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1 at hybrids and parental forms are adaptively nonequivalent.
2 domains in these two halves are functionally nonequivalent.
3 posal that these two halves are functionally nonequivalent.
4  fact that DNA strands are complementary and nonequivalent.
5 ogous halves of the ArsA may be functionally nonequivalent.
6 ary components of the ligand-binding site is nonequivalent.
7 nit of CPS are functionally and structurally nonequivalent.
8 PLP sites in cystathionine beta-synthase are nonequivalent.
9 t isotherms and indicates that the hemes are nonequivalent.
10 n this region are important for function and nonequivalent.
11 exonic and intronic replacements between two nonequivalent 5'splice sites in the 469 nt long rbcS3A i
12 which bears primary, secondary, and tertiary nonequivalent abstractable gamma-hydrogens, dramatically
13 roceeds with high selectivity between subtly nonequivalent acetal oxygen atoms.
14 l muscle acetylcholine receptor contains two nonequivalent acetylcholine binding sites, one each at t
15 dition reactions involving 1,3-disubstituted nonequivalent allene dienophiles were studied, and some
16 sition alpha2 beta gamma delta are formed by nonequivalent alpha-gamma and alpha-delta subunit interf
17  elements in the HTLV-1 LTR are functionally nonequivalent and suggest that Sp1 can influence HTLV-1
18 ions are all contributors to activation, are nonequivalent, and are additive.
19 rtzite CdS nanorods are crystallographically nonequivalent, asymmetric heterostructures can be produc
20  a spectroscopic characterization of the two nonequivalent beta-carotene molecules in the photosystem
21                          For tobramycin, two nonequivalent binding sites were found with K(D1) = 352
22  potential nucleotide binding sites that are nonequivalent both in the absence and in the presence of
23  causes development of healthy, functionally nonequivalent brain hemispheres.
24 ffluxing pump Anabaena AztA are functionally nonequivalent, but only with respect to zinc resistance.
25 body rely on interactions among distinct and nonequivalent cell types.
26                  Surprisingly, unprecedented nonequivalent chemical shift values (up to 2.052 ppm) of
27 DOR spectroscopy confirm the presence of two nonequivalent CN(-) ligands and delocalized spin density
28  and precursors for graphenic C phases, five nonequivalent CO species have been distinguished, eviden
29 eries, and nonrandomized experiments using a nonequivalent comparison group.
30  use were also included to the analysis as a nonequivalent concurrent control group.
31 ts of 60 copies each of P1(A) and P1(B), two nonequivalent conformers of the P1 protein.
32 risingly, meta-substituted phenyl rings with nonequivalent constitutions (i.e., O(4)O(5) oxazole term
33                                          The nonequivalent coordination environment of copper stabili
34 hium atoms in all crystal structures adopt a nonequivalent coordination protocol and exist in two dif
35 ht to be essential in binding one of the two nonequivalent copper atoms.
36  interactions of the 180-subunit capsid plus nonequivalent CP-CP interactions.
37 s in situ, we show that these enzymes act as nonequivalent decision gates, determining context-depend
38 remia with same species was also analyzed as nonequivalent dependent controls.
39                              We identify two nonequivalent DNA-binding sites and propose a model in w
40 ctions are the result of binding of multiple nonequivalent domains.
41  translocating potential are cooperative and nonequivalent due to the interaction-dependent reorganiz
42 rified that 32 (74%) of the 43 patients with nonequivalent durations of response (> 30 days differenc
43 supramolecular species composed of a pair of nonequivalent Dy(III)-radical complexes exhibits single-
44 ension of this approach to proteins with two nonequivalent EF-hand Ca(2+)-binding sites--rat beta par
45                            We found that the nonequivalent electron distribution within an asymmetric
46 ach such dimer contains two CPs in distinct, nonequivalent environments, in contrast to the quasi-equ
47 al and rotational behavior because its three nonequivalent equilibrium structures have nearly identic
48   A sample of 10 000 pairs of ED visits with nonequivalent ESI scores, balanced for each of the 10 po
49 ws five distinct peaks for each magnetically nonequivalent exchangeable proton in the molecule.
