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1 xperiments suggest the intermediacy of Ni(0)-ate complexes, leaving some doubt that a canonical catal
2 d with early satiety (P = 0.0002, R = 0.74), eating symptoms (P = 0.007, R = 0.54), and trouble enjoy
3 ENTIFIC COMMENTARY ON THIS ARTICLE: Abnormal eating behaviour and metabolic parameters including insu
4 emporal dementia is associated with abnormal eating behaviour characterized by increased sweet prefer
5 nts and proportions of macronutrients across eating patterns on meal or dietary glycemic index (GI) a
7 ures; however, no cases of anaphylaxis after eating a Citrus unshiu, the albedo of which is rich in p
11 he felt abdominal pain and nausea only after eating fruit, along with the albedo, of Citrus unshiu.
12 uinoa could also be detected in plasma after eating quinoa, indicating that some of these unique AR c
16 fin by a mechanism involving formation of an ate complex, 1,2-metalate rearrangement, and beta-elimin
20 direction of the association between BMI and eating disorders (EDs) in adults via a two-sample MR app
22 related and addictive disorders, feeding and eating disorders, schizophrenia, anxiety disorder, OCD,
23 earch is needed to facilitate the liking and eating of these foods by mothers, which will, in turn, i
25 hether the distinct and shared metabolic and eating changes represent a component of the proposed spe
26 tions were observed between gut microbes and eating behaviors, including eating frequency, early ener
27 a core feature of some forms of obesity and eating disorders, as well as of the recently proposed di
30 he number of OBE days, abstinence rates, and eating disorder psychopathologic findings and may be a b
31 outcomes included energy self-regulation and eating behaviors assessed with questionnaires at 6, 12,
34 iation between environmental stimulation and eating performance among nursing home residents with dem
36 when feeling full more than once a week, and eating continuously during the day, a participant who po
37 necrosis, and, by lacking the "find me" and "eat me" signals that are a feature of apoptosis, necropt
39 y was partially mediated by the "appetitive" eating behavior traits (uncontrolled and emotional eatin
40 are well known to feed on honeybees that are eaten by spiders, which we thus predicted as the model c
45 no history of jellyfish stings and had been eating commercially available jellyfish products twice y
49 were used to examine the association between eating performance and environmental stimulation, adjust
50 ia, suggesting a complex interaction between eating behaviour, autonomic function and energy homeosta
52 ks), lisdexamfetamine responders (</=1 binge eating day per week for 4 consecutive weeks and CGI-S sc
57 ention deficit hyperactivity disorder, binge eating disorder, cocaine addiction, obesity, and type 2
58 isorders, including gambling disorder, binge eating disorder, compulsive sexual behaviour, and compul
60 volved protective mechanisms including binge eating and increased metabolic efficiency and fat storag
62 e in the number of days with objective binge eating episodes (OBEs) during the previous 28 days betwe
63 esults suggested that higher levels of binge eating and overeating in males at age 13 y likely cause
65 age 7 y likely causes higher levels of binge eating and overeating, weight and shape concerns, and we
66 he criterion standard for treatment of binge eating disorder (BED), most individuals do not have acce
68 er criteria and had moderate to severe binge eating disorder (>/=3 binge-eating days per week for 14
69 significant genetic factor underlying binge eating and provide a behavioral paradigm for future geno
70 2 as a major genetic factor underlying binge eating in heterozygous knockout mice on a C57BL/6N backg
71 ade endocannabinoid signaling, whereas binge eating resulted in the downregulation of a gene set enri
74 utcome variable, time to relapse (>/=2 binge-eating days per week for 2 consecutive weeks and >/=2-po
75 to severe binge eating disorder (>/=3 binge-eating days per week for 14 days before open-label basel
77 owed flexibility in foraging patterns, binge-eating less and using feeders more when they experienced
82 genesis caused by dysregulation of so-called eat me ligands, which govern the edibility of cells unde
84 er controlling for resident characteristics, eating performance was significantly associated with sti
86 nges in appetite that result in compensatory eating, which may initially dissuade potential success i
87 ia experience increased risk for compromised eating performance due to intrapersonal, interpersonal,
91 need to improve understanding of compulsive eating through the integration of complex motivational,
92 re, we present evidence to relate compulsive eating behavior and addiction and to characterize their
94 The most prevalent subtype was compulsive eating, followed by punding, compulsive sexual behaviour
95 ammatory marker or adipokine concentrations, eating behaviors and changes in waist circumference duri
96 ammatory marker or adipokine concentrations, eating behaviors, comorbid psychiatric disorders or life
97 y dieting, the experiences of out-of-control eating, increased appetite, and increased fat storage ar
98 coral bleaching, and outbreaks of the coral-eating crown-of-thorns starfish (COTS), losing much of i
100 lancing selection on at least one case (Crab-eating monkey retrocopy 6, or CER6) in both species.
