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1  22 S dynein regulatory light chain, p29, in Paramecium.
2 ation of swimming behaviour in the protozoan Paramecium.
3 magnification factor = 1.4) to its predator, paramecium.
4 ses produced by some calmodulin mutations in Paramecium.
5 , we obtain a model of autonomously behaving Paramecium.
6 iliar ciliate models, such as Tetrahymena or Paramecium.
7 e the swimming and bending powers exerted by Paramecium.
8  for infected Paramecium than for uninfected Paramecium.
9 ng triplet microtubules in Chlamydomonas and Paramecium.
10 e responses of unicellular protists, such as Paramecium [1, 2], to complex animal neuromuscular activ
11 rotein kinases previously characterized from Paramecium (52 kDa CaPK-1, and 50 kDa CaPK-2) are activa
12                                           In Paramecium, a bacterial homospermidine synthase replaced
13 l body duplication in both Chlamydomonas and Paramecium, adding to the list of new tubulin family mem
14                  The germline chromosomes in Paramecium and other ciliated protozoa contain regions o
15 e more tandem stop codons downstream of both Paramecium and Tetrahymena genes than expected by chance
16           Within a single class of ciliates, Paramecium and Tetrahymena species have long been known
17  the abundance of the intermediate consumer (Paramecium), and parasitism indirectly reduced the abund
18 nimals, the discharge of defensive spikes in Paramecium, and the secretion of insulin from pancreatic
19                                          The Paramecium aurelia complex is a group of 15 species that
20 eproductive isolation between species in the Paramecium aurelia complex.
21 ation in the Rab GTPase gene family in three Paramecium aurelia species.
22 ber on Pavlovian conditioning in the ciliate Paramecium aurelia, and suggest that criticisms of her f
23 es, possible mechanisms, and implications in Paramecium biology are discussed.
24  the model facultative endosymbiosis between Paramecium bursaria and Chlorella spp., we demonstrate t
25 ing the interaction between the protist host Paramecium bursaria and the algal symbiont Chlorella sp.
26       Specifically, predation of the protist Paramecium bursaria by copepods resulted in a >100-fold
27 dy, the feasibility of using the algal virus Paramecium bursaria chlorella virus (PBCV-1) as an adeno
28                                              Paramecium bursaria chlorella virus (PBCV-1) is a large
29                                              Paramecium bursaria chlorella virus (PBCV-1) is the prot
30                                              Paramecium bursaria chlorella virus (PBCV-1) is the prot
31 lycans of the major capsid protein (Vp54) of Paramecium bursaria chlorella virus (PBCV-1) were recent
32  protein Vp54 from the prototype chlorovirus Paramecium bursaria chlorella virus 1 (PBCV-1) contains
33                                              Paramecium bursaria chlorella virus 1 (PBCV-1) elicits a
34                      The 331-kbp chlorovirus Paramecium bursaria chlorella virus 1 (PBCV-1) genome wa
35                                              Paramecium bursaria chlorella virus 1 (PBCV-1) infects c
36                              The chlorovirus Paramecium bursaria chlorella virus 1 (PBCV-1) is a larg
37                                              Paramecium bursaria chlorella virus 1 (PBCV-1) is the pr
38                                              Paramecium bursaria chlorella virus 1 (PBCV-1), a large
39                                              Paramecium bursaria chlorella virus 1 (PBCV-1), a member
40 n icosahedrally averaged capsid structure of Paramecium bursaria chlorella virus 1 (PBCV-1).
41                The prototype of the genus is Paramecium bursaria chlorella virus 1 (PBCV-1).
42 he bacteriophage PRD1 and eukaryotic viruses Paramecium bursaria Chlorella virus 1 and adenovirus, su
43 histone lysine methyltransferase (vSET) from Paramecium bursaria chlorella virus 1 bound to cofactor
44 sequence and the structure of the homologous Paramecium bursaria chlorella virus 1 Vp54 MCP.
