ライフサイエンスコーパス: Tetrahymena thermophila

1 and in vivo nucleosome maps for the ciliate Tetrahymena thermophila.

2 d Ca(2+) binding protein, has been cloned in Tetrahymena thermophila.

3 metallothionein (MTT1) gene was cloned from Tetrahymena thermophila.

4 s populations of Saccharomyces cerevisiae or Tetrahymena thermophila.

5 nd double-strand break repair in the ciliate Tetrahymena thermophila.

6 of the somatic nucleus during development of Tetrahymena thermophila.

7 germline micronucleus of the model organism Tetrahymena thermophila.

8 G-DNA-binding protein TGP1 from the ciliate Tetrahymena thermophila.

9 tes of phosphorylation of macronuclear H1 in Tetrahymena thermophila.

10 olecules found in ciliated protozoa, such as Tetrahymena thermophila.

11 TGP1, a G-DNA specific binding protein from Tetrahymena thermophila.

12 eloping amitotic macronucleus of the ciliate Tetrahymena thermophila.

13 d from macronuclei of the ciliated protozoan Tetrahymena thermophila.

14 hat regulate rRNA gene (rDNA) replication in Tetrahymena thermophila.

15 ly folding domain of the Group I intron from Tetrahymena thermophila.

16 cretory granule-like vesicles in the ciliate Tetrahymena thermophila.

17 uing process has been extensively studied in Tetrahymena thermophila.

18 regions, during macronuclear development in Tetrahymena thermophila.

19 hromosome breakage and telomere formation in Tetrahymena thermophila.

20 urs in the P5 helix of the group I intron of Tetrahymena thermophila.

21 he genome during macronuclear development of Tetrahymena thermophila.

22 ne H2A variant hv1 in the ciliated protozoan Tetrahymena thermophila.

23 n reactions of the self-splicing intron from Tetrahymena thermophila.

24 otic linkage data for the ciliated protozoan Tetrahymena thermophila.

25 RNase T2 genes (RNT2A-RNT2H) in the ciliate Tetrahymena thermophila.

26 the first canonical PARG from the protozoan Tetrahymena thermophila.

27 re proteins, Tpt1 and Pat1, from the ciliate Tetrahymena thermophila.

28 the structural maintenance of centrioles in Tetrahymena thermophila.

29 istone H2B in the single-cell model organism Tetrahymena thermophila.

30 matic macronucleus in the ciliated protozoan Tetrahymena thermophila.

31 ogress in genome closure and reannotation of Tetrahymena thermophila.

32 al body components in the ciliated protozoan Tetrahymena thermophila.

33 ed to programmed DNA deletion in the ciliate Tetrahymena thermophila.

34 ced ciliate genomes: Oxytricha trifallax and Tetrahymena thermophila.

35 earchers studying the model ciliate organism Tetrahymena thermophila.

36 ide-binding domain (NBD) of gamma-tubulin in Tetrahymena thermophila.

37 xcised from the developing somatic genome of Tetrahymena thermophila.

38 s and exconjugant development in the ciliate Tetrahymena thermophila.

39 tion-deletion polymorphisms among strains of Tetrahymena thermophila.

40 ess of conjugation in the ciliated protozoan Tetrahymena thermophila.

41 on cell pair formation during conjugation in Tetrahymena thermophila.

42 We have cloned the RAD51 homolog from Tetrahymena thermophila , a ciliated protozoan.

43 We show here that Tetrahymena thermophila, a bacterivorous predator, is ki

44 tified and cloned the parafusin homologue in Tetrahymena thermophila, a ciliate in which protein func

45 However, its presence in Tetrahymena thermophila, a ciliated protozoan with seven

46 Here we describe, using the ciliate Tetrahymena thermophila, a previously unidentified respo

47 Tetrahymena thermophila, a widely studied model for cell

48 ndary ion mass spectrometry images of mating Tetrahymena thermophila acquired at various stages durin

