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1 opods are radically different from any other invertebrate.
2 e rotifer, Brachionus manjavacas, an aquatic invertebrate.
3 e development of both axons and dendrites in invertebrates.
4 s for studies on bees and other understudied invertebrates.
5 g to their in vivo generation in terrestrial invertebrates.
6 ways conform to expectations, especially for invertebrates.
7 ication of blood-meal hosts of hematophagous invertebrates.
8 as not been previously described in deep-sea invertebrates.
9 s known as to how internalization happens in invertebrates.
10 cellular matrix (ECM) in various contexts in invertebrates.
11 egulate normal sleep in both vertebrates and invertebrates.
12 hough the concepts are broadly applicable to invertebrates.
13  of endocrine-disrupting chemicals (EDCs) to invertebrates.
14 iours remain speculative, in vertebrates and invertebrates.
15 7 family and is conserved in vertebrates and invertebrates.
16 mental management, especially for fishes and invertebrates.
17  has become a model of adult neurogenesis in invertebrates.
18 ecting microplastic ingestion by terrestrial invertebrates.
19  be limited to fish, but should also include invertebrates.
20 hways that regulate aging were discovered in invertebrates.
21 anisms, including freshwater and terrestrial invertebrates.
22 to be the most cognitively advanced group of invertebrates.
23 arctic is a diversity hotspot for freshwater invertebrates.
24 y expressed proteins between vertebrates and invertebrates.
25 g of habitat, primary producers, and aquatic invertebrates.
26 rporation and storage in mammalian cells and invertebrates.
27 ivation in vertebrates, but not necessary in invertebrates.
28 oductive processes and energy homeostasis in invertebrates.
29 tes the recruitment and settlement of marine invertebrates.
30  organic contaminants by benthic and sessile invertebrates.
31  interrogating gene function in other marine invertebrates.
32 aping olfactory responses in vertebrates and invertebrates.
33 are strongly conserved in mammals but not in invertebrates.
34  of its glycans, as observed in other marine invertebrates.
35 led communities of aquatic fungi and benthic invertebrates.
36 gical) effects [1] in vertebrates [2, 3] and invertebrates [4, 5].
37 tropical region, predation decreased sessile invertebrate abundance, richness and diversity on both n
38 1 taxonomic groups including vertebrates and invertebrates across 199,957 protected areas at the glob
39 use impacts on a comprehensive range of soil invertebrates across New Zealand, measured using DNA met
40 i-SmSEA IgG antibodies eluted from the three invertebrate allergens reacted with S. mansoni egg antig
41 ecies, with flowering plants and terrestrial invertebrates also represented; however, vertebrate spec
42              The effects of land use on soil invertebrates - an important ecosystem component - are p
43                              Octopamine, the invertebrate analog of norepinephrine, is known to modul
44  activates neurons that release tyramine, an invertebrate analogue of adrenaline and noradrenaline.
45 ate that vertebrate TIMP genes arose from an invertebrate ancestor through 3 successive duplications,
46 ut, respectively.SIGNIFICANCE STATEMENT Both invertebrate and vertebrate nervous systems display syna
47 "intrinsic plasticity") has been observed in invertebrate and vertebrate neurons, coinduced with syna
48 similar to pathways previously described for invertebrates and certain non-mammalian vertebrates.
49 nding of cross-sensitization among different invertebrates and design of suitable T-cell peptide-base
50 luded a diverse range of other taxa (plants, invertebrates and fish) suggesting there is scope to bro
51             CTA is common to vertebrates and invertebrates and is an important survival response: eat
52  endosymbiosis) is widely distributed across invertebrates and is recognized as a major driving force
53 he ancestral pterosaur diet was dominated by invertebrates and later pterosaurs evolved into piscivor
54 ved small interfering RNAs in fungi, plants, invertebrates and mammals, detailing the mechanisms for
55 rs known to regulate a range of behaviors in invertebrates and mammals, such as learning and memory.
56 ect development of neuronal circuits in both invertebrates and mammals.
