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1 elate with temporal variation in volcanic or metamorphic activity.
2         The MGC forms during early stages of metamorphic adult development through a stereotyped sequ
3 sets of centrally derived glial cells during metamorphic adult development.
4  contributed by met: continuous variation of metamorphic age and expression of discrete, alternate mo
5  Bd infection is limited to the skin in post-metamorphic amphibians, routine skin sloughing may regul
6 evolution of novel paedomorphic species from metamorphic ancestors via selection of TH-response allel
7 val period, is rapidly elaborated during the metamorphic and early juvenile periods to form the adult
8 ed in our work emphasize the need to include metamorphic and fluid transport processes in geodynamic
9                                         Both metamorphic and igneous models of apatite formation sugg
10 lpha and TRbeta genotypes was determined for metamorphic and non metamorphic offspring from backcross
11 amorphic core complexes are domal uplifts of metamorphic and plutonic rocks bounded by shear zones th
12 mental expression of Sox2 and Sox19 genes in metamorphic and postmetamorphic specimens and young adul
13 age specificity is reiteratively used during metamorphic and reproductive responses to ecdysone.
14 re completed in bedrock composed of granite, metamorphic, and mafic rocks.
15  this study we present new in situ U-Pb age, metamorphic, and morphological data on these titanite mi
16  including obligate metamorphic, facultative metamorphic, and obligate metamorphic-failure taxa.
17  outgassing from ocean ridges, volcanoes and metamorphic belts and increased carbon burial.
18                                     Although metamorphic cell death is perturbed in Atg7 mutants, the
19 ic profile of bite-force performance in post-metamorphic Ceratophrys cranwelli.
20                           In winged insects, metamorphic changes either are limited to a few tissues
21  process reported to date in the sequence of metamorphic changes in anurans.
22                                              Metamorphic changes in the amphibian olfactory system pr
23 d D2 expression contributes to the timing of metamorphic changes in these tissues.
24 ndicate that the intestine undergoes similar metamorphic changes in X. laevis and X. tropicalis, maki
25 alpha are resistant to a wide variety of the metamorphic changes induced by TH.
26 luding wing discs and eye primordia initiate metamorphic changes, such as pupal commitment, patternin
27  growing tissues nearing completion of their metamorphic changes, suggesting a role for the deiodinas
28                  XCL1/lymphotactin, a unique metamorphic chemokine, was recently identified as a broa
29 n mRNA is down regulated at the beginning of metamorphic climax (NF62) and reexpressed again near the
30  TH secretion) but was present just prior to metamorphic climax (stage 58, during TH secretion).
31  peak concentration of T4 that is reached at metamorphic climax cannot induce the final morphological
32 re down-regulated in the tail at the peak of metamorphic climax just before it is resorbed are suppre
33                                       During metamorphic climax when the exocrine pancreas dedifferen
34                                       During metamorphic climax, best frequencies significantly incre
35                                           At metamorphic climax, both TH-induced cell division and D2
36                                           By metamorphic climax, limb movement is impaired, ranging f
37                                   Before the metamorphic climax, most of the cells have already trans
38                  Shortly before the onset of metamorphic climax, there is a brief "deaf" period durin
39 rmis and finally appears in the tail only at metamorphic climax.
40 evelopment revealed greater expression after metamorphic climax.
41 as soon as they became free-swimming through metamorphic climax.
42 loproteinase 11) in the exocrine pancreas at metamorphic climax.
43 s lateral line projections degenerate during metamorphic climax.
44 fifth instar and coincided with the onset of metamorphic competence of these discs.
45                                          The metamorphic conditions and mechanisms required to induce
46 nd TC if the temperature and age at the peak metamorphic conditions are known.
47                                          For metamorphic conditions of cooling from 612 degrees +/- 1
48 e possible only with moderate diagenetic and metamorphic conditions.
49 ions in metasomatized ophicarbonates at peak metamorphic conditions.
