ライフサイエンスコーパス: a delay in

1 It seems to be driven mainly by a delay in achieving viral suppression.

2 exposure to pathway agonists, hESCs exhibit a delay in activation of beta-catenin signaling, which l

3 ranged from 3-fold to 30-fold and was due to a delay in activation of early sporulation genes.

4 However, a delay in additional diagnostic capacity with provision

5 xpression of PtAIL1 expression, which led to a delay in adventitious root formation.

6 FAS possibly due to the higher flow rate and a delay in aerobic bacterial degradation.

7 murine GC-B cells results in larger GCs and a delay in affinity maturation, demonstrating the import

8 minant-negative ATO1(G53D) allele results in a delay in alkalinization, a defect in hyphal formation,

9 mic control post-transplant and demonstrated a delay in allograft rejection.

10 oesin clearance from cell poles at anaphase, a delay in anaphase elongation, together with defects in

11 ably, we find that pk2 knockdown larvae show a delay in anterograde transport.

12 ouse embryo is significantly extended due to a delay in APC/C activation.

13 of B6-MRL Fas lpr/j-RAGE(-/-) mice exhibited a delay in apoptosis and expressed significantly less ac

14 A delay in application of the label of multiple myeloma

15 fibroblasts had a basal autophagy defect and a delay in autophagic flux, possibly due to unsealed aut

16 ults in exuberant VSN axonal projections and a delay in axonal coalescence into well defined glomerul

17 beta-catenin loss-of-function mutations show a delay in axonal sorting; conversely, gain-of-function

18 The photopic ERGs showed a delay in b-wave time to peak, but the photopic hill, i

19 IRKOGFAP males and females showed a delay in balanopreputial separation or vaginal opening

20 e phenotype, and neither genotypes exhibited a delay in behavioural timing in responses to dLAN.

21 Cells without centrioles exhibited both a delay in bipolar spindle assembly and a high rate of c

22 r ALAT2 caused unexpected phenotypes such as a delay in blood digestion, a massive accumulation of ur

23 entirely unclear how a lack of Ano6 leads to a delay in bone mineralization by osteoblasts.

24 lysis, with virion-associated CD55 providing a delay in both aggregation and lysis more substantial t

25 pared to diploid embryos, haploids exhibited a delay in both zygotic gene expression and cell cycle l

26 This commentary discusses how to balance a delay in cancer diagnosis or treatment against the ris

27 A delay in cardiac repolarization is characteristic of t

28 poptotic nuclear morphology correlating with a delay in caspase-3 activation.

29 PC maturation in the vaginal mucosa leads to a delay in CD8 T cell activation in the draining lymph n

30 This phenotype is associated with a delay in cell cycle progression and ectopic DNA elemen

31 mediates reversion of T(EM) into T(CM), via a delay in cell cycle progression at the G2/M stage.

32 nificant reduction in cell proliferation and a delay in cell cycle progression.

33 the precocious inhibition of mitosis due to a delay in cell cycle progression.

34 accumulation of Aurora A at centrosomes and a delay in centrosome separation.

35 e mechanism underlying these observations is a delay in channel opening after application of protons,

36 a Thus, we have demonstrated that, following a delay in chlamydial spreading caused by FTY720, genita

37 at cells without functional centrosomes have a delay in chromosome congression and anaphase onset, wh

38 e delay in fruit ripening is associated with a delay in climacteric respiration and reduced synthesis

39 n the alpha tocopherol group translates into a delay in clinical progression of 19% per year compared

40 A multidomain intervention showed a delay in cognitive decline (low-strength evidence).

41 The double mutant exhibits a delay in cohesin removal during anaphase I.

42 Furthermore, low-dose combination caused a delay in colonic adenocarcinoma progression.

43 ults in reduction of the fracture callus and a delay in conversion of cartilage to bone.

44 ing proteins at the CR, which in turn led to a delay in CR formation and sensitivity to other perturb

45 ptin receptor deficiency, which also induced a delay in cryptal epithelial proliferation.

46 ic division and failure in cytokinesis, with a delay in daughter cell abscission revealed by a fluore

47 red patients were least likely to experience a delay in definitive surgery, followed by Medicare and

48 tions were acquired prenatally and linked to a delay in dentate gyrus maturation in the ventral hippo

49 + complement-mediated cell lysis resulted in a delay in development of MBP cells and myelination.

