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1 e previously shown that the seemingly static paracrystalline actin core of hair cell stereocilia unde
2                            Here we construct paracrystalline amyloid surfaces through the self-propag
3 es revealed, in both cases, Rho organized in paracrystalline and raftlike structures.
4         The structures are best described as paracrystalline, and many of the concepts of conventiona
5          Each stereocilium is supported by a paracrystalline array of parallel actin filaments that a
6 in a surface layer (S-layer) consisting of a paracrystalline array of repeating lattice-forming prote
7 nd carbohydrate polymers and forms an almost paracrystalline array on the cell surface.
8                           In infected cells, paracrystalline arrays (PAs) of virions were observed in
9 nsisting of cytoplasmic vacuoles surrounding paracrystalline arrays and amorphous rod-like inclusions
10  accretion (in approximately 2% of cells) of paracrystalline arrays containing mutant chaperonin comp
11  inclusion bodies and their arrangement into paracrystalline arrays gives the gut of infected insects
12 RCs) that are assembled into two-dimensional paracrystalline arrays in the endoplasmic/sarcoplasmic r
13 electron microscopy contained densely packed paracrystalline arrays of 30- to 32-nm diameter viral pa
14  phase separation, and are distinct from the paracrystalline arrays of virions observed by transmissi
15 S-layers) are proteinaceous, two-dimensional paracrystalline arrays that constitute a major component
16 pound membrane vesicles and highly geometric paracrystalline arrays, which may represent viral replic
17 mplete virus particles, but these now formed paracrystalline arrays.
18 form structural dimers that are organized in paracrystalline arrays.
19  open helical structures that accumulated as paracrystalline arrays.
20 acis spore, the exosporium, is composed of a paracrystalline basal layer and an external hair-like na
21 re is the exosporium, which is composed of a paracrystalline basal layer and an external hair-like na
22       Confirming the location of CsmA in the paracrystalline baseplate, cross-linking showed that Csm
23 ically bind to crystalline (CBM2a-RRedX) and paracrystalline (CBM17-FITC) cellulose, were used to dif
24 velope is completely replaced by a different paracrystalline coat as the poxvirus matures.
25  cells contained rhomboid protogranules with paracrystalline contents, dilated rough endoplasmic reti
26      Coiled-coil dimers of paramyosin form a paracrystalline core of these filaments, and the motor p
27                             The discovery of paracrystalline diamond adds an unusual diamond form to
28 ecular dynamics simulation. The formation of paracrystalline diamond is a result of densely distribut
29                                          The paracrystalline diamond reported in this work, consistin
30        The structural characteristics of the paracrystalline diamond were identified through a combin
31  Bacillus thuringiensis) are surrounded by a paracrystalline flexible yet resistant layer called exos
32 spontaneously assembled into two-dimensional paracrystalline hexagonal lattices comprising open, six-
33 iated with loss of mitochondrial cristae and paracrystalline inclusions in 9 of 10 subjects, compared
34 l abnormalities were identified including i) paracrystalline inclusions, ii) linearization of cristae
35 h ragged red muscle fibers and mitochondrial paracrystalline inclusions.
36               BinAB is a naturally occurring paracrystalline larvicide distributed worldwide to comba
37 ing striated muscle, taking advantage of the paracrystalline lattice that would ultimately allow unde
38                         This protein forms a paracrystalline lattice, called the S-layer, surrounding
39                         This protein forms a paracrystalline lattice, called the surface layer (S-lay
40 osphate carboxylase/oxygenase (RuBisCO) in a paracrystalline lattice, making it possible for these or
41 e the unique ability to self-assemble into a paracrystalline layer on the surface of bacilli and form
42 beta-1,4-linked glucan chains assembled into paracrystalline microfibrils that are synthesized by pla
43                                          The paracrystalline model has implications for understanding
44 sed on a continuous random network and on a 'paracrystalline' model, respectively-the latter defined
45 al and local-energy descriptors to show that paracrystalline models are consistent with experiments i
46 or and cell envelope support structure whose paracrystalline nature is essential for its function.
47 pendent upon molecular packing; however, the paracrystalline nature of these materials limits the amo
48                                          The paracrystalline order parameter, g, is calculated to cha
49 ertheless, the PR- MuLV particles do exhibit paracrystalline order with a spacing between Gag molecul
50         Because of the pleomorphic shape and paracrystalline packing of the Gag-RNA complexes, we rai
51 -C spikes showed reflections consistent with paracrystalline packing of the NP molecules in a lattice
52 roteins contribute to the maintenance of the paracrystalline PLB morphology and are necessary for eff
53  development, the regular tubular network of paracrystalline prolamellar bodies (PLBs) and the flatte
54 and all archaeal cells are encapsulated by a paracrystalline, protective, and cell-shape-determining
55                 The cell surface comprises a paracrystalline proteinaceous S-layer encoded by the slp
56                Surface layers (S-layers) are paracrystalline, proteinaceous structures found in most
57                             Here we report a paracrystalline state of diamond that is distinct from e
58 MSP is sequestered through its assembly into paracrystalline structures called fibrous bodies (FBs).
59                   We find that inhomogeneous paracrystalline structures containing local cubic orderi
60 oelectron microscopy, mTim44 was seen in the paracrystalline structures within the mitochondria, as w
61  microtubules but re-aggregates tubulin into paracrystalline structures.
62 ns, is mediated in part by the presence of a paracrystalline surface layer (S-layer) that confers ser
63  into well-defined amyloid phases and define paracrystalline surfaces able to catalyse specific enant
64 es that account for noncrystalline disorder, paracrystalline theory (PT) and modified Caille theory (