ライフサイエンスコーパス: Caenorhabditis

1 nt cytoplasmic RNA that is conserved across Caenorhabditis and possesses three essential secondary s

2 es on stomatal shapes in the model nematodes Caenorhabditis and Pristionchus.

3 Caenorhabditis bovis is a particularly unusual species t

4 A new study analyzes the genome of Caenorhabditis bovis, a nematode that may be evolving a

5 ht C. elegans (Orsay virus) and its relative Caenorhabditis briggsae (Santeuil virus, Le Blanc virus,

6 and Santeuil, which both specifically infect Caenorhabditis briggsae, were also found to form fibrous

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

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

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

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

11 We find that Caenorhabditis elegans aggregates are observed in large

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

13 Caenorhabditis elegans alternate between local search an

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

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

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

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

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

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

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

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

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

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

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

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

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

27 Caenorhabditis elegans and related Caenorhabditis spp. c

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

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

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

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

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

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

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

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

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

37 We employed Caenorhabditis elegans as a heterologous host to underst

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

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

40 The Caenorhabditis elegans AWC olfactory neuron pair asymmet

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

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

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

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

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

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

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

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

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

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

51 Caenorhabditis elegans consumes bacteria, which can supp

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

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

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

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

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

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

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

59 Caenorhabditis elegans early embryos generate cell-speci

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

61 The Caenorhabditis elegans embryo is an important model for

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

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

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

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

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

67 In Caenorhabditis elegans embryos, chromodomain protein CEC

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 The nematode Caenorhabditis elegans has an alternate dispersal life s

85 Caenorhabditis elegans has long been a laboratory model

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

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

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

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

90 Young Caenorhabditis elegans hermaphrodites use their own sper

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

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

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

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

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

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

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

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

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

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

101 The nematode Caenorhabditis elegans is a bacterivore filter feeder.

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

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

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

105 Caenorhabditis elegans is a valuable model organism in b

106 Caenorhabditis elegans is an animal with few cells but a

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

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

109 Caenorhabditis elegans is used extensively as a medical

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

132 Caenorhabditis elegans must distinguish pathogens from n

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

134 d nucleus deformation dynamics within living Caenorhabditis elegans nematodes.

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

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

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

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

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

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

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

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

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

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

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

146 Caenorhabditis elegans possess a mild inflammatory respo

147 The nematode Caenorhabditis elegans possesses glial types similar to

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

149 Caenorhabditis elegans primordial germ cells (PGCs) jett

150 The nematode Caenorhabditis elegans produces a broad family of pherom

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

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

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

154 The spermatheca of the Caenorhabditis elegans reproductive system enables study

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

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

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

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

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

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

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

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

163 In Caenorhabditis elegans sleep occurs during a larval tran

164 During Caenorhabditis elegans sleep, energetic stores are alloc

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

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

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

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

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

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

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

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

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

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

175 Here, we used Caenorhabditis elegans to systematically functionally ch

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

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

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

179 The Caenorhabditis elegans vulva has been a paradigm for und

180 Caenorhabditis elegans was the first multicellular eukar

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

200 In Caenorhabditis elegans, and possibly other organisms, wh

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

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

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

204 In Caenorhabditis elegans, ascaroside pheromones can dictat

205 In the nematode Caenorhabditis elegans, axonal regeneration can proceed

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

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

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

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

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

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

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

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

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

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

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

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

218 In Caenorhabditis elegans, Katanin MT-severing activity is

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

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

221 In Caenorhabditis elegans, neural excitation increases with

222 In Caenorhabditis elegans, piRNA loci are clustered within

223 In Caenorhabditis elegans, RBPs control the translation, st

224 In Caenorhabditis elegans, reduced mitochondrial electron t

225 In Caenorhabditis elegans, regulation of piRNA target genes

226 In Caenorhabditis elegans, RNA interference (RNAi) response

227 In Caenorhabditis elegans, RNAi can be achieved by feeding

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

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

230 In Caenorhabditis elegans, signals from the germline initia

231 In Caenorhabditis elegans, the avoidance response to gentle

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

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

234 In Caenorhabditis elegans, the closest BUBR1 orthologue lac

235 In Caenorhabditis elegans, the heterochronic pathway contro

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

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

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

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

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

241 In the nematode Caenorhabditis elegans, the transcription regulators DAF

242 In the nematode Caenorhabditis elegans, this highly efficient regenerati

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

261 In Caenorhabditis elegans, wounding the epidermis triggers

262 we address this question using heteroplasmic Caenorhabditis elegans.

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

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

265 of proteins to chemosensory cilia in living Caenorhabditis elegans.

266 homologous recombination-mediated repair in Caenorhabditis elegans.

267 rous iron accumulates over adult lifetime in Caenorhabditis elegans.

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

269 e molecular bases of this organization using Caenorhabditis elegans.

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

271 ll ferroptosis and sterility in the nematode Caenorhabditis elegans.

272 cleavage to attract glia during migration in Caenorhabditis elegans.

273 during embryonic development of the nematode Caenorhabditis elegans.

274 ween Pseudomonas aeruginosa and the nematode Caenorhabditis elegans.

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

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

277 mentally identified piRNA targeting sites in Caenorhabditis elegans.

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

279 educe lipid storage and promote longevity in Caenorhabditis elegans.

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

281 , followed by functional characterization in Caenorhabditis elegans.

282 thereof on the reproduction of the nematode Caenorhabditis elegans.

283 with the membraneless organelle P granule in Caenorhabditis elegans.

284 hoprim exhibited increased virulence against Caenorhabditis elegans.

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

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

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

288 nactive one, controls checkpoint strength in Caenorhabditis elegans.

289 terograde synaptic organizer in the nematode Caenorhabditis elegans.

290 scales of hierarchical locomotion control in Caenorhabditis elegans.

291 The Caenorhabditis hosts were found defective in degrading e

292 imized to measure activity and quiescence in Caenorhabditis larvae and adults and in Drosophila larva

293 Several species of Caenorhabditis nematodes have evolved a mating system in

294 omosome in hemizygous (XY) males, whereas in Caenorhabditis nematodes, expression is halved for both

295 ing cell fate among vulva precursor cells in Caenorhabditis nematodes, that of P3.p.

296 logenetic relationships of C. bovis to other Caenorhabditis species and reveal the changes in genome

297 All of the ~65 Caenorhabditis species currently in culture are free-liv

298 preserving, are more highly conserved across Caenorhabditis species, and are enriched in specific cis

299 ncement in our understanding of this unusual Caenorhabditis species.

300 Caenorhabditis elegans and related Caenorhabditis spp. contain LTR retrotransposons and, as