ライフサイエンスコーパス: brain stem

1 mpus, thalamus, tectum, tegmentum, and lower brain stem).

2 tioning and examining the entire tissue (0/6 brain stems).

3 rons, which are located primarily within the brain stem.

4 ic resonance imaging (MRI) of the orbits and brain stem.

5 mygdala, hippocampus, putamen, thalamus, and brain stem.

6 ls, and HSV-1-specific CD8(+) T cells to the brain stem.

7 esencephalic trigeminal nucleus (Me5) of the brain stem.

8 e hippocampus, amygdala, olfactory bulb, and brain stem.

9 rinB3, but not ephrinB2, is expressed in the brain stem.

10 linked to productive HSV-2 infection in the brain stem.

11 tonergic and adrenergic projections from the brain stem.

12 tory neurotransmitter in the spinal cord and brain stem.

13 eral terminals and its site of origin in the brain stem.

14 increased sensory afferent discharge to the brain stem.

15 of approximately 20 microm were found in the brain stem.

16 nd internal capsule, and infrequently in the brain stem.

17 ectious virus could not be identified in the brain stem.

18 nvolve asymmetries in cortical inputs to the brain stem.

19 e spinal cord or in CNS areas outside of the brain stem.

20 or beta-endorphin in specific regions of the brain stem.

21 3 patients with diffuse axonal injury of the brain stem.

22 g in rostral structures and less abundant in brain stem.

23 on than in the frontal lobes, cerebellum, or brain stem.

24 er estimates for the thalamus, striatum, and brain stem.

25 or examination of PP receptor binding in the brain stem.

26 nigra and other neurons of the midbrain and brain stem.

27 in the basal ganglia, centrum semiovale, or brain stem.

28 and diencephalon, and in the medulla of the brain stem.

29 within the mouse hypothalamus, amygdala, and brain stem.

30 rons in the immediate vicinity of the caudal brain stem.

31 ebrain synaptically linked to neurons in the brain stem.

32 cated on neurons within the hypothalamus and brain stem.

33 ting from the cerebellum and the surrounding brain stem.

34 vation in the periaqueductal gray and caudal brain stem.

35 putamen, pallidum, caudate, hippocampus, and brain stem.

36 eatest involvement noted in the thalamus and brain stem.

37 reads from the cortex and hippocampus to the brain stem.

38 hed regions of the cortex, limbic system and brain stem.

39 h cerebellar hemispheres and the ipsilateral brain stem.

40 erves that transmit taste information to the brain stem.

41 Cav2.1 and Cav2.2 in cortex, cerebellum, and brain stem.

42 n brain, especially that associated with the brain stem.

43 emporal cortices, hippocampus, thalamus, and brain stem.

44 ime within respiratory-related nuclei of the brain stem.

45 greater in the TG than that detected in the brain stem.

46 f large motor neurons in the spinal cord and brain stem.

47 circuitries residing in the spinal cord and brain-stem.

48 m (71%), endocardium (93%), cerebrum (183%), brain stem (177%), renal cortex (53%), ileal mucosa (69%

49 esser increases occurred in the midbrain and brain stem (2-4-fold).

50 0.7 vs. 3.6 +/- 1.2 mg/100 g/min, P < 0.05), brain stem (2.2 +/- 0.4 vs. 2.8 +/- 0.5 mg/100 g/min, P

51 .8 vs. 3.5 +/- 0.8 mg/100 g/min, P = NS) and brain stem (2.5 +/- 0.5 vs. 2.6 +/- 0.5 mg/100 g/min, P

52 icant elevation in cGMP concentration in the brain stem 3 days after application of KCl.

53 interval (CI) 97.15-100%) than IHC of obex (brain stem, 76.56%, CI 57.00-91.46%) or retropharyngeal

54 oral and spatial movement of prions from the brain stem along cranial nerves into skeletal muscle as

55 ad and retrograde transport to the brain and brain stem along descending spinal tracts (i.e., lateral

56 turtles, and, generally, for the function of brain stem and cerebellar neural circuits in vertebrates

57 malformations that significantly affect the brain stem and cerebellum (pathogenesis partly or largel

58 plastic or dysplastic neuronal tissue in the brain stem and cerebellum can become epileptogenic in pe

59 tamate receptor subunits was examined in the brain stem and cerebellum of the pond turtle, Chrysemys

60 utamate receptor subunit distribution in the brain stem and cerebellum of turtles is similar to that

61 Considerable immunoreactivity in the turtle brain stem and cerebellum was observed with regional dif

62 t mice results in pathogenic invasion of the brain stem and cerebellum with attendant clinical sympto

63 sed to identify immunoreactive nuclei in the brain stem and cerebellum.

