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1 gions (periventricular white matter and both hippocampi).
2 suppression of spontaneous seizures in both hippocampi.
3 al-like discharges induced in vitro in mouse hippocampi.
4 ask in epileptic compared with non-epileptic hippocampi.
5 oven to depend on the presence of functional hippocampi.
6 57BL/6J mice and increased IL-1beta in their hippocampi.
7 re hypothalamic specific, with no changes in hippocampi.
8 al set of tissue samples from prenatal human hippocampi.
9 ronal loss, inflammation, and gliosis in the hippocampi.
10 ary hippocampal neuron cultures and in mouse hippocampi.
11 ctions of HFOs rates were found in epileptic hippocampi.
12 d methylation of the histone H3 in E17 fetal hippocampi.
13 ion were also increased in astrocytes in NBD hippocampi.
14 e) glycohydrolase mRNA were decreased in NBD hippocampi.
15 es in spared ipsi- and contralateral ventral hippocampi.
16 oligomers also increased in PS2APP;Trem2(ko) hippocampi.
17 in synaptic plasticity in eed and Mll mutant hippocampi.
18 lish or depress recurrent seizures in 70% of hippocampi.
19 RNA and protein levels were increased in NBD hippocampi.
20 nto SGs and away from polyribosomes, in both hippocampi.
21 were compared in epileptic and non-epileptic hippocampi.
22 uced by 44% in area CA1 of MTLE vs. non-MTLE hippocampi.
23 ficantly down-regulated in the neurons of AD hippocampi.
24 rd deviation in the Sommer sector of the MTS hippocampi.
25 ell as NFT formation, was observed in the AD hippocampi.
26 was associated with systemic hypoxia in both hippocampi.
27 lex families, had significantly smaller left hippocampi.
28 he brain, enhances neuronal survival in both hippocampi.
29 associated with increased activation of the hippocampi.
30 ulate white matter (WM), and the thalami and hippocampi.
31 tionalize the function of the left and right hippocampi.
32 188C>T) in postmortem AD olfactory bulbs and hippocampi.
33 Voxels were tailored to the individual hippocampi.
34 ere differences in T2 between right and left hippocampi.
35 ced by a mean of 42.7% compared with control hippocampi.
36 regions of interest within the head of both hippocampi.
37 r granule cell between control and sclerotic hippocampi.
38 eductions were not observed in non-epileptic hippocampi.
39 ong-term depression in USP6 transgenic mouse hippocampi.
40 ers reflect the extent of sclerosis in human hippocampi.
41 in brain metabolites characterize epileptic hippocampi.
42 quences predominantly involving the pons and hippocampi.
43 fferent spiking trains among eight different hippocampi.
44 e selectively reduced in the TFEB-transduced hippocampi.
45 o date comparing epileptic with normal human hippocampi.
46 es as well as in the thalami, amygdalae, and hippocampi.
47 cannot be used alone to distinguish between hippocampi.
48 lvement of the brainstem, basal ganglia, and hippocampi.
49 he largest effects seen in the amygdalae and hippocampi.
50 12 of 15 had abnormally low NAA in sclerotic hippocampi; 3 of these 12 also had abnormally low NAA co
51 iation (LTP) could not be induced in injured hippocampi; (3) GFAP and inducible NO synthase (iNOS) im
53 synchrony of neural oscillations between the hippocampi, a measure of brain function that indexed cog
54 First, metabolite changes occurring in brain hippocampi after application of 3 h of DBS to the animal
55 hermore, impaired growth of normal-appearing hippocampi after FSE suggests subtle injury even in the
57 rom this study of monkeys suggest that small hippocampi also reflect an inherited characteristic of t
58 G allele predicted lower volume of bilateral hippocampi among cannabis users relative to controls (bo
59 identified differentially expressed genes in hippocampi and amygdalae of the endogenous depression an
60 w that FNDC5/irisin levels are reduced in AD hippocampi and cerebrospinal fluid, and in experimental
61 n gray matter (GM) volume in their posterior hippocampi and concomitant changes to their memory profi
62 injured but also the contralateral uninjured hippocampi and correlated with the lesion induced atroph
64 decreased in DS fibroblasts, and in both the hippocampi and cortices of young (age 15-40 years old) a
65 its cleavage products was also increased in hippocampi and cultured hippocampal neurons lacking Fbxo
66 Risk adjustment correlated with DOC in the hippocampi and deliberation time with DOC in the medial
68 refrontal cortex, retroesplenial cortex, and hippocampi and elevated connectivity between anterior an
69 and a pattern of atrophy including bilateral hippocampi and entorhinal cortex, right inferior parieta