50 as that underlie the detachment fault in the metamorphic core complex of the Whipple Mountains yielde
51 t, at least in this case, the development of metamorphic core complexes and the accommodation of high
52                                              Metamorphic core complexes are domal uplifts of metamorp
53 nds of Papua New Guinea are actively forming metamorphic core complexes located within a continental
54 ast, here we present seismic observations of metamorphic core complexes of the western Woodlark rift
55 r crust exhumes mid-crustal rocks, producing metamorphic core complexes.
56 es have addressed this problem and therefore metamorphic decarbonation in subduction zones remains la
57 to high pore pressure that might result from metamorphic dehydration.
58 tinental foreland basin sediments containing metamorphic detritus eroded from the Himalaya orogeny th
59             The effects of BR-C mutations on metamorphic development are highly pleiotropic, yet litt
60 iscs showed that BRC-Z1 expression and early metamorphic development are rendered steroid-independent
61                                        Early metamorphic development in Drosophila melanogaster is in
62 sted the hypothesis that BRC is required for metamorphic development of MN1-MN5.
63 med cell death (PCD) of neurons during early metamorphic development of the central nervous system (C
64 n the glomeruli during the last one-third of metamorphic development were revealed.
65                   During the final stages of metamorphic development, auditory function and neural co
66                                       During metamorphic development, ranid frogs exhibit rapid reorg
67 in the developing Drosophila eye is an early metamorphic, ecdysteroid-dependent event.
68  distinct populations of melanophores: early metamorphic (EM) melanophores arise widely dispersed and
69   A full characterization of low-temperature metamorphic events and alternative biosignatures in gree
70 u geochemistry will allow us to date ancient metamorphic events and determine the terrestrial Pu/U ra
71 enes have putative functions relevant to key metamorphic events including the differentiation of smoo
72  an ancient martian meteorite record thermal metamorphic events with ages that group around and/or do
73 on formation and axonal outgrowth, two early metamorphic events, also occur prematurely.
74 e established a sequence of bacteria-induced metamorphic events: MACs induce larval settlement; then,
75 an obligate metamorphic-failure species) and metamorphic F1 hybrids (A. mexicanum x A. tigrinum tigri
76 d salamander populations, including obligate metamorphic, facultative metamorphic, and obligate metam
77 mode of development that is characterized by metamorphic failure (paedomorphosis), an adaptation for
78 ses between Ambystoma mexicanum (an obligate metamorphic-failure species) and metamorphic F1 hybrids
79 rphic, facultative metamorphic, and obligate metamorphic-failure taxa.
80                        These minerals buffer metamorphic fluids to extremely reducing conditions that
81  idea that this tremor is excited by flow of metamorphic fluids.
82 hing events seen in some marginally stable ("metamorphic") folded proteins in response to mutation or
83 ee were expressed widely throughout the post-metamorphic frog nervous system, but with distinctly dif
84 notactic responses as animals developed from metamorphic froglets to reproductive adults.
85 rocks of prehnite-pumpellyite to greenschist metamorphic grade between 3.2 and 2.75 billion years ago
86 the progressive decrease in delta(66)Zn with metamorphic grade is correlated with a decrease in sulfu
87 hat felsic rocks in both Archaean high-grade metamorphic ('grey gneiss') and low-grade granite-greens
88  other appendages, it is required for normal metamorphic growth of the mandibles.
89 ision, indicating that conductive models for metamorphic heat transfer in Barrovian terrains are inco
90 stent larval neurons exhibiting two distinct metamorphic histories.
91 ns have been preserved despite a complicated metamorphic history.
92                                              Metamorphic hydration and oxidation of ultramafic rocks
93 pentinization of Martian crust suggests that metamorphic hydration reactions played a critical part i
94 aining on opposite sides of the head in post-metamorphic individuals.
95                                              Metamorphic inefficiency and compositional relationships
96  to show that the early atrial siphon of the metamorphic juvenile, including its aperture and lining,
97 eveloping embryos, tornaria larvae, and post-metamorphic juveniles and show that the tornaria larva o
98 site pattern with the highest levels in post-metamorphic juveniles.
99 s and cell numbers in late embryonic and pre-metamorphic larval stages.
