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1 rchical order (from the periphery and up the neuraxis).
2 ted to originate from different parts of the neuraxis.
3  regulator of axonal crossing throughout the neuraxis.
4 aterals to other sites along the ventricular neuraxis.
5 commissural tracts at multiple levels of the neuraxis.
6 of Hensen's node, the organizer of the avian neuraxis.
7 erentiate into more posterior regions of the neuraxis.
8 rlie induction and patterning of the forming neuraxis.
9 e cortex that are common to all parts of the neuraxis.
10 ex neural circuits at multiple levels of the neuraxis.
11 pina bifida in the lumbosacral region of the neuraxis.
12 transmission through different levels of the neuraxis.
13  expression increased throughout most of the neuraxis.
14 graft contributes extensively to the ectopic neuraxis.
15 orders, affecting one or more regions of the neuraxis.
16 n the alar and basal plates along the entire neuraxis.
17 brain showed labelled neurons throughout the neuraxis.
18  nociceptive processing at all levels of the neuraxis.
19 R-B mRNA was widely expressed throughout the neuraxis.
20 mesoderm, endoderm and ventral aspect of the neuraxis.
21 t the level of the injury and throughout the neuraxis.
22  subtypes located at different levels of the neuraxis.
23 uts, can influence processing throughout the neuraxis.
24 nd on their location along the somatosensory neuraxis.
25 n activity changes across the pain circuitry neuraxis.
26 the diversity of neurons generated along the neuraxis.
27  produce neurodegeneration across the entire neuraxis.
28 rd and brain locations of the pain circuitry neuraxis.
29 atent in ganglionic neurons along the entire neuraxis.
30 m for the spread of degeneration through the neuraxis.
31 ent progression to more rostral parts of the neuraxis.
32 selectivity first emerges along the auditory neuraxis.
33 indgut, arises from the sacral region of the neuraxis.
34  morphogenic signals along the length of the neuraxis.
35 n of synaptic proteins in the rostral-caudal neuraxis.
36  behind that from more caudal regions of the neuraxis.
37 ation of neural progenitors along the entire neuraxis.
38 hogen Shh, has distinct properties along the neuraxis.
39 ated at multiple locations along the sensory neuraxis.
40  phenotypes of SIRT1-expressing cells in the neuraxis.
41 uclear boundaries at different levels of the neuraxis.
42 acids converge somewhere along the gustatory neuraxis.
43 ability at multiple levels along the sensory neuraxis.
44 ects along the length of the anteroposterior neuraxis.
45 nhibition at distinct sites of the pyramidal neuraxis.
46 ients had metastatic disease confined to the neuraxis.
47 lopment of ventral structures throughout the neuraxis.
48 loor plate formation along the length of the neuraxis.
49 lei to pervasive degeneration throughout the neuraxis.
50 l cells in discrete locations throughout the neuraxis.
51 tube, is regulated along the anteroposterior neuraxis.
52 g at spinal versus supraspinal levels of the neuraxis.
53 tems at the following multiple levels of the neuraxis: (1) through altering transmission in spino-oli
54 ivity is differentially regulated across the neuraxis; (2) sex differences in proliferation were pres
55 dose craniospinal RT regimen (23.4 Gy to the neuraxis, 32.4-Gy boost to the posterior fossa) and adju
56 S), the first relay in the central gustatory neuraxis, a rich variety of sensory inputs generated by
57 ing themselves throughout the deficient host neuraxis after perinatal allograft, and giving rise to a
58 s in the hypothalamus project throughout the neuraxis and are involved in regulation of the sleep/wak
59 of its neural correlates within the auditory neuraxis and associated structures.
60 NPs to achieve widespread delivery along the neuraxis and highlight IT administration as a potentiall
61 lastic meningitis is a disease of the entire neuraxis and is pleomorphic in its clinical presentation
62 y at median doses of 36.0 and 59.4 Gy to the neuraxis and pineal region, respectively.