101 ting disease in experimentally infected crab-eating macaques, while simian hemorrhagic fever virus (S
102 browsers for three species (brown kiwi, crab-eating macaque and Malayan flying lemur); eight updated
103 nonhuman primate cell cultures and then crab-eating macaques with either simian hemorrhagic fever vir
104 s of wakefulness and ingestion events, daily eating pattern offers a new potential target for lifesty
108 the first time the influence of disinhibited eating and vagal tone (heart rate variability (HRV)) on
110 n, attention-deficit/hyperactivity disorder, eating disorders, autism spectrum disorder, substance us
111 sociated with posttraumatic stress disorder, eating disorders, and anxiety disorders other than speci
112 tion of causality between BMI and disordered eating in childhood, adolescence, and adulthood.MR analy
116 ausal effect of BMI at age 7 y on disordered eating patterns at age 13 y with the use of data from th
118 o estimate the effect of the same disordered eating patterns at age 13 y on BMI at age 17 y via a spl
119 ly adolescence, which can lead to disordered eating behaviors, and future cardiometabolic health is,
120 1; 2001-2003) was associated with disordered eating behaviors at time 2 (2004-2006), as well as weigh
123 regulated weight-management behaviors (i.e., eating even in the absence of hunger), which were predic
124 ion, we tested for interactions between each eating behavior and the BMI-GRS on BMI.The association b
126 that perceived hunger, importance of eating, eating frequencies, and liking ratings of food pictures
127 (P = 0.03 and P = 0.012) with the effective eating duration and maximum food intake (adjusted R(2) =
129 behavior traits (uncontrolled and emotional eating) and, in 3 of the 4 population groups studied, wa
131 I-GRS and BMI was mediated by both emotional eating (EDEN: P-Sobel = 0.01; Fenland: P-Sobel = 0.02) a
132 ating this reaction is two-fold: it enables "ate" complex formation and overcomes catalytic inhibitio
133 tion trial findings suggested that a low-fat eating pattern may reduce breast cancers with greater mo
136 ary GI and GL values that are calculated for eating patterns, which may alter the interpretation of t
139 multi-faceted approach to estimate how fruit-eating bats (Uroderma bilobatum) manage a high-energy li
142 (CVD), can gain health benefits from healthy eating behaviors and appropriate physical activity.
143 ing is a prominent policy to promote healthy eating.We aimed to evaluate the effects of 2 interpretiv
144 rends in prevalence of 6 barriers to healthy eating (taste, price, daily habits, time, lack of willpo
145 This may be because of barriers to healthy eating hampering adherence, but whether these barriers h
146 valence of self-reported barriers to healthy eating in Switzerland overall and according to sex, age,
147 Diet quality estimated adherence to healthy eating recommendations and was assessed by using the 201
148 e.Between 1997 and 2012, barriers to healthy eating remained highly prevalent (>/=20%) in the Swiss p
149 variance in concordance with the WHO healthy eating guidelines that aim to prevent non-communicable d
151 lations, and can be applied to determine how eating behavior factors influence total food intake.
