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1 FA composition, measured as percentages of total FA of t
2 FA patients develop oral squamous cell carcinoma (OSCC)
3 FA proteins regulate replication dynamics, coordinate re
4 FA signaling is crucial in the DNA damage response (DDR)
5 FA-AKI in mice associates with lipid peroxidation and do
6 FA-APOE gene interactions at baseline and following chan
7 FA-PVSK films are processed via a two-step deposition pr
8 FA-treated cells also had higher amounts of small activa
10 e, we review how aberrant function of the 22 FA genes and their signaling network contributes to mali
12 tion, and the optimal balance of n-6 and n-3 FAs depends on the cognitive function and developmental
13 was to explore the salivary microbiome of 61 FA patients regarding their oral health status and OSCC
15 um with light-dye treatment midway between a FA and its primary arteriole eliminated ROV in the FA al
16 l access (RA), compared with femoral access (FA), mitigates the risk of acute kidney injury (AKI).
21 When crossed into germline liver fatty acid (FA) binding protein null mice (Mttp-LKO, i.e., double kn
22 ial aquaculture, but data on its fatty acid (FA) composition are still controversial, especially rega
23 relative to the wild type, total fatty acid (FA) content 1.8-fold to 8.3% dry weight, and TAG more th
24 f HIG2 enhanced LD breakdown and fatty acid (FA) oxidation, leading to increased ROS production and a
25 abundance were peptidoglycan and fatty acid (FA) synthesis, translation processes, methylglyoxal meta
27 parative study is reported where folic acid (FA) and boronic acid (BA) based cytosensors and their an
31 he synthesis of cholesterol and fatty acids (FA) in the liver is independently regulated by SREBP-2 a
32 To investigate the impact of fatty acids (FA) on sex determination and reproductive development, w
34 ich in long-chain n-3 (omega-3) fatty acids (FAs) [e.g., docosahexaenoic acid (DHA, 22:6n-3) and eico
37 s used to assimilate even-chain fatty acids (FAs) and has been implicated in persistence of Mycobacte
38 onse of macrophages to elevated fatty acids (FAs) and their contribution to metabolic inflammation in
39 interactions between Abeta and fatty acids (FAs) by two independent tool-sets such as reduced order
40 ocaloric replacement of dietary fatty acids (FAs) in quintiles (1-5) and continuously (per 5% of ener
42 pha signaling and catabolism of fatty acids (FAs) when simultaneously subjected to hypoglycemia and h
44 of the contents of carotenoids, fatty acids (FAs), and phytoprostanes (PhytoPs) on four enzymes: alph
46 Src substrate localized in focal adhesions (FAs) and functions in integrin signaling to promote cell
53 trated ambient PM2.5 (CAPs) or filtered air (FA) throughout pregnancy [6 h/d from gestational day (GD
58 ese studies demonstrate that cholesterol and FA synthesis in hepatocytes are coupled and that flux th
59 and no significant difference between HA and FA was found for major chemical groups, that is, carbohy
61 tential adverse effects of FA overdoses, and FA protection during processing and storage could lead t
65 eremia/fungemia in four bottle types, SA and FA Plus (aerobic) and SN and FN Plus (anaerobic), was pe
66 vealed associations between ASD severity and FA, RD, and MD in more extended portions of the corpus c
67 orufin scaffold, is the most red-shifted and FA sensitive in this series in terms of signal-to-noise
68 trients induce the accumulation of BCAAs and FAs that activate mTOR signaling and stimulate apoptosis
69 Fancd2 is a component of the Fanconi anemia (FA) DNA repair pathway, which is frequently found defect
70 in the cancer-prone disorder Fanconi anemia (FA) ensure the maintenance of chromosomal stability duri
76 he gold standard of fluorescein angiography (FA) and OCT was determined for structural SD-OCT alone,
79 retinal imaging and fluorescein angiography (FA) were performed at an average of 4 years after treatm
81 gital color images, fluorescein angiography (FA), and optical coherence tomography (OCT) in eyes with
82 ures obtained using fluorescein angiography (FA), indocyanine green angiography (ICGA), structural op
83 , autofluorescence, fluorescein angiography (FA), optical coherence tomography (OCT) of the retinal n
86 Amygdala-vPFC pathway fractional anisotropy (FA) from 669 diffusion magnetic resonance images was use
87 Purpose To analyze if fractional anisotropy (FA) in nonenhancing peritumoral regions (NEPTRs) at base
88 ificant reductions in fractional anisotropy (FA) in schizophrenia patients were widespread, and detec
89 etwork with decreased fractional anisotropy (FA) in the right hemisphere and a subnetwork with increa
90 trols (p < 0.05), and fractional anisotropy (FA) was lower within the left uncinate fasciculus, right
91 n outcome measure was fractional anisotropy (FA), a measure of WM tract integrity, in a priori region
92 line to first analyze fractional anisotropy (FA), the most commonly employed metric for assessing whi
96 onclusion, the contents of various bioactive FA were higher in milk fat of cows grazing a CSP compare
97 recurrence in the NEPTR may be predicted by FA metrics at baseline in patients with glioblastoma.
