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

1 suppressor-related protein of Chlamydomonas (Chlamydomonas reinhardtii).

2 ophy and photo-autotrophy in the green alga (Chlamydomonas reinhardtii).

3 he microbodies of the unicellular green alga Chlamydomonas reinhardtii.

4 he flagellar axoneme in the unicellular alga Chlamydomonas reinhardtii.

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

6 tive cation channel originally discovered in Chlamydomonas reinhardtii.

7 croalgae Pseudokirchneriella subcapitata and Chlamydomonas reinhardtii.

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

9 synchronized cell division in the green alga Chlamydomonas reinhardtii.

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

11 n the photosynthesis of the freshwater algae Chlamydomonas reinhardtii.

12 regulation of lipid biosynthesis in the alga Chlamydomonas reinhardtii.

13 ene expression in the unicellular green alga Chlamydomonas reinhardtii.

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

15 particularly in model microorganisms such as Chlamydomonas reinhardtii.

16 carefully examined for the freshwater alga, Chlamydomonas reinhardtii.

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

18 ssion in the photosynthetic unicellular alga Chlamydomonas reinhardtii.

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

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

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

22 tes in the eukaryotic unicellular green alga Chlamydomonas reinhardtii.

23 lementary approaches for the living cells of Chlamydomonas reinhardtii.

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

25 tivation in the model unicellular green alga Chlamydomonas reinhardtii.

26 algae closely related to the model organism Chlamydomonas reinhardtii.

27 rs that bind ciliary doublet microtubules in Chlamydomonas reinhardtii.

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

29 ible chloroplast gene expression in the alga Chlamydomonas reinhardtii.

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

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

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

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

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

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

36 against antigens in total cell lysates from Chlamydomonas reinhardtii.

37 of uniciliated mutants of the swimming alga, Chlamydomonas reinhardtii.

38 reproduction in the unicellular green alga, Chlamydomonas reinhardtii.

39 d insertion mutants for the unicellular alga Chlamydomonas reinhardtii.

40 present the structure of procentrioles from Chlamydomonas reinhardtii.

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

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

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

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

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

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

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

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

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

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

51 Chlamydomonas reinhardtii, a unicellular alga, is a good

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

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

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

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

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

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

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

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

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

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

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

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

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

65 on three types of genomes (Escherichia coli, Chlamydomonas reinhardtii and human genomes).

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

67 cetate-requiring) DNA insertional mutants of Chlamydomonas reinhardtii and isolated cpsfl1 The cpsfl1

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

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

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

71 ncommon glycans stemming from the green alga Chlamydomonas reinhardtii and the archaeon Haloferax vol

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

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

74 plast-localized TF (TIG1) in the green alga (Chlamydomonas reinhardtii) and the vascular land plant A

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

76 fferent components of axonemes purified from Chlamydomonas reinhardtii, and characterize their proper

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

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

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

80 We study phototaxis of single-celled algae Chlamydomonas reinhardtii as a function of cell number d

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

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

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

84 We used Chlamydomonas reinhardtii as a reference organism for a

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

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

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

88 served in the model photosynthetic microalga Chlamydomonas reinhardtii, but the substrates of TOR kin

89 nologically useful mutants of the green alga Chlamydomonas reinhardtii by incoherent neutron scatteri

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

91 We report here that Chlamydomonas reinhardtii can accumulate manganese (Mn)

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

93 nds selected by high-throughput screening in Chlamydomonas reinhardtii can induce lipid accumulation

94 for the in-depth study of arsenate uptake by Chlamydomonas reinhardtii cells and of the effect this t

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

96 Chlamydomonas reinhardtii cells exposed to abiotic stres

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

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

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

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

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

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

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

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

105 ermittent-light conditions in the green alga Chlamydomonas reinhardtii Chlororespiration, which is lo

106 asuring the lipid composition of microalgae, Chlamydomonas reinhardtii (ChRe) and Euglena gracilis (E

107 The Chlamydomonas reinhardtii Compromised Hydrolysis of Tria

108 In the alga Chlamydomonas reinhardtii, condensation is mediated by t

109 Here we show that the green alga Chlamydomonas reinhardtii contains a 5mC-modifying enzym

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

111 In Chlamydomonas reinhardtii, conventional actin is found i

112 -response relationships in Chlorococcum sp., Chlamydomonas reinhardtii CPCC 12 and 243 than Asterococ

113 native, heterogeneous thylakoid membranes of Chlamydomonas reinhardtii (Cr) and on Cr light-harvestin

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

115 The animal-like cryptochrome of Chlamydomonas reinhardtii (CraCRY) is a recently discove

116 was tested in a heterologous assay using the Chlamydomonas reinhardtii CrATG8 protein as a substrate.

