ライフサイエンスコーパス: be delayed

1 efore, diagnosis and treatment of sepsis may be delayed.

2 ce antigen-but anticancer therapy should not be delayed.

3 terococcal bloodstream infections (EBSI) can be delayed.

4 nces for patients, especially when diagnosis is delayed.

5 solution of the ribosomal DNA (rDNA) repeats is delayed.

6 ced, but also the onset of pancreatic cancer is delayed.

7 nting perinatal HIV infection when treatment is delayed.

8 ation of de novo methyltransferases Dnmt3a/b is delayed.

9 early after transplant, although the effect is delayed.

10 mutants, the degradation of apoptotic cells is delayed.

11 ult, expression of the incoming viral genome is delayed.

12 impairment or blindness if medical attention is delayed.

13 repair of patients with open-globe injuries is delayed.

14 ular comorbidities, if free flap anastomosis is delayed.

15 sitivity, and consequently, EVL-YSL movement is delayed.

16 is increased and osteoblast differentiation is delayed.

17 e when results from definitive viral testing are delayed.

18 h this effect decreased the longer treatment was delayed.

19 by US28; however, UL33-induced tumor growth was delayed.

20 cted BHK-21 or Vero cells, virus replication was delayed.

21 t transplantation; however, survival benefit was delayed.

22 on yielded similar protection when treatment was delayed.

23 doplasmic reticulum to and through the Golgi was delayed.

24 cosidase H resistance in Rab6 depleted cells was delayed.

25 eral regions of late-replicating euchromatin were delayed.

26 pFUS/MSC treatments were delayed 14 days, when surgical inflammation subside

27 Local calcium upstroke was delayed (23.9+/-4.9 versus 10.3+/-1.7 milliseconds;

28 ings revealed that proteasome inhibition can be delayed 3-4 days after denervation but is required th

29 discharged in the next 6 hours; 17,656 (2%) were delayed 48-72 hours; 31,389 (3.1%) died in hospital

30 Diagnoses were delayed a median of 27 days.

31 ord contains many instances where speciation is delayed-a phenomenon about which we have a poor under

32 tion of the repressive histone mark H3K27me3 is delayed after DNA replication, indicative of a decond

33 in the PH tail, global value maximum signals are delayed and sustained in the AH body.

34 of anaphylaxis, where reactions to alpha-gal are delayed and thus may be overlooked.

35 Hence, the diagnosis can be delayed and even missed without a high degree of susp

36 .g., fungal cultures and histopathology) can be delayed and insensitive.

37 adoption of this surgical technique may have been delayed and its potential benefits possibly under-e

38 regulatory system results in CCP maturation being delayed and/or stalled, hence impairing global rat

39 nt (Csf2(-/-)) mice, inflammation resolution is delayed and conditioning-lesion-induced regeneration

40 The increase in pre-mRNA is delayed and due to enhanced transcription and likely

41 beta cells, whereas beta cell failure in T2D is delayed and progressive.

42 opment of the membrane excitability of PVINs is delayed and reaches maturity only by adulthood, while

43 gut of Ascl1(-/-) mutant mice, neurogenesis is delayed and reduced, and posterior gliogenesis impair

44 When feedback was delayed and blurred based on the hemodynamics of fMR

45 The onset of biofouling was delayed and minimized in rectangular reactors operat

46 pression of some cell wall-modifying enzymes was delayed and others increased in the absence of RIN.

47 logy was grossly intact, but CNS myelination was delayed and overall myelin volume was decreased.

48 pha was rapid and transient in WT MGCs, this was delayed and prolonged and correlated with increased

49 t (KO) animals wherein EAE disease induction was delayed and reduced disease severity was observed.

50 erexpression of ARGOS8, nodal root emergence was delayed and the promotional effect of ACC on nodal r

51 aximum time of plasma flavanol concentration was delayed and these animals presented higher levels of

52 and tumor necrosis factor alpha (TNF-alpha) were delayed and low in CAST mice compared to BALB/c mic

53 than rTg4510, atrophy and tau histopathology are delayed, and a different behavioral profile is obser

54 HSF1 in germ cells, transcription occurs but is delayed, and progeny of stressed C. elegans mothers f

55 The juvenile-to-adult transition is delayed, and proximal distal-patterning is abnormal i

56 Maturation of sensory receptor precursors is delayed, and they never attain a fully differentiated

57 argely in hepatocytes, canalicular secretion was delayed, and 6-CF appeared in the blood.

