ライフサイエンスコーパス: Chlamydomonas reinhardtii

1 with the oxygen-evolving complex of PSII in Chlamydomonas reinhardtii.

2 n the photosynthesis of the freshwater algae Chlamydomonas reinhardtii.

3 regulation of lipid biosynthesis in the alga Chlamydomonas reinhardtii.

4 ene expression in the unicellular green alga Chlamydomonas reinhardtii.

5 olic model for the widely-studied microalga, Chlamydomonas reinhardtii.

6 carefully examined for the freshwater alga, Chlamydomonas reinhardtii.

7 of photosystem I (PSI) in the chloroplast of Chlamydomonas reinhardtii.

8 ssion in the photosynthetic unicellular alga Chlamydomonas reinhardtii.

9 state (Hhyd) of the [FeFe]-hydrogenase from Chlamydomonas reinhardtii.

10 two in vitro translation assays and the alga Chlamydomonas reinhardtii.

11 avy metals in the cytoplasm of the microalga Chlamydomonas reinhardtii.

12 -related protein encoded by the MAT3 gene in Chlamydomonas reinhardtii.

13 tes in the eukaryotic unicellular green alga Chlamydomonas reinhardtii.

14 lementary approaches for the living cells of Chlamydomonas reinhardtii.

15 n the nonsaturating range in the algal model Chlamydomonas reinhardtii.

16 tivation in the model unicellular green alga Chlamydomonas reinhardtii.

17 algae closely related to the model organism Chlamydomonas reinhardtii.

18 ive to D1:1 were expressed in the green alga Chlamydomonas reinhardtii.

19 ible chloroplast gene expression in the alga Chlamydomonas reinhardtii.

20 IFT complex B protein in mammalian cells and Chlamydomonas reinhardtii.

21 table marker for use in the model green alga Chlamydomonas reinhardtii.

22 nscriptome, proteome, and cellular levels of Chlamydomonas reinhardtii.

23 e of actin dynamics in flagellar assembly in Chlamydomonas reinhardtii.

24 (Cd) uptake kinetics in the freshwater alga Chlamydomonas reinhardtii.

25 d state transition mutant 6 (Stm6) mutant of Chlamydomonas reinhardtii.

26 against antigens in total cell lysates from Chlamydomonas reinhardtii.

27 nt NPQ, in contrast with previous reports in Chlamydomonas reinhardtii.

28 red mCherry) in the popular model microalga Chlamydomonas reinhardtii.

29 in the eyespot of the unicellular green alga Chlamydomonas reinhardtii.

30 wth and the expression of anaerobic genes in Chlamydomonas reinhardtii.

31 ing and wild type) and the biflagellate alga Chlamydomonas reinhardtii.

32 eous mutations in the unicellular green alga Chlamydomonas reinhardtii.

33 SI) biogenesis in the unicellular green alga Chlamydomonas reinhardtii.

34 in a plant cryptochrome from the green alga Chlamydomonas reinhardtii.

35 e cadmium (Cd) uptake in the freshwater alga Chlamydomonas reinhardtii.

36 manipulating the light harvesting system of Chlamydomonas reinhardtii.

37 the chloroplast genome from the green alga, Chlamydomonas reinhardtii.

38 ble component of NPQ, qE, in living cells of Chlamydomonas reinhardtii.

39 te, we investigated the function of VIPP1 in Chlamydomonas reinhardtii.

40 nt following N deprivation in the model alga Chlamydomonas reinhardtii.

41 he microbodies of the unicellular green alga Chlamydomonas reinhardtii.

42 vibrations in [FeFe]-hydrogenase HYDA1 from Chlamydomonas reinhardtii.

43 he flagellar axoneme in the unicellular alga Chlamydomonas reinhardtii.

44 f fluorescent protein-tagged EB1 (EB1-FP) in Chlamydomonas reinhardtii.

45 tive cation channel originally discovered in Chlamydomonas reinhardtii.

46 croalgae Pseudokirchneriella subcapitata and Chlamydomonas reinhardtii.

47 ery of this mechanism is the eukaryotic alga Chlamydomonas reinhardtii.

48 of PSI-LHCI and PSI-LHCI-LHCII complexes of Chlamydomonas reinhardtii.