64 on in the cerebellum and lower levels in the brain stem and cortex.

65 n in the cerebellum with lower levels in the brain stem and cortex.

66 hways related to balance control in both the brain stem and forebrain.

67 50 mg/kg, i.p.) can penetrate into the shrew brain stem and frontal cortex; 3) whether GR73632 (2.5 m

68 increases Kv2 currents in both the auditory brain stem and hippocampus (>3-fold) transforming synapt

69 espite marked elevations in Ang II levels in brain stem and hypothalamus at these later time points.

70 hine-induced receptor desensitization in the brain stem and hypothalamus, consistent with exon 7 invo

71 The expression of Nhlh1 in the developing brain stem and in the vagal nuclei in the wild-type mous

72 neuropathies, cerebellar ataxia, myelopathy, brain stem and limbic encephalopathy.

73 virus from the brain, and clearance from the brain stem and lumbar spinal cord was delayed, followed

74 hemangioblastomas of the cerebellum, spine, brain stem and retina.

75 ed by progressive atrophy of the cerebellum, brain stem and spinal cord and sensory axonal neuropathy

76 activation of microglia and monocytes in the brain stem and spinal cord during disease progression.

77 spongiform neurodegeneration throughout the brain stem and spinal cord.

78 pothalamus, such as autonomic regions of the brain stem and spinal cord.

79 mediate inhibitory neurotransmission in the brain stem and spinal cord.

80 Coordinated development of brain stem and spinal target neurons is pivotal for the

81 ting in neurodegeneration in the cerebellum, brain stem and spinocerebellar tracts.

82 more NK cells (NK1.1+ CD3-) residing in the brain stem and spleen of infected wild-type mice.

83 demonstrate HSV-1 gains access to the murine brain stem and subsequently brain ependymal cells, leadi

84 ized in subsets of neurons, including in the brain stem and the ventricular zone.

85 tected more frequently in the TG than in the brain stem and, in all but one case, the amount of virus

86 and cerebellum and leukoencephalopathy with brain-stem and spinal cord involvement and elevated whit

87 and cerebellum, and leukoencephalopathy with brain-stem and spinal cord involvement and elevated whit

88 rence in glucose metabolism in the thalamus, brain stem, and cerebellum between comatose and noncomat

89 nsciousness, CMRglc values for the thalamus, brain stem, and cerebellum significantly correlated with

90 cal bilirubin staining of the basal ganglia, brain stem, and cerebellum, and is associated with hyper

91 r, thalamus, basal ganglia, cerebral cortex, brain stem, and cerebellum.

92 tic disorder that affects the limbic system, brain stem, and cerebellum.

93 lls (NSCs) from perinatal murine cerebellum, brain stem, and forebrain.

94 i, the hippocampus, the amygdala, the caudal brain stem, and midbrain dopaminergic neurons.

95 GlyR are found in the spinal cord and brain stem, and more recently they were reported in high

96 eration of motor neurons in the spinal cord, brain stem, and motor cortex.

97 lial activation in the facial nucleus in the brain stem, and on axon degeneration and immune cell inf

98 chemotherapeutic options for supratentorial, brain stem, and optic track gliomas are discussed.

99 Ventral striatal, amygdala, brain stem, and orbitofrontal responses to hypoglycemia

100 d in sleep, and insults to the hypothalamus, brain stem, and reticular activating system are some of

101 ia of the corpus callosum, a small flattened brain stem, and specific cystic lesions in the white mat

102 ative disease where motor neurons in cortex, brain stem, and spinal cord die progressively, resulting

103 d synaptotagmin-2 levels in mouse forebrain, brain stem, and spinal cord.

104 of the motor neurons in the cerebral cortex, brain stem, and spinal cord.

105 d SINV infection and clearance in the brain, brain stem, and spinal cords of severe combined immunode

106 death was observed in the cerebral cortices, brain stems, and cerebella of caspase 3(-/-) mice.

