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1 arters of acute hepatitis C (HCV) infections evolve to a chronic state, while one quarter are spontan
2 catastrophic failures, the plastic flow can evolve to a critical dynamics, making the catastrophic f
3 implicit assumption that cancer cells never evolve to a fitness maximum because they can always acqu
4 to transmit in a mammalian host and quickly evolve to a more virulent strain is cause for concern.
5 od-carved landscapes in fractured rock might evolve to a threshold state for bedrock erosion, thus im
6 cal nodular hyperplasia (FNH), which finally evolved to a giant hepatocellular-cholangiocarcinoma (HC
7 The liver transplant allocation system has evolved to a ranking system of "sickest-first" system ba
8 atheter aortic valve implantation (TAVI) has evolved to a treatment of choice in high-risk patients a
9 or may manifest severe panencephalitis that evolves to a minimally conscious state and diffuse corti
11 ase with recurrent flare-ups of inflammation evolving to a chronic phase leading to restrictive heart
12 DNA polymerase, SFM4-3, which was previously evolved to accept nucleotides with 2'-modifications, we
13 cade, business models for these clinics have evolved to accept public and private health insurance, a
14 at the C-terminal Bag6-binding groove, which evolved to accommodate Bag6, a unique metazoan factor.
15 eage, suggesting these enzyme complexes have evolved to accomplish unique tasks within metazoan genom
17 strains, sophisticated strategies have been evolved to achieve the complete degradation of dietary p
19 ined largely unknown why microorganisms have evolved to acquire such proteases and how the host respo
24 LAR is a consistent entity that does not evolve to allergic rhinitis with systemic atopy over tim
25 x computation, the chunking structure should evolve to allow progressively more efficient movements (
26 en mRNAs and their encoded proteins may have evolved to allow efficient and accurate protein folding.
27 rs to promote HBoV1 replication and may have evolved to allow HBoV1 to establish persistent infection
38 hance our understanding of how AGMs may have evolved to avoid transmission through breastfeeding.
40 temperature variability: tropical ectotherms evolve to be 'thermal specialists' because their environ
41 However, with a connection cost, networks evolve to be both modular and hierarchical, and these ne
42 at networks without a connection cost do not evolve to be hierarchical, even when the task has a hier
43 less frequently required, the lag-phase will evolve to be longer whereas, in frequently changing envi
45 ervals around transcription start sites have evolved to be considerably wider in primates and dog tha
50 folding and unfolding; both modern RNases H evolved to be more kinetically stable than their most re
52 ross the animal kingdom, visual systems have evolved to be uniquely suited to the environments and be
53 e (describing the products of nature as they evolved to be) rather than normative (construing process
57 t set of metabolic strategies, the grain has evolved to become an almost perfect entity for carbon st
58 hogenic H7N9 influenza viruses have recently evolved to become highly pathogenic, raising concerns of
59 inase 1/2 (JAK1/2) inhibitor ruxolitinib has evolved to become the centerpiece of therapy for myelofi
61 propose that these strategies have initially evolved to benefit humans but are now maladaptive and in
62 the glucocorticoid receptor and its paralogs evolved to bind activating response elements [(+)GREs] a
63 GalR family of transcription regulators have evolved to bind diverse DNA sequences and allosteric reg
67 bipartite or two-signal mechanism has likely evolved to both sustain protective immunity and avoid au
69 idence for the existence of a natural enzyme evolved to catalyze a Diels-Alder reaction and shows how
70 sults highlight how a prevalent scaffold has evolved to catalyze quorum signal synthesis and provide
73 In this context, HEV infection frequently evolves to chronic infection with a rapid progression of
75 Our results revealed that linear peptides evolved to coadapt specificity and affinity to functiona
77 odevelopmental sequelae in children with CHD evolve to cognitive decline or dementia during adulthood
78 vores are no exception and the majority have evolved to colonise a small number of closely related ho
79 aboratory-adapted H3 strains tested may have evolved to compensate for the faster HA deactivation at
82 ecificity, paradigms of cardiac disease have evolved to conceptualize myocardial disease and patient
84 part of an adaptive mechanism that may have evolved to conserve energy until more food becomes avail
85 at temperature control of flowering time has evolved to constrain seed set environment and therefore
86 hly successful members of the microbiota has evolved to consume sterically-restricted yeast glycans,
87 This may suggest that miR-1 and miR-21 have evolved to contain distinct sequence elements that are m
88 vel mechanisms of Fat4-Dchs1 signalling have evolved to control cell proliferation within the develop
89 mammals cannot excrete iron, mechanisms have evolved to control iron acquisition, storage, and distri
90 and some of the diverse mechanisms that have evolved to control this critical developmental decision,
94 ect cell-to-cell transmission, yet many have evolved to counteract an antiviral protein called tether
95 ravels the intricate ways in which HSV-1 has evolved to counteract the host immune response and revea
98 Type III protein secretion machines have evolved to deliver bacterially encoded effector proteins
