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1 , 10 invertebrates, 12 vascular plants and a green alga.
2 as food, as now demonstrated in an ancestral green alga.
3 n preventing transposon mobilization in this green alga.
4 sembly of the PSII holocomplex in this model green alga.
5 r physiological processes in this eukaryotic green alga.
6 een acquired by secondary endosymbiosis of a green alga.
7  by secondary endosymbiosis, probably from a green alga.
8 iRNA-mediated CDS-targeting operates in this green alga.
9 sing our knowledgebase by 10% for this model green alga.
10 t of RNA polymerase II from two red algae, a green alga and a relatively derived amoeboid protist.
11  used affinity reagents for lipid A to probe green alga and tissues of the garden pea for a light mic
12 phosphate formation in several eubacteria, a green alga, and plant chloroplasts has been demonstrated
13 ion during photoacclimation for the colonial green alga Botryococcus braunii and made a comparison wi
14 ated derivatives (C31-C37), generated by the green alga Botryococcus braunii race B have received sig
15 to Chlamydomonas, a biflagellate fresh water green alga, but intense autofluorescence from photosynth
16              Under nitrogen deprivation, the green alga C. reinhardtii showed substantial triacylglyc
17  of 5 nm with a polyacrylate coating) by the green alga C. reinhardtii was investigated in order to a
18        During the atypically fast IFT in the green alga C. reinhardtii, on average, 10 kinesin-2 moto
19 ates for the absence of an active Rca in the green alga C. reinhardtii.
20 ce of this signaling complex in a charophyte green alga, Chara braunii, proposed to be the closest li
21                                       In the green alga Chlamydomonas (Chlamydomonas r einhardtii), c
22 s (P) regulates TORC1 signaling in the model green alga Chlamydomonas (Chlamydomonas reinhardtii) via
23 in gamete membrane fusion in the unicellular green alga Chlamydomonas and the malaria pathogen Plasmo
24                         Recent work with the green alga Chlamydomonas and the nematode C. elegans dem
25 -type minus (mt-) gametes of the unicellular green alga Chlamydomonas are mixed together, binding int
26              By contrast, the photosynthetic green alga Chlamydomonas can grow more than 8-fold durin
27 ium caudatum (P-trHb) and the other from the green alga Chlamydomonas eugametos (C-trHb).
28 parison to the truncated hemoglobin from the green alga Chlamydomonas eugametos also suggested how th
29               Among the eight organisms, the green alga Chlamydomonas has the most unusual pattern of
30  FUS1 gene in the unicellular, biflagellated green alga Chlamydomonas is one of the few sex-specific
31           In a culture of a B(12) -dependent green alga Chlamydomonas nivalis, we found a contaminati
32                                          The green alga Chlamydomonas proliferates by "multiple fissi
33                                       In the green alga Chlamydomonas reinhardtii (Cr), three genes e
34 tructures of PRK from two model species: the green alga Chlamydomonas reinhardtii (CrPRK) and the lan
35 /beta-barrel active site of Rubisco from the green alga Chlamydomonas reinhardtii (methyl-Cys-256, Ly
36 t it may not be closely related to the model green alga Chlamydomonas reinhardtii A detailed survey o
37                              The unicellular green alga Chlamydomonas reinhardtii acclimates to a low
38                              The unicellular green alga Chlamydomonas reinhardtii adapts to anaerobic
39 cytochrome b(6)f from the chloroplast of the green alga Chlamydomonas reinhardtii and cytochrome bc(1
40 oredoxins from Escherichia coli and from the green alga Chlamydomonas reinhardtii and for a number of
41 sure studies on the well-characterized model green alga Chlamydomonas reinhardtii and identified temp
42 e control of the photoperiod response in the green alga Chlamydomonas reinhardtii and its influence o
43 omes with uncommon glycans stemming from the green alga Chlamydomonas reinhardtii and the archaeon Ha
44                              The unicellular green alga Chlamydomonas reinhardtii and the vascular pl
45 was isolated from the unicellular eukaryotic green alga Chlamydomonas reinhardtii as a light-induced
46                           The success of the green alga Chlamydomonas reinhardtii as a model organism
47 type and in the cell wall free mutant of the green alga Chlamydomonas reinhardtii at pH 7.5.
