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1 furo[2,3-d]pyrimidin-2(3H)-ones in which the rodlike acetylene spacer replaces the 4-substituted-phen
2                                   Instead, a rodlike aggregate that mimics microtubules is complexed
3 dendron rodcoils (DRC) containing dendritic, rodlike, and coillike segments are described.
4 d NMR approaches is limited because of their rodlike anisotropic shape and repeating sequence.
5                                          The rodlike arrays are composed of zinc porphyrins at the te
6 pearance change abruptly from spherulitic to rodlike as temperature is increased.
7      The induction time for the formation of rodlike assemblies is sensitive to oligomerization.
8 sition involves an initial formation of thin rodlike assemblies, which then evolve to form crystals.
9 -120 nm) and had morphologies (spherical and rodlike) associated with the polymer chain stiffness.
10      We explicitly treat bulk excursions for rodlike chains arranged in parallel and consider a simpl
11 ange lyotropic ordering as a result of their rodlike character.
12  glucose/ADP/Mg2+/AlF3 are consistent with a rodlike conformation for the monomer similar to that obs
13 ar peptides considered here adopt a helical, rodlike conformation in aqueous solution.
14                 In both cases, the as-grown, rodlike crystal shape is maintained during the solid-sta
15  electrode-supported crystallites, where the rodlike crystallites are either oriented largely normal
16                                          The rodlike cTnI bends sharply at the end interacting with t
17 ed cTnC that sits at one end of an elongated rodlike cTnI, covering about one-third of its length.
18 ems is acid-base switchable to either an ON (rodlike dendronized polymers) or an OFF (flexible polyme
19  different architectures, including spheres, rodlike, disclike, or any other shape.
20  dependent upon the structure of the central rodlike domain and have implications for the design of d
21 tractable glycosylated polymers that possess rodlike extended conformations similar to natural mucins
22 ymerization of deoxyhemoglobin S into stiff, rodlike fibers that deform and rigidify red cells.
23 cular pattern and assembles with IMPDH2 into rodlike filaments, in which IMPDH2 is stable.
24 eneous initial protofibrils that became more rodlike following the elongation reaction.
25 rough side-by-side interactions); elongated, rodlike geometries (where subunits are bound end-to-end)
26                                              Rodlike guests possessing two or three binding stations,
27 ne equivalent of LiClO(4) or LiBF(4) to form rodlike ionic polymers.
28 was performed in the presence and absence of rodlike ligand 2b, which exhibits an affinity for the he
29 ile rigidification of nonmacrocycles lead to rodlike ligands that bind well to groove-shaped binding
30 ence of nutrients, the forespore can exhibit rodlike, longitudinal growth when SpoIIQ and SpoIIP are
31 ory of channel-facilitated transport of long rodlike macromolecules through thin membranes under the
32  In this work, a series of tailored uniaxial rodlike mesogens disfavouring the formation of blue phas
33                                              Rodlike micelle formation and swelling with toluene were
34 mes, aggregates of Janus glycodendrimers and rodlike micelles named glycodendrimer aggregates and gly
35 nfold when the preference for spherical over rodlike micelles was not strong enough to overcome the t
36 transmitting the stability signal along this rodlike molecule.
37          In continuing our investigations on rodlike molecules composed of bicyclo[2.2.2]octane units
38  part to the change in rotational entropy of rodlike molecules on dimerization and in part to the inc
39 ikely to be present, cholesteric stacking of rodlike molecules seemed to be the predominant contribut
40          Lateral association of the flexible rodlike monomers involves a multiple-step process that i
41  characterized by weakness and eosinophilic, rodlike (nemaline) inclusions in muscle fibers.
42 f f for both fragments was consistent with a rodlike particle having a diameter of 33-45 nm and a len
43                The model we use is that of a rodlike particle with an attractive (hydrophobic) stripe
44 ercritical fluids and gases formed by sparse rodlike particles.
45 In addition, viral infection of conelike and rodlike photoreceptors and amacrinelike cells suggest th
46  suggest that the pineal gland may contain a rodlike phototransduction cascade.
47 acrylamide to an aqueous solution of a stiff rodlike polymer molecule of xanthan gum, a popular emuls
48 ine the physics of orientational ordering of rodlike polymers and the microphase separation of coil-c
49                                    The novel rodlike polymers mimic the architecture of mucin glycopr
50 eometrically suitable for the preparation of rodlike polymers.
51 s that could endow Kalirin with the flexible rodlike properties characteristic of spectrin and dystro
52 otoxicogenic Escherichia coli is mediated by rodlike, rigid, highly hydrophobic proteins designated f
53 0 did not diminish binding to HDV unbranched rodlike RNA.
54  to small unilamellar phospholipid vesicles, rodlike SDS micelles, or lipid bicelles.
55 darkly stained puncta of either spherical or rodlike shape in the olfactory cortex, nucleus isthmi, a
56 nfocal microscopy, we found that the typical rodlike shape of the Weibel--Palade body is missing in v
57 r irradiation, transitioning from spheres to rodlike shapes, mimicking energy-dependent functions nor
58 tion of the oligomers were consistent with a rodlike structure comprised of six-membered, [RGaNH](3)
59  require interactions between the unbranched rodlike structure of HDV RNA and hepatitis delta antigen
60 what is called the top end of the unbranched rodlike structure predicted for the genomic RNA template
61 T-like twisted fibril morphology, unlike the rodlike structure that lRPT normally adopts.
62 we suggest that the b subunit is not a rigid rodlike structure, but has an inherent flexibility compa
63 that is predicted to fold into an unbranched rodlike structure.
64 elta virus (HDV) can fold into an unbranched rodlike structure.
65 and HU, promote the condensation of DNA into rodlike structures by providing the free energy necessar
66  rotary shadowing revealed the appearance of rodlike structures with multiple sharp bends, a small no
67 olgi glycosyltransferases to become extended rodlike structures.
68  IHF, polyamines condense DNA primarily into rodlike structures.
69 ds relative to the protein backbone in these rodlike systems.
70 ynamics of the spontaneous reconstitution of rodlike tobacco mosaic virus particles in solutions cont
71 ers, such as DNA, protein alpha-helices, and rodlike virus particles, remains elusive.
72       Aqueous suspensions of mixtures of the rodlike virus tobacco mosaic virus (TMV) with globular m