ライフサイエンスコーパス: polycephalum

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 arkable exception in the slime mold Physarum polycephalum.

9 e prototypical vascular networks of Physarum polycephalum.

10 ed organisms such as the slime mold Physarum polycephalum.

11 Among them, the slime mold Physarum polycephalum, a giant single cell, is ideally suited to

12 interest due to its resemblance to Physarum polycephalum, ability to leverage parallel processing, a

13 dless of the absence or presence of food, P. polycephalum achieves superdiffusive migration by perfor

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

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

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

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

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

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

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

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

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

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

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

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

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

27 icellular organisms, the slime mold Physarum polycephalum forms a giant network-shaped plasmodium whi

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

29 The P. polycephalum genome contains >20,000 U12-type introns-25

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

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

32 criptome analysis of the slime mold Physarum polycephalum in the plasmodium state under different env

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

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

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

36 Physarum polycephalum is a large multinucleated amoeboid cell tha

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

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

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

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

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

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

43 dy and quantify the migration behavior of P. polycephalum plasmodia on the time scale of days in the

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

45 The acellular slime mold Physarum polycephalum provides an excellent model to study networ

46 ow the giant unicellular slime mold Physarum polycephalum responds to a nutrient source.

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

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

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

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

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

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

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

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

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

56 g decentralized units in slime mold Physarum polycephalum, we introduce a combination of surfactants,

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

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