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1 ynthetic roles, mechanisms of catalysis, and evolutionary origin.
2 tributed mode of cell crawling with a single evolutionary origin.
3 a sequences suggests that they have a common evolutionary origin.
4 Petromyzon marinus) to gain insight into its evolutionary origin.
5 etals, despite these organs sharing a common evolutionary origin.
6 ibody-antigen interfaces is related to their evolutionary origin.
7 sectivorous bats, consistent with an ancient evolutionary origin.
8 belong to a single protein family of ancient evolutionary origin.
9  a finding consistent with their independent evolutionary origin.
10 nts such as Arabidopsis, which have a recent evolutionary origin.
11 eins, which may not solely arise from shared evolutionary origin.
12 romeres indicate their unique, and separate, evolutionary origin.
13 l limb molecular circuitry owing to a common evolutionary origin.
14  cerebral cortex and their developmental and evolutionary origin.
15 esistance such as AvrPiz-t may have a common evolutionary origin.
16 nsory-motor modules that may have an ancient evolutionary origin.
17 ollen-transcribed genes independent of their evolutionary origin.
18 peculate that it derives from a longstanding evolutionary origin.
19 ylinositol biosynthesis, suggesting a common evolutionary origin.
20 er plant species may also have more than one evolutionary origin.
21  bracts in this genus may not share a single evolutionary origin.
22 iversified doubly-wound superfold of ancient evolutionary origin.
23 gest that the two nodule types have a shared evolutionary origin.
24 gests they form a distinct clade with common evolutionary origin.
25 itherto undescribed protein folds of unknown evolutionary origin.
26 usters are protein cofactors with an ancient evolutionary origin.
27  importance, there is still debate about its evolutionary origins.
28  locus alleles can have distinctly different evolutionary origins.
29  neural circuits, and consider its potential evolutionary origins.
30 ferential words in humans likely has ancient evolutionary origins.
31 th groups although they likely have multiple evolutionary origins.
32 about skin B-cell responses as well as their evolutionary origins.
33 mon catalytic mechanisms and probably common evolutionary origins.
34  movements by virtue of their biological and evolutionary origins.
35 stem cells (SSCs) may have had shared common evolutionary origins.
36 rd groups, and analyzes them in reference to evolutionary origins.
37 rphisms, there is little discussion of their evolutionary origins.
38 t of archaeal flagellin, establishing common evolutionary origins.
39 hypotheses compete to explain the parasites' evolutionary origins: (1) the interspecific hypothesis p
40 est owing to their large genomes and complex evolutionary origins(3-6), but it is not yet known wheth
41  diazotrophic Frankia spp. bacteria share an evolutionary origin about 110 million years ago.
42  question of how enzymes with such different evolutionary origins achieved structural similarity and
43 iability across species, and identifying the evolutionary origins (analogous or homologous) of manipu
44 nd there is little information regarding the evolutionary origin and ancestral function of TLR signal
45 is functional change, and characterize their evolutionary origin and behavioural importance.
46 3' end processing raised questions about the evolutionary origin and conservation of this mechanism.
47 g a critical data point in understanding the evolutionary origin and developmental basis of nectaries
48                            Insights into the evolutionary origin and diversification of crop species
49 RNAs) can regulate chromatin states, but the evolutionary origin and dynamics driving lncRNA-genome i
50 creasing our ability to fully understand the evolutionary origin and fitness effects of trade-offs an
51             In this study, we focused on the evolutionary origin and functional specialization of kin
52 GSs constitute a trait characteristic of the evolutionary origin and functionality of different genom
53 Here we uncover the history of the monarch's evolutionary origin and global dispersal, characterize t
54 es and low abundances, suggests their recent evolutionary origin and participation in highly speciali
55  MUC4, MUC12, MUC13, and MUC17 have a common evolutionary origin and share a common structural organi
56 st nematode Heterodera avenae share a common evolutionary origin and that they evolved to parasitise
57  this raises questions with respect to their evolutionary origin and the factors allowing their maint
58                                 However, the evolutionary origin and the relative role of neural spec
59 ompasses several sets of genes with a common evolutionary origin and which form a branch of the immun
60    The Toll receptor superfamily has ancient evolutionary origins and a universal function in innate
61 known about stomata in bryophytes, and their evolutionary origins and ancestral function remain poorl
62                                 However, the evolutionary origins and causes of kin-discriminatory be
63 l (G&K) provide an interesting discussion of evolutionary origins and consequences of ultrasociality,
64 & Krall provide an interesting discussion of evolutionary origins and consequences of ultrasociality.
