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1 her organismal characteristics (here: colour morph).
2 tor, which is heterozygous in the red colour morph.
3 in lakes initially colonized by the littoral morph.
4 reased zooplanktivory, than for the Littoral morph.
5 sed that habitat 19.3% more than the Pelagic morph.
6  alternative, genetically identical nonmimic morph.
7 ic that prevents complete fixation of either morph.
8 R2 results in development of the long-winged morph.
9 r-mediated selection favored the long-scaped morph.
10 out deleterious effects in either homozygous morph.
11 n the Caribbean basin found in several color morphs.
12 ar reward differed across genders and colour morphs.
13 ted with one another and define two discrete morphs.
14 ate of their embryos from wingless to winged morphs.
15 ing the unique symbiont population in orange morphs.
16 ntained at low frequencies alongside cryptic morphs.
17 te preferences of the different wing-pattern morphs.
18  This includes midshipman that have two male morphs.
19 ective wild-type (WT) proteins and the other morphs.
20 d body size amongst the larger, 'weaponised' morphs.
21 pecies and to a lesser extent between colour morphs.
22 ns between light intensity and maternal wing morphs.
23 gical differences between the fruit and seed morphs.
24 e teeth that occur in either of two discrete morphs.
25 nificantly induced the development of winged morphs.
26 tal of 60 SNPs associated with dorsal colour morphs.
27 ism that generates incompatibilities between morphs.
28 o realize the significance of the two floral morphs.
29 lly possess higher fecundity than the winged morphs.
30 and Ilp3 triggers development of long-winged morphs.
31 he functional significance of the two floral morphs.
32 inantly on the perceptual difference between morphs.
33 rgone a mimetic radiation into four distinct morphs.
34 r, though less extensively, between the male morphs.
35  that enhance differentiation between colour morphs.
36 permutation" has deleted color loci in green morphs.
37 rate earlier during ontogeny of these female morphs.
38 morph and multiple populations of blind cave morphs.
39 st electronic connectivity, and active shape morphing.
40 e obtained when showing the pictures without morphing.
41 ng, evaluation, and structure-based scaffold morphing.
42 endent) selection, which favours hosts rarer morphs [1-3,7].
43 as individual mechanical entities can act to morph a tissue reliably and efficiently into three dimen
44 pt for the design of this series centered on morphing a quinoline series recently disclosed in the pa
45 ve organs and total number and proportion of morphs a, c and f on an individual.
46        This species of tetra is found in two morphs: a seeing surface fish and a blind cavefish.
47 strikingly different alternative male mating morphs (aggressive 'independents', semicooperative 'sate
48 inspire innovative directional fasteners and morphing aircraft.
49 idence of plasticity in life-phase and fruit-morph along a stressful environmental gradient.
50  adaptive plasticity in life-phase and fruit morphs along laboratory environmental stress gradients f
51 e we present a kinematics-based procedure to morph an RNA molecule between conformational substates,
52 lour variation among the three dorsal colour morphs analysed.
53 notypes, a slim, putatively pelagic-dwelling morph and a robust, putatively littoral-dwelling general
54 the survival advantage enjoyed by the yellow morph and assumes that relative mating success follows o
55 in size but there is no relationship between morph and body size amongst the larger, 'weaponised' mor
56  solvated soft matter nanoassemblies as they morph and evolve in time and space, enabling us to captu
57 which consists of a sighted surface-dwelling morph and multiple populations of blind cave morphs.
58 e just noticeable difference (JND) between a morph and original image.
59 nct from the host medium, though they can be morphed and reconfigured by weak stimuli under condition
60  platform for programming light-driven shape morphing and materials assembly.
61 lso served as the basis for further scaffold morphing and optimization, detailed in the following man
62 ential temperature sensitivity of the female morphs and faster sexual maturation of the male mimic in
63 n immunoreactivity in the brain of both male morphs and females with a focus on vocal-acoustic and ne
64 or, testis size and steroid metabolism among morphs and identify polymorphic genes within the inversi
65 ortionally increased the number of dehiscent morphs and non-dormant seeds germinating in autumn.
66 atterns of behavioral categorization of face morphs and search performance that were common across su
67 terial in a cantilever setup is used to show morphing, and analytical modeling shows good correlation
68 for applications such as camouflage, surface morphing, and soft robotic grippers.
69 'legitimate' pollinations between compatible morphs, and hence reproductive fitness.
70  early reproduction and life span than green morphs; and red consistent (non)droppers had highest lif
71 ight structures, shape-changing soft robots, morphing antenna and RF devices, and biomedical devices.
