1 We attribute this to 2F5 interacting more stably than 4E
2 We attribute both peaks to a single excited state becaus
3 We attribute the dynamics to a storage effect, where toa
4 We attribute these changes to a metaboreflex originating
5 We attribute these characteristics to a transition from
6 We attribute these effects to a reduction in small condu
7 We attribute these results to a catalytically relevant r
8 observed changes only at H1, H5, and H6, and
we attribute these to a slight change in the position of
9 We attribute these transitions to a combination of size,
10 , containing only one nitrogen redox center;
we attribute this band to a bridge-to-N(+) transition.
11 We attribute this behaviour to a momentary collapse of t
12 We attribute this difference to a change in the rate-lim
13 We attribute this finding to a positive reward predictio
14 inelastic electron tunnelling spectroscopy,
we attribute this finding to a strain-induced shift of t
15 We attribute this result to a linkage between CH-pi inte
16 actually improve at cryogenic temperatures;
we attribute this to a transition from planar-slip dislo
17 neous DNA sequences, as in native chromatin,
we attribute this variation to a dependence of the unrav
18 We attributed these defects to a caudal shift of the rho
19 lier structure of the poliovirus polymerase,
we attributed this conformation to a crystal packing art
20 We attribute this effect to abolition of the hypercapnia
21 We attribute these results to accessibility of the mutat
22 We attribute this delay to all processes leading to the
23 We attribute these differences to an additional mechanis
24 We attribute this discrepancy to an additional role for
25 bioavailability comparable to that of FeSO4
We attribute this effect to an in situ generation of sol
26 We attribute this to an antagonistic effect of PVDPf-5 o
27 We attribute this to an extension of TnI linking the tro
28 We attributed this to an increased turnover rate.
29 Mechanistically,
we attribute this sensitization to anti-cancer treatment
30 We attribute this relationship to asymmetric mantle upwe
31 We attribute this to auditory-visual interaction since s
32 We attribute this discrepancy to burial of the apolar su
33 We attributed this effect to central-resource competitio
34 We attribute these findings to charge transfer interacti
35 We attribute this to compensation of solvation terms fro
36 We attribute this discrepancy to convergence of SAR11 an
37 ere not shortened at all by gld-1 mutations;
we attribute this finding to decreased cell division and
38 We attribute this to decreasing fugitive emissions from
39 We attribute these changes to differences in the electro
40 We attribute this effect to differential phosphorylation
41 We attribute these effects to direct, PKA-dependent phos
42 We attribute the latter to domain heterogeneities that c
43 We attribute this defect to E2F/DP-dependent control of
44 We attribute this maximum to either elimination of a rec
45 We attribute these observations to electron transfer occ
46 omes infinite at full hydration (unbinding);
we attribute this both to electrostatic repulsion of the
47 ues ranging from -5.0 to -17.2 per thousand;
we attribute this result to ethanol's origin from corn a
48 We attribute this emission to excimers formed during ann
49 We attribute the sol-to-
gel transition to the formation
50 We attribute these observations to high rates of female-
51 We attribute the shift to higher energy seen for I to a
52 We attribute this effect to hydrogen bond formation.
53 ell as premature centrosome splitting, which
we attribute in part, to improper localisation of the nu
54 illate out of phase with a period of 280 fs;
we attribute these oscillations to impulsively excited l
55 We attribute these observations to increased levels of t
56 We attributed these changes to increased MLC2v and MYPT1
57 We attribute it to intrinsic superconductivity of heavil
58 We attribute this observation to large size differences
59 We attribute such localization to local changes in the t
60 We attribute the survival to lowering of expression of t
61 e alphaKG-dependent dioxygenase superfamily,
we attribute this spectrum to metal chelation by the sub
62 We attribute this relationship to "
MHC-guided processing
63 tion records from South Greenland ice cores,
we attribute this expansion to multi-decadal summer cool
64 We attribute this effect to myosin's action as a 'molecu
65 We attributed this phenotype to osteoclastic sensitizati
66 We attribute our results to overwhelming effects of much
67 inverse dependence on histone concentration;
we attribute this to partitioning to a faster pathway le
68 Psychological theories disagree on how
we attribute emotions to people.
69 We attribute this uncertainty to physico-chemical hetero
70 We attribute this phenomenon to point-defect migration f
71 We attribute these properties to polyvalent engagement b
72 ng a partial defect in coupling to G(q), and
we attribute it to potentiation of a non G(q)-pathway, u
73 orld is complex and multidimensional; how do
we attribute rewards to predictive features when surroun
74 We attribute this effect to protein-flexibility mediated
75 We attribute this to pulsed accretion associated with an
76 In the present study
we attribute this delay to reduced production of the mac
77 We attribute this discrepancy to regional differences in
78 We attribute this phenomenon to repetitive changes in th
79 ends on the charge-carrier concentration and
we attribute this to scattering by interfacial phonons i
80 Here
we attribute the discrepancy to species differences.
