1 Here
we prove that 1D fermionic and bosonic systems with stro
2 Here,
we prove that a class of hierarchical architectures and
3 sing biochemical and biophysical approaches,
we prove that a gene upstream from tubZ encodes the part
4 We prove that a group of anonymous agents randomly walki
5 Furthermore,
we prove that a maximally coherent network with constant
6 We prove that all algebras in a very large axiomatically
7 By using the MIR form
we prove that all rank 1 topologies with a given number
8 Here,
we prove that all the physics of every classical spin mo
9 We prove that alpha-SYN strains amplify in vivo.
10 In the present work
we prove that an increase in the strength of the diamagn
11 We prove that an untrusted server can implement a univer
12 We prove that any regular integral invariant of volume-p
13 We proved that any motif with four or more edges can be
14 We prove that,
as a result, the stochastic QSSA becomes
15 Assuming the continuum hypothesis,
we prove that Bernoulli function(H) has a pure state who
16 Interestingly,
we proved that CA-4 treatment induced significant cell a
17 Here
we prove that cascades operating near saturation have ou
18 catenane remains intact after RCA reactions,
we prove that certain DNA polymerases can carry out the
19 By doing so,
we prove that commercial dispensers of codling moth pher
20 We prove that DACTAL is guaranteed to produce the true t
21 Additionally,
we proved that deketene curcumin, compared to curcumin,
22 Importantly,
we proved that deleting the Sost gene (a potent inhibito
23 Hence,
we prove that deterministic decisions can be reached, e.