63 he distribution of Sirt1 mRNA throughout the neuraxis and suggest a previously unrecognized role of b
64 dy includes nontelencephalic portions of the neuraxis and suggest that the generation and maintenance
65 y of these solutions when injected along the neuraxis and the development of formulations without pre
66  which the cortex influences the rest of the neuraxis and thus are essential for proper cortical func
67 t (PT) neurons, which project throughout the neuraxis, and intratelencephalic (IT) neurons, which pro
68 , becomes latent in ganglia along the entire neuraxis, and reactivates to produce shingles (zoster).
69 s initiated by signals that posteriorize the neuraxis, and then secondarily restricted dorsally in re
70         NM is a disease affecting the entire neuraxis, and therefore clinical manifestations are pleo
71 resentation strength throughout the auditory neuraxis as a function of sleep state, as well as neural
72 s at multiple levels of the central auditory neuraxis as well as limbic and non-auditory cortical cen
73 lopment of central sensitization in the pain neuraxis, associated with allodynia and hyperalgesia obs
74 the tracking of secondary changes across the neuraxis at the microstructural level.
75 e was administered, and (c) the level of the neuraxis at which the behavioral assay was organized.
76 SVV DNA in ganglia at multiple levels of the neuraxis but not in the lung or liver tissue of any of t
77 ly increasing to adult levels throughout the neuraxis by postnatal day 26.
78 lls in the DRN rostrocaudal and mediolateral neuraxis by using a capsaicin challenge paradigm (50 mg/
79 ing sympathetic output to the heart from the neuraxis can protect against ventricular arrhythmias.
80 her-order sensory cortices and an evaluative neuraxis composed of the hypothalamus, amygdala, and orb
81 duce while notochord from all lengths of the neuraxis continues to induce.
82 mbryos with a well-formed and well-patterned neuraxis develop in the complete absence of notochord ce
83 x1a is expressed in the roof plate along the neuraxis during development of the CNS.
84 dherin in positioning cells along the caudal neuraxis during neurulation.
85  to examine neural activation throughout the neuraxis during sleep deprivation and recovery.
86 e targeting different sites of the autonomic neuraxis (experiment 1) or AIH (experiment 2).
87 ; (2) vagal NCC transplanted into the sacral neuraxis extensively colonised the hindgut, migrated in
88 puts from regions distributed throughout the neuraxis from frontal neocortex to the mesencephalon.
89 f EBV to affect multiple parts of the entire neuraxis from meninges and brain to the spinal cord and
90 hat afferents from different portions of the neuraxis have overlapping functions.SIGNIFICANCE STATEME
91               At all levels of the gustatory neuraxis, however, there are many cells that are broadly
92 nted to an ectopic site, induces a secondary neuraxis, identical to that induced by Hensen's node.
93 d it is expressed widely along the mammalian neuraxis, implying that there are undiscovered electrica
94 y Bodies/neurites) and spread throughout the neuraxis in a pattern that aligns with disease progressi
95 associated activation at three levels of the neuraxis in individual subjects.
96 till expressed along the adult zebrafish CNS neuraxis in most locations seen in larvae.
97  of Plp1 mRNA and PLP protein throughout the neuraxis in vivo.
98  of noradrenergic innervation to the central neuraxis, in Mecp2 mutant mice.
99 ticity occurring in all stations of the pain neuraxis, including cortical regions of the pain matrix.
100 e LHA and provide diffuse innervation of the neuraxis, including monosynaptic projections to the cere
101 ptides are widely distributed throughout the neuraxis, including regions associated with energy balan
102 d cells were found at multiple levels of the neuraxis, including septum, thalamus, hypothalamus, and
103 f neurological syndromes affecting the whole neuraxis, including the cerebral vasculature and, in som
104 erative ventricular zone at any level of the neuraxis, indicating that lamp is expressed in postmitot
105 analyzing early signaling events involved in neuraxis initiation and patterning.