50 , Caspase-3 and Caspase-6-knockout mice show a delay in developmental pruning of retinocollicular axo

51 icant morbidity and mortality as a result of a delay in diagnosis and initiation of circulatory suppo

52 hose of normal pregnancy, often resulting in a delay in diagnosis and preventable complications.

53 oms and multiple hospitalizations leading to a delay in diagnosis caused by incomplete initial workup

54 for systemic infection is warranted because a delay in diagnosis is associated with increased mortal

55 Results Tumor stage did not indicate a delay in diagnosis of breast cancer in women previousl

56 scribed a problem with medical care, such as a delay in diagnosis or treatment; 47% described a commu

57 tation in this age group sometimes can cause a delay in diagnosis.

58 d found that mutant mice had smaller testes, a delay in differentiation of pre-meiotic germ cells, de

59 eed, miR-223(-/-) eosinophil progenitors had a delay in differentiation.

60 SATB1 knockdown caused a delay in DNA repair following exposure to H2O2, an inc

61 o show that the absence of seipin results in a delay in droplet appearance with concomitant accumulat

62 Global deletion of Twsg1 leads to a delay in ductal elongation, reduced secondary branchin

63 rD-ALL blasts are low proliferative and show a delay in early mitosis at prometaphase, associated wit

64 in Rab7-positive late endosomes, suggesting a delay in early-to-late endosome maturation.

65 otype resulted from enhanced growth rate and a delay in ecdysteroid elevation during the mid-third in

66 The results showed a delay in elongation and disorganization of the HERS in

67 ndosperm development that are accompanied by a delay in embryo development followed by embryo arrest

68 However, a delay in EMG induction was observed, which became more

69 The loss of Pan1 caused a delay in endocytic progression and weakened connection

70 ay early developmental phenotypes, including a delay in epiboly, depleted S1P levels, elevated levels

71 n with an "eyes open at birth" defect due to a delay in epithelial sheet extension.

72 Coated plums showed a delay in ethylene production and respiration rate at 2

73 We show this cell death correlates with a delay in expression of Fgf8 in branchial arch ectoderm

74 lay increased sensitivity to mitomycin C and a delay in FANCD2 foci formation compared with their wil

75 gat2(-/-) mice, Mogat2(IKO) mice also showed a delay in fat absorption, a decrease in food intake, an

76 Col12a1 gene showed decreased grip strength, a delay in fiber-type transition and a deficiency in pas

77 season length were associated primarily with a delay in first frost of the fall season and lengthenin

78 s in unmanipulated plots showed no change or a delay in flowering over the 21-year period, despite mo

79 d lines and show that tropical lines exhibit a delay in flowering transition of more than 3 weeks und

80 ic Arabidopsis plants led to reduced growth, a delay in flowering, and strongly attenuated senescence

81 collagen in affected horse fibroblasts shows a delay in folding and secretion and a decrease in hydro

82 the first hair follicles is responsible for a delay in follicular destruction, which results in lowe

83 he Ras-related protein R-Ras2/TC21 displayed a delay in formation of neurofibromas but an acceleratio

84 A delay in G(1) to S phase of cell cycle was also seen t

85 many different aneuploid strains exhibiting a delay in G1, a cell cycle stage governed by extracellu

86 ks Tom1-mediated turnover of Dia2 and causes a delay in G1-to-S phase progression.

87 f the Tmtcs in Xenopus laevis embryos caused a delay in gastrulation that was rescued by the addition

88 olonged repression of housekeeping genes and a delay in gene activation at inducible loci.

89 er progenitor proliferation rate, along with a delay in gliogenesis, is also observed in Gdf11(-/-) s

90 utamate receptor subunit 1 (GluA1), there is a delay in GluA1 increase in the trained hemisphere of t

91 MeJA application led to a delay in grape technological maturity and a significan

92 es, hmp and nor hmp mutants both experienced a delay in growth initiation, whereas the nor mutant's a

93 less acm deletion mutant and did not observe a delay in growth.

94 mall fiber neuropathy and is associated with a delay in healing of shallow, but not deep wounds.