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

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

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

120 the [FeFe] hydrogenase from the green algae Chlamydomonas reinhardtii ( CrHydA1) was exchanged with

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

122 ases from Clostridium pasteurianum (CpI) and Chlamydomonas reinhardtii (CrHydA1) we have conducted si

123 ediate states in the [FeFe] hydrogenase from Chlamydomonas reinhardtii (CrHydA1), using a laser-induc

124 troscopy to an [FeFe] model hydrogenase from Chlamydomonas reinhardtii (CrHydA1), we have discovered

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

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

127 f PRK from two model species: the green alga Chlamydomonas reinhardtii (CrPRK) and the land plant Ara

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

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

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

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

132 mproved performance than existing methods on Chlamydomonas reinhardtii data.

133 Here, we characterized Chlamydomonas reinhardtii DEG1C, which together with DEG

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

135 ependent phosphorylation pattern compared to Chlamydomonas reinhardtii despite comparable levels of t

136 t the identification and characterization of Chlamydomonas reinhardtii diacylglycerol acyltransferase

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

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

139 The unicellular green alga Chlamydomonas reinhardtii displays metabolic flexibility

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

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

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

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

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

145 Chlamydomonas reinhardtii encodes eight different sHsps

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

147 spectroscopy on the [FeFe]-hydrogenase from Chlamydomonas reinhardtii evaluating dynamic changes in

148 The green alga Chlamydomonas reinhardtii evolved blue light-excited cha

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

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

151 The unicellular alga Chlamydomonas (Chlamydomonas reinhardtii) exhibits oriented movement re

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

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

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

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

156 he chloroplast genome of the green microalga Chlamydomonas reinhardtii for the expression of a dsRNA

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

158 We sequence a human genome HX1 and a Chlamydomonas reinhardtii genome using Nanopore sequenci

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

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

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

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

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

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

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

166 n animal-like cryptochrome in the green alga Chlamydomonas reinhardtii has expanded the spectral rang

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

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

169 t (SSU) of Rubisco and pyrenoid formation in Chlamydomonas reinhardtii has previously suggested that

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

171 ironmental variability, green algae, such as Chlamydomonas reinhardtii, have evolved multiple physiol

172 ysiological studies using the model organism Chlamydomonas reinhardtii, have revealed the function an

173 erredoxin protein in the alga Chlamydomonas (Chlamydomonas reinhardtii), helps maintain thylakoid mem

174 ng cytochrome b (559) Complementation of the Chlamydomonas reinhardtii (hereafter Chlamydomonas) RBD1

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

176 as validated with a suspension of green alga Chlamydomonas reinhardtii in interaction with an exogeno

177 al evolution of the non-B(12)-requiring alga Chlamydomonas reinhardtii in media supplemented with B(1

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

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

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

181 Chlamydomonas reinhardtii insertion mutants disrupted fo

182 In the bi-ciliated, unicellular alga Chlamydomonas reinhardtii, interactions between cilia of

183 The unicellular alga Chlamydomonas reinhardtii is a classical reference organ

184 The green alga Chlamydomonas reinhardtii is a leading model system to s

185 The green alga Chlamydomonas reinhardtii is a leading unicellular model

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

187 Chlamydomonas reinhardtii is a motile single-celled fres

188 Chlamydomonas reinhardtii is a unicellular green alga ex

189 Chlamydomonas reinhardtii is a unicellular green alga th

190 Chlamydomonas reinhardtii is a unicellular green alga th

191 Chlamydomonas reinhardtii is a unicellular, soil-dwellin

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

193 Chlamydomonas reinhardtii is a widely used reference org

194 The green alga Chlamydomonas reinhardtii is an invaluable reference org

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

196 The unicellular green alga Chlamydomonas reinhardtii is capable of photosynthetic H

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

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

199 The unicellular green alga Chlamydomonas reinhardtii is evolutionarily divergent fr

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

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

202 Chlamydomonas reinhardtii is one among such photosynthet

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

204 Chlamydomonas reinhardtii is the leading model system fo

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

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

207 at NPQ activation by high light treatment in Chlamydomonas reinhardtii leads to energy quenching in b

