ライフサイエンスコーパス: morph

1 her organismal characteristics (here: colour morph).

2 alternative, genetically identical nonmimic morph.

3 ic that prevents complete fixation of either morph.

4 R2 results in development of the long-winged morph.

5 r-mediated selection favored the long-scaped morph.

6 ype, or are carried out only on the inactive morph.

7 reased zooplanktivory, than for the Littoral morph.

8 sed that habitat 19.3% more than the Pelagic morph.

9 o realize the significance of the two floral morphs.

10 lly possess higher fecundity than the winged morphs.

11 and Ilp3 triggers development of long-winged morphs.

12 he functional significance of the two floral morphs.

13 ate of their embryos from wingless to winged morphs.

14 inantly on the perceptual difference between morphs.

15 rgone a mimetic radiation into four distinct morphs.

16 tantial gene flow between some color pattern morphs.

17 nstrated in species with discrete phenotypic morphs.

18 s that cause mortality of freezing-sensitive morphs.

19 n differences in relative fitness of the two morphs.

20 n the Caribbean basin found in several color morphs.

21 ing the unique symbiont population in orange morphs.

22 attern reveal substantial divergence between morphs.

23 lations with reduced numbers of throat color morphs.

24 ficantly brighter in island than in mainland morphs.

25 ntained at low frequencies alongside cryptic morphs.

26 te preferences of the different wing-pattern morphs.

27 ective wild-type (WT) proteins and the other morphs.

28 d body size amongst the larger, 'weaponised' morphs.

29 pecies and to a lesser extent between colour morphs.

30 ns between light intensity and maternal wing morphs.

31 gical differences between the fruit and seed morphs.

32 e teeth that occur in either of two discrete morphs.

33 ar reward differed across genders and colour morphs.

34 nificantly induced the development of winged morphs.

35 tal of 60 SNPs associated with dorsal colour morphs.

36 ism that generates incompatibilities between morphs.

37 e obtained when showing the pictures without morphing.

38 endent) selection, which favours hosts rarer morphs [1-3,7].

39 pt for the design of this series centered on morphing a quinoline series recently disclosed in the pa

40 ng by focusing on the timing of responses to morphs after facial expression adaptation.

41 strikingly different alternative male mating morphs (aggressive 'independents', semicooperative 'sate

42 sted in a straight alley maze to a series of morphed ambiguous appetitive (chick silhouette) to avers

43 e we present a kinematics-based procedure to morph an RNA molecule between conformational substates,

44 lour variation among the three dorsal colour morphs analysed.

45 notypes, a slim, putatively pelagic-dwelling morph and a robust, putatively littoral-dwelling general

46 l sulcus (STS) reflect the degree to which a morph and adapted expression deviate.

47 ages, as well as interactive effects of sex, morph and age, in response to both host and repellent od

48 the survival advantage enjoyed by the yellow morph and assumes that relative mating success follows o

49 in size but there is no relationship between morph and body size amongst the larger, 'weaponised' mor

50 solvated soft matter nanoassemblies as they morph and evolve in time and space, enabling us to captu

51 st false discovery rate overall, followed by morph and vsn.

52 aded versions of the training stimuli, while morphing and cell exchange were used to manipulate the r

53 Possible further applications of deactivated morphing and implications for force field development ar

54 or, testis size and steroid metabolism among morphs and identify polymorphic genes within the inversi

55 atterns of behavioral categorization of face morphs and search performance that were common across su

56 , which controls development into the Faeder morph, and draw further conclusions about candidate gene

57 expressed in the horns of the large, horned morph, and RNAi-mediated knockdown of dsx dramatically a

58 for controlling cell adhesion, tissue shape morphing, and cell tissue migration.

59 'legitimate' pollinations between compatible morphs, and hence reproductive fitness.

60 opment, including differences between sexes, morphs, and species.

61 early reproduction and life span than green morphs; and red consistent (non)droppers had highest lif

62 ight structures, shape-changing soft robots, morphing antenna and RF devices, and biomedical devices.

63 Two years later, the silent morph appeared on the neighboring island of Oahu.

64 genus Tetramorium, aphids of the alternative morph are transported by the ants to their brood chamber

65 Remarkably, the satellite and faeder morphs are controlled by dominant alleles.

66 ack changing resources, whereas short-winged morphs are flightless, but usually possess higher fecund

67 re predicted by gonadal phenotype (both male morphs are sensitive to androgen receptor blockade, wher

68 ent near-perfect disassortative mating among morphs, as well as the fitness consequences of rare asso

69 yield rather uniform frequencies of melanic morphs at around 20% along the whole transect by 2004.

