ライフサイエンスコーパス: Paramecium

1 ation of swimming behaviour in the protozoan Paramecium.

2 ses produced by some calmodulin mutations in Paramecium.

3 e the swimming and bending powers exerted by Paramecium.

4 magnification factor = 1.4) to its predator, paramecium.

5 for infected Paramecium than for uninfected Paramecium.

6 iliar ciliate models, such as Tetrahymena or Paramecium.

7 ng triplet microtubules in Chlamydomonas and Paramecium.

8 22 S dynein regulatory light chain, p29, in Paramecium.

9 rotein kinases previously characterized from Paramecium (52 kDa CaPK-1, and 50 kDa CaPK-2) are activa

10 In Paramecium, a bacterial homospermidine synthase replaced

11 l body duplication in both Chlamydomonas and Paramecium, adding to the list of new tubulin family mem

12 The germline chromosomes in Paramecium and other ciliated protozoa contain regions o

13 e more tandem stop codons downstream of both Paramecium and Tetrahymena genes than expected by chance

14 Within a single class of ciliates, Paramecium and Tetrahymena species have long been known

15 the abundance of the intermediate consumer (Paramecium), and parasitism indirectly reduced the abund

16 nimals, the discharge of defensive spikes in Paramecium, and the secretion of insulin from pancreatic

17 The Paramecium aurelia complex is a group of 15 species that

18 eproductive isolation between species in the Paramecium aurelia complex.

19 ation in the Rab GTPase gene family in three Paramecium aurelia species.

20 es, possible mechanisms, and implications in Paramecium biology are discussed.

21 ing the interaction between the protist host Paramecium bursaria and the algal symbiont Chlorella sp.

22 Specifically, predation of the protist Paramecium bursaria by copepods resulted in a >100-fold

23 Paramecium bursaria chlorella virus (PBCV-1) is a large

24 Paramecium bursaria chlorella virus (PBCV-1) is the prot

25 Paramecium bursaria chlorella virus (PBCV-1) is the prot

26 lycans of the major capsid protein (Vp54) of Paramecium bursaria chlorella virus (PBCV-1) were recent

27 protein Vp54 from the prototype chlorovirus Paramecium bursaria chlorella virus 1 (PBCV-1) contains

28 Paramecium bursaria chlorella virus 1 (PBCV-1) elicits a

29 The 331-kbp chlorovirus Paramecium bursaria chlorella virus 1 (PBCV-1) genome wa

30 Paramecium bursaria chlorella virus 1 (PBCV-1) infects c

31 Paramecium bursaria chlorella virus 1 (PBCV-1) is the pr

32 Paramecium bursaria chlorella virus 1 (PBCV-1), a large

33 Paramecium bursaria chlorella virus 1 (PBCV-1), a member

34 The prototype of the genus is Paramecium bursaria chlorella virus 1 (PBCV-1).

35 he bacteriophage PRD1 and eukaryotic viruses Paramecium bursaria Chlorella virus 1 and adenovirus, su

36 histone lysine methyltransferase (vSET) from Paramecium bursaria chlorella virus 1 bound to cofactor

37 sequence and the structure of the homologous Paramecium bursaria chlorella virus 1 Vp54 MCP.

38 Kcv, a 94-aa protein encoded by Paramecium bursaria chlorella virus 1, is the smallest k

39 wo minor capsid proteins are absent, causing Paramecium bursaria chlorella virus and the cellular con

40 A unique homolog of this family, the Paramecium bursaria Chlorella virus arginine decarboxyla

41 Paramecium bursaria Chlorella virus type 1 (PBCV-1) is a

42 diameter, icosahedral, internally enveloped Paramecium bursaria chlorella virus was used to interpre

43 ical to the MCP structures of the eukaryotic Paramecium bursaria Chlorella virus, and the bacteriopha

44 To test this hypothesis, the ability of Paramecium bursaria chlorella virus-1 (PBCV-1) and chlor

45 Topoisomerase II from Paramecium bursaria chlorella virus-1 (PBCV-1) and chlor

46 ANK proteins from the prototypic chlorovirus Paramecium bursaria chlorella virus-1 (PBCV-1) that func

47 , a novel topoisomerase II was discovered in Paramecium bursaria chlorella virus-1 (PBCV-1) that has

48 clease V was identified from chlorella virus Paramecium bursaria chlorella virus-1 (PBCV-1).