58 cking of the mutant Dsg2 to the cell surface was delayed, and a pool of the non-palmitoylated Dsg2 co

59 p following the weekend, the circadian phase was delayed, and after-dinner energy intake and body wei

60 The reduction of both As and Fe was delayed, and As(III) accumulated in birnessite-rich

61 sure after sunset was increased, sleep onset was delayed, and nocturnal sleep duration was reduced.

62 Clinical ECM progression was delayed, and overall survival was significantly prol

63 required neurosurgical intervention, 25 (9%) were delayed, and 7 (3%) were asymmetric.

64 ast, the axon degeneration and demyelination were delayed, and macrophage accumulation was reduced in

65 lower risk of linked partner infection than was delayed ART (hazard ratio, 0.07; 95% CI, 0.02 to 0.2

66 high fox density habitat, bait uptake might be delayed as other food and prey options for foxes are

67 Conclusions about the prognosis should be delayed at least 72 h after arrest to allow for the c

68 This quadruple mutant is delayed at cell separation upon release from mitotic

69 s revealed that sugaring in Thompson raisins was delayed at low temperatures (5 & 15 degrees C) compa

70 The wound healing process was delayed at the 3(rd) and 7(th) days after wounding i

71 activate GL promoters but that this activity is delayed, at least in part, by the CTCF insulator, whi

72 Empirical antimicrobial therapies should not be delayed based on the presumption of noninfectious syn

73 ntroduction in the remaining 2 countries has been delayed because of the global shortage of IPV, maki

74 ) and an increase in reports of medical care being delayed because of wait times for appointments (di

75 of all-oral direct-acting antivirals (DAAs) is delayed because of differing regulatory requirements.

76 hase transition, MPS1 S281 dephosphorylation is delayed because PP2A-B55 is negatively regulated by C

77 standing of the recent West African outbreak were delayed because of late recognition and because aut

78 cation of the first GES-5 K. oxytoca isolate was delayed, being identified by WGS.

79 cation of the first GES-5 K. oxytoca isolate was delayed, being identified on WGS.

80 Presentation was delayed beyond infancy with proximal muscle weakness

81 nction in C. elegans, cytokinetic abscission is delayed but can be completed, suggesting the existenc

82 Tumor xenograft growth was delayed but not suppressed in xCT-KO cells, which in

83 ME recruitment of leukocytes was delayed but persisted far longer than in WT mice.

84 (CP) development in the somatosensory cortex is delayed, but it is unclear how this contributes to al

85 sed in adiponectin-deficient mice, mortality was delayed, but not decreased, in mice deficient in bot

86 travenous tissue plasminogen activator would be delayed by 12 minutes, but MT would be performed 91 m

87 travenous tissue plasminogen activator would be delayed by 7 minutes and MT performed 94 minutes earl

88 years, disappearance of the ozone hole will be delayed by a few years, although there are significan

89 line in tissues throughout the body that may be delayed by caloric restriction (CR).

90 ow that the diagnosis of type 1 diabetes can be delayed by treatment with a FcR non-binding monoclona

91 The disastrous shear avalanches have, then, been delayed by forming a stable plastic-flow stage in t

92 withdrawal of life-sustaining treatment had been delayed by up to a further 36 hours.

93 tamate receptors (mGluR1s) when the CF input is delayed by 100-150 ms from the first PF input in both

94 ale fruit flies, onset of the daytime siesta is delayed by ambient temperatures above 29 degrees C.

95 in creates these by loop extrusion, until it is delayed by CTCF in a manner dependent on PDS5 protein

96 xes are stabilized and ILV membrane scission is delayed by Doa4, which is the ubiquitin hydrolase tha

97 human immunodeficiency virus type 1 (HIV-1) is delayed by HIV type 2 (HIV-2) in individuals with dua

98 If action to reduce per capita steel stocks is delayed by more than five years, then it is likely in

99 growth to investigate how the invasion front is delayed by resection, and how this depends on the den

100 ne-dependent ACx plasticity even when the US is delayed by several seconds following CS offset.

101 utic efficacy of traditional antidepressants is delayed by several weeks.

