ライフサイエンスコーパス: AV

1 AV differences existed between SOSDEs with different gal

2 AV has anti-inflammatory, antioxidant, antimicrobial, hy

3 AV-1451 tau binding in the medial temporal, parietal, an

4 g conditions of this case, recapitulated 2:1 AV block and arrhythmia.

5 We quantified in vivo retention of [F-18]-AV-1451 and performed autoradiography, [H-3]-AV-1451 bin

6 radiography failed to show detectable [F-18]-AV-1451 binding in multiple brain regions examined, with

7 The three subjects exhibited [F-18]-AV-1451 in vivo retention predominantly in basal ganglia

8 1451 phosphor screen autoradiography, [F-18]-AV-1451 nuclear emulsion autoradiography, and [H-3]-AV-1

9 They all underwent [F-18]-AV-1451 PET imaging before death.

10 We applied [F-18]-AV-1451 phosphor screen autoradiography, [F-18]-AV-1451

11 Our data suggest that [F-18]-AV-1451 strongly binds to tau lesions primarily made of

12 gnificant correlation between in vivo [F-18]-AV-1541 retention and postmortem in vitro binding and ta

13 18F-AV-1451 binding to the basal ganglia was strong in all g

14 eimer's disease slices with 11C-PBB3 and 18F-AV-1451 were noted.

15 differential affinities for 11C-PBB3 and 18F-AV-1451, and higher availability of binding sites on pro

16 ndent regressions were performed between 18F-AV-1451 binding and each cognitive domain, and we used t

17 n association between cognition and both 18F-AV-1451 uptake and grey matter volume.

18 ve to patients with Alzheimer's disease, 18F-AV-1451 binding was elevated in the midbrain (t = 2.1, P

19 line with moderate 11C-PBB3 versus faint 18F-AV-1451 autoradiographic labelling of these tissues.

20 tomography tracers such as flortaucipir (18F-AV-1451, also known as 18F-T807) have made it possible t

21 ed highly associated patterns of greater 18F-AV-1451 binding and increased annualized change in corti

22 rain regions was associated with greater 18F-AV-1451 PET retention most prominently in the inferior t

23 We found that: (i) 18F-AV-1451 positron emission tomography retention was diffe

24 There was increased 18F-AV-1451 binding in multiple regions in living patients w

25 in each domain was related to increased 18F-AV-1451 binding in specific brain regions conforming to

26 showed, relative to controls, increased 18F-AV-1451 uptake in the putamen, pallidum, thalamus, midbr

27 Overall, we confirm the potential of 18F-AV-1451 as a heuristic biomarker, but caution is indicat

28 elanin is an insufficient explanation of 18F-AV-1451 positron emission tomography data in vivo, at le

29 ng may contribute to disease profiles of 18F-AV-1451 positron emission tomography, especially in prim

30 rect and grey matter-mediated effects of 18F-AV-1451 uptake on cognitive performance.

31 We assessed the radiotracer 18F-AV-1451 with positron emission tomography imaging to com

32 More specifically, 18F-AV-1451 binding was significantly increased in patients

33 B) positron emission tomography and tau (18F-AV-1451) positron emission tomography, and episodic and

34 ear palsy tau deposits for 11C-PBB3 than 18F-AV-1451.

35 We suggest that 18F-AV-1451 positron emission tomography is a useful biomark

36 mortem autoradiographic data showed that 18F-AV-1451 strongly bound to Alzheimer-related tau patholog

37 We also examined the 18F-AV-1451 autoradiographic binding in post-mortem tissue f

38 palsy, and a control case to assess the 18F-AV-1451 binding specificity to Alzheimer's and non-Alzhe

39 e-associated variability; and (iii) this 18F-AV-1451 positron emission tomography retention pattern s

40 mission tomography binding antecedent to 18F-AV-1451 positron emission tomography scans, and to what

41 in florbetapir retention, antecedent to 18F-AV-1451 positron emission tomography scans, in the parie

42 the positron emission tomography tracer 18F-AV-1451) associated with well-established Alzheimer's di

43 between tau pathology, as measured with 18F-AV-1451-PET imaging, and cognitive deficits in Alzheimer

