戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 human immunodeficiency virus-1 encephalitis (HIVE).
2 tiviral T-cell response in HIV encephalitis (HIVE).
3 human brain tissues with HIV-1 encephalitis (HIVE).
4  human brain tissue with HIV-1 encephalitis (HIVE).
5 t, neurological damage and HIV encephalitis (HIVE).
6 nt (SCID) mouse model of HIV-1 encephalitis (HIVE).
7 topathologic features of HIV-1 encephalitis (HIVE).
8 n human immunodeficiency virus encephalitis (HIVE).
9 an animal model of HIV-induced encephalitis (HIVE).
10 d human immunodeficiency virus encephalitis (HIVE).
11 mmatory condition known as HIV encephalitis (HIVE).
12 led monocyte migration into the brain during HIVE.
13 an underlying cause of BBB impairment during HIVE.
14 il than did age-matched bees confined to the hive.
15         Honey bees begin life working in the hive.
16 ed the effects of regular HAART treatment on HIVE.
17 values similar to those observed in cases of HIVE.
18 caudate and putamen of SCID mice, generating HIVE.
19 cking and homeostasis in the pathogenesis of HIVE.
20  nonobese diabetic (NOD)-SCID mouse model of HIVE.
21 lly restricted to a narrow sector around the hive.
22 d in brain tissue from an adult patient with HIVE.
23  both neurons and microglia in patients with HIVE.
24 rtical gray matter in patients who died with HIVE.
25 lesions in the brain of children with severe HIVE.
26 g their stop signaling and time spent in the hive.
27 bees with 2D barcodes in a small observation hive.
28 ving only brood, food, and few adults in the hive.
29 (HIVE); D) Infected with substantial NCI and HIVE.
30 vae spores can be distributed throughout the hive.
31 uropsychologically impaired subjects without HIVE.
32 te the cognitive impairments associated with HIVE.
33 on in the mechanisms of neurodegeneration in HIVE.
34  behaviour were determined using observation hives.
35 celerometers placed in the heart of honeybee hives.
36 xidant derived from the propolis of honeybee hives.
37 e learning and memory of honeybees in normal hives.
38 cterial genera was also greater in surviving hives.
39  "bioethics," they break out in intellectual hives.
40 ion of bees' behaviours in small observation hives.
41 spectively, where we placed 120 experimental hives.
42 the social environments of small observation hives.
43 monly by robbing sugar resources from within hives.
44 cterized by relapsing appearance of pruritic hives.
45 relative to the sun(1) and distance from the hive.(2)(,)(3) Moreover, they appear capable of doing so
46 ver, reported nausea, vomiting, and systemic hives 20 to 30 minutes after ingestion of antipasto made
47 h other honey bees to steal honey from their hives.(27)(,)(28)(,)(29)(,)(30) Despite attacks from vic
48  and used the resulting outcomes to train BE-Hive, a machine learning model that accurately predicts
49 ut metabolism of coumaphos, a widely used in-hive acaricide, by approximately 60%.
50                              Bumblebees with hive access had significantly higher survival than bumbl
51 ntly higher survival than bumblebees without hive access.
52               Analyses of brain tissues from HIVE, AD and FTD patients showed that PINCH is increased
53  whether A. apicola's presence could protect hives against Galleria infestations, and second, to util
54 ts than those from mountain sites, but those hives also had higher and more constant temperatures fro
55 to releasing them in front of their maternal hive and allowing them to fly back unaided.
56 Young bees perform nursing duties within the hive and have high Vg and low JH; as older bees transiti
57  health and signaling genes occurred in both HIVE and HIV+ microglia.
58 ain endothelial cells in the mouse model for HIVE and human HIVE brains featuring mononuclear cell in
59 fferentiating between pesticide exposures in-hive and in agricultural fields.
60 ulted in decreased survivorship, both in the hive and in laboratory experiments in which bees were ex
61 that can be transported by honey bees to the hive and incorporated into the honey.