45              Kcv, a 94-aa protein encoded by Paramecium bursaria chlorella virus 1, is the smallest k
46 -resolution, five-fold averaged structure of Paramecium bursaria chlorella virus 1, we unexpectedly f
47 wo minor capsid proteins are absent, causing Paramecium bursaria chlorella virus and the cellular con
48         A unique homolog of this family, the Paramecium bursaria Chlorella virus arginine decarboxyla
49                                              Paramecium bursaria Chlorella virus type 1 (PBCV-1) is a
50  diameter, icosahedral, internally enveloped Paramecium bursaria chlorella virus was used to interpre
51 ical to the MCP structures of the eukaryotic Paramecium bursaria Chlorella virus, and the bacteriopha
52      To test this hypothesis, the ability of Paramecium bursaria chlorella virus-1 (PBCV-1) and chlor
53                        Topoisomerase II from Paramecium bursaria chlorella virus-1 (PBCV-1) and chlor
54                                              Paramecium bursaria chlorella virus-1 (PBCV-1) is a larg
55 ANK proteins from the prototypic chlorovirus Paramecium bursaria chlorella virus-1 (PBCV-1) that func
56 , a novel topoisomerase II was discovered in Paramecium bursaria chlorella virus-1 (PBCV-1) that has
57 clease V was identified from chlorella virus Paramecium bursaria chlorella virus-1 (PBCV-1).
58                                              Paramecium bursaria Chlorella virus-1 is an icosahedrall
59 ich corresponds to the C-terminal residue of Paramecium bursaria chlorella virus-1 topoisomerase II a
60 mbled into arrays that have either p6 (as in Paramecium bursaria Chlorella virus-1) or p3 symmetry (a
61 found in a strain of Chlorella virus (strain Paramecium bursaria Chlorella virus-1), which contains a
62                                     Notably, paramecium bursaria chlorella viruses encode a conserved
63                         The ciliate protist, Paramecium bursaria, offers a valuable insight into how
64 lic mechanisms of two independent origins of Paramecium bursaria-Chlorella photosymbiosis [9-11] usin
65 lated 22 S dynein from either Tetrahymena or Paramecium but not to 14 S dynein from either ciliate.
66 cium kinases shared sequence similarity with Paramecium calmodulin (30-34% identity).
67 tion of five interdomain residues to rat and Paramecium calmodulin N-domain fragments (residues 1-75)
68     Although a structure of Ca(2+)-saturated Paramecium CaM at 1.0 A resolution (1EXR.pdb) provides t
69             Studies of N-domain fragments of Paramecium CaM showed that residues 76-80 increased ther
70                 A CaM-binding protein, PCM1 (Paramecium CaM-binding membrane-bound protein), from a d
71 an fragments of the same length derived from Paramecium CaM.
72 HSQC NMR to monitor more than 40 residues in Paramecium CaM.
73 m two trHbs, one from the ciliated protozoan Paramecium caudatum (P-trHb) and the other from the gree
74       Here, we show that the trajectories of Paramecium caudatum align with intense static magnetic f
75                    The unicellular protozoan Paramecium caudatum contains a monomeric hemoglobin (Hb)
76 lia are made up of variable repeats, whereas Paramecium caudatum telomeric repeats are largely invari
77 (E. coli)) as a prey and ciliated protozoan (Paramecium caudatum) as a predator organism to determine
78 a fonticola), (ii) an intermediate consumer (Paramecium caudatum), (iii) a top predator (Didinium nas
79                               We apply it to Paramecium caudatum, a single-cell protozoan that varies
80 materials by a model aquatic microoraganism, Paramecium caudatum.
81 ever, by localizing specific Rab proteins in Paramecium cells, we found that paralogues from the two
82  mechanisms of intergenomic epistasis in the Paramecium-Chlorella symbiosis and test whether compensa
83 lipid binding properties similar to those of Paramecium copine.