102 insulins are suboptimal: The onset of action is delayed by slow dissociation of the insulin hexamer i

103 l factor dlg-1 Accumulation of DLG-1 protein is delayed by ZEN-4, acting in concert with its binding

104 Excess mortality was delayed by 1-2 years in 18 countries (46%).

105 days earlier by cobas CMV, whereas clearance was delayed by 12.8 days.

106 Final identification of the NB-PC pathogen was delayed by 2 days (P < 0.01) versus the PB-PC group.

107 Onset of cognitive decline was delayed by 3 years in individuals with higher educat

108 ding, infertility onset in knock-out females was delayed by 4 weeks.

109 IPV except Egypt, where introduction of IPV was delayed by a global shortage.

110 we show that the establishment of the virus was delayed by a year and that the ensuing outbreak was

111 activity, the timing of RhCMV seroconversion was delayed by an average of 12 weeks.

112 Muscle regeneration was delayed by angiotensin II infusion, mimicking aging

113 movement (ERS period), the first beta burst was delayed by approximately 100 milliseconds when an in

114 preexisting clots, even when administration was delayed by as little as 10 minutes, while it concurr

115 TE transposition in fly fat body cells that was delayed by dietary restriction.

116 ound-healing model demonstrated that closure was delayed by EVs released under the control of TBC1D3.

117 e was strongly down-regulated, and flowering was delayed by high temperatures irrespective of Ppd-H1

118 of somatic cells in milk after LPS treatment was delayed by HS.

119 hile the conventional electroencephalography was delayed by several hours (median [interquartile rang

120 tery dilation observed in untreated MFS mice was delayed by SIL treatment, and the severe emphysema-l

121 This discovery was delayed by the current paradigm confusing viruses wi

122 This fast relapse was delayed by the further addition of anti-PD-1.

123 terioration of all parameters studied, which was delayed by the use of LP.

124 Formation of MDA and HHE was delayed by tocopherols, the tocopherol mix Covi-ox(R

125 In adipose tissue, PER2 mRNA rhythms were delayed by 0.97 +/- 0.29 hr (p < 0.01), indicating

126 Detected rate shifts were delayed by 5-15 Myr with respect to the acquisition

127 late meals, however, plasma glucose rhythms were delayed by 5.69 +/- 1.29 hr (p < 0.001), and averag

128 he timing of emergence of consecutive leaves were delayed by exposure to radiation.

129 it in 2 (8%), were terminated in 2 (8%), and were delayed by more than 1 year in 3 (13%).

130 Thus, sequence evolution is delayed compared to genome evolution by gene gain and

131 n after infection via the ocular conjunctiva is delayed compared with infection via the standard intr

132 thermore, the onset of PREX1 phosphorylation was delayed compared with the phosphorylation of AKT, su

133 Growth of mutants was delayed compared with WT.

134 tion of fish oil in the sorghum wax oleogels were delayed considerably compared to free fish oil, whi

135 acute care of cardiovascular conditions may be delayed, deferred, or abbreviated during the COVID-19

136 ropriate staging is essential and should not be delayed due to pregnancy, management guidelines are l

137 Endoscopy or urgent surgery should not be delayed during pregnancy if indicated.

138 Timing was delayed following one cold winter.

139 cological diversification of marine reptiles was delayed following the EPME.

140 Oncologically urgent cases may be delayed for 6(-12) weeks without jeopardizing oncolog

141 corrosion of bR integrated Cu(2)O electrodes is delayed for about 36 times; The photocurrent of bR in

142 studies, the administration of EBOTAb dosing was delayed for 48 or 72 hours after challenge, resultin

143 Flowering time was delayed for most grass species with increasing mean

144 growing NSN in one patient in whom diagnosis was delayed for over 3 years.

145 Recovery was delayed for the miR-216a and miR-216b KOs following

146 Crucial treatments were delayed for many patients during the COVID-19 pande

147 Such contact-inhibition can be delayed from Day 21 to Day 42 by switching EGF-contai

148 The initiation of this sliding window is delayed further north, which may be a response to a p

149 ife was poor; diagnosis of wild-type ATTR-CM was delayed >4 years after presentation with cardiac sym

150 r in group 2, if the implantation of kidneys was delayed >48 hours (P < 0.01).

151 ients with GTR had worsened survival when RT was delayed >8 weeks.