57 ess is known about the trends affecting most invertebrates and other neglected taxa, and it is unclea
58 omes related with viral families that infect invertebrates and plants, suggesting that they might be
59 l systems by reducing populations of benthic invertebrates and releasing kelp forests from grazing pr
60 ms are likely to be widely distributed among invertebrates and to have broad influence on morphologic
61  of immune memory, such as immune priming in invertebrates and trained immunity in vertebrates.
62 , our data position the brittle star between invertebrates and vertebrates and confirm the high diver
63 lum (ER) calcium stores, a process common to invertebrates and vertebrates, is central to physiologic
64 rients numerous morphogenetic events in both invertebrates and vertebrates.
65 mer; Austriadactylus as a consumer of 'hard' invertebrates) and direct evidence of sympatric niche pa
66 tic and disease processes in vertebrates and invertebrates, and a carcinogenic role has been observed
67 s were the most potentially toxic to benthic invertebrates, and of the 9 pyrethroids detected, 7 occu
68 e psychopathologies, irrational decisions in invertebrates, and some aspects of evolution by means of
69             Distinct lineages infect plants, invertebrates, and vertebrates, including humans.
70 f fungicides on microorganisms, macrophytes, invertebrates, and vertebrates.
71 of this species' N-glycosylation reveal both invertebrate- and vertebrate-like features.
72 thetic gene cluster inhibits virulence in an invertebrate animal infection model.
73 acteria, phytoplankton, macroalgae, and some invertebrate animals, and both may be similarly impacted
74                                 Predation by invertebrates appears to select for only some aspects of
75                        Spermatozoa of marine invertebrates are attracted to their conspecific female
76 anges of broadband sounds produced by marine invertebrates are not known.
77 metazoans, even though components present in invertebrates are often found as multiple paralogous pro
78 mediated inducible defenses in other aquatic invertebrates are triggered by the same compound.
79 ies (including seabirds, plants, lichens and invertebrates) are found in one or more protected areas.
80 f conservation importance and sessile marine invertebrates as model prey, we tested the hypothesis th
81 ure experienced by nontarget benthic aquatic invertebrates as well as potential means to mitigate neo
82 abundance, and community composition of soil invertebrates, as well as fundamental soil properties su
83                                       Marine invertebrate ascidians display embryonic reproducibility
84 itical soil functions and the composition of invertebrate assemblages, by comparing invertebrate dive
85 wed higher but variable consumption rates on invertebrates at tropical relative to temperate latitude
86                                    Using the INVertebrate Automated Phenotyping Platform (INVAPP) and
87 re bdelloid rotifers, microscopic freshwater invertebrates believed to have completely abandoned sexu
88 itat features, ocean physical processes, and invertebrate bioconcentration.
89 peatland erosion, significant alterations to invertebrate biodiversity can be expected where these er
90                                 Nonarthropod invertebrate biomass and fecal material were also distin
91 etection of microplastics within terrestrial invertebrate biomass and fecal material.
92 ng of endogenous organic molecules in fossil invertebrate biominerals provides an ancient record of c
93 ual-based culture experiments on the aquatic invertebrate, Brachionus manjavacas (Rotifera).
94 he UK distributions of over 5,000 species of invertebrates, bryophytes and lichens, measured as chang
95 that TRPM2 Nudix motifs are canonical in all invertebrates but vestigial in vertebrates.
96 e is altering habitats for marine fishes and invertebrates, but the net effect of these changes on po
97      Convergent exploitation of hard-shelled invertebrates by different subclades of ichthyosauriform
98 stablish the relaxed helices of IHMs: one in invertebrates, by either regulatory light-chain phosphor
99 nses in mammals (mice and humans) as well as invertebrates (Caenorhabditis elegans and Drosophila mel
100 teomics to mollusc shells (and indeed to any invertebrate calcified tissue).
101                     Gravitational effects on invertebrate cardiovascular and respiratory systems are
102 results form the basis for developing marine invertebrate cell models to better understand early anim
103                                    Plant and invertebrate cells utilise mostly RNA interference (RNAi
104 expression in the larvae of a model sediment invertebrate Chironomus riparius.
105 eduction) and adverse effects on the benthic invertebrates Chironomus riparius and Lumbriculus varieg
106                                          The invertebrate chordate amphioxus, which expresses Hh in i
107  with a new chromosome-scale sequence of the invertebrate chordate amphioxus.