65                             Despite distinct evolutionary origins and differences in time scales, cel
66 we offer a conceptual framework to study the evolutionary origins and ecological circumstances of spe
67 ts importance, little is known regarding the evolutionary origins and emergence of this syntactic abi
68 the development of numerous theories for its evolutionary origins and genomic distribution.
69 ow strong statistical support for convergent evolutionary origins and massively parallel evolution of
70                                          The evolutionary origins and medical relevance of this polym
71                                          The evolutionary origins and molecular mechanisms underlying
72                                    Uncertain evolutionary origins and phylogenetic relationships amon
73 l as terrestrial vertebrates; however, their evolutionary origins and phylogenetic relationships are
74 or group of eukaryotic TEs and explore their evolutionary origins and relationships.
75 e superfamily were used to reconstruct their evolutionary origins and selection histories.
76                                          The evolutionary origins and substrate specificities of PONs
77 ward the evolution of complex organisms, the evolutionary origins and the genetic underpinnings of co
78 ir vast genomic diversity has obscured their evolutionary origins, and phylogenetic analyses have tra
79 reveal that regions in oprF are of different evolutionary origins, and the mosaic gene structure resu
80 i) the prevalence of monogamy at the time of evolutionary origin; and (iii) the female-biased sex all
81 l significance of these cell types and their evolutionary origin are often unknown.
82                               However, their evolutionary origins are much debated.
83 iverse and successful group today, but their evolutionary origins are obscure.
84  are integral to human society [1] and their evolutionary origins are of great interest.
85 comotion on land but their developmental and evolutionary origins are unclear.
86 the genetic causes and consequences of their evolutionary origins are unknown.
87 ween these MYBs, miR828, and TAS4, but their evolutionary origins are unknown.
88 nce is conserved among haplorhines, with its evolutionary origin as a splice acceptor site.
89 hese domains have a common developmental and evolutionary origin, as supported by functional experime
90 ave been of limited use in unravelling their evolutionary origin, as the earliest recognized examples
91 t paleontological evidence supports a deeper evolutionary origin, before the occurrence of salamander
92 y theories have been proposed to explain its evolutionary origin, but understanding has been limited
93                                        Their evolutionary origin can be traced back to prebilaterian
94 ests that these receptors may share a remote evolutionary origin, despite their lack of sequence simi
95 n Guyana, with genome analysis indicating an evolutionary origin distinct from Southeast Asia.
96 d annotates their properties (duplicability, evolutionary origin, expression profile, function and in
97                         Despite their shared evolutionary origin, extensive genetic decay has resulte
98                    The data suggest a common evolutionary origin for both inhibitory mechanisms, call
99 ion-like" aggressive behavior, suggesting an evolutionary origin for compulsive aggression.
100       Our results therefore suggest a common evolutionary origin for P-proteins found in the sieve el
101 These results support the idea of bats as an evolutionary origin for PEDV, implicate PEDV as a potent
102 shmania subgenus, indicative of pre-subgenus evolutionary origin for similar genetic deficiencies in
103 rowing body of evidence pointing to a common evolutionary origin for these virions.
104 e genomic analysis indicates a likely recent evolutionary origin for Tlp11.
105 d genomic cDNA-like sequences that implicate evolutionary origins for brain SGR.
106  with high catalytic efficiency and distinct evolutionary origin from other lipolytic enzymes.
