ライフサイエンスコーパス: restriction

1 ary from inception to 2017 (with no language restrictions).

2 nts were performed before and after fructose restriction.

3 ure and of energy expenditure during calorie restriction.

4 ation through a mechanism resembling caloric restriction.

5 rewiring, which can be prevented by calorie restriction.

6 of receptor-less lymphoma cells to nutrient restriction.

7 th a mechanism most likely mimicking calorie restriction.

8 more susceptible to Delta20 IFITM2-mediated restriction.

9 possibly without the need of dietary protein restriction.

10 and we found no evidence for MHC II or HLA-E restriction.

11 1, however, relieved this glucose and energy restriction.

12 le the remaining 71% displayed resistance to restriction.

13 delays age-related kidney disease is caloric restriction.

14 is largely resistant to changes during sleep restriction.

15 tions, including stillbirth and fetal growth restriction.

16 n hierarchy, and had similar profiles of HLA restriction.

17 There was no language restriction.

18 omotes longevity in a manner akin to caloric restriction.

19 in reduced placental weight and fetal growth restriction.

20 ear lamina during cardiac progenitor lineage restriction.

21 determination or subject to APOBEC3 and Fv1 restriction.

22 on rates in populations with and without TFA restrictions.

23 l use, prescriber type, and HIV co-infection restrictions.

24 ly between NP models applicable to marketing restrictions.

25 temporal trends, compared with those without restrictions.

26 ploits CD169 to attenuate type I IFN-induced restrictions.

27 de data from before and after national sales restrictions.

28 e for residents has decreased with duty hour restrictions.

29 Evidence is less consistent for sales restrictions.

30 studies, without language, time, or quality restrictions.

31 in the Cochrane Library database without any restrictions.

32 EMBASE and MEDLINE without language restrictions (1 January 2008 to 14 December 2016).

33 The restriction was termed lentiviral restriction 2 (Lv2).

34 fied Mrr (Methylated adenine Recognition and Restriction), a Type IV restriction endonuclease (REase)

35 acid concentrations as a biomarker for sleep restriction, acute phase protein concentrations and mala

36 However, whether and how dietary restriction affects hematopoietic malignancies is unknow

37 However, K(+) restriction also enhanced ENaC expression in Nedd4L(Pax8

38 ential factors that are regulated by caloric restriction and act as caloric restriction mimetics.

39 he hypothesis that implementation of caloric restriction and aerobic exercise is feasible and can imp

40 behavior after 7 consecutive nights of sleep restriction and after 1 night of acute sleep deprivation

41 g DNA as confirmed by partial resistance to restriction and by liquid chromatography-mass spectromet

42 y required for lifespan extension by dietary restriction and by modulation of the TORC1 pathway compo

43 signaling regulates inner cell mass lineage restriction and cell commitment during preimplantation d

44 Both directions of the relation between restriction and child body composition were examined wit

45 sence of atypical features such as diffusion restriction and hemorrhage were also recorded.

46 e to conditions associated with fetal growth restriction and iatrogenic preterm birth.

47 SERINC5 restriction and Nef antagonism were not associated with

48 adjusted for age, sex, and commuting between restriction and nonrestriction counties.

49 es in body composition during dietary energy restriction and resistance training.In a randomized para

50 In rodents, caloric restriction and young blood-induced revitalization rever

51 Numerous dietary restrictions and endoscopies limit the implementation of

52 cted last on September 6, 2016, with no date restrictions and limited to articles published in Englis

53 red 8 weeks of MR (80% restriction), LR (80% restriction) and control diet in 10-month-old C57BL/6J m

54 esis pathway, genomic clustering, and tissue restriction, and even identified flux heterogeneity amon

55 embryos exhibit gene dosage-dependent growth restriction, and homozygous mutants exhibit upper GU def

56 primary metabolic effect of dietary protein restriction, and requires both UCP1 and FGF21 but is ind

57 We did not apply any language restrictions, and searched the full time period availabl

58 For almost two decades Mexico City's driving restrictions applied during weekdays only.

59 Public health implications of TFA restrictions are not well understood.

60 We defined fetal growth restriction as a combination of estimated fetal weight o

61 Terminal selectors mediate this restriction at least partially by organizing chromatin.

62 ber 2016 in the PubMed database with no date restrictions, but were limited to studies published in E

63 age scrambling that is disconnected from TCR restriction by MHC.