70 n a set of 110 manually segmented atlases of hippocampi and find the manifold learning technique and
71 steady-state levels are reduced in human AD hippocampi and in the brain of an AD mouse model versus
72 en and women had significantly smaller right hippocampi and larger cerebrospinal fluid volumes than h
73 ated caspase 3 protein were increased in NBD hippocampi and localized to nuclei, mossy fibers, and de
75 levels of BDNF were associated with smaller hippocampi and poorer memory, even when controlling for
76 with bumetanide abolished seizures in 70% of hippocampi and significantly reduced the frequency, dura
77 dine 10 mg/kg/day) for 5 days, and cortices, hippocampi and spinal cords were collected for immunoblo
78 RNA miR-124 was increased in demyelinated MS hippocampi and targets mRNAs encoding 26 neuronal protei
79 exhibited greater activity in both posterior hippocampi and the right fusiform gyrus during smooth pu
83 ysis included both the MTS and contralateral hippocampi, and covariance for changes in brain parenchy
84 response in the posterior cerebellar cortex, hippocampi, and lenticular nuclei bilaterally and the ri
86 ed significantly lower NAA in right and left hippocampi, and significantly higher Glu and Glu/NAA in
88 ansgene spontaneously develop RIDNs in their hippocampi, and the formation of RIDNs correlates with t
89 lifetime of seizures on both left and right hippocampi, and the presence of any co-existing malforma
90 tionality of remaining tissue in the damaged hippocampi, and to appreciate the neural basis of a dist
91 induces tPA activity and cell death in both hippocampi, and unilateral treatment of rats with neuros
92 plasma, young mouse plasma, and young mouse hippocampi, appears in the brain after systemic administ
93 in triple-transgenic AD mice, CAR levels in hippocampi are low and further reduced after systemic in
95 ed significant neuronal damage in KA-treated hippocampi at 16 h post-injection in both maternal and v
96 on microscopic analyses confirm that PS-cDKO hippocampi at 2 months postnatal do not yet exhibit syna
98 or densities significantly decreased in both hippocampi (binding potential: controls 1.62 +/- 0.07; A
100 were significantly decreased in demyelinated hippocampi, but not in demyelinated motor cortices from
101 vulnerable regions of the brain, notably the hippocampi, but was not sufficient to result in the more
102 AE by performing in vivo recordings from the hippocampi (CA1 and CA3) of moderate PAE and control adu
103 46), temporal cortices (Brodmann's area 22), hippocampi, caudate nuclei, and cerebella of schizophren
104 les, but volume changes in dorsal or ventral hippocampi, caudate-putamen, or thalamus were not detect
105 0 mRNA levels were elevated in tetanized rat hippocampi compared with those of sham controls that rec
106 ipitation assays in NG108-15 cells and mouse hippocampi confirmed specific Egr1 binding to the Ca(V)3
108 /B, was selectively increased in 4E-BP2(-/-) hippocampi, consistent with unaltered I-V relation of EP
109 LTP induced in chronic nicotine-treated hippocampi contained a component that is immune to rever
111 better spatial learning abilities and larger hippocampi containing more and larger neurons compared t
112 uggests that radiation-induced injury to the hippocampi could play an important role in this cognitiv
113 s, and subcortical regions such as bilateral hippocampi depended predominantly on the perceptual diff
114 Inhibition of the MAPK/ERK cascade in dorsal hippocampi did not impair acquisition, but blocked the f
115 nome miRNA sequencing in surgically resected hippocampi did not reveal obvious differences in express
119 zure reduction greater than 98% in bilateral hippocampi during stimulation and greater than 50% seizu
120 e changes were attenuated in parkin-injected hippocampi, even in the presence of Tau pathology, sugge
121 n in an interface chamber were compared with hippocampi fixed by perfusion or by immersion of the who
123 s homolog NMNAT1, but not NMNAT3, in rTg4510 hippocampi from 6 weeks of age using recombinant adeno-a
124 62 were observed in cytoplasmic fractions of hippocampi from chronically stressed rats, and immunoflu
129 interneuronal synapse formation, we studied hippocampi from mutant mice that completely lack the z+
131 this pathway to experimental seizures and in hippocampi from patients with intractable temporal lobe
132 NA profiles from myelinated and demyelinated hippocampi from postmortem MS brains and performed valid
137 c human epilepsy were validated by examining hippocampi from the pilocarpine model of chronic TLE.