107 teraceae is connected with their independent evolutionary origins from separate branching systems.
108 urrently available data on cytoarchitecture, evolutionary origin, gene expression, cell types, birthd
109                               We discuss the evolutionary origins, genetic mechanisms and functional
110                                        Their evolutionary origin has attracted much attention from ev
111                                 However, its evolutionary origin has remained elusive.
112 tumor-associated ncRNAs, typically of recent evolutionary origin, has motif use that is often indicat
113 nal-muscle-based ventilatory apparatus whose evolutionary origins have remained mysterious.
114                      This is thought to have evolutionary origins, highlighting objects likely to pro
115 in, in several bilaterian clades, indicating evolutionary origin in a common ancestor of Bilateria.
116 cellular choanoflagellates, indicating their evolutionary origin in a common ancestor of Choanoflagel
117 cated that the nodulation trait has a shared evolutionary origin in all 10 lineages.
118 een in Saccharomyces cerevisiae had a single evolutionary origin in budding yeasts, simpler "flip/flo
119 al tissues by determining its occurrence and evolutionary origin in Eumetazoa and its essentiality in
120 challenges this view and proposes an earlier evolutionary origin in the most recent common ancestor o
121  findings could imply that feathers had deep evolutionary origins in ancestral archosaurs, or that th
122  in mice and characterized its phenotype and evolutionary origins in humans.
123 nd demonstrate retention of eyes of separate evolutionary origins in modern harvestmen [10-12].
124       The relative contributions of distinct evolutionary origins, in particular from nonviral elemen
125                             Therefore, their evolutionary origin is also reviewed in relation to over
126 nserved in virtually all eukaryotes, but its evolutionary origin is unclear because bacterial ortholo
127 e cycle of Saccharomyces cerevisiae, but its evolutionary origin is unknown.
128 damental for bilaterian musculature, but its evolutionary origin is unsolved.
129 ions in multiple genomes that share a common evolutionary origin, is a crucial, yet difficult task fa
130 d with localization within the mitochondria, evolutionary origin, location of protein-encoding, and u
131 lk between biological processes of different evolutionary origins may thus present powerful and broad
132              The evidence indicates a single evolutionary origin of 4-Cl-IAA synthesis in the Fabacea
133                          We also discuss the evolutionary origin of a novel class of knotted membrane
134                                          The evolutionary origin of amino acid occurrence frequencies
135             Our results demonstrate a common evolutionary origin of animal excretory systems and esta
136 ween RlmN and Cfr prompted us to investigate evolutionary origin of antibiotic resistance in this enz
137          These studies reveal the remarkable evolutionary origin of Arc and provide a structural basi
138 ss answers long-standing questions about the evolutionary origin of asymmetry, but it also provides i
139 st photosynthesis; it also suggests that the evolutionary origin of bioluminescence in nonphotosynthe
140 naptome of swimming tadpoles and tracing the evolutionary origin of cell types such as the vertebrate
141  of an inquiry into the metric structure and evolutionary origin of cognitive maps, the task should f
142 ttachment relationships, suggesting a shared evolutionary origin of cortisol coregulation in vertebra
143 esults contribute to an understanding of the evolutionary origin of cyclic nucleotide-modulated ion c
144 is essential to understand their role in the evolutionary origin of developmental novelties.
145 he goal of phylostratigraphy is to infer the evolutionary origin of each gene in an organism.
146 lar techniques enable the precise studies on evolutionary origin of endophytic Epichloe species, thei
147             We tested two hypotheses for the evolutionary origin of flatwings in Hawaii: (1) that the
148 r thorax of H. sapiens, pointing to a recent evolutionary origin of fully modern human body shape.
149                   We sought to determine the evolutionary origin of GPBP isoforms.
150 -terminal 2'-O-methylation, and the possible evolutionary origin of Hen1 present in bacterial and euk
151 acean wing homologues, which supports a dual evolutionary origin of insect wings (that is, novelty th
152  the acceptance of proline substitutions and evolutionary origin of kinks.