49 synchronized cell division in the green alga Chlamydomonas reinhardtii.

50 Discovery of this intracellular process in Chlamydomonas reinhardtii 20 years ago led to a rapid di

51 t be closely related to the model green alga Chlamydomonas reinhardtii A detailed survey of biologica

52 In the model green alga Chlamydomonas reinhardtii, a carbon-concentrating mechan

53 In the green alga Chlamydomonas reinhardtii, a luminal carbonic anhydrase,

54 In the model microalga Chlamydomonas reinhardtii, a membrane protein HLA3 is pr

55 Here, we study Se methylation by Chlamydomonas reinhardtii, a model freshwater alga, as a

56 e have studied the acclimation strategies of Chlamydomonas reinhardtii, a model green alga that can g

57 In the green alga Chlamydomonas reinhardtii, a photosynthetic model organi

58 Chlamydomonas reinhardtii, a unicellular alga, is a good

59 Chlamydomonas reinhardtii, a unicellular green alga, oft

60 explore the thylakoid membrane components of Chlamydomonas reinhardtii acclimated to high and low lig

61 n systems biology approach to understand how Chlamydomonas reinhardtii acclimates to long-term heat s

62 The unicellular green alga Chlamydomonas reinhardtii adapts to anaerobic or hypoxic

63 on detected via metabolism/photosynthesis of Chlamydomonas reinhardtii algal cells (algae) in tap wat

64 ted RNA silencing in the model algal species,Chlamydomonas reinhardtii Among the mutants from this sc

65 se STN7/STT7, orthologous protein kinases in Chlamydomonas reinhardtii and Arabidopsis (Arabidopsis t

66 al levels in two biological models, cells of Chlamydomonas reinhardtii and Arabidopsis thaliana.

67 the two most studied FeFe hydrogenases, from Chlamydomonas reinhardtii and Clostridium acetobutylicum

68 ata obtained with the FeFe hydrogenases from Chlamydomonas reinhardtii and Clostridium acetobutylicum

69 pp.　CLD resemble cytoplasmic droplets from Chlamydomonas reinhardtii and contain major lipid drople

70 spp. CLD resemble cytoplasmic droplets from Chlamydomonas reinhardtii and contain major lipid drople

71 Results for two enzymes, CrHydA1 from Chlamydomonas reinhardtii and CpI from Clostridium paste

72 b(6)f from the chloroplast of the green alga Chlamydomonas reinhardtii and cytochrome bc(1) from beef

73 SAS-6 from Chlamydomonas reinhardtii and Danio rerio was shown to f

74 d and purified the nonameric IFT-B core from Chlamydomonas reinhardtii and determined the crystal str

75 pectroscopic study of two cryptochromes from Chlamydomonas reinhardtii and Drosophila melanogaster.

76 Gene expression was studied in Chlamydomonas reinhardtii and human airway epithelial ce

77 structure and defective ciliary movement in Chlamydomonas reinhardtii and humans.

78 s on the well-characterized model green alga Chlamydomonas reinhardtii and identified temporal change

79 f the photoperiod response in the green alga Chlamydomonas reinhardtii and its influence on starch me

80 ndium accumulation by two unicellular algae, Chlamydomonas reinhardtii and Pseudokirchneriella subcap

81 ake of silver by two species of green algae, Chlamydomonas reinhardtii and Pseudokirchneriella subcap

82 Expression of NtRbcS-T in Chlamydomonas reinhardtii and purification of the full R

83 S) for biosensing intact eukaryotic cells of Chlamydomonas reinhardtii and Saccharomyces cerevisiae.

84 dbreaking research on the genetic mapping of Chlamydomonas reinhardtii and the use of mutant strains

85 The unicellular green alga Chlamydomonas reinhardtii and the vascular plant Arabido

86 which 43,783 compounds were screened against Chlamydomonas reinhardtii, and 243 compounds were identi

87 ave been demonstrated in the model microalga Chlamydomonas reinhardtii, and many questions still rema

88 ion in natural accessions of the model alga, Chlamydomonas reinhardtii, and test the hypothesis that

89 opsis (Arabidopsis thaliana), the green alga Chlamydomonas reinhardtii, and the cyanobacterium Prochl

