1 From these results,
we infer that 1) laforin is responsible for glycogen dep
2 Under the variable effects model,
we infer that 11% of synonymous mutations are subject to
3 Genome-wide,
we infer that 20,000 to 60,000 residues have been modifi
4 From our measurements,
we infer that 70% of 50S subunits are engaged in transla
5 We infer that a chronic hyperaldosteronic status, whethe
6 We infer that a DA-dependent signaling system operates i
7 We infer that a general strategy for a promiscuous prote
8 We infer that a primary antiviral function of IFN-gamma
9 We infer that a reversible diffusion of oxygen ions in t
10 We infer that a similar mechanism may apply to other mic
11 We infer that a single wild-type alpha subunit is capabl
12 We infer that a wide variety of amphipaths can displace
13 ns Arg-126-Gln, Asp-49-Asn, and Arg-126-Lys,
we inferred that a crystallographic water acts as a gene
14 We inferred that a small fraction of the renal Na,K-ATPa
15 We infer that abnormal peripheral C nociceptor ongoing a
16 We infer that abrupt warming triggered expansion of the
17 We infer that activation by anesthetics and GABA induces
18 We infer that AGO8 plays a central role in the induction
19 We infer that an imperfect purine/purine/pyrimidine (R.R
20 We infer that an increase of >1 megapascal in pore press
21 We infer that,
as the channel opens, the distance and/or
22 We infer that at least seven of these events, common to
23 We infer that at least some of this reduction in diversi
24 asured with average atom number N=1.1+/-0.4,
we infer that atoms are localized within the waveguide b
25 From the timing and pattern of effects,
we infer that back-projections from extrastriate cortex
26 We infer that background effects may hamper the search f
27 ecame oligomerized after membrane insertion,
we infer that Bax oligomers are present at pore edges.
28 We infer that BCRs with IgH chain from the Emu-deficient
29 We infer that belemnites adapted to environmental change
30 We infer that beta cell glucose-transporter glycosylatio
31 Based on this analysis,
we inferred that Bicc1 was involved in osteoblast differ
32 We infer that binding of the ordered population reflects
33 We infer that BNRF1 is also a latent Ag that could be ta
34 We infer that both mutant and wild-type proteins also ca
35 We infer that C signaling partially overcomes the negati
36 We infer that California seismicity rates are modestly m
37 We infer that CAP discriminates between consensus and no
38 We infer that carbon, helium, argon and highly incompati
39 We infer that carbonaceous chondrite matrices are not pr
40 We infer that cell cycle control of the V(D)J recombinas
41 We infer that cell cycle progression in cyanobacteria sl
42 We infer that CFS is based on modulating the gain of neu
43 We infer that coacquisition of multiple strains is commo
44 We infer that cross-talk between S(4) and S(6), not seen
45 We infer that crystal growth of wurtzite is kinetically
46 We infer that crystal plasticity precludes failure and c
47 the pattern of the S-S and Trp Raman bands,
we infer that Cys32 is likely to be involved in the cros
48 We infer that D(k)-licensed G2(+) NK cells efficiently d
49 We infer that degassing during decompression of water-sa
50 We infer that Delta-domains not only guide assembly but
51 tructures and distributions of sand and mud,
we infer that deposition occurred in normal open shallow
52 We infer that differences between plumes and the upper-m
53 omposing gene-by-aging (G x A) interactions,
we infer that different genes influence some neurocognit
54 Further,
we infer that dispersal limitation may also influence fu
55 We infer that doping up to the optimum level does not sh
56 From these data,
we infer that during large magnitude earthquakes a step-
57 We infer that E. coli is highly susceptible to radiation
58 virtue of these language group differences,
we infer that early cortical processing of pitch contour
59 Thus
we infer that EDA signaling is needed for the determinat
60 By manipulating MGC precursor availability,
we infer that elevated MGC in opa3 mutants derives from
61 We infer that European and Chinese populations had very
62 We infer that "
exotic" Neolithic domesticated plants wer
63 Additionally and unexpectedly,
we infer that extension and retraction are accompanied b
64 We infer that eye-specific expression predates the diver
65 information about human brain activity, and
we infer that features of the field potential that are u
66 We infer that for the smaller molecular mass, PEG entere
67 We infer that functional FtsZ rings can form in ftsI- an
68 Considering our results and those of others,
we infer that germ-line Piwi functions downstream of piR
