戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 e with massive growth of cyanobacteria (blue-green algae).
2 g have led to the dominance of chlorophytes (green algae).
3 tid genomes yet observed from photosynthetic green algae.
4 evolution of isogamy and anisogamy in marine green algae.
5 mages of several elements in frozen-hydrated green algae.
6 ips among land plants and (other) charophyte green algae.
7  strictly freshwater lineage, the charophyte green algae.
8 e a monophyletic lineage embedded within the green algae.
9 lated to land plants than to other groups of green algae.
10 tion in prasinophytes will differ from other green algae.
11 re unlikely crown-group animals or volvocine green algae.
12 elopment-specific expression were present in green algae.
13 ore ancestral third form (SLP3) was found in green algae.
14 rotein complex-based signaling mechanisms in green algae.
15 ay not explain the coexistence of freshwater green algae.
16 elrhodopsins are light-gated ion channels of green algae.
17 discriminating chlorophyte from streptophyte green algae.
18 s described in higher plants is conserved in green algae.
19 onophyletic clade of homologs descended from green algae.
20 for regulation of "steering" motility in the green algae.
21 ht-harvesting antenna size relative to other green algae.
22 s previously described in yeast, humans, and green algae.
23 isomal-based pathways observed in plants and green algae.
24 n-evolving PSII complex in higher plants and green algae.
25 ic endosymbiont related to prasinophyte-like green algae.
26  to achieve prolonged hydrogen production in green algae.
27 er virus that infects unicellular eukaryotic green algae.
28 r specific high-throughput gene silencing in green algae.
29 nt role for phosphotyrosine signaling in the green algae.
30 hat infect certain eukaryotic chlorella-like green algae.
31 s and a propionate detoxification pathway in green algae.
32 o-cytochrome present in land plants and some green algae.
33 germ-soma differentiation in the volvocalean green algae.
34 major land plant taxa and in closely related green algae.
35 of all species rather than being confined to green algae.
36 randed DNA virus that infects chlorella-like green algae.
37 rtain unicellular, eukaryotic chlorella-like green algae.
38  land plants, preceding the emergence of the green algae.
39 to that found for Cab proteins in plants and green algae.
40  a feature shared only with some chlorophyte green algae.
41 rtain unicellular, eukaryotic chlorella-like green algae.
42 yanobacteria, soon joined by eukaryotic blue-green algae.
43 light regulate GS transcript accumulation in green algae.
44 to earth ecosystems-the advent of eukaryotic green algae.
45 d even in ancient plants such as single-cell green algae.
46 esidues could explain pyrenoid occurrence in green algae.
47 n possible biotechnological applications for green algae.
48 utative orthologous relationships with other green algae.
49 h are not closely related to land plants and green algae.
50  in land plants, with none recognizable from green algae.
51 rent pesticides on Chlamydomonas reinhardtii green algae.
52 d be widely applicable to research involving green algae.
53 allmark of terrestrial plants and charophyte green algae.
54 table nucleus-encoded proteins deriving from green algae.
55 14L-PITPs evolved in land plants compared to green algae.
56 s conserved in dicots, monocots, mosses, and green algae.
57 ascular plants from the avascular plants and green algae.
58 known proteins modulated by short-term -N in green algae.
59 from glaucophytes, red algae and chlorophyte green algae.
60  organisms, from angiosperms and monocots to green algae.
61 ly known channelrhodopsins from chlorophyte (green) algae.
62  ago from a lineage of freshwater charophyte green algae(1).
63 s as a photoreceptor linked to phototaxis in green algae [2, 3] and has been implicated by chemical m
64                             In chlorophytes (green algae), a protein termed major lipid-droplet prote
65 sing a data set of 14 taxa: 6 land plants, 2 green algae, a diatom, 2 red algae and a cryptophyte, th
66 isting of isolated nuclei of the unicellular green algae Acetabularia acetabulum.
67 ar protists, mesomycetozoean-like holozoans, green algae akin to Volvox, and blastula embryos of earl
68                                In plants and green algae, ALB3 proteins interact with members of the
69 ion as sensory photoreceptors in flagellated green algae, allowing these algae to identify optimal li
70  occurs also in homologous proteins in other green algae, amoebae, and pathogenic fungi.