108                         The notochord of the invertebrate chordate Ciona forms a tapered rod at tailb
109        Species of reptiles, fish, and marine invertebrates clustered in the predation selection categ
110 itions.SIGNIFICANCE STATEMENT From humans to invertebrates, cognitive processes are influenced by org
111 we conduct a large-scale network analysis of invertebrate communities across 502 UK farm sites to GMH
112  of native forest and plantations, both soil invertebrate communities and physical soil properties di
113 rovide insights into the functioning of soil invertebrate communities and their role in decomposition
114 by reviewing published literature on aquatic invertebrate communities from stream ecosystems.
115 aluate the environmental pressures affecting invertebrate communities in two ecoregions (north, south
116 tematic characterization of deep-sea benthic invertebrate communities of the Galapagos, across a rang
117 southeastern US salt marsh geomorphology and invertebrate communities with a predator exclusion exper
118 ive impacts of agricultural land use on soil invertebrate communities.
119 for the adverse impact of peat deposition on invertebrate community biodiversity.
120 revealed significant differences in fish and invertebrate community composition across adjacent habit
121                        We explored trends in invertebrate community functional traits along a gradien
122       We identified a specialized cold-water invertebrate community restricted to the highest elevati
123 n a better condition when fed on fruits than invertebrates, confirming that innate immunity is nutrie
124                                          The invertebrates consist of ~95% of all known animals and p
125 a Anoteropora latirostris, a colonial marine invertebrate, constructs its skeleton from calcite and a
126 s a piscivore; Pterodactylus as a generalist invertebrate consumer).
127                               In terrestrial invertebrate consumers, PFAS concentrations increased wi
128                             For example, the invertebrate counterpart of norepinephrine, octopamine,
129 her level of genomic organization than their invertebrate counterparts.
130               Thus, we employed a freshwater invertebrate, Daphnia magna, to investigate the chronic
131 ding directly from the benthos when drifting invertebrates declined, a behaviour enhanced by morpholo
132 g the first global comparison for a deep-sea invertebrate, demonstrate that V. infernalis has an onto
133 erochronic genes Lin28a/b and let-7 regulate invertebrate development, but their functions in pattern
134 on of invertebrate assemblages, by comparing invertebrate diversity and soil physico-chemical propert
135                                       Marine invertebrates dominated the list of highest risk species
136  vertebrates (zebrafish and salamanders) and invertebrates (Drosophila) offer insights into brain rep
137 me the most investigated brain region of any invertebrate due to novel genetic strategies that relate
138 obust, something that we show rings true for invertebrate ears too.
139 eDNA, our findings suggest that the state of invertebrate eDNA is much smaller than previously suspec
140 ons that distinguish the vertebrate from the invertebrate enzyme, thereby thereby supporting a role f
141 ajor groups analysed, terrestrial non-insect invertebrates, exhibits the declining trend reported amo
142 advances have been made through the study of invertebrate experimental organisms, including Caenorhab
143 ethyl ester derivative was explored in crude invertebrate extracts spiked with an S-adenosylmethionin
144 atory insect is a major threat to the native invertebrate fauna, in particular to the endemic wingles
145 a decrease in body mass and delayed moult in invertebrate-fed bulbuls, while fruit-fed bulbuls mainta
146  for two of the three immune PCs compared to invertebrate-fed bulbuls.
147 th of the subsistence base-pine nuts, marine invertebrates, fish, marine birds and mammals, tortoises
148 ealized, they will exceed the annual loss to invertebrate fisheries (-$7.3 million CA$).
149 ubstances in nature, is present in bacteria, invertebrates, fishes, and amphibians.
150     Stickleback consume benthic and limnetic invertebrates, focusing on the former in small lakes, th
151  wild-caught bulbuls ad libitum on fruits or invertebrates for 24 weeks, switching half of each group
152  overall (gamma) diversity of benthic marine invertebrates for Phanerozoic geological formations.
153 e, and mirex) were detected in the Antarctic invertebrates for the first time.
154 ukaryotes and 5-hydroxymethylcytosine (5hmC) invertebrates from vertebrates.
155 ewater-derived micropollutants in freshwater invertebrates (Gammarus spp.).