152 actor for adverse metabolic health; yet, how eating at a later circadian time influences body composi
154 wel disease (IBD) is, "Doctor, what should I eat?" Findings from epidemiology studies have indicated
155 utrients to the brain, initiating changes in eating behavior and energy expenditure, to maintain ener
156 l correlates overlap the network involved in eating behaviour in frontotemporal dementia, suggesting
160 ly controlled research of brain structure in eating disorders, which will ultimately help predict the
161 gut microbes and eating behaviors, including eating frequency, early energy consumption, and overnigh
162 time of day or behavioral factors, including eating frequency, percentage of energy consumed early in
163 Potentially modifiable mechanisms, including eating behaviors, are of particular interest to public h
166 ntake using 3 key parameters: 1) the initial eating rate, 2) the effective duration of eating, and 3)
167 cal and practical importance - since insects eat 20% of crops - no exhaustive analysis of gene repert
170 technique of low amylose/waxy paddy that is eaten after soaking in water and requires no cooking.
171 results show that OSU6162 reduces binge-like eating behavior and attenuates the impact of cues on see
172 sults show that RO5256390 blocked binge-like eating in rats responding 1 h per day for a highly palat
173 fects of OSU6162 on consummatory (binge-like eating) and appetitive (cue-controlled seeking) behavior
176 R1 may have a role in compulsive, binge-like eating; we tested this hypothesis by assessing the effec
177 ore, RO5256390 fully blocked compulsive-like eating when the palatable diet was offered in an aversiv
180 teeth to assess whether these notorious man-eating lions scavenged carcasses during their depredatio
182 assessed whether variations in midchildhood eating attitudes influence the future development of ove
185 patterns that reduce or eliminate nighttime eating and prolong nightly fasting intervals may result
186 Among infants aged 12 months who did not eat fish or seafood, the geometric mean total urinary As
187 97 microg/L) compared with those who did not eat rice or rice products (2.85 microg/L; all P < .01).
190 These include psychological determinants of eating behaviours, the decline in physical activity lead
191 ne the effects of the timing and duration of eating a variety of vegetables during breastfeeding on t
193 ng meal significantly modified the effect of eating litchis on illness (odds ratio [OR] 7.8 [95% CI 3
194 ful attention to the timing and frequency of eating occasions could lead to healthier lifestyle and c
195 strated that perceived hunger, importance of eating, eating frequencies, and liking ratings of food p
198 Recently, an increasingly popular method of eating anchovies has been to eat it in a cleaned, evisce
199 The aims were to assess the prevalence of eating difficulties in infants born LMPT at 2 y correcte
200 habits, including the number and quality of eating occasions, are potential targets for primary prev
201 nic tone, which resulted in a faster rate of eating carrot-flavored cereal than that in infants who w
204 Behavioral factors, including timing of eating and overnight-fast duration, were also predictive
206 d with sham tDCS) has an immediate effect on eating behavior during ad libitum food intake, resulting
207 d that parenting practices have an impact on eating styles which determine obesity levels in children
215 versible formation of a pentavalent peroxide ate complex, prior to rate-limiting aryl migration, has
217 marshes experiencing a severe drought, plant-eating grazers eliminated drought-stressed vegetation th
221 bserved positive associations of problematic eating attitudes at age 11.5 y with new-onset obesity (O
222 /=85th percentile (indicative of problematic eating attitudes) compared with scores <85th percentile
223 or body mass index at age 6.5 y, problematic eating attitudes remained positively associated with new
226 rs - even mildly defended mimics were rarely eaten by a community of invertebrate and vertebrate pred
229 ty, the least fattening of widely recognised eating patterns needs to be measured and supported.