152 When blocking of TLR4 signaling after injury was delayed, however, this treatment failed to reduce po

153 CAPT should be delayed if receiving systemic steroids or antihistami

154 Diagnosis of osteoid osteoma may be delayed if secondary radiological findings such as mu

155 ddition, flowering phenology in a given year was delayed if summer temperatures were high the previou

156 rly hallmarks of Wallerian degeneration (WD) are delayed in aged flies.

157 A velocity, we find that activation kinetics are delayed in aged MuSCs, suggesting that changes in st

158 CD4(+) T cells lose their location bias and are delayed in antigen recognition, proliferative expans

159 , a large population of host hypocotyl cells are delayed in cell cycle exit and maintained in the pro

160 (fbRF) elicits responses that are slower and are delayed in comparison with those resulting from the

161 in variants with an AAA motif instead of EAL are delayed in development, similar to null mutants.

162 demonstrate that: (i) language N400 effects are delayed in onset by concurrent music processing only

163 ivation of MAPKs and PI3K signaling pathways are delayed in P2-deficient mouse bone marrow-derived ma

164 induced by oral P2Y(12) receptor antagonists are delayed in patients with ST-segment-elevation myocar

165 transitions of polarised cell intercalation are delayed in sdk mutants, in particular in rosettes.

166 This analysis identified mutants that are delayed in the initiation of sporulation, defective

167 -derived myogenic cells from EphA7(-/-) mice are delayed in their expression of differentiation marke

168 O-8 supports the recommendation that PBC not be delayed in favor of an NPBC in patients with partiall

169 on suggests that large transport cargoes may be delayed in passage through the nuclear pore channel,

170 thers of heavier infants were less likely to be delayed in subsequent reproduction, but the estimated

171 Colectomy should not be delayed in this setting.

172 f onchocerciasis or lymphatic filariasis has been delayed in Central Africa because of the occurrence

173 ancer follow-up or imaging appointments have been delayed in many clinics around the world.

174 the Qinghai-Tibetan Plateau, whereas it has been delayed in others.

175 eased during cold storage, all these changes being delayed in treated fruit, with the greatest differ

176 The in situ phenotypic switch of macrophages is delayed in acute injury following irradiation.

177 e the timing of activity onset and acrophase is delayed in aged mice compared to younger mice.

178 ic MDSC (M-MDSC), although tumor development is delayed in E0771 tumor-bearing mice.

179 Neutrophil recruitment is delayed in early wounds (12 hours and day 1), whereas

180 rt for the first time that micropore closure is delayed in elderly subjects in a manner that is depen

181 hat transitioning from mitosis into G1 phase is delayed in galectin-8-knockout HaCaT cells after cell

182 or acn1 mutants, the acs acn1 double mutant is delayed in growth and sterile, which is associated wi

183 usually go through an all-female stage), and is delayed in males.

184 we additionally reveal that axon initiation is delayed in posterior vagus motor neurons independent

185 e development of Southern Hemisphere warming is delayed in reconstructions, but this apparent delay i

186 e showed that light-induced stomatal opening is delayed in three TAG catabolism mutants (sdp1, pxa1,

187 eak of the systolic forward compression wave was delayed in AS, consistent with a delayed peak aortic

188 Nonetheless, leukemogenesis was delayed in both models with a shared core set of DNA

189 LRP growth was delayed in cell-death-deficient mutants lacking the

190 Comet assays demonstrated that DNA repair was delayed in cells silenced for the expression of ZNF2

191 Muscle injury repair was delayed in CX3CR1(GFP/GFP) mice as compared with wil

192 he clearance of these newly identified acids was delayed in fatal cases.

193 This species-conserved peak was delayed in females and marked a reorganization of ex

194 milar in both groups, but puberty completion was delayed in GHRH(DeltaERalpha) females.

195 Early motor development was delayed in half of the patients.

196 generation) in control mice, but this effect was delayed in interleukin 6-deficient mice.

197 Recurrent parasitaemia was delayed in patients treated with ACTs containing mef

198 Dynamic analyses showed that VL decay was delayed in PICU patients, especially in those treate

199 Mobilisation of endosperm alpha-cruciferin was delayed in prt6 seedlings.

200 torage but the rate of changes significantly was delayed in Put- and Spd-treated fruits.