104 The incidences of SPB for women consuming FA, IFA, and MMN were 5.7%, 5.6% and 5.1%, respectively.
105 l spreading and RhoA GTPase activity control FA formation through YAP to stabilize the anchorage of t
106 treatment, and ocular characteristics on CP/FA and optical coherence tomography (OCT) as candidate r
109 in the same region correlated with decreased FA (Mann-Whitney U, P = 0.037) as well as confounding co
110 with PD and MCI had a network with decreased FA, including basal ganglia and frontotemporoparietal re
111 advances our understanding of how defective FA signaling contributes to aging and cancer at the ener
112 amics distinctively in three broadly-defined FA concentration regimes containing non-micellar, pseudo
114 , we report a new mechanism by which dietary FAs, in particular, saturated FAs (sFAs), are able to di
116 h the amount of adducts formed by endogenous FA, raising the possibility that epigenetic mechanisms m
119 tic steatosis (a model of enhanced exogenous FA delivery) yet developed steatosis upon induction of h
120 Recent studies have shown that exogenous FA causes only a modest increase in DNA adduct formation
122 H-eGFP mice we found that DA neurons express FA transporter and binding proteins, and are capable of
123 ular free-water (FW) and cellular tissue FA (FA-t), were estimated and compared across the entire whi
125 ellsml(-1) with incubation time of 20min for FA based electrode, and for BA based electrode detection
126 c cell transplantation (HCT) is curative for FA-related marrow failure or leukemia, but both radiatio
127 firm this interaction in cells deficient for FA complementation group I and D2 (FANCI and FANCD2) tha
130 this context, fluorescence-based probes for FA imaging are emerging as potentially powerful chemical
134 ietic stem and progenitor cells (HSPCs) from FA patients, either after autologous transplantation or
135 we demonstrate that (13)C patterns of fungal FAs recapitulate those of wild-type hosts, indicating cr
137 HEK 293) as normal cells and Au/Fc-PAMAM(G2)/FA electrode showed two times better selectivity than BA
138 to achieve a consensus interpretation of GES FA, 4 readers interpreted FA in 148 GES studies from nor
142 0) discrimination of normal FA from impaired FA was 0.568 (sensitivity, 86.7%; specificity, 91.7%).
143 B population and activity after implementing FA treatment was less than 5% of those without FA treatm
146 analysis revealed a significant increase in FA in bilateral uncinate fasciculus and right inferior l
147 and the expression of all genes involved in FA and triglyceride synthesis that are normally regulate
150 haviors in AD and RD values, although not in FA values, including the splenium of corpus callosum, le
153 ions, slow onset vasodilatation (10-15 s) in FAs remained intact following loss of ROV and was elimin
159 erpretation of GES FA, 4 readers interpreted FA in 148 GES studies from normal volunteers and patient
161 tified ACS-4, an acyl-CoA synthetase and its FA-CoA product, as key germline factors that mediate the
162 protein, in the adg1suc2 mutant doubled leaf FA content and increased TAG content to 2.3% dry weight,
163 T1) selectively channels autophagy-liberated FAs into new, clustered LDs that are in close proximity
167 s with more than three concussions had lower FA in a broadly distributed area of white matter compare
170 s, microscopic phase composition, and the MA/FA ratio, in (MA)x(FA)1-xPbI3 between 100 and 330 K.
172 We examined combined exposures to maternal FA and pesticides in relation to autism spectrum disorde
175 nce of ASD diagnosis on several DTI metrics (FA, MD, RD, and AD), primarily in the corpus callosum.
