1 From these results,
we infer that 1) laforin is responsible for glycogen dep
2 , immunostaining, and in situ hybridization,
we infer that 1) the dominant effector response in Aire
3 Under the variable effects model,
we infer that 11% of synonymous mutations are subject to
4 Genome-wide,
we infer that 20,000 to 60,000 residues have been modifi
5 From our measurements,
we infer that 70% of 50S subunits are engaged in transla
6 We infer that a chronic hyperaldosteronic status, whethe
7 We infer that a DA-dependent signaling system operates i
8 We infer that a general strategy for a promiscuous prote
9 are predicted to lower the selectivity, and
we infer that a rational design strategy in selective ac
10 We infer that a reversible diffusion of oxygen ions in t
11 We infer that a similar mechanism may apply to other mic
12 We infer that a single wild-type alpha subunit is capabl
13 We infer that a wide variety of amphipaths can displace
14 ns Arg-126-Gln, Asp-49-Asn, and Arg-126-Lys,
we inferred that a crystallographic water acts as a gene
15 We inferred that a small fraction of the renal Na,K-ATPa
16 We infer that abnormal peripheral C nociceptor ongoing a
17 We infer that abrupt warming triggered expansion of the
18 We infer that accelerated retreat from 17.77 +/- 0.13 ca
19 We infer that activation by anesthetics and GABA induces
20 We infer that AGO4-dependent smRNAs play a central role
21 We infer that AGO8 plays a central role in the induction
22 We infer that an increase of >1 megapascal in pore press
23 We infer that ash dieback resistance in F. excelsior is
24 We infer that at least some of this reduction in diversi
25 asured with average atom number N=1.1+/-0.4,
we infer that atoms are localized within the waveguide b
26 ecame oligomerized after membrane insertion,
we infer that Bax oligomers are present at pore edges.
27 We infer that BCRs with IgH chain from the Emu-deficient
28 We infer that belemnites adapted to environmental change
29 We infer that Bennu's metre-sized boulders record its hi
30 Based on this analysis,
we inferred that Bicc1 was involved in osteoblast differ
31 We infer that binding of the ordered population reflects
32 We infer that BNRF1 is also a latent Ag that could be ta
33 hich occur in mice completely lacking LRP6),
we infer that bone mass accrual and dental patterning ar
34 We infer that both mutant and wild-type proteins also ca
35 We infer that California seismicity rates are modestly m
36 We infer that CAP discriminates between consensus and no
37 We infer that carbon, helium, argon and highly incompati
38 We infer that cell cycle control of the V(D)J recombinas
39 We infer that cell cycle progression in cyanobacteria sl
40 We infer that CFS is based on modulating the gain of neu
41 We infer that combining the NIR-I/II spectral windows an
42 We infer that continuous individual improvement could be
43 We infer that crystal plasticity precludes failure and c
44 the pattern of the S-S and Trp Raman bands,
we infer that Cys32 is likely to be involved in the cros
45 We infer that D(k)-licensed G2(+) NK cells efficiently d
46 We infer that D. biarmipes relies instead on a recombina
47 Overall,
we infer that deep-sea sediments experiencing thermogeni
48 We infer that degassing during decompression of water-sa
49 We infer that delivery of water to the bed transiently i
50 We inferred that difference in reactivity, coupled with
51 omposing gene-by-aging (G x A) interactions,
we infer that different genes influence some neurocognit
52 Further,
we infer that dispersal limitation may also influence fu
53 We infer that doping up to the optimum level does not sh
54 timing events using phylogenetic distances,
we inferred that duplications in cytoskeletal and membra
55 From these data,
we infer that during large magnitude earthquakes a step-
56 We infer that E. coli is highly susceptible to radiation
57 Accordingly,
we infer that EAAT5 may well be a player in modulating n
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 information about human brain activity, and