49 In Tetrahymena thermophila-ag in natural isolates is the re

50 The Tetrahymena thermophila Ago/Piwi protein Twi12 is essent

51 ated reaction, intron-derived ribozymes from Tetrahymena thermophila and Candida albicans, which are

52 oding kinesin-II homologues from the ciliate Tetrahymena thermophila and constructed strains lacking

53 Protein components from the Tetrahymena thermophila and human RNase P holoenzymes fo

54 , is characterized in the ciliated protozoan Tetrahymena thermophila and is shown to be responsible f

55 w that the ectodomain of HAP2 orthologs from Tetrahymena thermophila and other species adopt a protei

56 s spectrometric analyses of H3 purified from Tetrahymena thermophila and Saccharomyces cerevisiae (ye

57 The rDNA minichromosomes of Tetrahymena thermophila and Tetrahymena pyriformis share

58 terium Trichodesmium erythraeum, the ciliate Tetrahymena thermophila, and the viruses Enterobacteria

59 Arabidopsis thaliana, Plasmodium falciparum, Tetrahymena thermophila, Archaeoglobus fulgidus, and Myc

60 regulated secretory granules in the ciliate Tetrahymena thermophila are crystal lattices composed of

61 es of the macronuclear (expressed) genome of Tetrahymena thermophila are generated by developmental f

62 e macronuclear DNA of the ciliated protozoan Tetrahymena thermophila are modified to N 6-methyladenin

63 m the developing macronucleus in the ciliate Tetrahymena thermophila are released as linear fragments

64 The genetics of the ciliate Tetrahymena thermophila are richer than for most other e

65 r linker histones of the ciliated protozoan, Tetrahymena thermophila, are extensively phosphorylated

66 quantify these NPs in the ciliated protozoan Tetrahymena thermophila as a model aquatic organism.

67 re we analyze the actions of telomerase from Tetrahymena thermophila assembled in vivo with mutated o

68 In Tetrahymena thermophila, brief exposure to secretagogue

69 s were efficiently ingested by the protozoan Tetrahymena thermophila but were neither digested nor ki

70 n-binding protein profilin was isolated from Tetrahymena thermophila by affinity chromatography, and

71 demonstrated that the group I ribozyme from Tetrahymena thermophila can perform trans-splicing react

72 Tetrahymena thermophila cells contain three forms of H2A

73 In logarithmically growing Tetrahymena thermophila cells, for example, H3 phosphory

74 e ciliate Glaucoma chattoni was expressed in Tetrahymena thermophila cells.

75 The Tetrahymena thermophila CNA1 gene encodes the centromeri

76 During Tetrahymena thermophila conjugation, new somatic macronu

77 veloping somatic genome are generated during Tetrahymena thermophila conjugation.

78 The genome of Tetrahymena thermophila contains 39 loci encoding NIMA-r

79 The macronucleus of the ciliate Tetrahymena thermophila contains a fragmented somatic ge

80 The ciliate Tetrahymena thermophila contains at least four centrin g

81 The macronucleus of the binucleate ciliate Tetrahymena thermophila contains fragmented and amplifie

82 The ciliate protozoan Tetrahymena thermophila contains two types of structural

83 In telomeric DNA mutants of Tetrahymena thermophila, created by expression of a telo

84 he H2A.F/Z variant of the ciliated protozoan Tetrahymena thermophila, cross-react with proteins from

85 ation of a novel G4-DNA binding protein from Tetrahymena thermophila, designated TGP2.

86 In Tetrahymena thermophila, developmentally regulated DNA e

87 In binuclear ciliates, including Tetrahymena thermophila, DNA elimination occurs during t

88 The ciliate Tetrahymena thermophila encodes numerous PPD proteins ex

89 In the ciliated protozoan Tetrahymena thermophila, extensive DNA elimination is as

90 icient than the amber suppressor tRNA THG73 (Tetrahymena thermophila G73), which has been used extens

91 The gene (GTU1) encoding Tetrahymena thermophila gamma-tubulin was cloned and ana

92 e now report the cloning and sequencing of a Tetrahymena thermophila gene whose encoded protein has t

93 We cloned a Tetrahymena thermophila gene, IFT52, encoding a homolog

94 entified the centromeric histone gene in the Tetrahymena thermophila genome (CNA1).