50 nated receptors or by incorporating multiple nonequivalent fluorine atoms in a single receptor.
51           The styrene methylene protons were nonequivalent for both adducts, suggesting hydrogen bond
52 interactions with corepressor components are nonequivalent for these otherwise similar oncoproteins,
53  subtle differences in MAPK signaling confer nonequivalent functions that influence tumor spectra ind
54                      With substrates bearing nonequivalent gamma-C-H bonds, the factors governing sit
55                  When the substrate contains nonequivalent gamma-methylenes, the site-selectivity for
56         Mutants carrying double mutations in nonequivalent genes (i.e., motA motD or motB motC) retai
57 re used for comparison in a pretest-posttest nonequivalent group design.
58 drogen-bonded to a wide set of energetically nonequivalent groups.
59      The two hydrogen bonds were found to be nonequivalent, having different directions and different
60        The problems posed by the presence of nonequivalent hydrogen bond acceptor sites in molecular
61 tion for molecular structures with multiple, nonequivalent hydrogen bond acceptors are presented.
62 of NAC and EEC were temporally different and nonequivalent in magnitude, immunologic responses were s
63 peats bind distinct regions of RAD51 and are nonequivalent in their mode of interaction.
64 indications that the two domains of CFTR are nonequivalent in their nucleotide interactions.
65      Thus, signal sequences are functionally nonequivalent in vivo, with intrinsic inefficiency of th
66 americ structure as a "dimer of dimers" with nonequivalent interactions between subunits.
67 orders of flexible ethyl groups coupled with nonequivalent intra- and interlayer interactions are the
68  cisternae at equivalent levels, but none at nonequivalent levels.
69                                     We found nonequivalent lipid panel test results between Theranos
70                    The duplex assay detected nonequivalent molar ratios as high as 100-fold.
71  classes studied relies on interactions with nonequivalent N-H bonds that break symmetry.
72 an ATP dependent manner by utilizing its two nonequivalent nucleotide binding domains (NBDs) to bind
73 an ATP-dependent manner by utilizing its two nonequivalent nucleotide binding domains (NBDs) to bind
74 nd that CaMKIIgamma and -delta isoforms have nonequivalent, opposing functions.
75 rms the presence of a radical containing two nonequivalent oxygens as required for a superoxide in ma
76 domains in the elongated Gag subunits, whose nonequivalent packing is reflected in subtly different m
77 ylene protons of the hydroxymethyl group are nonequivalent protons and the hydroxymethyl group is not
78 d rearrangement of disulfide bonds using two nonequivalent redox active-sites, located in two differe
79    Our studies reveal that MyoR contains two nonequivalent repression domains.
80 rboxylate ligands (both crystallographically nonequivalent), resulting in a 173.3-angstrom cubic unit
81 d sites on the proteasome and play specific, nonequivalent roles in the asymmetric assembly and activ
82                     Here, we demonstrate the nonequivalent roles of the C termini of six AAA subunits
83              However, the two glutamates are nonequivalent since EbrA E15 is required for substrate b
84             These stems are connected by two nonequivalent single-stranded loops.
85 Wnt-dependent reiterative switch to generate nonequivalent sister cells that are born by anterior-pos
86 ing the differential nuclear POP-1 levels in nonequivalent sister cells.
87 " by a novel strand-specific imprint so that nonequivalent sister chromatids are produced.
88 hile the asymmetric distribution of POP-1 in nonequivalent sisters apparently requires a 124-amino-ac
89                                  hGH has two nonequivalent sites, called site 1 and site 2, that bind
90 -terminal inactivation domain (NTID) at four nonequivalent sites.
91                 The cardiac TF (cTF) has two nonequivalent strands, each comprised of actin, tropomyo
92 ers when the bridging carbon substitution is nonequivalent (X not equal Y).
93 g sites on PLD2 was found to be functionally nonequivalent: Y(169) serves to modulate the activity of