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1 and AAV-expressing Cre in C7/C8 dorsolateral funiculus.
2 ntral nucleus of Herrick, and in the lateral funiculus.
3 lcineurin-positive cells in the dorsolateral funiculus.
4 venting transportation of nutrients from the funiculus.
5 ally supports nutrient transport through the funiculus.
6 2 and found a completely disorganized dorsal funiculus.
7  rhombomeres 2-5 and extended in the lateral funiculus.
8 out mice results in a wild-type-like lateral funiculus.
9 t away from the floor plate into the lateral funiculus.
10 CST fibers that project via the dorsolateral funiculus.
11  was found in the middle of the dorsolateral funiculus.
12 e expressed on axons that compose the dorsal funiculus.
13 ibuted in the cuneate fasciculus and lateral funiculus.
14 e (LPS; 200 ng) directly into the rat dorsal funiculus.
15 5% of the cross-sectional area of the dorsal funiculus.
16 l column lesions by traveling in the lateral funiculus.
17  and/or branches entering the dorsal lateral funiculus.
18 superficial dorsal horn and the dorsolateral funiculus.
19 face between the floor plate and the ventral funiculus.
20 ase during silique development is within the funiculus.
21 superficial dorsal horn and the dorsolateral funiculus.
22 ly projecting axons constituting the lateral funiculus.
23 ral horn and the white matter of the lateral funiculus.
24 s of which travel in the ventral part of the funiculus.
25 ransported from the maternal tissues via the funiculus, accumulated in the central region of the imma
26 EPSPs elicited by stimulation of the lateral funiculus, an effect blocked by the A1R antagonist 8-cyc
27 ne is required for normal development of the funiculus, an umbilical-cord-like structure that connect
28                                    The plant funiculus anchors the developing seed to the placenta wi
29 jections into the white matter of the dorsal funiculus and dorsolateral fasciculus, respectively.
30 entral horn as well as fibers in the lateral funiculus and lamina X, but practically no fibers in the
31 PNs were identified laterally in the lateral funiculus and medially in the intercalated and central a
32      The afferents ascend in the dorsomedial funiculus and move laterally after they pass the obex.
33 Arg-Met-enkephalin, labeled the dorsolateral funiculus and numerous puncta in laminae I-III and V of
34 nt junction in mature flowers, and the ovule-funiculus and peduncle-silique boundaries in elongating
35 se inputs projected through the dorsolateral funiculus and primarily innervated layers I, II, and V o
36 a (I-III) were found to course in the dorsal funiculus and terminate bilaterally in the caudal zone o
37               The dorsal part of the lateral funiculus and the dorsal funiculus contained few labeled
38  axons prevents the formation of the lateral funiculus and the spinocerebellar tract, and simultaneou
39 eter of the spinal cord, in the dorsolateral funiculus, and adjacent to the central canal.
40  distinct positions within the ventrolateral funiculus, and never reenter the floor plate.
41  axon segments projecting within the ventral funiculus, and on ipsilaterally projecting axons constit
42  dorsolateral (DLFX) or ventrolateral (VLFX) funiculus, and with rats with a sham operation.
43 nges at 8 h, reached a maximum in the dorsal funiculus at 7 days, and were rare at 14 days.
44  to the ventral marginal area and the dorsal funiculus at birth (P0).
45               IS (60 Hz) of the dorsolateral funiculus at L1-L3 (depth of 0.5-1.0mm from the dorsal s
46  Therefore, the lack of myelin in the dorsal funiculus at lumbar levels does not enhance the growth o
47 timulation of the contralateral dorsolateral funiculus at the L2 level.
48  Ipsi- or contralateral lesion of the dorsal funiculus at the spinal level T8/T9 had no effect on dep
49 king Ntn1 had axons escaping from the dorsal funiculus at the time of bifurcation.
50 part of the lateral funiculus and the dorsal funiculus contained few labeled axons, in contrast to al
51  evoked via stimulation of the ventrolateral funiculus (contralateral to injury) were recorded in bot
52 e spinal cord and the pathways of the dorsal funiculus contralaterally.
53                    Rats received a C4 dorsal funiculus cut followed by chondroitinase ABC or penicill
54 l-distal domains - the nucellus, chalaza and funiculus - demarcated by developmental fate and specifi
55 s expected that a lesion to the dorsolateral funiculus (DLF) at C5 would interrupt the corticospinal
56 h sham bilateral lesions of the dorsolateral funiculus (DLF) but not in rats with DLF lesions.
57               After cutting the dorsolateral funiculus (DLF) contralateral to the stimulated hindpaw
58       Similarly, lesions of the dorsolateral funiculus (DLF) did not prevent the onset of SNL-induced
59 l root, the dorsal horn, or the dorsolateral funiculus (DLF) in spinal cord slices while superfusing
60  ventromedial medulla (RVM), or dorsolateral funiculus (DLF) lesion, abolishes opioid-induced hyperal
61  Transection of the ipsilateral dorsolateral funiculus (DLF) removed a descending inhibition of multi
62 ne, or bilateral lesions of the dorsolateral funiculus (DLF), did not change response thresholds in p
63 e and after interruption of one dorsolateral funiculus (DLF).
