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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 onder rejects the proposal, both players get nothing.
4 for 90 d, whereas control subjects received nothing.
5 The control group received nothing.
6 rable even when in vivo examination detected nothing.
7 sus the negative control PEU films releasing nothing.
8 ects swallow up whatever comes near and emit nothing.
9 ter than those who were punished or received nothing.
10 vy financial burden while arguably achieving nothing.
11 in which starvation corresponded to winning nothing.
12 atory reverberations create something out of nothing: A third flash where there are only two.SIGNIFIC
13 to indicate only which region is nearer, but nothing about how much the regions are separated in dept
22 al the onset of a light step with 1-3 all-or-nothing action potentials that attain a peak amplitude o
25 t steering can be detected by the all-versus-nothing argument experimentally even in the presence of
26 -Podolsky-Rosen steering based on all-versus-nothing argument, offering a strong condition to witness
28 Multivariate analysis revealed that all-or-nothing behaviour was the key predictor for the onset of
29 ions, stress, anxiety, depression and all-or-nothing behaviour were associated with the risk of PCS.
30 o create mirrors for space telescopes, using nothing but microscopic particles held in place by light
36 ic theories that allow everything but demand nothing, cases where seeing and thinking conflict, menta
37 binding triggers a highly localized, all-or-nothing change of water accessibility to the transport s
39 ene guests was observed to effect the all-or-nothing cooperative templation of an S6-symmetric host s
40 ered at FLC in individual cells in an all-or-nothing (digital) manner or is continuously varying (ana
46 bit of information to coordinate the all-or-nothing expression of early genes, but also over a longe
47 ure, cells respond autonomously in an all-or-nothing fashion, with the fraction of cells that stably
48 he complex at the cost of its normal, all-or-nothing functionality.IMPORTANCECaudovirales encode cell
50 ss from their assets or opt for a "double-or-nothing" gamble that would either avoid or double it.
52 e neural and muscular systems, and virtually nothing has been reported about their embryogenesis.
57 ty scale was collapsed into four categories: nothing in bed, in-bed activity, out-of-bed activity, an
59 nts might argue that we are advocating doing nothing instead, but we are not; we are only advocating
63 e their known wide distribution in primates, nothing is currently known about the occurrence, frequen
64 e cell types including conventional T cells, nothing is currently known concerning Notch function in
66 own for its role in olfaction, but virtually nothing is known about a clade of approximately 35 membe
68 gulate CIITA in B cells have been described, nothing is known about additional distal elements that m
71 on by bacteria is well described, but almost nothing is known about bacterial iron export even though
81 ted traffic to and from the plasma membrane, nothing is known about GORK, its distribution and traffi
82 s do not transfer to other tasks, and almost nothing is known about how activation in IC-related brai
84 s of DISC1-binding proteins reported, almost nothing is known about how DISC1 interacts with other pr
85 e Gi and abrogate PI3K-Akt signals; however, nothing is known about how GIV's GEF function is regulat
86 ied camphor elicits a sensation of cool, but nothing is known about how it affects cold temperature s
87 ories on aging on the cellular scale, nearly nothing is known about how microscopic failures cascade
89 ons as a modulator of inflammation; however, nothing is known about how Rc3h1 expression is regulated
90 s the formation of cohesion, and essentially nothing is known about how sister chromatid cohesion is
91 signaling remain incompletely understood, as nothing is known about how superficial dorsal horn neuro
99 contributor to periodontal bone loss, almost nothing is known about immune responses to this organism
102 cell wall alpha(1-3)glucan is essential, but nothing is known about its localization and function in
103 sent in all examined vertebrate genomes, but nothing is known about its molecular or cellular functio
105 muscle cell contraction in several tissues, nothing is known about its possible role in tracheal smo
106 eceptor CXCR1 shares ligands with CXCR2, yet nothing is known about its potential role in liver patho
109 or (HIF) in vitro and in cultured cells, but nothing is known about its roles in mammalian erythropoi
111 al infections has only recently emerged, and nothing is known about MDSC function in the context of S
112 , 2 and 4 have been characterized, virtually nothing is known about members of cluster 3 (ACA12 and A
115 studied in extant and fossilized organisms, nothing is known about secondary cartilage in fossils.