90 kinase (PGK1) from the eukaryotic green alga Chlamydomonas reinhardtii, and we show that C. reinhardt

91 The six FDXs identified in Chlamydomonas reinhardtii are not fully characterized in

92 parently, de novo-synthesized fatty acids in Chlamydomonas reinhardtii are, at least partially, first

93 The success of the green alga Chlamydomonas reinhardtii as a model organism is to a la

94 Using the related Chlamydomonas reinhardtii as a reference genome, 588 alg

95 Here we focus on Chlamydomonas reinhardtii as a reference model for LDs i

96 We used Chlamydomonas reinhardtii as a reference organism for a

97 ructs to express genes in the chloroplast of Chlamydomonas reinhardtii as an example, we show that a

98 ight-dark (12 h:12 h) cycles in synchronized Chlamydomonas reinhardtii at air-level CO(2).

99 the cell wall free mutant of the green alga Chlamydomonas reinhardtii at pH 7.5.

100 (modifier of inner arms) complex within the Chlamydomonas reinhardtii axoneme that physically links

101 ne expression system in the unicellular alga Chlamydomonas reinhardtii based mainly on a vitamin-repr

102 e D (PLD) accumulates abnormally in cilia of Chlamydomonas reinhardtii bbs mutants.

103 The problem has been studied in Chlamydomonas reinhardtii because the flagella are easy

104 ic reactions and stoichiometry were based on Chlamydomonas reinhardtii , but experiments for model ca

105 ion, a mutant (npq4 stt7-9) was generated in Chlamydomonas reinhardtii by crossing the state transiti

106 Here we report, a one-step transformation of Chlamydomonas reinhardtii by the DNA-free CRISPR-Cas9 me

107 s SSUs containing the SSU alpha-helices from Chlamydomonas reinhardtii can form hybrid Rubisco comple

108 n a synchronized photoautotrophic culture of Chlamydomonas reinhardtii, cell size, cell number, and t

109 changes in gene expression that occurs when Chlamydomonas reinhardtii cells are shifted from high to

110 ervation that the strong photosensitivity of Chlamydomonas reinhardtii cells depleted of the chloropl

111 Chlamydomonas reinhardtii cells exposed to abiotic stres

112 Acclimation of Chlamydomonas reinhardtii cells to low levels of singlet

113 l populations were observed after perturbing Chlamydomonas reinhardtii cells via nitrogen deprivation

114 structure of the COPI coat within vitrified Chlamydomonas reinhardtii cells.

115 ing both Homo sapiens centrin 2 (Hscen2) and Chlamydomonas reinhardtii centrin (Crcen).

116 ily divergent, although the unicellular alga Chlamydomonas reinhardtii (Chlamydomonas throughout) has

117 position of chloroplast lipids suggests that Chlamydomonas reinhardtii (Chlamydomonas) does not use t

118 in a model photosynthetic organism, the alga Chlamydomonas reinhardtii (Chlamydomonas), using mass sp

119 In Chlamydomonas reinhardtii (Chlorophyceae), a C17 alkene,

120 Two pathways increase the capacity of the Chlamydomonas reinhardtii chloroplast to detoxify supero

121 The Chlamydomonas reinhardtii chloroplast-localized poly(A)-

122 ves in association with IFT particles inside Chlamydomonas reinhardtii cilia.

123 The unicellular alga Chlamydomonas reinhardtii contains many types of small R

124 In Chlamydomonas reinhardtii, conventional actin is found i

125 he central gate residue Glu(130) (Glu(90) in Chlamydomonas reinhardtii (Cr) ChR2) (i) undergoes a hyd

126 In the green alga Chlamydomonas reinhardtii (Cr), three genes encode chape

127 f the cation channel channelrhodopsin-2 from Chlamydomonas reinhardtii (CrChR2) was selectively label

128 extensively studied channelrhodopsin-2 from Chlamydomonas reinhardtii (CrChR2).

129 most frequently used channelrhodopsin-2 from Chlamydomonas reinhardtii (CrChR2).

130 Channelrhodopsin-2 from Chlamydomonas reinhardtii, CrChR2, is the most widely us

131 ctrochemistry on the [FeFe] hydrogenase from Chlamydomonas reinhardtii (CrHydA1) at different pH valu

132 te ligands, in [FeFe]-hydrogenase HydA1 from Chlamydomonas reinhardtii (CrHydA1).

