ライフサイエンスコーパス: encystment

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1 traclonal propagation and regeneration after encystment.

2 iates the developmental pathway resulting in encystment.

3 hat putrescine induces protozoan trophozoite encystment and adversely affects cyst viability.

4 After encystment and attachment to the host cells, the parasit

5 binogalactan proteins of both species induce encystment and prevent germination, the effects of both

6 ations in the rhizosphere to induce zoospore encystment and thereby deter taxis to the root surface.

7 nts following incubation in water and amoeba encystment and was required for delay of phagosome acidi

8 ty chromatography from supernatant fluids of encystment cultures.

9 electrical fields, influence zoospore taxis, encystment, cyst germination, and hyphal chemotropism in

10 The 26-kDa form appeared early during encystment followed by the appearance of the 22-kDa form

11 arensis has a reduced ability to both induce encystment in A. castellanii and invade human macrophage

12 Following encystment in Acanthamoeba castellanii and reversion of

13 standpoint because death of the mouse before encystment interrupts the parasite life cycle.

14 Encystment is essential to the pathogen's long term intr

15 ay represent specific adaptation for oceanic encystment life cycles, preventing the cells from rapid

16 and used to produce cysts either with Neff's encystment medium (NEM) or starvation on nonnutrient aga

17 ever, dexamethasone treatment did not affect encystment of Acanthamoeba trophozoites.

18 ptides, previously shown to effect premature encystment of Phytophthora capsici zoospores, were fused

19 Although AH induced encystment of the amoebae, cysts remained viable.

20 ve identified a requirement for somatic cell encystment of the germline in promoting GSC abscission.

21 phosphate on excystment, proliferation, and encystment of trophozoites and cysts of A. castellanii w

22 he effects of incubation in water and amoeba encystment on L. pneumophila strain JR32 and null mutant

23 mor (AH) contains factors that either induce encystment or kill the amoebae.

24 n F. tularensis proteins that induce a rapid encystment phenotype (REP) in the free-living amoeba, Ac

25 e temperatures (19-22 degrees C) had greater encystment success across temperatures than either cold-

26 of non-encysting cells and that by 48 h into encystment the level of glucosamine 6-phosphate has decr

27 sizes UDP-GalNAc during cyst wall formation (encystment) via a pathway of inducible enzymes similar t

28 varied depending on the stage of infection (encystment vs. clearance): warm- (22-28 degrees C) and c

29 Amoeba encystment was inhibited by addition of beta(1)-adrenerg

30 Zoospore encystment was unaffected by silencing, but cysts germin

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