we infer that features of the field potential that are u
65 We infer that fluids are naturally injected into the fau
66 We infer that for the smaller molecular mass, PEG entere
67 In the suborder Ensifera,
we infer that forewing-based stridulation and tibial tym
68 We infer that functional FtsZ rings can form in ftsI- an
69 Considering our results and those of others,
we infer that germ-line Piwi functions downstream of piR
70 From the present results,
we infer that glutamate is released with GABA from inhib
71 We inferred that goats are the ancestral hosts for BTV b
72 We infer that Golgi compartments form at ERES and then p
73 We infer that gp140 proteins may always contain a variab
74 We infer that Gpa1 serves as a positional determinant fo
75 neuropeptide Y, parvalbumin, or calretinin,
we infer that graft-derived cells integrate into local c
76 as indicators of the pathogen's environment,
we inferred that granulocytic inflammation generates a n
77 a lipase mutant that does not bind to Grb2,
we inferred that Grb2 serves to hijack PLD2 to the perin
78 We infer that H3F3B is more similar to the ancestral H3.
79 We infer that high local interhost correlations in paras
80 Using MR,
we inferred that higher triglyceride (TG) and LDL choles
81 bining genetic and phylogenetic information,
we infer that hlx-Su(hlx) hybrid lethality is likely cau
82 We infer that hydrological variability in this part of I
83 We infer that hydrolysis leads to a compaction around th
84 From these results
we infer that (
i) P-deficient growth causes some interna
85 We infer that Ichthyostega underwent greater locomotory
86 We infer that IM symptoms arise as a consequence not of
87 From these data,
we infer that in female mice, PKCalpha normally serves t
88 We infer that in wild-type mice, Aag excises damaged DNA
89 e from silicon and nitrogen isotope changes,
we infer that,
in contrast to the modern situation, the
90 We infer that increased NlSPATA5 expression may be one m
91 We infer that increased reliance on wild plants rich in
92 Despite this,
we infer that Indian Zoroastrians (Parsis) intermixed wi
93 We infer that inhibition of nitrite oxidation resulted i
94 We infer that iron is the prosthetic metal in vivo.
95 proximal regulator of sigX in S. mutans, and
we infer that it controls competence in a parallel way i
96 densed DNA structure is not well ordered and
we infer that it is formed by many looping interactions
97 Thus
we infer that it is the positions of splice junctions in
98 Using Wiki-Pi,
we infer that its association to diabetic retinopathy ma
99 tep in binding is concentration independent,
we infer that JBP1 undergoes a conformational change upo
100 We inferred that K = 2 reflects the footprint of agricul
101 We infer that Lak phages are widespread in gut communiti
102 We infer that Lanzhousaurus had a rapid rate of tooth en
103 d the volcanic history of the Lhasa terrane,
we infer that large-magnitude surface uplift of the nort
104 We infer that levels of crossover interference are signi
105 We infer that loss of DGKE function results in a prothro
106 We infer that M2 is tightly associated with the adjacent
107 We infer that macromolecular synthesis in the forespore
108 We infer that major shifts occurred rapidly in the after
109 star formation rate and size of this galaxy
we infer that many star-forming cores may be heavily obs
110 We infer that melanoma risk is more strongly related to
111 From native gels,
we inferred that MET1 associates with PSII subcomplexes
112 We infer that Mg ions are complexed and dewatered by sur
113 We infer that modern humans proved a greater competitive
114 We infer that modified susceptibility due to natural inf
115 We infer that most cancer cells are differentiated along
116 We infer that most of the 267 lines show mutant effects
117 m the initial speed (after the load change),
we inferred that motors running at very low loads are dr
118 centrations near the surface in this region,
we infer that much of the secondary organic aerosol in t
119 We infer that Mus81-dependent crossing over occurs in a
120 Based on multiple measures,
we infer that Narp knockout mice undergo normal seizure
121 We infer that neural sonifications of speech-evoked brai
122 ressed in the rod photoreceptor lineage, and