156 tential and toxicity in two keystone aquatic invertebrates: Gammarus pulex and Hyalella azteca.
157 pecially strong increases were projected for invertebrates globally.
158 higher vertebrates as well as some classical invertebrate glycan structures.
159 diversity revealed bacteria, microalgae, and invertebrate groups adhered to debris.
160 a powerful tool to characterize hyperdiverse invertebrate groups such as the Acari (mites).
161 re was key evidence that EDCs were impacting invertebrates groups.
162 ant dominance, plant traits, soil biota, and invertebrate herbivores and measured indicators of carbo
163 ale restoration that includes enhancement of invertebrate herbivores can reverse the ecological phase
164 clear if the similarities of symbiosis in an invertebrate host would result in functionally similar m
165 member of a widespread monophyletic group of invertebrate host-associated microbes that has independe
166  BMPs has been found in both vertebrates and invertebrates, however the mechanisms that regulate grad
167             This atlas of medically relevant invertebrate immune cells at single-cell resolution iden
168 many signals involved in both vertebrate and invertebrate immune responses.
169 posomes as an important tool in the study of invertebrate immunity.
170 e for the CCDs shared by the schistosome and invertebrates in inducing an allergy-protective effect,
171 n taxonomic and functional diversity of soil invertebrates in pine plantation sites.
172     These differ from the nervous systems of invertebrates in several ways, including the evolution o
173                                         Most invertebrates in the ocean begin their lives with plankt
174 applied to twelve species of diverse aquatic invertebrates, including both pelagic and benthic organi
175                                  It feeds on invertebrates, including honey bees, and represents a th
176 viruses that infects the cells of the gut in invertebrates, including insects and crustaceans.
177 as been well studied in both vertebrates and invertebrates, including molluscs.
178 ensoviruses cause lethal epidemic disease in invertebrates, including shrimp, cockroaches, crickets,
179 line (trona) pan show that beetles and other invertebrates inhabit this extreme environment when cond
180 rated an RNAi suppressor-defective mutant of invertebrate iridescent virus 6 (IIV6), a large DNA viru
181 vity affects the open circulatory systems of invertebrates is unknown, partly due to technical measur
182  site of action potential (AP) initiation in invertebrates is unknown.
183  biodiversity (bacteria, fungi, protists and invertebrates) is significantly and positively associate
184 oup of parasitic annelids that live in other invertebrates, is the smallest animal genome ever report
185      However, Fam20 kinases are conserved in invertebrates lacking bone and enamel, suggesting other
186      The innate immune response is active in invertebrate larvae from early development.
187                               While numerous invertebrate lineages were eradicated at the last major
188 e-scale taxonomic resolution in poorly-known invertebrate lineages.
189 olutionary conserved between vertebrates and invertebrates, making any discovery easily translatable.
190          Recent studies suggest that aquatic invertebrates may be good biomonitors for REEs, yet ther
191 This cohabitation of birds and nest-dwelling invertebrates may foster symbiotic relationships between
192 biodiversity (bacteria, fungi, protists, and invertebrates) may change as soils develop over centurie
193 aracterization of Galapagos deep-sea benthic invertebrate megafauna across a range of ecosystems repr
194                      For many marine benthic invertebrates, migration happens during reproduction bec
195 ature can modulate cell fate decisions in an invertebrate model of stem cell patterning.
196 rotein is highly conserved in vertebrate and invertebrate model organisms and is currently not associ
197    CDK19 is conserved between vertebrate and invertebrate model organisms, but currently abnormalitie
198  the roots of which might be unearthed using invertebrate model systems.
199 d the evolution of priming specificity in an invertebrate model, the beetle Tribolium castaneum Using
200 ental infections in two genetically modified invertebrate models (Drosophila melanogaster) that devel
201 iched in modulators of defective behavior in invertebrate models of HD pathogenesis, validating their
202 itous molecule, in WS patient samples and WS invertebrate models.
203 we characterized synapsin transcripts in the invertebrate mollusk Octopus vulgaris and present eviden
204                                              Invertebrates molt, furry mammals shed, and human skin e
205 anisms except microbial extremophiles, a few invertebrates (mostly insects), highly adapted fish (Alc
206 c model for single motoneuron stimulation of invertebrate muscle.