107 Their axon tracts through the brain stem are established by a simple set of pioneer ax

108 abundantly expressed in forebrain limbic and brain stem areas that regulate stress and emotional beha

109 n primary cultures from the hypothalamus and brain stem areas to study the role of ROS on the cellula

110 r; alterations in metabolic signaling to the brain stem as a result of chronic liver disease could in

111 in pituitary, cerebellum, and in portions of brain stem associated with sensorimotor function.

112 results of IHC staining of sections from the brain stem at the convergence of the dorsal motor nucleu

113 After bilateral CSX, transection of the brain stem at the mid-pontine level abolished PD in resp

114 control of the pupil, and transection of the brain stem at the mid-pontine level blocks access of vag

115 atory infiltrates were seen in the lungs and brain stems at day 2 and day 6 after infection, respecti

116 rological status, along with measurements of brain stem auditory evoked potential (BAEP) changes.

117 nificant delay in the FIV-induced effects on brain stem auditory evoked potentials, and demonstrated

118 d [3H]strychnine binding activity in several brain stem auditory nuclei.

119 s part of acoustic information processing in brain stem auditory pathways and contributes to the regu

120 using a brain slice preparation of the avian brain stem auditory system have shown that activation of

121 In contrast, FIV-associated changes in brain stem auditory-evoked potentials were slow to devel

122 e examined the embryonic origins of cells in brain-stem auditory nuclei with particular emphasis on N

123 ex ("barrels"), thalamus ("barreloids"), and brain stem ("barrelettes").

124 on the other of more diffuse afferents from brain stem, basal forebrain, and other regions.

125 l disorder characterized by hydranencephaly; brain stem, basal ganglia, and spinal cord diffuse clast

126 ed and normalized by the whole-brain (WB) or brain stem (BS) average values as SUV ratio (SUVR((WB))

127 to 5 structures (thalamus [TH], cortex [CX], brain stem [BS], cerebellum [CB], and half brain).

128 sive transsynaptic infection not only of the brain stem but also of areas of the forebrain synaptical

129 of SP selectively and rapidly penetrated the brain stem but not the frontal cortex.

130 s individuals, this surge of activity in the brain stem, but also in medial wall cortical regions pro

131 9 mice results from widespread damage in the brain stem caused by destructive inflammatory responses

132 hat are similar to the processes observed in brain stem cells and lung progenitors.

133 olecular mechanisms preventing self-renewing brain stem cells from oncogenic transformation are poorl

134 le in driving a tumor suppressor response in brain stem cells upon oncogenic insult.

135 N-cadherin to stabilize apical junctions in brain stem cells.

136 ers the specific effects of high iron on the brain, stem cells, and the process of erythropoiesis and

137 om hemorrhagic lesions), striatum, thalamus, brain stem, cerebellar cortex, and whole brain was compa

138 neuritis, incomplete transverse myelitis, or brain-stem/cerebellar syndrome) and at least two charact

139 somes and other cellular organelles from the brain stem, cerebellum and spinal cord of the mouse brai

140 lls and astrocytes were present in thalamus, brain stem, cerebellum and spinal cord, indicating regio

141 st in the caudate nuclei, putamena, thalami, brain stem, cerebellum, and occipital cortex of each sub

142 ter only within the CNS, particularly in the brain stem, cerebellum, and spinal cord.

143 rominent involvement of large neurons in the brain stem, cerebellum, basal ganglia, thalamus, and spi

144 ised balance) could be representative of the brain stem/cerebellum dysfunction.

145 This increase in brain stem cGMP was abolished by tonabersat pre-treatmen

146 elect vagal subnuclei that may represent the brain stem circuit involved in the abdominal vagal-affer

147 r control because they are precise and their brain-stem circuitry is already well understood.

148 These observations suggest that different brain stem circuits are involved in swallow-induced and

149 control pathways in enabling spinal cord and brain stem circuits to generate meaningful motor pattern

150 Therefore, thalamic and brain stem CMRglc may have a closer correlation than doe

151 P < 0.05.) but was not related to GCSpet and brain stem CMRglc.

152 Keywords: Adults and Pediatrics, Brain/Brain Stem, CNS, Computer Aided Diagnosis (CAD), Compute

153 infection in the trigeminal ganglia (TG) and brain stem compared to the control-vaccinated group.