48  of biotechnologically useful mutants of the green alga Chlamydomonas reinhardtii by incoherent neutr
49 system II core dimers were isolated from the green alga Chlamydomonas reinhardtii by Ni(2+)-affinity
50              The [FeFe] hydrogenase from the green alga Chlamydomonas reinhardtii can catalyze the re
51                                          The green alga Chlamydomonas reinhardtii can grow photoautot
52                 The unicellular biflagellate green alga Chlamydomonas reinhardtii can perceive light
53 e [FeFe] hydrogenases HydA1 and HydA2 in the green alga Chlamydomonas reinhardtii catalyze the final
54 role in intermittent-light conditions in the green alga Chlamydomonas reinhardtii Chlororespiration,
55   Mutations at the APM1 and APM2 loci in the green alga Chlamydomonas reinhardtii confer resistance t
56                        Here we show that the green alga Chlamydomonas reinhardtii contains a 5mC-modi
57 his study shows that the cpSRP system in the green alga Chlamydomonas reinhardtii differs significant
58                              The unicellular green alga Chlamydomonas reinhardtii displays metabolic
59                              The unicellular green alga Chlamydomonas reinhardtii divides by multiple
60 by the screening and sorting of cells of the green alga Chlamydomonas reinhardtii encapsulated in dro
61 Chlorophycean VDE (CVDE) gene from the model green alga Chlamydomonas reinhardtii encodes an atypical
62                                          The green alga Chlamydomonas reinhardtii evolved blue light-
63                         In anaerobiosis, the green alga Chlamydomonas reinhardtii evolves molecular h
64 mple, we detect the release of H2O2 from the green alga Chlamydomonas reinhardtii exposed to either 1
65                                       In the green alga Chlamydomonas reinhardtii flagellar adhesion
66                                          The green alga Chlamydomonas reinhardtii has a network of fe
67                              The unicellular green alga Chlamydomonas reinhardtii has become an inval
68 directly light-gated cation channel from the green alga Chlamydomonas reinhardtii has been shown to b
69                       The chloroplast of the green alga Chlamydomonas reinhardtii has been shown to c
70 covery of an animal-like cryptochrome in the green alga Chlamydomonas reinhardtii has expanded the sp
71   The animal-like cryptochrome (aCRY) of the green alga Chlamydomonas reinhardtii has extended our vi
72                            The genome of the green alga Chlamydomonas reinhardtii has multiple genes
73                                          The green alga Chlamydomonas reinhardtii has numerous genes
74 thodology was validated with a suspension of green alga Chlamydomonas reinhardtii in interaction with
75 lar phosphatases produced by the terrestrial green alga Chlamydomonas reinhardtii in response to phos
76  The eyespot of the biflagellate unicellular green alga Chlamydomonas reinhardtii is a complex organe
77                                          The green alga Chlamydomonas reinhardtii is a leading model
78                                          The green alga Chlamydomonas reinhardtii is a leading unicel
79               The eyespot of the unicellular green alga Chlamydomonas reinhardtii is a photoreceptive
80                                          The green alga Chlamydomonas reinhardtii is a useful model o
81                              The unicellular green alga Chlamydomonas reinhardtii is a widely used mo
82                                          The green alga Chlamydomonas reinhardtii is an invaluable re
83                              The unicellular green alga Chlamydomonas reinhardtii is capable of accli
84                              The unicellular green alga Chlamydomonas reinhardtii is capable of photo
85                              The unicellular green alga Chlamydomonas reinhardtii is evolutionarily d
86 usly established that the Rh1 protein of the green alga Chlamydomonas reinhardtii is highly expressed
87                         One such gene in the green alga Chlamydomonas reinhardtii is MCD1, whose prod
88                              The unicellular green alga Chlamydomonas reinhardtii is the premier expe