70 haracterize the spatial organization of male morphs at each site and quantified male aggressive behav

71 gence in microhabitat use and diet among the morphs at the frequently burned site that reflected the

72 spatial network structure and differences in morph behaviour.

73 d different nectar reward, with intermediate morphs being midway between the other genders.

74 and independently in the face and voice via morphing between angry and happy expressions.

75 nts viewed images from continua generated by morphing between faces posing different expressions such

76 The ambiguous images were morphs between the faces of two familiar individuals, ch

77 al differences in the categorization of face morphs between two identities could be decoded from the

78 ication approach, based on printing of shape-morphing biopolymer hydrogels, is developed for the fabr

79 ficant genetic differentiation between color morphs both the composition of the Symbiodinium spp. com

80 e modest genetic differentiation between two morphs, but this level of differentiation is nonetheless

81 Long-winged morphs can fly, which allows them to escape adverse habi

82 MORPH candidates ranked for the carotenoid pathway from

83 uence variant associated with the carbonaria morph, carrying a signature of recent strong selection.

84 es, we find that categorization training (on morphed "cars") induced a significant release from adapt

85 In animals, the frequency of alternative morphs, characterized by different morphologies and mati

86 Pelagic morph charr exhibited significantly greater deltaC(13) d

87 We show that two morphs clonally produced by the aphid Paracletus cimicif

88 hism (where different genetically determined morphs co-occur in sympatry within the same population)

89 e we show, with a novel paradigm using audio morphing combined with multimodal neuroimaging and brain

90 cipants were shown six faces (F1-F6) along a morph continuum, and selectivity was quantified by const

91 first (F1-F3) or second (F4-F6) half of the morph continuum.

92 Along with sex and age of individual, adult morph could be an important variable determining the bio

93 forms are required for fertilization; within-morph crosses are impeded by a sporophytic self-incompat

94 nds, the molecular mechanism underlying wing morph determination in insects has remained elusive.

95 candidate gene involved in alternative male morph determination in ruffs.

96 candidate to play a role in alternative male morph determination.

97 thoppers have revealed that alternative wing morphs develop in response to various environmental cues

98 trial and outer-space structures, as well as morphing devices.

99 s in A. imperialis is accompanied by between-morph differences in pollen and seed dispersal.

100 h biotic and abiotic factors affect the wing morph differentiation of a bethylid parasitoid Scleroder

101 als is sufficient to maintain a diversity of morphs displaying accurate mimicry with other local prey

102 By comparing current data on morph distribution with that observed in the early 1970s

103 cluding locally adapted ecotypes and cryptic morphs, divergent social behaviours in birds and insects

104 idiosyncratic representations of famous face morphs during an identity categorization task; data from

105 The series emerged from scaffold morphing efforts and was demonstrated to noncovalently i

106 rate, but such aphids can produce the winged morph, even at low insect density, which can fly and col

107 Although one of these morphs exhibits the conventional trophobiotic (mutualist

108 Red morphs experienced stronger trade-offs between early rep

109 The microbiome of orange color morphs expressed significantly more nitrogenase (nifH) t

110 for each identity in the "crowd" of another morphed face in a separate search task.

111 (adaptation) induces perception of ambiguous morph faces as a category different from the adapted cat

112 Pelagic morph fish were significantly more active, further from

113 was driven by higher pollen export from male morph flowers as a result of greater pollen production a

114 differences between hermaphroditic and male morph flowers in P. incarnata and explored the fruiting

115 * The production of male morph flowers in P. incarnata appears to be a flexible a

116 * Male morph flowers in P. incarnata were of similar size to he

117 On average, male morph flowers sired twice as many seeds as hermaphroditi

118 Male morph flowers were less capable of producing fruit, even

119 By contrast, male morph flowers were more successful in siring seeds.

120 eve unimpeded fertilization only on opposite-morph flowers.

121 Remarkably, these continued to morph for months, long after session-averaged reward and

122 of transcript abundance across reproductive morphs for ERbeta1, ERbeta2, ERalpha, and aromatase in t

123 We present an algorithm called MORPH (for module-guided ranking of candidate pathway ge

124 to be understood about the process by which morphs found new species.