62 bees with repeated opportunities to view the hive and landscape features from different viewpoints, s
63 ethism, in which young workers remain in the hive and perform tasks there, whereas old workers perfor
64 es hippocampal synaptic impairment in murine HIVE and provide a rationale for its use in infected hum
65 eled IDV-NP was readily observed in areas of HIVE and specifically in brain subregions with active as
66 changes in cell cycle proteins occur in both HIVE and the simian model and that these changes have fu
67 ignificant increase in E2F1 and ppRb in both HIVE and the simian model.
68 long-term vibrational recordings of honeybee hives and additionally provide the first quantification
69 py/allergies, asthma, eczema, hay fever, and hives and childhood/adolescent leukemia, acute lymphobla
70 ic honey samples collected directly from the hives and find that a large proportion (37%) of Manuka h
71 rs and no audit of hives, low maintenance of hives and hives distributed in large groups) on the mean
72  dominant vibratory urticaria have localized hives and systemic manifestations in response to dermal
73 ition characterized by spontaneous, pruritic hives and/or angioedema that persists for 6 weeks or lon
74                          HIV-1 encephalitis (HIVE) and its associated dementia can occur in up to 20%
75 l cortex from individuals with encephalitis (HIVE) and without (HIV+).
76 untered by foraging honeybees and within the hive, and are additive with combined application.
77                     Efficacy (itch severity, hive, and urticaria activity scores) was evaluated at we
78 ch to survey microflora in CCD hives, normal hives, and imported royal jelly.
79                     Flora that surrounds the hives, and the apicultural practices also influence in t
80                            Their matriarchal hives are headed by queens, backed by an all-female work
81                          More than 1 million hives are transported to California each year just to po
82 human immunodeficiency virus-1 encephalitis, HIVE) are associated with oxidative stress and inflammat
83  CI, 1.92-3.16), with risk being highest for hives (aRR, 3.81; 95% CI, 2.33-6.22) and angioedema (aRR
84 y lower on farms with wildflower strips with hives as well.
85 inal landscapes differed in size in October, hive assessments revealed no differences between the gro
86                     In contrast, Li restored HIVE-associated loss of microtubule-associated protein-2
87 ive contributions of dance communication and hive-based olfactory information transfer to honeybee re
88  that the increase in JH that influences the hive bee-forager transition may cause many of these chan
89 f stores of food that are consumed by within-hive bees that convert stored pollen and honey into roya
90  exposome by analyzing residues from live in-hive bees, stored pollen, and wax in migratory colonies
91                    This holds true for small hive beetles (Aethina tumida), which are parasites of so
92 e colonies were used to attract flying small hive beetles at fixed spatial intervals from a central r
93 ficant effects on dispersal, with more small hive beetles being recaptured when temperatures were hig
94             Our findings show that the small hive beetles is capable of long-distance flights, and hi
95                                   Most small hive beetles were collected closest to the release point
96                                        Small hive beetles were recaptured (N = 770) at a maximum dist
97                 The database is available at hive.biochemistry.gwu.edu/review/codon .
98  IDV levels and reduced HIV-1 replication in HIVE brain regions.
99  microglia comprising 0.33% of all nuclei in HIVE brain.
100  findings was evaluated in HIV-encephalitis (HIVE) brain samples in which decreased levels of MCP-2 a
101  cells in the mouse model for HIVE and human HIVE brains featuring mononuclear cell infiltration acro
102 rty-nine plant taxa were recorded from three hives but only ten at greater than 1%.
103  miticides to eliminate Varroa in commercial hives, but these chemicals can diminish bee health and i
104 e nutritional profile of pollen brought into hives by foraging bees in crop fields and nut orchards c
105 human immunodeficiency virus encephalopathy (HIVE) by immunohistochemistry in an effort to gain insig
106 y of pesticide distribution on a comb in the hive can be driven by worker behaviors.
107 t direct experience of the world outside the hive causes mushroom body neuropil growth in bees.
108  such as queen clipping and the opening of a hive, causes strong interferences with important mechani
109           A large proportion of CD16+ MPs in HIVE CNS tissue were PCNA+, but do not appear to be prol
110 ome endothelial cells and ependymal cells in HIVE CNS.