89  generated a pgrl1 npq4 double mutant in the green alga Chlamydomonas reinhardtii lacking both PGRL1
90 otosynthetic apparatus using a mutant of the green alga Chlamydomonas reinhardtii lacking carotenoids
91 the low pH is the PsbS protein, while in the green alga Chlamydomonas reinhardtii LhcSR proteins appe
92                                          The green alga Chlamydomonas reinhardtii mutant 76-5EN lacks
93       CCS4 was genetically identified in the green alga Chlamydomonas reinhardtii on the basis of the
94 e redox regulation of autophagy in the model green alga Chlamydomonas reinhardtii Our results indicat
95                                          The green alga Chlamydomonas reinhardtii possesses a CO(2) c
96  the preexisting centriole proteome from the green alga Chlamydomonas reinhardtii revealed additional
97  dissection of xanthophyll metabolism in the green alga Chlamydomonas reinhardtii revealed functions
98                     State transitions in the green alga Chlamydomonas reinhardtii serve to balance ex
99 agenesis of cytochrome f from the eukaryotic green alga Chlamydomonas reinhardtii showed that a Phe4
100 anobacterium Mastigocladus laminosus and the green alga Chlamydomonas reinhardtii showed the presence
101                                     When the green alga Chlamydomonas reinhardtii swims, it uses the
102 splay for isolating genes of the unicellular green alga Chlamydomonas reinhardtii that exhibit elevat
103  Here, we have created a minimal cell of the green alga Chlamydomonas reinhardtii that is able to und
104 identified a gene (MUT68) in the unicellular green alga Chlamydomonas reinhardtii that is required fo
105 ve cloned a gene (Mut6) from the unicellular green alga Chlamydomonas reinhardtii that is required fo
106                       Here, we report in the green alga Chlamydomonas reinhardtii that UVR8 induces a
107  of the animal-like cryptochrome aCRY in the green alga Chlamydomonas reinhardtii This finding was ex
108 loned and characterized from the unicellular green alga Chlamydomonas reinhardtii to begin to underst
109 enesis and chloroplast transformation of the green alga Chlamydomonas reinhardtii to create D473A and
110                        Here we use the model green alga Chlamydomonas reinhardtii to discover that a
111 sponsive fluorescent dyes in the unicellular green alga Chlamydomonas reinhardtii to examine the spec
112 ble draft genome sequence of the unicellular green alga Chlamydomonas reinhardtii to guide clustering
113  critical for acclimation of the unicellular green alga Chlamydomonas reinhardtii to phosphorus starv
114 is of the evolutionarily distant unicellular green alga Chlamydomonas reinhardtii to quantify the eff
115 ed outcrossed populations of the unicellular green alga Chlamydomonas reinhardtii to selection by the
116                   Gametes of the unicellular green alga Chlamydomonas reinhardtii undergo sexual adhe
117                                          The green alga Chlamydomonas reinhardtii undergoes gametogen
118 ays of PS I in whole cells of the deuterated green alga Chlamydomonas reinhardtii using high-time-res
119           The 2pac mutant of the unicellular green alga Chlamydomonas reinhardtii was isolated and fo
120 translational acetylation in the unicellular green alga Chlamydomonas reinhardtii was studied by trit
121 further, we have used one such organism, the green alga Chlamydomonas reinhardtii We found that altho
122             Here, we crossed MA lines of the green alga Chlamydomonas reinhardtii with its unmutated
123  cellular organization, using mutants of the green alga Chlamydomonas reinhardtii with known alterati
124 We have investigated a cryptochrome from the green alga Chlamydomonas reinhardtii with sequence homol
125                                 In the model green alga Chlamydomonas reinhardtii, a carbon-concentra
126                                       In the green alga Chlamydomonas reinhardtii, a Leu(290)-to-Phe
127                                       In the green alga Chlamydomonas reinhardtii, a luminal carbonic
128                                       In the green alga Chlamydomonas reinhardtii, a mutant, pmp1, wa
129                                       In the green alga Chlamydomonas reinhardtii, a photosynthetic m
