 mature flowers, and the ovule-funiculus and peduncle-silique boundaries in elongating siliques; and
93 aoptic decussations or the inferior thalamic peduncle-stria terminalis pathway from the posterior tha
94 72 patients, 112 (65%) had middle cerebellar peduncle T2 lesions and 74 (43%) had superior cerebellar
96 thalamus, and along the superior cerebellar peduncle, thalamic fasciculus, and ansa peduncularis fro
97 ypoplasia with prominent superior cerebellar peduncles (the "molar tooth sign" [MTS] on axial magneti
98 ropy (FA) in ten brain regions: the cerebral peduncle, the anterior and posterior limbs of the intern
99 kinase gene expressed in the ectoderm of the peduncle, the end of the body column adjacent to the bas
101 nucleus of the MLF, the superior cerebellar peduncle, the oculomotor nucleus, and the interstitial n
103 of the internal capsule, and in the cerebral peduncle; the thalamus; the region of the red nucleus; t
105 asal disk without passing through a stage as peduncle tissue comes from LiCl-induced formation of pat
107 audally through the tegmentum and cerebellar peduncle to terminate just below the Purkinje cell layer
109 um via the anterior aspect of the cerebellar peduncles, to contribute to the generation of ventral st
110 ceptors suggests that the changes found with peduncle transection may have resulted from something mo
111 omponent of the motor system to the cerebral peduncle using diffusion-weighted imaging and probabilis
113 asures of the middle and superior cerebellar peduncles were derived from 172 patients with MS and 46
114 ty of the left and right superior cerebellar peduncles were found (F2,23 range, 5.555-3.450; P = .036
115 esions in the middle and superior cerebellar peduncles were more common in clinically impaired patien
116 lities of the middle and superior cerebellar peduncles were more severe in clinically impaired patien
117 the corpus callosum and superior cerebellar peduncles were of great importance to motor functioning,
118 and traverse the midsection of the cerebral peduncle, where SMA fibers are medial, and face, arm, an
119 rons retain only their main processes in the peduncle, which then project into the adult gamma lobe w
120 t Z score 4.12, p=0.0004) and right cerebral peduncle (Z score 3.89, p=0.0302) and of grey matter in
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