ライフサイエンスコーパス: polycephalum

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1 rved in the mitochondrial genome of Physarum polycephalum.

2 al regulation of DNA replication in Physarum polycephalum.

3 the mitochondrion of the slime mold Physarum polycephalum.

4 rome c oxidase subunit 3 mRNA (cox3) from P. polycephalum.

5 nd nuclear matrix from plasmodia of Physarum polycephalum.

6 ase was I-PpoI from the slime mould Physarum polycephalum.

7 up I intron found in the slime mold Physarum polycephalum.

8 group I intron in the rRNA genes of Physarum polycephalum, also can home into yeast chromosomal ribos

9 the PAF-AH from the lower eukaryote Physarum polycephalum although pPAF-AH and PAF-AH(II) tolerate th

10 anisms from the Myxomycetes, namely Physarum polycephalum and Didymium iridis, allows us to test hypo

11 encoded on the mitochondrial DNA of Physarum polycephalum and Didymium nigripes require insertional e

12 molds (Dictyostelium discoideum and Physarum polycephalum), and the roundworm (Caenorhabditis elegans

13 ranscriptional nature of editing in Physarum polycephalum, and will certainly provide future opportun

14 ed from the mitochondrial genome of Physarum polycephalum are edited by the insertion of nonencoded n

15 ed from the mitochondrial genome of Physarum polycephalum are heavily edited.

16 show that the brainless slime mold Physarum polycephalum constructs a form of spatial memory by avoi

17 Within P. polycephalum, cytoplasm is shuttled in a peristaltic wav

18 the patterns exhibited by individuals of P. polycephalum demonstrate that individuals maximize inter

19 n-3 headgroup better than the PAF-AH from P. polycephalum does.

20 ound in the ribo-somal RNA genes of Physarum polycephalum, encodes the I-PpoI homing endonuclease.

21 lling commitment and sporulation of Physarum polycephalum from experimental results using a hierarchi

22 The slime mold Physarum polycephalum grows as a random network of tubes, and our

23 s its network remains a puzzle, but Physarum polycephalum has emerged as a novel model used to explor

24 oint is the mitochondrial genome of Physarum polycephalum in which only about one-third of the number

25 the myxomycetes Didymium iridis and Physarum polycephalum, indicating evolutionary conservation of th

26 Insertional RNA editing in Physarum polycephalum is a complex process involving the specific

27 Slime mould Physarum polycephalum is a single cell visible by the unaided eye

28 Physarum Polycephalum is a single cell visible by unaided eye.

29 ome b apoprotein in mitochondria of Physarum polycephalum is created by the insertion of 43 nucleotid

30 ng endonuclease from the slime mold Physarum polycephalum, is a small enzyme (2 x 20 kDa) of known th

31 ed endonuclease from the slime mold Physarum polycephalum, is a small enzyme (2 x 20 kDa) that cataly

32 In the myxomycete Physarum polycephalum, nucleotides that are not specified by the

33 The yeast and P. polycephalum proteins bind actin, suggesting that the no

34 the peristaltic wave to organism size and P. polycephalum's ability to find the shortest route betwee

35 A simple feedback seems to give rise to P. polycephalum's complex behaviors, and the same mechanism

36 We first track P. polycephalum's response to a localized nutrient stimulus

37 We employ the P. polycephalum thermic switch to prototype hybrid electric

38 the naturally synchronous organism Physarum polycephalum to examine the fate of core histones in G2

39 of the foraging behaviour of slime mould P. polycephalum to solve the network design problem and con

40 omycetes Stemonitis flavogenita and Physarum polycephalum using a modified anchor PCR approach.

41 We annotate the mitochondrial genome of P.polycephalum using several different approaches for gene

42 Plasmodial transglutaminase of Physarum polycephalum was purified by anion exchange and hydropho

43 uclei in G2 phase of the slime mold Physarum polycephalum, when transplanted, by plasmodial coalescen

44 within the mitochondrial genome of Physarum polycephalum, which had gone undetected by existing prog

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