44 aging with fluorine 18-labeled AV-1451 ([18F]AV-1451) (formerly known as [18F]T807), [11C]PiB PET, ma

45 easured by fluorine 18-labeled AV-1451 ([18F]AV-1451) positron emission tomographic (PET) imaging are

46 Elevated cortical [18F]AV-1451 binding was observed in 4 of 17 patients with Le

47 Results: In patients with DLB, cortical [18F]AV-1451 uptake was highly variable and greater than in t

48 r DLB and PD-impaired patients, greater [18F]AV-1451 uptake in the inferior temporal gyrus and precun

49 Foci of increased [18F]AV-1451 binding in the inferior temporal gyrus and precu

50 rongly correlated with the magnitude of [18F]AV-1451 binding (3 patients with amnesic Alzheimer disea

51 18F]AV-1451 binding, the association of [18F]AV-1451 binding with [11C]PiB binding, and the associati

52 11C]PiB binding, and the association of [18F]AV-1451 binding with cognitive impairment.

53 on of diagnostic groups on the basis of [18F]AV-1451 binding, the association of [18F]AV-1451 binding

54 vivo evidence that distribution of the [18F]AV-1451 signal as seen on results of PET imaging is a va

55 d with the regional distribution of the [18F]AV-1451 signal.

56 Patients underwent [18F]AV-1451 PET imaging to measure tau burden, carbon 11-lab

57 An [18F]-AV-1451 SUVR cutoff value of 1.19 (sensitivity, 100%; sp

58 Abeta+ was associated with an elevated [18F]-AV-1451 SUVR in AD cortical signature regions (Abeta+ pa

59 An elevated [18F]-AV-1451 SUVR was associated with volumetric loss in both

60 nverse association between hippocampal [18F]-AV-1451 SUVR and volume was seen in Abeta+ participants

61 The observed [18F]-AV-1451 SUVR volumetric association was modified by Abet

62 Use of [18F]-AV-1451 has a potential for staging of the preclinical a

63 ndardized uptake value ratio (SUVR) of [18F]-AV-1451 in the hippocampus and a priori-defined AD corti

64 The [18F]-AV-1451 SUVR in the hippocampus and AD cortical signatur

65 in mice vaccinated with AV-1959R or AV-1959R/AV-1980R combination, anti-tau titers were significantly

66 on when compared to the AV-1980R or AV-1959R/AV-1980R.

67 AV-1451 and performed autoradiography, [H-3]-AV-1451 binding assays, and quantitative tau measurement

68 nuclear emulsion autoradiography, and [H-3]-AV-1451 in vitro binding assays to the study of postmort

69 The in vivo thoracic and abdominal AV-750 fluorescent signal was attributed to the thymus,

70 cided to generate vaccines, targeting Abeta (AV-1959R), Tau (AV-1980R) or Abeta/tau (AV-1953R) B cell

71 ac mutant photoreceptor terminals accumulate AV-lysosomal fusion intermediates, suggesting that Cac i

72 ncreased collagen content but did not affect AV calcification.

73 ti-tau titers were significantly lower after AV-1953R injection when compared to the AV-1980R or AV-1

74 While anti-Abeta antibody titers after AV-1953R immunization were similar to that in mice vacci

75 An AV fistula attempt strategy was found to be superior to

76 Overall, the advantages of an AV fistula attempt strategy lessened considerably among

77 te an arteriovenous (AV) fistula or place an AV graft.

78 AVs and would be less willing to buy such an AV.

79 ebo gel was locally delivered to group 1 and AV gel to group 2.

80 In sum, AV-1959R and AV-1980R formulated with Advax(CpG) adjuvant were identi

81 AV-1953R, or the combination of AV-1959R and AV-1980R vaccines formulated with Advax(CpG) induced rob

82 Ictal asystole, bradycardia and AV-conduction block were self-limiting in all but one of

83 tion of the phenolic compounds in HS, CA and AV extracts and was compared along with ten standard phe

84 =12.34 +/- 2.3 mug/mL) as compared to CA and AV extracts.