153 perceive rhizobium LCOs, suggesting a shared evolutionary origin of LCO-driven nodulation.
154 n the focus of recent work investigating the evolutionary origin of limb-specific morphologies.
155 ction has implications for understanding the evolutionary origin of major egalitarian transitions, sy
156 phytes and seedless vascular plants, and the evolutionary origin of mannan O-acetyltransferases in la
157 independently numerous times in animals, the evolutionary origin of many toxins remains unknown.
158 on of matched alphabeta heterodimers and the evolutionary origin of matched isotype mixed dimer forma
159 a, led to a paradigm shift, pushing back the evolutionary origin of methanogenesis to predate that of
160 the chemistry of the Archean environment and evolutionary origin of microbial metabolisms.
161                                              Evolutionary origin of muscle is a central question when
162                                 Although the evolutionary origin of myxozoans has been elusive, a clo
163 code progenitors and may explain the ancient evolutionary origin of neuropeptides, predating a comple
164 uli to initiate protective behavior, but the evolutionary origin of nociceptive systems is not well u
165                                          The evolutionary origin of non-allometric prefrontal enlarge
166    Collectively, our findings support a deep evolutionary origin of paired appendage regeneration in
167           Classical hypotheses regarding the evolutionary origin of paired appendages propose transfo
168                           Here we review the evolutionary origin of polydnaviruses, the organization
169             Here, we review the physical and evolutionary origin of protein allostery, as well as its
170                                          The evolutionary origin of rhythm perception, a cognitive ab
171      These results provide insights into the evolutionary origin of ruminant headgear as well as mamm
172 nderstanding of normal developmental and the evolutionary origin of senescence.
173 reover, they have been proposed to be at the evolutionary origin of several groups of large eukaryoti
174 offer an alternative null hypothesis for the evolutionary origin of SSB that, through a subtle shift
175                          We investigated the evolutionary origin of SVZ neural precursor cells in the
176          In this review, we will discuss the evolutionary origin of symbiotic LCO recognition.
177 narios that could explain the paradox of the evolutionary origin of TA elements and argue that these
178  in jawed vertebrates is well supported, the evolutionary origin of teeth and their relationship with
179  neurulation and thus may help elucidate the evolutionary origin of the brain.
180                                          The evolutionary origin of the Canadian outbreak strain and
181 ferences we propose a partially common early evolutionary origin of the cells that become claustrum a
182 speculations on the common developmental and evolutionary origin of the claustrum and the subplate.
183 in architecture, providing insights into the evolutionary origin of the contemporary gene set.
184 ediate by lateral mesoderm recapitulates the evolutionary origin of the diaphragm in mammals.
185 a large body of evidence supporting a single evolutionary origin of the eukaryotic flagellum, an orig
186 ore, the startle response is the most likely evolutionary origin of the female lebinthine vibrational
187                These results reveal an early evolutionary origin of the insect chemosensory receptor
188 rgan movement and deformation and suggest an evolutionary origin of the large leaf movements seen in
189  structural information and insight into the evolutionary origin of the LIC as well as revealing how
190          This has major implications for the evolutionary origin of the organisms, turnover of recalc
191                                          The evolutionary origin of the six-layered mammalian neocort
192               We study the morphogenesis and evolutionary origin of the spectacular erectile ruff of
193           However, little is known about the evolutionary origin of these neurons and their interacti
194                                          The evolutionary origin of these widespread phenomena is unc
195                                          The evolutionary origin of this branch was located within Po
196                               To explore the evolutionary origin of this layer, we have examined the
197 ike' (GRL) proteins across Animalia, but the evolutionary origin of this novel class of ion channels
198 ith prophages provides clues to the possible evolutionary origin of this phenomenon and the levels of
199     Phylogenetic analysis sheds light on the evolutionary origin of this rare enzyme family and ident
200     Despite its high clinical relevance, the evolutionary origin of USA300 remained unclear.
201                               To explain the evolutionary origin of vertebrate teeth from odontodes,
202 ggest that this co-option may facilitate the evolutionary origin of vertebrate vascular vessels.
