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1 quality, and within-canopy variation in leaf longevity).
2 RNA3/5, CDKN2A/B, SH2B3 and FOXO3A influence longevity.
3 ivate an adaptive stress response to promote longevity.
4 s the risk of many diseases and, ultimately, longevity.
5  make them fit for purpose will increase the longevity.
6 hat may link SES to age-related diseases and longevity.
7 interventions that improve public health and longevity.
8 olite acting on host mitochondria to promote longevity.
9 ychological maternal stress can affect human longevity.
10 of which also demonstrated associations with longevity.
11 ociated with various pathologies and reduced longevity.
12  cardioverter-defibrillators do not increase longevity.
13 s that promote metabolic health and organism longevity.
14  the UPR(mt) to improve metabolic health and longevity.
15 nogaster and Caenorhabditis elegans promotes longevity.
16 ar size varies, but is highly predictive for longevity.
17 ns for islet survival and transplanted graft longevity.
18 , and can promote both stress resistance and longevity.
19 important for RNA quality control to promote longevity.
20  reproductive success, rather than health or longevity.
21 hallenge the universal concept of microglial longevity.
22 ed on high dietary glucose limits C. elegans longevity.
23 ic hydrogen production through the radical's longevity.
24  and CHRNA5) might be causally implicated in longevity.
25 -1/NRF1,2,3 to promote stress resistance and longevity.
26 ents for energy, molecular biosynthesis, and longevity.
27  homeostatic proliferation, maintenance, and longevity.
28 atory influence of the flora on myeloid cell longevity.
29 n (CR) is a feeding paradigm known to extend longevity.
30 e cell wall component of BB68 contributed to longevity.
31 nes and metabolites correlating with species longevity.
32 uding MDL-1/MAD-like HLH factor required for longevity.
33 e training improve cardiovascular health and longevity.
34 1+ cells does not affect their quiescence or longevity.
35 inment are useful in the prediction of human longevity.
36 environmental stress play key roles in human longevity.
37 iated motor symptoms and improved health and longevity.
38 rs between areas with the highest and lowest longevity.
39 t with slow childhood growth and exceptional longevity.
40 ere followed up for mortality predictors and longevity.
41 oint to a role for this protein in promoting longevity.
42  in these cells can alter their function and longevity.
43 d downstream outputs that regulate aging and longevity.
44 elopment, and metabolism to reproduction and longevity.
45 insulin resistance and, conversely, improved longevity.
46 ociated with many health outcomes, including longevity.
47 ity, and is also an important determinant of longevity.
48 s for restorations with potentially enhanced longevity.
49 ir progeny can be a mechanism for modulating longevity.
50 stemic level to ensure organismal health and longevity.
51 icantly reducing lesion burden and extending longevity.
52  of extracellular H2O2 stress on replicative longevity.
53 ities, may impact mitochondrial function and longevity.
54 cal trade-offs that facilitate their greater longevity.
55  in the environmental influence on molecular longevity.
56 n and abrogated the effect of heat stress on longevity.
57 consequences of improved health and extended longevity.
58 ranscript, by daf-2 mutations contributes to longevity.
59 xplains a small fraction of the variances in longevity (5.9%), age at first reproduction (3.7%) and l
60 pecies (ROS) are not the key determinants of longevity, a number of studies have highlighted the key
61 cy at birth in women will be due to enhanced longevity above age 65 years.
62 d substantially across areas; differences in longevity across income groups decreased in some areas a
63 fibroblast profiling captures differences in longevity across mammals at the level of global gene exp
64  We identify lipids associated with species' longevity across the three clades, uncoupled from other
65 as biological links between mood, stress and longevity/aging, that may be biomarkers as well as targe
66 i.e., per-area photosynthetic capacity), and longevity all influence the photosynthetic seasonality o
67 results raise the prospect that variation in longevity and age-related traits could be traced to proc
68                  We used data from the Rugao Longevity and Ageing Study, a population-based cohort st
69                               The magnitude, longevity and avidity of IgG differed significantly amon
70 sient population dynamics and differences in longevity and behavioural flexibility can help reconcile
71       Our results indicate that increases in longevity and BMI are insufficient to explain the approx
72  seeds revealed that both the acquisition of longevity and dormancy were severely impaired.
73                                          The longevity and downstream propagation of these effects as
74 he soluble inner matrix through increases in longevity and fecundity.
75 sal associations of triglyceride levels with longevity and frailty in elderly populations.
76 est associations of triglyceride levels with longevity and frailty.