85 e was similarly increased in both MI-CHF and AV-CHF rats compared to control.

86 ssociations between mean visit frequency and AV fistula creation or graft placement in the first 90 d

87 sitron emission tomography ligands, PBB3 and AV-1451, by fluorescence, autoradiography and homogenate

88 of non-ghost and ghost tangles with PBB3 and AV-1451, while dystrophic neurites were more clearly det

89 state (peroxide and anisidine value, PV and AV) required for refined oils.

90 Rescuing of SAN and AV dysfunction could be obtained also by pharmacological

91 sed only in MI-CHF rats compared to Sham and AV-CHF rats.

92 undergo surgery to create an arteriovenous (AV) fistula or place an AV graft.

93 A side-to-side arteriovenous (AV) shunt was created between the distal stump of one of

94 ional flortaucipir F 18 (previously known as AV 1451, T807) positron emission tomography (FTP-PET) im

95 including bradycardia and atrioventricular (AV) dysfunction (heart block).

96 dycardia (25 cases), ictal atrioventricular (AV)-conduction block (11 cases), postictal AV-conduction

97 ion (AF) without producing atrioventricular (AV) block remains a clinical challenge.

98 longitudinal motion of the atrioventricular (AV) plane.

99 e, auditory enhancement of visual attention (AV) and visual enhancement of auditory speech (VA).

100 stem (T3SS) is a well-studied and attractive AV target, given that it is widespread in more than 25 s

101 Audiovisual (AV) integration is essential for speech comprehension, e

102 In this study, we examined audiovisual (AV) processing in normal and visually impaired individua

103 ness, in the context of natural audiovisual (AV) speech processing, relies on crossmodal integration

104 imize the behavioral benefit of audiovisual (AV) speech.

105 ides act on purinoceptors on cardiomyocytes, AV and SA nodes, cardiac fibroblasts, and coronary blood

106 ntricular response during AF without causing AV block.

107 al area and marked effects on AV conduction, AV block did not occur.

108 other RCC subtypes are aorta-based corrected AV and aorta-based corrected relative contrast enhanceme

109 9-95 HU and renal parenchyma-based corrected AV of 87-95 HU showed a diagnostic accuracy of 81-86%, 8

110 ut-off AV of 86-89 HU, aorta-based corrected AV of 89-95 HU and renal parenchyma-based corrected AV o

111 cin/vincristine/prednisone/cyclophosphamide (AV-PC).

112 PR prolongation (first degree AV block) was present at 4 weeks, 7 months, and 17 month

113 clinical effectiveness of locally delivered AV gel used as an adjunct to scaling and root planing (S

114 Adjunctive use of locally delivered AV gel, in comparison to locally delivered placebo gel,

115 in the SMART-AV study (SmartDelay Determined AV Optimization: A Comparison to Other AV Delay Methods

116 lure, left ventricular systolic dysfunction, AV block, atrial or ventricular arrhythmias, and sudden

117 as sufficient to induce formation of ectopic AV junction-like tissue as assessed by morphology, gene

118 senchymal protrusion (DMP) and the embryonic AV canal.

119 lation at presynaptic terminals by enhancing AV retrograde transport.

120 Conclusion:(18)F-AV-133 had substantial management impact in patients wit

121 tion 2 h after injection of 250 MBq of (18)F-AV-133, and the resulting images were quantitatively ass

122 The tau tangle ligand (18)F-AV-1451 ((18)F-T807) binds to neuromelanin in the midbra

123 ges were calculated from 80-100 minute (18)F-AV-1451 (also known as T807) positron emission tomograph

124 dults using the radioactive tau ligand (18)F-AV-1451 (previously known as T807) who also underwent a

125 erent strategies for quantification of (18)F-AV-1451 (T807) tau binding, including models with blood

126 l syndrome) underwent 180-min PET with (18)F-AV-1451 and arterial blood sampling.

127 l syndrome) underwent 180-min PET with (18)F-AV-1451 and arterial blood sampling.

