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1  a high frequency of deletions advancing our understanding of how a RAD51 paralog is involved in main
2                          Our data expand our understanding of how a single neuroendocrine cell coordi
3 60 data sets show that GRACE can improve our understanding of how a transcriptional network is re-wir
4                        Despite our increased understanding of how abiotic factors influence plant phe
5 s the canonical nucleosome structure for the understanding of how accessibility to genomic DNA is reg
6           However, there is currently little understanding of how accounting for unreported catches (
7                       The study improves our understanding of how adenoviruses establish infection in
8 essionals have a comprehensive knowledge and understanding of how adolescents experience living with
9                                A mechanistic understanding of how adolescents optimize social predict
10                                     A better understanding of how aging promotes CVD is therefore urg
11 physiology and may have implications for our understanding of how altered folate availability causes
12 These findings may have implications for our understanding of how altered folate availability causes
13                          However, we lack an understanding of how an interface can select some ligand
14 ch developments require detailed mechanistic understanding of how an SNP influences phenotype (and th
15                             However, we lack understanding of how and to what extent climate has shap
16  this experimental therapy, we need a better understanding of how and which mtDNA is tagged for repli
17 wledge of the surface structure will aid the understanding of how and which type of interface will be
18 ponses to these materials, and improving our understanding of how and why certain particulate materia
19 l of these species requires a well-developed understanding of how animals use these new landscapes to
20                                           An understanding of how antibiotic resistance mutations sha
21                                 However, our understanding of how AP1 signaling changes may underlie
22 on modelling (SEM) to achieve a system-level understanding of how aridity, mean annual temperature an
23  fundamental unanswered questions that limit understanding of how arrestin-dependent GPCR signaling c
24 es, and osmotic stress; however, a molecular understanding of how ASK proteins are controlled remains
25 inesin conformation that revises the current understanding of how ATP binding is coupled to forward s
26 iod as one of significant progress toward an understanding of how attitudes form and change in three
27     Furthering the mechanistic and molecular understanding of how bacteria affect the nervous system
28    Surprisingly, we still lack a fundamental understanding of how bacteria build, maintain and expand
29                      This study broadens the understanding of how bacteria diversify at the genomic l
30 y remains poorly characterized, impeding our understanding of how basal processes and endfeet influen
31 ural circuits are perturbed, and the limited understanding of how basic circuit functions relate to t
32 l feedback (PSF) framework has catalyzed our understanding of how belowground microbiota impact plant
33 cept to symbiotic fungi facilitated a better understanding of how biodiversity can be jointly shaped
34 's On Growth and Form, we review our current understanding of how biological forms are created and ma
35 ns between bacterial cells has broadened our understanding of how both pathogens and non-pathogens in
36 elling techniques, could greatly enhance our understanding of how cancer responds to treatment, and a
37 sed cooperative loops have also inspired our understanding of how catalytic loops appear in ecologica
38 mmunotherapeutic platform demands a thorough understanding of how cell death induced in the context o
39                         This requires a deep understanding of how cell signaling pathways converge on
40           We focus on recent advances in our understanding of how cells actively sculpt tissues and h
41 he potential to pave the way toward a better understanding of how cells function at the molecular lev
42          Optogenetics promises to deepen our understanding of how cells perceive and respond to compl
43 vers of aggregation and toxicity adds to the understanding of how cellular homeostasis can be deterio
44 e single-cell level, thus providing a fuller understanding of how changes at single synapses translat
45        Collectively, this study augments our understanding of how cholesterol metabolism can modulate
46 s in different tissues and can assist in the understanding of how chromatin states affect gene regula
47 in sub-Saharan Africa (SSA) require a better understanding of how climate and other drivers influence
48                             Despite detailed understanding of how climate influences N-fixation enzym
49                Our review illustrates how an understanding of how climate model outputs are derived a
50 marine ecosystems, and facilitates a greater understanding of how climate-driven changes in freshwate
51 y the groundwork for an improved mechanistic understanding of how colonization influences development
52 ly defined IAT class, and contributes to our understanding of how commensal and pathogenic E. coli co
53                Our results contribute to our understanding of how communities assembly and how specie
54 which can confound cataloging of members and understanding of how communities function.