69 From the present results,
we infer that glutamate is released with GABA from inhib
70 We infer that gp140 proteins may always contain a variab
71 We infer that Gpa1 serves as a positional determinant fo
72 neuropeptide Y, parvalbumin, or calretinin,
we infer that graft-derived cells integrate into local c
73 as indicators of the pathogen's environment,
we inferred that granulocytic inflammation generates a n
74 a lipase mutant that does not bind to Grb2,
we inferred that Grb2 serves to hijack PLD2 to the perin
75 We infer that high local interhost correlations in paras
76 bining genetic and phylogenetic information,
we infer that hlx-Su(hlx) hybrid lethality is likely cau
77 We infer that hydrological variability in this part of I
78 We infer that hydrolysis leads to a compaction around th
79 From these results
we infer that (
i) P-deficient growth causes some interna
80 From these studies,
we infer that (
i) Pols eta, iota, and kappa have the abi
81 We infer that Ichthyostega underwent greater locomotory
82 From these
we infer that,
if the fault is weak, seismic waves cause
83 We infer that IM symptoms arise as a consequence not of
84 From these data,
we infer that in female mice, PKCalpha normally serves t
85 We infer that in wild-type mice, Aag excises damaged DNA
86 e from silicon and nitrogen isotope changes,
we infer that,
in contrast to the modern situation, the
87 We infer that increased NlSPATA5 expression may be one m
88 We infer that increased reliance on wild plants rich in
89 Despite this,
we infer that Indian Zoroastrians (Parsis) intermixed wi
90 We infer that iron is the prosthetic metal in vivo.
91 proximal regulator of sigX in S. mutans, and
we infer that it controls competence in a parallel way i
92 densed DNA structure is not well ordered and
we infer that it is formed by many looping interactions
93 Thus
we infer that it is the positions of splice junctions in
94 Using Wiki-Pi,
we infer that its association to diabetic retinopathy ma
95 tep in binding is concentration independent,
we infer that JBP1 undergoes a conformational change upo
96 We inferred that K = 2 reflects the footprint of agricul
97 From these data,
we infer that key signaling and adhesion genes were in p
98 We infer that Lanzhousaurus had a rapid rate of tooth en
99 d the volcanic history of the Lhasa terrane,
we infer that large-magnitude surface uplift of the nort
100 We infer that loss of DGKE function results in a prothro
101 We infer that M2 is tightly associated with the adjacent
102 We infer that macromolecular synthesis in the forespore
103 We infer that mammalian cells have preserved and extende
104 star formation rate and size of this galaxy
we infer that many star-forming cores may be heavily obs
105 From native gels,
we inferred that MET1 associates with PSII subcomplexes
106 We infer that Mg ions are complexed and dewatered by sur
107 We infer that modern humans proved a greater competitive
108 We infer that most cancer cells are differentiated along
109 We infer that most of the 267 lines show mutant effects
110 m the initial speed (after the load change),
we inferred that motors running at very low loads are dr
111 We infer that MscS gate, which is similar to that of the
112 centrations near the surface in this region,
we infer that much of the secondary organic aerosol in t
113 We infer that Mus81-dependent crossing over occurs in a
114 Based on multiple measures,
we infer that Narp knockout mice undergo normal seizure
115 We infer that neural sonifications of speech-evoked brai
116 ressed in the rod photoreceptor lineage, and
we inferred that neuroD is also expressed in a subset of
117 Based on their somatic locations,
we inferred that neurons with only ipsilaterally project
118 We infer that NlPHF7 play a role important in stimulatin
119 We infer that Nlst6 acts in BPH growth and fecundity, an
120 We infer that Notch signalling has at least two function
121 We infer that off-line rTMS caused an additional dysfunc
122 We infer that oligomerization via the C-terminal domain
123 ume of 4.9 x 10(-4) (lambda/n)(3) from which
we infer that only ~2,400 electrons per resonator partic
124 From these data,
we infer that P(i) release commits myosin V to undergo a
125 before diverging below approximately 230 K,
we infer that PA in ice remains cooperatively hydrated w
126 We infer that para-substituted benzylamines are good rea
127 We infer that past plankton turnover occurred when a war
128 We infer that phosphorylation of one subunit of wild-typ
129 We infer that pilus polymerization involves the formatio
130 We infer that PIP2 participates in the initial trimer fo
131 We infer that Pk(Pk) is sufficient to mediate the interc