we inferred that neuroD is also expressed in a subset of
123 Based on their somatic locations,
we inferred that neurons with only ipsilaterally project
124 We infer that NlPHF7 play a role important in stimulatin
125 We infer that Nlst6 acts in BPH growth and fecundity, an
126 We infer that off-line rTMS caused an additional dysfunc
127 We infer that oligomerization via the C-terminal domain
128 ume of 4.9 x 10(-4) (lambda/n)(3) from which
we infer that only ~2,400 electrons per resonator partic
129 From these data,
we infer that P(i) release commits myosin V to undergo a
130 before diverging below approximately 230 K,
we infer that PA in ice remains cooperatively hydrated w
131 From these data,
we infer that PAC are therefore unlikely to be attractiv
132 We infer that para-substituted benzylamines are good rea
133 We infer that past plankton turnover occurred when a war
134 nse of the bulk soil and the heavy fraction,
we infer that phosphate has a greater contribution to th
135 We infer that phosphorylation of one subunit of wild-typ
136 We infer that pilus polymerization involves the formatio
137 We infer that PIP2 participates in the initial trimer fo
138 We infer that Pk(Pk) is sufficient to mediate the interc
139 However,
we infer that platelet activation and binding of activat
140 We infer that pro- and anti-inflammatory activities of b
141 We infer that projections forced by RCP8.5 underestimate
142 Thus,
we infer that Protein C002 is crucial in the feeding of
143 We infer that protonation of X = Y = Z at central atoms
144 We infer that protrusive F-actin, induced by the frontne
145 ping cellular environments for PrPC and Sho,
we inferred that PrPC levels might also be altered as pa
146 From this disease-association overlap,
we infer that PTV is the likely mechanism by which eight
147 Using mutant cycle analysis,
we inferred that Q226E induces activation via an enhance
148 Based on earlier molecular genetic studies,
we inferred that R. capsulatus CcmF, CcmH, and CcmI inte
149 We infer that reduced vegetation cover during glacials d
150 dered along with higher levels of cyclin D1,
we infer that relative to gamma radiation exposure to (5
151 uble knock-out mice resemble reeler mutants,
we infer that Reln(CTRdel)/Apoer2(null) double homozygot
152 From the studies presented here,
we infer that replication through the 3meA lesion in yea
153 In this work,
we infer that retrogenes do not generally carry regulato
154 We infer that rostral PPC areas do not code single effec
155 assemble into virus-like particles in vitro,
we infer that RSV Gag is biologically active.
156 We infer that selection acted mainly on young archaic va
157 We infer that selective stabilization of key recombinati
158 We infer that sex chromosome gene expression directly in
159 ombined with a small sex-determining region,
we infer that sexual conflict may be effectively stymied
160 We infer that Sgs1 always functions in the context of th
161 and in accord with some reports for PrP(C),
we infer that Sho's activity will prove germane to the m
162 From our measurements
we infer that Sid2p and Mob1p both exist as monomeric, h
163 We infer that sigma(E) compartmentalization is partially
164 We infer that similar principles underlie carrier protei
165 d to survive only in the outer Solar System,
we infer that,
similarly to cometary bodies, metal-rich
166 nown to be subject to a bistable switch, and
we infer that SinI reaches levels sufficient to trigger
167 king the size dependence of the jump number,
we infer that skyrmions are assembled into cluster state
168 We infer that snaR evolved from the left monomer of the
169 Further,
we infer that Soay and Sarda sheep carry introgressed mo
170 We infer that some of the ascribed functions are seconda
171 We infer that southwest Greenland will become a major fu
172 ring analysis and hybridization simulations,
we infer that Spanish teosinte is of admixed origin, mos
173 We infer that spatial and temporal variation of DNA supe
174 We infer that stem eukaryotes shared functionally modern
175 We infer that such CD4(+) T cells recognize cellular ant
176 We infer that such redirection of spatial attention enga
177 We infer that the 16S rRNA has evolved to undergo large-
178 and the micro- and macrofauna at this site,