130 ences from flowering plants with that of the green alga Chlamydomonas reinhardtii, a small number of
131 e 80S cytosolic ribosome from the eukaryotic green alga Chlamydomonas reinhardtii, and accompany this
132 similar to that recently demonstrated in the green alga Chlamydomonas reinhardtii, and for the first
133 lant Arabidopsis (Arabidopsis thaliana), the green alga Chlamydomonas reinhardtii, and the cyanobacte
134 oglycerate kinase (PGK1) from the eukaryotic green alga Chlamydomonas reinhardtii, and we show that C
135 ring plant, Commelina communis, cells of the green alga Chlamydomonas reinhardtii, and zygotes of the
136  optical spectroscopy in living cells of the green alga Chlamydomonas reinhardtii, between 277 and 31
137          In transformants of the unicellular green alga Chlamydomonas reinhardtii, expression of a eu
138                           In the unicellular green alga Chlamydomonas reinhardtii, GTR and GSAT were
139                                       In the green alga Chlamydomonas reinhardtii, Mut11p, related to
140                                       In the green alga Chlamydomonas reinhardtii, non-photochemical
141 hat a qE-deficient mutant of the unicellular green alga Chlamydomonas reinhardtii, npq4, lacks two of
142 e found on unicellular organisms such as the green alga Chlamydomonas reinhardtii, on sperm cells, an
143 ) showed a dramatic daily oscillation in the green alga Chlamydomonas reinhardtii, peaking once each
144                        We report that in the green alga Chlamydomonas reinhardtii, PPO and FeC are ea
145 onal, photosynthesis-deficient mutant of the green alga Chlamydomonas reinhardtii, previously recover
146 gly, a SU(VAR)3-9 homolog in the unicellular green alga Chlamydomonas reinhardtii, SET3p, functions i
147                           In the unicellular green alga Chlamydomonas reinhardtii, single-copy transg
148                           In the unicellular green alga Chlamydomonas reinhardtii, sRNAs derived from
149                                 In the model green alga Chlamydomonas reinhardtii, the capacity for r
150                           In the unicellular green alga Chlamydomonas reinhardtii, the epigenetic sil
151                                       In the green alga Chlamydomonas reinhardtii, the LHCSR pigment-
152                    In the chloroplast of the green alga Chlamydomonas reinhardtii, two discontinuous
153  of native chloroplast ClpP complex from the green alga Chlamydomonas reinhardtii, using a strain tha
154                        Using the unicellular green alga Chlamydomonas reinhardtii, we developed a gen
155                                    Using the green alga Chlamydomonas reinhardtii, we developed an ef
156 a heterologous psbA expression system in the green alga Chlamydomonas reinhardtii, we have measured g
157 chanisms exist in the evolutionarily distant green alga Chlamydomonas reinhardtii, we identified Chla
158 vivo, by manipulating the chloroplast of the green alga Chlamydomonas reinhardtii, where the translat
159 on two [FeFe]-hydrogenases, CrHydA1 from the green alga Chlamydomonas reinhardtii, which contains onl
160 remains poorly understood in the unicellular green alga Chlamydomonas reinhardtii, which contains thr
161 f these additional residues, a mutant of the green alga Chlamydomonas reinhardtii, which lacks both s
162                        The AMT4 locus of the green alga Chlamydomonas reinhardtii, which we mapped to
163 anobacterium Mastigocladus laminosus and the green alga Chlamydomonas reinhardtii, whose appearance i
164 nsertion sites in the eukaryotic unicellular green alga Chlamydomonas reinhardtii.
165 utophagy activation in the model unicellular green alga Chlamydomonas reinhardtii.
166 hat are native to D1:1 were expressed in the green alga Chlamydomonas reinhardtii.
167 ative selectable marker for use in the model green alga Chlamydomonas reinhardtii.
168 t is found in the eyespot of the unicellular green alga Chlamydomonas reinhardtii.
169 new spontaneous mutations in the unicellular green alga Chlamydomonas reinhardtii.
170 system I (PSI) biogenesis in the unicellular green alga Chlamydomonas reinhardtii.
171 e formation in a plant cryptochrome from the green alga Chlamydomonas reinhardtii.