55 s observation could prove significant to our understanding of how crystallisation ages are evaluated
56 ve preparedness, it is critical to have some understanding of how CSF would spread should it be intro
57 tion of Notch signaling, contributing to our understanding of how CSL functions as a transcriptional
58 ng cellular ATP production, and advances our understanding of how defective FA signaling contributes
59 ation is well established, we have a limited understanding of how differences in diversity are relate
60 eighboring mesenchymal partners provides new understanding of how different cell types are maintained
61  refined spatial perspective provides unique understanding of how different components of landscape s
62                                           An understanding of how different domains of the environmen
63 ding strong support for the local and global understanding of how different dopants influence the pro
64                      However, we have a poor understanding of how disease-specific methylation change
65                   These findings further our understanding of how diversity loss will reduce the host
66 man CNS-derived cells and contributes to our understanding of how DMF may act clinically to ameliorat
67 roposed catalytic mechanism provide a better understanding of how DMSP is catabolized to generate the
68 iseases, such studies leave us with a lesser understanding of how DNA viruses adapt to hosts and how
69  in clinical use, perhaps due to our lack of understanding of how drugs access this complex cell type
70 s regulation provides a new dimension in our understanding of how DSF-dependent microorganisms modula
71                                              Understanding of how each of these processes contributes
72     This has significant implications on our understanding of how early life events in childhood infl
73                       To further improve our understanding of how ecosystems might respond to future
74 he remaining challenges to achieve a unified understanding of how effector activities work together t
75                       A detailed mechanistic understanding of how environmental microbes influence th
76 ogy has the potential to greatly enhance our understanding of how environmental toxicants affect brai
77                           However, a limited understanding of how epilepsy develops, particularly in
78  and presents a barrier; however, a complete understanding of how EPS structure relates to biological
79                    These findings expand our understanding of how evolution driven by interactions oc
80           Their study has contributed to our understanding of how evolution modifies protein scaffold
81  computational biology have enabled a deeper understanding of how excitatory amino acid transporters
82 umulated by M. australiense and improves our understanding of how exposure duration will influence th
83           These findings help to enhance our understanding of how expression of the inflammatory modu
84 racellular transducer and contributes to our understanding of how FGF signaling plays diverse develop
85 ploited by species, thus limiting a complete understanding of how fish associate with reef structure.
86 ey Insight focuses on recent advances in our understanding of how flowers manipulate physical forces
87 vior may have important implications for our understanding of how fluid flow influences biofilm biolo
88 y knowledge gaps remain and gaining a better understanding of how freshwater pCO2 levels are regulate
89 etic questions and pave the road to a better understanding of how fundamental features of animal body
90 ummarise the current state-of-the-art in our understanding of how general features of amacrine cell i
91 y in cancer networks and will illuminate our understanding of how genes are modulated in a tissue-spe
92                 Here were review our current understanding of how genes, growth, mechanics, and evolu
93                                          Our understanding of how genetic changes underlie the evolut
94 tudies and have the potential to advance our understanding of how genetic networks regulate sophistic
95 ntractions have been predicted; however, our understanding of how genetic variation may promote adapt
96 mes in greater depth, leading to an enhanced understanding of how genome sequence variants underlie p
97 y rewriting the genetic code will deepen our understanding of how genomes are designed and how the ca
98             This might contribute to further understanding of how genomic variations contribute to ca
99 ection of selection targets provide a better understanding of how geography and selection may have sh
100          However, there is little scientific understanding of how global patterns of future urban exp
101 tes tumor invasiveness, and also advance the understanding of how Golgi structure and transport can b
102               Despite this, there is limited understanding of how HBV establishes chronic infections.
103                     This study furthered our understanding of how HCMV evades inhibition by PKR and i
104 ng cardiac specification is critical for our understanding of how heart formation is initiated during
105 eins have yielded vital contributions to our understanding of how hematopoietic stem and progenitor c
106 nces of apoptotic cell sampling, advance our understanding of how homeostasis is maintained within th
107 skin microbiome structure contributes to our understanding of how host-associated bacteria are distri
108                    These findings add to our understanding of how HPV replicates and the host cell pa
109 ce in the western Gulf of Alaska, but little understanding of how human foragers integrated into and
110 humans and toward robots, leading to greater understanding of how humans think, feel, and behave in t
111                                 However, our understanding of how hypoxia modulates the response of A
112                                  This deeper understanding of how immune cells and neurons interact t
113                    These results advance the understanding of how independent but converging influenc
114 gaps that should be addressed to improve our understanding of how individual and group-level factors
115  offers a rare opportunity to seek a dynamic understanding of how individual-, group- and population-
116 review will highlight recent advances in our understanding of how inflammation resolution may become
117                    There is currently little understanding of how initial community structure may dri
118 or regenenerative medicine, and enhances our understanding of how intrinsic and extrinsic signals sha
119 icant threat to global biodiversity, but our understanding of how invasive species impact native comm
120                               A quantitative understanding of how ion transport is integrated and con
121    This study therefore provides a molecular understanding of how kinase-substrate recognition acts a
122                   Here we review the current understanding of how lncRNAs help coordinate gene expres
123          These findings therefore inform our understanding of how local oscillatory activity may unde
124  tuberculosis enzyme, augmenting our current understanding of how M. tuberculosis meets its nutrient
125                                       Deeper understanding of how macroscopic structure affects visco
126 ation of vascularized 3D tissues requires an understanding of how material properties govern endothel
127            This study provides a mechanistic understanding of how MCPH1 controls neural stem cell fat
128 -kappaB is regulated and greatly expands our understanding of how MCV so effectively evades human imm
129 llular heterogeneity of the brain impedes an understanding of how MECP2 mutations contribute to RTT.