95 The haploid Tetrahymena thermophila genome contains a single alpha-t

96 We have found that the Tetrahymena thermophila genome contains two POT1 gene ho

97 e P5b stem loop from the P4-P6 domain of the Tetrahymena thermophila group I intron and a 58-nt fragm

98 independently folding P4-P6 domain from the Tetrahymena thermophila group I intron by single molecul

99 An RNA comprising the two domains of the Tetrahymena thermophila group I intron catalytic core re

100 bdomain (tP5abc, a 56-nucleotide RNA) of the Tetrahymena thermophila group I intron ribozyme changes

101 of the P5abc subdomain (a 56-nt RNA) of the Tetrahymena thermophila group I intron ribozyme has been

102 zyme constructs consist of the self-splicing Tetrahymena thermophila group I intron ribozyme that is

103 to define the folding landscape of the L-21 Tetrahymena thermophila group I intron structurally and

104 for Mg(2+) and Na(+)-mediated folding of the Tetrahymena thermophila group I intron using this combin

105 or exemplary RNA sequences (hairpins and the Tetrahymena thermophila group I intron), we compute the

106 In particular, the P456 domain of the Tetrahymena thermophila group I intron, and a 58 nt 23s

107 ent of the 5 S rRNA and the P5c helix of the Tetrahymena thermophila group I intron.

108 The Mg2+-induced folding of Tetrahymena thermophila group I ribozyme shows the capab

109 independently folding tertiary domain of the Tetrahymena thermophila group I ribozyme, is known to fo

110 lete sequence of the mitochondrial genome of Tetrahymena thermophila has been determined and compared

111 The unicellular eukaryote Tetrahymena thermophila has seven mating types.

112 In Tetrahymena thermophila, highly phosphorylated histone H

113 A truncated cDNA clone encoding Tetrahymena thermophila histone H2A2 was isolated using

114 H2A.Y is an essential, divergent Tetrahymena thermophila histone variant.

115 ure of one of these, the P4-P6 domain of the Tetrahymena thermophila intron, is described.

116 crystal structure of the P4-P6 domain of the Tetrahymena thermophila intron.

117 Conjugation in the freshwater ciliate Tetrahymena thermophila involves a developmental program

118 yme derived from the self-splicing intron of Tetrahymena thermophila involves at least two steps.

119 The ciliate Tetrahymena thermophila is a useful model organism that

120 As a unicellular model organism, Tetrahymena thermophila is among the first eukaryotes re

121 The SerH locus of Tetrahymena thermophila is one of several paralogous loc

122 Tetrahymena thermophila is the best studied of the cilia

123 Tetrahymena thermophila is the only ciliate in which a s

124 the H2A.Z variant of the ciliated protozoan TETRAHYMENA: thermophila is able to rescue the phenotype

125 hv2, an H3 variant in the ciliated protozoan Tetrahymena thermophila, is synthesized and deposited in

126 f various guanosine, or G, substrates to the Tetrahymena thermophila L-21 ScaI ribozyme have been inv

127 The Tetrahymena thermophila L-21 ScaI ribozyme utilizes Mg2+

128 into a site within a variable region in the Tetrahymena thermophila large subunit rRNA gene.

129 secondary and/or tertiary structures in the Tetrahymena thermophila large subunit rRNA-DeltaP5abc gr

130 ersally conserved site in this region of the Tetrahymena thermophila LSU rRNA confers anisomycin resi

131 ed by the recently completed sequence of the Tetrahymena thermophila macronuclear genome.

132 Tetrahymena thermophila macronuclear histone H1 is phosp

133 T).d(AACCCC) repeat tracts (G4T2 repeats) in Tetrahymena thermophila macronuclei were shown previousl

134 oper S-phase progression and division of the Tetrahymena thermophila macronucleus.

