ライフサイエンスコーパス: Chlamydomonas

1 l gene silencing relies primarily on AGO3 in Chlamydomonas.

2 normally has a growth-stimulatory effect on Chlamydomonas.

3 ssibilities for biotechnological research in Chlamydomonas.

4 conduct and interpret their experiments with Chlamydomonas.

5 fied the 6mA modification in 84% of genes in Chlamydomonas.

6 overcome the transgene expression problem in Chlamydomonas.

7 vation and investigation of gene function in Chlamydomonas.

8 e membrane, the location of MGDG synthase in Chlamydomonas.

9 flagella in protists, such as Paramecia and Chlamydomonas.

10 nuclear factors act on chloroplast mRNAs in Chlamydomonas.

11 let number 1, which completely lacks ODAs in Chlamydomonas.

12 erize genome-wide diurnal gene expression in Chlamydomonas.

13 iology of the multiple-fission cell cycle of Chlamydomonas.

14 of ISA1 and ISA2 from starch producing alga Chlamydomonas.

15 e photomobility of microalgae from the genus Chlamydomonas.

16 that facilitates flagellar length control in Chlamydomonas.

17 nd thereby influence flagellar shortening in Chlamydomonas.

18 ence suggests that this is not applicable to Chlamydomonas, a biflagellate fresh water green alga, bu

19 amydomonas as a model, and to illustrate how Chlamydomonas acclimates to limiting CO2 conditions and

20 ar transport (IFT) in humans and the protist Chlamydomonas, accompanied by destabilization of the ret

21 The Chlamydomonas alkene was identified as 7-heptadecene, an

22 Interestingly, Chlamydomonas also possesses two PsbS genes, but so far

23 ts as cpSRP43 is not complexed to cpSRP54 in Chlamydomonas and cpSRP54 is not involved in LHCP recogn

24 ng amidated bioactive signaling peptides, in Chlamydomonas and mammalian cilia.

25 eramide that is critical for ciliogenesis in Chlamydomonas and murine ependymal cells, respectively.

26 igating a variety of biological processes in Chlamydomonas and other eukaryotes.

27 Recent work with the green alga Chlamydomonas and the nematode C. elegans demonstrated t

28 as to identify chloroplast-targeted sHsps in Chlamydomonas and to obtain a comprehensive list of the

29 More than 25 years after its development for Chlamydomonas and tobacco, the transformation of the chl

30 ong constitutive expression of transgenes in Chlamydomonas, and develops a general approach for ident

31 ior; this includes phase locking, as seen in Chlamydomonas, and metachronal wave formation in the res

32 repair capacity, including Xenopus oocytes, Chlamydomonas, and Stentor coeruleus Although many open

33 etic relatives, Chlamydomonas leiostraca and Chlamydomonas applanata In fact, at approximately 230 kb

34 n with carbon assimilation, based largely on Chlamydomonas as a model, and to illustrate how Chlamydo

35 f the long timescale phototactic motility of Chlamydomonas at both single cell and population levels.

36 Channelrhodopsin-1 from Chlamydomonas augustae (CaChR1) exhibits a red-shifted a

37 Channelrhodopsin-1 from the alga Chlamydomonas augustae (CaChR1) is a low-efficiency ligh

38 the intricacies of dark anoxic metabolism in Chlamydomonas, but also discuss aspects of dark oxic met

39 Inhibition of SPT in Chlamydomonas by myriocin led to loss of flagella and re

40 In Chlamydomonas, calmodulin and spoke-associated complex (

41 Labeling kinetics indicate that Chlamydomonas can import lipid precursors from the ER, a

42 n steady-state systems, endogenous miRNAs in Chlamydomonas can regulate gene expression both by desta

43 blastoma cell cycle regulator in unicellular Chlamydomonas causes it to become colonial.

44 Recent advances in our understanding of the Chlamydomonas CCM 55 III.

45 Current gaps in our understanding of the Chlamydomonas CCM 58 IV.

46 to rapidly advance our understanding of the Chlamydomonas CCM 58 V.

47 The Chlamydomonas cell cycle consists of a long G1 phase, fo

48 The Chlamydomonas cell cycle has a striking temporal and fun

49 The Chlamydomonas cell cycle is synchronized by light-dark c

50 review the current status of studies of the Chlamydomonas cell cycle.

51 henotype for further characterization of the Chlamydomonas cell cycle.

52 recent genetic approaches and insights into Chlamydomonas cell-cycle regulation that have been enabl

53 ncoding glycerol kinase were up-regulated in Chlamydomonas cells exposed to high salinity.

54 Vitreous Chlamydomonas cells were thinned by cryo-focused ion bea

55 ng cryo-focused ion beam milling of vitreous Chlamydomonas cells with cryo-electron tomography, we ac

56 Accordingly, incubation of intact Chlamydomonas cells with per-deuterated D31-16:0 (palmit

57 esired trait as part of a mechanism enabling Chlamydomonas chloroplasts to rapidly react to thermal s

58 This makes the single septin from Chlamydomonas (CrSEPT) a particularly attractive model f

59 that is located in the thylakoid lumen, the Chlamydomonas CVDE protein is located on the stromal sid

60 ted with WDR34, a mammalian homologue of the Chlamydomonas cytoplasmic dynein 2 intermediate chain th

61 ve this conundrum, we identified a mutant of Chlamydomonas deleted in the TGD2 gene and characterized

62 s are of particular interest with respect to Chlamydomonas development and behavior.