172 dy of an unusual heteroplasmic strain of the green alga Chlamydomonas reinhardtii.
173 sociated with flagellar length change in the green alga Chlamydomonas reinhardtii.
174 es, including 6 eudicots, 5 monocots and the green alga Chlamydomonas reinhardtii.
175 1 and sac3 sulfur acclimation mutants of the green alga Chlamydomonas reinhardtii.
176 oved by conversion of each Tyr to Phe in the green alga Chlamydomonas reinhardtii.
177 aining protein cytochrome c6 (cyt c6) in the green alga Chlamydomonas reinhardtii.
178 ntly identified in the hydEF-1 mutant of the green alga Chlamydomonas reinhardtii.
179  basal bodies (centrioles) isolated from the green alga Chlamydomonas reinhardtii.
180 ntify proteins in purified flagella from the green alga Chlamydomonas reinhardtii.
181 ype and mutant forms of photosystem I in the green alga Chlamydomonas reinhardtii.
182 ned and characterized the psbW gene from the green alga Chlamydomonas reinhardtii.
183 A from the chloroplast to the nucleus in the green alga Chlamydomonas reinhardtii.
184 subunit of the chloroplast ribosome from the green alga Chlamydomonas reinhardtii.
185 edominant components of the cell wall of the green alga Chlamydomonas reinhardtii.
186 properties similar to acidocalcisomes in the green alga Chlamydomonas reinhardtii.
187 ia the reversible hydrogenase pathway in the green alga Chlamydomonas reinhardtii.
188 ent, Tcr3, was identified in the unicellular green alga Chlamydomonas reinhardtii.
189 ) from non-Solanaceae species, including the green alga Chlamydomonas reinhardtii.
190 ated from the chloroplast of the unicellular green alga Chlamydomonas reinhardtii.
191 use observed in the chloroplast genes of the green alga Chlamydomonas reinhardtii.
192 volved in the microbodies of the unicellular green alga Chlamydomonas reinhardtii.
193 ges during synchronized cell division in the green alga Chlamydomonas reinhardtii.
194 f nuclear gene expression in the unicellular green alga Chlamydomonas reinhardtii.
195                              The unicellular green alga Chlamydomonas sp. ICE-L thrives in polar sea
196                                The Antarctic green alga Chlamydomonas sp. UWO 241 (UWO 241) is adapte
197                              The unicellular green alga Chlamydomonas swims with two flagella that ca
198                  We screened the unicellular green alga Chlamydomonas using insertional mutagenesis t
199 ere, by use of gene discovery methods in the green alga Chlamydomonas, gene disruption in the rodent
200            In the unicellular, biflagellated green alga Chlamydomonas, the early steps in zygote deve
201                  During fertilization in the green alga Chlamydomonas, the plus gamete-specific membr
202  biflagellated phytoplanktons resembling the green alga Chlamydomonas.
203 ontrol zygote development of the unicellular green alga Chlamydomonas.
204  counterparts of cilia) of the biflagellated green alga Chlamydomonas.
205 e to environmental cues in the biflagellated green alga Chlamydomonas.
206 and receptors) in ciliary ectosomes from the green alga Chlamydomonas.
207 nd Fe) modified the response of a freshwater green alga ( Chlamydomonas reinhardtii) to copper.
208 on of chloroplast-localized TF (TIG1) in the green alga (Chlamydomonas reinhardtii) and the vascular
209 s (Physcomitrella patens), and a unicellular green alga (Chlamydomonas reinhardtii), encode proteins
210 der heterotrophy and photo-autotrophy in the green alga (Chlamydomonas reinhardtii).
211 esulted in identification of KCBP in another green alga, Chlamydomonas reinhardtii, and several flowe
212                        The model unicellular green alga, Chlamydomonas reinhardtii, employs diverse s
213                              Here we use the green alga, Chlamydomonas reinhardtii, which regulates b
214 nd modifying the chloroplast genome from the green alga, Chlamydomonas reinhardtii.
215  animals are also present in the unicellular green alga, Chlamydomonas reinhardtii.