84 etic susceptibility, Deltachi(p), of a whole Paramecium: Deltachi(p) = (6.7+/- 0.7) x 10(-23) m(3).
85                                           In Paramecium, developmentally programmed genome rearrangem
86 ted that there are two distinct types of the Paramecium enzyme, each synthesizing perfect telomeric r
87 these simulated gravities, denoted by f(gm), Paramecium exhibits a linear response up to f(gm) = 5 g,
88 cium genes, and the sequences encoded in the Paramecium genes differ from those in the plant CDPK gen
89  amino acid residues are the same in the two Paramecium genes, and the sequences encoded in the Param
90 K-alpha and PCaPK-beta, were isolated from a Paramecium genomic DNA library.
91 shown that the cam2 mutant (Ile136-->Thr) of Paramecium has a decreased level of methylated Lys115.
92                                      Because Paramecium has a transcriptionally silent germ-line nucl
93 for membrane excitation and ionic control in Paramecium has been facilitated by the availability of g
94 lasma gondii, and the contractile vacuole in paramecium have been demonstrated.
95  the effect of the distal pocket residues of Paramecium Hb in stabilizing the heme-bound ligands.
96            We postulate that the function of Paramecium Hb is to supply oxygen for cellular oxidative
97                  Unlike a previously studied Paramecium IES, the presence of this IES in the macronuc
98 terative integration support the theory that Paramecium IESs evolved from transposable elements.
99                                           In Paramecium, IESs are generally short (28-882 bp), AT ric
100 hysiological basis of autonomous behavior of Paramecium in ecological environments.
101     We investigate various swimming modes of Paramecium in geometric confinements and a non-swimming
102                                              Paramecium is a large unicellular organism that swims in
103                 The C-terminal region of the Paramecium kinases shared sequence similarity with Param
104 nd that free-living ciliates Tetrahymena and Paramecium lost the eukaryotic genes encoding spermidine
105 on dynamics, modelling and analyses of host (Paramecium) morphology and behaviour.
106 cies, similar to findings from the alveolate Paramecium multimicronucleatum.
107 uglena, Micromonas, Naegleria, Nephroselmis, Paramecium, Pavlova, Phaeodactylum, Porphyra, Pseudendoc
108 sent in a wide range of organisms, including Paramecium, plants, Caenorhabditis elegans, mouse, and h
109                                  The protist Paramecium presents opportunities to compare how groups
110                                        How a paramecium's cilium produces off-propulsion-plane curvat
111                               In the ciliate Paramecium, secondary small RNAs are produced after the
112  main target, originally described as p29 in Paramecium, seems to increase ciliary beat frequency (CB
113                       In the sibling species Paramecium septaurelia, mating type O is determined by c
114                         Therefore, unlike in Paramecium, small RNA amplification occurs before IES ex
115 m other species, including that from another Paramecium species that does not make a high percentage
116 velopmental Cell the discovery of a class of Paramecium sRNAs, produced by a unique Dicer-like enzyme
117 e synthesis of variable telomeric repeats by Paramecium telomerase are discussed.
118                                          All Paramecium telomerase RNAs examined include a template s
119                                              Paramecium telomeric DNA consists largely of a random di
120 n C. uncinata with those of 'model' ciliates-Paramecium, Tetrahymena, Euplotes, Oxytricha and Stylony
121  [Tetrahymena piggyBac-like 2] and LIA5) and Paramecium tetraurelia (PiggyMac).