63 ailed functional and biochemical analyses of Chlamydomonas DGTTs.

64 ids suggests that Chlamydomonas reinhardtii (Chlamydomonas) does not use the ER pathway; however, the

65 pression and PsbS and LhcSR3 accumulation in Chlamydomonas during high light stress.

66 We tested the time-of-flight model using Chlamydomonas dynein mutant cells, which show slower ret

67 We show for the first time that Chlamydomonas expresses serine palmitoyl transferase (SP

68 Tyr-216-GSK3 (pYGSK3) at the base and tip of Chlamydomonas flagella and motile cilia in ependymal cel

69 nd interdoublet shear stiffness of wild-type Chlamydomonas flagella in vivo, rendered immotile by van

70 t accords best with the bending waveforms of Chlamydomonas flagella.

71 blet sliding resistance in these immobilized Chlamydomonas flagella.

72 three-dimensional structure of the N-DRC in Chlamydomonas flagella.

73 movement of single IFT trains and motors in Chlamydomonas flagella.

74 We study 6mA at base resolution in the Chlamydomonas genome and apply the new method to two oth

75 s) does not use the ER pathway; however, the Chlamydomonas genome encodes presumed plant orthologues

76 ng of 6mA and its unique distribution in the Chlamydomonas genome suggest potential regulatory roles

77 found in the Nannochloropsis, Chlorella, or Chlamydomonas genomes.

78 In Chlamydomonas, GFP-tagged alpha-tubulin enters cilia as

79 Recombinant Chlamydomonas GPD2 showed both reductase and phosphatase

80 tions and, surprisingly, also suggested that Chlamydomonas has other pathways that generate acetate i

81 Here, we present the Chlamydomonas high-lipid sorting (CHiLiS) strategy, whic

82 Despite the demonstration of gene editing in Chlamydomonas in 1995, the isolation of mutants lacking

83 w source of genetic diversity for studies of Chlamydomonas, including naturally occurring alleles tha

84 we showed that cilium-generated signaling in Chlamydomonas induced rapid, anterograde IFT-independent

85 Screening of a Chlamydomonas insertional mutant library identified a st

86 Our data support previous observations that Chlamydomonas is among the most diverse eukaryotic speci

87 oteins in the nucleocytosolic compartment of Chlamydomonas is greatly hampered by the inefficiency of

88 han 50% increase in coverage of the enriched Chlamydomonas kinome over coverage found with no enrichm

89 Homologs of GUN4 from Synechocystis and Chlamydomonas lack the conserved phosphorylation site fo

90 its closest known photosynthetic relatives, Chlamydomonas leiostraca and Chlamydomonas applanata In

91 ht harvesting AcpPC protein with homology to Chlamydomonas LHCSR2.

92 Additionally, Chlamydomonas miRNAs were not conserved, even in algae o

93 We characterized a Chlamydomonas mutant defective in the N-DRC subunit DRC3

94 In a previously generated Chlamydomonas mutant, gravimetric measurements of crude

95 We previously reported a Chlamydomonas mutant, ift46-1, that fails to express the

96 We show that flagella of Chlamydomonas mutants deficient in filamentary connectio

97 The flagella in Chlamydomonas ndk5 mutant were paralyzed, albeit only de

98 genes has been successfully expressed in the Chlamydomonas nuclear genome, including transformation m

99 images of chloroplast structure in the alga Chlamydomonas offer new insights into photosynthesis.

100 lga Chlamydomonas reinhardtii, we identified Chlamydomonas orthologs of UVR8 and the key signaling fa

101 our understanding of carbon concentration in Chlamydomonas, outlines the most pressing gaps in our kn

102 Chlamydomonas PAM knockdown lines failed to assemble cil

103 ow that pCRY is involved in gametogenesis in Chlamydomonas pCRY is down-regulated in pregametes and g

104 iated Antigen 6 (SPAG6) is the orthologue of Chlamydomonas PF16, a protein localized in the axoneme c

105 Mammalian Spag6 is the orthologue of Chlamydomonas PF16, which encodes a protein localized in

106 rmal assembly of motile and primary cilia in Chlamydomonas, planaria and mice.

107 Thus, starch biosynthesis in Chlamydomonas plays a critical role as a principal carbo

108 served lattice arrangement of Rubisco in the Chlamydomonas pyrenoid.

109 e to antimycin A than the mesophile control, Chlamydomonas raudensis SAG 49.72.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 Chlamydomonas reinhardtii encodes eight different sHsps

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

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

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

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

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

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

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

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

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

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

165 74 and its domains in vivo, we have utilized Chlamydomonas reinhardtii ift74 mutants.

