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1             The proposed model overlooks the contribution of a relational/prosocial dimension to the
2 fect the metabolic response to exercise, the contribution of a self-selected diet to the interindivid
3  delta(13) C of CH4 suggesting an increasing contribution of acetoclastic methanogenesis to total CH4
4             In this study, we focused on the contribution of acquired MHC-class I on recipient DCs du
5                    However, the longitudinal contribution of adipocyte size reduction and fatty acid
6 discuss these emerging themes, including the contributions of aging, selective vulnerability and non-
7  patient's epilepsy, one should consider the contribution of all hyperperfused regions, as these are
8  experimental pulmonary emboli, assessed the contribution of alpha2-antiplasmin to fibrinolytic failu
9                   The model shows a combined contribution of altered biotic interactions and dispersa
10 t lamins dictate nuclear morphology, but the contributions of altered chromatin compaction remain unc
11 e to the different stimuli revealed that the contribution of an applied stimulus current exceeded tha
12 ry events, the strongest and most widespread contributions of anthropogenic climate forcing occur in
13                                     Relative contributions of AOA and AOB to N2 O production, therefo
14                         However, the precise contribution of apoptosis to GC biology and selection is
15 city trade-offs are governed by the relative contribution of arginine CDR residues to the overall ant
16 omatin accessibility at enhancers, while the contribution of ARID1B is evident only in the context of
17 ntation studies were performed to define the contribution of As3MT-mediated methylation in different
18                                 However, the contribution of autophagy to FK866-conferred hepatoprote
19 as been established, less is known about the contribution of B cells.
20 affects physiology and disease; however, the contribution of bacteria to the response to chemotherape
21                          The effect of DW on contribution of bacterial and fungal residues to N trans
22                                          The contribution of Bacteroides spp. to metabolism of the pe
23    Rare genetic syndromes have uncovered the contribution of barrier disruption, mediated in part by
24 s been studied intensively to understand the contribution of BB to radiative forcing.
25 ingle doses, showing the relative additional contribution of BEV, but also indicate negative drug int
26      The model simulations indicate that the contribution of biogenic VOC emissions to ozone formatio
27 yo is presented in relation to the potential contribution of BMAA to neurodegenerative disease.
28      Despite considerable research, specific contributions of BMAA toxicity to neurodegenerative dise
29                                 However, the contribution of both regulation mechanisms to oxygen up-
30 mulus value updating indicating a comparable contribution of both signals to reward learning.
31 roteome profiling (DPP), we investigated the contribution of both synthesis and breakdown to changes
32 val and pupal stages due to a large maternal contribution of CaMKII mRNA, which consists of a short 3
33 mple techniques do not exist to quantify the contribution of capillary flux to crop water use.
34                   Understanding the relative contributions of cardiovascular disease event types to t
35                                 However, the contribution of CD19 in the context of CNS infections ha
36                       Our data highlight the contribution of CD69 as a nonredundant key regulator of
37 ll activation and effector function, but the contribution of Cdk5 activity to the development of GVHD
38 loyed a cell-mixing approach to evaluate the contributions of cell populations to bioengineered tooth
39  we used murine models of AMD to examine the contribution of CFH to disease etiology.
40 lusively dependent on size exclusion and the contribution of charge exclusion is weak.
41  context of earlier groundwork exploring the contribution of chemokines to T cell development, recent
42                  We aimed to investigate the contribution of chymase to systemic GBS infection and ra
43                           Information on the contribution of chytrids to trophic interactions, as wel
44                        Herein, we review the contribution of clinical, pathological, and genetic risk
45   We used Phytotyping(4D) to investigate the contribution of clock and light signaling to the diurnal
46  origin of cometary matter and the potential contribution of comets to inner-planet atmospheres are l
47 ent complex and provide in vivo evidence for contributions of complement-dependent membrane perturbat
48                             We find that the contribution of conformational entropy can range from fa
49                   Here, we have examined the contributions of conserved salt-bridging residues in sta
50 mediated by mechanisms in addition to direct contributions of contact residues to binding affinity.