133 ases from Clostridium pasteurianum (CpI) and Chlamydomonas reinhardtii (CrHydA1).

134 mical studies of the [FeFe] hydrogenase from Chlamydomonas reinhardtii, CrHydA1, maturated with the p

135 we have overexpressed and purified ISA1 from Chlamydomonas reinhardtii (CrISA1) and solved the crysta

136 yrosine is able to fulfill this very role in Chlamydomonas reinhardtii cryptochrome.

137 In this study, we show that exposing a Chlamydomonas reinhardtii culture to saturating light (S

138 ynthetic function were recorded for cells of Chlamydomonas reinhardtii cultured under nine different

139 ained hydrogen production in sulfur-deprived Chlamydomonas reinhardtii cultures.

140 ana, Oryza sativa, Physcomitrella patens and Chlamydomonas reinhardtii, demonstrated the utility and

141 t the identification and characterization of Chlamydomonas reinhardtii diacylglycerol acyltransferase

142 hows that the cpSRP system in the green alga Chlamydomonas reinhardtii differs significantly from tha

143 involving a serine/threonine kinase (Stt7 in Chlamydomonas reinhardtii) directs light energy distribu

144 The unicellular green alga Chlamydomonas reinhardtii divides by multiple fission, w

145 The Chlamydomonas reinhardtii DNA-Binding with One Finger (C

146 ks the synthesis of ATP synthase subunits in Chlamydomonas reinhardtii does not exist in maize.

147 A cpld38 mutant of Chlamydomonas reinhardtii does not grow on minimal mediu

148 Chlamydomonas reinhardtii does not require B(12) for gro

149 The model unicellular green alga, Chlamydomonas reinhardtii, employs diverse strategies of

150 ening and sorting of cells of the green alga Chlamydomonas reinhardtii encapsulated in droplets.

151 an VDE (CVDE) gene from the model green alga Chlamydomonas reinhardtii encodes an atypical VDE.

152 Chlamydomonas reinhardtii encodes eight different sHsps

153 tic plant tissues, mouse liver, and cells of Chlamydomonas reinhardtii, Escherichia coli and baker's

154 In anaerobiosis, the green alga Chlamydomonas reinhardtii evolves molecular hydrogen (H(

155 sulfur (S) deprivation, the unicellular alga Chlamydomonas reinhardtii exhibits increased expression

156 riodic beating of an isolated flagellum from Chlamydomonas reinhardtii exhibits probability flux in t

157 tect the release of H2O2 from the green alga Chlamydomonas reinhardtii exposed to either 180 nM funct

158 at position 169 proximal to the H-cluster of Chlamydomonas reinhardtii [FeFe]-hydrogenase (CrHydA1) a

159 Investigations of the reaction of Chlamydomonas reinhardtii [FeFe]-hydrogenase with formal

160 Chlamydomonas reinhardtii figures remarkably in this res

161 rane inlet mass spectrometer to characterize Chlamydomonas reinhardtii flvB insertion mutants devoid

162 Here, we show that FtsH from Chlamydomonas reinhardtii forms heterooligomers comprisi

163 The Chlamydomonas reinhardtii genome encodes all the enzymes

164 Of the five GPDH enzymes in the model alga Chlamydomonas reinhardtii, GPD2 and GPD3 were shown to b

165 of toxic effects of different pesticides on Chlamydomonas reinhardtii green algae.

166 tallographic studies on the unicellular alga Chlamydomonas reinhardtii HAP2 that reveal homology to c

167 The unicellular green alga Chlamydomonas reinhardtii has become an invaluable model

168 igh-level expression of dicistronic genes in Chlamydomonas reinhardtii has been developed.

169 The chloroplast of the green alga Chlamydomonas reinhardtii has been shown to contain the

170 The [FeFe] hydrogenase HydA1 from Chlamydomonas reinhardtii has been studied using (1)H NM

171 l-like cryptochrome (aCRY) of the green alga Chlamydomonas reinhardtii has extended our view on crypt

172 The genome of the green alga Chlamydomonas reinhardtii has multiple genes encoding ty

173 The green alga Chlamydomonas reinhardtii has numerous genes encoding en

174 Sulfur-deprived cells of Chlamydomonas reinhardtii have been shown to produce hyd

175 74 and its domains in vivo, we have utilized Chlamydomonas reinhardtii ift74 mutants.

