ライフサイエンスコーパス: Caenorhabditis elegans

1 erves this function in human cells (LEM-3 in Caenorhabditis elegans).

2 obes in a complex multicellular model (i.e., Caenorhabditis elegans).

3 f two new SC components, SYP-5 and SYP-6, in Caenorhabditis elegans.

4 of proteins to chemosensory cilia in living Caenorhabditis elegans.

5 homologous recombination-mediated repair in Caenorhabditis elegans.

6 rous iron accumulates over adult lifetime in Caenorhabditis elegans.

7 tol's effects on fatty acid metabolism using Caenorhabditis elegans.

8 e molecular bases of this organization using Caenorhabditis elegans.

9 g m(5)C at position C2381 on the 26S rRNA in Caenorhabditis elegans.

10 ll ferroptosis and sterility in the nematode Caenorhabditis elegans.

11 cleavage to attract glia during migration in Caenorhabditis elegans.

12 during embryonic development of the nematode Caenorhabditis elegans.

13 ween Pseudomonas aeruginosa and the nematode Caenorhabditis elegans.

14 n an in vivo system using the model organism Caenorhabditis elegans.

15 e been best described for the model organism Caenorhabditis elegans.

16 mentally identified piRNA targeting sites in Caenorhabditis elegans.

17 ting the speed of locomotion of the nematode Caenorhabditis elegans.

18 educe lipid storage and promote longevity in Caenorhabditis elegans.

19 n structural analysis in vivo (IV-FPOP) with Caenorhabditis elegans.

20 alpha-synuclein-driven neurodegeneration in Caenorhabditis elegans.

21 , followed by functional characterization in Caenorhabditis elegans.

22 thereof on the reproduction of the nematode Caenorhabditis elegans.

23 with the membraneless organelle P granule in Caenorhabditis elegans.

24 tic protein phosphofructokinase-1/PFK-1.1 in Caenorhabditis elegans.

25 hoprim exhibited increased virulence against Caenorhabditis elegans.

26 y small silencing RNAs in the model nematode Caenorhabditis elegans.

27 A (ncRNA) essential for axon regeneration in Caenorhabditis elegans.

28 nactive one, controls checkpoint strength in Caenorhabditis elegans.

29 terograde synaptic organizer in the nematode Caenorhabditis elegans.

30 scales of hierarchical locomotion control in Caenorhabditis elegans.

31 we address this question using heteroplasmic Caenorhabditis elegans.

32 tivity in the nervous system of the nematode Caenorhabditis elegans.

33 transposon silencing and RNA interference in Caenorhabditis elegans(1-4).

34 we report that mitochondrial dysfunction in Caenorhabditis elegans activates RNAi-directed silencing

35 We find that Caenorhabditis elegans aggregates are observed in large

36 rmation, and emergence of swarming in active Caenorhabditis elegans aggregates.

37 Caenorhabditis elegans alternate between local search an

38 s involved in glial size regulation, we used Caenorhabditis elegans amphid sheath (AMsh) glia as a mo

39 ere we develop tests for IIA in the nematode Caenorhabditis elegans, an animal with only 302 neurons,

40 Remarkably, RAD-51 from Caenorhabditis elegans, an organism without Dmc1, has ac

41 Using an in vivo model of Caenorhabditis elegans anchor cell invasion, we characte

42 of the dosage compensation complex (DCC) in Caenorhabditis elegans and demonstrate that loop anchors

43 e mechanisms underlying UPR(mt) signaling in Caenorhabditis elegans and discuss emerging connections

44 as leveraged simple model organisms, such as Caenorhabditis elegans and Drosophila melanogaster larva

45 d aging, including stem cell dysfunction, in Caenorhabditis elegans and Drosophila melanogaster model

46 (mice and humans) as well as invertebrates (Caenorhabditis elegans and Drosophila melanogaster).

47 vertebrate experimental organisms, including Caenorhabditis elegans and Drosophila melanogaster.