177 vestigated the impact of the monounsaturated FA oleate in the VTA on feeding, locomotion, food reward
181 ise to electrophilic nitro-fatty acids (NO2 -FAs), such as nitro oleic acid (OA-NO2 ) and nitro linol
182 l cutoff for IMD(0) discrimination of normal FA from impaired FA was 0.568 (sensitivity, 86.7%; speci
184 primarily on the Kennedy pathway and de novo FA synthesis with limited, defined input from acyl editi
187 radiology physicians) visual assessments of FA from solid-meal GES; develop software to quantify GES
188 est that ferroptosis is the primary cause of FA-AKI and that immunogenicity secondary to ferroptosis
190 ools to help disentangle the complexities of FA homeostasis and its physiological and pathological co
192 aphic interferences for the determination of FA and 5-MTHF in milk formulae than enzymatic treatments
195 have indicated potential adverse effects of FA overdoses, and FA protection during processing and st
198 rrent perspectives regarding the genetics of FA, indicating that FA plays a role in a myriad of molec
200 pment, we examined and observed an impact of FA synthesis and mobilization by lipolysis in somatic ti
203 ytokines are required to induce our model of FA, whereas any pro-TH2 cytokine can maintain establishe
205 as a review and update on the prevention of FA and focuses on recently published randomized controll
207 thod, which allows precise quantification of FA profile using small (<24 mm(2) for mice and <12 mm(2)
208 The limits of detection and quantitation of FA were 1.4ng/mL and 3.1ng/mL, respectively; 7.5ng/mL an
212 ey germline factors that mediate the role of FA in promoting oocyte fate through protein myristoylati
213 OCTA approaches that of the gold standard of FA with OCT, and it is better than en face OCTA alone.
220 is an important consideration in the role of FAs in cognitive function, and the optimal balance of n-
225 rait anxiety and right amygdala-vPFC pathway FA was strongest in women carrying the Met allele, which
227 s at baseline and following change in plasma FA were assessed using adjusted general linear models.
228 Whilst elevated plasma n-3 polyunsaturated FA (PUFA) was associated with a beneficially lower conce
229 vation, 16:4 and omega-3 C18 polyunsaturated FAs accumulated into de novo synthesized TAGs while DHA-
234 h first-episode psychosis had lower regional FA in multiple commissural, corticospinal, and associati
236 emental FA intake was based on self-reported FA-supplement use.UMFA was detectable in the milk of 96.
239 which dietary FAs, in particular, saturated FAs (sFAs), are able to directly trigger macrophage cell
240 , HIG2 acts downstream of HIF-1 to sequester FAs in LDs away from the mitochondrial pathways for oxid
242 tical and grey matter patient regions showed FA decreases greater than the 99% PI for zero change.
243 ate with traction force magnitudes at single FAs, and this was consistent across different ECM stiffn
245 and vinculin-paxillin localization to single FAs in the context of substrate stiffness and actomyosin
254 inuous 8:2 ratio between de novo synthesized FA and acyl chain transfer from pre-stressed membrane li
255 y of filtered air (FA)-exposed Scnn1b-Tg(+) (FA-Tg(+)) mice successfully cleared spontaneous bacteria
256 rger size and weaker affinity with SnI2 than FA+ ions will facilitate the intramolecular exchange wit
258 egarding the genetics of FA, indicating that FA plays a role in a myriad of molecular and cellular pr
262 ession and random-effects meta-analysis, the FA-pattern score was associated with lower incident T2D.
264 y: following ICL detection on chromatin, the FA core complex monoubiquitinates and recruits the centr
265 its primary arteriole eliminated ROV in the FA along with conducted vasodilatation of the FA initiat
269 network promotes the proximal growth of the FA and contributes to a traction peak near the FA's dist
270 NCI and FANCD2) that function as part of the FA I-D2 complex, indicating that this interaction is not
271 A along with conducted vasodilatation of the FA initiated on the arteriole using ACh microiontophores
273 that this interaction is not limited to the FA core complex, hence demonstrating that systematic gen
276 cellular free-water (FW) and cellular tissue FA (FA-t), were estimated and compared across the entire
277 responding not only to hormones but also to FA nutrient signals to modulate food-directed behavior.
281 omposition, measured as percentages of total FA of triploids and immature diploid females significant
282 R [EPA: beta = -0.62 kg/1% increase of total FAs (95% CI: -1.18, -0.05); DHA: beta = -0.24 kg/1% incr
283 scent probe is a powerful tool to understand FA utilization within the tumor, thereby providing an un
284 intake) for 3 days, enriched in unsaturated FA (78 energy % [E%] fat) (UNSAT) or carbohydrates (80 E
285 trated that excess sFAs, but not unsaturated FAs, induced the production of cytotoxic ceramides (Cers
288 ncover a likely conserved mechanism by which FA, an environmental factor, regulates sex determination
289 broadens the ECM stiffness range over which FAs can accurately adapt to traction force generation.
291 15.4%) with RA and 712 patients (17.4%) with FA (odds ratio [OR]: 0.87; 95% confidence interval [CI]:
293 mal lymphopoietin (TSLP) are associated with FA, and mAbs to these cytokines are reported to suppress
294 FA growth and maturation thus culminate with FA traction oscillation to drive efficient FA mechanosen
295 facilitate the intramolecular exchange with FA+ ions, thereby enabling the formation of dense and co
297 e sn-1/sn-3 positions but when together with FAs 20:1, 20:2, 18:2, 14:1, 12:0 or 10:0 the positioning
298 LM data indicates that the structures within FAs, characterized as a Gaussian mixture, typically have
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