49 Paramecium bursaria Chlorella virus-1 is an icosahedrall

50 ich corresponds to the C-terminal residue of Paramecium bursaria chlorella virus-1 topoisomerase II a

51 mbled into arrays that have either p6 (as in Paramecium bursaria Chlorella virus-1) or p3 symmetry (a

52 found in a strain of Chlorella virus (strain Paramecium bursaria Chlorella virus-1), which contains a

53 Notably, paramecium bursaria chlorella viruses encode a conserved

54 lated 22 S dynein from either Tetrahymena or Paramecium but not to 14 S dynein from either ciliate.

55 cium kinases shared sequence similarity with Paramecium calmodulin (30-34% identity).

56 tion of five interdomain residues to rat and Paramecium calmodulin N-domain fragments (residues 1-75)

57 Although a structure of Ca(2+)-saturated Paramecium CaM at 1.0 A resolution (1EXR.pdb) provides t

58 Studies of N-domain fragments of Paramecium CaM showed that residues 76-80 increased ther

59 A CaM-binding protein, PCM1 (Paramecium CaM-binding membrane-bound protein), from a d

60 HSQC NMR to monitor more than 40 residues in Paramecium CaM.

61 an fragments of the same length derived from Paramecium CaM.

62 m two trHbs, one from the ciliated protozoan Paramecium caudatum (P-trHb) and the other from the gree

63 Here, we show that the trajectories of Paramecium caudatum align with intense static magnetic f

64 The unicellular protozoan Paramecium caudatum contains a monomeric hemoglobin (Hb)

65 lia are made up of variable repeats, whereas Paramecium caudatum telomeric repeats are largely invari

66 (E. coli)) as a prey and ciliated protozoan (Paramecium caudatum) as a predator organism to determine

67 a fonticola), (ii) an intermediate consumer (Paramecium caudatum), (iii) a top predator (Didinium nas

68 We apply it to Paramecium caudatum, a single-cell protozoan that varies

69 ever, by localizing specific Rab proteins in Paramecium cells, we found that paralogues from the two

70 lipid binding properties similar to those of Paramecium copine.

71 etic susceptibility, Deltachi(p), of a whole Paramecium: Deltachi(p) = (6.7+/- 0.7) x 10(-23) m(3).

72 In Paramecium, developmentally programmed genome rearrangem

73 ted that there are two distinct types of the Paramecium enzyme, each synthesizing perfect telomeric r

74 these simulated gravities, denoted by f(gm), Paramecium exhibits a linear response up to f(gm) = 5 g,

75 cium genes, and the sequences encoded in the Paramecium genes differ from those in the plant CDPK gen

76 amino acid residues are the same in the two Paramecium genes, and the sequences encoded in the Param

77 K-alpha and PCaPK-beta, were isolated from a Paramecium genomic DNA library.

78 shown that the cam2 mutant (Ile136-->Thr) of Paramecium has a decreased level of methylated Lys115.

79 Because Paramecium has a transcriptionally silent germ-line nucl

80 for membrane excitation and ionic control in Paramecium has been facilitated by the availability of g

81 lasma gondii, and the contractile vacuole in paramecium have been demonstrated.

82 the effect of the distal pocket residues of Paramecium Hb in stabilizing the heme-bound ligands.

83 We postulate that the function of Paramecium Hb is to supply oxygen for cellular oxidative

84 Unlike a previously studied Paramecium IES, the presence of this IES in the macronuc

85 terative integration support the theory that Paramecium IESs evolved from transposable elements.

86 In Paramecium, IESs are generally short (28-882 bp), AT ric

87 We investigate various swimming modes of Paramecium in geometric confinements and a non-swimming

88 The C-terminal region of the Paramecium kinases shared sequence similarity with Param

89 nd that free-living ciliates Tetrahymena and Paramecium lost the eukaryotic genes encoding spermidine

90 on dynamics, modelling and analyses of host (Paramecium) morphology and behaviour.

91 uglena, Micromonas, Naegleria, Nephroselmis, Paramecium, Pavlova, Phaeodactylum, Porphyra, Pseudendoc

92 sent in a wide range of organisms, including Paramecium, plants, Caenorhabditis elegans, mouse, and h

93 The protist Paramecium presents opportunities to compare how groups

94 How a paramecium's cilium produces off-propulsion-plane curvat

95 main target, originally described as p29 in Paramecium, seems to increase ciliary beat frequency (CB

96 In the sibling species Paramecium septaurelia, mating type O is determined by c

97 m other species, including that from another Paramecium species that does not make a high percentage

98 velopmental Cell the discovery of a class of Paramecium sRNAs, produced by a unique Dicer-like enzyme

99 e synthesis of variable telomeric repeats by Paramecium telomerase are discussed.