230 at diurnal size changes in the liver require eating during a mouse's normal awake time and that these
231 ing appetite ratings (visual analog scales), eating behavior traits (Three-Factor Eating Questionnair
232 Autophagy is the process of cellular self-eating by a double-membrane organelle, the autophagosome
233 fter autophagy) is a catabolic cellular self-eating process by which unwanted organelles or proteins
237 o this end, apoptotic cells express specific eat-me signals, such as externalized phosphatidylserine
238 e cardiometabolic health effects of specific eating patterns: skipping breakfast, intermittent fastin
239 1 point increase in stimulation specificity, eating performance increased by 8.78 points (95% CI=0.59
240 topped eating when feeling full, and stopped eating continuously during the day after surgery would b
241 stoperatively started to self-weigh, stopped eating when feeling full, and stopped eating continuousl
245 ency preserved the expression of CD47 (don't eat me signal) on cardiac MSCs after both TLR4 stimulati
246 ic immune checkpoint that engages the "don't eat me" signal CD47 expressed on tumors and normal tissu
247 uces anti-phagocytic signals from the 'don't eat me' CD47 ligand through negative Shp1 signaling, the
248 oplastic cells generate this dominant 'don't eat me' signal, we analyse the CD47 regulatory genomic l
249 posed of what has become known as the 'don't-eat me' signal CD47, which is a protein broadly expresse
252 odels assessed associations between temporal eating patterns, nutrient intakes, diet quality, and adi
253 was to examine associations between temporal eating patterns, nutrient intakes, diet quality, and mea
254 I.This study found that a "grazing" temporal eating pattern was modestly but significantly associated
255 rences in morphology and diet of the termite-eating gecko Gymnodactylus amarali between five such new
256 er on a treadmill than did control rats that ate an isocaloric diet that was supplemented with either
257 score, 77.7%); however, 48.6% believed that eating a healthy diet precluded the need for HCC surveil
258 of evidence also support the hypothesis that eating patterns that reduce or eliminate nighttime eatin
260 ulum stress with consequent exposure of the "eat-me" signal calreticulin on the cell surface, thereby
261 Alzheimer disease) were recruited, and their eating behavior was compared with that of 25 healthy con
264 kg/m(2)): 27-35; age: 18-45 y] were asked to eat either a main meal at lunch (LM) or a main meal at d
266 ass, ie, weekly self-weighing, continuing to eat when feeling full more than once a week, and eating
268 fects of increasing the homeostatic drive to eat on feeding behavior during appetite suppressing cond
270 es in cortex for enhancing the motivation to eat are discriminable from those for hedonic impact.
271 eed.SIGNIFICANCE STATEMENT The motivation to eat depends on the relative balance of activity in disti
272 ons about where, when, what, and how much to eat are not merely reflexive responses to food-relevant
273 se persuasive appeals to encourage people to eat healthier, purchase a particular product, or vote fo
277 roup, VAS ratings for hunger and the urge to eat declined significantly more (P = 0.01 and P = 0.05,
282 ncluding the vesicular glutamate transporter eat-4/VGLUT, induction of neuropeptide expression, chang
283 1; Fenland: P-Sobel = 0.02) and uncontrolled eating (EDEN: P-Sobel = 0.04; Fenland: P-Sobel = 0.0006)
284 ing behaviors-emotional eating, uncontrolled eating, and cognitive restraint-were measured through th
287 nergy intake was measured with the universal eating monitor in a test meal.In mice, AITC administrati
288 ondary outcomes included OBEs at follow-ups, eating disorder and general psychopathologic findings, b
290 te that, in a limited sense, "we are what we eat" and provide a perspective on a nutrition-driven mod
293 est to public health.Here we explore whether eating behaviors mediate or modify genetic susceptibilit
296 r, most of the questionnaire respondents who ate untreated meals knew how to prevent Anisakis infecti
297 s concentrations were higher among those who ate infant rice cereal (9.53 microg/L) or rice snacks (4
299 is a highly heritable trait associated with eating disorders that is comorbid with mood and substanc
301 sus arctos) hibernate for 5-7 months without eating, drinking, urinating, and defecating at a metabol
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