77   While the effects of hypoxia on neutrophil longevity and function have been widely studied, little
78 BP5 have a critical role in the maintenance, longevity and function of CD8(+) TRM cells, and suggest
79 hereby creating the opportunity for extended longevity and good quality of life.
80 towards answering this question, we compared longevity and health of Snuppy, the world's first cloned
81 ishment through low-level viral replication, longevity and homeostatic proliferation of memory T cell
82 us observations on the relationships between longevity and immunity.
83 rmittent silencing dynamics is important for longevity and is dependent on the conserved Sir2 deacety
84 ge at puberty is a predictive factor for sow longevity and lifetime productivity, but not routinely m
85 ual variance in demographic outcomes such as longevity and lifetime reproduction.
86 at small nucleoli are a cellular hallmark of longevity and metabolic health conserved across taxa.
87 sly unidentified molecular mechanism linking longevity and metabolic pathways to neural mechanisms of
88 conditions during development, also modulate longevity and metabolism.
89  an epigenetic mechanism that modulates both longevity and mitochondrial proteostasis throughout life
90  system and is believed to improve the graft longevity and patency rates at distal graft anastomoses.
91 aging reveals deeply conserved mechanisms of longevity and population structure regulation.
92 n, by which IDO is known to influence T cell longevity and proliferation, was not involved in its eff
93                               Based on their longevity and proliferative potential, CD4(+) T memory s
94 rturbation, we uncover abundant variation in longevity and reproduction-induced mortality among genot
95 es displayed more than fourfold variation in longevity and reproduction-induced mortality that can be
96 ting that TSCM cells, owing to their extreme longevity and robust potential for immune reconstitution
97 n as in berries, with an important impact on longevity and sensorial characters of wines.
98  splicing homeostasis in dietary restriction longevity and suggest that modulation of specific splice
99 thers have powerful influences on health and longevity and that lacking social connection qualifies a
100 etary history of an animal regulates its own longevity and that of its conspecific neighbours.
101 s stable to shear instability, suggestive of longevity and the ability to carry water far distances w
102 epigenetic contribution to healthy aging and longevity and the molecular basis of the DNA methylation
103 tion of the demethylases potently suppresses longevity and UPR(mt) induction, while gain of function
104 onserved roles of the mammalian orthologs in longevity and UPR(mt) signaling.
105 n efficiencies, (ii) gains in photocatalytic longevity, and (iii) insights into the ET mechanism at t
106 4, higher income was associated with greater longevity, and differences in life expectancy across inc
107     Being taller is associated with enhanced longevity, and higher education and earnings.
108      Autophagy is associated with health and longevity, and is critical for protecting haematopoietic
109 hat include curly hair, infertility, reduced longevity, and kidney abnormalities.
110 tes characterized by function, localization, longevity, and the capacity for self-renewal.
111  Our projections show continued increases in longevity, and the need for careful planning for health
112 ve natural compounds that promote health and longevity, and understanding how they act, will provide
113  mechanism by which H3K4me3 modifiers affect longevity, and whether this mechanism involves metabolic
114 bstantial impacts on health, well-being, and longevity, and, at least in animals, on reproductive fit
115                                    Aging and longevity are controlled by a multiplicity of molecular
116 increased xenobiotic resistance and enhanced longevity are not causally connected.
117 e pressure and exaptation of traits for tree longevity are potential explanations, highlighting the c
118 he main regulators of metabolism, aging, and longevity, are components of the same pathway.
119 molecular mechanisms underlying reproduction-longevity associations remain a matter of debate.
120 need without sacrificing quality of life and longevity because of drug-based immunosuppression.
121  activity in the adult gut achieves the full longevity benefit of systemic TORC1 inhibition.
122  a physiologically low heart rate may confer longevity benefits.
123                               Differences in longevity between sexes is a mysterious yet general phen
124 s of absolute and relative brain volume with longevity (both juvenile period and reproductive lifespa
125 ed with antiretroviral therapy have improved longevity but face an elevated risk of myocardial infarc
126 orrelation between antigen-specific IgGs for longevity but not for magnitude and avidity.
127 s have been repeatedly associated with human longevity, but online interactions might have different
128 itochondrial fusion is not a major driver of longevity, but rather is essential to allow the survival
129 s autotoxins can influence the regulation of longevity by other factors including diet, sex, insulin
130 irus and then assessed cellular turnover and longevity by quantifying deuterium dilution kinetics in
131  decreasing costs, and potentially improving longevity by reducing our patients' risk of death and tr
132  is sufficient to extend lifespan; in flies, longevity can be achieved by Pol III inhibition specific
133 k-controlled transcriptional factors and the longevity candidate genes.
