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1 r 12, independent of the time when the cells encysted.
2 loped a robust and reproducible protocol for encysting A. castellanii as well as a high-throughput, q
3 undergo stage conversion to bradyzoites that encyst and persist predominantly in the brain.
4  environmental conditions, infected FLA will encyst and provide an intracellular niche allowing their
5 rophosphorylase immunoaffinity purified from encysting and non-encysting cells exhibited the same mol
6 licable paradigm for treatment of active and encysted apicomplexan and other infections, and a generi
7  p70S6k in early preemergence development of encysted Artemia.
8 orylase protein is present constitutively in encysting as well as non-encysting cells.
9 3-19 degrees C) tadpoles had fewer parasites encyst at warm and cold performance temperatures, respec
10 ease in IOP, as well as the possibility that encysted blebs form cytokines.
11 of all the cytokines in the aqueous from the encysted blebs, in which the IOP was the highest, sugges
12 arasite differentiation to the slow-growing, encysted bradyzoite form.
13 e form during acute infection to a quiescent encysted bradyzoite stage that persists inside long-live
14 nct from the dense granules; however, in the encysted bradyzoite stage, TgPL1 localizes to the parasi
15  sequences (SRSs) from that displayed by the encysted bradyzoite stage.
16 rms: a rapidly replicating tachyzoite and an encysted bradyzoite.
17 ing tachyzoite and the more slowly dividing, encysted bradyzoite.
18 e for acute illness, whereas slowly dividing encysted bradyzoites can remain latent within the tissue
19 es and hypersensitivity and do not eliminate encysted bradyzoites that recrudesce.
20 ranes to enter intracellular tachyzoites and encysted bradyzoites.
21 nine enter Toxoplasma gondii tachyzoites and encysted bradyzoites.
22 ~2 billion persons chronically infected with encysted bradyzoites.
23 -phosphate increases 3-fold over that of non-encysting cells and that by 48 h into encystment the lev
24 h kinases were expressed in trophozoites and encysting cells as 44- and 41-kDa polypeptides, respecti
25 munoaffinity purified from encysting and non-encysting cells exhibited the same molecular weight, ami
26 es were regulated with the cell cycle and in encysting cells giActin was recruited to the Golgi-like
27 -terminal region, fewer ESVs were stained in encysting cells, and there was no staining in cysts.
28 hether the enzyme came from encysting or non-encysting cells, the change in its circular dichroism sp
29 pression of cyst wall protein transcripts in encysting cells.
30 rase 1 gene (gglct-1) is transcribed only in encysting cells.
31 sion level of either one of these kinases in encysting cells.
32 t constitutively in encysting as well as non-encysting cells.
33 fied hundreds of small secretory vesicles in encysting E. invadens parasites and in E. histolytica tr
34 metabolism and growth of the parasite in the encysted form and represents a substantial body of infor
35 nus Entamoeba travel from host to host in an encysted form.
36 regulatory point in amino sugar synthesis in encysting Giardia and that its allosteric anabolic activ
37 anscribed differentially in nonencysting and encysting Giardia trophozoites.
38 ne pyrophosphorylase activity, purified from encysting Giardia, is allosterically activated anabolica
39           In such hosts virulent strains can encyst, hinting at an explanation for the evolution of v
40 od stream and lymphatics, but preferentially encyst in the eye and other parts of the central nervous
41  an obligate parasitic stage in which larvae encyst in the tissues of finfish, offering a plausible e
42       Giardia trophozoites were persuaded to encyst in vitro by mimicking physiological stimuli.
43 ese parasites is limited because they do not encyst in vitro.
44  immune response to a nematode parasite that encysts in the small intestine.
45                    Unicellular protozoa that encyst individually upon starvation evolved at least eig
46 tal muscle is increased and the frequency of encysted larvae exhibiting necrosis is reduced.
47 t present in the skeletal muscle adjacent to encysting larvae.
48 glucosamine 6-phosphate has decreased to non-encysting levels or below.
49  host or, more commonly, establish resistant encysted life forms before the emergence of protective i
50 pidly and subsequently develop low levels of encysted muscle larvae.
51  when they ingest aquatic insects containing encysted N. risticii-infected trematodes.
52 , regardless of whether the enzyme came from encysting or non-encysting cells, the change in its circ
53           One paper shows that nuclei in the encysted organism can temporarily fuse and exchange gene
54                            EVs isolated from encysting parasites promoted encystation in other parasi
55 undergoing stage conversion from a primarily encysted, quiescent bradyzoite to a fast-replicating, hi
56 ating spermatocytes in eya mutant testes are encysted, ruling out a role for eya in cyst cell viabili
57 ithin 24 h after trophozoites are induced to encyst, the level of glucosamine 6-phosphate increases 3
58                         Giardia lamblia must encyst to survive in the environment and subsequently in
59 ghly stable, is secreted in large amounts by encysting trophozoites, and correlates well with O&P.
60 differentially expressed in nonencysting and encysting trophozoites, the giardial ceramide glucosyltr
61 is released when the cells are stimulated to encyst with galactose-terminated ligands.
62 rged, dumped, or carried in runoff, bringing encysted zoonotic protozoan parasites to estuaries and c
63          At pH 7.7, up to 99% and 96% of the encysted zoospores were removed in IOCS and uncoated san
64                           Significantly more encysted zoospores were retained in IOCS than in uncoate
65 zoospores were more readily transported than encysted zoospores, thus posing a greater dispersal and