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1 to plant growth and productivity which could negatively affect carbon sequestration capacity of North
2 Parasitism can cause clonal integration to negatively affect fitness in clonal plants because paras
3 Previous evidence suggests shift work can negatively affect health and wellbeing (increased accide
5 AL, but not overall complications, after MIE negatively affect long-term survival of esophageal cance
6 is able to induce neuroinflammation and may negatively affect neuronal morphology, synaptic plastici
10 anges to social networks, and discrimination negatively affect the mental and physical health of undo
12 While some H. bacteriophora isolates seemed negatively affected by benzoxazinoids, most showed to be
15 the hypothesis that specialist predators are negatively affected by urbanisation, we also show that a
16 proteolysis occurring during storage, light negatively affected milk flavour especially after longer
20 rhinosinusitis with nasal polyposis (CRSwNP) negatively affects health-related quality of life (HRQoL
22 nstrates that although functional p53 status negatively affects identification of significantly deple
24 modulatory cytokine that both positively and negatively affects the differentiation of individual Th
26 of mTORC1, by small interfering RNA (siRNA) negatively affects ZIKV protein expression and viral rep
27 H(2)S, methanethiol) which impact the smell negatively, and volatile thiols with higher boiling poin
28 ethnic majorities and cis-heterosexuals) but negatively associated among disadvantaged groups (ethnic
29 ex and caudal anterior cingulate cortex were negatively associated to ADHD symptoms when controlling
30 le rostral anterior cingulate cortex GMV was negatively associated to CD symptoms when controlling fo
31 y associated with woody biomass turnover and negatively associated with aboveground biomass and the d
33 child (aOR 1.10 [1.03-1.19], p=0.0080), and negatively associated with any financial cost of travel
35 rheal frequency, duration, and severity were negatively associated with bacterial diversity and richn
36 t aromatase availability in the amygdala was negatively associated with body mass index (BMI) (in kil
37 tosome-specific cytokine responses that were negatively associated with CD4+CD25+FOXP3+ T-cells and a
39 al (aHR 1.03, 95% CI 1.01-1.06, p=0.006) and negatively associated with distance from the transplant
44 l mass gain between breeding seasons was (a) negatively associated with lagged North Atlantic Oscilla
46 DENV (OR, 1.09; CI, 1.03-1.14; P = .001) and negatively associated with nonfebrile DENV (OR, 0.89; CI
48 genetic effective population size, which is negatively associated with organism size, can have a sub
49 ion, viral detection, and comorbidities were negatively associated with Pn-IST carriage (odds ratios,
52 n bed the night before cognitive testing was negatively associated with response times during the mos
53 Cardiac inflammation before implantation was negatively associated with response to CRT (25% of respo
56 confirmed, probable, or suspect EVD case was negatively associated with seroreactivity [0.23 (95% CI:
61 with prothrombin activity less than 70% and negatively associated with the initiation of renal repla
63 .0437-0.333], p < 0.0001) were independently negatively associated with time to ADA development, wher
64 ants who were not currently taking PrEP, and negatively associated with transgender women community c
69 ) ; it shows constitutive activity regulated negatively by Ca(2+) and positively by phosphoinositol a
70 higher energy barrier for partitioning into negatively charged (phosphatidylserine or phosphatidylch
71 harged (amine-modified polystyrene; a-PS) or negatively charged (polystyrene; PS) particles that flow
72 The structure shows that cGAS binds to a negatively charged acidic patch formed by histones H2A a
73 fixed charge density due to the presence of negatively charged aggrecan glycosaminoglycans that prov
75 reby raising pe, and by making hematite more negatively charged and hence impeding NTO adsorption.
76 electron-rich radicals, together with both a negatively charged and strongly electron-donating outer
77 rginine in extracellular loop 2 (K210) and a negatively charged aspartate (D112) in extracellular loo
78 rotubule-binding proteins can diffuse on the negatively charged biopolymers, the unique molecular fea
80 f the method was achieved by the coupling of negatively charged carboxylate groups present at the sur
84 l interphasial chemistry; in particular, the negatively charged electrode surface repels salt anions
85 hen echium oil emulsions were prepared using negatively charged emulsifier under acidic conditions.
86 lular experiments, we show that a conserved, negatively charged groove on B56 mediates dynamic bindin
90 ed in net positively charged compared to net negatively charged liposomes in low-salt buffer solution
92 reveals association between our polymers and negatively charged NG2 chondroitin sulfate proteoglycans
95 the direct extracellular interaction with a negatively charged phospho-tyrosine on the receptor tyro
96 roteins, which bind to membranes that expose negatively charged phospholipids in a Ca(2+)-dependent m
97 f DGKepsilon, our work reports the effect of negatively charged phospholipids on DGKepsilon activity
99 wed differential sensitivity to positive and negatively charged PS nanoparticles, illustrating their
102 functional groups, to produce membranes with negatively charged subnanometer-sized confined ionic cha
104 and seedling development more strongly than negatively charged sulfonic-acid-modified nanoplastics.