106                                 Reduced-dose neuraxis irradiation (23.4 Gy) is associated with increa
107 eas eligible patients receiving reduced-dose neuraxis irradiation had 52% event-free survival at 5 ye
108 s, eligible patients receiving standard-dose neuraxis irradiation had 67% event-free survival (EFS) a
109 for mixed motor-sensory loss when the entire neuraxis is considered, rather than a model primarily fo
110 l, the pattern of alpha 2C-LI throughout the neuraxis is consistent with previously published reports
111 on of A2A-AR immunoreactivity throughout the neuraxis is consistent with the receptors' role in modul
112 at the action of mGlu5 receptors in the pain neuraxis is not homogenous, and suggest that blockade of
113 l disease or metastatic disease localised to neuraxis) medulloblastoma.
114 expression domains along the anteroposterior neuraxis, midline, and streak/tailbud.
115 s as signposts for particular lesions of the neuraxis must be tempered by a working knowledge of fals
116 channels are widely expressed throughout the neuraxis, obscuring identification of the critical netwo
117 y and heterogeneously distributed across the neuraxis of the Syrian hamster brain.
118 ocalization of 5-HT(3A) receptors across the neuraxis of the Syrian hamster forebrain using immunohis
119 mbesin has similar functions in the visceral neuraxis of these two species.
120    PIST is distributed widely throughout the neuraxis, predominantly associated with neuronal cell bo
121 est that the various brain regions along the neuraxis previously implicated in the lordosis reflex ar
122 hibits ascending impulse transmission in the neuraxis projecting to the hypothalamus.
123 t essentially all rostrocaudal levels of the neuraxis; prospective mesoderm from the caudolateral epi
124 reased risk of early relapse, early isolated neuraxis relapse, and lower 5-year EFS and overall survi
125 ajor pathways beyond this canonical auditory neuraxis remains unclear.
126 developing embryo while patterning along the neuraxis remains unperturbed.
127 anized at medullary and spinal levels of the neuraxis, respectively.
128 dentification of neural cells throughout the neuraxis showing somatically generated mosaic aneuploidy
129    During early patterning of the vertebrate neuraxis, the expression of the paired-domain transcript
130 cently confirmed that a second region of the neuraxis, the sacral neural crest, also contributes to t
131 n-associated activity in three levels of the neuraxis: the medullary dorsal horn, thalamus, and prima
132  in the cortex and at multiple levels in the neuraxis; the underlying autoimmunity and involvement of
133 ects motor systems at multiple levels of the neuraxis through the following: (1) differential control
134                      Retinal axons cross the neuraxis to form the optic chiasm on the hypothalamus in
135 g activates a gut-brain-brown adipose tissue neuraxis to regulate thermogenesis.
136 CC, transplanted to the sacral region of the neuraxis, to colonise the chick hindgut and form the ENS
137 owed that patients randomized to the reduced neuraxis treatment had increased frequency of relapse.
138  to a total dose of 54 Gy in addition to the neuraxis treatment.
139 s transplanted into the sacral region of the neuraxis, vagal-derived ENS precursors immediately migra
140    After a survival period of 7-10 days, the neuraxis was examined for anterograde labelling.
141 haviors organized at different levels of the neuraxis was examined in the rat.
142  distal components of the sensory peripheral neuraxis was studied and related to disorders in structu
143 r radiation therapy (XRT) (54 Gy tumor/36 Gy neuraxis) was compared with vincristine, lomustine (CCNU
144 ove patients' lives different regions of the neuraxis were ablated.
145 ization afterdischarges, VADs) levels of the neuraxis were elicited by noxious tailshock.
146 s are also expressed throughout central pain neuraxis, where their functional contributions to neural
147 he dorsal and ventral midlines of the entire neuraxis, whereas anteroposterior patterning is controll
148 ing rapidly through the SAS along the entire neuraxis with reproducible, anatomically defined pattern
149 istributed in sensory ganglia throughout the neuraxis, with higher numbers noted in the sixth lumbar
150 as observed in neurons in all regions of the neuraxis, with particularly prominent localizations in t
151 to receptors at each level of the peripheral neuraxis without any apparent anatomical preference for

 
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