51 an be used in future studies to decouple the contributions of contaminant partitioning and diffusion
52 lines to further characterize the functional contributions of Cre defined populations.
53                          Here, we assess the contribution of CsrA to gene expression in Escherichia c
54 ch advances our understanding of the complex contribution of CtsB to angiogenesis.
55  different CXCL10 levels and to evaluate the contribution of CXCL10 to the described cytokine/proteas
56 shed light on the intricacies underlying the contribution of cytokines to peripheral tolerance and co
57 g, it will be of great interest to study the contribution of cytoplasmic Esrp1 in maintenance of epit
58 tudied here revealed the overall fundamental contribution of D2R in motor functions and explains some
59 tly enhanced the ability to characterize the contribution of different cells and circuits to neural f
60             Our BMI paradigm can dissect the contribution of different elements in the sensorimotor p
61                                          The contribution of different IgG isotypes to protection aga
62                                 However, the contribution of different Ras isoforms has not been inve
63          This modeling ignores the different contributions of different memory and decision-making sy
64                     Here, we investigate the contributions of different noise sources in well-known p
65 for linguistic processing, may depend on the contributions of distinct brain rhythms.
66                    To determine the relative contributions of distinct phototransduction systems, we
67 ns of the optogenetic assay, we examined the contribution of dynein to the motility of an endogenous
68 for the two major subtypes, but the relative contribution of each factor was strongly subtype-specifi
69          Here, we systematically dissect the contribution of each gene to growth on chitin as well as
70                                          The contribution of each ionic pathway to the calcium kineti
71                                          The contribution of each ionic pathway to the calcium kineti
72 ned risk statistic to calculate the relative contribution of each level of adjustment to the risk of
73                   Systematically mapping the contribution of each organ quantitatively will allow us
74                        However, the relative contribution of each process to neuronal polarity remain
75 g reduces this complexity by quantifying the contribution of each taxon topology to the full tree.
76                                 The relative contributions of each are still to be determined.
77 cal examination data as well as to learn the contributions of each feature that impact a patient's ri
78                         The relative in vivo contributions of each glycosylase remain elusive.
79 ly useful for interrogating the differential contributions of each individual cue to cell signaling.
80  growing interest in identifying the partial contributions of each of these stressors to programming
81        INTERPRETATION: Our findings show the contributions of ecological and demographic factors to t
82  This can then be applied to quantifying the contribution of electron interactions and screening to l
83 ocytosis delivers cargo for degradation, the contribution of ELMO1 to the lysosome degradation pathwa
84                                          The contributions of endocannabinoid signaling in the PL to
85 ance signal, and we were able to predict the contribution of endocytosis to the measured exocytotic r
86                       To define the relative contribution of endogenous TGF-beta proteins to the nega
87 heter-associated UTI (CAUTI), delineated the contribution of enhanced urease activity to coinfection
88                                          The contribution of epistasis to human disease remains uncle
89 e therefore set out to determine the precise contributions of Esco1 and Esco2 to cohesion in vertebra
90 Overall, our results establish the oncogenic contributions of EVI1 in ER- and HER2-negative subsets o
91 linically achievable PTX concentrations, the contribution of exosomes to active drug efflux increased
92 rved associations reflect direct detrimental contributions of exposure to bullying to mental health r
93  and an integrative analysis quantifying the contribution of factors critical to epitope presentation
94 to the CNS has been studied extensively, the contribution of fibroblastic stromal cells as portals of
95                             To elucidate the contribution of FOXP1-mediated signaling to brain develo
96                                          The contribution of frailty was important; adjusting for fra
97 uronal regulation and strongly implicate the contribution of fundamental sensory and motor processing
98 result, it has been largely assumed that the contribution of fungi to allergic disease is mediated th
99 of genetic patterning mutants identified the contribution of gene activity towards their construction
100            We aimed to estimate the relative contributions of genetic and environmental factors to th
101 ple genetic loci associated with AF, but the contributions of genome-wide variation to AF susceptibil
102         Furthermore, we demonstrated the key contribution of growth plate chondrocytes and articular
103 er- and RNAi-based approach to phenotype the contribution of > 1000 genes to the rounding of single m
104 al adiposity, suggesting a possible specific contribution of hepatic steatosis to subclinical vascula
105 of patients with AF, as well as the relative contributions of heritability and shared and nonshared e
106 asma of a human twin cohort and assessed the contribution of heritable, environmental and longitudina
107                      These results prove the contribution of high densities of CD11d to macrophage ar
108 eosinte (Zea mays ssp. parviglumis), but the contribution of highland teosinte (Zea mays ssp. mexican
109                                The potential contribution of His48 to the catalytic activity of BT368
110                                 However, the contribution of HMGA2 in the pathogenesis of MF remains
111 etween PrP(Sc) and cytotoxicity suggests the contribution of host factors.