154 raining lymph nodes, spleen, spinal cord, or brain stem comparing HSV-2-infected wild-type to CCR5-/-

155 ccompanied by increasing infiltration of the brain stem, cortex and thalamus by CD68 positive microgl

156 The results from bovine brain stem, cortex, and cerebellum demonstrated the repr

157 lity of analysis of HS, 15 mum frozen bovine brain stem, cortex, and cerebellum tissue sections were

158 hyperphosphorylated TAU in the spinal cord, brain stem, cortex, hippocampus and cerebellum of adult

159 of cannabinoids in CB(1)(-/-) membranes from brain stem, cortex, hippocampus, diencephalon, midbrain,

160 ng in intensive care units who were possibly brain stem dead (comatose, apparently apnoeic with unres

161 Cadaveric kidneys from brain-stem-dead donors continue to be limited because th

162 d rates for harvested kidneys is higher than brain-stem-dead donors.

163 Data on bowel offering from 657 donors after brain stem death (DBD) and on 46 patients on the active

164 after cardiac death (DCD) and donation after brain stem death (DBD) cohorts.

165 Donor after cardiac death and donor after brain stem death (DBD) had equivalent 1-, 3-, and 5-year

166 splantation using organs from donation after brain-stem death (DBD) donors.

167 se include migraine, encephalopathy, chorea, brain stem dysfunction, myelopathy, mononeuritis multipl

168 e serum of patients with subacute limbic and brain-stem dysfunction and testicular cancer contains an

169 patients with cancer, symptoms of limbic and brain-stem dysfunction may result from a paraneoplastic

170 red neuronal activity in the neurons of both brain stem emetic nuclei and the enteric nervous system

171 sticular cancer and paraneoplastic limbic or brain-stem encephalitis (or both), 10 had antibodies in

172 Paraneoplastic limbic or brain-stem encephalitis occurs more frequently with test

173 Although brain-stem evoked responses and distortion product otoac

174 , in which the largest increases are seen in brain stem, followed by striatum, thalamus, and frontal

175 ified in the trigeminal ganglia (TG) and the brain stem from the same latently infected animal using

176 ren with a newly diagnosed diffuse intrinsic brain stem glioma (BSG) and to investigate associations

177 trocytoma (n = 7), low-grade glioma (n = 9), brain stem glioma (n = 4), medulloblastoma (n = 2), and

178 intense uptake throughout the tumor, whereas brain stem gliomas (BSGs) had low uptake in less than 50

179 The auditory nuclei of the chick brain stem have distinct morphologies and highly specifi

180 of sympathetic activation that occurs after brain stem herniation and are not associated with allogr

181 wer interpreted the first ECG obtained after brain stem herniation in 980 potential organ donors mana

182 cord (wild type [WT]) or the cerebellum and brain stem (IFN-gamma deficient).

183 rt of reactivated virus from the TG into the brain stem.IMPORTANCE Latent herpes simplex virus (HSV)

184 The ratio of striatum to brain stem in mice and the binding potential (BP) in the

185 in the parasympathostimulatory nuclei of the brain stem in normal young and aged animals were measure

186 ped primarily on the ipsilateral side of the brain stem, in the cerebellum, and contralateral side of

187 Within neurons of the cerebellum and brain stem, in the context of WNV infection, a deficienc

188 , RaD, and MD in all major tracts except the brain stem, indicating that age-related changes in white

189 d other causes, including neoplasm, GCA, and brain stem infarction.

190 ers to undetectable levels but did not alter brain stem inflammation or mortality.

191 pinal cord invasion and block cerebellar and brain stem invasion.

192 The findings suggest brain stem involvement as an additional site of neurodeg

193 uggest that infectious virus detected in the brain stem is primarily the result of transport of react

194 The regional CMRglc of the brain stem is relatively unaffected by the TBI.

195 6) mice developed intense focal inflammatory brain stem lesions of primarily F4/80(+) macrophages and

196 calized to areas in the hypothalamus and the brain stem located outside the blood-brain barrier in a

197 els show autonomic dysfunction involving the brain stem locus coeruleus (LC).

198 e largest population of LepRb neurons in the brain stem, mediate this process.

199 ins, including cerebral cortex, hippocampus, brain stem, mid brain, cerebellum, and hypothalamus.

200 cing of mRNA and miRNA from cerebral cortex, brain stem, midbrain and cerebellum of 4L;C* mice.

201 ole for the vestibular system and descending brain stem motor pathways to the erectores spinae muscle

202 The cerebellum, brain stem, neocortex, hippocampus and adrenal gland med

203 entry and pathology may underlie the severe brain stem neuronal dysfunction seen in fatal Nipah vira

204 rasympathetic information from preganglionic brain stem neurons to the heart.