71 tous green algae (Cladophora genus) and blue-green algae (Anabaena genus).
72 mon lichen-forming genus of aero-terrestrial green algae and all its species are desiccation tolerant
73 ts, but are entirely absent from liverworts, green algae and all other eukaryotes.
74          Bioinformatics of 1,000 oleosins of green algae and all plants emphasizing biological implic
75 rameterized model of a planktonic ecosystem, green algae and cyanobacteria coexist over a wide range
76 omponent of photosystem II in higher plants, green algae and cyanobacteria.
77  metabolites in an extract of (13)C-enriched green algae and demonstrated at low field strength (80 M
78 tially decreased the colonization biomass of green algae and diatoms, with estimated EC(20) values we
79 harvesting complex stress-related (LHCSR) in green algae and diatoms.
80  inhibition in the diatoms, prymnesiophytes, green algae and dinoflagellates of >2-3 mum cell sizes a
81 us 1 (PBCV-1) infects certain chlorella-like green algae and encodes a 120-kDa protein with a similar
82 231 members were present in the charophycean green algae and evolved to form overlapped and divergent
83 lypeptides was identified that is present in green algae and flowering and nonflowering plants but is
84 s in photosynthetic bacteria, cyanobacteria, green algae and gymnosperms, dark-operative protochlorop
85           The oleosin gene first appeared in green algae and has evolved in enhancing promoter streng
86 A viruses known to infect certain eukaryotic green algae and have not been previously shown to infect
87 binding antenna of photosystem I (LHCI) from green algae and higher plants binds specific low energy
88                                           In green algae and higher plants, less efficient energy cou
89 nt and mobility, may also occur in wild-type green algae and higher plants.
90 for lipid A in free-living and endosymbiotic green algae and in the chloroplasts of vascular plants,
91 sponsible for light absorption in plants and green algae and is involved in photoprotective mechanism
92 ute polypeptides after the divergence of the green algae and land plant lineages.
93 two domains are mainly present in charophyte green algae and land plants but absent from glaucophytes
94 f myosins diverged prior to the radiation of green algae and land plants from a common ancestor and t
95                                              Green algae and land plants trace their evolutionary his
96 , an early divergent streptophyta (including green algae and land plants) in which both proteins are
97           CLMP1-like sequences are unique to green algae and land plants, and the CLMP1 sequence sugg
98                               In contrast to green algae and land plants, inverted repeat regions in
99 e of phytochrome in the common progenitor of green algae and land plants.
100 teins in 20 model organisms, with a focus on green algae and land plants.
101 s indicates that KCBP is highly conserved in green algae and land plants.
102 TALE HD TFs) act as life cycle regulators in green algae and land plants.
103 ic plant ancestor, prior to the evolution of green algae and land plants.
104  Our protein sequence analyses indicate that green algae and major lineages of fungi were present 100
105 ein, which is responsible for dissipation in green algae and moss.
106 nary gap that exists between the chlorophyte green algae and most basal land plants, the bryophytes,
107 (31)P NMR detection, and low cytotoxicity on green algae and murine fibroblasts cell cultures.
108 representative land plant species but not in green algae and nonplant species, suggesting it is speci
109 vance general understanding of the Antarctic green algae and offer potential explanations for how gre
110 n of entire mitochondrial genomes from three green algae and one moss.
111 nverted into zeaxanthin, is ubiquitous among green algae and plants and is necessary for the regulati
112 reenCut" gene set, a group of genes found in green algae and plants but not in non-photosynthetic org
113 cation of this information to sequences from green algae and plants suggested that a subset of the IT
114 imilar to that of metazoans but is absent in green algae and plants, facilitates rapid recovery from
115 e that was present in the common ancestor of green algae and plants, providing evidence of unexpected
116 enes, named GreenCut2, that are conserved in green algae and plants.
117  (AtCGL160) protein (AtCGL160), conserved in green algae and plants.