24 We proved that during combined treatment, inhibition of
25 In this article,
we prove that each of these scores can be computed in li
26 Here,
we prove that energy is indeed produced in the cochlea o
27 We prove that,
even for the simplest two-step mechanism
28 entangling the quantum kinetic complexities,
we prove that fcc lithium is the ground state, and we sy
29 Moreover,
we prove that fitting to canonical form preserves detail
30 tand the typical structure of random graphs,
we prove that for a generalization of the Erdos-Renyi mo
31 of interleaved hexagons and pentagon pairs,
we prove that for all n > 60, the head-to-tail exclusion
32 We prove that for friendly graphs, the convex relaxation
33 Here
we prove that for generic initial conditions, these are
34 We prove that for infinite (translationally invariant) s
35 We prove that,
for any two proteins, this measure can be
36 In addition,
we prove that heterospecific mating is the only option f
37 Here,
we prove that hot spot dominated systems show little dep
38 nolayer of intestinal epithelial HT29 cells,
we proved that HS loss directly causes protein leakage a
39 ociated with a well-behaved integral kernel,
we prove that I is invariant under arbitrary volume-pres
40 We prove that if the highest telomere class is exempted
41 We prove that if the probabilities of elementary expansi
42 exception was single ascertainment, in which
we proved that ignoring ascertainment does not bias the
43 We prove that inflammatory cytokine production by microg
44 We prove that information on spike amplitude and frequen
45 We prove that IsoSpec is optimal in terms of time comple
46 We prove that it is possible to design small peptides ba
47 We proved that it was directly targeted by miR-124-3p wi
48 using knockout mice for single JNK isoforms,
we proved that JNK2 is the essential isoform in mediatin
49 We prove that lim(n--> infinity )(log c(n)(Lambda)/((log
50 Here,
we prove that maintaining control of the curvature will
51 We prove that maximal steered coherence vanishes for qua
52 Here,
we prove that metabolic programming of MSCs by oxygen te
53 We proved that miR-142-3p promoted the IL-1beta-dependen
54 We prove that,
modulo certain conjectures, the category
55 fusion product of such representations, and
we prove that,
modulo certain conjectures, the Drinfel'd
56 We prove that mutant IMS-targeted SOD1 causes neuronal t
57 We prove that nodes are a consequence of the orthorhombi
58 We proved that Noxa was phosphorylated at Ser(13) residu
59 We prove that observing that the presented state is an [
60 Besides,
we prove that on SL3 the cluster algebra and the upper c
61 Among them,
we proved that one nonstructural protein is critical to
62 We prove that our extended space of local hidden variabl
63 We prove that our extended space of local hidden variabl
64 We prove that our models are often identifiable and demo
65 While
we prove that our problems are NP-hard, we also describe
66 Using atropine,
we proved that our findings with dobutamine were not sec
67 Likewise,
we proved that our systems did not suffer from interfere
68 Here
we prove that parameters for several such models, with f
69 We prove that,
per the EFD hypothesis, the multi-quantum
70 d the surrogate MsmRv3242c infection models,
we proved that phosphoribosyltransferase is involved in
71 Here,
we prove that Ramanujan's examples do indeed satisfy his
72 We prove that retinal microglia have a unique CD45(lo) C
73 Finally,
we proved that RUNX1/MTG8 and DNMT1 were functionally in
74 We proved that SERPINE-1 is its biochemical target.
75 We prove that sets of MeSH terms provide a highly descri
76 mensional (2D) water-wave equation for which
we prove that smoothness of the interface breaks down in
77 and the expectation-maximization algorithm,
we prove that spectrotemporal pursuit converges to the g
78 With this approach,
we prove that stochastic differentiation can result in t
79 We prove that strong-coupling is impossible with monolay
80 and without using a priori selected regions,
we prove that structural and functional abnormality in B
81 In particular,
we prove that summing up PEC/PNEC ratios might serve as
82 arithmetic mean operations on ideals, e.g.,
we prove that the am-closure of a sum of ideals is the s
83 For the case of beta > 3,
we prove that the average distance of the power law grap
84 We prove that the bi-level framework is robust against b
85 In this paper,
we prove that the Boltzmann probability of all k-neighbo
86 We prove that the construction is thermally robust, show
87 ngularity" blow-up scenario; in other words,
we prove that the contours evolving from either of these
88 Here
we prove that the DBDI can be applied to exchange fluori
89 We prove that the deep coalescence consensus tree proble
90 Here
we prove that the emergence of classical features along
91 constituted on a 5 S rRNA gene tandem array,
we prove that the enzyme attacks chromatin in the intern
92 In combination with GW-BSE theory,
we prove that the excitons are of Wannier type, meaning
93 We prove that the exponential stability depends on relat
94 We prove that the facet degree distribution yielded by G
95 In this paper
we prove that the GNARLED gene encodes a homolog of the
96 We prove that the histone H3K4 methyltransferase SETD1A
97 ally have highly skewed singular values, and
we prove that the many small singular values cannot be e
98 nerated from a uniform mixture of two trees,
we prove that the Markov chains take an exponentially lo
99 Upon revisiting these claims,
we prove that the mathematical definition of equitabilit
100 We prove that the method yields consistent estimates in
101 We prove that the multiparticle Schrodinger operator, as
102 Using these lines
we prove that the NC give rise to the olfactory ensheath
103 Using Lyapunov indirect method,
we prove that the new control system is input-output sta
104 In particular,
we prove that the only derivation that maps a Murray-von
105 We prove that the optical transmission spectra are highl
106 There is structure to this diversity:
we prove that the optimal correlation structures must li
107 In doing so,
we prove that the pluripotent spectrum can encompass mul
108 cale modeling and crystal plasticity theory,
we prove that the preferred bimetal interface arising fr
109 In the present work
we prove that the problem of scoring the parsimony of a
110 We prove that the RDI method is an accurate and versatil
111 rical objects in the quasistatic limit, then
we prove that the scattering of bending waves from an ob
112 We prove that the second law of thermodynamics holds in
113 We prove that the statement "there exists a counterexamp
114 ic administration of a MET kinase inhibitor,
we prove that the therapeutic benefit of MET targeting i
115 We prove that the tubular structure of the PLB transform
116 Using in vivo electrophysiology,
we prove that the tVTA is a major inhibitory control cen
117 In this paper,
we prove that the u, v method provides asymptotically ef
118 We prove that the ultimate fate of both clonotypes is ex
119 Moreover,
we prove that the upper cluster algebras of Berenstein e
120 We proved that the 5' splice sites of CD46 cassette exon
121 We proved that the behavior of KIEobs for a reversible t
122 Finally,
we proved that the CD157-fibronectin interaction occurs
123 y absorption and photoelectron spectroscopy,
we proved that the dominant role of the less reducible c
124 We proved that the rate constants of inhibitor release a
125 On the other hand,
we proved that the spectral contribution centered at app
126 We proved that the tumor blood flow in this model was ex
127 We prove that there exist k in and 0 < epsilon in such t
128 In this article,
we prove that there exists an analytical solution of par
129 ease biology and epidemiologic study design,
we prove that there is a one-to-one correspondence betwe
130 We prove that there is a one-to-one correspondence betwe
131 We prove that there is a trade-off with the uncertainty
132 We prove that these cannot be older than Phobos' current
133 We prove that these eight phases form a complete list of
134 Finally,
we prove that these films are useful for the constructio
135 We prove that this decomposition extends to higher order
136 Using site-directed mutants of thrombin
we prove that this effect is mediated by the RGD sequenc
137 Here
we prove that this is an undecidable problem.
138 We prove that this new procedure allows a simplified pro
139 We prove that this structural similarity is a consequenc
140 Thus,
we prove that this task is computationally feasible, alt
141 We proved that this process led to the preferential coup
142 We proved that this was because of the presence of anoth
143 umulation in neutrophils from knockout mice,
we prove that TLR7 is essential for influenza viral reco
144 Thanks to the assay optimization,
we proved that tuning the NSs surface coverage with DNA
145 asymptotic limit of many signals exchanged,
we prove that two-way Gaussian protocols are immune to c
146 We prove that under very weak assumption, the nonlinear
147 We prove that with parameter input consistent with exper