95 paired erythroid maturation characterized by a delay in hemoglobin accumulation, larger mean cell are

96 ificantly increased hepatocyte apoptosis and a delay in hepatocyte regeneration after injury, which w

97 Deletion of AIM44 results in a delay in Hof1p phosphorylation and altered Hof1p local

98 ermined that mild disease is associated with a delay in host expression of genes linked to virulence,

99 Here, we test for such a delay in impact by relating numbers of threatened spec

100 A delay in implementation had a differential effect on t

101 e show that at CB1 1, 10, 13, and 18 display a delay in inhibiting CP55,940-mediated cAMP inhibition,

102 er, larger droplets that are consistent with a delay in initiation but are otherwise normal in morpho

103 s waiting for laboratory tests and therefore a delay in initiation of chemotherapy.

104 ctive recovery from hematological stress and a delay in initiation of HSPC proliferation.

105 the peak of morphologic differentiation and a delay in initiation of myelination.

106 d defects in replication and spread, and had a delay in innate immune cytokine responses in primary,

107 susceptibility in diabetic mice results from a delay in innate immune response to inhaled Mycobacteri

108 the formation of defective viral DNA ends or a delay in integration, suggesting that the compound inh

109 ntly different in GF and SPF mice, there was a delay in intestinal epithelial repair to DSS-induced i

110 ts of the cholinergic-evoked inhibition, and a delay in IPSC latency.

111 itude of the apical Ca(2+) signal and caused a delay in its initiation.

112 n the Barnes maze test, mSOD1 mice displayed a delay in learning, outperformed wild-type mice during

113 rms this role, and DeltaDslA strains exhibit a delay in leaving from prey.

114 that myeloid-specific Foxm1 deletion caused a delay in liver repair.

115 with cyclin A2-deficient hepatocytes, where a delay in liver tumor formation was observed.

116 (-/-)) mice resulted in increased mortality, a delay in lung bacterial clearance, increased L. pneumo

117 inatal hypoxia alters development is through a delay in maturation of affected cell types, including

118 els, less severe histologic alterations, and a delay in mean time to death, compared with MARV-Ang in

119 14 of whom were considered ICU boarders with a delay in medical ICU transfer over 2 hours.

120 A delay in mesophyll differentiation apparent both in th

121 aptor protein complex 2 binding site, caused a delay in MHC I recycling to the plasma membrane withou

122 grouped PV-KO and wild-type mice, suggesting a delay in microglial activation when PV is absent from

123 Shp2-depleted cells exhibited a delay in mitotic entry and an earlier mitotic exit.

124 nation revealed that these filaments exhibit a delay in mitotic exit mediated by the checkpoint prote

125 cts in spindle assembly, pole splitting, and a delay in mitotic progression.

126 e marrow microenvironmental cell can lead to a delay in MM tumor progression.

127 (lox/lox) mice heterozygous for Agr2 exhibit a delay in mPanIN initiation and progression to PDAC.

128 elopmental pattern seen in wild type matches a delay in myelination of the superficial tracts of the

129 ic D2 inactivation (ALB-D2KO) is followed by a delay in neonatal expression of key lipid-related gene

130 One SD below the mean established a delay in neurodevelopment (score <85).

131 a reduced postmitotic layer, consistent with a delay in neurogenesis.

132 he intermediate forms of SMA presenting with a delay in neuromuscular junction maturation and a decre

133 TCF4 haploinsufficiency mice exhibit a delay in neuronal migration, and a significant increas

134 e initiation of a biofilm infection in which a delay in neutrophil recruitment to an abiotic surface

135 Without these reconnaissance cells, there is a delay in neutrophil recruitment to the lymph node and

136 e in promoting nodal root emergence and that a delay in nodal root development has a negative effect

137 Furthermore, A2BAR KO mice display a delay in normal fracture physiology with lower express

138 Trailing chromatids induce a delay in nuclear envelope reassembly concomitant with

139 gs from observational studies have suggested a delay in nursing home placement with dementia drug tre

140 t throughout gastric digestion, which caused a delay in nutrient emptying, slower digestion and leuci

141 e association between nutritional status and a delay in nutrition initiation was independent of poten

142 n warthog RELA were not resilient to ASF but a delay in onset of clinical signs and less viral DNA in

143 ns in pacman result in small imaginal discs, a delay in onset of pupariation and lethality during the

144 ed inhibition in tumor incidence, as well as a delay in onset of tumorigenesis.

145 POPs measurements (to our knowledge) reveals a delay in onset with higher concentrations.

146 aused by mating in blood-fed females, causes a delay in oocyte development, and impairs the function

147 losure of the palatal shelves accompanied by a delay in ossification along the fusion area of seconda

148 ults in a more reduced Mia40 redox state and a delay in oxidative folding and mitochondrial import of

149 is delayed by 48 hours; this corresponds to a delay in p38MAPK activation.