72                  Two years later, the silent morph appeared on the neighboring island of Oahu.
73 genus Tetramorium, aphids of the alternative morph are transported by the ants to their brood chamber
74        Recent realizations of time-dependent morphing are limited to the actuation of few, discrete h
75         Remarkably, the satellite and faeder morphs are controlled by dominant alleles.
76 ack changing resources, whereas short-winged morphs are flightless, but usually possess higher fecund
77 ent near-perfect disassortative mating among morphs, as well as the fitness consequences of rare asso
78     These lakes harbor up to three different morphs associated with the three major lake habitats: li
79 haracterize the spatial organization of male morphs at each site and quantified male aggressive behav
80 gence in microhabitat use and diet among the morphs at the frequently burned site that reflected the
81                                  We envision MORPH becoming a valuable tool for controlling nanoscale
82 netic composite film, whose responsive shape-morphing behaviors induced by a magnetic field can be di
83 spatial network structure and differences in morph behaviour.
84 d different nectar reward, with intermediate morphs being midway between the other genders.
85                                     Next, we morphed between these patterns and determined the just n
86  and independently in the face and voice via morphing between angry and happy expressions.
87                    The ambiguous images were morphs between the faces of two familiar individuals, ch
88 al differences in the categorization of face morphs between two identities could be decoded from the
89 r pairs of JND stimuli along the spectrum of morphs between two original images.
90 ication approach, based on printing of shape-morphing biopolymer hydrogels, is developed for the fabr
91 ficant genetic differentiation between color morphs both the composition of the Symbiodinium spp. com
92 an alternative strategy for prescribed shape-morphing by programming the magnitude of stretch ratio i
93                                  Long-winged morphs can fly, which allows them to escape adverse habi
94                                  First, in a morph categorisation task, participants made binary deci
95 Three hemizygous genes appear to determine S-morph characteristics in T. subulata.
96                                      Pelagic morph charr exhibited significantly greater deltaC(13) d
97                             We show that two morphs clonally produced by the aphid Paracletus cimicif
98 hism (where different genetically determined morphs co-occur in sympatry within the same population)
99 e we show, with a novel paradigm using audio morphing combined with multimodal neuroimaging and brain
100 esent an electrically controlled solid-state morphing composite material that is lightweight and has
101 de binary decisions about faces drawn from a morph continuum that blended incrementally an average ma
102  life-phase (vegetative vs sexual) and fruit morph (dehiscent [DEH] vs indehiscent fruits [IND]).
103 rphic Finland, where the attack risk of moth morphs depended on the local avian community.
104 nds, the molecular mechanism underlying wing morph determination in insects has remained elusive.
105  candidate gene involved in alternative male morph determination in ruffs.
106 thoppers have revealed that alternative wing morphs develop in response to various environmental cues
107 trial and outer-space structures, as well as morphing devices.
108 applications such as soft robotics and shape-morphing devices.
109  and transcriptomic analyses reveal that the morphs differ solely in cyanidin pigments, which are lin
110 h biotic and abiotic factors affect the wing morph differentiation of a bethylid parasitoid Scleroder
111 als is sufficient to maintain a diversity of morphs displaying accurate mimicry with other local prey
112 cluding locally adapted ecotypes and cryptic morphs, divergent social behaviours in birds and insects
113 are an attractive platform for dynamic shape-morphing due to their ability to rapidly undergo large d
114 idiosyncratic representations of famous face morphs during an identity categorization task; data from
115 xes into discrete units of diversity such as morphs, ecotypes, or species.
116             The series emerged from scaffold morphing efforts and was demonstrated to noncovalently i
117    During the fastest growth period in rats, morphing electronics caused minimal damage to the rat ne
118                                              Morphing electronics offers a path toward growth-adaptiv
119                               The ability of morphing electronics to self-heal during implantation su
120         We design and fabricate multilayered morphing electronics, consisting of viscoplastic electro
121        Here, we address this limitation with morphing electronics, which adapt to in vivo nerve tissu
122                                In the winged morph, energy needed for wing maintenance may lead to tr
123 onsidered a precursor to speciation in which morphs evolve into different species.
124                        Although one of these morphs exhibits the conventional trophobiotic (mutualist
125                                          Red morphs experienced stronger trade-offs between early rep
126               The microbiome of orange color morphs expressed significantly more nitrogenase (nifH) t
127  for each identity in the "crowd" of another morphed face in a separate search task.
128 first while they discriminated repetition of morphed faces or voices and either directed their attent
129                                      Pelagic morph fish were significantly more active, further from
130 eve unimpeded fertilization only on opposite-morph flowers.