125 tilis), re-established with perturbed colour morph frequencies and followed for >20 generations.

126 ing classical data sets of moth pigmentation morph frequencies, but it has wide applications in setti

127 and yellow male moths under three different morph frequencies.

128 pulations was associated with differences in morph frequency change, and the experimental removal of

129 ocially transmitted defenses depend on enemy morph frequency.

130 ays when group mean fitness is a function of morph frequency.

131 strong need to understand how pavement cells morph from a simple polyhedral shape into highly lobed a

132 The field of single-cell biology has morphed from a philosophical digression at its inception

133 e gaits of walkers whose gender is digitally morphed from male to female [1, 2], we show that smellin

134 For non-rebound cases, droplets can be morphed from spheres to complex shapes--without unwanted

135 ous expectations, as a pattern is gradually "morphed" from one stored pattern to another, a sharp tra

136 istromellaceae and the two purported asexual morphs--Fusicladium and Aposphaeria--in the Venturiaceae

137 Symbiodinium spp. transcriptomes from orange morphs had significantly increased expression of genes r

138 The carbonaria morph has declined across the region following 1960s leg

139 Development into independent or satellite morphs has previously been shown to be due to a single-l

140 one particular male strategy, the "sneaker" morph, has been lost in all cases.

141 ntributing to phenotypic differences between morphs have accumulated within the inverted region.

142 The morph highlights similarities in tRNA conformational cha

143 with the hosts with a newly acquired mimetic morph, host polymorphism should be maintained through ap

144 hree permanent alternative male reproductive morphs: (i) territorial 'Independents', (ii) non-territo

145 signalling cascade, leads to the long-winged morph if active and the short-winged morph if inactive.

146 -winged morph if active and the short-winged morph if inactive.

147 ks later, 82 participants viewed the CS+ and morphed images resembling the CS+ in an MRI scanner.

148 Here, we measured the neural response to morphed images to directly address how facial expression

149 discovered that the production of the winged morph in asexual clones of the rosy apple aphid, Dysaphi

150 and dark, whereas males have only one color morph in each species.

151 hid virus (RAAV), did not produce the winged morph in response to crowding and poor plant quality.

152 ascomycete families: the Microcyclus sexual morph in the Planistromellaceae and the two purported as

153 enerator (VPG) diverges between reproductive morphs in a teleost fish.

154 subdivision associated with sympatric colour morphs in A. imperialis is accompanied by between-morph

155 s and aromatase varied significantly between morphs in and around the sexually polymorphic vocal moto

156 combined with independent origins of similar morphs in different lineages and secondary loss of polym

157 ated the genetic differentiation between two morphs in Lake Thingvallavatn relative to historically e

158 differences between flower gender and colour morphs in nectar rewards.

159 ikely to contribute to the differences among morphs in reproductive traits.

160 polymorphism, uniformity of respective host morphs in single host nests stochastically prevents para

161 role of morphologically male flowers ('male morph') in andromonoecious Passiflora incarnata.

162 mal kingdom, comprising three different male morphs (independents, satellites and faeders) that diffe

163 ing which "protein crystallography" began to morph into "structural biology." The course of the resea

164 Nucleic acids transiently morph into alternative conformations that can be difficu

165 beta's tumor-suppressive roles may appear to morph into tumor-promotion during cancer progression.

166 hat followed, the same genetic material also morphed into a wide spectrum of viruses and other parasi

167 s, the malleobactin pathway was successfully morphed into an ornibactin assembly line.

168 erin, which enables retained ectosomes to be morphed into discs.

169 eneric bone architecture of the MS model was morphed into the segmented bones.

170 d structured as a tubular network capable of morphing into flat cisternae, mainly at three-way juncti

171 The gray morph is a Batesian mimic whose hawk-like appearance det

172 Morph is determined by alternative alleles at a balanced

173 lation is large or the mutation rate between morphs is high enough.

174 where reproductive isolation between mimetic morphs is incomplete but evident.

175 velop fluorescence-inducing reporter RNA and morph it into remotely related sequences without prior s

176 Morphing leads to complex transformations of the stimuli

177 es, females have alternative abdominal color morphs, light and dark, whereas males have only one colo

178 tion of responses to one prototype along the morph line) served as a reference when, in a second phas

179 corded place cell activity in rats exploring morphing linear tracks that allowed us to dissociate the

180 da), the gene that underlies the major plate-morph locus [11].

