ライフサイエンスコーパス: cytoplasmic filament

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1 first step to determine the function of the cytoplasmic filaments.

2 nd electron microscopy confirmed the lack of cytoplasmic filaments.

3 RE3] cells, nor do the control cells exhibit cytoplasmic filaments.

4 g compaction of the NPC and extension of the cytoplasmic filaments.

5 requires Dbp5 interaction with Nup159 in NPC cytoplasmic filaments and activation of Dbp5's ATPase ac

6 n-specific nucleoporin that localizes to the cytoplasmic filaments and provides several binding sites

7 alysis suggests that it is unlikely that the cytoplasmic filaments and the flagellar apparatus are ph

8 to assess the structural relationship of the cytoplasmic filaments and the PFF.

9 Treponemal cytoplasmic filaments are composed of one protein, CfpA,

10 Unique cytoplasmic filaments are found in the treponeme genus o

11 NPC's central channel rather than on distal cytoplasmic filaments, as previously supposed.

12 e unique structures, the gene coding for the cytoplasmic filaments, cfpA, was identified in various t

13 induction also occurs in response to keratin cytoplasmic filament collapse, absence, or ablation of K

14 ic ring component Nup107, and only later the cytoplasmic filament component Nup358.

15 NPC has cytoplasmic filaments composed of RanGAP1 and RanBP2 wit

16 Cytoplasmic filaments converged from their attachment po

17 Moreover, chains of cells are formed by the cytoplasmic filament-deficient mutant, and those cells s

18 for Ran in altering the conformation of the cytoplasmic filaments during transport.

19 domain and the NLS proved necessary for both cytoplasmic filament formation and nuclear targeting.

20 These cytoplasmic filaments have a ribbon-like profile and con

21 nderstanding of the involvement of bacterial cytoplasmic filaments in cell division requires the eluc

22 y condensed chromosomal DNA suggest that the cytoplasmic filaments may be involved in chromosome stru

23 Thus, the cytoplasmic filament network of the NPC is robust, consi

24 The cytoplasmic filament nucleoporins of the nuclear pore co

25 Nup) and 4000-fold higher than to Nup42p (a cytoplasmic filament Nup), revealing a steep gradient of

26 The cytoplasmic filaments of T. pallidum and other spirochet

27 f the NPC and is implicated in anchoring the cytoplasmic filaments of the NPC and recruiting the RNA

28 Nup358/RanBP2 is a constituent of the cytoplasmic filaments of the NPC specific to higher euka

29 itment of the DEAD-box helicase Ddx19 to the cytoplasmic filaments of the NPC that is mediated by the

30 m a trimeric complex with a component of the cytoplasmic filaments of the NPC, Nup358.

31 RanBP2/Nup358, the major component of the cytoplasmic filaments of the nuclear pore complex (NPC),

32 ther set of components appears to bridge the cytoplasmic filaments on the cytoplasmic side, and to be

33 The number of cytoplasmic filaments per cell of T. phagedenis (mean, 5

34 a ribbon-like profile and consist of a major cytoplasmic filament protein subunit (CfpA, formerly cal

35 The cytoplasmic filament protein-deficient mutant exhibited

36 pha/CAS complexes after export occurs in the cytoplasmic filament region of the NPC.

37 -deficient mutant of T. phagedenis possessed cytoplasmic filaments similar to those of the wild type,

38 ponema denticola, a ribbon-like structure of cytoplasmic filaments spans the cytoplasm at all stages

39 se proteins cause apoptosis by forming novel cytoplasmic filaments that recruit and activate pro-casp

40 Spirochaeta, and Leptonema contain multiple cytoplasmic filaments that run the length of the organis

41 The cytoplasmic filaments were also analyzed by electron mic

42 leoplasmin-gold along the length of extended cytoplasmic filaments, whereas RanGDP caused accumulatio

43 ed in large irregular bodies associated with cytoplasmic filaments while at late stages, vRNA was dis

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