1 t coding strategies shall be incorporated in
a revised model.
2 leaf-out by the end of the 21st century for
the revised model.
3 rence was not statistically significant when
a revised model accounted for random state effects.
4 The revised model accounts for the magnitude and wavefor
5 The revised model also accounts for selective effects of
6 The revised model also does a better job of representing
7 In
the revised model,
conserved Tyr-157 makes contact with
8 por sensor response data is demonstrated and
a revised model developed from SAW vapor sensor response
9 otein-ligand-solvent interactions to propose
a revised model for allostery in LacI, where ligand bind
10 Based on these observations we present
a revised model for assembly of the E. coli division app
11 may be essential after this step, supporting
a revised model for assembly of the mitochondrial fissio
12 Our studies support
a revised model for assembly of the mitochondrial fissio
13 n vivo connections between these enzymes and
a revised model for CTD-mediated small nuclear RNA termi
14 Based on these data, we present
a revised model for ESCRT-0 function in cargo recruitmen
15 Based on this new evidence we propose
a revised model for establishing anteroposterior polarit
16 n binding in the structure led us to propose
a revised model for FGFR dimerization.
17 We propose
a revised model for FSHD in which FAT1 levels might play
18 his review we integrate new information into
a revised model for further understanding this important
19 Taken together, these findings yielded
a revised model for HMW2 in terminal organelle architect
20 We provide
a revised model for how actin structures position nuclei
21 e conditions for actinopterygians, providing
a revised model for interpreting brain evolution in a ma
22 Our findings suggest
a revised model for Lgl regulation and function in both
23 d dynamical modeling to develop and validate
a revised model for lipopolysaccharide (LPS)-induced mac
24 These results suggest
a revised model for major aspects of ESX-1-mediated host
25 nd computational docking studies, we propose
a revised model for MAPK interaction with substrates con
26 These observations lead to
a revised model for NiV fusion activation and provide a
27 We describe
a revised model for P(i) signal transduction of the E. c
28 his article incorporates these findings into
a revised model for pathway activation.
29 Our results lead to
a revised model for platelet activation that establishes
30 A revised model for predicting stabilities of 3 x 3 loop
31 A revised model for predicting stabilities of internal l
32 These results precipitate
a revised model for pulmonary T cell trafficking and dif
33 Our results support
a revised model for salivary gland homeostasis based pre
34 Based on these results, we propose
a revised model for selenocysteine incorporation where S
35 nations for these results are discussed, and
a revised model for SrtA catalysis is presented.
36 Based on these data, we proposed
a revised model for storage and secretion of cytokines a
37 s, is relatively limited in vivo and support
a revised model for T(H)1 memory differentiation.
38 Based on our findings, we propose
a revised model for T4 middle promoter activation, with
39 ly based on a micellar structure, we propose
a revised model for the association of transmembrane dom
40 We propose
a revised model for the checkpoint response to HU that a
41 We suggest
a revised model for the conformation of DNA bound to the
42 Here, we present
a revised model for the establishment of asymmetric gene
43 sil, and biogeochemical evidence, we propose
a revised model for the evolution of thecal tabulations
44 hese results are discussed in the context of
a revised model for the fatty acid synthase.
45 xtend stretch-buffering capacity and support
a revised model for the function of EHDs at the caveolar
46 Here I describe
a revised model for the function of three tubulin cofact
47 Based upon these results,
a revised model for the loop A tertiary interaction with
48 Based on these data, we present
a revised model for the mechanism by which Srv2 promotes
49 A revised model for the mechanism of the allosteric acti
50 phohistidyl enzymes is described, as well as
a revised model for the mechanism of the uridylyltransfe
51 A revised model for the origin of enantio- and diastereo
52 A revised model for the regulation of comK expression is
53 mechanism for polymerase exchange and offer
a revised model for the replication reaction that emphas
54 Based on our findings we propose
a revised model for the role of Gbx in cerebellar develo
55 We present
a revised model for the role of small RNAs in dorsiventr
56 This idea is discussed within the context of
a revised model for the structure of the lactose permeas
57 ilus is required for DNA uptake and we offer
a revised model for the transformation process.