128 R30-150 < 1.5), and for ROIs with high (18)F-AV-1451 binding (hROIs, mean of BPND + 1 and DVR30-150 >

129 in), for all values, for ROIs with low (18)F-AV-1451 binding (lROIs, mean of BPND + 1 and DVR30-150 <

130 bjective of this study was to evaluate (18)F-AV-1451 binding with full kinetic analysis using a metab

131 Quantitative region-based analysis of (18)F-AV-1451 images yielded region of interest and voxel leve

132 fter injection with the tau PET tracer (18)F-AV-1451 in 19 subjects.

133 the novel tau-specific PET radioligand (18)F-AV-1451 in cognitively healthy control (HC) and Alzheime

134 (18)F-AV-1451 is currently the most widely used of several exp

135 Methods:(18)F-AV-1451 PET brain imaging was completed in 16 4 young he

136 Methods:(18)F-AV-1451 PET brain imaging was completed in 16 subjects:

137 (18)F-AV-1451 PET imaging was performed on 43 subjects (5 youn

138 In vivo (18)F-AV-1451 positron emission tomography images across the A

139 (18)F-AV-1451 positron emission tomography may be the first ra

140 We investigated the utility of (18)F-AV-1451 positron emission tomography to visualize the co

141 - and sex-matched control subjects had (18)F-AV-1451 positron emission tomography using a Siemens hig

142 Results: AD demonstrated increased (18)F-AV-1451 retention compared with YHV and AHV based on bot

143 AD demonstrated increased (18)F-AV-1451 retention compared with YHV and AHV based on bot

144 displayed visually apparent decreased (18)F-AV-1451 signal in the midbrain.

145 as decreased by 45% and the mean total (18)F-AV-1451 substantia nigra volume of distribution was decr

146 Our data suggest that although (18)F-AV-1451 SUVR curves do not reach a plateau and are still

147 lusion: Our data suggest that although (18)F-AV-1451 SUVR curves do not reach a plateau and are still

148 The kinetics of the (18)F-AV-1451 tracer in cortical areas, as examined in this sm

149 here was no correlation between nigral (18)F-AV-1451 volume of distribution and age or time since dia

150 ed a 30% mean decrease in total nigral (18)F-AV-1451 volume of distribution compared with controls (P

151 hether (18)F-flortaucipir (also called (18)F-AV-1451) PET, targeting tau aggregates, detects these di

152 Using the tau PET agent (18)F-AV-1451, we examined retention patterns in cognitively n

153 e not able to describe the kinetics of (18)F-AV-1451, with poor fits in 33%-53% of cortical regions a

154 e not able to describe the kinetics of (18)F-AV-1451, with poor fits in 33%-53% of cortical regions a

155 ssion tomography (PET) tracer known as (18)F-AV-1451; and (2) amyloid-beta, quantified with (11)C-PiB

156 s studied using the novel tau tracer [(18) F]AV-1451 in conjunction with [(11) C]Pittsburgh compound

157 nd throughout association neocortex, [(18) F]AV-1451 was selectively retained in posterior brain regi

158 We used [(18)F]AV-1451 and [(11)C]PiB positron emission tomography, str

159 nalysis, based on the distribution of [(18)F]AV-1451 binding potential, separated semantic dementia f

160 [(18)F]AV-1451 binds in vivo regions that are likely to contain

161 ll be useful to assess the utility of [(18)F]AV-1451 to differentiate and track different types of fr

162 oposed 'off target' binding sites for [(18)F]AV-1451, such as neuronal monoamine oxidase or neuromela

163 le this suggests a non-tau target for [(18)F]AV-1451, the pathological regions in semantic dementia d

164 vo binding of the putative tau ligand [(18)F]AV-1451, which is elevated in frontotemporal lobar degen

165 mission tomography brain imaging with [(18)F]AV-1451.

166 phoid cell death was detected by fluorescent AV-750 accumulation in the thorax and abdomen (in vivo),

167 cantly improved long-term survival following AV surgery.

168 ac, indicating that the VGCC is required for AV-lysosomal fusion.

169 ove of enforcing utilitarian regulations for AVs and would be less willing to buy such an AV.