111                                     Internal hive CO(2) concentration was higher on average in coloni
112                       Building on our recent HIVE-Codon Usage Tables, we constructed a new database t
113             Using longitudinal data from the HIVE cohort from 2010-11 through 2017-18, we estimated d
114  choice pollen types, predominantly choosing hive-collected mixed species pollen (MSP), followed by a
115                                          The hive-collected MSP was chemically diverse, richest in ch
116 rved in cerebellar tissue from patients with HIVE compared to HIV-seronegative patients or HIV-1-infe
117  of children with severe HIV-1 encephalitis (HIVE) compared with children with mild HIVE or non-AIDS
118  pediatric patients with HIV-1 encephalitis (HIVE) compared with those without HIVE, or that were HIV
119 cant differences in alpha diversity based on hive condition, but there was a highly significant diffe
120 equency with which these pesticides occur as hive contaminants and suggests that they present a great
121 sample confirmed exposure of Galleria in the hive context.
122 5 alleles with bystander nucleotides that BE-Hive correctly predicted would not be edited.
123 nces on various outdoor routes from the same hive could be considerably different.
124        This work demonstrates that honey bee hives could detrimentally affect fruit count and wild be
125 ated Virtual Environment-Codon Usage Tables (HIVE-CUTs), to present and analyse codon usage tables fo
126 th substantial NCI without HIV encephalitis (HIVE); D) Infected with substantial NCI and HIVE.
127 esticides coordinated with growers, audit of hives, dietary supplementation and individual distributi
128 audit of hives, low maintenance of hives and hives distributed in large groups) on the mean level of
129 netic shaker attached to the outer wall of a hive, driven by a computer with a 0.1 s long, monochroma
130 on the hind legs and mass upon return to the hive, during the lifelong foraging career of individual
131 on of collection or land use surrounding the hive (e.g. agricultural, rural, urban).
132  delaying the transition from working in the hive (e.g., brood care, or "nursing") to foraging.
133  between entering foragers and guards at the hive entrance.
134                                  A nurturing hive environment and a mutualistic relationship with pla
135  imidacloprid, highly stable in honey in the hive environment over several months.
136 ere open-mated and then placed into standard hive equipment in an "artificial swarm" to measure subse
137                                        Thus, hives exhibited short-term resilience.
138 eased when samples from the location with no hive failures were excluded from analysis.
139  encephalitis (SHIVE) with several classical HIVE features that include astrocyte infection.
140 , and beekeeping in skep, log, box, and tree hives flourished to meet the demand.
141 on through p.C492Y-ADGRE2, causing localized hives, flushing, and hypotension.
142  to 2022, 1755 participants were followed in HIVE for 7785 person-years with 7833 illnesses documente
143  A worker honeybee performs tasks within the hive for approximately the first 3 weeks of adult life.
144 ion, because foragers bring food back to the hive for storage rather than eating it themselves.
145 ng repeatedly to collect food outside of the hive for the remainder of its 5-6 week life.
146  also continuously monitored for 20 of those hives for 6 weeks for both years, during commercial poll
147 he rate of resolution (defined as absence of hives for at least 1 year with no treatment) and the ass
148  These can then be introduced into queenless hives for natural mating or insemination, both of which
149 d to treat symptoms of allergy and long-term hives for over 25 years.
150                                       Though hives from different original landscapes differed in siz
151 mperatures from September until January than hives from mountain sites.
152 e monitoring was effective at distinguishing hive groups and had the best overall value in terms of e
153 in two millennia, beekeeping with horizontal hives had spread throughout the Mediterranean.
154 ean+/-SE: 6.61 +/- 0.88 ppb clothianidin per hive) had seven times greater concentrations than nectar
155                                  Traditional hive has no negative effect on quality factors of honey
156 l agriculture, but dramatic losses of entire hives have been reported in numerous countries since 200
157 elatively warm temperatures inside honey bee hives have prevented these fungi from becoming effective
158 y be used as a diagnostic tool in evaluating hive health prior to the onset of winter.
