ライフサイエンスコーパス: brain stem

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

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

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

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

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

6 tonergic and adrenergic projections from the brain stem.

7 tory neurotransmitter in the spinal cord and brain stem.

8 eatest involvement noted in the thalamus and brain stem.

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

10 increased sensory afferent discharge to the brain stem.

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

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

13 nvolve asymmetries in cortical inputs to the brain stem.

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

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

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

17 3 patients with diffuse axonal injury of the brain stem.

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

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

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

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

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

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

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

25 ebrain synaptically linked to neurons in the brain stem.

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

27 cated on neurons within the hypothalamus and brain stem.

28 ting from the cerebellum and the surrounding brain stem.

29 rigeminal mesencephalic nucleus (MNV) in the brain stem.

30 ctable in rostral areas of the Unc5h3 mutant brain stem.

31 nd the cortex by 22%, but did not affect the brain stem.

32 erves that transmit taste information to the brain stem.

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

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

35 vation in the periaqueductal gray and caudal brain stem.

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

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

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

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

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

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

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

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

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

45 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

46 .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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

61 50 mg/kg, i.p.) can penetrate into the shrew brain stem and frontal cortex; 3) whether GR73632 (2.5 m

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

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

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

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

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

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

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

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

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

71 t progressive action tremor, degeneration of brain stem and spinal cord neurons, and juvenile death.

72 spongiform neurodegeneration throughout the brain stem and spinal cord.

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

74 fast inhibitory synaptic transmission in the brain stem and spinal cord.

75 ted with severe loss of motor neurons in the brain stem and spinal cord.

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

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

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

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

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

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

82 Within the brain stems and brains of three paralyzed animals examin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

99 cluding hippocampus, thalamus, hypothalamus, brain stem, and spinal cord.

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

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

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

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

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

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

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

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

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

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

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

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

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

113 paired cognition") were the most impaired on brain stem auditory evoked potentials (P=.005); those (n

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

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

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

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

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

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

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

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

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

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

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

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

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

127 9 mice results from widespread damage in the brain stem caused by destructive inflammatory responses

128 cDNA clones, VL1, VL2 and VL3, from a human brain stem cDNA expression library using four tandem rep

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 stly in the cervical spinal cord, and in the brain stem cranial motor nuclei.

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

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

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

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

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

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

161 Clinically, the field of brain stem death is reasonably defined and consistently

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

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

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

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

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

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

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

169 Although brain-stem evoked responses and distortion product otoac

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

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

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

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

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

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

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

177 several different neurotransmitters from the brain stem, hypothalamus, basal forebrain, and cerebral

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

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

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

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

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

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

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

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

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

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

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

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

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

191 ctory bulb (high nNOS) as well as cortex and brain stem (low nNOS).

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

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

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

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

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

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

198 tine as well as in cerebral, cerebellar, and brain stem neurons but not in glial cells.

199 virions spread to the brain in long axons of brain stem neurons that give rise to the tenth cranial n

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

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

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

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

204 egeneration of cerebellar Purkinje cells and brain stem neurons.

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

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

207 heteropentameric glycine receptors in these brain stem nuclear groups.

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

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

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

211 form degeneration of the cortex and specific brain stem nuclei associated with gliosis and intramyeli

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

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

214 , ventral tegmentum, geniculate, and certain brain stem nuclei, a striking inverse pattern of express

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

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

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

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

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

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

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

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

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

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

225 20% higher than in either the cortex or the brain stem (p < 0.05).

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

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

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

229 ism and oxidative phosphorylation than other brain stem populations.

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

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

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

233 gh levels of 5-HTT mRNA were detected in all brain stem raphe nuclei, with variations in labeling amo

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

235 The brain stem region containing the nucleus magnocellularis

236 01 showed bilateral attenuated activation of brain stem regions and less deactivation in lateral orbi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

254 orated patch-clamp technique in a visualized brain stem slice.

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

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

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

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

259 Brain stem-spinal cord recordings reveal reduced neurona

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

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

262 Brain stem subnuclei including interstitial, intermediat

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

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

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

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

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

268 ed after 48 microwires were implanted in the brain stem, thalamus, and somatosensory cortex of rats.

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

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

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

285 (200 microg/kg) and c-fos expression in the brain stem was examined.

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

287 1-weighted MRI scans, the GM fraction of the brain stem was reduced in all HTLV-1-infected patients c

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

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

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

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

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

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

294 tors are expressed on nerve terminals in the brain stem, where they increase the spontaneous release

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

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

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

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

299 neuronal cocultures of rat hypothalamus and brain stem with Ang II elicits an Ang II type 1 (AT1) re

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