100 All Paramecium telomerase RNAs examined include a template s

101 Paramecium telomeric DNA consists largely of a random di

102 n C. uncinata with those of 'model' ciliates-Paramecium, Tetrahymena, Euplotes, Oxytricha and Stylony

103 [Tetrahymena piggyBac-like 2] and LIA5) and Paramecium tetraurelia (PiggyMac).

104 holipid-binding proteins first isolated from Paramecium tetraurelia and found in a wide range of orga

105 analyze the genomes of two ciliate species--Paramecium tetraurelia and Tetrahymena thermophila--that

106 The telomeres of Paramecium tetraurelia are made up of variable repeats,

107 e, we present the 1.0 A crystal structure of Paramecium tetraurelia Ca(2+)-CaM, including 36 discrete

108 plication in the otherwise compact genome of Paramecium tetraurelia displays the early forces driving

109 n of a simple avoidance reaction behavior in Paramecium tetraurelia has shown that ion channels are a

110 Paramecium tetraurelia internal eliminated sequences (IE

111 The micronuclear DNA of Paramecium tetraurelia is estimated to contain over 50,0

112 Telomeric DNA in the ciliate Paramecium tetraurelia is synthesized by an error-prone

113 Pawn mutants of Paramecium tetraurelia lack a depolarization-activated C

114 The ciliate Paramecium tetraurelia must eliminate approximately 60,0

115 The membrane of Paramecium tetraurelia passes a large Mg(2+)-selective c

116 The error-prone telomerase from the ciliate Paramecium tetraurelia stereotypically misincorporates T

117 Paramecium tetraurelia stock 51 can express at least 11

118 Paramecium tetraurelia telomerase has been isolated from

119 cloned and sequenced a SEC7-related gene in Paramecium tetraurelia that contains an open reading fra

120 ut here we report a genome-wide estimate for Paramecium tetraurelia that is more than an order of mag

121 fusin, a major phosphoprotein in the ciliate Paramecium tetraurelia that undergoes rapid and massive

122 Three mutant strains of Paramecium tetraurelia with an enhanced sensitivity to m

123 the maternal inheritance of mating types in Paramecium tetraurelia, a long-standing problem in epige

124 tudied Ca2+/CaM-binding membrane proteins in Paramecium tetraurelia, a unicellular model system.

125 oned and sequenced telomerase RNA genes from Paramecium tetraurelia, P. primaurelia, P. multimicronuc

126 two domains were demonstrated by mutants of Paramecium tetraurelia, some of which have altered calci

127 es coding for rRNA (ribosomal DNA [rDNA]) of Paramecium tetraurelia, stock 51, are arranged in polyme

128 ding proteins were isolated from extracts of Paramecium tetraurelia.

129 e transcriptome of the intron-rich eukaryote Paramecium tetraurelia.

130 algal origin in the ciliates Tetrahymena and Paramecium tetraurelia.

131 ochondrial ATP synthase dimer of the ciliate Paramecium tetraurelia.

132 ncodes K(+)-channel pore-forming subunits in Paramecium tetraurelia.

133 these modifications were higher for infected Paramecium than for uninfected Paramecium.

134 dem stop codons is larger in Tetrahymena and Paramecium than in yeast.

135 in cloning other unknown DNA sequences from Paramecium that are functionally responsible for various

136 g (self-bending) of the cell body allows the Paramecium to reorient its anterior end and explore a co

137 In the ciliate Paramecium, transposable elements and their single-copy

138 ound in a wide range of species from Homo to Paramecium use calmodulin (CaM) as their constitutive or

139 A new study has revealed how Paramecium uses short RNAs to delete information from th

140 Paramecium was found to accumulate homospermidine, sugge

141 Paramecium was found to have two closely related copine

142 bserved that 29% of bacterivory potential of paramecium was lost, including an approximately 12 h del

143 ing the model predator-prey system (Didinium-Paramecium) we support our hypothesis, by examining repl

144 by others on the distantly related ciliate, Paramecium, we propose a molecular model of template-gui