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1 oid hormone signalling), and eat-2 (putative dietary restriction).
2 of long-lived eat-2 mutant worms, a model of dietary restriction.
3 germline signalling, sensory perception, or dietary restriction.
4 ons, including mitochondrial dysfunction and dietary restriction.
5 m line largely insensitive to the effects of dietary restriction.
6 echanism by which SIRT3 regulates IDH2 under dietary restriction.
7 therefore does not explain the responses to dietary restriction.
8 athways that reveal a more genetic basis for dietary restriction.
9 ing full feeding and limits fecundity during dietary restriction.
10 p-7 and cup-4 mediate longevity increases by dietary restriction.
11 pan in Caenorhabditis elegans in response to dietary restriction.
12 n-like growth factor 1 (IGF-1) signaling and dietary restriction.
13 hat lead to bacterial avoidance behavior and dietary restriction.
14 lterations in the insulin/IGF pathway and by dietary restriction.
15 ht/obese subjects undergoing weight-loss via dietary restriction.
16 anisms associated with lifespan extension by dietary restriction.
17 y reverse the longevity-extending effects of dietary restriction.
18 fasting (ADF) represent 2 different forms of dietary restriction.
19 ould increase with leptin administration and dietary restriction.
20 te can sometimes be altered, for example, by dietary restriction.
21 a possible link between the TOR pathway and dietary restriction.
22 dy mass index, presumably indicating greater dietary restriction.
23 male SENCAR mice made vitamin A deficient by dietary restriction.
24 B6C3F1 mice are eliminated by apoptosis with dietary restriction.
25 ng protein-2 levels, a pattern suggestive of dietary restriction.
26 greater increase in longevity in response to dietary restriction.
27 daptation to maintain barrier immunity under dietary restriction.
28 on in fly fat body cells that was delayed by dietary restriction.
29 This may operate by a mechanism similar to dietary restriction.
30 c progression that was further attenuated by dietary restriction.
31 a key metabolite that mediates longevity by dietary restriction.
32 onsistent gene expression changes induced by dietary restriction.
33 00 g peas each week for 12 wk, with no other dietary restrictions.
34 ng pregnant or breastfeeding or having major dietary restrictions.
35 vere allergic reactions; however, it reduced dietary restrictions.
36 may cause confusion and lead to unnecessary dietary restrictions.
37 use it has prognostic implications and eases dietary restrictions.
38 augmented in the livers of mice subjected to dietary restriction, a known longevity-extending regimen
41 he most well-studied longevity intervention, dietary restriction, acts in-part through a cell non-aut
43 s indicate that peptone deprivation mediated dietary restriction affects lifespan in C. elegans in a
44 sing various aspects of calorie restriction, dietary restriction, aging, longevity, life span, adipos
45 associated with insulin/IGF-1 signaling and dietary restriction allow us to understand longevity fro
50 esembles the anti-ageing response induced by dietary restriction (also known as caloric restriction).