112                                          The contribution of host genetic and nongenetic factors to i
113 he rat motor cortex to determine the percent contribution of HS and LS alpha4beta2 receptors in this
114 d mice may provide a framework to assess the contribution of human-specific toxins and better explore
115  lineages across Iberia, however the genetic contribution of hunter-gatherers is generally higher tha
116  regional air pollution control policies and contributions of hypothetical Ni sources (industrial and
117                   Nevertheless, the relative contribution of IKur to AP repolarization increases at h
118 model provides an opportunity to analyze the contribution of immune cells to brain atrophy in a syste
119                                          The contribution of indirect effects differs among types of
120 DP-43; however, the mechanistic basis of the contribution of individual domains in the process remain
121 ution 7 T fMRI, we delineated the functional contribution of individual hippocampal subfields during
122                            To understand the contribution of individual phenolics to an antioxidant a
123                        Here, we explored the contribution of individual receptor-activated SMADs in h
124 e some of these intricacies to highlight the contributions of inflammation, angiogenesis, and the ECM
125                                 However, the contribution of innate receptor engagement on epithelial
126                                 However, the contribution of integrin and Src kinase interaction to l
127 we discuss evidence supporting the important contribution of intergenerational parental stress in off
128 cs provide a framework for interrelating the contribution of internal friction observed in the two ty
129 stigate these alternatives, we evaluated the contributions of intersex genetic correlations, ecologic
130 tures of psoriasis lesions, but the specific contributions of KCs to plaque formation are not fully u
131 ession eliminates the phenomenon, indicating contributions of Kir2.1 and K2P1 channels to two levels
132 d developmental stages we observe a relative contribution of KRas4B > > NRas >/= KRas4A > HRas to tot
133  use this variation to evaluate the relative contributions of leader social influence versus follower
134 ng of bulk skin may inadequately capture the contribution of less abundant cell types.
135 ed in CX3CR1-deficient mice and involves the contribution of LFA-1 (lymphocyte-associated antigen 1)
136                                 However, the contributions of lipid interactions to the function and
137               Little is understood about the contribution of lncRNA to epithelial-to-mesenchymal tran
138               In this review, we discuss the contribution of lncRNAs in the development and activatio
139                   However, the functions and contributions of lncRNAs remain largely unknown.
140 echnology enable focused explorations on the contribution of low-frequency and rare variants to human
141    Our findings add empirical support to the contribution of low-frequency variants in complex traits
142                   Here, we have assessed the contribution of LRH-1 SUMOylation to the development of
143 a support a further, and hitherto unreported contribution of magma mingling to highly explosive erupt
144              In this study, we evaluated the contribution of major histocompatibility complex class I
145 ies have been instrumental in disclosing the contributions of major pathways for central carbon and a
146 ma, it has not been possible to evaluate the contribution of malaria infection to retinopathy-negativ
147                                          The contribution of mammary-derived serotonin to circulating
148 reted by mast cells that are relevant to the contribution of mast cells in diseases.
149 tegy on the task, corroborating the parallel contribution of MB and MF systems in reinforcement learn
150 (N) into amino sugars (AS) could reflect the contribution of microbial residues to soil N transformat
151  must be minimized to confidently assess the contributions of microbiota to human health.
