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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
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

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