170 The effect of Aloe vera gel (AV) and Aloe arborescens gel (AA) alone or in combinatio

171 Patients with probable DLB had greater AV-1451 uptake in the posterior temporoparietal and occi

172 Defining the algorithms that will help AVs make these moral decisions is a formidable challenge

173 e AD dementia group had significantly higher AV-1451 uptake than the probable DLB group, and medial t

174 Center underwent magnetic resonance imaging, AV-1451, and Pittsburgh compound-B (PiB) PET examination

175 that regulates key mechanosensitive gene in AV such as TGFbeta1.

176 reduced in the CBs of MI-CHF rats but not in AV-CHF rats.

177 The role of VGCC in AV-lysosomal fusion is evolutionarily conserved, as the

178 but they would themselves prefer to ride in AVs that protect their passengers at all costs.

179 resting aortic valve (AV) gradient, indexed AV area, METs, and heart rate recovery were 2.9+/-3%, 58

180 INTERPRETATION: AV-1451 may have limited utility for in vivo selective a

181 tudies approved of utilitarian AVs (that is, AVs that sacrifice their passengers for the greater good

182 nts (66%) underwent AV surgery (36% isolated AV surgery, 16% concomitant coronary bypass, and 58% aor

183 operative mortality was 2% (0.6% in isolated AV surgery).

184 Exposures: Imaging with fluorine 18-labeled AV-1451 ([18F]AV-1451) (formerly known as [18F]T807), [1

185 gic findings measured by fluorine 18-labeled AV-1451 ([18F]AV-1451) positron emission tomographic (PE

186 at evaluating synchrony of auditory-leading (AV) versus visual-leading (VA) audiovisual stimulus pair

187 INTERPRETATION: Medial temporal lobe AV-1451 uptake distinguishes AD dementia from probable D

188 Medial temporal lobe AV-1451 uptake distinguishes AD dementia from probable D

189 ith diabetes, reflecting the effect of lower AV fistula success rates and lower life expectancy.

190 The AID deficiency inhibits DSA-mediated AV after aorta transplantation in mice.

191 odel (MI-CHF) and as a high output HF model (AV-CHF), respectively.

192 trast, HSulf-1 proficient cells exhibit more AVs and reduced LDs.

193 gration of unimodal (A or V) and multimodal (AV) sensory cues.

194 d to the group of iLVESD <2.5 cm/m(2) and no AV surgery, the 2 groups of iLVESD <2.5 cm/m(2) with AV

195 ated posterior temporoparietal and occipital AV-1451 uptake in probable DLB and its association with

196 +/- 13 versus 91 +/- 9 ms, P < 0.01), and of AV node Wenckebach cycle length (230 +/- 19 versus 213 +

197 the temporal and spatial characteristics of AV processing and assess differences in neural responses

198 ope vaccine, AV-1953R, or the combination of AV-1959R and AV-1980R vaccines formulated with Advax(CpG

199 ter isolating the multisensory components of AV-VA event-related potentials (ERPs) from the sum of th

200 e IIA LPHL were treated with three cycles of AV-PC.

201 networks learned from a clinical dataset of AV-45 PET image and compare network properties of both u

202 Formulation of AV-1959R in Advax(CpG) induced the highest cellular and

203 and visual cortices, as opposed to fusion of AV percepts in a multisensory integrator.

204 showed slower and less accurate judgments of AV and V stimuli but more accurate responses in the A-al

205 Measurement of AV integration was accomplished via quantification of th

206 ssociated with a 21% increase in the odds of AV fistula creation or graft placement during that perio

207 ms contribute to the efficient processing of AV speech in background noise.

208 ting that Cac is necessary for the fusion of AVs with lysosomes, a poorly defined process.

209 he number of LDs and increased the number of AVs compared to vector controls.

210 ing ccRCC from other RCC subtypes, a cut-off AV of 86-89 HU, aorta-based corrected AV of 89-95 HU and

211 s in the AV nodal area and marked effects on AV conduction, AV block did not occur.

212 d extend current mechanistic perspectives on AV speech perception.

213 Despite extensive studies on AV junction development, the genetic regulation of DMP d

214 s /ba/ and /fa/, presented in Auditory-only, AV congruent or incongruent contexts.