152  Here we describe a previously unappreciated contribution of microchannel deformation to such measure
153 he aim of this study was to characterize the contribution of microRNAs (miRs) delivered by microvesic
154  factors influence the nature and functional contributions of "microscale" mixing to the dynamic oper
155                     This study showcased the contribution of modeling to inform local health-care pla
156  from NRPSs and PKSs, thereby augmenting the contribution of molecular biology techniques to the acce
157 cologic approaches were used to evaluate the contribution of Mrgprs to SP-induced scratching behavior
158 e recent advances in dissecting the relative contributions of mTORC1 versus mTORC2 in cancer, their r
159  in viral control and contrast the potential contribution of mucosal plasma cells to mediate protecti
160 L/6J, BALB/cJ, and C3H-HeJ, and examined the contribution of multiple immune parameters, including TL
161 llowed us, for the first time, to assess the contributions of multiple low frequency cell lineages to
162 utational approaches allow us to disentangle contributions of multiple systems to learning and, conse
163 g a need for computational tools to separate contributions of multiple tumor clones and assorted stro
164 r genomes in providing new insights into the contribution of mutagenic exposures to cancer incidence.
165 and computationally evaluated the functional contributions of mutations acquired by a human variable
166 duced to 0.05 mm, but without an appreciable contribution of Na(+) At physiological concentrations of
167             However, changes in the relative contributions of NADW and AABW and their properties are
168                             To determine the contribution of naive T cell, memory stem T cell, centra
169 ies obscured the interpretation of cytotoxic contributions of nanosheet edges.
170  To achieve this goal, we need to understand contributions of natural and anthropogenic sources to th
171 be reasonably tested in humans, in which the contribution of neural maturation and experience cannot
172 cial defeat in mice and uncovered a critical contribution of neural projections from the medial prefr
173 ficacy, despite the growing awareness of the contribution of neuraminidase (NA) to influenza virus va
174  the present study, we examined the relative contributions of neuromuscular junction physiology and t
175 s) are often interpreted to reflect a causal contribution of neurons to task performance.
176 ghout segmentation, and examine the relative contribution of newly formed versus existing tissue to s
177 enia patients, consistent with the theorized contribution of NMDAR hypofunction to predictive coding
178                     To test the hypothesized contribution of NMDAR hypofunction to this disruption, w
179 feration during liver injury to evaluate the contribution of non-hepatocytes to parenchymal regenerat
180             This strongly suggests potential contribution of non-oceanic factors (e.g., land cover ch
181                                          The contribution of non-respiratory causes of death to globa
182             Here, we sought to determine the contributions of nsp14 ExoN activity in the induction of
183 ing results allowed to quantify the relative contribution of OC-complexed Fe to the total sediment ir
184 monary, LCH cases, suggesting organ-specific contribution of oncogenic RAS to LCH pathogenesis.
185                         Here, we discuss the contributions of organelles and the cytoskeleton to the
186 odel simulation results reveals the relative contributions of osmotic pressure, cell-cell adhesion an
187            Here, to determine the individual contributions of osteoclasts and osteoblasts to HCS oste
188 ether, our results highlight the specialized contribution of P/Q- and N-types VGCCs to neurotransmitt
189 ed by our screen, we compared the functional contributions of P. simiae genes to growth in 90 distinc
190                                  The complex contributions of p53 define a biological paradigm for th
191                                 However, the contribution of peripheral activation events in cervical
192           Our quantification of the relative contributions of pesticide exposure pathways in agricult
193  a negligible amount of consideration of the contribution of phagocytosis and other host defenses in
194 arious cortical brain areas, determining the contribution of phylogenetically older pathways is cruci
195                            To understand the contribution of plant-microbiota interactions, we studie
196 milar between genotypes, suggesting that the contribution of plasminogen was downstream of the T-cell
197                                          The contribution of plasmon resonance confinement to the abn
198 ifferences in birth outcomes, the individual contribution of PM2.5 is comparable in magnitude to any
199 population attributable risk to quantify the contribution of poor and rural populations to national t
200        Our results are the first to show the contribution of positively correlated CpG's for regulati
201 ween different cell-types, and highlight the contribution of post-transcriptional regulation to shapi
202 rties that define mature adipocytes, but the contribution of posttranscriptional factors to the adipo
203 c macrophages to tissue repair; however, the contribution of precursor monocyte phagocytic receptors,
204           However, little is known about the contribution of primary metabolism to the evolution of s
205           We investigate how the theoretical contributions of prospect theory, and specifically the e
206  connected with ASD-implicated circuits, the contribution of RCrusI dysfunction to ASD remains unclea
207                                 As such, the contribution of regeneration emissions from a growing fl
208 er the last decade, our appreciation for the contribution of resident gut microorganisms-the gut micr
209 s to make recommendations for maximizing the contributions of RNs in team-based primary care models.