134                                   Of ten pro-longevity chemicals tested, six significantly extend lif
135 sing both simulated and real datasets (Rugao longevity cohort mitochondrial DNA haplogroups and kidne
136 in the body weight, oviposition periods, and longevity compared to controls.
137  quality control process that contributes to longevity conferred by daf-2 mutations.
138 cted to) has been associated with fertility, longevity, disease and information transmission in a ran
139 ired at memory to maintain memory CD8 T-cell longevity, effector function, and Eomes expression.
140   Furthermore, the mitochondrial changes and longevity effects induced by CA are conserved across dif
141                                 The dramatic longevity-enhancing effect of cold has long been known i
142 identified 6 genetic markers associated with longevity for all 4 antigens, although the expression le
143 valuable opportunities to improve health and longevity for an aging global population.
144 vements in air quality may promote molecular longevity from birth onward.
145 herefore, those at high risk of SCD may gain longevity from successful implantable cardioverter defib
146 ors to contemporary Japan, Sweden, and other longevity frontrunners.
147 g missed out on decades of income growth and longevity gains, low-income Americans are increasingly l
148  and the first to discriminate anti- and pro-longevity genes, revealing new insights on aging-related
149 d triglycerides with two ageing phenotypes - longevity ( >/=95 years) and frailty (modified Fried fra
150 her hand, the biofilm exhibited much greater longevity (&gt;5 days) than the protein-film (<6 h), with t
151      Therapeutic advances, despite improving longevity, have increased the overlap between these dise
152 val, we discover two regions associated with longevity (HLA-DQA1/DRB1 and LPA).
153         Dampened flow seasonality, increased longevity (i.e., delayed reproduction), and decreased fi
154                       Aripiprazole increased longevity in a Drosophila model of Machado-Joseph diseas
155 Dead, Yet") gene in lower organisms promotes longevity in a manner akin to caloric restriction.
156      We also demonstrate that PACRG promotes longevity in C. elegans by acting upstream of the lifesp
157               Here we show that NMD mediates longevity in C. elegans strains with mutations in daf-2/
158 ry point for the modulation of autophagy and longevity in C. elegans with conserved effects in the mu
159 ifespan in Drosophila, and can also increase longevity in C. elegans, mice, and possibly humans.
160   Antidepressants have been shown to improve longevity in C. elegans.
161 ectiveness as a mechanism for improving bond longevity in dentin bonding.
162 production drives the evolution of decreased longevity in Drosophila whereas experimental selection f
163 he relationship of TL with these disease and longevity in humans.
164 restriction (CR) retards aging and increases longevity in many animal models.
165 UPS) and autophagy, appear indispensable for longevity in many long-lived invertebrate mutants.
166           Calorie restriction (CR) increases longevity in many species by unknown mechanisms.
167                 Autophagy has been linked to longevity in many species, but the underlying mechanisms
168 ) action can produce remarkable extension of longevity in mice.
169 regulator of cellular proteostasis linked to longevity in nematodes, but its biological function in m
170 ifespan, but also with a greater increase in longevity in response to dietary restriction.
171                      AMPK/SNF1 also promotes longevity in several model organisms, including yeast.
172     However, little is known about aging and longevity in symmetrically dividing eukaryotic cells bec
173 er environmental signals influence phagocyte longevity in the absence of inflammation remains unknown
174 reased mitochondrial fusion is essential for longevity in the diverse longevity pathways, as inhibiti
175 essful suppression of viremia with increased longevity in the era of combined antiretroviral therapy,
176 t 29 bacterial genes, when deleted, increase longevity in the host Caenorhabditis elegans.
177              How schistosomes maintain their longevity in this immunologically hostile environment is
178 vealing a genetic mechanism for cold-induced longevity in this model organism.
179 re, we investigated how heat stress promotes longevity in yeast.
180 f candidate genes previously implicated with longevity indicates physiological systems may undergo se
181 ike complex (MML-1/MXL-2) to be required for longevity induced by germline removal, as well as by red
182 , whereas genetic loci linked to exceptional longevity influence metabolism.
183 are rapidly ageing, evidence that increasing longevity is being accompanied by an extended period of
184 crose and xenobiotic metabolism pathway with longevity is consistent with the previous results from D
185 ve lifespan) and social group size, although longevity is generally the stronger predictor.
186 hs to expected lifespan.Variability in human longevity is genetically influenced.
187          A key obstacle to achieving optimal longevity is the progressive decline in physiological fu
188 whereas experimental selection for increased longevity leads to changes in reproduction.