81 We attribute this effect to SSTR2a restoration of the at
82 We attribute this to strong interactions between the ini
83 We attribute these properties to structural hierarchy at
84 We attribute fluorescence fluctuations to the interfacia
85 nd site was unaffected by bound thrombin and
we attribute it to the consensus Ca2+ site in EGF3.
86 We attribute our findings to the presence of proteins (s
87 ibbean more than for Mainland samples, which
we attribute primarily to the additional reference panel
88 he bound DNA in solution versus the crystal;
we attribute the difference to the presence of osmolytes
89 Therefore,
we attribute the enhancement to the PM metabolite of 4-H
90 We attribute the outburst to the 'break-out' of the supe
91 We attribute the results to the insensitivity of phase-m
92 We attribute these anomalies to the failure of both assu
93 We attribute these changes to the effect of lipid domain
94 We attribute these changes to the higher aggregation pro
95 We attribute these differences to the Mg(2+)-induced com
96 We attribute these differences to the rapid large energy
97 We attribute these discrepancies to the fact that the cu
98 We attribute these effect to the conversion between two
99 Based on the crystallographic data,
we attribute these effects to the competition between be
100 We attribute these effects to the reduction in intermole
101 We attribute these effects to the reversible protonation
102 We attribute these observations to the dominance of a fa
103 We attribute these observations to the existence of at l
104 We attribute these observations to the gradual and irrev
105 We attribute this activation to the attractive charge in
106 We attribute this behaviour to the fact that the attract
107 of our experimental and theoretical results,
we attribute this behaviour to the presence of a glass-l
108 We attribute this cooling to the interaction between the
109 We attribute this decrease to the absence of one nuclear
110 We attribute this difference to the ability of tandem ma
111 We attribute this difference to the Arabidopsis mating s
112 We attribute this difference to the decreased inter-ring
113 We attribute this difference to the distinct interlayer
114 We attribute this difference to the fact that the OVER t
115 We attribute this difference to the radiative impacts of
116 We attribute this discrepancy to the effects of double-l
117 Using theoretical models,
we attribute this effect to the generation of hot plasmo
118 We attribute this effect to the increased propensity of
119 We attribute this effect to the presence of nanoscale el
120 Instead,
we attribute this effect to the stable radical cation of
121 We attribute this enhancement to the weakened CO binding
122 domains is N-acetylglucosamine binding, and
we attribute this function to the G5 domain.
123 We attribute this observation to the magnetic-field sens
124 We attribute this observation to the pre-encapsulation d
125 We attribute this phenomenon to the particular redox-rea
126 We attribute this resistance to the tremendous temporal
127 ve changes in total body mass by midcentury;
we attribute this response to the fact that many low-ele
128 We attribute this result to the ability of the proton to
129 We attribute this result to the enforced use of an effor
130 We attribute this result to the formation of off-pathway
131 We attribute this result to the large lipid concentratio
132 We attribute this result to the recipient immunosuppress
133 We attribute this result to the strong dynamic dipole-di
134 We attribute this result to the strong interaction betwe
135 We attribute this sensitivity to the marginal stability
136 Thus
we attribute this stiffness to the foot, Achilles' tendo
137 We attribute this to the ability of cladribine to combin
138 We attribute this to the change of the surface of the ba
139 We attribute this to the crystal field interaction being
140 We attribute this to the effects of in vivo healing and
141 to those of the solution phase reaction, and
we attribute this to the effects of intermolecular inter
142 We attribute this to the enhanced electron-electron scat
143 We attribute this to the entropically more favorable int
144 We attribute this to the extreme flexibility of graphene
145 We attribute this to the greater activity of the reagent
146 We attribute this to the high entropic repulsion (electr
147 We attribute this to the inability of the central Lys to
148 We attribute this to the lack of nuclei in small MG nano
149 We attribute this to the necessary presence in the nucle
150 We attribute this to the number of excitatory neurons an
151 We attribute this to the shift in population of four res
152 We attribute this to the shift of the slip plane from be
153 We attribute this weakening to the observed increase in
154 We attributed this difference to the additional block at
155 We attributed this scenario to the nucleation process of
156 We attribute their cytotoxicity to their specific molecu
157 We attribute their hydrophobicity to their unique electr
158 We attribute the ECR to upwelling of cold deep waters fr
159 For a subset of 22 species,
we attributed these responses to variation in RAV.
160 We attribute tissue stiffening to Xlfc, a previously ide