53 ism whereby cognitive stimulation, exercise, dietary restriction and antidepressant drugs preserve br
54 cifically required for lifespan extension by dietary restriction and by modulation of the TORC1 pathw
55 xpression of 4E-BP1 mediates the benefits of dietary restriction and can counter metabolic stress, an
56 interleukin-6 were significantly reduced by dietary restriction and correlated with adipose interleu
61 ion of a single longevity gene downstream of dietary restriction and hypoxia markedly alters behavior
64 triction in Drosophila mimicks the effect of dietary restriction and is associated with decreased rep
65 s that coordinate the organismal response to dietary restriction and maintain homeostasis when nutrie
67 studies involving exercise training without dietary restriction and no weight loss demonstrate that
68 ssential enzyme and are currently treated by dietary restriction and other strategies to replace the
69 ith physiological metabolic stress caused by dietary restriction and profoundly suppressed leukemogen
71 understanding of the molecular mechanism of dietary restriction and suggest a role for counterintuit
72 gh prevalence of anxiety before the onset of dietary restriction and support proposals that in AN, CR
73 ges were the only cell population reduced by dietary restriction and that CD11c/CD206 (M2-type) and C
74 ns, show that NAE abundance is reduced under dietary restriction and that NAE deficiency is sufficien
75 were compared between patients treated with dietary restriction and those that received topical ster
77 ified in 65% to 85% of the patients, so some dietary restrictions and endoscopies after food challeng
79 ntake, which may be reinforced by prescribed dietary restrictions and inadequate monitoring of the pa
81 s, encompass an array of strategies (such as dietary restrictions and supplementations) aimed at opti
82 determinant of the sensitivity of tumours to dietary restriction, and activating mutations in the pat
84 ctively, the available data suggest the that dietary restriction, and physical and mental activity, m
86 ell as gene expression signatures of ageing, dietary restriction, and replicative senescence based on
90 -4 in lifespan determination is specific for dietary restriction, because it is not required for the
91 few years, greater ability to travel, fewer dietary restrictions, better preservation of residual ki
92 or lactation, use of soy products, or infant dietary restrictions beyond 4-6 months has any effect on
93 span of the eat-2 mutant, a genetic model of dietary restriction, but has no effect on the life span
94 interactions between the microbiome, ageing, dietary restriction (caloric restriction and fasting), h
100 opsies from individuals who underwent modest dietary restriction coupled with exercise also display s
102 y decades of animal experiments showing that dietary restriction delays the aging process and decreas
104 Very short-term caloric and saturated fat dietary restrictions do not lead to the same changes in
109 secondary lymphoid organs in the context of dietary restriction (DR) but dramatically accumulated wi
111 in insulin/IGF signaling (IIS) pathways and dietary restriction (DR) can extend lifespan in model or
115 o activate DAF-16 (FOXO orthologue) or mimic dietary restriction (DR) effects, but selectively induce
119 e retarded when the mice are maintained on a dietary restriction (DR) feeding regimen resulting in an
120 nging from humans to Caenorhabditis elegans, dietary restriction (DR) grants numerous benefits, inclu
125 ositive regulator of lifespan in response to dietary restriction (DR) in Caenorhabditis elegans.
146 sm through brief restriction of food intake (dietary restriction, DR) prevents neuropathology in expe
147 erm 20 to 40% restriction in calorie intake (dietary restriction, DR), whose effects on cancer progre
159 pies are now established treatments, namely, dietary restriction for phenylketonuria and miglustat fo
162 and the pathway that mediates the effects of dietary restriction have evolved to respond to the nutri
164 g insulin-like signaling and the response to dietary restriction, identified the cellular machineries
172 lternate-day fasting is a feasible method of dietary restriction in nonobese humans and whether it im
173 netic requirements for lifespan extension by dietary restriction in the nematode Caenorhabditis elega
174 e, a universal cellular energy generator and dietary restriction in the regulation of organismal life
175 In this Review, we discuss the effects of dietary restriction in these mammalian model organisms a
177 the role of oxalate, salt and animal protein dietary restrictions in the prevention of calcium stone
178 greatly inhibited in eat-2 worms, a model of dietary restriction, in daf-16/FOXO, sir-2.1, rsks-1 (ri
179 he role of environmental factors, other than dietary restriction, in developmental reprogramming thro
181 n ob/ob mice, both leptin administration and dietary restriction increased G5 and G8 protein and bili