64 nt profile (NP) models relevant to marketing restrictions by applying them in the Canadian context.Wi

65 However, there is also evidence that MHC restriction can be imposed on the TCR repertoire during

66 study has investigated whether chronic sleep restriction can influence implicit attitudes (e.g., towa

67 Severe early-onset fetal growth restriction can lead to a range of adverse outcomes incl

68 es, most notably exercise and dietary energy restriction, can increase the likelihood that the brain

69 carried out similar analyses for spirometric restriction, chronic cough and chronic phlegm.

70 rall, we found no association of spirometric restriction, chronic cough or chronic phlegm with the us

71 rom individuals who underwent modest dietary restriction coupled with exercise also display small nuc

72 Calorie restriction (CR) increases the lifespan of C57Bl/6 mice,

73 uggesting weight maintenance through calorie restriction (CR) may limit risk of HER2-positive breast

74 Calorie restriction (CR) retards aging and increases longevity i

75 Caloric restriction (CR) without malnutrition extends lifespan a

76 Short-term (9 days) isocaloric fructose restriction decreased liver fat, VAT, and DNL, and impro

77 cient mESCs are hypersensitive to methionine restriction/depletion-induced differentiation and apopto

78 ease in survival time in mice on a glutamine restriction diet.

79 om humans to Caenorhabditis elegans, dietary restriction (DR) grants numerous benefits, including enh

80 Dietary restriction (DR), a reduction in food intake without mal

81 e [Crete], South Korea, and Taiwan) or sales restrictions (eight studies of restrictions in five coun

82 nine Recognition and Restriction), a Type IV restriction endonuclease (REase), as instigator for this

83 The restriction endonuclease CglI from Corynebacterium gluta

84 tures to two structurally similar 'PD-D/ExK' restriction endonucleases (EcoRV and HincII) that also g

85 Although all Type II restriction endonucleases catalyze phosphodiester bond h

86 as (i) bisulfite treatment, (ii) cleavage by restriction endonucleases, and (iii) immuno/affinity rea

87 ge mechanism of AgeI is novel among Type IIP restriction endonucleases.

88 modification genes and an adjacent putative restriction enzyme (RE) operon likely form a restriction

89 erases generating 3-OH and 5-P ends, but one restriction enzyme (restriction glycosylase) excises unm

90 e performed a previously reported assay, the restriction enzyme hotspot mutation assay (IgkappaREHMA)

91 ral and regulatory chromatin interactions by restriction enzyme targeting and two-step proximity liga

92 e-wide analyses of DNA modifications rely on restriction enzymes capable of digesting genomic DNA at

93 All restriction enzymes examined are phosphodiesterases gene

94 method of genome reduction that employs two restriction enzymes to generate overhangs in opposite or

95 The NYS populations with TFA restrictions experienced fewer cardiovascular events, be

96 Gene expression and caloric restriction experiments in model organisms confirm the c

97 evels of SIV RNA, corresponding to the lower restriction factor expression in this subset relative to

98 ation, HIV coreceptor expression, and innate restriction factor expression.

99 r report, Ifit2, is found to be an important restriction factor for rabies virus, acting directly or

100 significantly greater mRNA levels of select restriction factor genes than CSF-1-Mphis.

101 The antiviral restriction factor IFN-induced transmembrane protein 3 (

102 ata point to Ccr7 as a critical host defense restriction factor limiting neuroinflammation during acu

103 idering the host immune system in studies of restriction factor mechanisms.

104 nt, based on the observation that the innate restriction factor MxA represents an effective species b

105 es cytosine (C) to uracil (U) and is a known restriction factor of HIV-1.