176 ternalization fluxes (Jint) were measured in Chlamydomonas reinhardtii in order to explore the applic

177 I (PSII) LHC protein LHCBM9 of the microalga Chlamydomonas reinhardtii in terms of expression kinetic

178 ed transient absorbance changes of ChR2 from Chlamydomonas reinhardtii in the visible and infrared re

179 the short-term toxicity for the green algae Chlamydomonas reinhardtii increased and reached EC50 val

180 Chlamydomonas reinhardtii insertion mutants disrupted fo

181 Chlamydomonas reinhardtii intraflagellar transport (IFT)

182 size3 (tla3) DNA insertional transformant of Chlamydomonas reinhardtii is a chlorophyll-deficient mut

183 The green alga Chlamydomonas reinhardtii is a leading unicellular model

184 Channelrhodopsin-2 from Chlamydomonas reinhardtii is a light-gated ion channel.

185 The eyespot of Chlamydomonas reinhardtii is a light-sensitive organelle

186 Chlamydomonas reinhardtii is a motile single-celled fres

187 Chlamydomonas reinhardtii is a unicellular green alga th

188 Chlamydomonas reinhardtii is a unicellular green alga th

189 Chlamydomonas reinhardtii is a unicellular, soil-dwellin

190 The green alga Chlamydomonas reinhardtii is a useful model organism for

191 Chlamydomonas reinhardtii is a widely used reference org

192 The green alga Chlamydomonas reinhardtii is an invaluable reference org

193 The unicellular green alga Chlamydomonas reinhardtii is capable of acclimating spec

194 nthetic hydrogen production in the microalga Chlamydomonas reinhardtii is catalyzed by two [FeFe]-hyd

195 The photosystem II antenna of Chlamydomonas reinhardtii is composed of monomeric and t

196 that the maturation of psaC mutant (mac1) of Chlamydomonas reinhardtii is defective in photosystem I

197 The model green microalga Chlamydomonas reinhardtii is frequently subject to perio

198 the pyrenoid matrix of the unicellular alga Chlamydomonas reinhardtii is not crystalline but behaves

199 Chlamydomonas reinhardtii is one among such photosynthet

200 Chlamydomonas reinhardtii is one of the most important m

201 and cytochrome b6f complex that occurs when Chlamydomonas reinhardtii is starved for nitrogen in the

202 Chlamydomonas reinhardtii is the leading model system fo

203 wing biflagellated single-celled chlorophyte Chlamydomonas reinhardtii is the most widely used alga i

204 a pgrl1 npq4 double mutant in the green alga Chlamydomonas reinhardtii lacking both PGRL1 and LHCSR3

205 c apparatus using a mutant of the green alga Chlamydomonas reinhardtii lacking carotenoids.

206 is the PsbS protein, while in the green alga Chlamydomonas reinhardtii LhcSR proteins appear to be ex

207 In the chloroplast of Chlamydomonas reinhardtii, maturation of psaA mRNA encod

208 In more efficient channelrhodopsins from Chlamydomonas reinhardtii, Mesostigma viride, and Platym

209 ion, we identify a B12-responsive element of Chlamydomonas reinhardtii METE using a reporter gene app

210 Here Chlamydomonas reinhardtii microalga-produced recombinant

211 In Chlamydomonas reinhardtii microtubules and associated pr

212 Mutations in CCDC114, an ortholog of the Chlamydomonas reinhardtii motility gene DCC2, were ident

213 a high similarity among oleaginous microbes Chlamydomonas reinhardtii, Mucor circinelloides and Rhiz

214 We isolated a Chlamydomonas reinhardtii mutant (dhc1b-3) with a temper

215 thesis and growth performances of a knockout Chlamydomonas reinhardtii mutant (pgrl1) deficient in PR

216 tivity in pam71 plants and the corresponding Chlamydomonas reinhardtii mutant cgld1 was restored by s

217 A Chlamydomonas reinhardtii mutant lacking CGL71, a thylak

218 id and starch accumulation is inhibited in a Chlamydomonas reinhardtii mutant lacking the transcripti

219 Surprisingly, a Chlamydomonas reinhardtii mutant null for the ferredoxin

220 The Chlamydomonas reinhardtii mutant stm6 is devoid of the m

221 report here the unanticipated isolation of a Chlamydomonas reinhardtii (mutant5 [mut5]).