48 ulfide reduction exclusively in endosomes in Caenorhabditis elegans and identified that exchange is m

49 e paralysis, we conducted genetic screens in Caenorhabditis elegans and isolated mutants that became

50 In numerous species including Caenorhabditis elegans and mammals, neural serotonin sig

51 al to organismal health in both the nematode Caenorhabditis elegans and mammals.

52 fication of Abeta oligomers in vitro, and in Caenorhabditis elegans and mouse hippocampal tissues.

53 mporal regulation of LAG-1/CSL expression in Caenorhabditis elegans and observed that an increase in

54 Caenorhabditis elegans and related Caenorhabditis spp. c

55 ptide F (NPF)-related neuropeptide system in Caenorhabditis elegans and show that this FLP-34/NPR-11

56 vensis is a natural pathogen of the nematode Caenorhabditis elegans and that parental exposure of ani

57 t method relying on the free-living nematode Caenorhabditis elegans and the infection of those nemato

58 mental inhibitor of the free-living nematode Caenorhabditis elegans and the plant-parasitic nematode

59 on of a long-term swim exercise protocol for Caenorhabditis elegans and we demonstrate its benefits t

60 ultured cells, acute mouse brain slices, and Caenorhabditis elegans and Xenopus laevis in vivo.

61 couple these key events of the cell cycle in Caenorhabditis elegans and zebrafish through live-cell i

62 dopsis thaliana), rice (Oryza sativa), worm (Caenorhabditis elegans), and human (Homo sapiens) cells

63 t organisms, including Arabidopsis thaliana, Caenorhabditis elegans, and Danio rerio.

64 bolism without affecting eating behaviors in Caenorhabditis elegans, and identified specific odors th

65 ciated protein misfolding toxicity in yeast, Caenorhabditis elegans, and mammalian cells.

66 In Caenorhabditis elegans, and possibly other organisms, wh

67 e, whereas Smn from Drosophila melanogaster, Caenorhabditis elegans, and Schizosaccharomyces pombe wa

68 of a related nonparasitic nematode species, Caenorhabditis elegans, and the parasitic nematode Haemo

69 europeptide Y/neuropeptide F in the nematode Caenorhabditis elegans, and we discovered that it is req

70 Indeed, in ARX/alr-1-deficient Caenorhabditis elegans animals, SAHA was shown to counte

71 Laboratory-conditioned 'wild-type' Caenorhabditis elegans are different from wild-isolated

72 rpose, we have designed a pipeline that uses Caenorhabditis elegans as a genetic model to screen for

73 We employed Caenorhabditis elegans as a heterologous host to underst

74 Using Caenorhabditis elegans as a model, here we report that h

75 ral, biochemical, and functional analyses in Caenorhabditis elegans As capsaicin elicits heat and pai

76 In Caenorhabditis elegans, ascaroside pheromones can dictat

77 The Caenorhabditis elegans AWC olfactory neuron pair asymmet

78 In the nematode Caenorhabditis elegans, axonal regeneration can proceed

79 RNAi-mediated knockdown of Caenorhabditis elegans bcat-1 is known to recapitulate P

80 We identified the Caenorhabditis elegans BK channel SLO-1 as a molecular t

81 tant proteins remain enriched at synapses in Caenorhabditis elegans, but show defects in active-zone

82 nd prodigiosin antibiotics, and infection in Caenorhabditis elegans, but up-regulating flagellar moti

83 ogical mechanisms that delay neuron aging in Caenorhabditis elegans by asking how neuron morphologica

84 We developed a glutamate spillover model in Caenorhabditis elegans by inactivating the conserved gli

85 However, for the infection of Caenorhabditis elegans by P. aeruginosa, the precise pat

86 Drosophila, Escherichia coli (E. coli), and Caenorhabditis elegans (C. elegan) datasets.

87 omatin and nucleoli during cell division and Caenorhabditis elegans (C. elegans) growth.

