ライフサイエンスコーパス: restore

1 rption and hydrogenation reactivity could be restored.

2 an regain normal orientation if SF length is restored.

3 nd bulk hBN, where the center of symmetry is restored.

4 the beta4 subunit into either the MHb or IPN restored a "stop" signal on nicotine self-administration

5 Co-depletion of POT1B or BRD2 with TRF2 restores a canonical DNA damage response at telomeres, r

6 eration in Xenopus embryonic aggregates that restores a mucociliated epithelium from mesenchymal cell

7 Few studies assess the potential for restoring a deteriorating ecosystem that is on a transit

8 afficking of several transmembrane proteins, restored Abeta-induced impaired gap junction coupling be

9 mogenetic inhibition of the PFC-BNST pathway restored abnormal responses to predator odor in alcohol-

10 omplex by antagonizing PD-L1 and, therefore, restores activation of T cells similarly to the antibodi

11 DAA treatment restored ADCC ability and reduced programmed death recep

12 Chronic leptin treatment of ob/ob mice restores adipose tissue sympathetic innervation, which i

13 initial P3HHT film thickness is essentially restored after de-doping while p(g2T-TT) remains substan

14 nule convergence and cytolytic function were restored after IL-2 stimulation.

15 ing hepatitis C virus (HCV) infection can be restored after viral eradication with direct acting anti

16 t therapeutic targeting of blood vessels may restore aged endocrine tissue function.

17 ) during apneas contributes to awakening and restoring airway patency.

18 1 recombinant virus expressing cpIAP did not restore all LAT functions.

19 Soils were sampled from intact, degraded and restored alpine grasslands at altitudes ranging between

20 While efforts to restore and protect mangroves appear to be effective ove

21 ich has consequences of blood flow not being restored and tissue damage being observed in histology.

22 Restoring animals to normoxic conditions results in cyto

23 patients, and may lead to a new strategy to restore anti-tumor immunity by inhibiting pathways of fo

24 the steroidogenesis pathway is sufficient to restore anti-tumor immunity.

25 , and immune checkpoint blockade effectively restores antitumor immunity and results in a significant

26 possibility that targeting this cytokine may restore antiviral mechanisms.FUNDINGThis study was suppo

27 Reduction of IP3R1 in epsin-deficient mice restores atherosclerotic progression.

28 for phosphotransfer activity were unable to restore atxA transcription to parent levels, suggesting

29 LAMTOR1 silencing or mTOR inhibition restores autophagy and induces apoptosis in p27(-/-) cel

30 this intermediate state and instantaneously restored awake dynamics and the top task performance whi

31 l striatum of D2R knockout mice, this mutant restored basal locomotor activity and cocaine-induced lo

32 reporter system, mutagenesis to disrupt and restore base pairing revealed that the MTE interacts wit

33 vity ameliorated the skin immunopathology by restoring beneficial AHR signaling.

34 EC-specific ablation of Gja1 restores beta-cell expansion in the aged pancreas.

35 +PL) to RN at 50% of standard concentrations restored blastocyst development, hatching, and cell numb

36 nhibition of adenylyl cyclase with SQ 22,536 restored BLT1(-/-) BMN apoptosis, FasL and CD36 expressi

37 of the affected lymphocytes with MAGT1 mRNA restored both N-glycosylation and receptor function.

38 e enzyme, fatty acid amide hydrolase (FAAH), restored both synaptic and behavioral alterations.

39 RESTORE BRAIN was an international, randomised, double-b

40 tagonist S44819 after Recent ischemic Event (RESTORE BRAIN) aimed to evaluate the safety and efficacy

41 tions are reverted when membrane fluidity is restored by a chemical fluidizer.

42 orf8-, Ccz1- and Mon1A/B-deficient cells and restored by a constitutively active Rab7.

43 The original 3D layered structure can be restored by a solvothermal process with pyridine, so tha

44 rway smooth muscle cell migration, which was restored by Abi1 rescue.

45 paired in vitro serum control of KP that was restored by adding healthy serum.

46 lines of affected individuals that could be restored by addition of heparin, a GAG similar to hepara

47 2 levels in lymphoid organs, and this can be restored by adoptive transfer of wild-type T cells or ad

48 he 22q11DS calcium abnormality could also be restored by application of antipsychotics.

49 hibition, increased by I(Kr) inhibition, and restored by combined I(NaL) and I(Kr) inhibitions.

50 hage were observed at 1 and 7 days, and were restored by day 28 post-blast.