181 pulations of this species include two floral morphs: long-scaped plants that present their flowers we

182 ss was positively frequency-dependent: white morph males had high relative fitness when common, likew

183 elative fitness when common, likewise yellow morph males had high relative fitness when instead they

184 Morphing materials have promising applications in variou

185 Many of the mechanically morphing materials systems found in nature are based on

186 This finding suggests that the two morphs may live in contact with each other in the same b

187 tions, and so did the frequency of the short morph (median 19%, range 0-100%; n = 69 populations).

188 We present a new morphing method that does not extrapolate linearly and c

189 in, using the recently developed deactivated morphing method to calculate free energy differences bet

190 sented as a prime, immediately before a test morph object.

191 y training rats to categorize a continuum of morph objects resulting from blending two object prototy

192 species could originate from the distinctive morphs observed in polymorphic populations.

193 shows that it is not merely a late-surviving morph of Au. africanus.

194 events parasites from targeting any specific morph of hosts and thus helps parents detect parasitism.

195 ecular probes to discriminate the rare black morph of Proteus from the closely related white morph, w

196 The wrinkly spreader morph of Pseudomonas fluorescens arises repeatedly durin

197 e in the frequency of the black (carbonaria) morph of the peppered moth (Biston betularia) across nor

198 g approach yielding controlled vectoring and morphing of droplets during and after impact.

199 We show how this can be used for morphing of macromolecules that can be heterogeneous in

200 within 360 deg is achieved via a topological morphing of the metasurface pattern from metallic patche

201 ctory and trigeminal sensations, resulted in morphing of the temporal dynamics of stimulus-evoked res

202 It is intriguing that conspicuous colour morphs of a prey species may be maintained at low freque

203 genotypic space separating two flower color morphs of Antirrhinum.

204 Winged morphs of aphids are essential for their dispersal and s

205 nce of adaptive phenotypic differences among morphs of Arctic charr, Salvelinus alpinus, in Iceland.

206 success, life span) in red and green colour morphs of clonal pea aphids, Acyrthosiphon pisum.

207 a task in which subjects were presented with morphs of fearful facial emotional expressions.

208 c incompatibilities between sympatric colour morphs of the Gouldian finch (Erythrura gouldiae), in wh

209 A cline in the frequency of melanic morphs of the two-spot ladybird, Adalia bipunctata, was

210 e genes responsible for producing different "morphs" of primrose flowers has been identified.

211 Because different morphs often display alternative strategies and exploit

212 We tested MORPH on 230 known pathways in Arabidopsis thaliana and

213 stened to non-speech-affective vocalizations morphed on a continuum between anger and fear.

214 typic mismatch (inaccuracy) of heterostylous morphs on a common scale.

215 pulations of place cells, recent experiments morphed one familiar context into another while observin

216 ompound, methyl salicylate, differed between morphs or sexes.

217 of flatwings in Hawaii: (1) that the silent morph originated on Kauai and subsequently introgressed

218 ly reduced the frequency of the short-scaped morph over 8 y.

219 ust, putatively littoral-dwelling generalist morph, over an annual cycle, using biotelemetry and stab

220 h, high volumetric change, and complex shape-morphing patterns are introduced.

221 ange in the point of subjective equality for morphed pictures of the two faces.

222 heterostyly in Primula described two floral morphs, pin and thrum, with reciprocal anther and stigma

223 geometries and precisely controllable shape morphing potential, while drastically reducing the requi

224 e polymorphic than if there is only a single morph present in the population.

225 selection for locally camouflaged seed color morphs, probably driven by seed predators, may maintain

226 On a large benchmark set, we show that our morphing procedure compares favorably to peer algorithms

227 Notably, as morphing proceeds, the activity pattern in the dentate g

228 ernative to N-methylation for the purpose of morphing protein-binding peptides into more serum-stable

229 hrombin by factor Xa by compressing Lnk2 and morphing prothrombin into a conformation similar to the

230 ntally changing shapes along a continuous 3D morph, ranging from a head ("face") to a house ("place")

231 se sexual polymorphisms, resulting in biased morph ratios and populations with a single mating group,

232 site sex on complementary (inter-compatible) morphs, reflecting the correspondence of locations of po

233 e cuticular hydrocarbon profile of the mimic morph resembles the profile of ant larvae more than that

234 raphy, conformational analysis, and scaffold morphing resulted in highly optimized difluorophenol pyr

235 ders have selected for entire and lobed leaf morphs resulting from a single locus, okra (l-D1), which

236 Using machine learning techniques, MORPH selects the best combination of data and analysis

237 pt transitions at different points along the morph sequence, and some displayed hysteresis which is a

238 de transitions at different points along the morph sequence.