88 ctivation of the UPR(ER) in the intestine of Caenorhabditis elegans (C. elegans) through release of a

89 ied by the dauer larva stage of the nematode Caenorhabditis elegans (C. elegans).

90 ibed a physiological program in the nematode Caenorhabditis elegans called the intracellular pathogen

91 how that bloating of the intestinal lumen of Caenorhabditis elegans caused by microbial colonization

92 fied a gain-of-function (gf) mutation in the Caenorhabditis elegans CaV2 channel alpha1 subunit, UNC-

93 oteins and an unexpected direct link between Caenorhabditis elegans CFP-1 and an Rpd3/Sin3 small (SIN

94 Here, using Caenorhabditis elegans chemosensory neurons as a model s

95 herefore, simple organisms like the nematode Caenorhabditis elegans, combining relevant advantages of

96 Caenorhabditis elegans consumes bacteria, which can supp

97 We show that in Caenorhabditis elegans COQ-2e is required for efficient

98 Here the role of human AMPK and its Caenorhabditis elegans counterpart AAK-2 was explored up

99 ry element activities across five tissues of Caenorhabditis elegans, covering ~90% of cells.

100 This subunit, dSol-1, is the homolog of the Caenorhabditis elegans CUB (Complement C1r/C1s, Uegf, Bm

101 e atomic cryo-EM structures of a full-length Caenorhabditis elegans cyclic GMP-activated channel TAX-

102 ve L3 larvae, an arrested stage analogous to Caenorhabditis elegans dauer larvae.

103 actors implicated in translation fidelity in Caenorhabditis elegans decreases lifespan, and eEF2K is

104 In Caenorhabditis elegans, deficiency of DCAP-1/DCP1, the e

105 Research in the nematode Caenorhabditis elegans demonstrates that retrieval of av

106 We show that the Caenorhabditis elegans DIP-2 maintains morphology of mat

107 is regard, we summarize recent studies using Caenorhabditis elegans, Drosophila melanogaster, Danio r

108 ets across species inclusive of Arabidopsis, Caenorhabditis elegans, Drosophila, human, mouse, rat, y

109 Caenorhabditis elegans early embryos generate cell-speci

110 namic responses of touch receptor neurons in Caenorhabditis elegans (Eastwood et al., 2015), which su

111 erotonin-dependent behavior of the roundworm Caenorhabditis elegans, egg laying, to perform a behavio

112 We followed the first nine divisions of Caenorhabditis elegans embryo development and demonstrat

113 The Caenorhabditis elegans embryo is an important model for

114 Here we use the early Caenorhabditis elegans embryo to explore how the actin f

115 ce in situ hybridization (smFISH) studies in Caenorhabditis elegans embryogenesis.

116 nvestigated cytokinesis during the invariant Caenorhabditis elegans embryonic divisions and found sev

117 ression levels of APA isoforms in individual Caenorhabditis elegans embryos at different stages throu

118 robe and control the cell-division timing in Caenorhabditis elegans embryos using a combination of lo

119 In Caenorhabditis elegans embryos, chromodomain protein CEC

120 ically infects the laboratory model nematode Caenorhabditis elegans, encodes a fibrous protein delta

121 Here, we show that the nematode Caenorhabditis elegans exhibits the key features of alco

122 report that the noncanonical sHsp HSP-17 of Caenorhabditis elegans facilitates aggregation of model

123 We show that FAMK-1, the Caenorhabditis elegans Fam20C orthologue, contributes to

124 Apoe(-/-) mice expressing the Caenorhabditis elegans Fat-1 transgene (Fat-1(tg)xApoe(-

125 hat govern the formation of gap junctions in Caenorhabditis elegans, five of which are already suppor

126 ng, we performed a forward genetic screen in Caenorhabditis elegans for genes involved in body size r