51 n diabetic rat corneas, which were partially restored by fenofibrate treatment.

52 ith a thymidine-kinase promoter but could be restored by fusion with the 100 bp minimum transcription

53 reduced axonal mitochondrial content that is restored by genetic inhibition of AMPK and autophagy.

54 ce in germ-free mice, but their presence was restored by gut re-colonization.

55 Capsid stability was restored by introduction of specific changes to the oute

56 e of oxygen consumption, which was partially restored by PDK4 inhibition with dichloroacetate.

57 iboly and microtubule defects were partially restored by pregnenolone treatment.

58 R responses in PI4KIIalpha-deficient DCs are restored by reexpression of wild-type PI4KIIalpha, but n

59 t in long-term object recognition memory was restored by the administration of a selective Kv7 channe

60 hibitors are effective immunotherapeutics to restore cancer- and virus-induced exhausted CD8(+) T cel

61 de and stands apart from the current DBOs in restoring carbapenem activity against OXA-CRAB as well a

62 ut not mice with established cardiomyopathy, restored cardiac myocyte mitochondrial membrane potentia

63 spensable for controlling viral replication, restoring CD4+ T cells, and preventing opportunistic inf

64 on therapy with CD40 agonist and Flt3 ligand restores cDC1 abundance to normal levels, decreases cDC1

65 Remarkably, iron supplementation restores cell proliferation under both pharmacologic and

66 icits well-orchestrated programs that either restore cellular homeostasis or induce cell death depend

67 o, upregulated glycolytic ATP production and restored cellular proliferation.

68 rocesses, could be compensatory responses to restore cerebellar GABAergic tone and cerebellar cortica

69 stance and provide a therapeutic strategy to restore chemosensitivity.

70 The addition of PS restores cholesterol transport to the ER.

71 improving contractility and relaxation while restoring coronary perfusion pressure.

72 D requires a multipronged approach, not only restoring cutaneous barrier function, microbial flora, a

73 invariably acquired revertant mutations that restored cysteine 181.

74 Spinal treatment can restore diaphragm function in all animals 1 month follow

75 Strategies to restore disrupted myocardial calcitonin signalling thus

76 d carriers were also able to deliver RNPs to restore dystrophin expression in DMD mice and significan

77 ur findings indicate that they may, in part, restore ecological functions reflective of the past seve

78 summer probably because increased meltwater restored efficient channelized flow.

79 Checkpoint inhibitors are effective in restoring exhausted CD8(+) T cell responses in persisten

80 morphine abstinent mice were correlated with restored expression of key MSN and neural activity marke

81 Optimal restored floodplain conditions for photolysis would maxi

82 These reductions were not restored following 12-weeks of exercise training implyin

83 bust regeneration of corticospinal axons and restore forelimb function after spinal cord injury(1); h

84 and proposed a novel algorithm to detect and restore fragmented ridges in incomplete fingerprints.

85 , the epitope expressed from the gB promoter restored full gB-CD8 immunodominance to 50%.

86 suggesting that restoring muscle BDNF might restore function.

87 preceding the A4G point mutation (2stop+A4G) restored G protein expression but retained lower F prote

88 rapeutic potential of stimulation of ChIs to restore gait and balance, and to prevent falls in PD.SIG

89 ety, of achieving some level of remission to restore generic and disease-related HRQoL and one's abil

90 Genetically restoring Gli3 repressor rescues the decreased indirect

91 ter-regulatory responses whose purpose is to restore glucose homeostasis.

92 at regulates tubulin acetylation, in CF mice restores growth and inflammatory phenotypes to wild type

93 o heart failure mice silences miR-370-3p and restores HCN4 mRNA and protein and I(f) in the sinus nod

94 become clear that ARV therapy does not fully restore health, leaving individuals at elevated risk for

95 ehavioral inhibition play different roles in restoring health.

96 Therapeutics that restore healthy mitochondrial function hold promise for

97 rythrophagocytes, and Nfe2l2/Nrf2 deficiency restored heme-suppressed inflammation.

98 nd exhibited p53 stabilization, successfully restored hepatocyte formation from hESCS.

99 Following TSD, two nights of recovery sleep restored hippocampal connectivity to baseline levels, bu

100 Lacritin monomer restores homeostasis via autophagy and mitochondrial fus

101 WE1 loss increases RAD51 levels to partially restore HR, whereas KAT5 depletion rewires double strand

102 , reintroduction of BRCA1 or 53BP1 depletion restored HR and rescued the ability of cells to maintain

103 ling mediator Traf6 in RLR deficient embryos restored HSPC numbers.

