ライフサイエンスコーパス: Chlamydomonas

1 rs) in ciliary ectosomes from the green alga Chlamydomonas.

2 tworks governed by the TOR kinase pathway in Chlamydomonas.

3 nd is essential for atpI mRNA translation in Chlamydomonas.

4 y low CO(2) (< 0.02% CO(2) ) state, exist in Chlamydomonas.

5 e photomobility of microalgae from the genus Chlamydomonas.

6 that facilitates flagellar length control in Chlamydomonas.

7 nd thereby influence flagellar shortening in Chlamydomonas.

8 l gene silencing relies primarily on AGO3 in Chlamydomonas.

9 normally has a growth-stimulatory effect on Chlamydomonas.

10 major mediator of P deprivation responses in Chlamydomonas.

11 iple-fission cycles and cell-size control in Chlamydomonas.

12 t TORC1 is a key component in P signaling in Chlamydomonas.

13 the adaptation of phototactic sensitivity in Chlamydomonas.

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

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

16 al characterization of filamentous actins in Chlamydomonas, allowing insights into the coordinated fu

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

18 pectrometry to compare axonemes of wild-type Chlamydomonas and a CA-less mutant.

19 Chloromonas, Chlamydomonas and Chlorella were found in green blooms b

20 length control in the single cell organisms Chlamydomonas and Giardia.

21 Using Chlamydomonas and human telomerase reverse transcriptase

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

23 ulates cell division in the mat3-4 mutant of Chlamydomonas and provides yet another important example

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

25 Our study in Chlamydomonas and the presence of PAM in mammalian cilia

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

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

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

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

30 Here, we characterize AGO2 and 3 in Chlamydomonas, and show that cytoplasmically enriched Cr

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

32 These findings indicate that the Chlamydomonas AOX proteins can participate in acclimatio

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

34 sessing a biallelic mating-type locus (e.g., Chlamydomonas, ascomycete fungi).

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 e a critical component of Mn accumulation in Chlamydomonas by driving Mn relocation from the cytosol

38 By contrast, the photosynthetic green alga Chlamydomonas can grow more than 8-fold during daytime a

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

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

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

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

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

44 e environment is a fundamental aspect in the Chlamydomonas CCM, and consists of CO(2) and HCO(3) (-)

45 of a "commitment point" during the growth of Chlamydomonas cells and hint at intriguing similarities

46 that in physiologically relevant conditions, Chlamydomonas cells are prepared to immediately activate

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

48 cs, and metabolomics data were acquired from Chlamydomonas cells grown in the presence of one of two

49 multiple-fission cycles and the response of Chlamydomonas cells to different light-dark regimes.

50 ate in cilia of mammalian photoreceptors and Chlamydomonas cells when BBSome function is compromised.

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

52 In Chlamydomonas cells, the assembly dynamics of its two fl

53 In the green alga Chlamydomonas (Chlamydomonas r einhardtii), chloroplast

54 The unicellular alga Chlamydomonas (Chlamydomonas reinhardtii) exhibits orien

55 ic screen for TAG homeostasis, we isolated a Chlamydomonas (Chlamydomonas reinhardtii) mutant (bkdE1a

56 ates TORC1 signaling in the model green alga Chlamydomonas (Chlamydomonas reinhardtii) via LST8, a co

57 ED HYDROLYSIS OF TRIACYLGLYCEROLS7 (CHT7) in Chlamydomonas (Chlamydomonas reinhardtii) was previously

58 DX5), a minor ferredoxin protein in the alga Chlamydomonas (Chlamydomonas reinhardtii), helps maintai

59 blastoma tumor suppressor-related protein of Chlamydomonas (Chlamydomonas reinhardtii).

60 Unexpectedly, division of the large Chlamydomonas chloroplast was delayed in the cells lacki

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

62 rotein MST1, to the extracellular surface of Chlamydomonas cilia.

63 ment of an in vitro SUMOylation system using Chlamydomonas components and use it to provide evidence

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

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

66 Unlike the model alga Chlamydomonas, de novo fatty acid synthesis in C. zofing

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

68 ailed functional and biochemical analyses of Chlamydomonas DGTTs.

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

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

71 Among the findings are the observations that Chlamydomonas exhibits lower respiratory activity at nig

72 contrast with what was recently observed in Chlamydomonas Experimental trends are quantitatively des

73 In addition to two actin genes, Chlamydomonas expresses a profilin (PRF1) and four formi

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

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

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

77 blet sliding resistance in these immobilized Chlamydomonas flagella.

78 Recombinant Chlamydomonas GPD2 showed both reductase and phosphatase

79 o date, the filamentous actin network within Chlamydomonas has remained elusive.