127 on developmental gene expression dataset for Caenorhabditis elegans from Bao, Murray, Waterston et al

128 lar range cysteamine bitartrate treatment in Caenorhabditis elegans gas-1(fc21) RC complex I (NDUFS2-

129 We performed a Caenorhabditis elegans genetic screen to find cellular f

130 We deleted mafr-1 from the Caenorhabditis elegans genome and found that animals lac

131 H Oligopaint library that targets the entire Caenorhabditis elegans genome at chromosome, three megab

132 onserved homeodomain proteins encoded by the Caenorhabditis elegans genome(2), that the complete set

133 Here, we use the Caenorhabditis elegans germline as a model to investigat

134 ins FBF-1 and FBF-2 have opposite effects on Caenorhabditis elegans germline stem cell dynamics: FBF-

135 In the Caenorhabditis elegans germline, fem-3 Binding Factor (F

136 e-like glia, which extended the life span in Caenorhabditis elegans Glial XBP-1s initiated a robust c

137 In the Caenorhabditis elegans gonad, the broad outlines of germ

138 pling between the soma and germ cells in the Caenorhabditis elegans gonad.

139 rain to induce CA production directly in the Caenorhabditis elegans gut, we reveal the local effect o

140 The nematode Caenorhabditis elegans has an alternate dispersal life s

141 Caenorhabditis elegans has long been a laboratory model

142 Some nematodes such as Caenorhabditis elegans have an XO sex determination syst

143 sed by all neurons in model systems, such as Caenorhabditis elegans have left still unresolved how ne

144 Hawaiian isolates of the nematode species Caenorhabditis elegans have long been known to harbor ge

145 netic studies on the excretory canal cell of Caenorhabditis elegans have revealed many proteins that

146 Young Caenorhabditis elegans hermaphrodites use their own sper

147 TFEB and TFE3, as well as their ortholog in Caenorhabditis elegans HLH-30, play an important role in

148 nd genetic analysis, we found that catp-6, a Caenorhabditis elegans homolog of ATP13A2, was responsib

149 UNC-104 is the Caenorhabditis elegans homolog of kinesin-3 KIF1A known

150 ere, we study the effect of different crh-1 [Caenorhabditis elegans homolog of mammalian cAMP respons

151 zing proteome-wide mass spectrometry data of Caenorhabditis elegans, however, we show that the levels

152 Here we show that in Caenorhabditis elegans HS induces up- and downregulation

153 regulates EV levels in the sensory organs of Caenorhabditis elegans in a cilia specific manner.

154 mechanical properties associated with ageing Caenorhabditis elegans in addition to capturing high-res

155 on in HD models (cells, primary neurons, and Caenorhabditis elegans) increases mutant HTT exon 1 phos

156 cells as well as Drosophila melanogaster and Caenorhabditis elegans, indicating suitability for use i

157 successfully reduced the fungal burdens in a Caenorhabditis elegans infection model by up to 96%.

158 Additionally, in a Caenorhabditis elegans infection model, the ospemifene-i

159 utative FAM173B orthologue from the nematode Caenorhabditis elegans Interestingly, lack of Lys-43 met

160 The nematode Caenorhabditis elegans is a bacterivore filter feeder.

161 The free-living nematode Caenorhabditis elegans is a key laboratory model for met

162 on the host strain.IMPORTANCE The roundworm Caenorhabditis elegans is a laboratory model organism in

163 The pharynx of the nematode Caenorhabditis elegans is a simple neuromuscular organ w

164 The nematode Caenorhabditis elegans is a useful model for studying th

165 Caenorhabditis elegans is a valuable model organism in b

166 Caenorhabditis elegans is an animal with few cells but a

167 The model nematode Caenorhabditis elegans is ideal to study these interacti

168 The endoderm GRN in Caenorhabditis elegans is initiated by the maternally su

169 Caenorhabditis elegans is used extensively as a medical

170 In Caenorhabditis elegans, Katanin MT-severing activity is

171 Upon sensing starvation stress, Caenorhabditis elegans larvae (L2d) elicit two seemingly

172 can modulate the developmental trajectory of Caenorhabditis elegans larvae by promoting entry into da

173 We generate CRISPR knockout strains for Caenorhabditis elegans lincRNAs and evaluate their pheno

174 In Caenorhabditis elegans, low vitamin B12, or genetic pert

175 -shared neurons in the nervous system of the Caenorhabditis elegans male is controlled by the tempora

176 g a conspicuous muscle change that occurs in Caenorhabditis elegans males.