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

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

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

211 Here Chlamydomonas reinhardtii microalga-produced recombinant

212 In Chlamydomonas reinhardtii microtubules and associated pr

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

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

215 ounts of Asc, we searched for an insertional Chlamydomonas reinhardtii mutant affected in theVTC2 gen

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 AG homeostasis, we isolated a Chlamydomonas (Chlamydomonas reinhardtii) mutant (bkdE1alpha) that is d

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

223 ooperative protection, here we characterized Chlamydomonas reinhardtii mutants lacking the mitochondr

224 We isolated Chlamydomonas reinhardtii mutants that disrupt cpUPR sig

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

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

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

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

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

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

231 ions, the kinase STATE TRANSITION7 (STT7) of Chlamydomonas reinhardtii phosphorylates components of l

232 s of three essential outlets associated with Chlamydomonas reinhardtii photosynthetic electron transp

233 The flagella of Chlamydomonas reinhardtii possess fibrous ultrastructure

234 The green alga Chlamydomonas reinhardtii possesses a CO(2) concentratin

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

236 The Chlamydomonas reinhardtii proton gradient regulation5 (C

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

238 Chlamydomonas reinhardtii, Pseudokirchneriella subcapita

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

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

241 Here we show that the green microalga Chlamydomonas reinhardtii reduces NO into N(2)O using th

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

243 Here, we reconstituted the Chlamydomonas reinhardtii RS head that abuts the CP and

244 Chlamydomonas reinhardtii's long established role in the

245 pecies in a lipid extract of a green algae ( Chlamydomonas reinhardtii) sample.

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

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

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

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

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

251 maximize rectification of initially uniform Chlamydomonas reinhardtii suspensions.

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

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

254 potential (TRP) channel crTRP1 from the alga Chlamydomonas reinhardtii that opens in response to incr

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

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

257 In the model green alga Chlamydomonas reinhardtii, the capacity for rapidly reve

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

259 In the green alga Chlamydomonas reinhardtii, the LHCSR pigment-binding pro

260 s and could also confirm that in contrast to Chlamydomonas reinhardtii, the scaffold Y complex is arr

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

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

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

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

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

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

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

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

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

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

271 orescence microscopy in the unicellular alga Chlamydomonas reinhardtii to reveal spatiotemporal organ

272 ed populations of the unicellular green alga Chlamydomonas reinhardtii to selection by the filter-fee

273 ed the response of a freshwater green alga ( Chlamydomonas reinhardtii) to copper.

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

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

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

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

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

279 The green alga Chlamydomonas reinhardtii undergoes gametogenesis and ma

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

281 Here we investigated NPQ in Chlamydomonas reinhardtii using an approach that maintai

282 aling in the model green alga Chlamydomonas (Chlamydomonas reinhardtii) via LST8, a conserved TORC1 s

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

284 The green photosynthetic algae Chlamydomonas reinhardtii was immobilized on carbon blac

285 F TRIACYLGLYCEROLS7 (CHT7) in Chlamydomonas (Chlamydomonas reinhardtii) was previously shown to affec

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

287 have used one such organism, the green alga Chlamydomonas reinhardtii We found that although F-actin

288 he properties of the single cellular species Chlamydomonas reinhardtii We show that B. braunii shares

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

290 molecular landscape of the unicellular alga Chlamydomonas reinhardtii, we discovered that the cytoso

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

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

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

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

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

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

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

298 The single-celled green algae Chlamydomonas reinhardtii with its two flagella-microtub

299 Here, we crossed MA lines of the green alga Chlamydomonas reinhardtii with its unmutated ancestral s

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