130  research questions to answer to enhance our understanding of how MedSD affects CVD risk or how these
131  the notion that there are major gaps in our understanding of how microbial communities degrade ligno
132  findings have important implications in the understanding of how microRNAs influence the co-expressi
133              While many studies advanced our understanding of how microtubule-associated proteins tun
134             Our results not only help in the understanding of how mitochondria cope with replicative
135 ctin-mitochondria interaction, enhancing our understanding of how mitochondria properly localize in a
136 in chromosome segregation, we have a limited understanding of how molecular features of tubulin prote
137              A key limitation is our lack of understanding of how molecular structure impacts on the
138 se results are a first step to gain a better understanding of how mood fluctuations in real life are
139 tiviral state, as well as providing a better understanding of how multiple arms of the immune system
140 nse to climate change requires a mechanistic understanding of how multiple factors interact to limit
141 either FTD or NCL, in part because of a poor understanding of how mutations in genes such as GRN cont
142 arget tissues and cells and by an incomplete understanding of how nanoparticle structure affects biod
143         Our results allow for a quantitative understanding of how natural calcium sulfate deposits ma
144 ks in higher organisms has prevented a clear understanding of how natural environmental conditions af
145 aluable but would be facilitated by a better understanding of how natural human CMV infection is acqu
146 d four distinct products, thus advancing our understanding of how neo-functionalization events have s
147 review highlights recent developments in our understanding of how neural circuits, pubertal hormones,
148  forms a foundation for a more comprehensive understanding of how neural information is directed and
149                Here we review our increasing understanding of how neuronal activity regulates oligode
150 process are not well described, limiting our understanding of how new species are created.
151         However, there are still gaps in our understanding of how nitrate signaling affects biologica
152 de formation are well characterized, but our understanding of how non-native disulfides are reduced s
153                      Our results further our understanding of how novel morphological and biochemical
154 ther histone chaperones, and it advances our understanding of how nucleosomes and their epigenetic in
155                           Results extend the understanding of how organic carbon and nitrite loads mo
156 e bacteria have developed as a model for the understanding of how organization of particles can influ
157 owing maternal loss has been documented, but understanding of how orphans allocate bonding to reconst
158 is in S. pyogenes reported here enhances our understanding of how other Gram-positive bacteria produc
159                             However, a clear understanding of how (p)ppGpp promotes virulence in E. f
160 sis approaches, however, are simplifying our understanding of how p53 functions as a transcription fa
161 maturation of beta-like cells.Our incomplete understanding of how pancreatic beta cells form limits t
162 model may reveal a better pathophysiological understanding of how PE transitions to CTEPH in human tr
163                                           An understanding of how perturbed mechanical properties imp
164 otics and immune modulators by expanding the understanding of how PG is processed by lytic enzymes.
165                              The fundamental understanding of how phonons move and the physical mecha
166 represents a significant step forward in our understanding of how physicochemical theories (such as C
167  and opportunity in developing a mechanistic understanding of how plants detect and respond to drough
168  review, we present an update on the current understanding of how plants recognize and respond to non
169                     This finding expands our understanding of how platelets attach to sites of vascul
170                                      Current understanding of how platelets localize coagulation to w
171                   Moreover, they enhance our understanding of how PMEs may be regulated by pH and pro
172  this single-cell approach provides a better understanding of how prostate cancer cells respond heter
173 popular, highlighting the need for a greater understanding of how proteins behave in the absence of s
174  to biochemistry to structural biology to an understanding of how proteins evolve interaction specifi
175 atomic details of these structures helps our understanding of how proteins work together, how mutatio
176     Here we summarize recent advances in our understanding of how PTMs and regulatory enzymes control
177 ence for microrefugia is hindered by lack of understanding of how rates of warming vary across a land
178              Our model enables an analytical understanding of how Red Queen dynamics emerge in our se
179 ociated gene loci to improve our mechanistic understanding of how resistance develops.