177 tion channel complex in the sensory cilia of Caenorhabditis elegans mechanoreceptor neurons.

178 ayer in coordinating these key events during Caenorhabditis elegans meiosis.

179 specific isoform of CREB1/CRH-1, CRH-1e, in Caenorhabditis elegans memory formation and chemosensati

180 In Caenorhabditis elegans, MET-2, the homologue of mammalia

181 -helix transcription factor 30 (hlh-30), the Caenorhabditis elegans MiT/TFE ortholog, to starvation f

182 beta-induced paralysis in a transgenic Abeta Caenorhabditis elegans model and specifically target and

183 To this end, we have generated a transgenic Caenorhabditis elegans model expressing both human Abeta

184 Previously, we generated a Caenorhabditis elegans model of ALS, in which the expres

185 ogical tau protein, we employed a transgenic Caenorhabditis elegans model of human tauopathy exhibiti

186 A genome-wide screen in a Caenorhabditis elegans model of SOD1-linked ALS identifi

187 re, we develop an experimental handle in the Caenorhabditis elegans model system, in which we uncover

188 MP resistance show enhanced virulence in the Caenorhabditis elegans model, an effect that is abolishe

189 rough CRISPR/Cas9-mediated gene editing in a Caenorhabditis elegans model.

190 en suggested to regulate tau inclusions in a Caenorhabditis elegans model.

191 In both amyloid-beta (Abeta) and tau Caenorhabditis elegans models of AD, mitophagy stimulati

192 hes to better understand the function of the Caenorhabditis elegans MORC-1 protein.

193 pmental expression of three conserved genes, Caenorhabditis elegans mpk-1, lag-1, and lag-3/sel-8, wh

194 e diseases, and we show that the lack of the Caenorhabditis elegans Msp1 homologue triggers an import

195 hondria are arrayed in a periodic pattern in Caenorhabditis elegans muscle, but this pattern is disru

196 Caenorhabditis elegans must distinguish pathogens from n

197 Here, we analyzed Caenorhabditis elegans mutants deleted of the sole SEIPI

198 In Caenorhabditis elegans, mutations in WDR-5 and other com

199 d nucleus deformation dynamics within living Caenorhabditis elegans nematodes.

200 e retraction is shown to be operative in the Caenorhabditis elegans nervous system.

201 In Caenorhabditis elegans, neural excitation increases with

202 to visualize alternative splicing in single Caenorhabditis elegans neurons, identifying complex spli

203 e in primary fibroblasts, murine neurons and Caenorhabditis elegans neurons.

204 ant for controlling levels of DCV cargoes in Caenorhabditis elegans neurons.

205 we discovered a novel coordinated action of Caenorhabditis elegans neuropeptide Y/neuropeptide F and

206 The Caenorhabditis elegans NPY/NPF ortholog FLP-34 displays

207 Here we report our investigations on three Caenorhabditis elegans orthologous proteins involved in

208 We also report that the Caenorhabditis elegans orthologs of 14-3-3zeta and MSec

209 subunits partially rescue sensory defects in Caenorhabditis elegans osm-9 and tax-4 knock-out strains

210 of Alzheimer's disease in the model organism Caenorhabditis elegans Our results pose and answer the q

211 In Caenorhabditis elegans, piRNA loci are clustered within

212 e we describe the emerging model system of a Caenorhabditis elegans polymodal neuron named PVD, whose

