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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
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
56 Young bees perform nursing duties within the hive and have high Vg and low JH; as older bees transiti
58 ain endothelial cells in the mouse model for HIVE and human HIVE brains featuring mononuclear cell in
60 ulted in decreased survivorship, both in the hive and in laboratory experiments in which bees were ex
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
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
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
85 inal landscapes differed in size in October, hive assessments revealed no differences between the gro
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
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
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
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
108 such as queen clipping and the opening of a hive, causes strong interferences with important mechani
114 choice pollen types, predominantly choosing hive-collected mixed species pollen (MSP), followed by a
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
125 ated Virtual Environment-Codon Usage Tables (HIVE-CUTs), to present and analyse codon usage tables fo
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
136 ere open-mated and then placed into standard hive equipment in an "artificial swarm" to measure subse
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.
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
152 e monitoring was effective at distinguishing hive groups and had the best overall value in terms of e
154 ean+/-SE: 6.61 +/- 0.88 ppb clothianidin per hive) had seven times greater concentrations than nectar
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
159 formed using brain tissue from patients with HIVE, HIV-1 infection without encephalitis, and seronega
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
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
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
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
178 in the start of foraging of 3.3 h, and whole-hive locomotor-activity rhythms were delayed by an avera
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
184 eybees, employed foragers recruit unemployed hive mates to food sources by dances from which a human
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
193 Here, we show that the neural damage in HIVE mice extends beyond the basal ganglia and is associ
203 nges in 3D genomic compartment structures in HIVE microglia were linked to the transcriptional activa
207 ammatory and neuroprotective responses in an HIVE model of human disease and as such warrants further
211 dy, blocking IFNalpha in a HIV encephalitis (HIVE) mouse model with intraperitoneal injections of IFN
214 escribes the direction and distance from the hive of a new food source, and this message is displaced
216 centration of all pesticide brought into the hive on that particular day, it is likely representative
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
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
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
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
239 asures included Skindex-29, current itch and hives scores, total leukocyte histamine content (an indi
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
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
254 frames of bees (adult bee mass) and internal hive temperature were monitored for 60 colonies for each
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)
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
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
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
281 sting in sites underneath foliage, bumblebee hive usage) and interactions (parasitism, predation) of
283 tributes to the neurodegenerative process in HIVE via abnormal tau phosphorylation; thus, reducing CD
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
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
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