122 holipid-binding proteins first isolated from Paramecium tetraurelia and found in a wide range of orga
123  analyze the genomes of two ciliate species--Paramecium tetraurelia and Tetrahymena thermophila--that
124                             The telomeres of Paramecium tetraurelia are made up of variable repeats,
125 e, we present the 1.0 A crystal structure of Paramecium tetraurelia Ca(2+)-CaM, including 36 discrete
126 plication in the otherwise compact genome of Paramecium tetraurelia displays the early forces driving
127 n of a simple avoidance reaction behavior in Paramecium tetraurelia has shown that ion channels are a
128                                              Paramecium tetraurelia internal eliminated sequences (IE
129                      The micronuclear DNA of Paramecium tetraurelia is estimated to contain over 50,0
130                 Telomeric DNA in the ciliate Paramecium tetraurelia is synthesized by an error-prone
131                              Pawn mutants of Paramecium tetraurelia lack a depolarization-activated C
132 s of Tetrahymena thermophila MTA1 (TthMTA1), Paramecium tetraurelia MTA9 (PteMTA9)-TthMTA1 binary com
133                                  The ciliate Paramecium tetraurelia must eliminate approximately 60,0
134                              The membrane of Paramecium tetraurelia passes a large Mg(2+)-selective c
135  The error-prone telomerase from the ciliate Paramecium tetraurelia stereotypically misincorporates T
136                                              Paramecium tetraurelia stock 51 can express at least 11
137                                              Paramecium tetraurelia telomerase has been isolated from
138  cloned and sequenced a SEC7-related gene in Paramecium tetraurelia that contains an open reading fra
139 ut here we report a genome-wide estimate for Paramecium tetraurelia that is more than an order of mag
140 fusin, a major phosphoprotein in the ciliate Paramecium tetraurelia that undergoes rapid and massive
141 ental metapopulations of the aquatic protist Paramecium tetraurelia to determine how network topology
142                      Three mutant strains of Paramecium tetraurelia with an enhanced sensitivity to m
143  the maternal inheritance of mating types in Paramecium tetraurelia, a long-standing problem in epige
144 tudied Ca2+/CaM-binding membrane proteins in Paramecium tetraurelia, a unicellular model system.
145 icha trifallax, Tetrahymena thermophila, and Paramecium tetraurelia, but only the Oxytricha lineage h
146 oned and sequenced telomerase RNA genes from Paramecium tetraurelia, P. primaurelia, P. multimicronuc
147  two domains were demonstrated by mutants of Paramecium tetraurelia, some of which have altered calci
148 es coding for rRNA (ribosomal DNA [rDNA]) of Paramecium tetraurelia, stock 51, are arranged in polyme
149  protein Ezl1 from the unicellular eukaryote Paramecium tetraurelia, which exhibits significant seque
150 ncodes K(+)-channel pore-forming subunits in Paramecium tetraurelia.
151 ding proteins were isolated from extracts of Paramecium tetraurelia.
152 e transcriptome of the intron-rich eukaryote Paramecium tetraurelia.
153 ochondrial ATP synthase dimer of the ciliate Paramecium tetraurelia.
154  to selection by the filter-feeding predator Paramecium tetraurelia.
155 algal origin in the ciliates Tetrahymena and Paramecium tetraurelia.
156 these modifications were higher for infected Paramecium than for uninfected Paramecium.
157 dem stop codons is larger in Tetrahymena and Paramecium than in yeast.
158  in cloning other unknown DNA sequences from Paramecium that are functionally responsible for various
159 For this reason, several authors have called Paramecium the "swimming neuron".
160 g (self-bending) of the cell body allows the Paramecium to reorient its anterior end and explore a co
161                               In the ciliate Paramecium, transposable elements and their single-copy
162 ound in a wide range of species from Homo to Paramecium use calmodulin (CaM) as their constitutive or
163                 A new study has revealed how Paramecium uses short RNAs to delete information from th
164                                              Paramecium was found to accumulate homospermidine, sugge
165                                              Paramecium was found to have two closely related copine
166 bserved that 29% of bacterivory potential of paramecium was lost, including an approximately 12 h del
167 ing the model predator-prey system (Didinium-Paramecium) we support our hypothesis, by examining repl
168  by others on the distantly related ciliate, Paramecium, we propose a molecular model of template-gui

 
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