207 tions between neurons in some regions of the invertebrate nervous system.
208                                           In invertebrate neuronal types multiple currents can be see
209                                              Invertebrate neurons are typically unipolar with dendrit
210      Where APs are initiated in the axons of invertebrate neurons is unclear.
211 aments in axon shafts in both vertebrate and invertebrate neurons, as well as the axon initial segmen
212                                       Within invertebrates, not only do they possess by far the large
213 orax pyrrhocorax) that are dependent on dung invertebrates on islands in the Inner Hebrides of Scotla
214 rward genetic screen, typically performed in invertebrates or mammalian cell lines, has been instrume
215 he teeth of reptiles with diets dominated by invertebrates, particularly invertebrates with hard exos
216 rtical [1-4] and subcortical [5-8] areas and invertebrate peripheral [9-11] and central [12-14] brain
217 cally guided biological control of 43 exotic invertebrate pests permitted 73-100% yield-loss recovery
218 ed in nociceptors across both vertebrate and invertebrate phyla and (2) there may be an interaction b
219 related signalling systems in a deuterostome invertebrate phylum - the Echinodermata.
220 ve in the future, including fish, tunicates, invertebrates, plants and protists.
221 g changes in the abundance of vertebrate and invertebrate populations relative to undisturbed old-gro
222                                              Invertebrates possess open circulatory systems, which co
223 ragonflies are sentinel species that are key invertebrate predators in both aquatic (as larvae) and t
224  (primary producers, mutualists, herbivores, invertebrate predators, and vertebrate predators) in 75
225 olf spiders, one of the most abundant arctic invertebrate predators, are becoming larger and therefor
226                                  As many top invertebrate predators, such as spiders and mantises, ar
227                                   Studies on invertebrate preparations usually examine synaptic chang
228    Soil contains a smorgasbord of nutritious invertebrate prey - hence all the tunneling.
229 at allows them to exploit a huge resource of invertebrate prey that is largely inaccessible to their
230  support for the temperature independence of invertebrate production and the necessary inclusion of r
231 ns, allowing comparison of modern and fossil invertebrate protein sequences, and will likely lead to
232 served example of convergent evolution among invertebrate PVs with respect to host-driven capsid stru
233 DV has a transcription strategy unique among invertebrate PVs, using extensive alternative splicing a
234 eriments demonstrated that predation reduced invertebrate recruitment in the tropics but not the temp
235 reveals that a representative of our closest invertebrate relatives, the tunicate Ciona, processes li
236 but is not suitable for separating them from invertebrate remains.
237                   Further, predation reduced invertebrate richness at both local and regional scales
238  we clear up this taxonomic ambiguity in the invertebrate RNA virosphere.
239                               The impacts of invertebrate RNA virus population dynamics on virulence
240 d deletion in the vertebrate relative to the invertebrate sequence unwinds an alpha-helix, placing th
241 te or calcite in biomineralization of marine invertebrate shells or avian eggshells, respectively.
242 tation of electrophysiological recordings in invertebrates.SIGNIFICANCE STATEMENT The site of action
243  approaches tested the hypothesis that small invertebrate size classes are more sensitive than large,
244 x (Asp + Asn) and Glx (Glu + Gln) typical of invertebrate skeletal proteins.
245  varies greatly between ingested and inhaled invertebrate sources.
246                      In both vertebrates and invertebrates, spatial patterning along the Dorsal-ventr
247                                       Marine invertebrate species are ectothermic and should be highl
248  the currently most commonly farmed fish and invertebrate species in the world's coastal and/or open
249                    Specimens of five benthic invertebrate species were collected at two distinct loca
250 at fluorotelomer compounds may accumulate in invertebrate species with limited metabolization.
251 animal models (that is, lower vertebrate and invertebrate species with low diversity microbiomes) are
252                                           In invertebrates, specific GPCRs instruct G proteins to pro
253 ide pigment dispersing factor (PDF), and the invertebrate-specific D1-like dopamine receptor (InvD1L)
254 ased vulnerability assessment to 36 fish and invertebrate stocks in the eastern Bering Sea (EBS), a d
255 nt of reproductive potential is unique among invertebrates studied to date and provides a potential m
256                         In contrast to other invertebrates studied, Trichoplax and Hoilungia have thr
257 priate assays, and generally low support for invertebrate studies.