100 acceleration, surface downdrop, and specific metamorphic lithologies and large plutonic intrusions.
101  and then migrate into stripes, whereas late metamorphic (LM) melanophores arise already within strip
102                                          The metamorphic Mad2 protein acts as a molecular switch in t
103 00 Ma magmatic core surrounded by a ~4070 Ma metamorphic mantle.
104 isotopic compositions for ultrahigh pressure metamorphic marbles and enclosed carbonated eclogites fr
105 how that kit functions during a late step in metamorphic melanophore development in both species.
106 re both autonomous and non-autonomous to the metamorphic melanophore lineage.
107  lineages, including a dramatic reduction of metamorphic melanophore precursors.
108 ow that one such mutant, picasso, lacks most metamorphic melanophores and results from mutations in t
109 ontributing to the evolutionary reduction in metamorphic melanophores and the increased contribution
110 o-adult transformation by the recruitment of metamorphic melanophores from latent precursors.
111  crest cells, as well as from post-embryonic metamorphic melanophores that are derived from latent pr
112 r tyrosine kinase, as well as late-appearing metamorphic melanophores that depend on both the G-prote
113 otes the development of both early-appearing metamorphic melanophores that depend on the kit receptor
114 phores are replaced by newly differentiating metamorphic melanophores that form the adult stripes.
115 orphosis at the same time as wild-type fish, metamorphic melanophores that normally appear during the
116  for erbb3b in the development of much later metamorphic melanophores, and suggest complex modes by w
117 s in five additional species also arise from metamorphic melanophores, identifying this as an ancestr
118  stages, with a diminished contribution from metamorphic melanophores.
119 maintain or recruit the latent precursors to metamorphic melanophores.
120                                          The metamorphic mineral assemblages in relatively FeO-rich M
121  extremely low delta(18)O records of igneous/metamorphic minerals from South China.
122                    Neither the timing of the metamorphic molt nor the duration of larval growth was a
123  by the pulse of ecdysone that initiates the metamorphic molt.
124 ought to have been eroded from the Himalayan metamorphic mountain belt.
125                                By the end of metamorphic nerve shortening, one-quarter of all myelin
126 types was determined for metamorphic and non metamorphic offspring from backcrosses between Ambystoma
127 ly abiotic porphyroblasts of thermal contact metamorphic origin that record late-stage retrograde coo
128 lance between carbon input from volcanic and metamorphic outgassing and its removal by weathering fee
129                                    Comparing metamorphic patterning in T. castaneum to embryonic and
130                           Here, we study the metamorphic patterning of mandibulate mouthparts of the
131         The collisional shortening, prograde-metamorphic phase of the Orogeny lasted 8 my, extensiona
132           Subsequently, they display a novel metamorphic phenotype, involving collapse of the head an
133       We used thyroid hormone (TH) to rescue metamorphic phenotypes in paedomorphic salamanders and t
134       HIV-1 reverse transcriptase utilizes a metamorphic polymerase domain that is able to adopt two
135 cations from postdepositional diagenetic and metamorphic processes.
136 s exhibit temporal misregulation of specific metamorphic processes.
137 5 results in temporal delays in two distinct metamorphic processes: the terminal cell-cycle exit in t
138                          They reveal how the metamorphic properties of KaiB, a protein that adopts tw
139            Thus, IscU may be classified as a metamorphic protein.
140 l heterogeneity, defining a new category of "metamorphic proteins".
141                                              Metamorphic proteins, including proteins with high level
142 d of the increasingly recognized concept of "metamorphic proteins."
143  transcripts within the liver of exposed pre-metamorphic R. catesbeiana tadpoles within 6 d.
144                While the LC50 of IBF for pre-metamorphic Rana catesbeiana tadpoles is 41.5 mg/L (95%
145 otopic and elemental compositions, degree of metamorphic re-equilibration and sulphide-rich nature of
146 ay microtomography we have imaged a complete metamorphic reaction and show how chemical transport evo
147                             High-temperature metamorphic reaction rates were measured using strontium
148                                              Metamorphic reactions influence the evolution of the Ear
149  arc magmatism, which reflect differences in metamorphic reactions occurring in subducting oceanic cr
150 in-building episode which is consistent with metamorphic reactions produced by long-term cooling.