210                                          The contribution of ruminant livestock to greenhouse gas (GH
211  efficacy of heterospecific pollination, the contribution of S. admonitor trees to paternity in seed
212 llectively, these findings demonstrate a key contribution of saNOS to S. aureus aerobic respiratory m
213 pulation genetics approaches to estimate the contribution of selection and genetic drift, and their i
214 prokaryotic genomes to estimate the relative contributions of selection and intrinsic loss bias to th
215                 Results demonstrate that the contribution of sensory evidence (size, color, and motio
216 n in FTR after multiple complications or the contribution of sequential complications to variation.
217 es from immune serum samples to estimate the contribution of serotype-cross-reactive and type-specifi
218               Herein, we address the diverse contributions of several recombination/repair proteins t
219                                          The contribution of shared environmental factors to the cros
220 n-forest types, and suggest a decline in the contribution of Sierra Nevada forests to U.S.
221 matory responses against GBS, as well as the contribution of signaling modulators involved in host im
222 her investigate the molecular mechanisms and contribution of single amino acids in OST interaction wi
223 t of ageing on individual muscle fibres, the contribution of single muscle fibre adaptations to agein
224 s of this research include discussion of the contribution of sleep disturbance to depression and espe
225  single nucleotide variants (SNVs), with the contribution of small insertions and deletions (indels)
226 ning by genic annotation indicated a greater contribution of SNPs in protein-coding regions and withi
227                                 The relative contribution of social, biologic, and clinical risk fact
228 ervational study design was used to test the contribution of sociodemographic, medical, psychological
229                                          The contribution of somatic mutations to metastasis of color
230 uld indicate that LTM training maximizes the contribution of spinal locomotor circuits as well as rem
231                                          The contribution of SSCT cells to fibrosis and the signaling
232  harnessing in vivo imaging to determine the contributions of striosomes and matrix to striatal circu
233                                          The contribution of TCR clonotype to inhibitory potency was
234 ds to seconds but also, reveals differential contributions of temporal channels across visual cortex.
235 ractions of plant and animal genomes yet the contribution of TEs to lincRNAs is largely unknown.