201 turonan-I recognized by the CCRC-M2 antibody was delayed in root hair cells (trichoblasts) compared w

202 The impact of the pandemic on mortality was delayed in several countries, pointing to a window o

203 This alpha-actin switch was delayed in systemic CAP2 mutant mice, and myofibrils

204 the promoters of the genes whose activation was delayed in the absence of Plag1.

205 Our analyses demonstrate that tumor growth was delayed in the absence of signaling by PDGF-DD.

206 nce from the lung tissue after LPS challenge was delayed in the aged group.

207 ision of the large Chlamydomonas chloroplast was delayed in the cells lacking F-actin; as this organe

208 The 28-day platelet recovery was delayed in the haploidentical group compared with th

209 The time to first brood was delayed in the highest FPW (0.04%) treatment.

210 Flowering was delayed in the hk5 hk6 mutant and the panicle was si

211 vitro, and that in vivo production of GM-CSF was delayed in the lungs of MR1(-/-) mice.

212 g from colonies grown on MacConkey soft agar was delayed in the mutant in comparison to the wild type

213 t the timing of spindles within the SO cycle was delayed in the patients.

214 n; however, time to source-control procedure was delayed in the prolonged and intermediate groups com

215 baseline HBV, HBV-R diagnosis and treatment were delayed in 7 cases and possibly 7 others.

216 onged inflammatory responses in the lung and were delayed in alveolar epithelial regeneration during

217 quency and flow cytometry, but the responses were delayed in older compared with young adults.

218 hyroid cancer development and local invasion were delayed in only the PVPV-Akt1 knock out (KO) mice i

219 Go condition, the onsets of beta ERD and ERS were delayed in PD patients.

220 ants contained more starch, less sucrose and were delayed in sprouting.

221 cally than those of mature T cells, but RTEs were delayed in their transition to central memory, disp

222 ot only visual, but also auditory plasticity is delayed, including the experience-dependent expansion

223 e find that homology-directed repair of DSBs is delayed, indicating antagonism between nuclear migrat

224 Chromatin compaction in mutants is delayed into developmental time periods when zygotic

225 During winter, the nap onset was delayed, its duration increased and its efficiency i

226 All implants were delayed loaded and were fixed with non-splinted scr

227 y mating, but these deleterious effects must be delayed long enough for successful reproduction.

228 DD), and the rate of retinal vascularization was delayed (mean, 0.11 DD/week vs. 0.23 DD/week) in tho

229 are removed by macrophages, but if apoptosis is delayed, neutrophils can cause extensive tissue damag

230 diagnosed at initial presentation; diagnosis was delayed, on average, by 29 months (range, 0.25-288 m

231 s of immune responses in PRRSV-infected pigs are delayed onset and low levels of virus neutralizing a

232 But, if regeneration is delayed or absent, blue-cone synaptogenesis increases

233 wake, induces DSBs, and their repair in mice is delayed or prevented by subsequent wake.

234 In addition, expression of SOST is delayed or suppressed; resulting in active WNT signal

235 We found that the Camui response is delayed or terminates earlier than the FRESCA respons

236 1, polarization was compromised, cytokinesis was delayed or failed, and 50% of embryos died during de

237 nrecipients (unexposed) for whom transfusion was delayed or not given.

238 In S-phase, the NF-kappaB response was delayed or repressed, while cell cycle progression w

239 individual's average, sleep onset and offset were delayed (p < 0.0001), duration was shorter (p < 0.0

240 0.01-0.26) for every 5 days that recurrence was delayed, p = 0.0407.

241 feedback channeled through the Ras1/2 GTPase is delayed, pinpointing its time scale and its contribut

242 Consequently, treatment is delayed, posing significant risks to maternal and fet

243 rt that in PML(-/-) cells, Sp100 degradation is delayed, possibly because colocalization and merger o

244 approach, we found that RUSH VSVG transport was delayed pre-trans Golgi.

245 The functional effect of complex formation was delayed procarboxypeptidase activation due to increa

246 ence of p35, oligodendrocyte differentiation was delayed, process outgrowth was truncated in vitro, a

247 In C57BL/6J mice podocyte effacement is delayed, prolonging normal renal function.

248 ontaneous and induced AD-like lesions, there was delayed re-epithelialization.

249 Continuous glucose monitor (CGM) readings are delayed relative to blood glucose, and this delay is

250 develop bilateral mechanical allodynia that is delayed relative to the onset of spontaneous pain.