106 The depletion of the restriction factor SAMHD1 resulted in a markedly increas

107 nally differentiated macrophages despite the restriction factor SAMHD1.

108 The viral restriction factor SERINC5 inhibits HIV-1 infection via

109 gies to counteract the human ortholog of the restriction factor tetherin.

110 protein 1 (SAMHD1) has been identified as a restriction factor, lowering the concentration of dNTP s

111 of both the long and short isoforms of this restriction factor.

112 T cells expressed higher levels of multiple restriction factors compared to naive cells.

113 Although multiple restriction factors have been shown to inhibit HIV/SIV r

114 the expression of 45 confirmed and putative restriction factors in primary CD4(+) T cells from rhesu

115 ents of many of these confirmed and putative restriction factors in primary cells or during the early

116 and suggest that the level of expression of restriction factors may contribute to the differential s

117 he expression of most confirmed and putative restriction factors substantially increased in all CD4(+

118 ression of 45 confirmed and putative HIV/SIV restriction factors was analyzed in CD4(+) T cells from

119 e to the disruptive effects of IFN, cellular restriction factors, and neutralizing antibodies compare

120 rs and another subset of APOBEC3G anti-viral restriction factors, both of which were upregulated.

121 ication is marked by expression of antiviral restriction factors, it was intuitive to find that IL-34

122 upregulation of distinct subsets of multiple restriction factors.

123 ability causes diseases such as fetal growth restriction, fetal malformations and cancer.

124 y causes human diseases such as fetal growth restriction, fetal malformations and cancer.

125 al age (AMA) are susceptible to fetal growth restriction (FGR) and stillbirth.

126 l vessel networks in normal and fetal growth restriction (FGR) complicated pregnancies.

127 ancies and those complicated by fetal growth restriction (FGR).

128 eight eukaryotic species, and we describe a restriction fragment length polymorphism (RFLP) assay th

129 es with TFA restrictions vs counties without restrictions from 2002 to 2013 using NYS Department of H

130 ently searched 13 databases with no language restrictions from inception to Aug 15, 2017, for randomi

131 4 bibliographic databases, without language restrictions, from 1 January 1999 to 1 February 2016.

132 To escape this restriction, Gag promotes secretase-dependent cleavage o

133 gag gene replacements are influenced by host restriction genes Fv1 and Apobec3 Pathogenic potential m

134 OH and 5-P ends, but one restriction enzyme (restriction glycosylase) excises unmethylated bases from

135 Here, we show that fasting or glucose restriction (GR) regulate PKA and AMP-activated protein

136 t had never been restricted or at times when restrictions had never been in place.

137 a determinant of lifespan in mammals.Caloric restriction has been shown to increase lifespan in mamma

138 Magnetic anisotropy removes this restriction, however, and enables, for instance, the occ

139 The genetic restrictions identified within the epitopes in the EDII

140 They also show that calorie restriction, IGF-1R signaling, and body temperature, thr

141 or component of the previously described Lv2 restriction.IMPORTANCE Measures taken by the host cell t

142 s significantly smaller (97 degrees ) due to restrictions imposed by the shorter linker.

143 d and Drug Administration plans a nationwide restriction in 2018.

144 oGRID data are directly downloadable without restriction in a variety of standardized formats and are

145 significantly prevented by long-term caloric restriction in aged mice.

146 Placental sO2 was lower in fetal growth restriction in an angiotensin-converting enzyme 2 knocko

147 T tracer uptake was identified after calorie restriction in diabetic rats (ZDF-CR).

148 odel in several cell types, we show that the restriction in E7 replication in mutants with increased

149 patterns in both males and females and food restriction in males at age 13 y.

150 promotes rapid fat mass loss without calorie restriction in obese mice.