150 B4049/emb30-1) (gnom(B)(/E)) mutant revealed a delay in papilla formation and reduced penetration res

151 Resistance in CD73 knockout mice was due to a delay in parasite differentiation in the central nervo

152 r regrowth in hepFXR-KO mice was unaffected, a delay in peak hepatocyte proliferation from day 2 to d

153 (Epid)CaR(-/-) mice exhibited a delay in permeability barrier formation during embryon

154 ffects may depend on age at vaccination, and a delay in pertussis vaccination has been linked to redu

155 played other early disease features, such as a delay in photoreceptor outer segment (POS) clearance a

156 Lrp4 mutant mice displayed a delay in placode initiation and changes in distributio

157 Our results showed a delay in plant senescence with an increase in the expr

158 dothelial cell (EC) migration contributes to a delay in postnatal development of the retinal vasculat

159 When CXCR4 is lacking, KikGR(+) B cells show a delay in PP egress.

160 ease or worse at diagnosis), likely owing to a delay in presentation, nonspecific presenting symptoms

161 s showed that corpora allata ablation caused a delay in production of the major female-specific sex p

162 logous genes in Nicotiana benthamiana led to a delay in programmed cell death normally associated wit

163 phase III studies and phase II studies where a delay in progression is expected in the absence of rad

164 mic reticulum (ER)-to-Golgi transport and/or a delay in protein exit from the Golgi.

165 In patients with diagnosed PDR, a delay in PRP treatment beyond 31 days was associated w

166 extension reduced lytic activity and led to a delay in rapid egress, but did not significantly decre

167 Absence of DraRnl elicts a delay in reconstitution of the 10 kGy IR-shattered D.

168 nsuspected and likely harmful consequence of a delay in recovering from acidification in boreal lakes

169 However, increased temperature resulted in a delay in recovery (72 hours) from dispersant exposure.

170 ficant increase in hepatocellular injury and a delay in recovery compared to control-treated mice.

171 Both mutations also cause a delay in recovery following bleaching.

172 epcidin rapidly after hemorrhage and exhibit a delay in recovery from blood loss.

173 ation resulted in increased facilitation and a delay in recovery from synaptic depression, indicating

174 Interestingly, APE2-deficient mice show a delay in recovery of B lymphocyte progenitors followin

175 tive to drought than WT plant, and exhibited a delay in recovery of floral organ development under pr

176 When B cells return to the MZ, there is a delay in recovery of SIGN-R1-expressing macrophages.

177 Analysis of muscle regeneration showed a delay in recovery, probably as a result of decreased a

178 All 4 of these cases had a delay in referral for surgical intervention.

179 clear activation, findings that characterize a delay in regenerative reprogramming.

180 creases CCL2-induced chemotaxis and mediates a delay in reinsertion of the CCL2 receptor, CCR2, into

181 nt of reovirus transit to late endosomes and a delay in reovirus disassembly.

182 We also observed a delay in reprogramming of the maternal allele of the i

183 Here, we directly demonstrate a delay in restriction endonuclease synthesis after tran

184 ectopic Foxp3 expression and correlated with a delay in retinoic acid-related orphan receptor gammat

185 ward their targets is impaired, resulting in a delay in RGC axons reaching the dorsal thalamus compar

186 omatin association of CDC6 and cyclin E, and a delay in S phase entry.

187 A deficiency of SIRT1 led to a delay in SC activation that could also be partially re

188 reduction in expression of myelin genes and a delay in Schwann cell differentiation.

189 We recently showed that a delay in sigma(E) activation resulted in the novel phe

190 nctional relevance as Tlr3-/- mice displayed a delay in skin barrier repair following UVB damage.

191 ickness skin wounds to beryllium only causes a delay in skin regeneration.

192 A delay in SMC differentiation was observed in Six1(-/-)

193 In the Fmr1 knockout mouse, we find a delay in somatosensory map formation, alterations in t

194 ed levels of spore-specific gray pigment and a delay in spore formation.

195 e-free and particle-modified surfaces reveal a delay in spreading rate after an elapsed time of about

196 Finally, a delay in stomatal conductance recovery during the peri

197 Scn1b(-/-) mice with bumetanide resulted in a delay in SUDEP onset compared to controls in a subset

198 tting of suspected macular holes may lead to a delay in surgical treatment, with attendant worse anat

199 in-1 gene have hair bundle dysmorphology and a delay in synapse maturation.