135 In conjugating Tetrahymena thermophila, massive DNA elimination occurs

136 The eight DRPs in the ciliate Tetrahymena thermophila might contribute to aspects of c

137 The ciliate Tetrahymena thermophila offers a simple system in which

138 The ciliated protozoan, Tetrahymena thermophila, offers an attractive medium for

139 ins that contained eRF1 domain 1 from either Tetrahymena thermophila or Euplotes octocarinatus fused

140 The Tetrahymena thermophila origin recognition complex (ORC)

141 Two telomerase proteins from Tetrahymena thermophila, p80 and p95, were identified on

142 In Tetrahymena thermophila, peptides secreted via dense-cor

143 The L-21 ScaI ribozyme derived from the Tetrahymena thermophila pre-rRNA group I intron catalyze

144 The targeted disruption of somatic genes in Tetrahymena thermophila presents the opportunity to dete

145 base pairing within the telomerase RNA from Tetrahymena thermophila prevent the stable assembly in v

146 resulted in cystic kidneys, and knockdown in Tetrahymena thermophila produced shortened or absent cil

147 an be transferred to and biomagnified in the Tetrahymena thermophila protozoa that prey on the bacter

148 enantiomer-specific toxicity in the case of Tetrahymena thermophila, protozoa that are utilized duri

149 Tetrahymena thermophila RAD51 encodes a 36.3 kDa protein

150 The Tetrahymena thermophila RAD51 gene was recently cloned,

151 The Tetrahymena thermophila rDNA exists as a 21 kb palindrom

152 Self-splicing of the group I IVS from Tetrahymena thermophila rDNA is limited by the time requ

153 tion fork movement, and transcription of the Tetrahymena thermophila rDNA minichromosome and are requ

154 f replication forks and transcription of the Tetrahymena thermophila rDNA minichromosome.

155 ation fork movement and transcription of the Tetrahymena thermophila rDNA minichromosome.

156 The model ciliate Tetrahymena thermophila removes 34% of its germline micr

157 into the genome of a somatic macronucleus in Tetrahymena thermophila requires several DNA rearrangeme

158 -nucleotide bulge of the group I intron from Tetrahymena thermophila results in an electrophoreticall

159 horesis was used to study replication of the Tetrahymena thermophila ribosomal DNA (rDNA) minichromos

160 C protein, TIF1, recognizes sequences in the Tetrahymena thermophila ribosomal DNA (rDNA) minichromos

161 The Tetrahymena thermophila ribosomal DNA (rDNA) replicon co

162 During macronuclear development the Tetrahymena thermophila ribosomal RNA gene is excised fr

163 lent cation-induced folding of the L-21 Sca1 Tetrahymena thermophila ribozyme and a selected mutant w

164 inding in the folding of the P4-P6 domain of Tetrahymena thermophila ribozyme by examining the Mg2+-i

165 e Mg(2+)-dependent folding of the L-21 Sca 1 Tetrahymena thermophila ribozyme has been followed using

166 The Mg2 +-mediated folding of the Tetrahymena thermophila ribozyme is characterized by rap

167 d the catalysis by and folding of individual Tetrahymena thermophila ribozyme molecules.

168 -helix junction, and the P5abc domain of the Tetrahymena thermophila ribozyme.

169 and fold during Mg2+-mediated folding of the Tetrahymena thermophila ribozyme.

170 compaction upon Mg2+-mediated folding of the Tetrahymena thermophila ribozyme.

171 ibosome entry sequence of hepatitis C virus, Tetrahymena thermophila rRNA intron, 100 tRNAs and 14 RN

172 The Tetrahymena thermophila self-splicing RNA is trapped in

173 In the self-splicing group I intron from Tetrahymena thermophila, several divalent metals can ser

174 The NMR structure of Tetrahymena thermophila stem-loop IV shows a highly stru

175 The Tetrahymena thermophila strain SB281 fails to synthesize

176 An active Tetrahymena thermophila telomerase complex can be recons

177 Tetrahymena thermophila telomerase contains two essentia

178 Here we describe the architecture of Tetrahymena thermophila telomerase holoenzyme determined

179 nce of telomere binding by each of the seven Tetrahymena thermophila telomerase holoenzyme proteins T

180 entification of three additional subunits of Tetrahymena thermophila telomerase holoenzyme.

