ライフサイエンスコーパス: Artemia

1 onding protein of human, Xenopus laevis, and Artemia.

2 n early preemergence development of encysted Artemia.

3 imaging application was also confirmed using Artemia as a model.

4 oth species significantly reduced feeding on Artemia but no significant decrease in microplastics ing

5 udget, biomass, lipids, protein, and maximum Artemia capture rate.

6 In-vivo bio-imaging in live brine shrimp Artemia confirmed that HL-FeNPs could be used as fluores

7 These studies identify activated Artemia cysts as a system for biochemical studies of p70

8 Halophilic bacteria were enriched from Artemia cysts, living in salt lakes, in different salt m

9 E-47/g Artemia) or high (392.59 mug BDE-47/g Artemia) dose of BDE-47 from fertilization to 34 days po

10 increased with toxicity of immature fruit to Artemia during germination and decreased with toxicity t

11 t pH fluctuations, metabolic state change of Artemia embryos, and kinetic insulation of fluctuations

12 Here Daphnia magna, Eisenia fetida and Artemia franciscana are used to demonstrate the potentia

13 amino acid polypeptide from the brine shrimp Artemia franciscana is 34 kDa.

14 Interestingly, the brine shrimp Artemia franciscana is the only animal known to express

15 this engineered pond system, brine shrimp ( Artemia franciscana Kellogg) and brine fly (Ephydridae s

16 ered carbon-black materials on brine shrimp (Artemia franciscana) as a model marine microcrustacean.

17 in experimental populations of brine shrimp (Artemia franciscana) was measured to assess hypothesized

18 t exclusively on superabundant brine shrimp (Artemia franciscana).

19 ., and reduced survivorship of brine shrimp, Artemia franciscana, across a range of concentrations of

20 In the branchiopod crustacean, Artemia franciscana, the trunk Hox genes are expressed i

21 rpureogenus CFRM02 pigments are non-toxic to Artemia franciscana.

22 ring anoxia-induced quiescence in embryos of Artemia franciscana.

23 one species of anostracan, the brine shrimp, Artemia franciscana.

24 insufficient to mitigate benzene toxicity to Artemia in coexposure experiments.

25 Thus an originally Artemia-like pattern of homeotic gene expression has app

26 programmed, was programmed with SBM-enriched Artemia nauplii during the live feed stage (4-26 dph) an

27 s C) temperature and then fed microplastics, Artemia nauplii, or both.

28 exposed to either a low (57.68 mug BDE-47/g Artemia) or high (392.59 mug BDE-47/g Artemia) dose of B

29 exhibited similar high toxicity against the Artemia ribosomes with IC50 values near 1 nM.

30 coli ribosomes, about the same as it had for Artemia ribosomes.

31 Partially purified Artemia S6 kinase was inactivated by treatment with prot

32 Likewise, Artemia salina (brine shrimps) was used to study cytotox

33 Dormant Artemia salina cysts contain desiccated gastrulae that a

34 city of seagrass extracts against nauplii of Artemia salina revealed that Syringodium isoetifolium ex

35 to reduce overall activity 500-fold against Artemia salina ribosomes.

36 er, it showed toxicity against brine shrimp (Artemia Salina) (LD50 of 66.26 mug/mL).

37 er, it showed toxicity against brine shrimp (Artemia Salina) (LD50 of 66.26 ug/mL).

38 onation using a brine shrimp toxicity assay (Artemia salina).

39 xicity was confirmed with micronucleus (MN), Artemia salina, and Allium cepa assays.

40 ring infection of an aquatic model organism, Artemia salina.

41 of 10 x 40 mum Nylon fibers to brine shrimp (Artemia sp).

42 amounts of adenine residues from ribosomal (Artemia sp. and rat ribosomes) and non-ribosomal substra

43 Half of the corals were fed Artemia sp. brine shrimp in a separate feeding tank to p

44 rtebrate- and wind-dispersed species reduced Artemia survivorship and hyphal growth of Fusarium durin

45 We found that, unlike the pattern seen in Artemia, these genes are expressed in well-defined discr

46 damicornis only ingested microplastics when Artemia were also present, providing evidence that micro