118 ochrome c6A is a unique dithio-cytochrome of green algae and plants.
119  organization of thylakoid membranes in both green algae and plants.
120 ein sequence and CCM distribution across the green algae and positive selection in RbcS was estimated
121           All these gene families emerged in green algae and show concurrent expansions via serial du
122 nt transposons in the CHG context extends to green algae and that exclusion of histone H2A.Z from met
123 egulated enzyme in ascorbate biosynthesis in green algae and that, together with the ascorbate recycl
124 e Streptophyta, which consists of freshwater green algae and the land plants.
125  photosynthetic bacteria and eventually blue-green algae (and protoplastids) is described.
126  secondary metabolite of cyanobacteria (blue-green algae) and cyclic heptapeptide cyanotoxin, are one
127 ght-harvesting complexes of prochlorophytes, green algae, and both nonvascular and vascular plants.
128 ause orthologs of ARC6 occur in land plants, green algae, and cyanobacteria but PDV2 occurs only in l
129 The oxygenic photosynthesis of green plants, green algae, and cyanobacteria is the major provider of
130  of photosystem II (PS II) in higher plants, green algae, and cyanobacteria, is encoded by the psbC g
131 es photosynthetic water oxidation in plants, green algae, and cyanobacteria.
132 omponent of photosystem II in higher plants, green algae, and cyanobacteria.
133  liverwort, and hornwort), from streptophyte green algae, and from a monocot (duckweed).
134 nctly different from those used by bacteria, green algae, and fungi to synthesize astaxanthin.
135 tida, consisting of glaucophytes, red algae, green algae, and land plants, share a common ancestor th
136 Thr-244 are conserved only in cyanobacteria, green algae, and land plants, whereas the other key amin
137                              In prokaryotes, green algae, and most plants, this enzyme is a heteromer
138                               In eubacteria, green algae, and plant chloroplasts, isopentenyl diphosp
139 nclude centrioles in humans, basal bodies in green algae, and spindle pole bodies in yeast.
140 east three independent times--in alveolates, green algae, and the ancestor of fungi and metazoans-acc
141 ble reactions of O(2) and H(2) production in green algae, and the second involves the use of classica
142 orophyta, which includes a wide diversity of green algae, and the Streptophyta, which consists of fre
143 esiccation in even more distantly related DT green algae, and, importantly, whether that up-regulatio
144                                The volvocine green algae are a tractable system for understanding the
145 he oral delivery of therapeutic proteins, as green algae are edible and do not contain endotoxins or
146 lectron transport rates in higher plants and green algae are light-saturated at approximately one qua
147 ecular studies have revealed that charophyte green algae are the closest relatives of the land plants
148          Cyanobacteria, formerly called blue-green algae, are abundant bacteria that carry out green
149 oducts, such as spirulina, derived from blue green algae, are believed to help reverse this effect du
150 , along with MSC1, a MscS family member from green algae, are implicated in the control of organelle
151                          Cyanobacteria, blue-green algae, are the most abundant autotrophs in aquatic
152                          Cyanobacteria, blue-green algae, are the most abundant autotrophs in aquatic
153                                              Green algae as a whole are among the oldest eukaryotic l
154 s of lichen species that exclusively include green algae as photobiont.
155 ding ulvophyte, charophyte, and prasinophyte green algae, as well as in diatoms.
156 hyceae/phaeophyceae) and frequent loss among green algae, as well as in the red algae and their secon
157  from a streptomycete strain found in a blue-green algae associated with the ascidian Ecteinascidia t
158 vans are cell wall matrix polysaccharides in green algae belonging to the genus Ulva.
159 enomena were previously observed in other DT green algae, bryophytes and resurrection plants, other t
160                  Both types of Glbs occur in green algae, bryophytes and vascular plants.
161    MET1 is conserved in C3 and C4 plants and green algae but is not found in prokaryotes.
162 eus-encoded proteins conserved in plants and green algae but not in non-photosynthetic organisms.