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

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

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

169 The green alga Chlamydomonas reinhardtii is a leading unicellular model

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

171 Chlamydomonas reinhardtii is a motile single-celled fres

172 Chlamydomonas reinhardtii is a unicellular green alga th

173 Chlamydomonas reinhardtii is a unicellular green alga th

174 Chlamydomonas reinhardtii is a unicellular, soil-dwellin

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

176 Chlamydomonas reinhardtii is a widely used reference org

177 The green alga Chlamydomonas reinhardtii is an invaluable reference org

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

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

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

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

182 Chlamydomonas reinhardtii is one among such photosynthet

183 Chlamydomonas reinhardtii is the leading model system fo

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

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

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

187 Here Chlamydomonas reinhardtii microalga-produced recombinant

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

189 A Chlamydomonas reinhardtii mutant lacking CGL71, a thylak

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

191 Surprisingly, a Chlamydomonas reinhardtii mutant null for the ferredoxin

192 The Chlamydomonas reinhardtii mutant stm6 is devoid of the m

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

209 The green alga Chlamydomonas reinhardtii undergoes gametogenesis and ma

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

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

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

213 Chlamydomonas reinhardtii's long established role in the

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

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

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

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

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

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

220 Chlamydomonas reinhardtii, a unicellular alga, is a good

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

250 he flagellar axoneme in the unicellular alga Chlamydomonas reinhardtii.

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

252 tive cation channel originally discovered in Chlamydomonas reinhardtii.

253 croalgae Pseudokirchneriella subcapitata and Chlamydomonas reinhardtii.

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

255 synchronized cell division in the green alga Chlamydomonas reinhardtii.

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

257 n the photosynthesis of the freshwater algae Chlamydomonas reinhardtii.

258 regulation of lipid biosynthesis in the alga Chlamydomonas reinhardtii.

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

260 ene expression in the unicellular green alga Chlamydomonas reinhardtii.

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

262 carefully examined for the freshwater alga, Chlamydomonas reinhardtii.

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

264 ssion in the photosynthetic unicellular alga Chlamydomonas reinhardtii.

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

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

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

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

269 he microbodies of the unicellular green alga Chlamydomonas reinhardtii.

270 In order to facilitate ongoing Chlamydomonas research and explain the phenotypic variat

271 targeted nuclear gene editing broadly hinder Chlamydomonas research.

272 Chlamydomonas RPL23 sequences also enabled transgene exp

273 y, ChlaMmeSeq allows genotyping of hits from Chlamydomonas screens on an unprecedented scale, opening

274 Chlamydomonas shows apparent UV-B acclimation in colony

275 Chlamydomonas sp. UWO 241 (UWO 241) is a psychrophilic g

276 Arabidopsis rbcs mutants expressing a Chlamydomonas SSU differed from wild-type plants with re

277 optimized gene-editing protocols for several Chlamydomonas strains (including wild-type CC-125) using

278 ble easy maintenance of tens of thousands of Chlamydomonas strains by propagation on agar media and b

279 Here we analyze Chlamydomonas strains expressing different amounts of th

280 We also reanalyzed miRNA expression data in Chlamydomonas subject to sulfur or phosphate deprivation

281 was detected at the base of the flagella in Chlamydomonas, suggesting that CrSEPT is involved in the

282 te that pCRY is a key blue light receptor in Chlamydomonas that is involved in both circadian timing

283 ntraflagellar Transport 172 Homolog [IFT172 (Chlamydomonas)] that underlie an isolated retinal degene

284 In Chlamydomonas, three assembly factors--ODA5, ODA8, and O

285 unicellular alga Chlamydomonas reinhardtii (Chlamydomonas throughout) has both an animal-like crypto

286 Here, we use the unicellular alga Chlamydomonas to characterize contributions of key regio

287 s, we have taken advantage of the biology of Chlamydomonas to isolate TZs.

288 hese new tools and explored the potential of Chlamydomonas to produce a recombinant biopharmaceutical

289 uce acclimation, led to broad changes in the Chlamydomonas transcriptome, including in genes related

290 f the time-of-flight model and suggests that Chlamydomonas uses another length-control feedback syste

291 notypes of two mutations in the DRC2 gene of Chlamydomonas Using high-resolution proteomic and struct

292 We screened the unicellular green alga Chlamydomonas using insertional mutagenesis to find muta

293 alysis of the 6mA landscape in the genome of Chlamydomonas using new sequencing approaches.

294 rganism, the alga Chlamydomonas reinhardtii (Chlamydomonas), using mass spectrometry-based label-free

295 utilization localizes mainly to 3' UTRs, in Chlamydomonas utilized target sites lie predominantly wi

296 Chlamydomonas UV-B acclimation preserved the photosystem

297 e role of PsbS in NPQ and photoprotection in Chlamydomonas, we generated transplastomic strains expre

298 rategy to identify highly expressed genes in Chlamydomonas whose flanking sequences were tested for t

299 oteins showed the ability to increase NPQ in Chlamydomonas wild-type and npq4 (lacking LhcSR3) backgr

300 The position of Chlamydomonas within the eukaryotic phylogeny makes it a