189  three UH groups, differing substantially in longevity, lifetime reproductive output, age at first re
190 nd are new attitudes and demand for 'optimal longevity' - living long, but with good health and quali
191                                         Leaf longevity (LL) varies more than 20-fold in tropical ever
192 ions, and APOE and 5q33.3 were replicated as longevity loci.
193 ntified molecular targets for developing pro-longevity microbes and a bacterial metabolite acting on
194 an extension across mechanistically distinct longevity nematode models.
195 interface between antidepressant effects and longevity, notably pathways involved in drug metabolism/
196 ced expiratory volume, grip strength, HbA1c, longevity, obesity, self-rated health, smoking status, t
197 es are required for the thermoresistance and longevity of animals exposed to hormetic heat shock or H
198                                          The longevity of asexual clades may be correlated with the m
199                                          The longevity of both the donor and the cloned dog was close
200 s to advance predictive understanding of the longevity of BPA and its transformation products in envi
201 fidobacterium longum strain BB68 affects the longevity of C. elegans were assessed.
202 es cell size, and suppresses the replicative longevity of cells lacking the Sch9p protein kinase regu
203 a unique opportunity to study the health and longevity of cloned animals compared with their cell don
204 mplies that women's fertility depends on the longevity of cohesin proteins that established cohesion
205                                    Thus, the longevity of dentin bonding can only be improved with en
206 composite restoration is unsatisfactory, and longevity of dentin bonding is one of the major culprits
207 represent mechanisms responsible for reduced longevity of dwarf mice exposed to GH treatment early in
208 ue to low spatiotemporal resolution and poor longevity of gradients utilizing microfluidic techniques
209 iquid phase, as well as the distribution and longevity of heat.
210                            With the improved longevity of HIV-positive individuals, a kidney transpla
211 l of serological memory based upon intrinsic longevity of human plasma cells.
212 olism and the differentiation, function, and longevity of immune cells.
213                           Characterising the longevity of immunological memory requires establishing
214 ls produce high condition larvae and rely on longevity of individuals for population persistence and
215            Dietary restriction increases the longevity of many organisms, but the cell signaling and
216 he physical state, spatial distribution, and longevity of melt in the crust.
217                 In contrast, SHM reduced the longevity of memory B cells by creating polyreactive spe
218                     Thus, BB68 increased the longevity of nematodes by activating the TIR-1 - JNK-1 -
219 f high-resolution data, qualitative metrics, longevity of records, and simultaneous multiwatershed an
220 bjective measure to assess independently the longevity of retinal GT.
221 ding smg-2/UPF1, are required to achieve the longevity of several long-lived mutants, including daf-2
222 em to improve the operational efficiency and longevity of SOFC-based energy generation systems.
223 ffold were also generally maintained for the longevity of the culture albeit with a higher level of c
224 and surgically related events increases with longevity of the implants.
225 cessary to predict both the severity and the longevity of the resulting environmental impacts.
226 icolour photometric observations confirm the longevity of the secondary variations, which we interpre
227 e next "generation" of learners, so that the longevity of the skill in the population could outlast t
228 e over millions of years and establishes the longevity of these genes in this genus.
229    These studies confirm the persistence and longevity of thin myelin sheaths and the importance of r
230                         The association with longevity of three of these four pathways (MAPK; immunit
231 have been developed to improve prognosis and longevity of transplanted teeth with complete root forma
232 ient benefits and its role in prolonging the longevity of treatment programs.
233 due to its impact on the sensory quality and longevity of wines.
234 fusion is necessary, but not sufficient, for longevity of worms with mutations that increase lifespan
235                          Genomic analysis of longevity offers the potential to illuminate the biology
236 id composition imbalance, and reduced animal longevity on a high-fat diet.
237 d autophagy pathways-processes implicated in longevity-on learning.
238 OI, and whether this is due to high density, longevity or high annual production in six study species
239 icted triglyceride levels and probability of longevity (OR: 0.61; 95% CI: 0.35, 1.07 per 1 mmol/L inc
240 K; calcium signaling) highly associated with longevity (P </= 0.006) in Han Chinese.
241 autophagic activity, indicating that the two longevity paradigms have distinct effects on autophagy d
242 e developments needed to improve restoration longevity past the average 10 y.
243                         We show that diverse longevity pathways exhibit increased levels of elongated
244     Long-lived animals representing distinct longevity pathways exhibit small nucleoli, and decreased
245 nt of target genes involved in key aging and longevity pathways including mTOR, FOXO and MAPK, most o
246 ribute to cell cycle, growth regulation, and longevity pathways to which MRPL12 has been linked.