200 At the human NMJ, a delay in synaptic maturation and an altered maintenanc

201 e retinas in postnatal development indicated a delay in synaptogenesis in Slitrk6-deficient animals.

202 This elimination process caused a delay in TEB outgrowth, after which the gland develope

203 PLK-1 and AIR-1 in C. elegans), which impose a delay in the activation of the PAR network so that it

204 The loss of endothelial IRs also resulted in a delay in the acute hypoglycemic effect of systemic ins

205 s of the liver because DeltaEGFR mice showed a delay in the appearance of diethyl-nitrosamine-induced

206 nregulated VEGFR expression, which may cause a delay in the bone repair/remodeling process.

207 to approximately 50% of normal levels causes a delay in the cell cycle and accumulation of cells in e

208 A delay in the completion of metaphase induces a stress

209 n IMP go through one extra division owing to a delay in the Delta-dependent S2 cleavage of Notch.

210 Finally, we demonstrated that there was a delay in the development and severity of inflammation

211 Furthermore, mice lacking CX3CR1 exhibited a delay in the development of allodynia following VCR ad

212 d with the low number of patients has led to a delay in the development of appropriate therapies.

213 junction barrier formation, as indicated by a delay in the development of peak transepithelial elect

214 When RHD3 is mutated, a delay in the development of TuMV infection is observed

215 These results thus suggest a delay in the differentiation process of Klhl6-deficien

216 A delay in the DOC mobilization became apparent as the a

217 inding of the virus to the cell, we detected a delay in the entry and subsequent delivery of virion D

218 diminished KGF expression in GFs, leading to a delay in the epithelial wound-healing process that was

219 e epitopes, and that this is associated with a delay in the epitope-specific CD8(+) T cells respondin

220 These phenotypes are correlated with a delay in the eviction of nucleosomes surrounding the D

221 aled a defect in uncoating, characterized by a delay in the exposure of a conformational epitope on L

222 the rate of T-cell division concurrent with a delay in the expression of PLK1, Cyclin A and pH3.

223 Furthermore, loss of Aplnr results in a delay in the expression of the cardiogenic transcripti

224 In vivo, a delay in the expression of the myelin protein MBP was

225 tilage was strongly suppressed, resulting in a delay in the formation of the secondary ossification c

226 tion that each intermediate hospital conveys a delay in the further spread of the pathogen.

227 Deletion of DIA2 rescues a delay in the G1-to-S phase transition in the tom1Delta

228 on, a change that positively correlates with a delay in the GABAergic response switch.

229 o 30 days post-primary infection, suggesting a delay in the generation of memory.

230 Phenotypic analysis revealed a delay in the germination of atlig6 mutants compared wi

231 different particle concentrations did cause a delay in the growth of P. aeruginosa, whereas impressi

232 A delay in the initiation of appropriate antifungal ther

233 Mutations in lep-2 cause a delay in the juvenile-to-adult transition, with adult

234 hereas lower concentrations resulted in only a delay in the lag phase.

235 catalytic reaction slows down, resulting in a delay in the lasing onset time, which is used as the s

236 Here we demonstrate that there is a delay in the maturation of the intrinsic properties of

237 Here we demonstrate a delay in the maturation of the properties and synaptic

238 ant ail6 mutants display a delay in the meristem identity transition and in LFY i

239 he relative density of laminar compartments, a delay in the neurogenesis of infragranular layers rela

240 nfragranular layers relative to layer 1, and a delay in the neurogenesis of supragranular layers rela

241 DSC showed a delay in the OCT peak that appeared after 200 degrees

242 characterized by an advance in the onset and a delay in the offset of daily activity, thus revealing

243 lopes slowly to reach their target, there is a delay in the onset of action that may be reduced by in

244 Computer modeling predicts that a delay in the onset of base generation can lead to impr

245 develop blood-stage parasitemia or exhibited a delay in the onset of blood-stage patency.

