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1 bles with constant outcome values (0.5 ml or nothing).
2 g the Nash equilibrium action, namely giving nothing).
3 e avoiding the overused approach of assuming nothing.
4 vy financial burden while arguably achieving nothing.
5 in which starvation corresponded to winning nothing.
6 onder rejects the proposal, both players get nothing.
7 The control group received nothing.
8 rable even when in vivo examination detected nothing.
9 sus the negative control PEU films releasing nothing.
10 ects swallow up whatever comes near and emit nothing.
11 and used only single antiplatelet therapy or nothing.
12 for 90 d, whereas control subjects received nothing.
14 atory reverberations create something out of nothing: A third flash where there are only two.SIGNIFIC
23 le for the clients to share a key and reveal nothing about what key has been agreed upon to the serve
24 , but not all veins, contrasting with all-or-nothing alternatives available with the single-order vei
26 ing among people otherwise inclined to share nothing and increases the proportion of participants wil
27 ductive dechlorination rates; however, a "do nothing" approach that relies on indigenous diazotrophs
29 t steering can be detected by the all-versus-nothing argument experimentally even in the presence of
30 -Podolsky-Rosen steering based on all-versus-nothing argument, offering a strong condition to witness
32 to disparity in procedural approach, "leave nothing behind" or "combination therapy," and vessel siz
33 been prepared via hydrothermal synthesis in nothing but H(2) O under high-pressure and high-temperat
34 o create mirrors for space telescopes, using nothing but microscopic particles held in place by light
41 ic theories that allow everything but demand nothing, cases where seeing and thinking conflict, menta
42 binding triggers a highly localized, all-or-nothing change of water accessibility to the transport s
43 us recombination DNA repair is not an all-or-nothing concept, but a spectrum, and that where a tumor
44 ene guests was observed to effect the all-or-nothing cooperative templation of an S6-symmetric host s
45 ered at FLC in individual cells in an all-or-nothing (digital) manner or is continuously varying (ana
50 bit of information to coordinate the all-or-nothing expression of early genes, but also over a longe
51 ure, cells respond autonomously in an all-or-nothing fashion, with the fraction of cells that stably
52 he complex at the cost of its normal, all-or-nothing functionality.IMPORTANCECaudovirales encode cell
54 creases, slot machine switches and double or nothing gambles) was associated with this self-reported
55 network was associated with more 'double or nothing' gambles, weighted by connections between the su
58 e neural and muscular systems, and virtually nothing has been reported about their embryogenesis.
64 ty scale was collapsed into four categories: nothing in bed, in-bed activity, out-of-bed activity, an
68 for a ruthenium catalyst, but since there is nothing in the mechanism restricting it to this metal, t
69 nts might argue that we are advocating doing nothing instead, but we are not; we are only advocating
72 gradation of all these compounds, yet almost nothing is currently known about what these fungi do or
73 e cell types including conventional T cells, nothing is currently known concerning Notch function in
74 (iv) there is two-sided irreversibility; if nothing is done and the problem proves serious, the clim
76 own for its role in olfaction, but virtually nothing is known about a clade of approximately 35 membe
80 on by bacteria is well described, but almost nothing is known about bacterial iron export even though
89 ted traffic to and from the plasma membrane, nothing is known about GORK, its distribution and traffi
90 s do not transfer to other tasks, and almost nothing is known about how activation in IC-related brai
92 s of DISC1-binding proteins reported, almost nothing is known about how DISC1 interacts with other pr
93 e Gi and abrogate PI3K-Akt signals; however, nothing is known about how GIV's GEF function is regulat
94 ied camphor elicits a sensation of cool, but nothing is known about how it affects cold temperature s
95 ories on aging on the cellular scale, nearly nothing is known about how microscopic failures cascade
97 ons as a modulator of inflammation; however, nothing is known about how Rc3h1 expression is regulated
98 signaling remain incompletely understood, as nothing is known about how superficial dorsal horn neuro
99 int and the spindle assembly checkpoint, and nothing is known about how T. brucei controls its cell c