216 obacterium, Mastigocladus laminosus, and the green alga, Chlamydomonas reinhardtii.
217 ibody in the chloroplast of the unicellular, green alga, Chlamydomonas reinhardtii.
218 ized a second [Fe]-hydrogenase gene from the green alga, Chlamydomonas reinhardtii.
219 us, (ii) spinach chloroplasts, and (iii) the green alga, Chlamydomonas reinhardtii.
220 were changed in six mutants generated in the green alga, Chlamydomonas reinhardtii.
221 uring sexual reproduction in the unicellular green alga, Chlamydomonas reinhardtii.
222                   Sexual reproduction in the green alga, Chlamydomonas, is regulated by environmental
223  in many aspects of flagella function in the green alga, Chlamydomonas.
224 stically related in higher plants and in the green alga Chlorella protothecoides.
225 e-forming virus that infects the unicellular green alga Chlorella sp. strain NC64A.
226 A (dsDNA) virus that infects the unicellular green alga Chlorella variabilis NC64A.
227 hlorophyte plastid genomes, only that of the green alga Chlorella vulgaris appears to share this feat
228 diuron on the photosynthetic activity of the green alga Chlorella vulgaris in presence of different m
229                         Experiments with the green alga Chlorella vulgaris presented here compared po
230 TCV-1, whose only known host is a eukaryotic green alga (Chlorella heliozoae) that is an endosymbiont
231 ntosa and two acetylated diterpenes from the green alga Chlorodesmis fastigiata as potent allelochemi
232         There is interest in the unicellular green alga Chromochloris zofingiensis, because it produc
233 f oxygenic photosynthesis in the unicellular green alga Chromochloris zofingiensis.
234                   The nuisance, macrophytic, green alga Cladophora (Chlorophyta; mostly Cladophora gl
235 ls B-I (5-12), were isolated from the Fijian green alga Cladophora socialis and identified by a combi
236                                          The green alga Desmodesmus armatus is an emerging biofuel pl
237 diolabeled EE2 ((14)C-EE2) by the freshwater green alga Desmodesmus subspicatus were investigated.
238  DNA (mtDNA) of Chlamydomonas reinhardtii, a green alga, does not encode subunit 6 of F(0)F(1)-ATP sy
239                             The halotolerant green alga Dunaliella bardawil is unique in that it accu
240  we investigated the DIC assimilation of the green alga Dunaliella tertiolecta after using artificial
241 diatom, Pseudonitzshia delicatissima and the green alga, Dunaliella tertiolecta .
242  (APS) reductase from the marine macrophytic green alga Enteromorpha intestinalis uses reduced glutat
243 iclosan in the presence of TiO(2) P25 to the green alga Eremosphaera viridis in Lake Erie.
244 inant phytochromes from a higher plant and a green alga exhibit serine/threonine kinase activity simi
245   Chlamydomonas reinhardtii is a unicellular green alga expressing a conventional and divergent actin
246 photoacclimation processes for this colonial green alga further extends the view of the diversity of
247 en plant lineage, including charophytes (the green alga group closest to the land plants), bryophytes
248     Chlamydomonas reinhardtii, a unicellular green alga, grows photoautotrophically at very low conce
249   In the model organism Dunaliella salina (a green alga), growth under low light (100 mol of photons
250                       The chlamydomonadalean green alga Haematococcus lacustris (strain UTEX 2505) ha
251 s (delta(18)O and delta(13)C) in the benthic green alga, Halimeda tuna.
252                                          The green alga Hematococcus pluvialis accumulates large amou
253 elicits a lytic infection of its unicellular green alga host.
254  in Chlamydomonas reinhardtii, a unicellular green alga in the land plant lineage.
255 B(12) -dependent Lobomonas rostrata, another green alga, in return for fixed carbon.
256 nas sp. UWO 241 (UWO 241) is a psychrophilic green alga isolated from Antarctica.