117 a number of biological functions, virtually nothing is known about structure-function relationships
119 ins are essential for this process; however, nothing is known about the arrangement of the subunits i
122 characterized to a limited extent and almost nothing is known about the behavior of these materials u
125 periplasmic domain of the binding protomer, nothing is known about the binding of many other ligands
126 ence suggests that IscS and Fdx interact but nothing is known about the binding site and the role of
128 nt biochemical function between GNC and GNL, nothing is known about the biological role of the four o
131 ains with short incubation periods; however, nothing is known about the conversion of the long-incuba
135 n numerous nonerythroid cells, but virtually nothing is known about the expression and potential sign
140 nello import studies and in silico analyses, nothing is known about the function and properties of pr
141 rane domains have been analyzed extensively, nothing is known about the function of CAR-D2 and the ex
142 e been investigated extensively, practically nothing is known about the function of NRG2, the closest
144 ishing reproductive mode remain unknown, and nothing is known about the genetic basis of postzygotic
147 ) triggers prominent motivation deficits but nothing is known about the impact of this exposure in th
148 y to deletion in P. falciparum in vitro, but nothing is known about the in vivo functions of PAT in P
150 o-inflammation and -degeneration, but almost nothing is known about the interactions between the peri
151 produce nitrous acid, HONO, but essentially nothing is known about the isomeric nitrosyl-O-hydroxide
152 nd ability to transmit vertically, virtually nothing is known about the life history of these endobac
153 ortant to achieving high toxicity, virtually nothing is known about the matrix that binds the toxin i
157 e leading causes of chronic pain, but almost nothing is known about the mechanisms and molecules that
159 ntially important physiological role, almost nothing is known about the mechanisms responsible for th
160 chwann cell development during this process, nothing is known about the mechanisms that mediate the m
162 ealth of information about archaeal biology, nothing is known about the molecular basis of DNA segreg
163 nd heart in humans and mice; however, almost nothing is known about the molecular downstream targets
166 o known as hypocretin) signaling, but almost nothing is known about the neural mechanisms through whi
167 spite these far-reaching behavioral effects, nothing is known about the neural processes impacted by
170 ssion has been observed in cancer cells, but nothing is known about the piRNA partners or the functio
171 lease contributes to the pathogenesis of AF, nothing is known about the potential role of JPH2 in atr
172 ed vaccine (LAV) to protect against measles, nothing is known about the primary cells in which the vi
173 linked to the flagellar basal body; however, nothing is known about the proteins encoding the collar
174 ngage a pseudo-ELR and an N-like loop motif, nothing is known about the regions of CXCR4 and MIF that
179 the other post-translational modifications, nothing is known about the role of SUMO conjugation to h
186 ion in other environmental compartments, and nothing is known about the stability of high-molecular-w
187 Apart from their identification, almost nothing is known about the structure and function of PRO
188 multimeric channel complex, although almost nothing is known about the structure or subunit composit
190 ell-established clinical syndrome, virtually nothing is known about the tumor cells responsible for t
193 icrobial functions of porcine cathelicidins, nothing is known about their ability to promote pDC acti
197 (11-42) make up one fifth of plaque load yet nothing is known about their interaction with full-lengt
198 lity, cell trafficking/adhesion, and cancer, nothing is known about their involvement in liver pathol
199 water bodies is relatively well studied, but nothing is known about their presence in most of the com
202 mbrane, the phagophore; however, essentially nothing is known about this process including the molecu
203 ociated factor 2 (TRAF2); however, virtually nothing is known about TRAF2 signaling in the adult mamm
204 nt arterialization of endothelial cells, yet nothing is known about what regulates COUP-TFII expressi
205 ough the RST is present postnatally in cats, nothing is known about when rubrospinal projections coul
207 hance neuronal form and function, but almost nothing is known about whether and how it alters the bra
211 corridors impact animal movement, virtually nothing is known for species dispersed by wind, which ar
216 in secretion, and social behavior in adults, nothing is known of its role during embryonic developmen
217 gical role is not completely understood, and nothing is known of the biology of these enzymes in Arch
218 ith the exception of one inconclusive study, nothing is known of the genetic basis of this phenomenon
219 l interactions, and in particular, virtually nothing is known of the molecular mechanisms that contro
220 eral inflammatory response to sepsis, almost nothing is known of the neuronal changes that cause asso
223 ically split across the plasma membrane, yet nothing is known of the transporters required for the tr
224 acaques on the binding of human (hu)IgG, and nothing is known of this interaction in the pig-tailed m
226 the molecular mechanism remains elusive and nothing is known on PIP(2) effect on other Kv such as th
227 ctors of hypersensitivity to betalactam, but nothing is known on the influence of NOD genes, despite
230 th human cardiovascular disease, essentially nothing is known regarding the molecular identity or fun
232 ated with deleterious clinical outcomes, but nothing is known to date about tissue protein carbamylat
238 t important sources of human arsenic intake, nothing is published about uptake, toxicity, or toleranc
240 ions of TNF mediated by engagement of TNFR1, nothing is yet known of their role in CD40-mediated even
242 this circuit to decision making, and almost nothing known about the whether any contribution is via
245 explain the experimentally observed 'all-or-nothing' LAX3 spatial expression pattern in cortical cel
246 ticated catalytic centre shows that there is nothing magical about the catalytic activities or mechan
247 eceptors are thought to operate in an all-or-nothing manner, existing in an immunologically active or
250 vital in animals that reproduce in an all-or-nothing mode, such as bristle worms: females committed t
253 h vigor and imagination, our pinnacle may be nothing more than an inflection point leading to decline
262 r's contention that a belief in free will is nothing other than a continuing belief in vitalism--some
264 6:1 at the branches, we observed the "all-or-nothing" phenomenon with plasma only entering the low fl
266 In this work, we show that the all-versus-nothing proof of Einstein-Podolsky-Rosen steering can be
267 nt (CABG surgery, PCI, medical treatment, or nothing) recommended by the catheterization laboratory c
268 Although initially considered an all-or-nothing reflex [1], numerous studies on freely diving ma
269 en identified in diverse organisms; however, nothing regarding their physiology in the context of cel
272 izable lactose analogues generates an all-or-nothing response, where some cells express the lac genes
275 ical control of the source of pathology, and nothing should be allowed to delay transfer to the opera
276 its the important neural functions of all-or-nothing spiking with signal gain and diverse periodic sp
278 6 to 15 minutes in a room by themselves with nothing to do but think, that they enjoyed doing mundane
279 ction, irrelevant events that government has nothing to do with and for which no government response
280 hould be an alternative explanation that has nothing to do with genetic continuity, but stresses the
284 e loading of a cofactor represents an all-or-nothing transition in regard to the enzymatic function a
285 ation are often assumed to involve an all-or-nothing two-state dissociation pathway, but deviations f
295 bon, nitrogen and phosphorous, but virtually nothing was previously known about how A. tumefaciens ac
296 nventional pathway enrichment tests detected nothing, while our approach discovered biological proces
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