151 ted participants to 3 weeks of chronic sleep restriction in the lab (i.e., 3 weekly cycles of 5 night

152 d are turning to license-plate based driving restrictions in an effort to address urban air pollution

153 wan) or sales restrictions (eight studies of restrictions in five countries- India, Denmark, Ireland,

154 fragments to overcome the placement and size restrictions in selenocysteine-mediated chemical ligatio

155 Moreover, K(+) restriction increased WNK1 and WNK4 expression and enhan

156 Dietary protein restriction increases adipose tissue uncoupling protein

157 Dietary restriction increases the longevity of many organisms, b

158 ion and are sensitive to maternal methionine restriction-induced lethality, whereas maternal methioni

159 LysoPC restriction induces a compensatory response, linking par

160 KEY POINTS: Maternal nutrient restriction induces intrauterine growth restriction (IUG

161 ABSTRACT: Maternal nutrient restriction induces intrauterine growth restriction (IUG

162 Chronic sleep restriction is highly prevalent in modern society and is

163 Starvation, or caloric restriction, is known to activate the transcription fact

164 ient restriction induces intrauterine growth restriction (IUGR) and leads to heightened cardiovascula

165 We hypothesized that intrauterine growth restriction (IUGR) offspring hearts would show impaired

166 lts who were affected by intrauterine growth restriction (IUGR) suffer from reductions in muscle mass

167 that is characterized by intrauterine growth restriction (IUGR) with gonadal, adrenal, and bone marro

168 ient restriction induces intrauterine growth restriction (IUGR), increasing later life chronic diseas

169 Metabolic factors such as caloric restriction, ketogenic diet, and hyperglycemia influence

170 f stem cell types and robustly track lineage restriction kinetics.

171 e subjected to dietary potassium loading and restriction, KS-WNK1 knockout mice were deficient in the

172 XR-TGR5 dual agonist INT-767 induced caloric restriction-like effects and reversed age-related increa

173 role for RNA splicing homeostasis in dietary restriction longevity and suggest that modulation of spe

174 etus and newborn include intrauterine growth restriction, low birth weight, and stillbirth.

175 d LR, this study compared 8 weeks of MR (80% restriction), LR (80% restriction) and control diet in 1

176 These findings suggest that chronic sleep restriction may "unmask" implicit racial or ethnic biase

177 ogies; therefore, we hypothesized that sleep restriction may perturb the gut microbiome to contribute

178 forming an understanding of the reassortment restriction mechanism.

179 y for L1 derepression arises, and additional restriction mechanisms become crucial.

180 Three reported dietary restriction mimetics are mainly effective across C. eleg

181 ed by caloric restriction and act as caloric restriction mimetics.

182 restriction enzyme (RE) operon likely form a restriction modification (RM) system for defence from fo

183 gest that DISARM is a new type of multi-gene restriction-modification module, expanding the arsenal o

184 Two restriction-modification systems have been previously di

185 ISARM (defence island system associated with restriction-modification), which is widespread in bacter

186 Dietary methionine restriction (MR) produces a rapid and persistent remodel

187 (one prolonged wake episode), chronic sleep restriction (multiple nights with insufficient sleep), a

188 Postnatal growth restriction occurred in pups in UPI/RA, but not in UPI/O

189 The greatest degree of restriction occurs when a contact is predicted between t

190 irms the importance of RNA binding for IFIT1 restriction of a human coronavirus mutant lacking viral

191 Kinetic restriction of a thermodynamically favourable equilibriu

192 lls, suggesting that TEX1- and TAS3-mediated restriction of ARF3 expression limits excessive megaspor

193 erned substrates of Nogo-A-Fc, KT5720 caused restriction of axon growth to areas devoid of Nogo-A-Fc.

194 However, growth restriction of bacteria lacking PlcA, PlcB, and ActA req

195 cellular identity is usually paralleled by a restriction of cellular plasticity.

196 Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and US High Production

197 Here, we demonstrate that basal restriction of ciliary structure dynamics is established

198 in stem cells enables self-renewal and rapid restriction of developmental potential following asymmet

199 Restriction of dietary serine and glycine can reduce tum

200 ion, a slowdown of transcript elongation and restriction of gene activity to the promoter-proximal ap

201 om Zambia, Malawi, and Mozambique revealed a restriction of gene flow between populations, in line wi

202 receptor) as central effectors of B-lymphoid restriction of glucose and energy supply.