247 nimal model of aging which shares many major longevity pathways with mammals.
248 on is essential for longevity in the diverse longevity pathways, as inhibiting mitochondrial fusion r
249 imits nucleolar size in the major C. elegans longevity pathways, as part of a convergent mechanism fo
250 rse genetic backgrounds may engage conserved longevity pathways.
251 mals beyond their normal lifespan in diverse longevity pathways.Mitochondria can undergo shape change
252                                          The longevity phenotype is associated with amelioration of a
253 prone background, Pml(-/-) animals display a longevity phenotype, likely reflecting decreased basal p
254 levels of these genes did not correlate with longevity phenotype.
255                                  The EFA and longevity phenotypes are ameliorated by a reduction of t
256 ing 58 disease-related GWA studies to derive longevity priors for all HapMap SNPs.
257 etin, vitamin D and resveratrol as potential longevity promoting compounds, along with a series of ex
258  and metformin (an antidiabetic and possible longevity promoting drug).
259                                          The longevity-promoting benefits of lactobacilli were hypoth
260                                              Longevity-promoting caloric restriction is thought to tr
261                                     Distinct longevity-promoting interventions, specifically genetic,
262 evel in mouse liver and tested the impact of longevity-promoting interventions, specifically the Ames
263 er epigenetic aging signatures are slowed by longevity-promoting interventions, we analyzed 28 additi
264  klotho transgene in mdx mice restored their longevity, reduced muscle wasting, improved function and
265 o environmental cues and sexual behaviors in longevity regulation, we examined Caenorhabditis male li
266   Evasion of forkhead box O (FOXO) family of longevity-related transcription factors-mediated growth
267  organisms the underpinnings of cold-induced longevity remain largely mysterious.
268 s between social learning, brain volume, and longevity remain when controlling for maternal investmen
269 entified 11 independent loci associated with longevity replicated in Southern-Northern regions of Chi
270 shape the great amount of variation in plant longevity, reproductive output and growth rate is fundam
271 nfirmed a role for ABI5 in the regulation of longevity, seed degreening, and RFO accumulation, identi
272 ve characteristics such as clonal expansion, longevity, self-renewal, and robust recall responses to
273                     INS-6 in turn relays the longevity signals to nonneuronal tissues by decreasing t
274 stem to explore the genetic underpinnings of longevity, since its generation time is brief and both t
275 ses with absolute and relative brain volume, longevity (specifically reproductive lifespan), and soci
276  them replicate (5% FDR) in five independent longevity studies combined; all but three are depleted o
277 .2% women, median age 66.5 years) and Leiden Longevity Study (N = 661; 50.5% women, median age 63.1 y
278 cated in 599 Dutch Europeans from the Leiden Longevity Study (p = 0.042) and in 1,173 Europeans of th
279  the Collaborative Breast Cancer and Women's Longevity Study, a population-based prospective observat
280 d data from the Chinese Longitudinal Healthy Longevity Study.
281 on rate of CDPs is inversely correlated with longevity, suggesting the occurrence of still unidentifi
282 onger in the fossil record than DNA, but the longevity, survival mechanisms and substrates remain con
283 ping but distinct phenotype from exceptional longevity that may be enriched with disease-protective g
284  of this key nutrient-signalling network for longevity; the growth-promoting anabolic activity of Pol
285 scovered that five bacterial mutants promote longevity through increased secretion of the polysacchar
286 t, higher income was associated with greater longevity throughout the income distribution.
287  cells maintain developmental plasticity and longevity to provide long-term immunity while other effe
288 These observations may explain the increased longevity typical of endurance athletes despite the pres
289      In contrast with studies of exceptional longevity, usually focused on centenarians, healthy agin
290 , healthy aging is not associated with known longevity variants, but is associated with reduced genet
291 is Intervention Testing Program in assessing longevity variation across 22 Caenorhabditis strains spa
292                                              Longevity varies among individuals, but how natural gene
293 rified CA polymers are sufficient to promote longevity via ATFS-1, the host UPR(mt)-responsive transc
294 ypes and then animal behavior, pathology and longevity were assessed.
295 andidate genes for mood and stress-modulated longevity were changed in expression in opposite directi
296  of bryozoans (rather than high densities or longevity), which were 2x, 3x and 5x higher than on the
297 a1-1 and bb/eod1-2 leaves showed a prolonged longevity, which was enhanced in the double mutant.
298        DNA, for example, combines remarkable longevity with high data storage densities and has been
299  growth and reproduction trading off against longevity, with trials of calorie restriction underway.
300 rsal trade-off between early growth and tree longevity within a species, although this result may als

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