131 d on a morphological transformation process (MORPH, for short) driven by the formation of supramolecu
132 tilis), re-established with perturbed colour morph frequencies and followed for >20 generations.
133 ing classical data sets of moth pigmentation morph frequencies, but it has wide applications in setti
134  and yellow male moths under three different morph frequencies.
135 tors on warning colour is predicted by local morph frequency and predator community composition.
136 strong need to understand how pavement cells morph from a simple polyhedral shape into highly lobed a
137         The field of single-cell biology has morphed from a philosophical digression at its inception
138               These unexpected findings have morphed from detours to main directions, changing how I
139 e gaits of walkers whose gender is digitally morphed from male to female [1, 2], we show that smellin
140       For non-rebound cases, droplets can be morphed from spheres to complex shapes--without unwanted
141 ous expectations, as a pattern is gradually "morphed" from one stored pattern to another, a sharp tra
142 istromellaceae and the two purported asexual morphs--Fusicladium and Aposphaeria--in the Venturiaceae
143 o key steps for optimization were (i) a core morph guided by a TLR7 sequence alignment to achieve a d
144 Symbiodinium spp. transcriptomes from orange morphs had significantly increased expression of genes r
145 ntributing to phenotypic differences between morphs have accumulated within the inverted region.
146                                          The morph highlights similarities in tRNA conformational cha
147 with the hosts with a newly acquired mimetic morph, host polymorphism should be maintained through ap
148 signalling cascade, leads to the long-winged morph if active and the short-winged morph if inactive.
149 -winged morph if active and the short-winged morph if inactive.
150                           The lavender color morph in corn snakes is characterized by gray, rather th
151  and dark, whereas males have only one color morph in each species.
152 e male mimic increases the frequency of this morph in the north.
153  ascomycete families: the Microcyclus sexual morph in the Planistromellaceae and the two purported as
154 combined with independent origins of similar morphs in different lineages and secondary loss of polym
155  situ emergence of the pelagic and profundal morphs in lakes initially colonized by the littoral morp
156        What selection pressures maintain the morphs in multiple daughter species?
157 differences between flower gender and colour morphs in nectar rewards.
158 ikely to contribute to the differences among morphs in reproductive traits.
159  polymorphism, uniformity of respective host morphs in single host nests stochastically prevents para
160 olymorphism with black, red and white floral morphs in the Alpine orchid Gymnadenia rhellicani.
161 t females differ dramatically from both male morphs in the number of galanin-expressing somata and in
162 mal kingdom, comprising three different male morphs (independents, satellites and faeders) that diffe
163                                      While l-morph individuals form flowers with long styles, short a
164 s, short anthers, and small pollen grains, S-morph individuals have flowers with short styles, long a
165 ing which "protein crystallography" began to morph into "structural biology." The course of the resea
166 Micron-scale robots require systems that can morph into arbitrary target configurations controlled by
167 we designed and printed planar lattices that morph into frequency-shifting antennae and a human face,
168  times this methodological device appears to morph into the substantive claim that humans are actuall
169 can be compressed by orders of magnitude and morphed into a Mobius strip or a simple origami at room
170 hat followed, the same genetic material also morphed into a wide spectrum of viruses and other parasi
171 s, the malleobactin pathway was successfully morphed into an ornibactin assembly line.
172 sheet of AuNR/LCE film (100 um thick) can be morphed into different shapes simply by varying the moti
173 erin, which enables retained ectosomes to be morphed into discs.
174 eneric bone architecture of the MS model was morphed into the segmented bones.
175 d structured as a tubular network capable of morphing into flat cisternae, mainly at three-way juncti
176                                              Morph is determined by alternative alleles at a balanced
177                                         Such morphing is problematic; the methodological approach use
178                   The difference between the morphs is controlled by an S-locus "supergene" consistin
179 where reproductive isolation between mimetic morphs is incomplete but evident.
180         The presence of different phenotypic morphs is sometimes considered a precursor to speciation
181 le Abl weakly modulates the ratio of the two morphs it does not greatly change their properties.
182 es, females have alternative abdominal color morphs, light and dark, whereas males have only one colo
183 corded place cell activity in rats exploring morphing linear tracks that allowed us to dissociate the
184 ny of these species maintain nonwhite winter morphs, locally adapted to less snowy conditions, which
185 ss was positively frequency-dependent: white morph males had high relative fitness when common, likew
186 elative fitness when common, likewise yellow morph males had high relative fitness when instead they
187 e mass and mechanical complexity solid-state morphing materials are desirable but are typically nonst
188                                Herein, shape-morphing materials called "kinomorphs" that rationally c
189                                              Morphing materials have promising applications in variou
190                     Many of the mechanically morphing materials systems found in nature are based on
191 des key new principles for designing shaping-morphing materials that avoid undesired distractor state
192                            Advances in shape-morphing materials, such as hydrogels, shape-memory poly
193 ise and paves the way for stiff, solid-state morphing materials.