163 odel system for studying lipid metabolism in green algae, but current methods for isolating mutants o
164 s have been well characterized in plants and green algae, but little is known about transporters or t
165       The work shows that cpftsy deletion in green algae, but not in higher plants, can be employed t
166 B contains 21 or more residues in plants and green algae, but only 10 residues in prokaryotes and non
167  stress is conserved between land plants and green algae, but the distinct spatial and temporal dynam
168 (Girella nigricans) fed primarily on red and green algae, but there was significant variation in the
169 lated with secondary endosymbiosis of red or green algae, but were acquired by horizontal gene transf
170 h core features similar to those of PSI from green algae, but with significant differences in shape a
171                          NPQ is catalyzed in green algae by protein subunits called LHCSRs (Light Har
172 complexes (LHCs) of higher plants, moss, and green algae can undergo dynamic conformational transitio
173 isiae (Tpa1p), Schizosaccharomyces pombe and green algae catalyze an unprecedented dihydroxylation mo
174 psins (CCRs), structurally distinct from the green algae CCRs used extensively for neural activation
175 lar landscapes of thylakoid membranes inside green algae cells.
176                               The charophyte green algae (CGA, Streptophyta, Viridiplantae) occupy a
177 ns, vertebrate rat rhodopsin 4 (RO4) and the green algae channelrhodospin 2 (ChR2), could be used to
178                                         Both green algae (charophytes) and cyanobacteria have also be
179  (Cys362) in the [FeFe] hydrogenase from the green algae Chlamydomonas reinhardtii ( CrHydA1) was exc
180 ed effluent, the short-term toxicity for the green algae Chlamydomonas reinhardtii increased and reac
181 -sensitive [FeFe]-hydrogenase HydA1 from the green algae Chlamydomonas reinhardtii was exposed to def
182                            The single-celled green algae Chlamydomonas reinhardtii with its two flage
183 tion-selective ion channel isolated from the green algae Chlamydomonas reinhardtii.
184 serine lipid species in a lipid extract of a green algae ( Chlamydomonas reinhardtii) sample.
185 hort-term uptake of silver by two species of green algae, Chlamydomonas reinhardtii and Pseudokirchne
186 itrate transport system from the unicellular green algae, Chlamydomonas reinhardtii required two gene
187 hat the observed phenomenon extends to other green algae (Chlorella kesslerii and Scenedesmus obliquu
188 rticles (NPs) interacting with single-celled green algae, Chlorella sp., have been found to be bilate
189      Upper shore epiphytes were dominated by green algae (Chlorophyta) and single-celled diatoms (pri
190 eophyceae), 23 red algae (Rhodophyta), and 3 green algae (Chlorophyta).
191 ants as well as the two distinct lineages of green algae, chlorophytes and charophytes.
192      Thus light-activated vertebrate RO4 and green algae ChR2 allow the antagonistic control of neuro
193              The calculated profiles of 96-h green algae chronic toxicity show that the overall toxic
194 imes (archamoebae, calonymphids, chlorophyte green algae, ciliates, foraminifera).
195 algal blooms, which consisted of filamentous green algae (Cladophora genus) and blue-green algae (Ana
196 ting in proliferation of filamentous benthic green algae (Cladophora glomerata).
197 ella spp. are free-living, nonphotosynthetic green algae closely related to the model organism Chlamy
198 hotspots coinciding with abundant freshwater green algae (Closterium spp.).
199                                 Both red and green algae colonized marine environments early in their
200 tions to three food treatments consisting of green algae combined with cyanobacteria able/unable of p
201 AT values are increased in nonphotosynthetic green algae compared to their closest photosynthetic rel
202           Volvox carteri and other volvocine green algae comprise an excellent model for investigatin
203            Chloroplast genomes in plants and green algae contain numerous group II introns, large rib
204 loroplast-localized holoenzyme of plants and green algae contains eight nuclear-encoded small subunit
205                  Freshwater with higher blue-green algae content produced higher number fractions of
206 ost cases, the blooms are predominantly blue-green algae (Cyanobacteria), which are favored by low ra
207 es form obligate symbiotic associations with green algae, cyanobacteria or with both photobionts.