132 However,
we infer that platelet activation and binding of activat
133 We infer that pro- and anti-inflammatory activities of b
134 We infer that propofol may bind near the extracellular e
135 Thus,
we infer that Protein C002 is crucial in the feeding of
136 We infer that protonation of X = Y = Z at central atoms
137 We infer that protrusive F-actin, induced by the frontne
138 ping cellular environments for PrPC and Sho,
we inferred that PrPC levels might also be altered as pa
139 From this disease-association overlap,
we infer that PTV is the likely mechanism by which eight
140 Using mutant cycle analysis,
we inferred that Q226E induces activation via an enhance
141 Based on earlier molecular genetic studies,
we inferred that R. capsulatus CcmF, CcmH, and CcmI inte
142 dered along with higher levels of cyclin D1,
we infer that relative to gamma radiation exposure to (5
143 uble knock-out mice resemble reeler mutants,
we infer that Reln(CTRdel)/Apoer2(null) double homozygot
144 From the studies presented here,
we infer that replication through the 3meA lesion in yea
145 We infer that residue His-225 is likely to modulate the
146 In this work,
we infer that retrogenes do not generally carry regulato
147 We infer that rostral PPC areas do not code single effec
148 assemble into virus-like particles in vitro,
we infer that RSV Gag is biologically active.
149 We infer that selective stabilization of key recombinati
150 We infer that sex chromosome gene expression directly in
151 ombined with a small sex-determining region,
we infer that sexual conflict may be effectively stymied
152 We infer that Sgs1 always functions in the context of th
153 and in accord with some reports for PrP(C),
we infer that Sho's activity will prove germane to the m
154 From our measurements
we infer that Sid2p and Mob1p both exist as monomeric, h
155 We infer that sigma(E) compartmentalization is partially
156 Thus,
we infer that signal transduction does not require bindi
157 We infer that signaling from the retina to the optic lob
158 We infer that similar principles underlie carrier protei
159 d to survive only in the outer Solar System,
we infer that,
similarly to cometary bodies, metal-rich
160 nown to be subject to a bistable switch, and
we infer that SinI reaches levels sufficient to trigger
161 We infer that sisters are initially linked and that loss
162 king the size dependence of the jump number,
we infer that skyrmions are assembled into cluster state
163 We infer that snaR evolved from the left monomer of the
164 Further,
we infer that Soay and Sarda sheep carry introgressed mo
165 From these results,
we infer that solvent restructuring, resulting from rele
166 We infer that some of the ascribed functions are seconda
167 ring analysis and hybridization simulations,
we infer that Spanish teosinte is of admixed origin, mos
168 We infer that spatial and temporal variation of DNA supe
169 We infer that stem eukaryotes shared functionally modern
170 We infer that such CD4(+) T cells recognize cellular ant
171 We infer that such redirection of spatial attention enga
172 We infer that TGFbeta is an essential morphogenic signal
173 We infer that the 16S rRNA has evolved to undergo large-
174 and the micro- and macrofauna at this site,
we infer that the 9-m-thick sequence was deposited at a
175 We infer that the ability of PcG proteins to compact chr
176 We infer that the abrupt changes in crustal properties r
177 We infer that the actomyosin-driven circumferential cont
178 We infer that the advent of eusociality led automaticall
179 We infer that the adventitious autoxidation of dihydrome
180 We infer that the agility of the medieval glassmaker all
181 We infer that the amide bond between the biotin and the
182 We infer that the amino acid substitutions in HoxA11 alt
183 Based on the results of this study,
we infer that the antiatherogenic properties of 4F may r
184 processes at opposite sides of the membrane,
we infer that the ATPase activity of OpuA in nanodiscs r
185 We infer that the auxiliary gamma subunit effectively in
186 We infer that the basic pitch relationships governing mu
187 We infer that the cells extrude the polysaccharide stran
188 s isomorphous presence in the native enzyme,
we infer that the channel is a diffusion pathway for O2
189 We infer that the charge selectivity filter is in the cy
190 on concentration of nucleotide triphosphate,
we infer that the combed DNA molecules capable of intera
191 ith oxygen isotope data from sediment cores,
we infer that the contributions from Antarctica and the
192 et genes in cell culture studies, from which
we infer that the cycle is cell permeable.
