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 Based on these observations we present
a revised model for assembly of the E. coli division app
10 Our studies support
a revised model for assembly of the mitochondrial fissio
11 may be essential after this step, supporting
a revised model for assembly of the mitochondrial fissio
12 n vivo connections between these enzymes and
a revised model for CTD-mediated small nuclear RNA termi
13 Based on these data, we present
a revised model for ESCRT-0 function in cargo recruitmen
14 Based on this new evidence we propose
a revised model for establishing anteroposterior polarit
15 n binding in the structure led us to propose
a revised model for FGFR dimerization.
16 We propose
a revised model for FSHD in which FAT1 levels might play
17 his review we integrate new information into
a revised model for further understanding this important
18 Taken together, these findings yielded
a revised model for HMW2 in terminal organelle architect
19 We provide
a revised model for how actin structures position nuclei
20 Our findings suggest
a revised model for Lgl regulation and function in both
21 nd computational docking studies, we propose
a revised model for MAPK interaction with substrates con
22 We describe
a revised model for P(i) signal transduction of the E. c
23 his article incorporates these findings into
a revised model for pathway activation.
24 Our results lead to
a revised model for platelet activation that establishes
25 A revised model for predicting stabilities of 3 x 3 loop
26 A revised model for predicting stabilities of internal l
27 These results precipitate
a revised model for pulmonary T cell trafficking and dif
28 Our results support
a revised model for salivary gland homeostasis based pre
29 Based on these results, we propose
a revised model for selenocysteine incorporation where S
30 nations for these results are discussed, and
a revised model for SrtA catalysis is presented.
31 Based on these data, we proposed
a revised model for storage and secretion of cytokines a
32 s, is relatively limited in vivo and support
a revised model for T(H)1 memory differentiation.
33 Based on our findings, we propose
a revised model for T4 middle promoter activation, with
34 ly based on a micellar structure, we propose
a revised model for the association of transmembrane dom
35 We propose
a revised model for the checkpoint response to HU that a
36 We suggest
a revised model for the conformation of DNA bound to the
37 Here, we present
a revised model for the establishment of asymmetric gene
38 sil, and biogeochemical evidence, we propose
a revised model for the evolution of thecal tabulations
39 hese results are discussed in the context of
a revised model for the fatty acid synthase.
40 xtend stretch-buffering capacity and support
a revised model for the function of EHDs at the caveolar
41 Here I describe
a revised model for the function of three tubulin cofact
42 Based upon these results,
a revised model for the loop A tertiary interaction with
43 Based on these data, we present
a revised model for the mechanism by which Srv2 promotes
44 A revised model for the mechanism of the allosteric acti
45 phohistidyl enzymes is described, as well as
a revised model for the mechanism of the uridylyltransfe
46 A revised model for the origin of enantio- and diastereo
47 A revised model for the regulation of comK expression is
48 Based on our findings we propose
a revised model for the role of Gbx in cerebellar develo
49 We present
a revised model for the role of small RNAs in dorsiventr
50 This idea is discussed within the context of
a revised model for the structure of the lactose permeas
51 ilus is required for DNA uptake and we offer
a revised model for the transformation process.
52 at a combination of a Model-Based system and
a revised Model-
Free system can account for the developm
53 The revised model identifies distinct roles for these tw
54 efining the carboxylase active site, suggest
a revised model in which the glutamyl substrate indirect
55 The findings suggest
a revised model in which the signal transduction cascade
56 nts that are designed to test predictions of
the revised model in a group II organism.
57 In
the revised model in this study, the lower part of the a
58 A revised model involving a cycle of disengagement and r
59 A revised model is presented for protein IX within the v
60 A revised model is proposed for Gam-induced radioresista
61 The data are consistent with
a revised model of AAV integration that includes prelimi
62 odeling based on the structure of rhodopsin,
a revised model of adenosine-A1AR interactions is propos
63 These data suggest
a revised model of AMPA receptor trafficking wherein a l
64 We propose
a revised model of arterial-venous differentiation that
65 py and crystallography are incorporated into
a revised model of channel gating.
66 a role in cognitive flexibility, and suggest
a revised model of dopamine-serotonin opponency with pot
67 Based on these data, we propose
a revised model of exosporium maturation and assembly an
68 A revised model of factor XIII activation is presented b
69 We present
a revised model of gastrulation movements in Xenopus lae
70 re, we reconcile this sea-level record using
a revised model of glacial isostatic adjustment characte
71 We propose
a revised model of gradient sensing, suggesting an impor
72 Taken together, these results provide
a revised model of how this and possibly other AAA ATPas
73 These findings result in
a revised model of lagging strand DNA synthesis where th
74 rs, these data have led to the generation of
a revised model of lineage commitment.
75 Based on these results, we propose
a revised model of long-patch BER and a new key regulati
76 Based on these data, we propose
a revised model of LTA structure: its polysaccharide rep
77 We propose
a revised model of optic nerve development and new mecha
78 We propose
a revised model of peptide processing for MHC class I by
79 Altogether, our results support
a revised model of PGC DNA demethylation in which the fi
80 unctional and PKR-P58(IPK) binding analyses,
a revised model of PKR regulation by P58(IPK) is present
81 Our results suggest
a revised model of skill learning: basal ganglia circuit
82 ct subset of effector CD4 T cells has led to
a revised model of the adaptive immune system.
83 ferred at the ends of both exons and support
a revised model of the interactions of the exons with U5
84 spatial and temporal localization, prompting
a revised model of the internal arrangement of the beta-
85 e use our temporal observations to construct
a revised model of the relative timing and duration of t
86 This leads to
a revised model of the SRR pathway in which the Ycks pri
87 V-ATPases and is discussed in the context of
a revised model of the topology of the 100-kDa subunit a
88 We propose
a revised model of TTX and STX binding in the Na+ channe
89 The revised model recognizes the salience of individual
90 The earlier spring leaf-out predicted by
the revised model resulted in enhanced gross primary pro
91 The revised model should facilitate investigation of the
92 forests (5.5 million km(2) ), we found that
the revised model substantially outperformed the standar
93 In this study, we propose
a revised model that is based on the ability of the BCR
94 al and temperate deciduous forest region for
the revised model,
whereas the standard model predicts e
95 Our findings demonstrate
a revised model whereby Myc promotes both proliferation
96 at the invasive front of human CRCs supports
a revised model wherein Axin2 acts as a potent tumor pro