104 mitochondrial antioxidant reduced AF burden, restored I(Na), I(Ca,L), I(Kur), action potential durati

105 arance of these same microbes in WT mice was restored if active thrombin was administered to the peri

106 Discrimination was restored if the face-like stimuli were presented upside-

107 ogated Ido1 expression and was sufficient to restore IgE production and worm expulsion in inulin-fed

108 CS3 in macrophage and T cells, respectively, restored IL-12 and IFN-gamma cytokine levels and BMM -T

109 utative receptor could provide strategies to restore immune homeostasis in these diseases.

110 th booster of subtype C pox-protein vaccines restored immune responses, and slowed response decay com

111 ating factors as a target of intervention to restore immunity.

112 PLA2 synergizes with fatty acid-free diet to restore immunogenicity and selectively reduce mutant PIK

113 Finally, NOX4 inhibition restored immunotherapy response in CAF-rich tumors.

114 a healthy microcirculation and suggest that restoring impaired microvascular supply, regardless of d

115 Postoperative EZ integrity was restored in 52 eyes (60%), ELM integrity was restored in

116 restored in 52 eyes (60%), ELM integrity was restored in 54 eyes (62%), and cystoid spaces of variabl

117 ng BETi treatment, c-Myc levels were rapidly restored in BETi-P/R sAML cells.

118 tly asymmetric during S phase but is rapidly restored in G2, whereas mCHG remains asymmetric througho

119 LRP growth was restored in ore1-2 knockout plants by genetically induci

120 is diminished in the Deltabb0326 mutant and restored in the complemented bb0326+ cells, leading us t

121 HER2 therapy sensitivity is restored in the fibroblast cocultures by combination tre

122 ondrial network morphology was substantially restored in the HVT-DeltavNr-13-infected cells.

123 sing sequence at the terminal break site was restored in the recircularized plasmid in control cells

124 Our algorithm can effectively restore incomplete fingerprints.

125 formances once a pure carbon dioxide feed is restored, indicating a negligible long-term impact of ni

126 ansfer of WT neutrophils into Par4(-/-) mice restored inflammation resolution, reduced cardiac ruptur

127 to switch off nuclear mechanotransduction to restore initial chromatin state.

128 s of mice treated with antibiotics partially restores intestinal motility.

129 , theoretically, collateral circulations may restore it.

130 s of BH3 mimetics were highly synergistic in restoring killing of CLL cells.

131 the glucocorticoid receptor antagonist RU486 restored KLF15 and POX expression levels in mutant BAT,

132 Restoring lipoprotein function with ApoA-I raising agent

133 immunotherapies that reverse CNS damage and restore lost neurological function across a spectrum of

134 ast cancer and prostate cancer spheroids and restored lumen filling in the presence of HR-targeting a

135 lasts from PSEN1 familial AD patients, which restores lysosomal proteolysis, calcium homeostasis, and

136 preventing Mad1 from binding to Megator/Tpr restores Mad1 accumulation at kinetochores, the fidelity

137 nights of recovery sleep are needed to fully restore memory function and hippocampal-memory associati

138 tivity to baseline levels, but did not fully restore memory performance nor its associations with hip

139 Importantly autophagy-restored mice still succumb earlier due to an increase i

140 evented platelet-neutrophil aggregation, and restored microvascular blood flow in lung arterioles of

141 Activation of PPAR-gamma partially restored mitochondrial membrane potential and IFN-gamma

142 The ensuing proteasomal degradation of FNIP1 restores mitochondrial activity to preserve redox homeos

143 Restoring mitochondrial bioenergetics in the colonic epi

144 cardiac L-type calcium channel (AID-TAT) on restoring mitochondrial metabolic activity, and preventi

145 tion with SR-17018 in morphine-tolerant mice restores morphine potency and efficacy, whereas the onse

146 SAP2 silencing fully restores mortality of the mosquitoes, whereas SAP2 overe

147 sh are able to repair spinal cord tissue and restore motor function after complete spinal cord transe

148 s priorities for protecting, connecting, and restoring mountain landscapes may otherwise be misguided

149 inc to cells harboring hibernating ribosomes restores Mrf instability and dissociates Mpy from the ri

150 e role of the interleukin-10 (IL-10) axis in restoring murine microglia homeostasis following a perip

151 Genetic ablation of the Cdkn2a locus restored muscle stem cell properties in lamin A/C-null d

152 s of Kennedy's disease (KD), suggesting that restoring muscle BDNF might restore function.