we infer that the 9-m-thick sequence was deposited at a
179 We infer that the ability of PcG proteins to compact chr
180 We infer that the abrupt changes in crustal properties r
181 We infer that the actomyosin-driven circumferential cont
182 We infer that the advent of eusociality led automaticall
183 We infer that the agility of the medieval glassmaker all
184 We infer that the amino acid substitutions in HoxA11 alt
185 We infer that the ancestral therian chewing stroke relie
186 Based on the results of this study,
we infer that the antiatherogenic properties of 4F may r
187 processes at opposite sides of the membrane,
we infer that the ATPase activity of OpuA in nanodiscs r
188 We infer that the auxiliary gamma subunit effectively in
189 We infer that the basic pitch relationships governing mu
190 Additionally,
we infer that the bound guanosine triphosphate cofactor
191 s isomorphous presence in the native enzyme,
we infer that the channel is a diffusion pathway for O2
192 We infer that the charge selectivity filter is in the cy
193 on concentration of nucleotide triphosphate,
we infer that the combed DNA molecules capable of intera
194 We infer that the concerted transition model can be used
195 et genes in cell culture studies, from which
we infer that the cycle is cell permeable.
196 We infer that the decomposition of TpT is initiated by t
197 We infer that the degeneracy of specific Fis binding sit
198 e ambiguity, and by performing PCR analysis,
we infer that the deletion breakpoints were most likely
199 We infer that the DFE is highly leptokurtic (L-shaped).
200 We infer that the differences between the two tandem pai
201 We infer that the differing trajectories in optimizing a
202 Thus,
we infer that the distinct gene profile of Wp-restricted
203 hanism of formation of this tetramer domain,
we infer that the domain folds by the docking of the int
204 Furthermore,
we infer that the electron transfer between cerium catio
205 We infer that the evolutionary advantage of RESA to the
206 We infer that the experimentally observed gradual change
207 We infer that the extreme interpersonal diversity of hum
208 Importantly,
we infer that the five epistatic interactions occurring
209 rom the DGIE scores of relevant subnetworks,
we infer that the functions of embryonic stem (ES) cells
210 s genetic perturbations to Notch1a and Emx2,
we infer that the gene-regulatory network determining ce
211 We infer that the GlnRS architecture has differentiated
212 We infer that the high binding affinity of HMGB1a for CP
213 ies of either group of crown Catarrhini, and
we infer that the hominoid-cercopithecoid split happened
214 We infer that the host originated first and that the par
215 Altogether,
we infer that the host that engulfed the proto-mitochond
216 We infer that the hypothesized transition-zone water fil
217 We infer that the IMF in massive star-forming galaxies i
218 We infer that the information obtained in steady-state s
219 ade in the absence of applied force, whereby
we infer that the initial assembly stage of FAs is force
220 We infer that the inter-tropical convergence zone of int
221 We infer that the interactions underlying misfolding are
222 genies and the synchrony of these key nodes,
we infer that the internal genes of avian influenza viru
223 Based on these findings,
we infer that the KCl denuder method underestimates atmo
224 We infer that the LAB beneath young plates consists of a
225 n old and metal-rich stellar population, and
we infer that the lifetime of long-period variables in M
226 We infer that the major meiotic role of BRCA1 is to prom
227 pact heating signatures in stony meteorites,
we infer that the Moon formed ~4.47 billion years ago, w
228 id regions) and twelve biogeographic models,
we infer that the most recent common ancestor of Cycnoch
229 Instead,
we infer that the MPT was initiated by a change in ice s
230 From these results,
we infer that the mutation reduces rates of transitions
231 volume and phase equilibrium considerations,
we infer that the niccolite-type phase may contain H wit
232 dyneins underlying the centering machinery,
we infer that the number is approximately 1000, consiste
233 We infer that the observed fluorescence increase on the
234 We infer that the occurrence of the giant earthquake at