205 Virus was cleared from spinal cord and brain stem neurons, but not from cortical neurons, and r

206 (CCK), has also been linked to activation of brain stem neurons, suggesting that it might act partial

207 pal pyramidal neurons and rapid infection of brain stem neurons.

208 egeneration of cerebellar Purkinje cells and brain stem neurons.

209 een observed in immature spiral ganglion and brain-stem neurons and is likely to depend on cochlear i

210 N-myc(T58A) cerebellar and brain stem NSCs generated medulloblastoma/primitive neur

211 heteropentameric glycine receptors in these brain stem nuclear groups.

212 was undertaken in seven respiratory-related brain stem nuclei and one nonrespiratory nucleus in P0-2

213 objective of this study was to determine the brain stem nuclei and physiological responses activated

214 egrates neural signals from hypothalamic and brain stem nuclei and regulates feeding behavior, autono

215 eurons in the cochlear ganglion and auditory brain stem nuclei preserve the relative timing of action

216 reflect impoverished cortical signals to the brain stem nuclei that control eye movements.

217 leucoagglutinin, with projections to over 50 brain stem nuclei.

218 l PET scanners allow for investigating small brain stem nuclei.

219 gal efferent neurons that originate from two brain stem nuclei: the nucleus ambiguus and the dorsal m

220 uron shows that the human locus coeruleus, a brain stem nucleus containing cell bodies of noradrenerg

221 Two groups of neurons in the brain stem, octopus cells in the posteroventral cochlear

222 ly, NK activity from cells isolated from the brain stem of HSV-2-infected wild-type mice was greater

223 red from both the trigeminal ganglia and the brain stem of latently infected mice following a reactiv

224 demonstrated a pathological signature in the brain stem of Stat1-deficient mice characterized by upre

225 udy, we compared host gene expression in the brain stems of mice infected with either FrCas(E) or the

226 PBS or HCl on c-fos immunoreactivity of the brain stem or on physiological variables, and the effect

227 neuritis, incomplete transverse myelitis, or brain-stem or cerebellar syndrome) and evidence of prior

228 ctivity in SMS, both at the bedside (cortex, brain stem, or spinal cord) and at the bench (neuronal c

229 , anterior cingulate cortex, caudate nuclei, brain stem periaqueductal gray matter, cerebellum, and o

230 s (cerebellar gray matter, whole cerebellum, brain stem/pons, eroded subcortical white matter [WM], a

231 ls of aldolase C mRNA than other midbrain or brain stem populations in both control and IPD material.

232 ism and oxidative phosphorylation than other brain stem populations.

233 ophysiological recordings within the ventral brain stem pre-Botzinger respiratory complex were also a

234 TME PrP(Sc) entry into the brain stem preceded PrP(Sc) detection in the rostral cer

235 In the working heart-brain stem preparation of the Cx36-KO mouse, respiratory

236 y 4 p.i. (24 h after HSV-1 first reaches the brain stem) reduced nervous system viral titers to undet

237 01 showed bilateral attenuated activation of brain stem regions and less deactivation in lateral orbi

238 uted abnormalities of midline cerebellum and brain stem regions associated with Joubert syndrome.

239 of the pedunculopontine nucleus and in other brain stem regions in a pattern similar to what has been

240 the expression of adenosine A(2A)Rs mRNA in brain stem regions where GABAergic neurons are located;

241 The localization of substance P in brain-stem regions associated with vomiting, and the res

242 aquaporins play a role in hearing, auditory brain stem response (ABR) thresholds were compared in wi

243 nd 10 weeks of age were measured by auditory brain stem response (ABR).

244 of otoacoustic emission testing and auditory brain stem response according to national guidelines, an

245 ants exhibit significantly elevated auditory-brain stem response thresholds and reduced distortion-pr

246 indicated by an elevation in auditory-evoked brain stem response thresholds at 3 or 7 days postinocul

247 Auditory-evoked brain-stem response thresholds were used to assess heari

248 inbred strains detected linkage of auditory brain-stem response thresholds with a locus on distal ch

249 aluate this hypothesis, we measured auditory brain stem responses (ABRs), hair cell loss, and free ra

250 bor/+) and C57BL/6J showed variable auditory brain-stem responses and cochlear coiling.

251 food intake and lower body weight through a brain-stem-restricted receptor.