153 direct cell transplantation into the CNS to restore myelin has been tested in animal models of sever

154 apacity of transplanted neural stem cells to restore myelin in the context of PLP overexpression.

155 etent tadpoles with immune-suppressing drugs restores myeloid lineage-controlled cellular mechanisms.

156 ubiquitin E3 ligases in NatB mutants did not restore NAD(+) levels.

157 m ATP synthesis or increasing ATP hydrolysis restores NAD(+)/NADH homeostasis and proliferation even

158 ases can be slowed down and even reversed by restoring NAD(+) levels.

159 tion by enhancing myelin regeneration, hence restoring nerve conduction and metabolic support to the

160 it nonfunctional, whereas its WT form could restore neuronal morphology and function in Drosophila l

161 -encapsulated with COOH-coated nanoparticles restore normal glycemia in immunocompetent diabetic mice

162 Endogenous homeostatic mechanisms can restore normal neuronal function following cocaine-induc

163 Blockade of G-CSF restored normal granulopoiesis in DeltaNC16A mice.

164 stration of peptide YY to EEC-deficient mice restores normal electrophysiology, improves glucose and

165 Consistently, Nep1 inhibition also restores normal PKA activation in amn mutant flies.

166 can be removed by tamoxifen administration, restoring normal gene expression systemically.

167 ght the utility of EE during adolescence for restoring normal hippocampal function.

168 mice had increased synaptic vesicle numbers, restoring normal neurotransmission.

169 nscription site, preventing their export and restoring normal SRSF7 protein levels.

170 in the device and implanted in diabetic mice restored normoglycaemia in the mice for over 75 days.

171 complement-like system through RNAi largely restores ookinete-to-oocyst transition but oocysts remai

172 Knee loading restores OPOA by regulating subchondral bone remodeling,

173 zed these effects, increasing oxygen supply, restoring optimal diaphragm functional properties.

174 taneous macrophage regeneration, which fully restored original macrophage distributions and morpholog

175 muscle activity reverses these alterations, restoring oxygen supply to the tissue and enabling recov

176 ting glucose levels, insulin sensitivity and restored pancreatic islet cell mass, neuronal innervatio

177 The angiogenic response to ischemia restores perfusion so as to preserve tissue.

178 that YAP/TAZ are required for mature SCs to restore peripheral myelination, but not to proliferate,

179 ion of ORP2, another truncated variant, also restored PM cholesterol in ORP1-null cells.

180 rendered the kinase refractory to MFH290 and restored Pol II CTD phosphorylation and DNA damage repai

181 respond to these eventualities in ways that restore population modification with functional genes, i

182 tensities ranged from 204% (stover) to 416% (restored prairie) for ethanol vehicles and from 329 to 5

183 benefits ranged from ~80% (stover) to 290% (restored prairie) reductions in CO(2)e compared to petro

184 ive grasses ~ poplar > early successional >= restored prairie; direct climate benefits ranged from ~8

185 In cystic cholangiocytes UDCA-HDAC6i #1 restored primary cilium length and exhibited potent anti

186 opulation with increased endogenous GLS2 and restored proliferative capacity.

187 overexpression of PYCR1 in PINCH-1 KO cells restores proline synthesis and cell proliferation, and s

188 to compromised function of the proteasome to restore proteostasis.

189 ould provide a novel therapeutic strategy to restore PTEN, thereby obliterating PTEN deficiency-induc

190 toxide (PBO), a synergist that can partially restore pyrethroid susceptibility in mosquito vectors.

191 ugh postmastectomy breast reconstruction can restore quality of life and body image, its morbidity re

192 network suppresses neurogenic competence and restores quiescence.

193 ormones were necessary for and sufficient to restore (R,S)-ketamine- and (2R,6R)-HNK-mediated prophyl

194 he metabolic/fluxomic redirection leading to restored redox balance imparted by palmitate helps expla

195 ed reduced podocyte migration rate (PMR) and restored reduced filopodia formation in shRNA-induced DA

196 nerves will help develop new treatments for restoring regulatory functions.

197 d great promise for penile reconstruction to restore reproductive capability of males.

198 ibition of NOX4 increased CD8(+) T cells and restored responsiveness to immune therapy, suggesting an

199 cardiovascular parameters, grafting RN-NSCs restored resting mean arterial pressure to normal levels

200 f artificial PM-PER tethers is sufficient to restore retention in inp1Delta cells.