80 Genetic screens in the model alga Chlamydomonas have demonstrated that transgene silencing

81 Our results include Chlamydomonas homologs of TOR signaling-related proteins

82 iliary roles of two mammalian orthologues of Chlamydomonas IFT-A gene, IFT139, namely Thm1 (also know

83 Deletion of residues 342-356 of Chlamydomonas IFT54 resulted in diminished anterograde t

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

85 limate in the low and very low CO(2) states, Chlamydomonas induces a sophisticated strategy known as

86 Screening of a Chlamydomonas insertional mutant library identified a st

87 Flagellar length control in Chlamydomonas is a tractable model system for studying t

88 contains exclusively conventional F-actin in Chlamydomonas is the fertilization tubule, a mating stru

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

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

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

92 ggesting that FDX5 may have other effects on Chlamydomonas metabolism through its interaction with mu

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

94 ext of a theoretical model for regulation of Chlamydomonas multiple fission, these results suggest th

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

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

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

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

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

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

101 ructural studies, including newly identified Chlamydomonas pacrg mutants.

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 structures supports a mechanosensory role of Chlamydomonas PKD2.

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

107 The green alga Chlamydomonas proliferates by "multiple fission": a long

108 In the green alga Chlamydomonas (Chlamydomonas r einhardtii), chloroplast gene expression

109 of the Chlamydomonas reinhardtii (hereafter Chlamydomonas) RBD1-deficient 2pac mutant with construct

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

145 The Chlamydomonas reinhardtii Compromised Hydrolysis of Tria

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

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

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

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

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

151 mproved performance than existing methods on Chlamydomonas reinhardtii data.

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

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

154 The unicellular green alga Chlamydomonas reinhardtii displays metabolic flexibility

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

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

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

158 Chlamydomonas reinhardtii encodes eight different sHsps

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

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

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

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

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

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

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

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

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

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

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

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

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

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

173 The unicellular alga Chlamydomonas reinhardtii is a classical reference organ

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

175 Chlamydomonas reinhardtii is a unicellular green alga ex

176 Chlamydomonas reinhardtii is a unicellular green alga th

177 The green alga Chlamydomonas reinhardtii is an invaluable reference org

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

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

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

181 The unicellular green alga Chlamydomonas reinhardtii is evolutionarily divergent fr

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

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

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

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

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

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

188 The Chlamydomonas reinhardtii mutant stm6 is devoid of the m

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

190 We isolated Chlamydomonas reinhardtii mutants that disrupt cpUPR sig

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

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

193 The flagella of Chlamydomonas reinhardtii possess fibrous ultrastructure

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

229 Chlamydomonas reinhardtii, a unicellular alga, is a good

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

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

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

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

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

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

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

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

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

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

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

241 Chlamydomonas reinhardtii, Pseudokirchneriella subcapita

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

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

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

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

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

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

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

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

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

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

252 reproduction in the unicellular green alga, Chlamydomonas reinhardtii.

253 d insertion mutants for the unicellular alga Chlamydomonas reinhardtii.

254 present the structure of procentrioles from Chlamydomonas reinhardtii.

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

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

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

258 he microbodies of the unicellular green alga Chlamydomonas reinhardtii.

259 he flagellar axoneme in the unicellular alga Chlamydomonas reinhardtii.

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

261 tive cation channel originally discovered in Chlamydomonas reinhardtii.

262 particularly in model microorganisms such as Chlamydomonas reinhardtii.

263 rs that bind ciliary doublet microtubules in Chlamydomonas reinhardtii.

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

265 targeted nuclear gene editing broadly hinder Chlamydomonas research.

266 nt classes of MTs in metaphase spindles from Chlamydomonas rheinhardti and two strains of cultured ma

267 Chlamydomonas RPL23 sequences also enabled transgene exp

268 In the unicellular alga Chlamydomonas, several metazoans, and land plants, emerg

269 Chlamydomonas shows apparent UV-B acclimation in colony

270 The unicellular green alga Chlamydomonas sp. ICE-L thrives in polar sea ice, where

271 The Antarctic green alga Chlamydomonas sp. UWO 241 (UWO 241) is adapted to perman

272 The Antarctic psychrophile Chlamydomonas sp. UWO241 evolved in a permanently ice-co

273 3)P]ATP labeling of thylakoid membranes from Chlamydomonas sp. UWO241 exhibited a distinct low temper

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

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

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

277 Wild-type and AZD-insensitive Chlamydomonas strains were treated with TOR-specific che

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

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

280 here we describe a mutant in the model alga Chlamydomonas that has on average 10 pyrenoids per chlor

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

282 In Chlamydomonas, the photoreceptors for phototaxis are the

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

284 cross species from the unicellular eukaryote Chlamydomonas to humans.

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

286 ics to investigate the effects of inhibiting Chlamydomonas TOR kinase on dynamic protein phosphorylat

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

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

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

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

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

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

293 Here we show that Chlamydomonas VIG1, an ortholog of the Drosophila melano

294 Much of the early appeal of Chlamydomonas was rooted in its promise as a genetic sys

295 We have now identified a Chlamydomonas wdr92 mutant that encodes a protein missin

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

297 trans-acting factors characterized so far in Chlamydomonas, which control the expression of a single

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

299 omography, we have compared the structure of Chlamydomonas wild-type flagella to that of strains with

300 on tomography to compare the CA of wild-type Chlamydomonas with CA mutants.