222 Forward genetics was used to isolate Chlamydomonas reinhardtii mutants with altered abilities

223 We analyzed two Chlamydomonas reinhardtii mutants, mia1 and mia2, which

224 cerol (TAG) accumulation in starchless (sta) Chlamydomonas reinhardtii mutants, we undertook comparat

225 nt nuclear mutations in the unicellular alga Chlamydomonas reinhardtii, ncc1 and ncc2 (for nuclear co

226 In the green alga Chlamydomonas reinhardtii, non-photochemical quenching b

227 gellates, represented by the green microalga Chlamydomonas reinhardtii, on microparticles.

228 unicellular organisms such as the green alga Chlamydomonas reinhardtii, on sperm cells, and on cells

229 Here we establish that Chlamydomonas reinhardtii, one of many chlorophyte speci

230 ulation of autophagy in the model green alga Chlamydomonas reinhardtii Our results indicate that the

231 Chlamydomonas reinhardtii PF22 is exclusively cytoplasmi

232 eals striking similarity to human PHD2 and a Chlamydomonas reinhardtii prolyl-4-hydroxylase.

233 The Chlamydomonas reinhardtii proton gradient regulation5 (C

234 Flagellar length control in Chlamydomonas reinhardtii provides a simple model system

235 f the ADHE from the photosynthetic microalga Chlamydomonas reinhardtii Purified recombinant ADHE cata

236 When testing with cells (Chlamydomonas reinhardtii), recovery rates as high as 98

237 ediated silencing of the orthologous gene in Chlamydomonas reinhardtii resulted in absent outer dynei

238 particularly abundant in flagellar lipids of Chlamydomonas reinhardtii, resulting in the purification

239 sensor (CAS) protein by an RNAi approach in Chlamydomonas reinhardtii results in strong inhibition o

240 Chlamydomonas reinhardtii's long established role in the

241 State transitions in the green alga Chlamydomonas reinhardtii serve to balance excitation en

242 d light-harvesting antenna2 (tla2) mutant of Chlamydomonas reinhardtii showed a lighter-green phenoty

243 ved fluorescence measured on intact cells of Chlamydomonas reinhardtii shows that independently of th

244 In the unicellular green alga Chlamydomonas reinhardtii, sRNAs derived from genome-int

245 thetic growth and carbon partitioning in the Chlamydomonas reinhardtii starchless mutant, sta6, which

246 algae in particular, like the model organism Chlamydomonas reinhardtii, steer either towards or away

247 To investigate this possible overlap, Chlamydomonas reinhardtii strains were engineered to ove

248 maximize rectification of initially uniform Chlamydomonas reinhardtii suspensions.

249 When the green alga Chlamydomonas reinhardtii swims, it uses the breaststrok

250 ave created a minimal cell of the green alga Chlamydomonas reinhardtii that is able to undergo NPQ.

251 Here, we report in the green alga Chlamydomonas reinhardtii that UVR8 induces accumulation

252 e, we screened for mutants of the model alga Chlamydomonas reinhardtii that, in contrast to wild-type

253 In the green unicellular alga Chlamydomonas reinhardtii, the cytosolic RNA-binding pro

254 mal-like cryptochrome aCRY in the green alga Chlamydomonas reinhardtii This finding was explained by

255 For the model microalga, Chlamydomonas reinhardtii, this has prompted a period of

256 Developed using Chlamydomonas reinhardtii, this method is also successfu

257 or a whole-genome view of the acclimation of Chlamydomonas reinhardtii to anoxic conditions imposed s

258 ied laboratory strains of the model organism Chlamydomonas reinhardtii to characterize genomic divers

259 We subject the alga Chlamydomonas reinhardtii to conditions that favour mult

260 ically grown wild-type and mutant strains of Chlamydomonas reinhardtii to determine the integration o