201 imaging to optically record optogenetically restored retinal ganglion cell activity in the fovea of

202 PARs or ryanodine receptors, was required to restore robust LTP.

203 Exogenous Pip partially restored SAR in jmj14 plants, suggesting that JMJ14 regu

204 erexpression of SAR1B but not of SAR1A could restore secretion, and a divergent cluster adjacent to t

205 t atrial fibrillation (defined as no plan to restore sinus rhythm) and dyspnea classified as New York

206 n G6pc-/- mice corrects defective autophagy, restores SIRT1/FoxO3a/AMPK/PPAR-alpha signaling and rect

207 emonstrate the potential of SCS as a tool to restore somatosensation after amputations.

208 le those of unilateral BKAs, suggesting that restoring somatosensation may improve locomotion for amp

209 inert cargo protein or reducing vesicle size restores sorting stringency.

210 iated block in oligodendrocyte generation by restoring Sox10 expression without affecting canonical H

211 Restored SOX17 expression, in addition to its tumor supp

212 CD4+ T cells were poorly restored specifically in the lung interstitium, despite

213 In response to MCC cells with restored STING, cocultured T cells expressing MCPyV-spec

214 human proSFTPB cDNA into SP-B deficient mice restores surfactant homeostasis, prevents lung injury, a

215 th a barley (cv. Conlon) orthologue, Hv2OGO, restored susceptibility to Fg.

216 (Lo) non-classical monocytes in this setting restored susceptibility to RRV-mediated disease.

217 t 4-AP-induced increase of neuronal activity restores synaptic connectivity and function in the senso

218 olved or compound errors into substitutions, restoring synchronization for correction via a standard

219 r xylem parenchyma cells of the rbohD mutant restores systemic ROS signaling, systemic stress-respons

220 orates exhausted CD8(+) T cells, it fails to restore T cell repertoire diversity.IMPORTANCE Checkpoin

221 ion of virus replication but failed to fully restore T-cell function and eliminate HBV.

222 Addition of IL-12 restored T-cell proliferation to baseline levels.

223 decreased expression of NKG2D and DAP12 and restored TCR signaling in senescent-like CD27(-)CD28(-)C

224 d colleagues identified small molecules that restore telomere maintenance in patient-derived stem cel

225 boosting the peripheral immune response can restore the balance between the brain and the immune sys

226 evelopment of drugs that target PfCRT and/or restore the efficacy of existing antimalarials.

227 and purse-string contraction orchestrate to restore the gap.

228 ify and test novel therapeutic approaches to restore the impaired epithelial repair mechanisms in COP

229 Interventions to treat reflux attempt to restore the integrity of the EGJ.

230 cleotide (ASO) that induces exon skipping to restore the open reading frame.

231 Re-irradiation of the samples can restore the radical concentration back to a similar maxi

232 firms the capability of LVAs to successfully restore the reading ability in patients with corneal dis

233 Prolonged ART may restore the richness of the microbiota closer to that of

234 The potentiating anti-FH Ab is able to restore the surface regulatory function of most of the t

235 A5 addition to choroid plexus cell cultures restored the Abeta-induced impairments on autophagy flux

236 tro and in vivo studies demonstrated that 20 restored the activity of beta-lactam antibiotics against

237 ith a pharmacologic inhibitor of SRC kinases restored the antiaggregative phenotype in the presence o

238 Off-label treatment with tocilizumab restored the cytotoxic potential of NK cells.CONCLUSIONT

239 ion of Dnase1l3 into Dnase1l3-deficient mice restored the end motif profiles to those seen in the pla

240 g AML cells with an EZH2 inhibitor partially restored the expression of approximately 50% of the gene

241 Flushing rapidly restored the total chlorine (as chloramine) residual and

242 Reconstitution of mast cells in W/W(V) mice restored the visceral hypersensitivity response.

243 kout of the key antiphagocytic molecule CD47 restores the ability of macrophages to sense and clear o

244 e indole, followed by a decarboxylation that restores the aromaticity of the phenyl.