203 y described and characterized an early-phase restriction of HIV-1 and -2 replication in human cell li

204 These results demonstrate that the restriction of HIV-1 particle infectivity by SERINC5 doe

205 rimental to the growth and survival of mice, restriction of hTetherin expression to hematopoietic cel

206 ansion of type 1 regulatory (Tr1) cells, and restriction of humoral immunity during malaria blood sta

207 R.CcoLI/R.PabI expression caused restriction of incoming bacteriophage/plasmid DNA and en

208 Restriction of infection via apical inoculation was over

209 ary PB2 627 domain, implicated in host range restriction of influenza A viruses, is still poorly unde

210 synchronization in the gamma band, the phase-restriction of informative spikes in principal neurons w

211 se between generation of motility forces and restriction of intercellular communication.

212 as no growth defect, arguing against ongoing restriction of its own DNA.

213 some elongation, in macrophages impaired the restriction of L. major replication in C57BL/6, but did

214 immediately following infection and for the restriction of leukocyte migration into the brain.

215 TRIM23 was critical for autophagy-mediated restriction of multiple viruses, and this activity was d

216 suggest that Namikonga's resistance involves restriction of multiplication of UCBSV within the host.

217 This may alleviate the restriction of N supply for increased primary productivi

218 s63-linked ubiquitination of the vacuole and restriction of parasite early replication without interf

219 ole of Dectin-1 for inflammasome activation, restriction of parasite replication in macrophages, and

220 f reactive oxygen species (ROS) accounts for restriction of parasite replication, Leishmania is known

221 To study restriction of plasticity, we ectopically expressed C. e

222 studies using a moderate 30% global calorie restriction of pregnant mothers and used cardiac magneti

223 TU, TM7-3a, was found to increase with sleep restriction of rats.

224 The increased survival following dietary restriction of serine and glycine in these models was fu

225 t mutants from Arabidopsis (especially after restriction of the cytochrome c pathway) but cannot comp

226 In data analysis, restriction of the mass range was considered and differe

227 on property that was attributed to both, the restriction of the molecular rotation at low temperature

228 eristics (ie, age and sex) resulted from the restriction of the original cohort to those with at leas

229 sis phagocytosis is important for macrophage restriction of the parasite replication and effectively

230 s a specific role in somite number and size, restriction of the presomitic mesoderm anterior border,

231 wever, there is evidence that conformational restriction of the substrate may play a role in catalysi

232 e then tested 39 patients with severe growth restriction of unknown etiology, and found hypomethylati

233 such as antibody diversification/maturation, restriction of viral infection, and generation of somati

234 doluminal CT colonography led to progressive restriction of visual search patterns.

235 about these substances and the recent legal restrictions of China in distillates import need a quick

236 tracing to define the lineage relations and restrictions of the mesenchymal and epithelial cell type

237 Unfortunately, hardware restrictions often limit the sensor performance.

238 tional in utero parental energy and nutrient restriction on offspring growth in rural Gambia.

239 vator paricalcitol (PARI) and dietary sodium restriction on residual albuminuria in CKD.

240 Lifting the restriction on the rate of the spin-selective recombinat

241 the size of the recognition repertoire, and restrictions on cis-interactions among Pcdh isoforms def

242 ating in their normal daily routines without restrictions on diet or physical activity.

243 es designed to overcome the stereoelectronic restrictions on homoallylic ring expansion in alkyne rea

244 y of photoelectrode materials impose serious restrictions on its advancement.

245 tors requires anomalous dispersion, imposing restrictions on materials and resonator design.