183 brought about by administration of leptin or dietary restriction increases biliary cholesterol excret
187 osapentaenoyl ethanolamide not only inhibits dietary-restriction-induced lifespan extension in wild-t
190 chanism underlying the beneficial effects of dietary restriction involves stimulation of the expressi
193 Identifying the most efficacious forms of dietary restriction is key for developing interventions
199 interaction between nutrition and longevity, dietary restriction is typically based on medium dilutio
200 Intermittent fasting, an alternative form of dietary restriction, is potentially more sustainable in
202 sential role in Orsay virus infection of the dietary restriction-like (drl-1) gene, which encodes a s
203 tion and suggest a role for counterintuitive dietary-restriction-like therapy for human progeroid gen
205 addressed in this article is whether or not dietary restriction long term is feasible or beneficial
206 trate a role for RNA splicing homeostasis in dietary restriction longevity and suggest that modulatio
209 ning both gene mutations that interfere with dietary restriction-mediated lifespan extension and cons
210 -4 and SKN-1, miRNAs transduce the effect of dietary-restriction-mediated lifespan extension in C. el
218 self-care (eg, adherence to medications and dietary restrictions, monitoring of symptoms and vital s
223 aintain their weight loss, including greater dietary restriction of fat and higher physical activity
227 induced in 12 healthy adult men and women by dietary restriction of phylloquinone (40 microg/d, days
228 rsed the effects of minidose warfarin and of dietary restriction of phylloquinone on hemostasis and v
229 y was manifest both in vitro and in vivo, as dietary restriction of serine and glycine in mice was ab
232 how that such inhibition can be augmented by dietary restriction of upstream amino acid substrates, l
236 e to flies in holidic medium and, similar to dietary restriction on oligidic food, amino acid dilutio
238 es have shown that the beneficial effects of dietary restriction on the brain result in part from inc
240 Here we demonstrate that under conditions of dietary restriction or growth factor starvation, where P
241 irect role for endocannabinoid signalling in dietary restriction or lifespan determination has yet to
243 striction of serum l-Met, either via partial dietary restriction or with bacterial l-Met-degrading en
244 are achieved without developing significant dietary restrictions or clinical metabolic or nutritiona
245 gned to receive either conventional therapy (dietary restriction) or intensive therapy (either sulfon
249 f gammaH2AX DNA damage foci, indicating that dietary restriction preserves genome function by allevia
252 tants (insulin/insulin-like growth factor-1, dietary restriction, protein translation, mitochondrial
253 eir side effects and prescription-associated dietary restrictions reduce their suitability as a first
254 al models of these disorders have shown that dietary restriction (reduced calorie intake or intermitt
259 epithelial carcinogenesis and this method of dietary restriction reduces many circulating proteins, i
260 nd fertility for the African killifish and a dietary restriction regimen where both feeding time and
263 intermittent fasting (alternate-day fasting) dietary-restriction regimen their overall food intake is
269 cancer cell line, is sufficient to convert a dietary-restriction-resistant tumour into one that is di
272 discuss accumulating data that suggest that dietary restriction results in many of the same physiolo
274 Treatments such as enriched environment, dietary restriction, running and anti-depressants increa
275 with few food triggers, avoiding unnecessary dietary restrictions, saving endoscopies, and shortening
279 bit a shortened lifespan that is extended by dietary restriction, the most potent aging intervention
281 anisms such as yeast and rodents is reduced (dietary restriction), they live longer than organisms fe
284 extension observed in wild-type N2 worms by dietary restriction using bacterial dilution is prevente
285 e-mRNA splicing with age that are reduced by dietary restriction via splicing factor 1 (SFA-1; the C.
286 d old animals fed ad libitum or subjected to dietary restriction, we find defects in global pre-mRNA
288 endent delay in anaphase onset, and inducing dietary restriction when the checkpoint is impaired incr
291 such as reduced insulin/IGF-1 signaling and dietary restriction, which are critical in determining t
292 to recapture the full potential benefits of dietary restriction, which humans can find difficult to
297 ssible to obtain the benefits to lifespan of dietary restriction without incurring a reduction in fec
298 his relation is of concern and suggests that dietary restrictions without attention to a possible res
299 The best avenue for humans to benefit from dietary restriction would be for pharmacological or bioa
300 y, we tested whether the loss of fat mass by dietary restriction would remove the major source of the