258 elanopsin, depolarize like photoreceptors of invertebrates such as Drosophila, discharge electrical s
259                          Soft-bodied aquatic invertebrates, such as sea slugs and snails, are capable
260 ird colonies are favorable habitats for soil invertebrates, such as springtails (Collembola), which m
261 iderable concentrations of 6:2 FTS in marine invertebrates, suggesting bioaccumulation.
262                      Aquatic and terrestrial invertebrates, surface water, sediments, soils, and plan
263 ammalian cells but are less commonly used in invertebrate systems, mostly due to low fluorescence yie
264 ssland, and perennial cropland for most soil invertebrate taxa, demonstrating pervasive impacts of ag
265 r evolutionary potential of the epigenome in invertebrates than there is in mammals.
266  the biofilm matrix and ecological health of invertebrates that depend on biofilms as a food source.
267 ilization of a representative marine benthic invertebrate, the red abalone Haliotis rufescens, to a h
268 iomineral proteins from a Pleistocene fossil invertebrate, the stony coral Orbicella annularis.
269                                           In invertebrates, the formation and function of epithelial
270 rial infection can induce IL-17D in fish and invertebrates, the role of mammalian IL-17D in antibacte
271 lished regulators of developmental timing in invertebrates, their role in mammalian organogenesis is
272                           For example, among invertebrates, there is typically a positive correlation
273 ties and likely other drought-sensitive soil invertebrates, thereby retarding litter decomposition an
274 ductance correlations are well documented in invertebrates, they have not been reported in vertebrate
275                               Vertebrate and invertebrate TnTs have conserved core structures, reflec
276         Here we use the accessible ear of an invertebrate to, for the first time in any animal, chara
277         The pre-conditioning of adult marine invertebrates to altered conditions, such as low pH, can
278 votal role of horizontal virus transfer from invertebrates to plants during the terrestrialization of
279 s, enhance the vulnerability of macrobenthic invertebrates to predation and strongly reduce secondary
280 pressors that act on conserved pathways from invertebrates to vertebrates to alleviate degeneration.
281 systems, revealing them to be divergent from invertebrates to vertebrates.
282 poxic event may weaken the ability of marine invertebrates to withstand elevated CO(2) conditions.
283 semblage (Prokaryota, Protozoa and Eumetazoa invertebrates) to understand the generality and efficien
284 he sensitivity (EC(50)-values) of 10 aquatic invertebrates toward a 24 h pulse of the pyrethroid cype
285                             An initial acute invertebrate toxicity assessment shows that exposure to
286 n scars on trilobites [7], directionality of invertebrate traces [8], and even behavioral asymmetry i
287      We mimic locomotion modes common to sea invertebrates using monolithic liquid crystal gels (LCGs
288          However, conventional monitoring of invertebrates via kick-sampling, is invasive and expensi
289 he detrital food web, including microbes and invertebrates, was not affected by fire.
290 red by lack of insight from commonly studied invertebrates where nervous system morphology and geneti
291 nderestimate the impacts of land use on soil invertebrates, whereas rarity provides clearer and more
292 e strongest effects are in annual plants and invertebrates, whereas vertebrates appear to benefit mos
293 e-F (NPF) have been identified in protostome invertebrates, whilst prolactin-releasing peptide (PrRP)
294             Further research on NF-kappaB in invertebrates will reveal information about the evolutio
295 ets dominated by invertebrates, particularly invertebrates with hard exoskeletons (e.g. beetles and s
296  diversity of bacteria, fungi, protists, and invertebrates with pedogenesis were strongly and positiv
297 y loss was driven by decreasing abundance of invertebrates with trait combinations sensitive to sedim
298 ntinent's terrestrial fauna consists only of invertebrates, with just two native species of insects,
299 gas-1(fc21) RC complex I (NDUFS2-/-) disease invertebrate worms significantly improved mitochondrial
300                                  The general invertebrate ZBJ primers were not appropriate for detect

 
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