99 protein secretion systems have specifically evolved to deliver bacterially encoded proteins into tar
100 inside cells, and a network of proteins has evolved to deliver this essential, but potentially toxic
106 tal insights into how molecules interact and evolve to enable the control of reaction chemistry and t
109 er, currently circulating pH1N1 viruses have evolved to encode 6 amino acid changes (E55K, L90I, I123
110 from currently circulating pH1N1 viruses has evolved to encode 6 amino acid changes (E55K, L90I, I123
111 ined, and this way, the genome has gradually evolved to encode for genes with multiple isoforms, ther
113 e activity of neurons in OFC and MFC rapidly evolved to encode the amount of reward associated with e
114 h mRNA abundance and splicing appear to have evolved to enhance developmental transitions in major cl
115 that codon choices and protein structures co-evolve to ensure proper protein folding in eukaryotic or
116 pose that sequence features within IDRs have evolved to ensure an optimal balance of sequence-encoded
118 wever, influenza viruses are able to rapidly evolve to escape immune pressure in a process known as "
119 t these unique features of ADAMDEC1 may have evolved to escape from inhibition by endogenous metallop
121 otably, certain avian influenza viruses have evolved to escape this restriction, possibly contributin
123 However, the molecular mechanisms that have evolved to establish these unparalleled developmental pr
127 ell understood how these events interact and evolve to evoke such a highly dynamic and heterogeneous
128 rchers to identify how migration routes have evolved to exploit predictable atmospheric and oceanic c
129 work elucidates how secreted proteases have evolved to exploit the pH of the secretory pathway by al
132 ariety of mechanosensitive ion channels have evolved to facilitate these responses, but the molecular
134 ucture and function of biomacromolecules has evolved to fill many essential roles in biological syste
135 t crosslinks generally have shapes that have evolved to fit precisely into binding pockets on their t
137 ion and in vitro measurements, this FADA was evolved to form a homodimer for the activation of MG dye
141 on mutants suggests that secondary replicons evolved to fulfil a specialized function, particularly h
142 ave been shaped by natural selection as they evolved to fulfill changing functional roles in their na
145 This work sets the stage to explore how MDRs evolved to generate structural and biological diversity
149 text] theory, by which small populations can evolve to higher densities in the absence of disturbance
150 ilayers and numerous accessory proteins, has evolved to house the genetic material of all eukaryotic
151 e whether this distinctive vocal feature has evolved to improve the perception of formants, key acous
154 ife host, suggesting that the disease may be evolving to include a wider spectrum of cloven-hoofed an
156 , a new C-mannosyltransferase has apparently evolved to increase glycosylation of TSRs, potentially t
157 king posture of white butterflies has indeed evolved to increase the temperature of their flight musc
158 To facilitate viral replication, Vpx has evolved to induce SAMHD1 degradation and Vpr to mediate
160 ophage-tropic (M-tropic) HIV-1 variants have evolved to infect macrophages, which have only low level
163 ese results also indicate that H. pylori has evolved to integrate expression of the major virulence g
164 t trigger disease resistance in the host can evolve to interfere with the resistance process and, thu
165 P. knowlesi invasion, but that parasites may evolve to invade human RBCs through the use of sialic ac
166 small deltaproteobacterial predator that has evolved to invade, reseal, kill, and digest other gram-n
167 understanding on why only some DCIS lesions evolve to invasive cancer whereas others appear not to d
168 fractionation of the epimer, the enzyme was evolved to invert stereoselectivity, producing the pharm
169 e present a simple model in which plants can evolve to invest in a range of defensive toxins, and her
171 ther, these results show that the shell also evolved to kill parasitic nematodes and this is the only
172 We conclude that synaptic proteins have evolved to limit possible contact site assemblies and mo
174 we suggest negative cooperativity might have evolved to maintain a residual conjugating activity of G
176 (TCR) are among the DNA repair pathways that evolved to maintain genome integrity by removing DNA dam
177 static modifiers of the cue polymorphism can evolve to make optimal use of the information in the gen
180 ce arises when the nutrient storage pathways evolved to maximize efficient energy utilization are exp
181 ession through the endocytic pathway and has evolved to maximize extraction of antigens from cell cor
182 ks of pores, with pore size ratios that have evolved to maximize mass transport and rates of reaction
183 uscle-tendon morphology of the human leg has evolved to maximize the metabolic efficiency of walking
185 ions between prokaryotes and eukaryotes have evolved to mediate microbe-dependent host physiology and
190 c resources, elaborate egress processes have evolved to minimize the time between escaping and invadi
191 drial mechanisms of bat physiology that have evolved to mitigate oxidative stress incurred during met
193 result of obstruction to bulk flow of CSF is evolving to models that incorporate dysfunctional cerebr
195 d public media speculated that the virus had evolved to more effectively transmit between humans.