138 itu hybridization and immunocytochemistry in hippocampi from three groups: TLE with hippocampal scler
139 activities of various apoptotic pathways in hippocampi from type 1 diabetic BB/Wor rats (hyperglycem
141 ding field and whole-cell patch recording in hippocampi from wild-type and transgenic mice, we show t
142 foundly upregulated KCNQ2/3 transcription in hippocampi from wild-type, but not AKAP150(-/-), mice af
144 ynapses or mtHSP70 was seen in myelinated MS hippocampi, further pointing toward a link between the c
145 Our results indicate that although both hippocampi generate HFOs with similar features that prob
151 he diagnostic potential of GSH estimation in hippocampi (HP) and frontal cortices (FC) as a biomarker
152 d in the head and body of the right and left hippocampi in 123 subjects: 62 patients with Alzheimer d
155 all samples, we found significantly smaller hippocampi in subjects with current PTSD compared with t
156 led activation of both TrkB and PLCgamma1 in hippocampi in the pilocarpine and kindling models in wil
157 uma exposure, we found evidence that smaller hippocampi indeed constitute a risk factor for the devel
158 t to left hippocampal volume ratios, smaller hippocampi initially, and reduced hippocampal growth.
159 tissue lactic acid and FFA were made in the hippocampi, ipsilateral cortex, contralateral cortex, an
161 anscriptome profiling by RNA-seq analysis of hippocampi isolated from neonatal pups prenatally expose
163 s +/- 0.31; right, 1.70 years +/- 0.37), and hippocampi (left, 1.93 years +/- 0.34; right, 1.78 years
164 matched cannabis users had smaller bilateral hippocampi (left, p=0.002; right, p=0.001) and left amyg
165 increased in myelinated and demyelinated MS hippocampi, mainly in the CA3/2 and CA1 subfields, which
166 rimary neuron-glia co-cultures from P0 mouse hippocampi, male neurons have more complex dendritic arb
168 s (HS; n = 16), non-HS (n = 10), and autopsy hippocampi (n = 9) were studied for NMDAR1 (NR1) and NR2
170 er cell of 29,201 from both fresh and frozen hippocampi, observing little difference in accessibility
171 lmodulin-dependent protein kinase II mRNA in hippocampi obtained during surgical resections for intra
172 n Illumina sequencing reads derived from the hippocampi of 10 colonial tuco-tucos housed in captivity
173 unit neuronal recordings were taken from the hippocampi of 10 male, New Zealand white rabbits during
174 Abeta and plaque loads were observed in the hippocampi of 11-month old Tg2576 mice born to mothers f
175 presynaptic and postsynaptic structures from hippocampi of 13 individuals aged 4 months to 71 years.
176 c imaging measurements were performed in the hippocampi of 14 control subjects and nine patients with
178 dentate granule cells acutely isolated from hippocampi of 28- to 35-day-old rats suggests that recep
179 Granule cells were acutely isolated from hippocampi of 7- to 14- and 45- to 52-day-old rats, and
182 ADAM10/AP2 association was increased in the hippocampi of AD patients compared with healthy controls
183 y of these deficits were also present in the hippocampi of adult Df(16)A(+/-) and Zdhhc8-deficient mi
190 l, FGF2 gene is delivered bilaterally to the hippocampi of APP+presenilin-1 bigenic mice via an adeno
191 sited amyloid in the vessels of cortices and hippocampi of APP/PS1DeltaE9/apoA-I(KO) mice, measured b
192 it and local field potential recordings from hippocampi of behaving rats with and without chronic epi
193 table metabolites can be quantified from the hippocampi of cognitively impaired individuals, and that
194 troscopy (MRS) studies of the left and right hippocampi of consenting Gulf War veterans (N=15; 10 wit
196 f the cannabinoid type 1 (CB(1)) receptor in hippocampi of epileptic rats following pilocarpine-induc
197 pared with NW piglets at 12 days of age, the hippocampi of EW piglets showed decreased gene expressio
202 hexin5 expression was highly elevated in the hippocampi of human AD patients, indicating its potentia
204 he differential expression of SNAP-25 in the hippocampi of infected neonates indicates a variable deg
210 021 prevented PSD95-positive synapse loss in hippocampi of mice with EAE but did not affect developme
211 1H MRS described a metabolite profile in the hippocampi of MRI-negative TLE patients that was differe
212 (MRS), we examined metabolic changes in the hippocampi of MS patients, compared the findings to perf
215 ) cannabinoid receptor protein levels in the hippocampi of patients with Alzheimer's disease remain u
216 e found significant volume reductions in the hippocampi of patients with schizophrenia compared with
220 how that promoting translational recovery in hippocampi of prion-infected mice is neuroprotective.
