ライフサイエンスコーパス: paracrystalline

1 e previously shown that the seemingly static paracrystalline actin core of hair cell stereocilia unde

2 es revealed, in both cases, Rho organized in paracrystalline and raftlike structures.

3 The structures are best described as paracrystalline, and many of the concepts of conventiona

4 Each stereocilium is supported by a paracrystalline array of parallel actin filaments that a

5 nd carbohydrate polymers and forms an almost paracrystalline array on the cell surface.

6 nsisting of cytoplasmic vacuoles surrounding paracrystalline arrays and amorphous rod-like inclusions

7 accretion (in approximately 2% of cells) of paracrystalline arrays containing mutant chaperonin comp

8 inclusion bodies and their arrangement into paracrystalline arrays gives the gut of infected insects

9 RCs) that are assembled into two-dimensional paracrystalline arrays in the endoplasmic/sarcoplasmic r

10 electron microscopy contained densely packed paracrystalline arrays of 30- to 32-nm diameter viral pa

11 pound membrane vesicles and highly geometric paracrystalline arrays, which may represent viral replic

12 form structural dimers that are organized in paracrystalline arrays.

13 open helical structures that accumulated as paracrystalline arrays.

14 mplete virus particles, but these now formed paracrystalline arrays.

15 acis spore, the exosporium, is composed of a paracrystalline basal layer and an external hair-like na

16 re is the exosporium, which is composed of a paracrystalline basal layer and an external hair-like na

17 Confirming the location of CsmA in the paracrystalline baseplate, cross-linking showed that Csm

18 velope is completely replaced by a different paracrystalline coat as the poxvirus matures.

19 cells contained rhomboid protogranules with paracrystalline contents, dilated rough endoplasmic reti

20 Coiled-coil dimers of paramyosin form a paracrystalline core of these filaments, and the motor p

21 Bacillus thuringiensis) are surrounded by a paracrystalline flexible yet resistant layer called exos

22 spontaneously assembled into two-dimensional paracrystalline hexagonal lattices comprising open, six-

23 iated with loss of mitochondrial cristae and paracrystalline inclusions in 9 of 10 subjects, compared

24 l abnormalities were identified including i) paracrystalline inclusions, ii) linearization of cristae

25 h ragged red muscle fibers and mitochondrial paracrystalline inclusions.

26 BinAB is a naturally occurring paracrystalline larvicide distributed worldwide to comba

27 ing striated muscle, taking advantage of the paracrystalline lattice that would ultimately allow unde

28 This protein forms a paracrystalline lattice, called the S-layer, surrounding

29 This protein forms a paracrystalline lattice, called the surface layer (S-lay

30 osphate carboxylase/oxygenase (RuBisCO) in a paracrystalline lattice, making it possible for these or

31 e the unique ability to self-assemble into a paracrystalline layer on the surface of bacilli and form

32 beta-1,4-linked glucan chains assembled into paracrystalline microfibrils that are synthesized by pla

33 The paracrystalline model has implications for understanding

34 The paracrystalline order parameter, g, is calculated to cha

35 ertheless, the PR- MuLV particles do exhibit paracrystalline order with a spacing between Gag molecul

36 Because of the pleomorphic shape and paracrystalline packing of the Gag-RNA complexes, we rai

37 -C spikes showed reflections consistent with paracrystalline packing of the NP molecules in a lattice

38 development, the regular tubular network of paracrystalline prolamellar bodies (PLBs) and the flatte

39 The cell surface comprises a paracrystalline proteinaceous S-layer encoded by the slp

40 Surface layers (S-layers) are paracrystalline, proteinaceous structures found in most

41 We find that inhomogeneous paracrystalline structures containing local cubic orderi

42 oelectron microscopy, mTim44 was seen in the paracrystalline structures within the mitochondria, as w

43 microtubules but re-aggregates tubulin into paracrystalline structures.

44 ns, is mediated in part by the presence of a paracrystalline surface layer (S-layer) that confers ser

45 into well-defined amyloid phases and define paracrystalline surfaces able to catalyse specific enant

46 es that account for noncrystalline disorder, paracrystalline theory (PT) and modified Caille theory (