159 formed using brain tissue from patients with HIVE, HIV-1 infection without encephalitis, and seronega
160                              Since 2010, the HIVE (Household Influenza Vaccine Evaluation) study has
161                                          The HIVE (Household Influenza Vaccine Evaluation) study was
162 g human immunodeficiency virus encephalitis (HIVE); however, the basis of these permeability changes
163 lpha has a major role in the pathogenesis of HIVE in mice and is likely important in the development
164 two decades it has encountered pesticides in-hive in the form of acaricides to control Varroa destruc
165                                Beebread from hives in agricultural sites had greater agrochemical div
166 otinoids brought back in pollen to honey bee hives in arable landscapes was from wildflowers, not cro
167 foragers at colonies, and wax from honey bee hives in blooming blueberry farms in southwest Michigan.
168 ated neuronal pathways strongly dominated in HIVE, including GABA receptors, glutamate signaling, syn
169       In the frontal cortex of patients with HIVE, increased levels of CDK5 and p35 expression were a
170 co of 121 pesticide contaminants of American hives into the active pocket of CYP9Q1, a broadly substr
171 n active component of propolis from honeybee hives, is known to have antimitogenic, anticarcinogenic,
172  place high value on immediate and sustained hive, itch, and swelling relief, particularly long-term
173 t with chronic urticaria that presented with hives lasting at least 6 weeks between 2013 and 2015 at
174 r relationship to SIV/HIV encephalitis (SIVE/HIVE) lesions and SIV-infected cells.
175 , and the mutant biofilms appeared loose and hive-like, whereas the biofilms of the wild type were sm
176 chemical properties vary with honey type and hive location, and suggests that Irish heather honey sho
177 , and whether properties varied according to hive location.
178 in the start of foraging of 3.3 h, and whole-hive locomotor-activity rhythms were delayed by an avera
179  gut microbial communities in driving winter hive loss has received little attention.
180 le the contribution of pesticides to current hive loss rates is debated, remarkably little is known r
181 bee gut microbiota is associated with winter hive loss, and can potentially be used as a diagnostic t
182 ut coordination with growers and no audit of hives, low maintenance of hives and hives distributed in
183                              We examined how hive mates interpret these dances.
184 eybees, employed foragers recruit unemployed hive mates to food sources by dances from which a human
185 f NP(EO)3-13 and OP(EO)3-13 oligomers in bee hive matrices.
186 ulation of immunosuppressive IDO activity in HIVE may enhance the generation of HIV-1-specific CTLs,
187 ation might improve NCI, whereas NCI without HIVE may not respond in kind; array results suggest that
188 Thus focal inflammation in brain tissue with HIVE may up-regulate neuronal FKN levels, which in turn
189 ent of astrocyte and microglia activation in HIVE mice (10-fold and 16-fold, respectively, compared w
190 ion were reduced by 14.1, 29.5, and 45.3% in HIVE mice compared with sham-injected or control animals
191 d with untreated or control antibody-treated HIVE mice during water radial arm maze behavioral testin
192                 By day 15, the CA2 region of HIVE mice expressed 3.8- and 2.6-fold less NF and SP tha
193      Here, we show that the neural damage in HIVE mice extends beyond the basal ganglia and is associ
194                  Here, CEP-1347 treatment of HIVE mice showed a dose-dependent reduction in microglio
195                            Memantine-treated HIVE mice showed significant improvements in synaptic fu
196 g-term potentiation in hippocampal slices of HIVE mice that were restored by Li.
197 ficantly in the CA2 hippocampal subregion of HIVE mice with limited neuronal apoptosis.
198 s of dendritic arborization in the brains of HIVE mice.
199 1(+) MDMs) and enhanced neuroinflammation in HIVE mice.
200 itive MDMs were unaltered by Li treatment of HIVE mice.
201 he CA1 region of hippocampal brain slices of HIVE mice.
202                          HIV-1 encephalitis (HIVE) mice, where human virus-infected monocyte-derived
203 nges in 3D genomic compartment structures in HIVE microglia were linked to the transcriptional activa
204                                    For human HIVE, microglial activation and virus infection correlat
205 l interactions that make up the fundamental "hive mind" of the tumor.