103 ges in vitro by a variety of mechanisms, but nothing is known about intracellular bacterial trafficki
105 d the neuroprotective properties of PEA-OXA, nothing is known about its effects on the gut-brain axis
107 muscle cell contraction in several tissues, nothing is known about its possible role in tracheal smo
110 or (HIF) in vitro and in cultured cells, but nothing is known about its roles in mammalian erythropoi
112 al infections has only recently emerged, and nothing is known about MDSC function in the context of S
113 , 2 and 4 have been characterized, virtually nothing is known about members of cluster 3 (ACA12 and A
114 ptor 2 (NPFFR2) mRNA is highest in placenta, nothing is known about NPFF-NPFFR2 functions in placenta
117 a number of biological functions, virtually nothing is known about structure-function relationships
120 characterized to a limited extent and almost nothing is known about the behavior of these materials u
123 ence suggests that IscS and Fdx interact but nothing is known about the binding site and the role of
124 nt biochemical function between GNC and GNL, nothing is known about the biological role of the four o
127 ains with short incubation periods; however, nothing is known about the conversion of the long-incuba
130 n numerous nonerythroid cells, but virtually nothing is known about the expression and potential sign
131 expression directly or indirectly, virtually nothing is known about the extent to which CodY exerts i
135 nello import studies and in silico analyses, nothing is known about the function and properties of pr
136 rane domains have been analyzed extensively, nothing is known about the function of CAR-D2 and the ex
138 e been investigated extensively, practically nothing is known about the function of NRG2, the closest
142 ) triggers prominent motivation deficits but nothing is known about the impact of this exposure in th
143 y to deletion in P. falciparum in vitro, but nothing is known about the in vivo functions of PAT in P
145 o-inflammation and -degeneration, but almost nothing is known about the interactions between the peri
146 known about epigenetic signaling in glia and nothing is known about the intersection of glial epigene
147 produce nitrous acid, HONO, but essentially nothing is known about the isomeric nitrosyl-O-hydroxide
148 nd ability to transmit vertically, virtually nothing is known about the life history of these endobac
149 ortant to achieving high toxicity, virtually nothing is known about the matrix that binds the toxin i
156 ntially important physiological role, almost nothing is known about the mechanisms responsible for th
157 chwann cell development during this process, nothing is known about the mechanisms that mediate the m
159 ealth of information about archaeal biology, nothing is known about the molecular basis of DNA segreg
162 o known as hypocretin) signaling, but almost nothing is known about the neural mechanisms through whi
163 spite these far-reaching behavioral effects, nothing is known about the neural processes impacted by
165 ssion has been observed in cancer cells, but nothing is known about the piRNA partners or the functio
166 lease contributes to the pathogenesis of AF, nothing is known about the potential role of JPH2 in atr
167 ed vaccine (LAV) to protect against measles, nothing is known about the primary cells in which the vi
168 linked to the flagellar basal body; however, nothing is known about the proteins encoding the collar
169 ngage a pseudo-ELR and an N-like loop motif, nothing is known about the regions of CXCR4 and MIF that
175 the other post-translational modifications, nothing is known about the role of SUMO conjugation to h
181 ion in other environmental compartments, and nothing is known about the stability of high-molecular-w
183 Apart from their identification, almost nothing is known about the structure and function of PRO
184 multimeric channel complex, although almost nothing is known about the structure or subunit composit
186 ell-established clinical syndrome, virtually nothing is known about the tumor cells responsible for t
188 icrobial functions of porcine cathelicidins, nothing is known about their ability to promote pDC acti
192 found in all members of this phylum, almost nothing is known about their identity, location and inte
193 (11-42) make up one fifth of plaque load yet nothing is known about their interaction with full-lengt
194 lity, cell trafficking/adhesion, and cancer, nothing is known about their involvement in liver pathol
195 water bodies is relatively well studied, but nothing is known about their presence in most of the com
196 cosylated chondroitin sulfate and fucoidan), nothing is known about their protein-linked glycosylatio
