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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
11 l body duplication in both Chlamydomonas and Paramecium, adding to the list of new tubulin family mem
13 e more tandem stop codons downstream of both Paramecium and Tetrahymena genes than expected by chance
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
21 ing the interaction between the protist host Paramecium bursaria and the algal symbiont Chlorella sp.
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
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
39 wo minor capsid proteins are absent, causing Paramecium bursaria chlorella virus and the cellular con
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
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
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
54 lated 22 S dynein from either Tetrahymena or Paramecium but not to 14 S dynein from either ciliate.
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
62 m two trHbs, one from the ciliated protozoan Paramecium caudatum (P-trHb) and the other from the gree
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
69 ever, by localizing specific Rab proteins in Paramecium cells, we found that paralogues from the two
71 etic susceptibility, Deltachi(p), of a whole Paramecium: Deltachi(p) = (6.7+/- 0.7) x 10(-23) m(3).
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
78 shown that the cam2 mutant (Ile136-->Thr) of Paramecium has a decreased level of methylated Lys115.
80 for membrane excitation and ionic control in Paramecium has been facilitated by the availability of g
89 nd that free-living ciliates Tetrahymena and Paramecium lost the eukaryotic genes encoding spermidine
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
95 main target, originally described as p29 in Paramecium, seems to increase ciliary beat frequency (CB
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
102 n C. uncinata with those of 'model' ciliates-Paramecium, Tetrahymena, Euplotes, Oxytricha and Stylony
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
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
116 The error-prone telomerase from the ciliate Paramecium tetraurelia stereotypically misincorporates T
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
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
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
138 ound in a wide range of species from Homo to Paramecium use calmodulin (CaM) as their constitutive or
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
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