194           This finding suggests that the two morphs may live in contact with each other in the same b
195 events parasites from targeting any specific morph of hosts and thus helps parents detect parasitism.
196 ecular probes to discriminate the rare black morph of Proteus from the closely related white morph, w
197                         The wrinkly spreader morph of Pseudomonas fluorescens arises repeatedly durin
198                       Two cycles of scaffold morphing of a high-throughput biochemical screening hit
199 g approach yielding controlled vectoring and morphing of droplets during and after impact.
200             We show how this can be used for morphing of macromolecules that can be heterogeneous in
201 within 360 deg is achieved via a topological morphing of the metasurface pattern from metallic patche
202 s the role of the mechanical feedback during morphing of tissue in three dimensions?
203     It is intriguing that conspicuous colour morphs of a prey species may be maintained at low freque
204  success, life span) in red and green colour morphs of clonal pea aphids, Acyrthosiphon pisum.
205  we show that the genomes of sympatric color morphs of the European common wall lizard (Podarcis mura
206 c incompatibilities between sympatric colour morphs of the Gouldian finch (Erythrura gouldiae), in wh
207  but recombining loci underlie cryptic color morphs of Timema chumash stick insects.
208 e genes responsible for producing different "morphs" of primrose flowers has been identified.
209                            Because different morphs often display alternative strategies and exploit
210 stened to non-speech-affective vocalizations morphed on a continuum between anger and fear.
211 typic mismatch (inaccuracy) of heterostylous morphs on a common scale.
212 uous trajectories that displace densities to morph one map into the other, instead of blending them.
213 pulations of place cells, recent experiments morphed one familiar context into another while observin
214       These species have three female colour morphs, one of which is a male mimic.
215 served during mating in cuckolders of either morph or females (none of which show parental care).
216  of flatwings in Hawaii: (1) that the silent morph originated on Kauai and subsequently introgressed
217 ust, putatively littoral-dwelling generalist morph, over an annual cycle, using biotelemetry and stab
218 h, high volumetric change, and complex shape-morphing patterns are introduced.
219  heterostyly in Primula described two floral morphs, pin and thrum, with reciprocal anther and stigma
220                        In Primula forbesii S-morph plants, GLO2 promotes growth by cell expansion in
221  geometries and precisely controllable shape morphing potential, while drastically reducing the requi
222 e polymorphic than if there is only a single morph present in the population.
223   On a large benchmark set, we show that our morphing procedure compares favorably to peer algorithms
224                                  Notably, as morphing proceeds, the activity pattern in the dentate g
225 trimentally altering its mechanical or shape-morphing properties.
226 ernative to N-methylation for the purpose of morphing protein-binding peptides into more serum-stable
227 hrombin by factor Xa by compressing Lnk2 and morphing prothrombin into a conformation similar to the
228 does sensing promote plasticity of dispersal morph ratio, individuals who can sense their sub-habitat
229 se sexual polymorphisms, resulting in biased morph ratios and populations with a single mating group,
230 site sex on complementary (inter-compatible) morphs, reflecting the correspondence of locations of po
231 e cuticular hydrocarbon profile of the mimic morph resembles the profile of ant larvae more than that
232 raphy, conformational analysis, and scaffold morphing resulted in highly optimized difluorophenol pyr
233 ders have selected for entire and lobed leaf morphs resulting from a single locus, okra (l-D1), which
234 pt transitions at different points along the morph sequence, and some displayed hysteresis which is a
235 de transitions at different points along the morph sequence.
236  phylogenetic evidence, with the Aposphaeria morph shown to have a spermatial rather than an infectiv
237 ana showing four clearly differentiated male morphs: small "Gammas", "Alphas" which express large, lo
238 isms of vertebrate social behavior including morph-specific actions on vocal neurophysiology in midsh
239  steroid receptor abundances likely regulate morph-specific behaviors in males and females of other s
240 ar evoked by, and their explicit memory for, morph stimuli with varying degrees of similarity to the
241  Although three-dimensional space-use of the morphs strongly overlapped, on average, the Littoral mor
242                                        Shape-morphing structured materials have the ability to transf
243 s are applicable to origami-inspired robots, morphing structures and devices, metamaterials, and mult
244 ra of applications, including soft robotics, morphing structures, and biomedical devices.