208  C. reinhardtii and other frequently studied green algae: decreased chlorophyll content, increased fr
209        The carbon material derived from blue-green algae demonstrated promising electrochemical perfo
210  lineages: animals, land plants, chlorophyte green algae, demosponges, slime molds and brown algae.
211                                           In green algae, diatoms, and mosses, NPQ depends on the lig
212 plexa, ciliates, land plants, and charophyte green algae--directly conflicts with the phylogeny of th
213 nce is eliminated or greatly restricted, and green algae dominate over a wide range of supply conditi
214  the natural organic ligands excreted by the green algae Dunaliella tertiolecta on the Fe(II) oxidati
215 ists representing Choanozoa, Archamoeba, and green algae efficiently suppressed all the phenotypes of
216 s 1 (PBCV-1), a large DNA virus that infects green algae, encodes a histone H3 lysine 27-specific met
217 rised nuclei of formerly independent red and green algae enslaved by separate eukaryote hosts over 50
218 ment analyses), particularly the diatoms and green algae, experienced only transient suppression then
219                                      Whereas green algae express many different OPR proteins, only a
220                                              Green algae expressing a carbon-concentrating mechanism
221             Heterokonts, Alveolata protists, green algae from Charophyta and Chlorophyta divisions, a
222 hat infect certain eukaryotic chlorella-like green algae from the genus Chlorovirus.
223 , including Charophyceae algae, the group of green algae giving rise to land plants.
224  sulfate deficiency of plants and freshwater green algae has been extensively analysed by system biol
225 protein homologs in the sequenced genomes of green algae has led to the hypothesis that, in plants, t
226 ished role in the field of basic research in green algae has paved the way for understanding algal me
227  as in the chloroplasts of higher plants and green algae, has been implicated in this process.
228                         Only land plants and green algae have a kinesin with the MyTH4 and talin-like
229  the spatial distribution of mitochondria in green algae have also been observed under CO(2) limitati
230                   Indeed, several charophyte green algae have historically been used as model systems
231 rce the cell walls of some red and siphonous green algae have not been well studied, yet they could p
232 t the bright promise studying the charophyte green algae holds for better understanding plant evoluti
233 the same interaction partners as their plant/green algae homologs.
234 major divisions of land plants as well as in green algae; homologs outside of the plant kingdom were
235 s are typically caused by the so-called blue-green algae in eutrophic waters.
236 e disturbance of triclosan on five nontarget green algae in Lake Erie.
237 ery different from those found in plants and green algae, including 3' poly(U) tail addition, and ext
238  chloroplast chaperonin system of plants and green algae is a curiosity as both the chaperonin cage a
239 f both mammalian sperm cells and unicellular green algae is primarily governed by direct ciliary cont
240 al diversity seen in the cyanobacteria (blue-green algae) is especially pronounced in the ubiquitous
241                                  Tiny marine green algae issued from two deep branches of the Chlorop
242                                  Compared to green algae, land plants have an extended set of SEC14L-
243 gae Pseudokirchneriella subcapitata and blue-green algae Microcystis aeruginosa were separately incub
244  reveal five oleosin lineages: primitive (in green algae, mosses, and ferns), universal (U; all land
245  of foreign mitochondrial DNA, acquired from green algae, mosses, and other angiosperms.
246 AE gene families in the sequenced genomes of green algae, mosses, and trees; the size of the respecti
247 erved in DT resurrection plants, mosses, and green algae most closely related to these Embryophytes.
248 11-kDa protein from the cyanobacterium (blue-green algae) Nostoc ellipsosporum with potent virucidal
249  by photosynthesizing cyanobacteria and blue-green algae of nearly three billion years appeared to ha
250                                  Among them, green algae of the genus Tetraselmis are extensively stu
251 , but recent studies of mating-type genes in green algae open a promising new way to explore molecula
252 genetic and genomic properties of charophyte green algae opens up new opportunities to study key prop
253                                   Plants and green algae optimize photosynthesis in changing light co
254 ontal acquisitions from organisms other than green algae or prokaryotes.