213 Caenorhabditis elegans possess a mild inflammatory respo

214 The nematode Caenorhabditis elegans possesses glial types similar to

215 of integrin-mediated collagen recruitment to Caenorhabditis elegans postembryonic gonadal and pharyng

216 Caenorhabditis elegans primordial germ cells (PGCs) jett

217 The nematode Caenorhabditis elegans produces a broad family of pherom

218 Here we identified the Caenorhabditis elegans protein huntingtin-interacting pr

219 re, we report the identification of PLP-1, a Caenorhabditis elegans protein related to the human sing

220 Here we describe a Caenorhabditis elegans quiescent behavior, post-response

221 In Caenorhabditis elegans, RBPs control the translation, st

222 In Caenorhabditis elegans, reduced mitochondrial electron t

223 In Caenorhabditis elegans, regulation of piRNA target genes

224 The spermatheca of the Caenorhabditis elegans reproductive system enables study

225 EB) transcription factor significantly slows Caenorhabditis elegans' reproductive decline, an early h

226 dbt-1 gene underlies natural differences in Caenorhabditis elegans responses to the toxin arsenic.

227 The expression of chimeric hnRNPA2 D290V in Caenorhabditis elegans results in stress-induced glutama

228 R-generated, fluorescently tagged endogenous Caenorhabditis elegans RHEB-1 and DAF-15/Raptor are expr

229 The Caenorhabditis elegans RIG-I-like receptor DRH-1 promote

230 In Caenorhabditis elegans, RNA interference (RNAi) response

231 In Caenorhabditis elegans, RNAi can be achieved by feeding

232 colleagues provide evidence that exposure of Caenorhabditis elegans roundworms to 2 simple nutrients,

233 l-angle x-ray scattering) and in vivo tools (Caenorhabditis elegans sarcomere structure).

234 We show that in Caenorhabditis elegans, serotonin released by maternal n

235 velopment in a subpopulation of synchronized Caenorhabditis elegans, sets processes in motion that in

236 repeated induction of the flight response in Caenorhabditis elegans shortens lifespan and inhibits co

237 gene expression analyses in P. univalens and Caenorhabditis elegans show that the intestine is the ma

238 In Caenorhabditis elegans, signals from the germline initia

239 In Caenorhabditis elegans sleep occurs during a larval tran

240 During Caenorhabditis elegans sleep, energetic stores are alloc

241 We use the myoepithelial cells of the Caenorhabditis elegans spermatheca to study the mechanis

242 to a brief 2 degrees C temperature increase, Caenorhabditis elegans spermatocytes exhibit up to a 25-

243 bservations were recapitulated in vivo, in a Caenorhabditis elegans strain deficient in the ATP13A2 o

244 A new study in Caenorhabditis elegans suggests the ubiquitin-proteasome

245 For example, in Caenorhabditis elegans, SUN protein UNC-84 binds to two

246 e for the whole-life culture of the nematode Caenorhabditis elegans that allows the scoring of animal

247 identify a neuronal circuit in the nematode Caenorhabditis elegans that processes information percei

248 he model agrees with experiments in the worm Caenorhabditis elegans that show the following: Life spa

249 We have recently shown in Caenorhabditis elegans that transcript levels of sqst-1/

250 In Caenorhabditis elegans, the avoidance response to gentle

251 Here, we show that in Caenorhabditis elegans, the axons of the ALA neuron cont

252 In Caenorhabditis elegans, the BMP ligand DBL-1 is a regula

253 In Caenorhabditis elegans, the closest BUBR1 orthologue lac

254 In Caenorhabditis elegans, the heterochronic pathway contro

255 To test this, we used Caenorhabditis elegans, the intestinal cells of which ar

256 ntrations in most studied species, including Caenorhabditis elegans, the molecular mechanisms behind

257 Here we show that in Caenorhabditis elegans, the neuromodulator tyramine prod

258 In Caenorhabditis elegans, the transcription factor HBL-1 (

259 In Caenorhabditis elegans, the transcription factor, SKN-1,

260 In the nematode Caenorhabditis elegans, the transcription regulators DAF

261 In the nematode Caenorhabditis elegans, this highly efficient regenerati

262 which male-specific neurons are generated in Caenorhabditis elegans through the direct transdifferent

263 omeric organization and muscle function from Caenorhabditis elegans to humans.