197 cent insights into the strategies cells have evolved to neutralize toxic aggregates by sequestering t
198 idered as an environmental pathogen that has evolved to occupy a diverse set of environmental niches
199 ous lesion known as Barrett's oesophagus can evolve to oesophageal adenocarcinoma in decades-long pro
200 apable of causing pneumonic plague before it evolved to optimally cause invasive infections in mammal
201 e results suggest that binding pathways have evolved to optimize rapid responses of AMPA-type iGluRs
203 e substrate-binding surface of LPMOs have co-evolved to optimize several of the interconnected proper
205 this spacer diversity, viruses can no longer evolve to overcome CRISPR-Cas by point mutation, which r
208 side of the clinic, gene therapy research is evolving to overcome the poor responses and toxicity ass
209 otection from pathogen invasion but has also evolved to participate in physiological processes to mai
211 propose that fungal NAT isoenzymes may have evolved to perform diverse functions, potentially releva
212 Consequently, specialized structures have evolved to permit rapid communication among cells, tissu
214 ome of the ways in which the PAR network has evolved to polarize cells in different contexts and in r
219 ults illustrate how two related species have evolved to precisely adjust their volatile content by mo
220 that membrane-interaction mechanisms of ABPs evolved to precisely fulfill their specific functions in
221 perhaps inevitable that some bacteria would evolve to preferentially grow in environments that harbo
222 ese data suggest that EBNA3A and EBNA3C have evolved to prevent differentiation to PCs after infectio
224 h radiologically isolated syndrome (RIS) who evolve to primary progressive multiple sclerosis (PPMS).
225 to unpredictable pollen availability, plants evolve to produce more ovules than they expect to be fer
227 at the wrapping mechanism of gyrase may have evolved to promote rapid removal of positive supercoils,
228 ural features used for reverse transcription evolved to promote the splicing of both group II and spl
230 mation as a physicochemical process that has evolved to protect the integrity of the human vasculatur
231 ANCE Restriction factors are genes that have evolved to provide intrinsic defense against viruses.
233 he treatment of hepatitis C virus (HCV) have evolved to provide shorter treatment duration and higher
234 the collective motion of the group of agents evolves to reach the most probable state with relatively
236 e solutions that the human immune system can evolve to recognize a conserved motif buried under a can
238 ptation or recycling of visual circuits that evolved to recognize everyday objects and shapes in our
239 data provide compelling evidence that ZFP809 evolved to recognize foreign DNA and establish histone m
242 e propose that these cone-like rods may have evolved to regain spectral sensitivity and chromatic dis
244 in the developing vertebrate nervous system evolved to regulate neurogenesis.SIGNIFICANCE STATEMENT
245 lts demonstrate that the PXY-CLE pathway has evolved to regulate secondary growth and manipulating th
246 Bud32, Cgi121, Pcc1 and Gon7 appear to have evolved to regulate the central t(6)A biosynthesis funct
248 NAP1L1 through NS5A.IMPORTANCE Viruses have evolved to replicate and to overcome antiviral counterme
249 are an unusual group of organisms that have evolved to replicate exclusively within the cytoplasm or
250 sory receptor cells are generally thought to evolve to respond to sensory cues as fast as they can.
252 is transcriptionally regulated and may have evolved to respond to distinct photoprotective needs und
255 TSA complex, indicating that the enzyme has evolved to restrict the conformational freedom along its
258 of regulatory mechanisms that bacteria have evolved to sense cellular RSS and mitigate their deleter
259 gregation prone Halo-tag mutant (AgHalo) was evolved to sense proteome stress through its aggregation
260 it instability and cognitive decline rapidly evolving to severe dementia and death within 3 months.
261 ise are therefore interdependent and have co-evolved to share an optimal physiological abundance poin
262 safe and effective when nonshockable rhythms evolve to shockable rhythms (ventricular fibrillation/pu
263 es in which the length of e ach displacement evolves to show a well-defined characteristic scale that
264 hnology and techniques, cataract surgery has evolved to small-incisional surgery with rapid visual re
267 a reveals how different neural circuits have evolved to solve the same problem, even when using diffe
268 lts reveal how interdomain interactions have evolved to stimulate the inhibitory activity of an integ
273 es, as well as in the neural circuitry, have evolved to suppress the noise and enhance the visual sig
274 nsequence, several restriction pathways have evolved to suppress their activity at both transcription
278 h produces cis-polyisoprene, E. ulmoides has evolved to synthesize long-chain trans-polyisoprene via
280 ibility that, like papillomaviruses, EBV has evolved to take advantage of epithelial differentiation
281 at the protein machinery in this process has evolved to take advantage of some set of physical design
282 g of the strategies human gut symbionts have evolved to target other members of this community may pr
285 that is distinct from the pathways that have evolved to the three other beta-lactam antibiotic famili
289 esents convergent lncRNAs that independently evolved to tune PRC1 repression at individual loci.
290 ample of a pathogen resistance gene that has evolved to underlie two types of resistance, yet ensure
291 cuss how solar-cell device architectures can evolve to use coherence-exploiting materials, and we spe
292 derstanding of how retroviruses enter cells, evolve to use new receptors, and maintain efficient entr
295 ng to speculate that gammaherpesviruses have evolved to usurp the type I interferon pathway to compen
300 tness is the extent to which an organism has evolved to withstand the effects of deleterious mutation
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