ライフサイエンスコーパス: zebra fish

1 e are examining its role in embryogenesis in zebra fish.

2 region of iipA, was completely avirulent to zebra fish.

3 rization of NF-kappa B/I kappa B proteins in zebra fish.

4 -scale insertional mutagenesis screen in the zebra fish.

5 Aspartate 44 (D44) of zebra fish AID has been proposed to compensate for the a

6 Some features of zebra fish AID other than D44 might compensate for the a

7 Paradoxically, zebra fish AID, which lacks a serine at the position cor

8 e report a biochemical analysis of TGIF from zebra fish and DROSOPHILA: Our study reveals an unpreced

9 nerally applicable to other systems, such as zebra fish and embryonic stem cells, and may enable tiss

10 gands were tested for teratogenic effects on zebra fish and Xenopus embryos, we found that coadminist

11 or many model (e.g. human, mouse, fruit fly, zebra fish) and non-model species.

12 human keratinocyte, monocyte, and embryonic zebra fish assays revealed no cytotoxicity.

13 GT virus, is nontoxic following injection of zebra fish blastulae and efficiently infects embryonic c

14 pha M), which is able to block NF-kappa B in zebra fish cells, interferes with the notochord differen

15 Zebra fish contain two genomic copies (zfAPEX1a and zfAP

16 Zebra fish (Danio rerio) were infected with the NV delet

17 tive erythropoiesis in the rps29(-/-) mutant zebra fish DBA model.

18 l imaging of H2S and in vivo imaging in live zebra fish demonstrated FEPO's potential biological appl

19 he H3K9 histone methyltransferase Suv39h1 in zebra fish development.

20 patterns of gene expression during the early zebra fish development.

21 dels exist for FPD/AML, as Runx11/2 mice and zebra fish do not develop bleeding disorders or leukemia

22 l with the N-terminal ADPR binding pocket in zebra fish DrTRPM2.

23 esterol efflux in endothelial cells controls zebra fish embryonic angiogenesis.

24 Knockdown of Dnmt1 in zebra fish embryos caused defects in terminal differenti

25 both mouse developing cerebral cortices and zebra fish embryos.

26 t resulted in elevated IGFBP-1 expression in zebra fish embryos.

27 in mouse macrophages as well as infection of zebra fish embryos.

28 ll line that yields virus at a high titer on zebra fish embryos.

29 imetry to measure heat dissipation by living zebra-fish embryos and to estimate the energetics of spe

30 The recombinant human and zebra fish enzymes hydrolyze fructose-2,6-bisphosphate a

31 AID, we assayed AID from Japanese puffer and zebra fish for class-switching activity in mouse B cells

32 We show that zebra fish I kappa B alphas are degraded in a time-depen

33 Although the zebra fish IGFBP-1 promoter contains 13 consensus hypoxi

34 dopsis thaliana, Drosophila melanogaster, or zebra fish, in which a majority of genes have broad-shap

35 4 domain bound to VH9 and those of human and zebra fish MDM4 bound to a p53 peptide.

36 a defective erythropoiesis phenotype using a zebra fish model.

37 pombe, D. melanogaster, C. elegans, Xenopus, zebra fish, mouse and human, for a total of 12,877 tRFs.

38 Biochemical assays indicate that zebra fish NF-kappa B proteins are able to bind consensu

39 s Dnmt1 morphants could be rescued by active zebra fish or human DNMT1 but not by catalytically inact

40 Alternatively, the zebra fish protein might function in a manner that is in

41 Zebra fish TGIF, like its mammalian relative, interacts

42 maging in positive ion mode of rat brain and zebra fish tissues allowed enhanced detection of compoun

43 Rat brain and zebra fish tissues were investigated with reactive DESI-

44 Vertebrates, from zebra fish to humans, have an innate immune recognition

45 Deletion of ILK in zebra fish using antisense morpholino oligonucleotides r

46 crystal structures of these compounds in the zebra fish zVDR ligand binding domain as complexes with