236 ted at the meeting highlighted the important contributions of TGFbeta family signaling to normal deve
237 of the NICS(1)zz value comes with the larger contribution of the aromatic zwitterionic mesomeric form
238 e tracking analysis was used to estimate the contribution of the breast milk and areolar skin microbi
239                          We suggest that the contribution of the C-NHEJ pathway to the formation of a
240                                 However, the contribution of the cannabinoid system to antihyperalges
241                         However, a potential contribution of the cardio-cardiac reflex control of car
242                                          The contribution of the COX-2 in IH-induced enhanced tumor m
243                         However, a potential contribution of the CSAR control of cardiac dysfunction
244 There are some important similarities in the contribution of the cytoskeleton to these different form
245  from plant organs are the reflection of the contribution of the different cell types composing the s
246                                          The contribution of the gap junctional protein connexin 36 (
247                                          The contribution of the gut microbiota to the metabolism of
248 ntaining A-U pairs in order to determine the contribution of the hydrogen bond involving the exocycli
249                        Here, we examined the contribution of the ipsilateral somatosensory cortex (iS
250                                          The contribution of the MEP pathway increased significantly
251 , it is necessary to continue to monitor the contribution of the mutations detected here as increasin
252            There is an ongoing debate on the contribution of the neuronal glutamate transporter EAAC1
253                     To determine the lineage contribution of the Nkx2.5+ cardiomyoblasts, we generate
254              The importance of assessing the contribution of the precursor ion within an isolation wi
255  in intracortical inhibition we assessed the contribution of the reticular system, which projects to
256                                 The specific contribution of the three actin isoforms, Actalpha, Actb
257                           To investigate the contribution of the TL to intrinsic termination, we deve
258 EIO fragment peaks to determine the relative contribution of the trans double-bond isomer in the mixe
259                             The differential contribution of the two FMOs to chlorination versus hydr
260               Here we determine the relative contribution of the two sugar-sensing pathways to pH reg
261   In the present work, we investigate causal contributions of the basolateral amygdala (BLA) and orbi
262             Our purpose is to comment on the contributions of the BRINDA to advance global knowledge
263                       Here, we elucidate the contributions of the Cas10-Csm complex toward maturation
264 s highlight the significance of the relative contributions of the damping and the IDMI from the heavy
265 of P in agricultural soils and to assess the contributions of the different drivers at the global sca
266                                          The contributions of the fraction of the ASCP-labile species
267              However, the actual mechanistic contributions of the motor system to sensory processing
268                      To dissect the relative contributions of the paracrine effects, we first establi
269 tially overlapping with previously described contributions of the recombination regulator Cst9 (also
270                 We investigated the relative contributions of the sympathetic and parasympathetic ner
271  was used to explore the characteristics and contributions of the two mutation mechanisms.
272  gating, and pharmacology of AMPARs, but the contribution of these auxiliary subunits to AMPAR-mediat
273 vous system led us to address the individual contribution of these Hoxa5 expression domains using a c
274 niculohypothalamic tract (GHT), although the contribution of these indirect projections to circadian
275          Our understanding of the biological contributions of these different chemical modifications
276  and nanoparticulate forms, but the relative contributions of these different forms to overall metal
277 lly reduced ACR, consistent with independent contributions of these disorders to renal disease.
278 ase, has broadened our view of the potential contributions of these essential nutrients in biology.
279     However, the precise nature and relative contributions of these features remain unclear.
280 ing sites, allowing us to rank the energetic contributions of these individual interactions.
281  CRF2R compounds were employed to assess the contributions of these receptors in modulating binge-lik
282    In this Perspective, we highlight the key contributions of these synthetic approaches and how the
283                                          The contributions of tracheid size and wall dimensions to de
284                    To determine the relative contribution of TTX-s and TTX-r channels to action poten
285            This study evaluates the relative contributions of two broad classes of carbonyl-containin
286 nique enabled us to investigate the mnemonic contributions of two direct hippocampal-medial prefronta
287 ize of the Bbaa1 interval, and confirmed the contribution of type I IFN genes to Lyme arthritis.
288                     To evaluate the relative contributions of urine kidney injury biomarkers and plas
289  phylogenetic resolution revealed a moderate contribution of variable selection across the whole N gr
290 and methods attempt to address each of these contributions of variation to reduce noise.
291                                          The contribution of various enzyme activities that collectiv
292 ed therapeutics have helped to elucidate the contribution of various immune axes to the disease pheno
293 model that provides in-depth analysis of the contribution of various molecular determinants to the vo
294                        However, the relative contribution of various Notch ligands, specifically jagg
295 rant urea to reveal the individual energetic contributions of various ligand-functional groups to the
296 associated with increased mortality, but the contributions of varying illness severity and admission
297 ulence-linked targets may be affected by the contribution of virulence-related genes to metabolism.
298 n in evaluating the data was determining the contribution of VOX to SOF/VEL and how this differed dep
299 e detection of ethanol while eliminating the contribution of water in a micro fuel cell sensor system
300 ability, functional cooperation and relative contributions of Wnt versus RSPO ligands to in vivo cano

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