257 osynthetic cell, because in this unicellular green alga LD dynamics can be readily manipulated by nit
258                              The unicellular green alga Lobomonas rostrata requires an external suppl
259 of phytochrome isolated from the unicellular green alga Mesotaenium caldariorum is blue-shifted.
260 ornithine decarboxylase in the single-celled green alga Micromonas.
261 is, we show that gametogenesis in the marine green alga, Monostroma angicava, exhibits equal size cel
262 DNA possesses 4 derived features relative to green alga mtDNAs--increased genome size, RNA editing, i
263 sis obtusa (starry stonewort) is a dioecious green alga native to Europe and Asia that has emerged as
264     Chlamydomonas reinhardtii, a unicellular green alga, often experiences hypoxic/anoxic soil condit
265   Dendroamide A (1) was isolated from a blue-green alga on the basis of its ability to reverse drug r
266   During embryonic development, cells of the green alga Oophila amblystomatis enter cells of the sala
267 g was associated with POT1 proteins from the green alga Ostreococcus lucimarinus and two flowering pl
268 phytoplankton virus, which infects the small green alga Ostreococcus tauri, a host-derived ammonium t
269 ferent frequencies using the bacterium-sized green alga Picochlorum SE3.
270 nced the 13.5 Mbp genome of the halotolerant green alga Picochlorum SENEW3 (SE3) that was isolated fr
271 hthoquinone aulosirazole, isolated from blue-green alga, possesses selective antitumor cytotoxicity,
272                                              Green alga POT1 exhibited a strong preference for the ca
273  As NoDGAT2A, 2C, and 2D originated from the green alga, red alga, and eukaryotic host ancestral part
274  Arthrospira (Spirulina) platensis is a blue-green alga, rich with bioactive components and nutrients
275 -PS) on the growth and photosynthesis of the green alga Scenedesmus obliquus and the growth, mortalit
276 iforme and Anabaena spp., in addition to the green alga Scenedesmus obliquus.
277 cation to homogeneity of the enzyme from the green alga, Scenedesmus obliquus.
278 ene functions as a hormone in the charophyte green alga Spirogyra pratensis Since land plants evolved
279 d KCBP from a gymnosperm, Picea abies, and a green alga, Stichococcus bacillaris.
280 he glaucocystophyte Cyanophora, and the blue-green alga Synechocystis as an outgroup.
281 tegies of Chlamydomonas reinhardtii, a model green alga that can grow using various carbon sources an
282   Chlamydomonas reinhardtii is a unicellular green alga that has attracted interest due to its potent
283 s a unicellular, soil-dwelling (and aquatic) green alga that has significant metabolic flexibility fo
284   Chlamydomonas reinhardtii is a unicellular green alga that is a key model organism in the study of
285 hardtii is a motile single-celled freshwater green alga that is guided by photosensory, mechanosensor
286 Chlamydomonas reinhardtii is a single-celled green alga that phototaxes toward light by means of a li
287 ed into a putative genome-scale model of the green alga to in silico test hypotheses of underlying ca
288 he robust and flexible biology utilized by a green alga to successfully inhabit a desert coastline.
289 ar plant (fern, Dryopteris crassirhizoma), a green alga (Ulva pertusa), and cyanobacteria (Anabaena v
290                            The multicellular green alga Volvox carteri and its morphologically divers
291                                          The green alga Volvox carteri possesses several thousand cel
292 (MT) of the sexually dimorphic multicellular green alga Volvox carteri specifies the production of eg
293 TIs is the origin of multicellularity in the green alga Volvox, a model system for the evolution of m
294 ly linked to the regA gene of the eukaryotic green alga Volvox.
295 poson called kangaroo from the multicellular green alga, Volvox carteri.
296   Chlamydomonas reinhardtii is a unicellular green alga whose lineage diverged from land plants over
297                Volvox carteri is a spherical green alga with a predominantly asexual mode of reproduc
298 n identified in Chlamydomonas reinhardtii, a green alga with a well-studied CCM.
299    Udotea flabellum is a marine, macroscopic green alga with C4-like photosynthetic characteristics,
300 complex of Botryococccus braunii, a colonial green alga with potential for lipid and sugar production

 
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