ライフサイエンスコーパス: rodlike

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 glucose/ADP/Mg2+/AlF3 are consistent with a rodlike conformation for the monomer similar to that obs

12 ar peptides considered here adopt a helical, rodlike conformation in aqueous solution.

13 In both cases, the as-grown, rodlike crystal shape is maintained during the solid-sta

14 The rodlike cTnI bends sharply at the end interacting with t

15 ed cTnC that sits at one end of an elongated rodlike cTnI, covering about one-third of its length.

16 ems is acid-base switchable to either an ON (rodlike dendronized polymers) or an OFF (flexible polyme

17 different architectures, including spheres, rodlike, disclike, or any other shape.

18 dependent upon the structure of the central rodlike domain and have implications for the design of d

19 tractable glycosylated polymers that possess rodlike extended conformations similar to natural mucins

20 ymerization of deoxyhemoglobin S into stiff, rodlike fibers that deform and rigidify red cells.

21 eneous initial protofibrils that became more rodlike following the elongation reaction.

22 Rodlike guests possessing two or three binding stations,

23 ne equivalent of LiClO(4) or LiBF(4) to form rodlike ionic polymers.

24 was performed in the presence and absence of rodlike ligand 2b, which exhibits an affinity for the he

25 ile rigidification of nonmacrocycles lead to rodlike ligands that bind well to groove-shaped binding

26 ence of nutrients, the forespore can exhibit rodlike, longitudinal growth when SpoIIQ and SpoIIP are

27 ory of channel-facilitated transport of long rodlike macromolecules through thin membranes under the

28 Rodlike micelle formation and swelling with toluene were

29 mes, aggregates of Janus glycodendrimers and rodlike micelles named glycodendrimer aggregates and gly

30 nfold when the preference for spherical over rodlike micelles was not strong enough to overcome the t

31 transmitting the stability signal along this rodlike molecule.

32 In continuing our investigations on rodlike molecules composed of bicyclo[2.2.2]octane units

33 part to the change in rotational entropy of rodlike molecules on dimerization and in part to the inc

34 ikely to be present, cholesteric stacking of rodlike molecules seemed to be the predominant contribut

35 Lateral association of the flexible rodlike monomers involves a multiple-step process that i

36 characterized by weakness and eosinophilic, rodlike (nemaline) inclusions in muscle fibers.

37 f f for both fragments was consistent with a rodlike particle having a diameter of 33-45 nm and a len

38 The model we use is that of a rodlike particle with an attractive (hydrophobic) stripe

39 In addition, viral infection of conelike and rodlike photoreceptors and amacrinelike cells suggest th

40 suggest that the pineal gland may contain a rodlike phototransduction cascade.

41 acrylamide to an aqueous solution of a stiff rodlike polymer molecule of xanthan gum, a popular emuls

42 ine the physics of orientational ordering of rodlike polymers and the microphase separation of coil-c

43 The novel rodlike polymers mimic the architecture of mucin glycopr

44 eometrically suitable for the preparation of rodlike polymers.

45 s that could endow Kalirin with the flexible rodlike properties characteristic of spectrin and dystro

46 otoxicogenic Escherichia coli is mediated by rodlike, rigid, highly hydrophobic proteins designated f

47 0 did not diminish binding to HDV unbranched rodlike RNA.

48 to small unilamellar phospholipid vesicles, rodlike SDS micelles, or lipid bicelles.

49 darkly stained puncta of either spherical or rodlike shape in the olfactory cortex, nucleus isthmi, a

50 nfocal microscopy, we found that the typical rodlike shape of the Weibel--Palade body is missing in v

51 tion of the oligomers were consistent with a rodlike structure comprised of six-membered, [RGaNH](3)

52 require interactions between the unbranched rodlike structure of HDV RNA and hepatitis delta antigen

53 what is called the top end of the unbranched rodlike structure predicted for the genomic RNA template

54 we suggest that the b subunit is not a rigid rodlike structure, but has an inherent flexibility compa

55 that is predicted to fold into an unbranched rodlike structure.

56 elta virus (HDV) can fold into an unbranched rodlike structure.

57 and HU, promote the condensation of DNA into rodlike structures by providing the free energy necessar

58 rotary shadowing revealed the appearance of rodlike structures with multiple sharp bends, a small no

59 IHF, polyamines condense DNA primarily into rodlike structures.

60 ds relative to the protein backbone in these rodlike systems.

61 ynamics of the spontaneous reconstitution of rodlike tobacco mosaic virus particles in solutions cont

62 ers, such as DNA, protein alpha-helices, and rodlike virus particles, remains elusive.

63 Aqueous suspensions of mixtures of the rodlike virus tobacco mosaic virus (TMV) with globular m