264 We have used RNA-seq in Caenorhabditis elegans to produce transcription profiles

265 Here, we used Caenorhabditis elegans to systematically functionally ch

266 icellular settings, from the model organism, Caenorhabditis elegans, to humans.

267 lls, a population of epidermal stem cells in Caenorhabditis elegans, to study the influence of temper

268 For example, in the annotation of the Caenorhabditis elegans transcriptome, more than half of

269 come well established that the nematode worm Caenorhabditis elegans triggers innate immune responses

270 usly shown that 2 paralogous tetraspanins in Caenorhabditis elegans, TSP-12 and TSP-14, function redu

271 In the nematode Caenorhabditis elegans, UNC-87 is a calponin-related pro

272 In Caenorhabditis elegans, unc-89 encodes a set of giant mu

273 s controlled by Munc18 (mammalian homolog of Caenorhabditis elegans uncoordinated gene 18) proteins.

274 The Caenorhabditis elegans vulva has been a paradigm for und

275 Caenorhabditis elegans was the first multicellular eukar

276 regulates its trafficking and degradation in Caenorhabditis elegans We found that the WD40-repeat pro

277 multipotent vulval precursor cells (VPCs) of Caenorhabditis elegans We have previously shown that thi

278 Using the touch receptor neurons (TRNs) of Caenorhabditis elegans, we find that mec-15(-) mutants d

279 ructions of spermatocyte meiotic spindles in Caenorhabditis elegans, we find the lagging X chromosome

280 ors of heat-shock-induced gene expression in Caenorhabditis elegans, we found a new allele of hsf-1 t

281 Using the in vivo model system Caenorhabditis elegans, we found that the highly conserv

282 Here, using Caenorhabditis elegans, we generated the first organism

283 n coupled with deep-sequencing (TRAP-seq) in Caenorhabditis elegans, we have obtained high coverage p

284 Using forward genetics in Caenorhabditis elegans, we identified a conserved orphan

285 encing and genomic and genetic approaches in Caenorhabditis elegans, we reveal an unprecedented role

286 Using optogenetics in Caenorhabditis elegans, we solved the presynaptic circui

287 and siRNAs in regulating gene expression in Caenorhabditis elegans, we subjected small RNAs and mRNA

288 In a forward genetic screen in Caenorhabditis elegans, we uncover that TALP-3, a homolo

289 increased in young amyloid B (AB) expressing Caenorhabditis elegans, whereas it is not in wild type s

290 odels zebrafish, Drosophila melanogaster and Caenorhabditis elegans, which command superb research re

291 ned by the number of traps after exposure to Caenorhabditis elegans While some strains were highly se

292 neuronal tissue, mouse embryonic tissue and Caenorhabditis elegans whole embryos.

293 In simple organisms such as Caenorhabditis elegans, whole brain imaging has been per

294 riation in the behavioral flexibility of two Caenorhabditis elegans wild strains.

295 measured touch-induced mechanical strain in Caenorhabditis elegans worms.

296 In Caenorhabditis elegans, wounding the epidermis triggers

297 During the asymmetric division of the Caenorhabditis elegans zygote, germ (P) granules are dis

298 Using the newly fertilized Caenorhabditis elegans zygote, we show that the mitotic

299 In Caenorhabditis elegans zygotes, PAR-1 localizes to the p

300 In wild-type Caenorhabditis elegans zygotes, symmetry breaking during