151 th in intact F protein and in 6HB, suggest a metamorphic region around these residues with dual struc
152 geting, branching patterns, territories, and metamorphic remodeling are controlled in specific ways,
153  To identify molecular mechanisms underlying metamorphic remodeling, we conducted a neuropeptidergic
154  nerve (ON) shortening during Xenopus laevis metamorphic remodeling.
155 n factors (BRC-Z1-Z4) that are essential for metamorphic reorganization of the central nervous system
156                                   During the metamorphic reorganization of the insect central nervous
157 ecdysone receptor isoforms induces different metamorphic responses in various larval tissues.
158 ding the roles of BR-C proteins in directing metamorphic responses to ecdysone.
159 nsiderations and N contents of high pressure metamorphic rocks imply massive addition of subducted N
160 icrom in size discovered in the 1980s within metamorphic rocks related to continental collisions clea
161 ons to produce eclogites and eclogite facies metamorphic rocks.
162           Our experiments indicated that the metamorphic role of T3 is through genomic action of the
163  into the relationship between embryonic and metamorphic segmental identity specification, we have co
164 the terminal growth zone that generates post-metamorphic segments, however, CapI-hes1 has a non-overl
165 ic deposits from magmatic, hydrothermal, and metamorphic settings.
166  of protein kinase C, two other steps in the metamorphic signal transduction pathway.
167 xamined larval (duration, survival) and post-metamorphic (size) traits of both species after manipula
168                                              Metamorphic species, such as C. riparius, may act as a v
169 he most heavily infected species at the post-metamorphic stage.
170 ion dose treatments at both larval and post- metamorphic stages and quantified infection load on day
171 tonergic cells in the embryonic, larval, and metamorphic stages of the life cycle of Aplysia.
172                                           At metamorphic stages Xenopus displays a superficial granul
173 f adult tissue progenitors during larval and metamorphic stages, and gametogenesis in adults.
174 n shown to shift the equilibrium between the metamorphic states.
175  superomniphobicity and shape memory effect, metamorphic superomniphobic (MorphS) surfaces that trans
176 ) and showed that it was present in pre- and metamorphic tadpoles.
177 tions of peak conditions in high-temperature metamorphic terranes define relatively narrow ranges of
178 ible with observations from high-temperature metamorphic terranes exhumed in orogens.
179 a minor component in many very high-pressure metamorphic terranes that formed during continental subd
180 ociated with amphibian life cycle evolution: metamorphic timing and adult body size.
181  selection of TH-response alleles that delay metamorphic timing and increase adult body size.
182 ge influence of Mendelian dominance on size, metamorphic timing and predation rate of hybrid tiger sa
183                 Repeatedly during evolution, metamorphic timing has been delayed to exploit growth-pe
184 s associated with genetic changes that delay metamorphic timing in biphasic life cycles.
185 locus (QTL) that contributes to variation in metamorphic timing.
186 lopment may occur through genetic changes in metamorphic timing.
187 n responsiveness to TH and additively affect metamorphic timing.
188 -history traits in amphibians: body size and metamorphic timing.
189 t study demonstrating Se transference during metamorphic tissue remodelling.
190 ella germanica, BgE93 is highly expressed in metamorphic tissues, and RNA interference (RNAi)-mediate
191 early in the season, and was not mediated by metamorphic traits (age and mass at emergence).
192  the larval stage and may not be captured by metamorphic traits, and (ii) be strongly modulated by eg
193 in premetamorphic tadpoles led to precocious metamorphic transformations.
194                                          The metamorphic translocation of ganglia, which included a c
195  growing and regenerating adult retina, of a metamorphic vertebrate, the winter flounder.
196 olatile contents could reflect post-magmatic metamorphic volatile addition or growth from a late-stag
197 ulation on Delta and Notch expression during metamorphic wing vein development, and that the resultan
198 ation after partial retinal resection in pre-metamorphic Xenopus laevis.

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