239 i) little or no response to the intermediate morphed shapes (predicted by the category model).

240 Given that these morphs show dissimilar biology, it is possible that they

241 phylogenetic evidence, with the Aposphaeria morph shown to have a spermatial rather than an infectiv

242 ana showing four clearly differentiated male morphs: small "Gammas", "Alphas" which express large, lo

243 changes in alpha power during the different morphs, source analysis, and graph-theoretic metrics ser

244 steroid receptor abundances likely regulate morph-specific behaviors in males and females of other s

245 ral traits, including the central control of morph-specific vocal behaviors.

246 es the duration, frequency, and amplitude of morph-specific vocalizations.

247 ical space were tackled by multiple scaffold morphing steps, which progressed through tricyclic pyrim

248 monstrates how fragment-growing and scaffold morphing strategies arising from a structure-based under

249 Although three-dimensional space-use of the morphs strongly overlapped, on average, the Littoral mor

250 ranging from biomedical devices to aerospace morphing structures.

251 materials for shape change applications like morphing structures.

252 This suggests that red morphs suffer the highest costs of dropping (they are mo

253 situ and in situ wetting transitions on the MorphS surfaces are solely due to transformations in mor

254 It is envisioned that the robust MorphS surfaces with reversible wetting transition will

255 Utilizing the MorphS surfaces, the distinctly different wetting transi

256 memory effect, metamorphic superomniphobic (MorphS) surfaces that transform their morphology in resp

257 Shape-morphing systems can be found in many areas, including s

258 s of biologically inspired composites, shape-morphing systems, soft sensors and robotics that only ad

259 ical architectures for self-motile and shape-morphing systems.

260 This species comprises two morphs, tan and white, that differ in pigmentation and c

261 In this study we applied a morphing technique to systematically vary intensities of

262 Morphing techniques were used to generate 888 models wit

263 Morphing techniques were used to produce 768 models with

264 ually addressed in an approximate way using 'morphing' techniques, which are linear interpolations of

265 at social learning is specific to the cuckoo morph that neighbors mob.

266 al image and video manipulation technique of morphing that allows these images to be compiled in such

267 a significant increase in the proportion of morphs that are sensitive to winter freezing.

268 strength of an immune response across aphid morphs that differ in life-history strategy but are gene

269 ), a teleost fish, has two male reproductive morphs that follow alternative mating tactics and diverg

270 rmediate environments, generated by linearly morphing the background landscapes of the familiar envir

271 ost abundant and best-protected wing-pattern morph, thereby limiting polymorphism.

272 of volume data from fluorescence microscopy, morphed three-dimensionally, onto a common spatial frame

273 ly break their shape symmetry several times, morphing through a series of complex regular shapes owin

274 We have genetically mapped the carbonaria morph to a 200-kilobase region orthologous to a segment

275 tes' mimicry can favour a newly emerged host morph to escape parasites' mimicry.

276 ect recognition with standard facial stimuli morphed to display varying intensities of happiness.

277 ative frequency-dependent selection for rare morphs to explain polymorphic (white and yellow) warning

278 is species frequently neglect to distinguish morph type, or are carried out only on the inactive morp

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 irection and magnitude of selection on scape morph varied among populations, and so did the frequency

283 "Morphed" versions of this potential, fitted to experimen

284 We present three morphed video data sets from ranid tadpoles that facilit

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 hways of Arabidopsis, genes ranked highly by MORPH were recently verified to be associated with these

290 e also considering differences between adult morphs where present in insect species.

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 invasion speed of a population that has two morphs which differ in their dispersal abilities.

294 ncreased selection for the completely plated morph, which we suggest could result from higher levels

295 l origin are significantly greater in orange morphs, which is also consistent with the significantly

296 s affecting plants' outcrossing rates or sex morphs will spread in populations.

297 eeding systems, there can exist intermediate morphs with a reduction in their male function (i.e. red

298 s, and among alternative, nutritionally-cued morphs within sexes.

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,