106 ions at positively charged surface sites and negatively charged surface sites and those participating
110 af tissues, PP2A-B'gamma is also required to negatively control the expression of salicylic acid-rela
112 results provide the first evidence that GITR negatively controls intestinal inflammation through NK c
113 binding of a second molecule of profilin is negatively cooperative, with the affinity reduced ~11-fo
114 Our work indicates that enFeLV-LTR elements negatively correlate with exogenous FeLV replication.
116 cterized by a transcriptomic gradient of two negatively correlated gene-expression profiles, each con
119 M(2.5) was positively correlated with CO and negatively correlated with 24-h cumulative precipitation
120 ed retrieval cues and this reinstatement was negatively correlated with accuracy for lure images, sug
121 , daily maximum and minimum temperature, and negatively correlated with atmospheric pressure, while t
122 revealing clusters where brain iron content negatively correlated with beta-amyloid and global cogni
124 ion was positively correlated with IL-10 and negatively correlated with concentrations of MMP-8 and I
125 ated with LHCII levels, while grana stacking negatively correlated with CURT1 and RIQ protein abundan
126 other diadromous species were significantly negatively correlated with distance from the river mouth
128 PET subgroup, brain iron in the hippocampus negatively correlated with episodic memory (beta = -0.24
129 Degeneration rates of S- and M-cones are negatively correlated with expression levels of FATP4 in
131 ild emphysema (normal CT, abnormal ADC) were negatively correlated with FEV(1) (r = -0.65 and -0.42,
132 .54 km m(-2) degrees C(-1) Soil moisture was negatively correlated with fine-root growth, highlightin
135 Retention of verbal memory over 1 week was negatively correlated with hippocampal spike frequency d
136 ngulate cortex and the ventral striatum that negatively correlated with increased nicotine dependence
137 iR-223 levels in the OFC were positively and negatively correlated with inflammatory and GABAergic ge
138 Fasting large, medium, and very small TRLPs negatively correlated with insulin sensitivity index and
141 Prohibitin (PHB) expression is significantly negatively correlated with mitochondrial ROS levels but
146 ntral attention and somatomotor networks and negatively correlated with salience and cingulo-opercula
147 co-occurrence of monosyllabic words in Jueju negatively correlated with speech segmentation, which pr
148 ha power modulations within participants was negatively correlated with strength of memorized informa
150 proportion and duration of microstate D were negatively correlated with symptom severity (Spearman's
151 n circuit strength between dACC and LSFG was negatively correlated with the change in withdrawal symp
153 tochondrial RNA catabolic processes and both negatively correlated with the overall survival of pancr
154 of volume change in the left hippocampus was negatively correlated with the period of treatment.
155 y regulator of integrins and cell adhesions, negatively correlated with the survival rate of colon ca
160 a activity in the orbitofrontal cortex (OFC) negatively correlates with physiological arousal induced
161 is increased and circulating PD-1 expression negatively correlates with sputum TNF-alpha concentratio
163 with that of activated p38; Skp2 expression negatively correlates with that of Tpl2 and activated p3
164 Our findings show that reproductive effort negatively covaries with remaining life expectancy, supp
165 ntal cortical glutamate were associated with negatively experienced ego dissolution, lower levels in
169 of the cholesterol biosynthesis pathway may negatively impact fish growth due to its large energy ex
173 ction reduces foraging opportunities and can negatively impact respiratory efficiency, our data sugge
174 lterations in future climatic conditions can negatively impact soil net N(min) across global grasslan
175 ients with retinal or systemic disease could negatively impact the accuracy and sensitivity of biomar
176 tory syndrome coronavirus 2 test results can negatively impact the clinical and public health respons
181 Intravital imaging of immune cells can be negatively impacted by surgical manipulation, exogenous
183 ure (heat*time) increased response times and negatively impacted executive functioning, spatial plann
191 Inactivation of the methyltransferase gene negatively impacts sporulation, a key step in C. diffici
192 by LCO disrupts metabolic homeostasis, which negatively impacts the growth and development, a mechani
193 ggest that the presence of gingival bleeding negatively impacts the social life of adolescents, causi
198 biota-pathogen interactions can favorably or negatively influence host survival during infection.