252 and executive regions, with its peak in the brain stem reticular activating system.

253 organized cell group closely related to the brain stem reticular formation, it can now be seen as a

254 rimary motor cortex (M1) strongly innervates brain stem reticular nuclei containing whisker premotor

255 Neural circuits connect brain stem sites that regulate vigilance state with the

256 sensory cortex (S1) strongly projects to the brain stem spinal trigeminal interpolaris nucleus, which

257 Axonal degeneration was evident in brain stem, spinal cord and white matter of cerebellum a

258 on of aggregated alpha-synuclein in specific brain stem, spinal cord, and cortical regions.

259 ically expressed, being detected only in the brain stem, spinal cord, and thalamic/hypothalamic areas

260 Brain stem-spinal cord recordings reveal reduced neurona

261 isions of patients who become locked-in with brain stem stroke or amyotrophic lateral sclerosis to be

262 have been shown to arise from somatosensory brain stem structures, but the nature of the projection

263 Brain stem subnuclei including interstitial, intermediat

264 tic target nuclei in the developing auditory brain stem, such a role for gamma-aminobutyric acid (GAB

265 found within the reticular formation of the brain stem, suggesting that MSCs also may have different

266 plex neurophysiological system involving the brain stem, superior colliculus, and several cortical ar

267 The CM pathway may act together with several brain-stem systems that also act directly with motoneuro

268 neurons with input from the motor-cortex and brain-stem systems.

269 and CCL5 in the vagina, spinal cord, and/or brain stem than did wild-type mice.

270 connections between neural structures in the brain stem that control eye movements.

271 parabrachial nucleus (PBN) is an area of the brain stem that controls eating and contains endogenous

272 bunit switching may be a common theme in the brain stem that may mediate different functional propert

273 the longitudinal (rostrocaudal) axis of the brain stem that was consistent with the classically desc

274 ripts and HSV-1 lytic cycle genes within the brain stem, the ependyma (EP), containing the limbic and

275 emotor neurons, which are located within the brain stem, the midbrain, and the neocortex.

276 SV-2 levels in the vaginal, spinal cord, and brain stem tissue of wild-type but not CCR5-/- mice.

277 oid analgesic, is known to act in the rodent brain stem to produce highly effective antinociception i

278 s, in part because tissue from low-grade and brain stem tumors is not readily available, and also bec

279 sEH expression in the hypothalamus and brain stem, two cardioregulatory brain areas, was increa

280 e among all gray matter regions, whereas the brain stem, uncus, and hippocampus had the lowest uptake

281 We aimed to identify the brain stem vagal subnuclei involved in these reflexes.

282 d a frequency-dependence that paralleled the brain stem velocity storage mechanism.

283 0), inferior orbital frontal lobe (area 11), brain stem (ventral tegmentum), anteromesial temporal lo

284 hyperintense bilateral lesions in the dorsal brain stem vestibular nucleus (VN) and cerebellum of sev

285 The earliest presence of infectivity in the brain stem was detected at 24 mpi, whereas PrP(Sc) accum

286 (200 microg/kg) and c-fos expression in the brain stem was examined.

287 ns, and the initial appearance of TME in the brain stem was found in the hypoglossal nucleus at 2 wee

288 ut a cellular source for reactivation in the brain stem was not identified, despite serially sectioni

289 1-weighted MRI scans, the GM fraction of the brain stem was reduced in all HTLV-1-infected patients c

290 acytoid dendritic cell infiltration into the brain stem was reduced in CD118(-/-) mice following infe

291 e use of functional genomics on the infected brain stems, we determined gene signatures that were rep

292 flammatory cells infiltrating the cornea and brain stem were isolated and stained for flow cytometric

293 G, tryptophan and 5-HIAA in hypothalamus and brain stem were not significantly altered.

294 Orbital structures and the brain stem were prepared for tracer detection and immuno

295 suggesting that pathways at the level of the brain stem were principally intact.

296 in the olfactory bulb, cerebral cortex, and brain stem; whereas HK483 was not recovered in these tis

297 viral replication were high in the brain and brain stem, while levels of viral genome equivalents wer

298 l, ethidium bromide-induced demyelination of brain stem white matter (with intervening recovery) on t

299 ) region of the cerebellum as well as in the brain stem with a relatively uniform distribution and ha

300 were elevated in the trigeminal ganglia and brain stem with virus disseminating rapidly to the drain