251 tion in FTC/TAF but not TAF-treated macaques was delayed relative to controls (P = .005 and P = .114)

252 However, these calcium signals were delayed relative to channel activation produced by

253 Synaptic changes in L2 were delayed relative to L5, requiring 48 h of SAT to dr

254 The key finding at physical examination was delayed relaxation after repetitive contractions.

255 4.1%) of 248, and 29 (11.7%) of 247 patients were delayed responders, respectively.

256 RISE, 9% to 10% of ranibizumab-treated eyes were delayed responders.

257 s against Candida, but their release of NETs is delayed, resulting in impaired control of fungal grow

258 We find that every day ART initiation is delayed results in a 39% increase in the recrudescenc

259 Hence, the likely mechanism of action is delayed RNA chain termination.

260 The standard approach to treat cataracts is Delayed Sequential Bilateral Cataract Surgery (DSBCS)

261 s challenging diagnosis, especially when PCR is delayed, shows negative results, or is not available.

262 The time to viremia was delayed significantly by treatment with a broadly ne

263 degeneration was complete at 1 mo of age but was delayed significantly in Nphp5(-/-);Nrl(-/-) (cone o

264 epopulation of the lesion site by astrocytes was delayed significantly.

265 Abeta fibrillization was delayed specifically in the presence of N-terminal d

266 l-cycle studies indicated that the CHH cells were delayed specifically in the passage from G2 phase t

267 Secondary outcome was delayed splenectomy rate.

268 The appearance of infected cells is delayed, the levels of intracellular viral proteins a

269 e Mreg(-/-) mouse where phagosome maturation is delayed, there was a temporal shift in the release of

270 Filament formation is delayed to a predetermined distance in space, defined

271 R-mediated up-regulation of GL transcription is delayed to the mature B-cell stage is presently unkno

272 networks was not achieved if IL-17A blockage was delayed two or more hours postreperfusion.

273 that turnover of the entire adhesion complex was delayed under these conditions.

274 ondrial protective miR-210 inhibition should be delayed until after the initial burst of proliferatio

275 Crucially, sister chromatid separation must be delayed until all the chromosomes have attached to th

276 Surgical intervention might be delayed until symptoms are severely limiting and cann

277 which the generation of BCR-bearing IgLkappa is delayed until after IgLlambda becomes the dominant is

278 To prevent genome instability, mitotic exit is delayed until all chromosomes are properly attached t

279 singly, EfnA1-stimulated EphA2-SOCS2 binding is delayed until EphA2 has been internalized into endoso

280 nfection in the animals, even when treatment is delayed until external signs of respiratory syncytial

281 ell undergoes superinfection, then the lysis is delayed until host/phage ratio becomes more favorable

282 unctions in Drosophila melanogaster gastrula is delayed until mesoderm is internalized, despite the e

283 h curative intent, in which active treatment is delayed until the cancer shows signs of significant p

284 le factor 1-alpha expression in the MP group was delayed until 20 h.

285 ary angiography or coronary angiography that was delayed until after neurologic recovery.

286 despite RPV LA PrEP, WT HIV-1 dissemination was delayed until genital and plasma RPV concentrations

287 over the weekend than those whose surgeries were delayed until a weekday (7.9% vs 3.1%, P = 0.02).

288 US population aged >=65 years if vaccination were delayed until October 1.

289 de deaf children whose first exposure to ASL was delayed up to 7 years (n = 12).

290 In mice, tumour progression is delayed upon pharmacologic or genetic inhibition of M

291 Liver regeneration in rodents is delayed when platelets are inhibited.

292 ases the mean environmental temperature, but is delayed when warming increases the amplitude of seaso

293 radation of PP2CA, however, such degradation was delayed when incubated with protein extract prepared

294 hotopic PDAC models, pancreatic tumor growth was delayed when iNOS inhibition was combined with radio

295 ral structure on appearance-evoked responses was delayed when listeners were focused on the scenes re

296 l diagnosis of ARN, but treatment should not be delayed while awaiting PCR results.

297 reduced in the stem and siliques and bolting was delayed, while the opposite phenotype was observed i

298 eruse of tryptase measurement; its treatment is delayed, with little use of epinephrine; and its unde

299 In addition, granulation phase resolution is delayed, with persistent blood vessels and reduced de

300 s, the degradation of accumulating fragments is delayed within natural protein aggregates such as pos