203                     Here, we investigate the evolutionary origins of adhesion and the emergence of gr
204                                          The evolutionary origins of arboviruses are unknown because
205 , and potential general implications for the evolutionary origins of binding specificity in multi-pro
206 ification models in better understanding the evolutionary origins of biodiversity.
207 s between Ciona and the mouse evoke the deep evolutionary origins of cardiopharyngeal networks in cho
208 ebrates, they also provide insights into the evolutionary origins of cell types such as cranial placo
209                                          The evolutionary origins of CNTs and their relationships to
210                                          The evolutionary origins of complex morphological structures
211 tigations for phylogenetic constructs of the evolutionary origins of culture.
212 erse leaf forms and account for the multiple evolutionary origins of cup-shaped leaves through simple
213                                              Evolutionary origins of derived morphologies ultimately
214                               To examine the evolutionary origins of Dicer helicase functions, we inv
215 sophila Erg homologs bring into question the evolutionary origins of distinct Erg K(+) channel functi
216  of EPEV, is discussed in the context of the evolutionary origins of EPEV in the New World.
217  little is known about the developmental and evolutionary origins of external genitalia.
218                      A new study reveals the evolutionary origins of fangs and venom in the Nemophini
219 ns, and rhesus monkeys similarly bear on the evolutionary origins of foresight as it pertains to tool
220 S signal transduction, which suggests common evolutionary origins of functional phenotypes and simila
221 , raises interesting questions regarding the evolutionary origins of gamete-specific functions in sex
222 also provides the opportunity to explore the evolutionary origins of genes by considering the functio
223 s in the land plant tree and investigate the evolutionary origins of genes that specify stomatal deve
224                    This study focuses on the evolutionary origins of green seaweeds, which play an im
225 n a fundamentally important precursor in the evolutionary origins of group living in the squamates.
226 s a coherent framework for understanding the evolutionary origins of HDT.
227                                          The evolutionary origins of how modern humans share and use
228 hese are exclusively 3' linked, and thus the evolutionary origins of human 2',3' cGAMP signaling are
229 living relatives is central to revealing the evolutionary origins of human culture.
230 mpirical assumptions concerning the adaptive evolutionary origins of human diseases.
231 ammals.SIGNIFICANCE STATEMENT To explore the evolutionary origins of human face-preference and its re
232 rgent evidence from many species reveals the evolutionary origins of human friendship.
233 le relevance for the ongoing debate over the evolutionary origins of human language [1, 4].
234 w crucial information for reconstructing the evolutionary origins of human mortuary practices may be
235                            To illuminate the evolutionary origins of human-like patterns of choice, w
236          In order to determine the number of evolutionary origins of kdr, kdr-his and super-kdr, we s
237   Developmental novelties often underlie the evolutionary origins of key metazoan features.
238 populations to test hypotheses regarding the evolutionary origins of kin discrimination.
239                                          The evolutionary origins of metabolism, in particular the em
240                      Despite the independent evolutionary origins of monogamous mating systems, sever
241 stinct protein families, but the genomic and evolutionary origins of most venom components are not un
242                                 However, the evolutionary origins of neurogenic placodes have remaine
243  as a tool for a better understanding of the evolutionary origins of our unique cognitive abilities.
244                              We consider the evolutionary origins of potential allergens, toxins and
245       These results provide insight into the evolutionary origins of primitive cell envelope structur
246 sed this key fossil taxon to investigate the evolutionary origins of seed development.
247                            Understanding the evolutionary origins of sexual features and preferences
248 gnificant implications for understanding the evolutionary origins of SH2 domain-phosphotyrosine signa
249                     Furthermore, independent evolutionary origins of short-necked, large-headed "plio
250                      Here we investigate the evolutionary origins of social instincts, as shaped by s
251 ogical factors may influence the independent evolutionary origins of sociality in Synalpheus shrimps.
