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1 a high frequency of deletions advancing our understanding of how a RAD51 paralog is involved in main
3 60 data sets show that GRACE can improve our understanding of how a transcriptional network is re-wir
5 s the canonical nucleosome structure for the understanding of how accessibility to genomic DNA is reg
8 essionals have a comprehensive knowledge and understanding of how adolescents experience living with
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
14 ch developments require detailed mechanistic understanding of how an SNP influences phenotype (and th
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
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
28 Surprisingly, we still lack a fundamental understanding of how bacteria build, maintain and expand
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
41 he potential to pave the way toward a better understanding of how cells function at the molecular lev
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
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
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
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
63 ding strong support for the local and global understanding of how different dopants influence the pro
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
72 This has significant implications on our understanding of how early life events in childhood infl
74 he remaining challenges to achieve a unified understanding of how effector activities work together t
76 ogy has the potential to greatly enhance our understanding of how environmental toxicants affect brai
78 and presents a barrier; however, a complete understanding of how EPS structure relates to biological
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
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
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
99 ection of selection targets provide a better understanding of how geography and selection may have sh
101 tes tumor invasiveness, and also advance the understanding of how Golgi structure and transport can b
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
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
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
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
121 This study therefore provides a molecular understanding of how kinase-substrate recognition acts a
124 tuberculosis enzyme, augmenting our current understanding of how M. tuberculosis meets its nutrient
126 ation of vascularized 3D tissues requires an understanding of how material properties govern endothel
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
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
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
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
152 de formation are well characterized, but our understanding of how non-native disulfides are reduced s
154 ther histone chaperones, and it advances our understanding of how nucleosomes and their epigenetic in
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
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
164 otics and immune modulators by expanding the understanding of how PG is processed by lytic enzymes.
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
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
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
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
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
200 er, and are modulated by drug therapies, our understanding of how such changes shape the properties o
202 esynaptic function for LRP4, enabling deeper understanding of how synapse organization is coordinated
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
211 reinstatement of alcohol seeking, expand our understanding of how the BLA-->NAc pathway regulates alc
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
223 Here, we highlight recent advances in our understanding of how the genome folds inside the 3D nucl
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
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
237 However, a quantitative and mechanistic understanding of how the signal is processed by the reci
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
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
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
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
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
262 n diverse actin-based processes [1], but our understanding of how they mechanistically contribute to
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
272 protein acetylation dynamics is critical for understanding of how this modification influences protei
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
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
283 re finding success; however, there is little understanding of how to translate monomer sequence to ph
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
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