245 ped flexure bearings, compliant prosthetics, morphing structures, and soft robots.
246 materials for shape change applications like morphing structures.
247 ranging from biomedical devices to aerospace morphing structures.
248                       This suggests that red morphs suffer the highest costs of dropping (they are mo
249 ph to support telechory, while the M(+) seed morph supports antitelechory.
250  situ and in situ wetting transitions on the MorphS surfaces are solely due to transformations in mor
251             It is envisioned that the robust MorphS surfaces with reversible wetting transition will
252                                Utilizing the MorphS surfaces, the distinctly different wetting transi
253  memory effect, metamorphic superomniphobic (MorphS) surfaces that transform their morphology in resp
254                                        Shape-morphing systems can be found in many areas, including s
255 s of biologically inspired composites, shape-morphing systems, soft sensors and robotics that only ad
256 ical architectures for self-motile and shape-morphing systems.
257                   This species comprises two morphs, tan and white, that differ in pigmentation and c
258 65 y all Faroese hares became winter-gray, a morph that occurs in the source population at low freque
259      We present a minimal physical model for MORPH that suggests a general mechanism which is potenti
260  strength of an immune response across aphid morphs that differ in life-history strategy but are gene
261 ), a highly vocal teleost fish with two male morphs that follow alternative reproductive tactics, sho
262 rpose to transform electromagnetic waves, we morph the shapes of FSS designs based on origami pattern
263 g flight feathers when the skeleton moves to morph the wing planform.
264 rmediate environments, generated by linearly morphing the background landscapes of the familiar envir
265 cribe the further expansion of our approach, morphing the fused, bicyclic system into a novel monocyc
266 longer and more branched, while in both cave morphs the ventral dendrites were smaller or absent.
267 -locus determines the long- and short-styled morphs, the genes were unknown in Turnera.
268    Variable feather overlap enables birds to morph their wings, unlike aircraft.
269 ost abundant and best-protected wing-pattern morph, thereby limiting polymorphism.
270 n a number of X-ray cocrystal structures, we morphed this hit class into potent imidazoles, exemplifi
271 of volume data from fluorescence microscopy, morphed three-dimensionally, onto a common spatial frame
272 ly break their shape symmetry several times, morphing through a series of complex regular shapes owin
273 tes' mimicry can favour a newly emerged host morph to escape parasites' mimicry.
274 lity and degree of dormancy on the IND fruit morph to support telechory, while the M(+) seed morph su
275    Remarkably, the local structure of portal morphs to compensate for symmetry-mismatch, forming simi
276 ative frequency-dependent selection for rare morphs to explain polymorphic (white and yellow) warning
277 late barycenters between EM maps and produce morphing trajectories.
278  The region is highly differentiated between morphs, unlike the rest of the genome, yet we find no ev
279 trongly overlapped, on average, the Littoral morph used that habitat 19.3% more than the Pelagic morp
280                That is, only more aggressive morphs usurped trees and consumed prey from higher troph
281              We conclude that while discrete-morph variation provides the most unambiguous cases of p
282 tress on number and mass of a dispersal unit morph varied by treatment, with dispersal unit f having
283                      The frequency of female morphs varies geographically, with higher frequency of t
284                                 We presented morph videos of the caregiver, a familiar person, and a
285 1-sulfonate (SPTZ) and 4-morpholinopyridine (MORPH) was used to enhance peroxidase-induced CL.
286  investigate the causes for brown and orange morphs we undertook a genomics approach on corals collec
287 ph of Proteus from the closely related white morph, we detected its eDNA at five new sites, thus more
288         Utilizing the same forces central to morphing, we demonstrate the ability to rebound orthogon
289 g the production of offspring of alternative morphs, we also explore the influence of symbionts acros
290 stal elastomers (LCEs) that reversibly shape-morph when cycled above and below their nematic-to-isotr
291  exerted by grazers favored the short-scaped morph, whereas pollinator-mediated selection favored the
292  flowers had higher sugar content than light morphs, whereas intermediate flowers did not.
293 l origin are significantly greater in orange morphs, which is also consistent with the significantly
294 demonstrate how both passive mechanisms make morphing wings robust to turbulence.
295                               However, shape morphing with dielectric elastomers has not been possibl
296 eeding systems, there can exist intermediate morphs with a reduction in their male function (i.e. red
297 hic architecture (both "baggy" and "compact" morphs), with diversification within Hyalophora for both
298 igher fitness (seed set) of the heterozygous morph without deleterious effects in either homozygous m
299 rical representations of the continuous face morphs would predict their distractability when searchin
300 rounding the pathogen that each of the spore morphs would, according to their present classification,

 
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