252  findings have implications not only for the evolutionary origins of SSB, but also for the evolution
253  under low later-life nutrition, leaving the evolutionary origins of such plasticity unexplored.
254  replicated our study across two independent evolutionary origins of the "competitive" ecotype.
255                   The complex and unresolved evolutionary origins of the 2009 H1N1 influenza pandemic
256                                          The evolutionary origins of the bacterial lineages that popu
257              Here we study theoretically the evolutionary origins of the capacity to internalize norm
258                          Here we discuss the evolutionary origins of the cGAS-STING pathway, and cons
259                           Here we reveal the evolutionary origins of the chemosensory machinery that
260 t of these findings, we discuss the possible evolutionary origins of the complex DPE2-heteroglycan pa
261 enetic patterns in current infections or the evolutionary origins of the disease due to the low quant
262 -depth molecular analysis to reconstruct the evolutionary origins of the enhanced pathogenicity of SA
263  important implications for the study of the evolutionary origins of the genetic code and protein-mRN
264 provide remarkable new information about the evolutionary origins of the human genome and the process
265                                          The evolutionary origins of the hypoxia-sensitive cells that
266                                          The evolutionary origins of the pathway and its regulators a
267  The results provide novel insights into the evolutionary origins of the pathways, suggesting that on
268 This has been taken as evidence for multiple evolutionary origins of the penis.
269  spots of biodiversity and endemism, but the evolutionary origins of their unique biotas are poorly u
270 sors in animals from fish to humans, but the evolutionary origins of these cells are only just becomi
271      In this issue, Foldi et al. explore the evolutionary origins of these cues and report that in Dr
272 s is likely to uncover information about the evolutionary origins of this key human signaling pathway
273               In an effort to understand the evolutionary origins of this multilateral system, we inv
274 ad in vertebrates, little is known about the evolutionary origins of this process, in part because of
275        Despite considerable speculation, the evolutionary origins of this species' remarkable tool be
276 behave as Na-hyperaccumulators, and multiple evolutionary origins of this trait can be identified wit
277                                          The evolutionary origins of this two-recombinase system rema
278 lineage, enabling valuable insights into the evolutionary origins of tool-using behaviour.
279 ient vertebrates might yield clues about the evolutionary origins of vertebrate brain lateralization.
280  improve understanding of the mechanisms and evolutionary origins of vocal learning.
281 o understand the structures, mechanisms, and evolutionary origins of widespread Na(+)-coupled transpo
282                                          The evolutionary origins of Yakutian horses and the genetic
283               With improved understanding of evolutionary origins of zoonotic IAV, we can inform publ
284 se adaptations complicates pinpointing their evolutionary origin or loss.
285 ted that these three proteins have different evolutionary origins, possibly explaining their differen
286  in leaf growth polarity and, therefore, its evolutionary origin remain unknown.
287 but their true functional specialization and evolutionary origins remain obscure.
288 is limited and their genetic variability and evolutionary origins remain poorly known.
289                                 However, its evolutionary origins remain speculative because few stud
290  vertebrate brain is highly complex, but its evolutionary origin remains elusive.
291 of the jawed vertebrate body plan, but their evolutionary origin remains unresolved.
292 owards the end of the Pre-Cambrian and their evolutionary origin represents a key transition in the g
293 ties of cancer genes, such as duplicability, evolutionary origin, RNA and protein expression, miRNA a
294  what algae are, their diversity in terms of evolutionary origin, size, shape and life cycles, and th
295 generated receptors and thus, of a different evolutionary origin than bona fide RRs.
296 ortex is a uniquely mammalian structure with evolutionary origins that remain in dispute.
297  stage ingrained in the gynoecium due to its evolutionary origin to a radially symmetric structure.
298                       Could there thus be an evolutionary origin to risk aversion?
299                 This structure likely shares evolutionary origins with the DA-enriched central comple
300 nservation of delta-HXTXs despite their deep evolutionary origin within funnel-web spiders, consisten

 
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