215 to that in mice vaccinated with AV-1959R or AV-1959R/AV-1980R combination, anti-tau titers were sign

216 R injection when compared to the AV-1980R or AV-1959R/AV-1980R.

217 complications than eyes with partial PPVs or AVs during the average 4 years of follow-up.

218 who underwent total PPVs and partial PPVs or AVs.

219 mined AV Optimization: A Comparison to Other AV Delay Methods Used in CRT).

220 All fish oils complied with a p-AV limit of 30, 98% with a PV limit of 10 meq O2/kg, and

221 Peroxide Value (PV), para-Anisidine Value (p-AV), and TOTOX, respectively.

222 cted for further investigation using porcine AV leaflets in an ex vivo shear system.

223 isolated from either side of healthy porcine AVs for microarray analysis.

224 (AV)-conduction block (11 cases), postictal AV-conduction block (2 cases), (post)ictal atrial flutte

225 ne the correlation of in vivo and postmortem AV-1451 binding patterns in three autopsy-confirmed non-

226 In this study, we examined postnatal AV conduction in the knockin mice.

227 The highly penetrant and progressive AV block phenotype seen in human heterozygous missense m

228 reases Cx30.2 expression by 50% and prolongs AV delay by 13%.

229 t regulatory circuit that establishes proper AV delay, and these findings may have wider implications

230 PV, AV and aroma of accelerated stored SOSDEs do not clearly

231 A total of 135 patients received AV-PC; 126 were treated at diagnosis and nine at relapse

232 Eleven patients receiving AV-PC had less than CR and received IFRT.

233 ts show that IRD individuals exhibit reduced AV integration for concurrent audio and visual (AV) stim

234 high heritability in first-degree relatives, AV genetic determinants remain incompletely understood.

235 Aaron CP, Chervona Y, Kawut SM, Diez Roux AV, Shen M, Bluemke DA, Van Hee VC, Kaufman JD, Barr RG.

236 rved peptide motifs, [GS]LFXG[ML]X[LV] and S[AV]F[SA]FLN, within its C-terminal unstructured region,

237 urvived for 4 weeks and significantly slowed AV conduction and ventricular rate in acutely induced AF

238 tively in 426 patients enrolled in the SMART-AV study (SmartDelay Determined AV Optimization: A Compa

239 x assembly with the SNARE motif mutant Stx1A(AV) (A240V, V244A) was not sufficient to rescue neurotra

240 In sum, AV-1959R and AV-1980R formulated with Advax(CpG) adjuvan

241 e vaccines, targeting Abeta (AV-1959R), Tau (AV-1980R) or Abeta/tau (AV-1953R) B cell epitopes, based

242 eta (AV-1959R), Tau (AV-1980R) or Abeta/tau (AV-1953R) B cell epitopes, based on immunogenic MultiTEP

243 Building upon this idea, we proposed that AV integration in spoken language reflects visually indu

244 Electrophysiology studies showed that AV nodal function and right ventricular effective refrac

245 eal data to index the similarity between the AV and VA maps at each time point (500 ms window after s

246 nal similarity analysis (tRSA) comparing the AV and VA ERP maps.

247 investigated if key microRNAs (miRNA) in the AV are differentially expressed due to disturbed blood f

248 despite a large number of injections in the AV nodal area and marked effects on AV conduction, AV bl

249 evealed presence of ADF-labeled cells in the AV nodal area at 28 days.

250 cted under electroanatomical guidance in the AV nodal area, with continuous 28-day ECG recording.

251 s dermal fibroblast (ADF) injection into the AV nodal area would reduce ventricular response during A

252 Based on our model we suggest that the AV response can be considered as an evolutionary extensi

253 fter AV-1953R injection when compared to the AV-1980R or AV-1959R/AV-1980R.

254 wnregulates canonical Wnt targets within the AV junction.

255 r separate neuronal mechanisms underlie this AV-VA dichotomy in humans.

256 ate distinct selectivity of PBB3 compared to AV-1451 for diverse tau fibril strains.

257 ced hypoxic ventilatory response compared to AV-CHF rats.