261 Here, we developed tools in the model alga Chlamydomonas reinhardtii to determine the localizations

262 Here we use the model green alga Chlamydomonas reinhardtii to discover that a low-complex

263 uorescent dyes in the unicellular green alga Chlamydomonas reinhardtii to examine the specificity of

264 mmalian neural tissue, Drosophila brain, and Chlamydomonas reinhardtii to illustrate the power of thi

265 volutionarily distant unicellular green alga Chlamydomonas reinhardtii to quantify the effects of miR

266 ations of the unicellular green chlorophyte, Chlamydomonas reinhardtii, to minimum inhibitory concent

267 a stress-related LHC from the model organism Chlamydomonas reinhardtii, to sense pH variations, rever

268 uration of the [FeFe] hydrogenase HydA1 from Chlamydomonas reinhardtii, to yield the enzyme selective

269 hed four nutritional zinc states in the alga Chlamydomonas reinhardtii: toxic, replete, deficient, an

270 We used RNA sequencing to query the Chlamydomonas reinhardtii transcriptome for regulation b

271 In the chloroplast of the green alga Chlamydomonas reinhardtii, two discontinuous group II in

272 yeast Saccharomyces cerevisiae and the alga Chlamydomonas reinhardtii--two model eukaryotes with ver

273 The green alga Chlamydomonas reinhardtii undergoes gametogenesis and ma

274 the changes the photosynthetic apparatus of Chlamydomonas reinhardtii undergoes upon acclimation to

275 eased by unicellular aquatic microorganisms, Chlamydomonas reinhardtii, upon cadmium exposure.

276 in whole cells of the deuterated green alga Chlamydomonas reinhardtii using high-time-resolution ele

277 e iron nutrition-responsive transcriptome of Chlamydomonas reinhardtii using RNA-Seq methodology.

278 chloroplast ClpP complex from the green alga Chlamydomonas reinhardtii, using a strain that carries t

279 oscopy revealed that MLDP in the chlorophyte Chlamydomonas reinhardtii was associated with endoplasmi

280 FeFe]-hydrogenase HydA1 from the green algae Chlamydomonas reinhardtii was exposed to defined concent

281 he 2pac mutant of the unicellular green alga Chlamydomonas reinhardtii was isolated and found to have

282 d orderly process as we are showing here for Chlamydomonas reinhardtii We conducted comparative trans

283 Using the unicellular green alga Chlamydomonas reinhardtii, we developed a genetic screen

284 Using the green alga Chlamydomonas reinhardtii, we developed an efficient pip

285 ous psbA expression system in the green alga Chlamydomonas reinhardtii, we have measured growth rate,

286 ist in the evolutionarily distant green alga Chlamydomonas reinhardtii, we identified Chlamydomonas o

287 to image the native cellular environment of Chlamydomonas reinhardtii, we observed that nuclear 26S

288 Using the model alga Chlamydomonas reinhardtii, we show that pyrenoid formati

289 Here, using the unicellular microalga Chlamydomonas reinhardtii, we study the impact of hetero

290 contaminated environments, on the microalga Chlamydomonas reinhardtii were assessed using both physi

291 r ciliary and flagellar function in mice and Chlamydomonas reinhardtii, where it localizes to the C1d

292 of total fatty acids in the green microalga Chlamydomonas reinhardtii, where they are present in bot

293 cyltransferase (PDAT) in the green microalga Chlamydomonas reinhardtii, which catalyzes TAG synthesis

294 e]-hydrogenases, CrHydA1 from the green alga Chlamydomonas reinhardtii, which contains only the activ

295 rly understood in the unicellular green alga Chlamydomonas reinhardtii, which contains three AGO para

296 AKOID ENRICHED FRACTION30 (TEF30) protein in Chlamydomonas reinhardtii, which is conserved in the gre

297 Here we use the green alga, Chlamydomonas reinhardtii, which regulates both thiazole

298 rganization, using mutants of the green alga Chlamydomonas reinhardtii with known alterations in cent

299 estigated a cryptochrome from the green alga Chlamydomonas reinhardtii with sequence homology to anim

300 cine algae include isogamous species such as Chlamydomonas reinhardtii, with two equal-sized mating t