200 ociated factor 2 (TRAF2); however, virtually nothing is known about TRAF2 signaling in the adult mamm
201 nt arterialization of endothelial cells, yet nothing is known about what regulates COUP-TFII expressi
202 ough the RST is present postnatally in cats, nothing is known about when rubrospinal projections coul
203 hance neuronal form and function, but almost nothing is known about whether and how it alters the bra
206 corridors impact animal movement, virtually nothing is known for species dispersed by wind, which ar
210 in secretion, and social behavior in adults, nothing is known of its role during embryonic developmen
211 gical role is not completely understood, and nothing is known of the biology of these enzymes in Arch
212 ith the exception of one inconclusive study, nothing is known of the genetic basis of this phenomenon
213 l interactions, and in particular, virtually nothing is known of the molecular mechanisms that contro
214 eral inflammatory response to sepsis, almost nothing is known of the neuronal changes that cause asso
216 acaques on the binding of human (hu)IgG, and nothing is known of this interaction in the pig-tailed m
218 ctors of hypersensitivity to betalactam, but nothing is known on the influence of NOD genes, despite
222 ated with deleterious clinical outcomes, but nothing is known to date about tissue protein carbamylat
229 t important sources of human arsenic intake, nothing is published about uptake, toxicity, or toleranc
231 ions of TNF mediated by engagement of TNFR1, nothing is yet known of their role in CD40-mediated even
233 this circuit to decision making, and almost nothing known about the whether any contribution is via
236 explain the experimentally observed 'all-or-nothing' LAX3 spatial expression pattern in cortical cel
237 ticated catalytic centre shows that there is nothing magical about the catalytic activities or mechan
238 eceptors are thought to operate in an all-or-nothing manner, existing in an immunologically active or
240 ion of CasX specificity, revealing an all-or-nothing mechanism where mismatches can be bound, but not
242 vital in animals that reproduce in an all-or-nothing mode, such as bristle worms: females committed t
243 for DNA loop formation are one-step, all-or-nothing models with a looped state and an unlooped state
246 h vigor and imagination, our pinnacle may be nothing more than an inflection point leading to decline
255 r participation costs and allowed for all-or-nothing orders to avoid fragmented share portfolios.
256 applied to intentionally exposed dentin with nothing over it in vivo, whether it affects microleakage
257 We predict that while there appears to be nothing particularly special about water with regard to
259 mologous recombination (HR) is not an all-or-nothing phenomenon, but that HR competency comes on a sp
260 6:1 at the branches, we observed the "all-or-nothing" phenomenon with plasma only entering the low fl
262 In this work, we show that the all-versus-nothing proof of Einstein-Podolsky-Rosen steering can be
264 Although initially considered an all-or-nothing reflex [1], numerous studies on freely diving ma
266 izable lactose analogues generates an all-or-nothing response, where some cells express the lac genes
271 s, such as ELISA and immunofluorescence, are nothing short of ubiquitous in biotechnology and medical
274 its the important neural functions of all-or-nothing spiking with signal gain and diverse periodic sp
275 properties of a neuron, including the all or nothing spiking, the threshold driven spiking of the act
276 w cooperative individuals to adopt an all or nothing strategy to tie strengthening based on the well-
277 ce pathway enabled transition from an all-or-nothing survival strategy to a hormone-modulated, compet
278 l genes and act as long-range enhancers, yet nothing that we know about their function explains the o
280 6 to 15 minutes in a room by themselves with nothing to do but think, that they enjoyed doing mundane
281 hould be an alternative explanation that has nothing to do with genetic continuity, but stresses the
283 d location of that item, despite there being nothing to look at and location memory never explicitly
286 e loading of a cofactor represents an all-or-nothing transition in regard to the enzymatic function a
287 ation are often assumed to involve an all-or-nothing two-state dissociation pathway, but deviations f
293 lt to believe that in about 1960 practically nothing was known about the thymus and some of its produ
295 nventional pathway enrichment tests detected nothing, while our approach discovered biological proces
300 ask that predicted whether reward, shock, or nothing would be delivered to the rat being recorded fro