180                        However, a precarious understanding of how resistance emerges and a lack of tr
181  of new and existing agents by advancing our understanding of how resistance evolves.
182                    In order to gain a better understanding of how resistance to DNA methylation from
183                                 The emerging understanding of how SCI cell biology differs across les
184          However, there still is not a clear understanding of how SecDF functions, its exact role in
185 ave played a major role in enhancing current understanding of how selection and demography can impact
186  behavior and pathology, but we lack a basic understanding of how sex differences in the human cerebe
187 ractions with heme and NCoR1 and advance our understanding of how signaling through HRMs affects the
188 tic classifications will help to further our understanding of how single amacrine cell circuits act t
189 f other class I fusion proteins enhances our understanding of how small molecules can function as fus
190 onary theoretical models that can deepen our understanding of how socioeconomic inequalities can beco
191 lts lay the foundation for a more predictive understanding of how soil microbial communities respond
192                         A better mechanistic understanding of how solid tumours are rejected may aid
193  results have important implications for our understanding of how spatial restriction is imposed on t
194 ploration of this technology may improve our understanding of how specific stromal composition could
195             These findings contribute to our understanding of how SPM synthesis is regulated during t
196 e acute setting, there is a lack of cohesive understanding of how staff experience and perceive the c
197 Together, these models provide a biophysical understanding of how stem cell scaling is maintained dur
198            Central to protein biology is the understanding of how structural elements give rise to ob
199                    To obtain a more detailed understanding of how structure influences the function a
200 er, and are modulated by drug therapies, our understanding of how such changes shape the properties o
201                                   A detailed understanding of how such interfaces can be used to tail
202 esynaptic function for LRP4, enabling deeper understanding of how synapse organization is coordinated
203                    This necessitates further understanding of how T follicular helper cells are regul
204        These findings not only transform our understanding of how T3 orchestrates adult brain lineage
205                                  The current understanding of how temperature affects mosquito and pa
206                                          Our understanding of how temporal variations of atmospheric
207 vents occur in the context of chromatin, our understanding of how TF-nucleosome interplay affects gen
208 ight recent advances that have increased our understanding of how the amount of tonic signal impacts
209 ecies.SIGNIFICANCE STATEMENT A comprehensive understanding of how the anatomical architecture of the
210                        Here we provide a new understanding of how the auditory system extracts behavi
211 reinstatement of alcohol seeking, expand our understanding of how the BLA-->NAc pathway regulates alc
212                                  An improved understanding of how the brain allocates mental resource
213 ed view of motor cortex may lead to a better understanding of how the brain controls movement.
214  necessary first step toward a circuit-level understanding of how the brain generates behavior.
215 nues to have great promise in furthering our understanding of how the brain works.
216                Two recent papers advance our understanding of how the cancer genome evolves as the pr
217                                          Our understanding of how the course of opportunistic bacteri
218  isotope heterogeneity in plants and for our understanding of how the delta(18) O signal is incorpora
219 of key factors that govern metabolism and an understanding of how the differential capacity to metabo
220  individual isoforms, necessitating a deeper understanding of how the distinct transcriptional progra
221               However, we still lack a clear understanding of how the endogenous activity of these ce
222                                          Our understanding of how the endoplasmic reticulum (ER)-asso
223    Here, we highlight recent advances in our understanding of how the genome folds inside the 3D nucl
224       This limitation especially hinders our understanding of how the gut microbiota interact with th
225                                     A better understanding of how the host inflammatory/immune respon
226                    These results advance our understanding of how the immune system limits NiV dissem
227  the first time a quantitative basis for our understanding of how the large population of definitive
228 agate actions in the cell, but an integrated understanding of how the lipid bilayer exerts its effect
229 gest volcanic systems, resulting in a better understanding of how the melt structure controls volcani
230 nition on perception would revolutionize our understanding of how the mind is organized; but without
231                       However, a mechanistic understanding of how the mitochondrial Ca(2+) signaling
232                                     A better understanding of how the mobilization process is regulat
233 ffects on sleep/wake behavior, improving our understanding of how the PPT nucleus regulates cortical
234 ral research in monkeys has offered a better understanding of how the primate brain processes this ty
235                   The research completes our understanding of how the repertoire of tetrapyrrole-base
236             These findings contribute to our understanding of how the SC processes visual inputs, a c
237      However, a quantitative and mechanistic understanding of how the signal is processed by the reci
238                            Our work advances understanding of how the TRF2(TRFH) domain orchestrates
239 x-trait association studies, and an in-depth understanding of how their genetic variation has been sh
240  across different temperatures would advance understanding of how thermally activated processes contr
