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1 ive P1 site forms a hydrogen bond and not an ionic bond.
2 iodine ions via the formation of strong Cd-I ionic bonds.
3 s different than covalent/polar-covalent and ionic bonds.
4 otential, and abilities to form covalent and ionic bonds.
5 n the Cu(100) surface to form Na-carboxylate ionic bonds.
6 e distinction of CSBs vis-a-vis covalent and ionic bonds.
7 clusters that are stabilized by hydrogen or ionic bonds.
8 than GA-CLEA owing to the presence of weaker ionic bonds.
9 terials but 1 angstrom more than covalent or ionic bonds.
10 ostatic interactions, involving hydrogen and ionic bonding.
11 s, which passivate defects due to the strong ionic bonding.
13 onate through a hydrogen bond rather than an ionic bond and that this interaction is much less import
14 howed that this interaction relies mostly on ionic bonds and does not involve the two C-terminal cyst
18 ving local loss of hydrophobic interactions, ionic bonds, and helical structure, leads to Urc inactiv
20 o bonds with significant covalent character, ionic bonds are of limited use for the spatial structuri
21 systems forming dative-covalent rather than ionic bonds, as exemplified here by NH(3) and CO, mu(S)
28 of a single critical interaction, the buried ionic bond between the phosphate of the pTyr and Arg bet
29 ative cell walls was dominated by the strong ionic bonding between the surface amine groups of CDs an
33 er of charged amino acids with potential for ionic bond formation between oppositely charged partners
36 tion of oxygen vacancies weaken the covalent/ionic bonds, giving rise to the unexpected plasticity.
37 e, nanosized (346-nm) complexes with GFX via ionic bond, hydrogen bond, and hydrophobic interactions.
38 ace chemistries-including hydrophobic bonds, ionic bonds, hydrogen bonds, self-assembled monolayers,
39 VHS domains suggests that this intrapeptide ionic bond in solution may reduce the change in binding
40 A167R double mutant, which re-establishes an ionic bond in the opposite orientation, reverses this po
42 is the local electric field that breaks the ionic bonds in mixed-halide nanocrystals, which could be
43 GF) spreading and attachment, as affected by ionic bonding interactions, may facilitate cell orientat
51 bundance of C=O in the CDs, the formation of ionic-bond networks around the CDs, and the spatial conf
52 ral rigidity to the tissue through extensive ionic-bonding networks; this matrix is highly permselect
55 llular structures are shaped by hydrogen and ionic bonds, plus van der Waals and hydrophobic forces.
57 alyse RG-II dimerization via co-ordinate and ionic bonding respectively (possible and impossible, res
59 n 2-4 A of the arginine, forming a favorable ionic bond that is largely unaltered upon activation.
60 ibe a predictable directional orientation of ionic bonds that contain concave nonpolar shields around
62 tural and dynamic roles; in particular, four ionic bonds that open in a sequential, zipper-like fashi
63 caine analogs has been assumed to provide an ionic bond to the aspartic acid residue on the dopamine
64 trong guest-host interaction beyond the pure ionic bonding, where a large extent of covalency may exi
65 ough an additional lysine-phosphate backbone ionic bond which makes a significant contribution to the
66 g due to their inherently strong covalent or ionic bonding, which usually leads to material crazing a
68 (D53) conserved in both beta 2ms to form an ionic bond with arginine residues at positions 35 and 48
69 e that the guanido group of Arg-120 forms an ionic bond with the carboxylate group of arachidonate an
70 s significant covalent Ir-B bonding and weak ionic bonding with charge transfer from B(3) to Ir, and
71 abilize H1 in PrP(C) yet form intermolecular ionic bonds with adjacent PrP molecules during conversio
72 th activation, the Asp3.49(138)-Arg3.50(139) ionic bond would break, and the unrestrained Arg would b
73 salts form anisotropic polar structures with ionic bonding, yet covalent-like directionality, akin to