181 lass of atypical RRM first identified in the Tetrahymena thermophila telomerase LARP7 protein p65.

182 the sequences and structures of recombinant Tetrahymena thermophila telomerase RNA necessary for phy

183 Here, using circularly permuted variants of Tetrahymena thermophila telomerase RNA, we identify the

184 structure of the TBE element (helix II) from Tetrahymena thermophila telomerase RNA.

185 tic activity and protein-RNA interaction for Tetrahymena thermophila telomerase.

186 first complete replacement of the nine base TETRAHYMENA: thermophila telomerase templating region in

187 e about the structure of the DNA terminus at Tetrahymena thermophila telomeres, we have devised a lig

188 In Tetrahymena thermophila, telomeres become long at 30 deg

189 We previously purified epitope-tagged Tetrahymena thermophila TERT and characterized two of th

190 such as Saccharomyces cerevisiae (yeast) and Tetrahymena thermophila (Tet), for example, contain more

191 We have identified a family of genes in Tetrahymena thermophila that encode proteins homologous

192 We identified a gene, TWI1, in Tetrahymena thermophila that is homologous to piwi and i

193 We report a pioneering approach using Tetrahymena thermophila that permits rapid identificatio

194 ciliate species--Paramecium tetraurelia and Tetrahymena thermophila--that reassign the stop codons T

195 In the ciliated protozoan Tetrahymena thermophila the ribosomal DNA (rDNA) minichr

196 In Tetrahymena thermophila, the development of a transcript

197 ker histone H1 knockout strain (delta H1) of Tetrahymena thermophila, the number of mature RNAs produ

198 In the genome of Tetrahymena thermophila, the only ORF sharing similariti

199 In the ciliate Tetrahymena thermophila, the polypeptides stored in secr

200 In ciliates such as Tetrahymena thermophila, the resulting crystals function

201 In the ciliate Tetrahymena thermophila, the telomerase holoenzyme consi

202 In the ciliate Tetrahymena thermophila, thousands of DNA segments of va

203 ere we describe a unique ORC-like complex in Tetrahymena thermophila, TIF4, which bound in an ATP-dep

204 lectron microscopy studies were performed in Tetrahymena thermophila to determine how proteins assemb

205 We used the ciliate protist Tetrahymena thermophila to gain a better understanding o

206 chers have manipulated the unique biology of Tetrahymena thermophila to generate a premier experiment

207 RNase P activity from the ciliate protozoan Tetrahymena thermophila to learn more about the biochemi

208 ted proteins from the macronuclear genome of Tetrahymena thermophila to query prokaryotic and eukaryo

209 lyzed the role of tubulin polyglycylation in Tetrahymena thermophila using in vivo mutagenesis and im

210 essed MWCNT bioaccumulation in the protozoan Tetrahymena thermophila via trophic transfer from bacter

211 acronuclear genome of the ciliated protozoan Tetrahymena thermophila was analyzed by indirect end lab

212 tagenesis and homologous gene replacement in Tetrahymena thermophila, we analyzed mutations, deletion

213 hnique and exploiting the unique genetics of Tetrahymena thermophila, we have identified and characte

214 In the ciliate Tetrahymena thermophila, we identified TXR1, encoding a

215 For the first time in Tetrahymena thermophila, we use comparative whole-genome

216 Mating Tetrahymena thermophila were bombarded with ribosomal DN

217 breakage has been most rigorously defined in Tetrahymena thermophila, where it consists of a 15-bp DN

218 To address this question we used Tetrahymena thermophila, which expresses two SAS-6 homol

219 truct is a modification of tRNAGln(CUA) from Tetrahymena thermophila, which naturally recognizes the