64 steps of ovule development as well as in the funiculus, embryo, and integuments of developing seeds.
65 , demyelination was restricted to the dorsal funiculus, i.e., axons undergoing Wallerian degeneration
66 fected mice induced lesions in the posterior funiculus in addition to the anterior/lateral funiculi.
67 outer integument, and a small portion of the funiculus in developing siliques.
68                 After lesions of one lateral funiculus in the lumbar cord the responses evoked by sti
69                            The ventrolateral funiculus in the spinal cord has been identified as cont
70                                   The dorsal funiculus in the spinal cord relays somatosensory inform
71  spinal cord gray matter, cupping the dorsal funiculus, in an anterior-to-posterior decreasing gradie
72                                 Dorsolateral funiculus lesion (DLF) or destruction of RVM neurons exp
73 expression, adult rats underwent a C3 dorsal funiculus lesion.
74 pinal Fos protein expression in dorsolateral funiculus-lesioned (DLFX) rats following hindpaw inflamm
75  at lumbar levels L4/5, and bilateral dorsal funiculus lesioning at thoracic levels T10/11 on NP-1 mR
76  < 0.001), but not after rhizotomy or dorsal funiculus lesioning.
77 salis, raphe magnus, and spinal dorsolateral funiculus lesions abolish antianalgesia.
78  into one hind paw of rats with dorsolateral funiculus lesions and sham-operated rats.
79                      Following either dorsal funiculus lesions at thoracic level 9 (T9) or lateral he
80 ated rats but not in those with dorsolateral funiculus lesions, indicating that lesioning blocked EA-
81  section) but not in those with dorsolateral funiculus lesions.
82  in ventrolateral funiculus (VLF) or lateral funiculus (LF) at the injured epicenter was significantl
83  revealed that the development of the dorsal funiculus occurs independently of EphA4 expression in de
84 al degeneration was induced in the posterior funiculus of mice by injecting the toxic lectin Ricinus
85 e gliotoxin ethidium bromide into the dorsal funiculus of the cervical spinal cord of the rat to indu
86 in the descending tracts of the dorsolateral funiculus of the cervical spinal cord was investigated i
87 ior olivary complex; and in the dorsolateral funiculus of the spinal cord.
88 trigeminal sensory zone and the dorsolateral funiculus of the spinal cord.
89 s via a stimulating electrode in the lateral funiculus of the T2 or T10 segment of spinal cord.
90 al half of the dorsal portion of the lateral funiculus on one side, dorsal and over-dorsal hemisectio
91 al cord on one side and transects the dorsal funiculus on the other side.
92 CAP-LI nerve fibers were seen in the lateral funiculus projecting into the intermediolateral cell col
93 econdary cell wall (SCW) biosynthesis in the funiculus remain elusive.
94 ventral roots and axons in the ventrolateral funiculus, respectively, were confined within a gray neu
95 ified them as mediated mainly via the dorsal funiculus-spino-olivocerebellar path (DF-SOCP).
96 e intermediolateral cell column, the lateral funiculus, the intercalated nucleus and the central auto
97 ects within the ventral aspect of the dorsal funiculus, the same location as the descending corticosp
98 esis is restricted to the vasculature of the funiculus to ensure proper seed loading in Arabidopsis.
99 eral ascending projection within the lateral funiculus to the L4 level.
100 rhythm depended on continuity of the ventral funiculus (VF) along the S2-L2 segments.
101 n of fibers in the superficial ventrolateral funiculus (VLF) at a site from which rhythmic locomotor-
102       The superficial thoracic ventrolateral funiculus (VLF) contains both ascending and descending a
103 n through intact fibers in the ventrolateral funiculus (VLF) contralateral to HX.
104  neurons ascending through the ventrolateral funiculus (VLF) have been shown to transmit nociceptive
105 heaths around the axons in the ventrolateral funiculus (VLF) of spinal cord.
106 er of OL-remyelinated axons in ventrolateral funiculus (VLF) or lateral funiculus (LF) at the injured
107 e whose axons project into the ventrolateral funiculus (VLF), in embryonic day 9 (E9)-E12 chick embry
108 tic inputs, L5 dorsal root and ventrolateral funiculus (VLF), were recorded intracellularly in L5 mot
109 ia reticulospinal axons in the ventrolateral funiculus (VLF).
110 hase of EN1 axon growth in the ventrolateral funiculus (VLF); however, En1 is not required for the ea
111 inal white matter [ipsilateral ventrolateral funiculus (VLF)] and muscle spindle afferents.
112 s generally weak, except in the dorsolateral funiculus, where strongly calcineurin-positive axons for
113  rats underwent T9 transection of the dorsal funiculus, which axotomizes the dorsal CST, and introduc
114 ctivated in the ventro-lateral aspect of the funiculus, while the elbow muscle maps spread to both do
115 rhombomeres 6-7 that elongated in the dorsal funiculus, while the other originated from rhombomeres 2
116 d2 spinal commissural axons join the lateral funiculus within the spinal cord and target the cerebell

 
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