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1 lization to an osmoregulatory organelle, the contractile vacuole.
2 but populate the tubules and bladders of the contractile vacuole.
3 asites and are linked to the function of the contractile vacuole.
4 osmoregulation, the Dictyostelium discoideum contractile vacuole.
5 cked AP180 or AP2 exhibited abnormally large contractile vacuoles.
6 roteins and limiting homotypic fusions among contractile vacuoles.
7  because of excessive homotypic fusion among contractile vacuoles.
8 er, AP180 null cells formed abnormally large contractile vacuoles.
9 olyphosphate, which were also present in the contractile vacuoles.
10 cted, macropinocytosis (myosin I-dependent), contractile vacuole activity (myosin V-dependent), and p
11   We also reveal that OCRL/Dd5P4 acts at the contractile vacuole, an exocytic osmoregulatory organell
12 ibution but enriched on the membranes of the contractile vacuole and Golgi-like structures in the cel
13 h use vacuolar-type proton pumps for filling contractile vacuoles and actin for osmoregulation, but n
14 len and rounded in shape, with hypertrophied contractile vacuoles and intense cytoplasmic vacuolizati
15 bited the carbonic anhydrase activity of the contractile vacuoles and prolonged their contraction cyc
16 lized to punctae at the plasma membrane, the contractile vacuole, and the cytoplasm and associated wi
17              The mass-dense granules and the contractile vacuole appeared to contact each other when
18                                     Although contractile vacuoles are essential to many species, incl
19                  Right before discharge, the contractile vacuole bladder sequentially recruits Draini
20                                              Contractile vacuole bladders were isolated by subcellula
21      Polyphosphate was also localized to the contractile vacuole by 4',6-diamidino-2-phenylindole sta
22 er (TcPho91) localized to the bladder of the contractile vacuole complex (CVC) of Trypanosoma cruzi,
23    The channel changes its location from the contractile vacuole complex in epimastigotes to the plas
24 y support a role for acidocalcisomes and the contractile vacuole complex in osmoregulation and identi
25 e of an aquaporin in acidocalcisomes and the contractile vacuole complex of T. cruzi, provides suppor
26                                          The contractile vacuole complex was characterized by two bla
27 MP-mediated fusion of acidocalcisomes to the contractile vacuole complex with translocation of this a
28 ied by immunogold electron microscopy as the contractile vacuole complex.
29                           Clathrin puncta on contractile vacuoles contained multiple accessory protei
30 ects Vamp7B into clathrin-coated vesicles on contractile vacuoles, creating an efficient mechanism fo
31                                          The contractile vacuole (CV) complex in Dictyostelium is a t
32                       Water expulsion by the contractile vacuole (CV) in Dictyostelium is carried out
33 ing mammalian lysosomes, phagosomes, and the contractile vacuole (CV) of the amoeba Dictyostelium.
34                                          The contractile vacuole (CV) system is the osmoregulatory or
35  cytoplasmic pressure is sufficient to drive contractile vacuole emptying for a wide range of cellula
36 ls was accompanied by a marked inhibition of contractile vacuole emptying.
37 icles to the expulsion of cellular waste via contractile vacuoles, exocytosis and its sequel, endocyt
38  Because vacuolar-type proton-pump-dependent contractile vacuole filling and pressure-dependent empty
39 46, encoding a Rab family GTPase involved in contractile vacuole function, is likely a direct target.
40   To identify the basic principles governing contractile vacuole function, we investigate here the mo
41              Osmotic tests revealed that the contractile vacuole functioned inefficiently in mutant c
42 s in bacteria and Toxoplasma gondii, and the contractile vacuole in paramecium have been demonstrated
43                                 The enlarged contractile vacuoles in AP180-null mutants formed becaus
44 , the cycle of expansion and contraction for contractile vacuoles in AP80 null cells was twice as lon
45 pressure is sufficient to drive water out of contractile vacuoles in these species, similar to findin
46 nt microscopy indicated that in mutant cells contractile vacuole membrane proteins were associated wi
47 , localizes to the endosomal pathway and the contractile vacuole membrane system in Dictyostelium dis
48  phagocytosis and contained abnormal looking contractile vacuole membranes.
49  AP180 plays a unique role as a regulator of contractile vacuole morphology and activity in Dictyoste
50                             Furthermore, the contractile vacuole network of membranes (probably conne
51  Vamp7B was mislocalized and enriched on the contractile vacuoles of AP180-null mutants.
52                                Dictyostelium contractile vacuoles offer a valuable system to study cl
53 clear envelopes, micronuclear envelopes, and contractile vacuole pores.
54 tes and in the flagellar pocket membrane and contractile vacuole/spongiome complex of amastigotes.
55 regulating the structure and function of the contractile vacuole system by facilitating communication
56  and the exocyst complex in tethering of the contractile vacuole to the plasma membrane, fusion, and
57                    Many eukaryotic cells use contractile vacuoles to collect excess water from the cy
58  zoospores use specialized organelles called contractile vacuoles to pump water out of the cell, ther
59 e clathrin accessory proteins influenced the contractile vacuole, we generated cell lines that carrie
60 membrane, in intracellular vacuoles, and the contractile vacuole where it colocalized with the vacuol