258 s with less than a complete response (CR) to AV-PC received 21-Gy involved-field radiation therapy (I

259 attempt strategy was found to be superior to AV grafts and CVCs in regard to mortality and cost for t

260 at positron emission tomography (PET) tracer AV-1451 exhibits high binding affinity for paired helica

261 ositron emission tomography (PET) tau tracer AV-1451 uptake in patients with probable DLB, compared t

262 to explain the neural mechanisms underlying AV integration.

263 Over 6.9+/-3 years, 341 (64%) underwent AV replacement (54% isolated), and there were 104 (20%)

264 .6 +/- 3 years, 933 patients (66%) underwent AV surgery (36% isolated AV surgery, 16% concomitant cor

265 Survival of patients who underwent AV surgery was similar to that of an age- and sex-matche

266 hanical Turk studies approved of utilitarian AVs (that is, AVs that sacrifice their passengers for th

267 cell death using a near-infrared annexin V (AV-750).

268 The dual-epitope vaccine, AV-1953R, or the combination of AV-1959R and AV-1980R va

269 droplets (LDs), reduced autophagic vacuoles (AVs) and less LC3B puncta.

270 of transporting nascent autophagic vacuoles (AVs) from distal axons toward the soma, where mature lys

271 pendent accumulation of autophagic vacuoles (AVs) in photoreceptor terminals and eventually a degener

272 cting conditions on aroma, anisidine values (AV) and peroxide values (PV) were determined.

273 evaluated in terms of CT attenuation values (AV) and differences in contrast density; the aorta or re

274 Aortic valve (AV) calcification is an inflammation driven process that

275 jection fraction, mean resting aortic valve (AV) gradient, indexed AV area, METs, and heart rate reco

276 action (LVEF) and the value of aortic valve (AV) surgery on long-term survival.

277 and Rac1, coordinate atrioventricular valve (AV) differentiation and morphogenesis.

278 simultaneity judgment task including various AV-VA asynchronies and unisensory control conditions (vi

279 ables suppression of allograft vasculopathy (AV) after aorta transplantation, a DSA-mediated process.

280 Autonomous vehicles (AVs) should reduce traffic accidents, but they will some

281 based model for estimating angular velocity (AV) in the bee brain, capable of quantitatively reproduc

282 ium anterius (AA), the arcopallium ventrale (AV), the arcopallium dorsale (AD), the arcopallium inter

283 Herbal agents such as Aloe vera (AV) have been used in medical and dental therapy for tho

284 ntella asiatica (CA) and Amaranthus viridis (AV) extracts and investigate their respective antioxidan

285 Anti-virulence (AV) compounds are a promising alternative to traditional

286 integration for concurrent audio and visual (AV) stimuli but increased brain activity during the unim

287 ory and visual stimuli into auditory-visual (AV) objects.

288 nding on the leading input: auditory-visual (AV) or visual-auditory (VA).

289 o had partial PPVs or anterior vitrectomies (AVs) at the time of KPro implantation (n = 26).

290 In vivo AV-750 fluorescent imaging provides spatially resolved a

291 Acne vulgaris (AV) affects most adolescents, and of those affected, mod

292 y PBB3 fluorescence in contrast to very weak AV-1451 signals.

293 d with higher longer-term mortality, whereas AV replacement (time-dependent covariate, hazard ratio,

294 sociated with longer-term mortality, whereas AV replacement was associated with improved survival.

295 sual-only, auditory-only) and tested whether AV and VA processing generate different patterns of brai

296 ilencing of miR-214 by anti-miR-214 in whole AV leaflets with the fibrosa exposed to OS significantly

297 ry, the 2 groups of iLVESD <2.5 cm/m(2) with AV surgery and iLVESD >/=2.5 cm/m(2) with AV surgery wer

298 th AV surgery and iLVESD >/=2.5 cm/m(2) with AV surgery were associated with improved survival (hazar

299 were similar to that in mice vaccinated with AV-1959R or AV-1959R/AV-1980R combination, anti-tau tite

300 myloid-beta (Abeta) oligomers associate with AVs in AD axons and interact with dynein motors.