246 at the full implications of locality and its restrictions on possible ground states may hold further

247 quirement of a gate electrode, which imposes restrictions on sensor device architectures and results

248 obiota composition as it imposes significant restrictions on the allowable community membership, comp

249 significant regulatory role, in fact impart restrictions on the developmental timing of gene express

250 Our results also impose restrictions on the potential role of atmospheric CO2 in

251 There were no restrictions on the study design.

252 Restrictions on their use were initiated in 11 New York

253 ns, including Prop1(df/df) dwarfism, calorie restriction or dietary rapamycin.

254 demonstrate that under conditions of dietary restriction or growth factor starvation, where PI3K/mTOR

255 zation of weight was mediated not by caloric restriction or increased activity, but by increased ener

256 stress, exercise-induced adaptation, caloric restriction, osmotic stress, mechanical stress, immune r

257 Additionally, calorie restriction partially restored the impaired BAT glucose

258 L1 retrotransposition, elucidate a novel L1 restriction pathway and illustrate how epigenetic silenc

259 to one of the oldest and best-known driving restriction policies.

260 fiber with placebo treatments without energy-restriction protocols.

261 n contrast, food availability following food restriction rapidly increased VPpp neuron activity withi

262 There is some evidence that calorie restriction reduces or delays many of the age-related de

263 Dietary restriction regimens, including fasting, have been consi

264 On a publicly available website without restriction, researchers should post 1) analysis code us

265 equately concentrate their urine after water restriction, resulting in susceptibility to prerenal azo

266 ns population and causes intrauterine growth restriction, severe microcephaly, craniofacial anomalies

267 Restriction site-associated DNA sequencing (RAD-seq) all

268 Large genomic data sets generated with restriction site-associated DNA sequencing (RADseq), in

269 ion sequencing data were generated using the restriction-site associated DNA (RAD-seq) method.

270 We used restriction-site associated DNA sequencing (RAD-seq) to

271 We employed restriction-site-associated DNA sequencing and integrate

272 of 31 mayfly (Ephemeroptera) communities and restriction-site-associated-DNA sequencing in the four m

273 se To investigate whether sinovenous outflow restriction (SOR) is more strongly associated with hemor

274 The restriction starch hydrolysis rate markedly reduced the

275 Conclusion Commonly practiced restrictions surrounding 6-MP ingestion might not influe

276 The defence systems include a single-subunit restriction system, a heterotypic exclusion system and a

277 lication associated with intrauterine growth restriction that may influence respiratory outcome at bi

278 d consider the role of regulatory and market restrictions that obstruct necessary ecological and gene

279 To evade this restriction, the HIV-1 Vif protein binds A3H and mediate

280 CU clinicians should be aware of any special restrictions their state places on medical information.

281 iets increase weight loss (WL) during energy restriction; therefore, it has been suggested that addit

282 olled Trials, were searched without language restrictions through July 30, 2016.

283 .956 to 0.983]; P < .01), and persisted upon restriction to men meeting strict AS inclusion criteria.

284 e.g. the need for intravenous infusions and restriction to short-term studies (hours) in controlled

285 equal value to iFR can be determined without restriction to the WFP.

286 entralized data sharing platforms with fewer restrictions to data access.

287 tumor growth, these signaling and metabolic restrictions triggered autophagy, which supplied the met

288 searched PubMed and MEDLINE without language restrictions up to Sept 18, 2017, for eligible trials.

289 post study of residents in counties with TFA restrictions vs counties without restrictions from 2002

290 ng impaired fear extinction via dietary zinc restriction was associated with differential expression

291 The R.PabI-mediated restriction was promoted by AP endonuclease action in vi

292 The restriction was termed lentiviral restriction 2 (Lv2).

293 Rescuing these metabolic restrictions was sufficient to reverse IDH1-mediated rad

294 More potent CA determinants for HIV-1 REAF restriction were identified at P38A, N74D, G89V, and G94

295 No age or language restrictions were applied.

296 No language restrictions were applied.

297 Donor pool restrictions were associated with worse 3-year outcomes,

298 0 bases) and although a few strong localised restrictions were observed, they contributed little to t

299 Restrictions were only implemented in highly urban count

300 eotides 784-820 is critical for the observed restriction; yet additional determinants reside in other