245 We conclude that re-expression of APC restores the cell-cell adhesion gene and posttranscripti

246 tic activation of beta-catenin in beta-cells restores the diabetes-like phenotypes induced by Kindlin

247 eptor agonist in conjunction with fluoxetine restores the efficacy of fluoxetine actions on D1 recept

248 overexpression corrects defective autophagy, restores the expression of FoxO3a and liver kinase B1 bu

249 Moreover, deletion of Foxo1 restores the expression of T-bet and corrects the abnorm

250 ar but non-phosphorylatable amino acid (Phe) restores the more dynamic cellular functions of NMII, su

251 Treatment with NS9283 restores the rapid onset of the postsynaptic cholinergic

252 This change restores the T-cell reactivity to the anti-PD-1 blockade

253 Restoring the levels and activity of cytotoxic T cells i

254 ay progression or replace damaged neurons by restoring the original neuronal structures.

255 treatments share the aim of facilitating or restoring the pursuit of individual valued life goals in

256 signaling rescued seizure-induced anxiety by restoring the tonic control of the eCB signaling over gl

257 rsely, for rats in which wakefulness was not restored, the functional gamma connectivity remained red

258 l in RPL-TSCs and rescue of TEAD4 expression restores their self-renewal ability.

259 To reduce rCDI, microbiota-restoring therapies are needed, particularly standardize

260 SMN-restoring therapies have recently emerged; however, prec

261 exposure to RUX, this apoptotic potential is restored, thereby sensitizing CD8 T cells to DEX-induced

262 that targeting this pathway could be used to restore thermogenic activity.

263 Molecular tools to restore this balance are highly desirable.

264 ghlights how the metastatic microenvironment restores this malignant property of cancer cells during

265 enescence-inducing combination of drugs, and restore tissue homeostasis in mice in which liver fibros

266 t increasing Gish activity in aging guts can restore tissue homeostasis.

267 re to eliminate physical discontinuities and restore tissue integrity is a fundamental process in nor

268 e upregulation of protective responses which restore tissue structure and metabolic function.

269 involving several mediators that is aimed at restoring tissue homeostasis.

270 nd ADSC-TM cells as a potential treatment to restore TM structure and function in glaucoma.

271 To establish a stem cell-based approach to restoring TM function and normalizing IOP, human adipose

272 reductase activity in C163S can be partially restored to 54% wild type by increasing Cu(II) concentra

273 These phenotypes were fully restored to those of the wild type when dksA mutation wa

274 All these phenotypes were restored to WT or near-WT levels when lon-2 mutation was

275 arrier surfaces or the host immune system to restore tolerance and homeostasis will be explored.

276 Treatment with recombinant Gal1 restored tolerogenic mechanisms and reduced salivary gla

277 ogy is altered, but not when it is normal or restored toward WT.

278 on of wild-type TRAPPC4 in these fibroblasts restored trafficking, suggesting that the trafficking de

279 Many introduced herbivores restore trait combinations that have the capacity to inf

280 To better monitor and restore tree cover, I call for re-interpretation and cor

281 xogenous glutamine or glutaminase inhibitors restores tRNA(Gln) charging and the levels of polyglutam

282 Lastly, pharmacologic NGFR inhibition restores tumor sensitivity to T cell attack in vitro and

283 es of equal duration and amplitude and fully restored (unipolar-equivalent response) when the delay b

284 activate RhoA/ROCK/pMLC but its activity was restored upon reoxygenation.

285 Conversely, normal numbers of PML NBs were restored upon transition to latency or by decreasing oxi

286 CP) has long been proposed as a strategy for restoring useful vision to the blind, under the assumpti

287 Cavities were restored using glass-hybrid material (Equia Forte, GC).

288 er scaffolds seeded with autologous cells to restore uterine structure and function in rabbits.

289 erefore a potential therapeutic strategy for restoring uteroplacental perfusion in pregnancy disorder

290 nofocal CT ASPHINA 409 IOL was beneficial to restore vision in eyes with or without concomitant ocula

291 t CiPCs could have therapeutic potential for restoring vision.

292 ngs showed that 9-cis-retinal administration restored visual pigment formation and decreased oxidativ

293 enerating all classes of retinal neurons and restoring visual function.

294 mportance of an accelerated peace process to restore well-being in Syria.

295 ctive Fe and Al minerals affect C cycling in restored wetlands.

296 chromosome in some isolates and this fusion restored wild-type growth.

297 eutic behavioral effects without necessarily restoring wild-type circuit states, while highlighting t

298 ) Oxygen content in arterial blood was fully restored with acclimatisation to 4330 m, but concurrent

299 isplay flexibility as their formation can be restored with select arginine precursors.

300 genes (OSK) in mouse retinal ganglion cells restores youthful DNA methylation patterns and transcrip