58 These observations demand
a revised model framework, which considers the potential
59 at a combination of a Model-Based system and
a revised Model-
Free system can account for the developm
60 However,
the revised model had a larger self-energy than the trad
61 The revised model identifies distinct roles for these tw
62 scale chromatin organization consistent with
a revised model in which compartments are more precise t
63 We present
a revised model in which NOG1 operates independently of
64 Our study supports
a revised model in which potentiation of PTI is an indis
65 efining the carboxylase active site, suggest
a revised model in which the glutamyl substrate indirect
66 The findings suggest
a revised model in which the signal transduction cascade
67 nts that are designed to test predictions of
the revised model in a group II organism.
68 In
the revised model in this study, the lower part of the a
69 A revised model involving a cycle of disengagement and r
70 A revised model is presented for protein IX within the v
71 A revised model is proposed for Gam-induced radioresista
72 We present
a revised model of 3D growth in which PpNOG2 comprises p
73 The data are consistent with
a revised model of AAV integration that includes prelimi
74 odeling based on the structure of rhodopsin,
a revised model of adenosine-A1AR interactions is propos
75 These data suggest
a revised model of AMPA receptor trafficking wherein a l
76 We propose
a revised model of arterial-venous differentiation that
77 We propose
a revised model of cell wall architecture which will imp
78 mous with medullary localization and support
a revised model of central tolerance in which CCR4 and C
79 py and crystallography are incorporated into
a revised model of channel gating.
80 Our findings prompt us to present
a revised model of CSS wherein the CCSSD:NTSD complex fo
81 These observations necessitate
a revised model of DNA damage response in G(1) phase and
82 a role in cognitive flexibility, and suggest
a revised model of dopamine-serotonin opponency with pot
83 We propose
a revised model of dynein's mechanochemical cycle which
84 We propose
a revised model of elongation control in this accelerati
85 Based on these data, we propose
a revised model of exosporium maturation and assembly an
86 A revised model of factor XIII activation is presented b
87 We present
a revised model of gastrulation movements in Xenopus lae
88 re, we reconcile this sea-level record using
a revised model of glacial isostatic adjustment characte
89 We propose
a revised model of gradient sensing, suggesting an impor
90 er, our results not only allow us to propose
a revised model of how CDK8 activity is regulated by MED
91 Taken together, these results provide
a revised model of how this and possibly other AAA ATPas
92 These findings result in
a revised model of lagging strand DNA synthesis where th
93 rs, these data have led to the generation of
a revised model of lineage commitment.
94 Based on these results, we propose
a revised model of long-patch BER and a new key regulati
95 Based on these data, we propose
a revised model of LTA structure: its polysaccharide rep
96 Our observations not only support
a revised model of Mtb Clp biology, where ClpP2 scaffold
97 We propose
a revised model of optic nerve development and new mecha
98 We propose
a revised model of peptide processing for MHC class I by
99 Altogether, our results support
a revised model of PGC DNA demethylation in which the fi
100 unctional and PKR-P58(IPK) binding analyses,
a revised model of PKR regulation by P58(IPK) is present
101 population and type of diabetes and leads to
a revised model of secretory changes in the diabetogenic
102 Our results suggest
a revised model of skill learning: basal ganglia circuit
103 ct subset of effector CD4 T cells has led to
a revised model of the adaptive immune system.
104 ferred at the ends of both exons and support
a revised model of the interactions of the exons with U5
105 spatial and temporal localization, prompting
a revised model of the internal arrangement of the beta-
106 e use our temporal observations to construct
a revised model of the relative timing and duration of t
107 These results support
a revised model of the Rut pathway and provide evidence
108 This leads to
a revised model of the SRR pathway in which the Ycks pri
109 V-ATPases and is discussed in the context of
a revised model of the topology of the 100-kDa subunit a
110 We propose
a revised model of TTX and STX binding in the Na+ channe
111 The revised model recognizes the salience of individual
112 The earlier spring leaf-out predicted by
the revised model resulted in enhanced gross primary pro
113 The revised model should facilitate investigation of the
114 forests (5.5 million km(2) ), we found that
the revised model substantially outperformed the standar
115 ons can account for this effect, and propose
a revised model that better describes pH-coupled partiti
116 In this study, we propose
a revised model that is based on the ability of the BCR
117 al and temperate deciduous forest region for
the revised model,
whereas the standard model predicts e
118 Our findings demonstrate
a revised model whereby Myc promotes both proliferation
119 at the invasive front of human CRCs supports
a revised model wherein Axin2 acts as a potent tumor pro
120 The revised model with SOC function better reproduces th