241 ated to PAH pathogenesis but without a clear understanding of how these abnormalities are initiated,
242 an be immunomodulatory, but there is limited understanding of how these contribute to inter-individua
243                                     A better understanding of how these enzymes interact with their s
244 , and our study provides further mechanistic understanding of how these enzymes maintain genome integ
245 ul algal blooms (CHABs), yet we have limited understanding of how these events affect freshwater bact
246 yed in physical therapy that can improve our understanding of how these factors change under patholog
247 ith, and provide validation for, the current understanding of how these factors influence ENM transpo
248 r interpretations of forest dynamics and our understanding of how these forests are responding to glo
249                        During this time, our understanding of how these kinases regulate DNA repair a
250                             We still lack an understanding of how these microbial communities are str
251 e of forest regeneration, yet we have a poor understanding of how these N fixers influence the trees
252     Recent studies in mice have advanced our understanding of how these neurons are specified, migrat
253 lar electron transfer proteins are known, an understanding of how these proteins bind to their metal
254   However, we currently lack a generalizable understanding of how these soil communities will change
255                                          Our understanding of how these spatial regulators are deploy
256 ts with malignant gliomas; however, a better understanding of how these tumors escape immune surveill
257 in that drive viral assembly, we further our understanding of how these viruses assemble and egress f
258                                  Our limited understanding of how these viruses interact with their h
259 American population, we still have a limited understanding of how they affect pregnancy and fetal dev
260 normal laboratory growth conditions, and our understanding of how they are silenced is in its infancy
261 s that have been overlooked due to a lack of understanding of how they function.
262 n diverse actin-based processes [1], but our understanding of how they mechanistically contribute to
263 tity of these genetic factors, improving our understanding of how they shape retinal function.
264                                      To gain understanding of how this binding process is modulated,
265 ists in plankton communities, we have little understanding of how this biodiversity influences the bi
266 recent advances that have contributed to our understanding of how this complex molecule is transporte
267  effective prevention strategies requires an understanding of how this condition develops and progres
268 e key to DNA virus adaptation, improving our understanding of how this group of pathogens evolves.
269  and suggest the next steps towards a better understanding of how this important group of disease vec
270                                 An increased understanding of how this is achieved is critical for id
271                   We do not yet have a clear understanding of how this metabolic activity changes dur
272 protein acetylation dynamics is critical for understanding of how this modification influences protei
273                         Although the current understanding of how this overlooked element improves pl
274 ing tissue homeostasis, yet there is limited understanding of how this process is regulated.
275                                           An understanding of how threonine phosphorylation regulates
276                Our findings lead to a better understanding of how TLR-ligand based adjuvants can alte
277 he nanoscale is a rich and dynamic area, our understanding of how to control and harness it and dial-
278 (RFS) strategy is still low due to a limited understanding of how to determine the best mutation cand
279                                To develop an understanding of how to interpret these signals and the
280 esistance that would be helpful for a better understanding of how to manage antibiotic-resistant bact
281  the data are that individuals vary in their understanding of how to maximize income, with misunderst
282       These findings advance our theoretical understanding of how to predict and enhance the wisdom o
283 re finding success; however, there is little understanding of how to translate monomer sequence to ph
284                                     A better understanding of how to uncouple anti-tumor activity fro
285           As a first step toward a molecular understanding of how Toc159 mediates preprotein import,
286                                   A complete understanding of how topographical properties affect cel
287 al components may be able to inform a deeper understanding of how traits evolve.
288      Nevertheless, we have a very incomplete understanding of how tropical arthropod communities are
289                                 However, our understanding of how tropical cyclones currently affect
290 h levels of species diversity hamper current understanding of how tropical forests may respond to env
291 D chromosome structure and function, but our understanding of how various factors contribute to the s
292 demiology, and genetics have led to a deeper understanding of how vascular disease affects cognition.
293      However, we presently lack a systematic understanding of how vegetation responds to asymmetric s
294 irus responses and enhancing our fundamental understanding of how viral manipulation of direct presen
295 terest and may well fundamentally change our understanding of how viral replication is regulated.
296 rporation.IMPORTANCE Our findings expand our understanding of how viruses utilize capping, suggesting
297  of additional experimentation to enrich our understanding of how vision works on a broad scale.
298                    These results provide new understanding of how widely used immunosuppressive drugs
299                           This more detailed understanding of how xylem and leaf hydraulic traits var
300                        Our study provides an understanding of how ZIKV initiates transmission in new

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