193 We infer that the death rate of HIV-infected cells is 80
194 We infer that the decomposition of TpT is initiated by t
195 We infer that the degeneracy of specific Fis binding sit
196 e ambiguity, and by performing PCR analysis,
we infer that the deletion breakpoints were most likely
197 We infer that the differences between the two tandem pai
198 We infer that the differing trajectories in optimizing a
199 Thus,
we infer that the distinct gene profile of Wp-restricted
200 hanism of formation of this tetramer domain,
we infer that the domain folds by the docking of the int
201 n computer modeling of the Kir6.2 structure,
we infer that the EET-Kir6.2 interaction may allosterica
202 Furthermore,
we infer that the electron transfer between cerium catio
203 We infer that the evidence is consistent with a frozen b
204 We infer that the evolutionary advantage of RESA to the
205 We infer that the experimentally observed gradual change
206 We infer that the extreme interpersonal diversity of hum
207 Importantly,
we infer that the five epistatic interactions occurring
208 We infer that the function of many 3'-to-3' overlaps is
209 We infer that the GlnRS architecture has differentiated
210 of rate constants at elevated temperatures,
we infer that the half-time at 25 degrees C for spontane
211 We infer that the high binding affinity of HMGB1a for CP
212 ies of either group of crown Catarrhini, and
we infer that the hominoid-cercopithecoid split happened
213 We infer that the host originated first and that the par
214 We infer that the hypothesized transition-zone water fil
215 We infer that the IMF in massive star-forming galaxies i
216 We infer that the Indian upper-mantle isotope signature
217 We infer that the information obtained in steady-state s
218 We infer that the inter-tropical convergence zone of int
219 We infer that the interactions underlying misfolding are
220 genies and the synchrony of these key nodes,
we infer that the internal genes of avian influenza viru
221 Using a multigene land plant phylogeny,
we infer that the intron underwent a transition from cis
222 Based on these findings,
we infer that the KCl denuder method underestimates atmo
223 We infer that the LAB beneath young plates consists of a
224 n old and metal-rich stellar population, and
we infer that the lifetime of long-period variables in M
225 )(NBD),Nle(12)] alpha-factor during binding,
we infer that the ligand associates with receptors via a
226 We infer that the magnitude of an earthquake can therefo
227 We infer that the major meiotic role of BRCA1 is to prom
228 pact heating signatures in stony meteorites,
we infer that the Moon formed ~4.47 billion years ago, w
229 id regions) and twelve biogeographic models,
we infer that the most recent common ancestor of Cycnoch
230 Instead,
we infer that the MPT was initiated by a change in ice s
231 From these results,
we infer that the mutation reduces rates of transitions
232 Thus,
we infer that the non-specific and nicked-site cleavage
233 dyneins underlying the centering machinery,
we infer that the number is approximately 1000, consiste
234 We infer that the observed aftershock density is consist
235 We infer that the observed fluorescence increase on the
236 We infer that the observed macroevolutionary increase in
237 We infer that the observed pattern of uplift and subside
238 )(3)N(g) is protonated only on pH < 4 water,
we infer that the outer surface of water is Bronsted neu
239 We infer that the Patagonian desertification was not sol
240 ng human and macaque monkey cerebral cortex,
we infer that the pattern of human evolutionary expansio
241 We infer that the patterns are structurally and opticall
242 We infer that the pdh-expressing subpopulation is able g
243 From this
we infer that the phosphorylation state of RsbV(1) and R
244 We infer that the physiologic level of germline transcri
245 tinct sequence types and their distribution,
we infer that the population is undergoing frequent gene