200 echanisms through which excess glutamate can negatively influence synaptic plasticity, and we discuss
201 species at biome ecotones are positively or negatively influenced by projected changes in global tem
202 lity, and long-term oncological outcomes are negatively influenced by the occurrence of anastomotic l
204 dy 8 found that declining creativity beliefs negatively influenced task persistence and creative perf
207 umatic stress disorder, being overweight and negatively loaded by pain self-efficacy and exercise lev
208 ed that histamine, acting at H(3) receptors, negatively modulates corticostriatal synaptic transmissi
209 entify unique features of a highly-absorbing negatively photochromic molecular switch, donor acceptor
210 about 50% less (i.e., 2.6 +/- 1.1 nN) for a negatively polarized probe at a hydrophilic OH-terminate
212 r, little is known about the mechanisms that negatively regulate CLR-induced NF-kappaB, and molecules
214 ese findings suggest the MT cytoskeleton may negatively regulate GSIS by both limiting the amount of
215 hich the ARF tumor suppressor binds PPM1G to negatively regulate its coactivator function in the NF-k
217 nal differentiation, and that the chaperones negatively regulate neuronal morphogenesis and functions
220 PIF1, PIF4, and PIF5 proteins, all of which negatively regulate plant freezing tolerance, were desta
222 d other key components of ethylene signaling negatively regulate RPW8.1-mediated cell death and disea
225 proteins that localize in cell membranes and negatively regulate superinfection and syncytium formati
226 (EGR 2 and EGR3), transcription factors that negatively regulate T-cell activation, may play a role i
227 ract with HLA-E(high) CD8 T cells, which may negatively regulate the expansion of CMV-specific CD8 T
228 o inhibit the DNA-binding ability of PIF1 to negatively regulate the expressions of PIF1 target genes
229 ion between PQLC2 and the C9orf72 complex is negatively regulated by arginine, lysine, and histidine,
230 thermore, ringer lies downstream from and is negatively regulated by the microtubule-associated deace
233 orted before, the light signaling factor HY5 negatively regulates ABA-mediated inhibition of post-ger
235 sis (Arabidopsis thaliana), hydrogen sulfide negatively regulates autophagy independently of reactive
236 activation of both mTORC1 and mTORC2, which negatively regulates autophagy to facilitate ZIKV replic
237 maintains root distal stem cell identity and negatively regulates auxin signaling by interacting with
238 a2 subunit of voltage-gated calcium channels negatively regulates axon growth and regeneration of cor
240 s (IPA) showed that LINC00313 overexpression negatively regulates cell movement and migration pathway
242 uman autosomal recessive cone-rod dystrophy, negatively regulates EV levels in the sensory organs of
246 ty protein Lethal (2) giant larvae [L(2)gl], negatively regulates Hippo-mediated transcriptional outp
249 , is proposed to act as a signaling hub that negatively regulates mitogenic signaling pathways, like
253 tions independently of PM depolarization and negatively regulates pathogen-associated molecular patte
254 w that in addition to IL-1beta, PSTPIP2 also negatively regulates pathways governing reactive oxygen
256 Collectively, our study reveals that SnRK1 negatively regulates phenylpropanoid biosynthesis, and K
258 hylene signaling, and the latter, in return, negatively regulates RPW8.1-mediated cell death and defe
259 an intricate post-translational network that negatively regulates the abundance of a conserved NADPH
260 The stimulation of dopamine D2 receptors negatively regulates the angiogenic process in normal de
261 time quantitative PCR indicated that PIERCE1 negatively regulates the gene expression of the AKT supp
262 igomerization and sequestration activity and negatively regulates the Keap1-Nrf2-mediated antioxidant
264 imuli such as cell-cell contact, the pathway negatively regulates YAP through cytoplasmic sequestrati
265 These findings suggest a role of GORAB in negatively regulating AKT phosphorylation, the expressio
268 lammatory cytokine and ferritin secretion by negatively regulating Erk1/2 and p38 activation downstre
270 2A (PP2A) functions as a tumor suppressor by negatively regulating multiple oncogenic signaling pathw
274 entry into the virtual memory compartment by negatively regulating tonic TCR triggering in response t
278 chemical transformation of plant remains was negatively related to temperature of the wettest quarter
279 is positively related to trip distance, but negatively related to the destination population density
280 only in the RYGB group that betatrophin was negatively related to the disposition index (rho = -0.53
281 and 2586 genes in total were positively and negatively, respectively, correlated to POP exposure, wh
282 724 uLMS-PCI procedures were analyzed with a negatively skewed distribution and an annualized median
283 precipitation 2 yr before (R(2) = 0.85), and negatively to precipitation in May (R(2) = 0.83) in the
284 ersifying the type of stimuli to account for negatively valenced chills and intercultural differences
286 subsets, which represent the positively and negatively valent polar-extremity of stimulus sets repor
287 the polar-extremity of their positively and negatively valent subsets, which represent the positivel
289 ce Test and Continuous Performance Test, but negatively with FA values in posterior thalamic radiatio
293 arnitine in plasma samples, which correlated negatively with plasma TG and positively correlated with
294 binding in the total presubiculm correlated negatively with Proximity (r = - 0.88) and Contact (r =
297 ory function of MDD appears to be correlated negatively with the age and the DeltaMRT of negative sti
298 ed human IFN-gamma in plasma that correlated negatively with the expansion of the human hematopoietic
299 rucially, glutamate concentration correlated negatively with the inhibitory influence on the excitato
300 ceric acid partitioning to the gas phase and negatively with the ratio of 2-methyltetrols to C(5)-alk