206 bling widespread novel contributions from a "hive mind."
207 ammatory and neuroprotective responses in an HIVE model of human disease and as such warrants further
208 munodeficiency virus-1 (HIV-1) encephalitis (HIVE) models.
209                       The human PBL-NOD-SCID HIVE mouse provides a new tool for studies of cellular i
210 e human PBL to generate a human PBL-NOD-SCID HIVE mouse.
211 dy, blocking IFNalpha in a HIV encephalitis (HIVE) mouse model with intraperitoneal injections of IFN
212 e CD40/CD40L dyad plays an important role in HIVE neuroinflammation.
213 genomic approach to survey microflora in CCD hives, normal hives, and imported royal jelly.
214 escribes the direction and distance from the hive of a new food source, and this message is displaced
215                                          The hive of the honey bee is a suitable habitat for diverse
216 centration of all pesticide brought into the hive on that particular day, it is likely representative
217                            Keeping honey bee hives on farms with wildflower strips could reduce conse
218 ted by managed honey bee (Apis mellifera L.) hives on farms.
219       Honeybees are known to fly a feeder-to-hive or hive-to-feeder vector according to whether or no
220 itis (HIVE) compared with children with mild HIVE or non-AIDS controls, whereas the frequency of CXCR
221 eepers collect pollen at the entrance to the hive or pollen is added to the honey after it is harvest
222 ounds (GH) and reared them in normal (within hives) or stressed (protein-deficient, asocial) conditio
223 ephalitis (HIVE) compared with those without HIVE, or that were HIV-1 seronegative.
224           This study measured part of the in-hive pesticide exposome by analyzing residues from live
225                                              Hives placed in commercial almond pollination gained on
226 ment to reduce honey bee viral infection and hive placement.
227 d outputs publication-quality Sashimi plots, hive plots and structure plots, enabling better investig
228      Using bees trained to a certain kind of hive pollen, we applied a binary scoring system, to test
229  and pollen carried by foragers returning to hives, preplanting and in-season soil samples, and wild
230                              Bee pollen is a hive product with a high content of antioxidants.
231  count by 18% across all farm with honey bee hives regardless of wildflower strip presence, and winte
232 ng-were remarkably invariant across distinct hive regions, suggesting a lack of direct environmental
233 as observed in CNS tissue from patients with HIVE, relative to seronegative controls and patients wit
234 ropathological features of HIV encephalitis (HIVE) remains unclear.
235                 Using previously reported in-hive residues from commercial colonies, we examined how
236  10) and 40% (4 of 10) had complete itch and hive resolution by FricTest, respectively, and 100% (7 o
237    To test this idea, an HIV-1 encephalitis (HIVE) rodent model was used where HIV-1-infected human m
238                                       In the HIVE SCID mice, a marked accumulation of murine MDM was
239 asures included Skindex-29, current itch and hives scores, total leukocyte histamine content (an indi
240                                  The type of hives significantly affected the moisture (p<0.01), redu
241 s overall experienced increased time delays, hive stay durations and a decreased number of transfer p
242  donors experienced reduced transfer delays, hive stay durations and an increased number of simultane
243  the Household Influenza Vaccine Evaluation (HIVE) study, acute respiratory infections (ARI) have bee
244  of patients affected by HIV-1 encephalitis (HIVE), suggesting an important role for the CD40/CD40L d
245 proximity to feral honeybee (Apis mellifera) hives, suggesting potential transmission routes for thes
246                                Expression in HIVE suggests that lowering brain HIV-1 replication migh
247 sella were positively associated with winter hive survival.
248 al exposures are linked to reduced honey bee hive survival.
249 hives; the balanced allocation of workers to hive tasks and foraging; the recovery of a colony from d
250 n activity rhythms; young adult bees perform hive tasks with no daily rhythms, whereas older bees for
251 d day lengths differed significantly between hive temperature and CO(2) after 15 d in the 12 l:12D li
252 y bee colonies produced circadian rhythms in hive temperature and CO(2) concentration with periods bo
253                                              Hive temperature average and daily variability were not
254 frames of bees (adult bee mass) and internal hive temperature were monitored for 60 colonies for each
255  treatment more than rhythms associated with hive temperature.