246 We infer that the protein hydration shell is more resist
247 We infer that the protein packing around the M2M3 loop i
248 We infer that the proximity-induced high-T c superconduc
249 We infer that the remaining New Madrid mainshock may hav
250 We infer that the role of MukBEF in stabilizing chromati
251 We infer that the sequence mutation rate is 1.4-2.3x10(-
252 Based on genome and relevant gene sequences,
we infer that the sweet, umami, and bitter tastes have b
253 We infer that the talc is forming as a result of the rea
254 Instead,
we infer that the temperature contrast across the equato
255 We infer that the trimer constitutes the vertex of the C
256 stently indicates eastward winds, from which
we infer that the troposphere is rotating faster than th
257 We infer that the unusually high set point of virus carr
258 dation/reduction and compositional unmixing,
we infer that the variation in Curie temperature arises
259 We infer that the vertebrate Hox bipartite regulatory sy
260 We infer that the volcano was probably poised in a near-
261 Finally,
we infer that the ZW sex chromosome pair had undergone a
262 We inferred that the ectodomain and CTD have protein int
263 We inferred that the exogenous GAs had inhibitory effect
264 We inferred that the LD-induced cholesterol enrichment o
265 Thus,
we inferred that the tested Bt rice varieties have negli
266 While a few such compounds are known,
we infer that their number is actually much larger.
267 Furthermore,
we infer that there is more than three times as much fun
268 We infer that these 'propeller'-shaped perturbations ari
269 From petrological modelling,
we infer that these changes reflect a cooling of the Gal
270 We infer that these findings are inconsistent with a non
271 We infer that these high initial air concentrations resu
272 We infer that these inconsistencies result from the proc
273 We infer that these lysine residues impede functional pr
274 ty have not been found with other expansins,
we infer that these novel activities are linked to the s
275 We infer that these represent the internal aldimine (lam
276 We infer that these residues, predicted to face beta2-M3
277 essed in R cells and their synaptic targets,
we infer that these three genes act at the same step in
278 Thus,
we inferred that these forests can respond differently t
279 We infer that they line a water-accessible surface, poss
280 We infer that this conformational change is required for
281 We infer that this group, which may comprise >15% of the
282 We infer that this highly conserved protein has no mitoc
283 We infer that this increased lethality limits adrenocort
284 doacrylate peracid in reaction mixtures, and
we infer that this is the direct product of RutA.
285 cal asparagine residue in the kinase domain,
we infer that this N-terminal domain functions as a sigm
286 We infer that this occurs prior to the conformational ch
287 We infer that this reproductive strategy was critical to
288 We infer that this secondary variability is driven by su
289 opulation dynamics at the base of the crypt,
we infer that this sensitivity is due to direct competit
290 We infer that this steric repulsion would tilt the top o
291 We infer that this was achieved by a sluggish deep overt
292 We infer that this, and selection for form II RuBisCOs,
293 Using covalently linked dimers of FtsK,
we infer that three gamma domains per hexamer are suffic
294 Furthermore,
we infer that two different movement patterns existed hi
295 From these observations,
we infer that value is decreased because of a negative r
296 In summary,
we infer that variant influenza viruses with deletions i
297 We infer that very low levels of Arf are tumor suppressi
298 ral arousal preceding a change in meal time,
we infer that VMH activation is involved in the increase
299 Based on our biochemical and genetic studies
we infer that yeast Poldelta can simultaneously utilize
300 We infer that zinc mobilization from intracellular zinc