246 e qoxAB mutants are attenuated in mice, with a delay in the onset of disease signs and with increased

247 derm development, that end-3(-) embryos have a delay in the onset of E lineage cell fate and that end

248 ncrease in the proportion of nonlearners and a delay in the onset of learning in both FX and conditio

249 s for development later in life and to cause a delay in the onset of menopause as measured by the num

250 nked an increase in aerosol concentration to a delay in the onset of rain, invigorated clouds and str

251 ions,in a subset of genes, that likely cause a delay in the onset of stationary phase, which appears

252 nts using a single bacterial species yielded a delay in the onset of transmission, which we hypothesi

253 There is a delay in the phasing of H3K4me3 relative to the peak i

254 problematic owing to its infrequency and/or a delay in the positivity of a cerebrospinal fluid (CSF)

255 AS and NOS inhibition caused a delay in the progress of neural differentiation, as su

256 t production from endothelial cells leads to a delay in the proliferative response after injury.

257 cells defective in DNA replication exhibited a delay in the prometaphase-to-metaphase transition and

258 This uncoating defect was accompanied by a delay in the proteolysis of both L1 and L2 in mutated

259 d levels of O-GlcNAc modification as well as a delay in the rate of wound closure in vitro.

260 For flucloxacillin, a delay in the reaction onset and identification of huma

261 In the presence of NAC, a delay in the recovery rate of the hemocyte number was

262 indicate that morphine treatment results in a delay in the recruitment of cellular events following

263 endent reduction of Mon1a levels resulted in a delay in the reformation of the Golgi apparatus after

264 These observations suggest that a delay in the release of cytochrome c or delay in ATP i

265 lanes relax under prolonged load that causes a delay in the reload curve which ultimately catches up

266 eage cell expansion and survival, leading to a delay in the remyelination process.

267 leting cells of HP1 caused genotoxic stress, a delay in the repair of DSBs and elevated levels of apo

268 esthetic treatment, time-trained bees showed a delay in the start of foraging of 3.3 h, and whole-hiv

269 These findings suggested a delay in the structural and functional maturation of R

270 The conjunctival route resulted in a delay in the time to peak organ burden in comparison t

271 rojected water temperatures at depth creates a delay in the timing of annual severe bleaching >= 10 y

272 SCs deficient in miRNAs manifested a delay in the transition between the distinct different

273 b INs results in hindlimb hyperextension and a delay in the transition from stance phase to swing pha

274 nd larger cell size and is not simply due to a delay in the transition to flowering.

275 Mechanistically, this corresponds with a delay in the transition to PI(3,4,5)P3 and phagocytic

276 s subject to a circadian gate that generates a delay in the TTFL, and this delay is thought to be cri

277 ghts and to identify factors associated with a delay in the workup of small children.

278 lium, partial absence of the thymic capsule, a delay in thymus and parathyroid separation, and failed

279 E-cadherin and ZO-1 to junctions, as well as a delay in tight junction barrier formation, as indicate

280 Thus, acute stress coupled with a delay in time from a negative experience may be a stro

281 (P < 0.05) in statin myalgic subjects due to a delay in time to reach peak power output.

282 nt by a medicine service was associated with a delay in time to surgical intervention (IRR = 1.84, 95

283 %) receiving ChAd63-MVA ME-TRAP demonstrated a delay in time to treatment, compared with unvaccinated

284 esidue located in CRD2 (TNFR1(F60V) ) causes a delay in TNFR1 transport to cell membrane, leading to

285 ch as the prion protein, and correlated with a delay in translocation initiation.

286 Our results demonstrate a delay in transmission of action potentials by the gang

287 odel of diffusive pathogen transfer predicts a delay in transmission that depends both on the distanc

288 Patients with a delay in treatment of 21 weeks or more compared to a d

289 Both interruptions led to a delay in triple-helix folding, with the 15-residue int

290 y, comparisons with other phyla suggest that a delay in trunk development is a feature of indirect de

291 lysis of normal melanocytes, associated with a delay in tumor progression.

292 bese diabetic (NOD.Ncf1(m1J)) mice exhibited a delay in type 1 diabetes (T1D) partially due to blunte

293 the offender population is a consequence of a delay in typical development, rather than a distinct a

294 f Obstetricians and Gynecologists recommends a delay in umbilical cord clamping in term neonates for

295 n to lung tight junctions in situ along with a delay in up-regulation of claudin-4.

296 lin-resistant S. aureus coinfection, despite a delay in viral clearance.

297 ups of New World begomoviruses, resulting in a delay in viral DNA accumulation and symptom appearance

298 bility of astrocytes to WNV-MAD78 was due to a delay in viral genome replication and an interferon-in

299 ction, reduced the HIV reservoir, and caused a delay in viral rebound after ART interruption.

300 e variation in population growth rates, such a delay in winter-onset would enable a population growth