235 )(3)N(g) is protonated only on pH < 4 water,
we infer that the outer surface of water is Bronsted neu
236 We infer that the Patagonian desertification was not sol
237 ng human and macaque monkey cerebral cortex,
we infer that the pattern of human evolutionary expansio
238 We infer that the patterns are structurally and opticall
239 We infer that the pdh-expressing subpopulation is able g
240 tinct sequence types and their distribution,
we infer that the population is undergoing frequent gene
241 We infer that the protein hydration shell is more resist
242 We infer that the protein packing around the M2M3 loop i
243 We infer that the proximity-induced high-T c superconduc
244 We infer that the same physics shapes both AGB winds and
245 We infer that the sequence mutation rate is 1.4-2.3x10(-
246 compared to purely hydrophobic interactions,
we infer that the six M101-F99 pairs in the hexameric ch
247 We infer that the structural features that develop below
248 Based on genome and relevant gene sequences,
we infer that the sweet, umami, and bitter tastes have b
249 We infer that the talc is forming as a result of the rea
250 We infer that the trimer constitutes the vertex of the C
251 We infer that the unusually high set point of virus carr
252 dation/reduction and compositional unmixing,
we infer that the variation in Curie temperature arises
253 We infer that the vertebrate Hox bipartite regulatory sy
254 Finally,
we infer that the ZW sex chromosome pair had undergone a
255 We inferred that the ectodomain and CTD have protein int
256 We inferred that the exogenous GAs had inhibitory effect
257 els of sperm competition in Pan Furthermore,
we inferred that the great ape common ancestor already p
258 We inferred that the LD-induced cholesterol enrichment o
259 Using phylogenetic analysis,
we inferred that the newly identified noncanonical LsrB
260 Thus,
we inferred that the tested Bt rice varieties have negli
261 While a few such compounds are known,
we infer that their number is actually much larger.
262 Furthermore,
we infer that there is more than three times as much fun
263 We infer that there is no single pathway that explains m
264 We infer that these 'propeller'-shaped perturbations ari
265 We infer that these amyloidogenic events occur only at a
266 We infer that these changes of body shape and centre of
267 From petrological modelling,
we infer that these changes reflect a cooling of the Gal
268 We infer that these findings are inconsistent with a non
269 We infer that these lysine residues impede functional pr
270 Moreover,
we infer that these municipalities experienced greater i
271 ty have not been found with other expansins,
we infer that these novel activities are linked to the s
272 We infer that these represent the internal aldimine (lam
273 We infer that these residues, predicted to face beta2-M3
274 Thus,
we inferred that these forests can respond differently t
275 We inferred that these founder events removed low freque
276 We infer that they line a water-accessible surface, poss
277 We infer that this conformational change is required for
278 We infer that this group, which may comprise >15% of the
279 We infer that this increased lethality limits adrenocort
280 We infer that this inversion was transferred between lin
281 doacrylate peracid in reaction mixtures, and
we infer that this is the direct product of RutA.
282 cal asparagine residue in the kinase domain,
we infer that this N-terminal domain functions as a sigm
283 We infer that this pattern is caused by retention of cat
284 Using modelling,
we infer that this pile-up arises from the release of la
285 We infer that this reproductive strategy was critical to
286 We infer that this secondary variability is driven by su
287 opulation dynamics at the base of the crypt,
we infer that this sensitivity is due to direct competit
288 We infer that this steric repulsion would tilt the top o
289 We infer that this was achieved by a sluggish deep overt
290 We infer that this, and selection for form II RuBisCOs,
291 Using covalently linked dimers of FtsK,
we infer that three gamma domains per hexamer are suffic
292 We infer that TLAs convey feedforward mechanosensory sti
293 We inferred that tolerant alloreactive B cells retained
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