256 survived, germinated, and grew better at bee hive temperatures (35 C).
257 ight junction disruption is a key feature of HIVE that occurs in regions of histopathological alterat
258 e past 15 years, the proportion of honey bee hives that fail to survive winter has averaged ~ 30% in
259 ymmetric chemical gradient grow close-packed hives that reach a steady-state size tunable through lig
260 rofiling (QMP), was significantly greater in hives that survived winter 2022 than in those that faile
261 -performance Integrated Virtual Environment (HIVE) that encapsulates Curated Short Read archive (CSR)
262                                         With HIVE the HIV-1 RNA load in brain tissue was three log(10
263                                           In HIVE, the transcripts for TLR3, IFN-beta, IDO, and viper
264 e tested whether a natural inhabitant of bee hives, the wax moth Galleria mellonella, was a suitable
265  first forages and how this age varies among hives; the balanced allocation of workers to hive tasks
266 Third, immunohistochemical analyses of human HIVE tissue defined the relationships between astroglios
267  nestmates a distance and direction from the hive to a valuable resource, usually nectar or pollen(2)
268  of pesticide location/deposition within the hive to compare with exposure levels estimated by averag
269            Finally, we used insights from BE-Hive to engineer novel CBE variants that modulate editin
270 lly regulated transition from working in the hive to foraging that has been previously associated wit
271 lly regulated transition from working in the hive to foraging, which is associated with changes in th
272 asuring exposure of individual bees within a hive to pesticide is at least as difficult as assessing
273            Clinical presentation ranges from hives to anaphylaxis; episodes typically occur 2-6 h aft
274  bloom for many crops, as growers often rent hives to ensure successful pollination.
275 mitraz is a formamidine acaricide applied to hives to manage Varroa destructor, an ectoparasite of ho
276 nally at the tumor site, forming a "cellular hive" to recruit anti-PD-1 antibody (aPD-1)-conjugated p
277 neybees are known to fly a feeder-to-hive or hive-to-feeder vector according to whether or not they h
278 oring system to record mass on departing the hive, trip duration, presence of pollen on the hind legs
279 etic xenobiotics that frequently contaminate hives-two herbicides (atrazine and glyphosate) and three
280  and acceptability tests not observed due to hive types and locations.
281 sting in sites underneath foliage, bumblebee hive usage) and interactions (parasitism, predation) of
282          However, for larger cell sizes, the hive uses adaptive strategies such as tilting for founda
283 tributes to the neurodegenerative process in HIVE via abnormal tau phosphorylation; thus, reducing CD
284  The overall time foragers spent outside the hive was significantly reduced post-exposure.
285 d, a SCID mouse model of HIV-1 encephalitis (HIVE) was used to determine in vivo monocyte blood-to-br
286 mbined immunodeficient (SCID) mouse model of HIVE, we determined the effects of regular HAART treatme
287                      Using a murine model of HIVE, we investigated the effects of alcohol abuse on th
288                             Using a model of HIVE, we investigated whether IDO inhibitor 1-methyl-d-t
289                                Average daily hive weight losses per day in the 5-ppb clothianidin col
290                                              Hive weight was also continuously monitored for 20 of th
291 ried according to floral origin, and whether hives were in urban or rural sites.
292 al abundance was not affected by whether the hives were stored outside or in constant temperature ind
293 dicators of honey from traditional and frame hives were within the criteria set by Codex Alimentarus
294 Nurses were most likely to be present in the hive with their tag still attached when introduced using
295 pplementation and individual distribution of hives) with conventional practices (i.e., pesticides app
296                          The transition from hive work to foraging has been shown to be socially regu
297 he age-related transition by honey bees from hive work to foraging is associated with an increase in
298 -related transition by adult honey bees from hive work to foraging is associated with changes in mess
299 lore how increased mortalities of larvae, in-hive workers, and foragers, as well as reduced egg-layin
300 tle, losing anywhere from 40 to 90% of their hives yearly, often by brood diseases caused by bacteria

 
Page Top