223 ired IRS-1 signaling was also present in the hippocampi of Tg mice with a brain condition that models
224 ignificant increase of new mature neurons in hippocampi of TgCRND8 compared with WT mice, suggesting
226 primary cultures of neurons derived from the hippocampi of the embryonic brain, suggesting that the a
231 presence of dystrophic neurites in both the hippocampi of transgenic mice overexpressing amyloid pre
232 ffect in vivo, lactate was perfused into the hippocampi of unanesthetized rats while recording the fi
233 ndritic spines of CA1 pyramidal cells in the hippocampi of water maze-trained rats vs. controls.
240 romoter heat shock elements by HSF1 in APP23 hippocampi, primary murine hippocampal neurons, and SH-S
242 n AQP4 levels in MTLE compared with non-MTLE hippocampi, quantitative ImmunoGold electron microscopy
245 tive assessments of mRNA levels in epileptic hippocampi relative to autopsy controls were made by usi
246 ongation of T2 relaxation time identified in hippocampi remote from the seizure focus in all patient
247 of having 50% volume loss bilaterally in his hippocampi, retrieval in Jon was associated with increas
248 Magnetic resonance spectra measured in the hippocampi revealed a significantly lower glutamate conc
249 [3H]L-655,708 binding sites in rat and human hippocampi revealed a strong correlation with the affini
250 ed distant areas, including the neocortices, hippocampi, rostral migratory stream, and olfactory bulb
254 rying with brain parenchymal volume, the MTS hippocampi showed significant volume loss (P < 0.0001),
255 to autopsies both sclerosis and mass lesion hippocampi showed that, in the stratum granulosum, the g
256 l of TLE using 100 epileptic and 100 control hippocampi shows the proconvulsive module is preserved a
257 orded at rest in epileptic and non-epileptic hippocampi suggests that they cannot be used alone to di
258 cutely dissociated from slices prepared from hippocampi surgically removed for the treatment of tempo
259 APOE4 carriers, GM volume loss affected the hippocampi, temporal and parietal lobes, right caudate n
260 cannabis users display smaller amygdalae and hippocampi than controls, and genetic variation accounts
264 ent of prolongation of T2 relaxation time in hippocampi that are not the primary epileptogenic focus,
268 solute concentrations of metabolites in both hippocampi, the sites of early Alzheimer's disease, in p
269 ation of a white matter tract connecting the hippocampi, the ventral hippocampal commissure (VHC), wi
270 r piriform cortex and the dorsal and ventral hippocampi underwent MS: electrical stimulation of the l
272 ciated viral delivery of the channel to both hippocampi was also effective in a model of temporal lob
276 lobe epilepsy model) and 100 healthy control hippocampi, we identified 256 RNA sites (overlapping wit
278 e imaging (MRI) studies of the amygdalas and hippocampi were conducted in 50 non-epileptic controls (
289 tal and temporal lobe regions (including the hippocampi) were associated with the decline in PIQ.
290 s callosum, anterior commissure, and fimbria hippocampi, were investigated for structural and functio
291 as required to saturate LTD in primed mutant hippocampi, whereas multiple low-frequency stimuli were
292 articularly in the left hemisphere; (2) that hippocampi will be smaller in multiplex relatives as com
293 will be positively correlated; and (4) that hippocampi will be smaller in patients with schizophreni
295 g early posthatching development had smaller hippocampi with fewer neurons and performed worse in a c
297 ure of rat hippocampal neurons and the mouse hippocampi with morphine or fentanyl for 3 days, seven m
298 ype II focal cortical dysplasia (IIa and b), hippocampi with or without hippocampal sclerosis (HS), a
300 ippocampal sclerosis (HS; n = 17), epileptic hippocampi without HS, or non-HS (NHS; n = 10), and auto