255 d colonial organisms such as the volvocalean green algae, organized beating by the somatic cells' fla
256 at support the expected monophyly of red and green algae/plants (i.e. the Plantae hypothesis) and 19
257 d mitochondrial ATP synthase dimers from the green algae Polytomella sp. and the yeast Yarrowia lipol
258                Several charophytes (advanced green algae) possessed low levels of transcripts encodin
259 l hormone during the evolution of charophyte green algae, prior to land colonization.
260 ever, it is not known if avascular plants or green algae produce this enzyme.
261 l algal blooms (HABs) of Cyanobacteria (blue-green algae) produce toxins that impact human health.
262                               The freshwater green algae Pseudokirchneriella subcapitata and blue-gre
263 ent chloroplast genomes from land plants and green algae recovers the phylogeny congruent with prior
264 ation in chloroplasts of vascular plants and green algae, respectively.
265 e virus PBCV-1 that infects a chlorella-like green algae revealed an open reading frame, A98R, with s
266              Comparison with other sequenced green algae revealed unique protein families involved in
267                            Analysis of other green algae reveals species-specific repeated elements t
268 nse to high CO(2) environmental variability, green algae, such as Chlamydomonas reinhardtii, have evo
269 roup of spore-forming parasites that share a green algae symbiont and a predilection for causing chro
270 s obliquus) and at least one species of blue-green algae (Synechococcus leopoliensis).
271 yococcus braunii race B is a colony-forming, green algae that accumulates triterpene oils in excess o
272 he planet and they infect certain eukaryotic green algae that are mutualistic endosymbionts in a vari
273         Evidence is accumulating that in the green algae the evolution of female and male gametes dif
274                                In plants and green algae the fastest response to high light is non-ph
275  is a spherical shell, such as the volvocine green algae, the current (molecules per second) of neede
276 Although state transitions are also found in green algae, the detailed architecture of the extant see
277 P. margaritaceum, a member of the charophyte green algae, the immediate ancestors of land plants, was
278  compounds have been identified in primitive green algae, the presence of true lignins in nonvascular
279      The accepted view is that in plants and green algae, the three extrinsic proteins are PsbO, PsbP
280 re the plastid genomes of two "transitional" green algae: the photosynthetic, mixotrophic Auxenochlor
281 ports on auxin function in basal lineages of green algae, these results suggest that auxin function p
282 despread endogenization of NCLDVs in diverse green algae; these giant EVEs reached sizes greater than
283 lvania, USA, including fourteen Chlorophyta (green algae), three Bacillariophyta (diatoms) and one cy
284 tilization in taxa ranging from protozoa and green algae to flowering plants and invertebrate animals
285  is highly conserved from cyanobacteria, and green algae to land plants but not existing in the other
286 e the phenomic and genomic traits that allow green algae to survive in deserts, we characterized a ub
287 or understanding the transition from aquatic green algae to terrestrial plants.
288 plastids, photosynthesis spread from red and green algae to unrelated eukaryotes by secondary and ter
289 ted the organellar genomes of photosynthetic green algae, we generated the complete plastid genome (p
290 entified as a biotransformation product when green algae were exposed to environmentally relevant con
291  in situ hybridization images suggested that green algae were predominant in both the anode-based bio
292 se mediated by the two sensory rhodopsins in green algae were recorded.
293 ned by acid hydrolysis of ulvans from marine green algae, were sprayed on leaves of Arabidopsis thali
294                      These include volvocine green algae, where sexual cycles and sex-determining mec
295          To assess the role of Asc in NPQ in green algae, which are known to contain low amounts of A
296 ider aspects of the biology of the volvocine green algae, which contain both unicellular and multicel
297 s a phycobiliprotein extracted from the blue-green algae, which has been shown to have various pharma
298  deviant chloroplast genome of Cladophorales green algae, which is entirely fragmented into hairpin c
299  Auxenochlorella spp. are diploid oleaginous green algae whose streamlined genomes can be readily man
300 tes, recent efforts to purify molecules from green algae with structural features unique to lipid A h

 
Page Top