ライフサイエンスコーパス: PSV

1 PSV and VICA/VCCA helped classify, respectively, 185 and

2 PSV neutralization assays are safer than live virus neut

3 PSV patients' SF-36 scores, except for mental health, we

4 PSV was more common in males (23.5/million; 95% CI 17.3-

5 PSVs were directly purified from mature seeds by differe

6 r confirming alpha2,3-linked SA on GD1a as a PSV receptor.

7 xample involving thermodynamic dispersion, a PSV parameter inference effort requiring 7,500,000 simul

8 ibuted to the cisternal ER as expected for a PSV-localized protein, but instead are targeted to the p

9 mately 80 proteins, and we have identified a PSV-specific GTP-binding protein that may be involved in

10 The addition of a PSV threshold resulted in significant decrease in overal

11 Patients were randomized to a PSV protocol (n = 62), VSV protocol (n = 60), or no prot

12 ults suggest that as the LV transitions to a PSV, the tonoplast remodels before the large vacuole lum

13 inguishable with high specificity by using a PSV greater than 10 cm/sec and an RI greater than 0.65 a

14 hese internal membrane structures to yield a PSV morphology different from that of tomato or tobacco.

15 veloped a new method to detect low-abundance PSVs with improved sensitivity.

16 Aleurone PSVs contain zein-rich protein inclusions, a matrix, and

17 the ER, zeins are delivered to the aleurone PSVs in atypical prevacuolar compartments that seem to a

18 oninvasive mechanical ventilation algorithm (PSV-NIV+), neurally adjusted ventilatory assist without

19 oninvasive mechanical ventilation algorithm (PSV-NIV-), pressure support ventilation with a noninvasi

20 in neurally adjusted ventilatory assist and PSV-NIV+ than in PSV-NIV- (p < .05).

21 ystole was shortened, EDV was decreased, and PSV was increased.

22 ESA and PSV were significantly lower in the renal artery than in

23 significant association between farming and PSV has been identified for the first time.

24 Among patients having CXRs on both IMV and PSV breaths, 15 of 67 (22%) had their overall degree of

25 ology resembling an amalgamation of a LV and PSV.

26 nd 23 patients were entered into the PAV and PSV groups, respectively, and had similar diagnoses and

27 ction and metabolic signature observed in AP-PSV could be largely mitigated with the OP procedure.

28 In five arteries, PSV ratios exceeded a threshold of 1.8 (suggesting > or

29 nal parameters, ICA-to-common carotid artery PSV ratio and ICA end-diastolic velocity may also be use

30 rface carbohydrates could not be utilized as PSV receptors for binding and infection.

31 gas exchange and avoid intubation as well as PSV and be more comfortable and tolerable for patients.

32 ficant inverse correlation was seen between %PSV and the percent change of intrastent volume (P<0.000

33 scribed family of proteins, the Brassicaceae PSV-embedded proteins (BPEPs), associated with 'crystall

34 These results demonstrate that Brassicaceae PSVs contain internalized membranes, and raise the possi

35 CCA PSV and EDV ranges averaged 23.1 cm/sec +/- 15.7 (SD) an

36 Right-to-left CCA PSV ratios were abnormal in up to 26 patients (suggestin

37 enting there was a drop in the contralateral PSV and EDV of 60.3 cm/s (p = 0.005) and 15.1 cm/s (p =

38 erapies that interfere with the conventional PSV assay.

39 CPAP(PSV) provides a straightforward and effective alternativ

40 CPAP(PSV) resulted in an alveolar-arterial partial pressure o

41 PaO(2)) was significantly higher during CPAP(PSV) compared with CPAP or IPPV (98+/-10, 61+/-27, and 7

42 (VO(2)) was significantly higher during CPAP(PSV) than with the other ventilation modes (P<0.05) and

43 t of cardiac output was 76+/-17% during CPAP(PSV), 61+/-21% during CPAP (P<0.01), and 54+/-13% during

44 n was recorded in 8 of 8 animals in the CPAP(PSV) group, in 6 of 8 in the CPAP group, and in 3 of 8 i

45 nced with pressure support ventilation (CPAP(PSV)) during CPR.

46 o ventricular fibrillation and CPR with CPAP(PSV), CPAP, or IPPV.

47 Detecting PSVs and determining their origins, either by DNA mutati

48 an Arabidopsis thaliana mutant that disrupts PSV trafficking identified TERMINAL FLOWER 1 (TFL1), a s

49 tically significant differences in MFV, EDV, PSV and RI (all p > 0.05).

50 hing trials performed with the use of either PSV (with a pressure-support level of 8 cm of water and

51 As expected, %PSV directly correlated with %VV (P<0.0001, r=0.935), wi

52 Seventy-five PSV cases and 273 controls (220 nonvasculitis, 19 second

53 5% confidence interval [CI]: 0.95, 1.00) for PSV and 0.86 (95% CI: 0.78, 0.95; P = .011) for RI.

54 ide, the difference averaged 1.0 +/- 1.3 for PSV ratios and 2.7 +/- 6.9 for EDV ratios, depending on

55 weaning was not significantly different for PSV (1.6 days), VSV (1.8 days), and no protocol (2.0 day

56 e rates were not significantly different for PSV (15%), VSV (24%), and no protocol (17%) (P =.44).

57 ACH homologs acted in a cascading manner for PSV trafficking.

58 l surface GD1a ganglioside could be used for PSV binding and infection as a receptor.

59 We biochemically fractionated PSVs from Brassica napus and defined a crystalloid-like

60 rity (NHA) who were >15 years of age and had PSV first diagnosed between January 1, 1988 and December

61 On the other hand, PSVs had no binding affinity for synthetic histo-blood g

62 or technical factors raise concern that ICA PSV may not be representative of the extent of disease.

63 is visible; (iii) 50%-69% stenosis when ICA PSV is 125-230 cm/sec and plaque is visible; (iv) > or =

64 or =70% stenosis to near occlusion when ICA PSV is greater than 230 cm/sec and visible plaque and lu

65 A should be diagnosed as (i) normal when ICA PSV is less than 125 cm/sec and no plaque or intimal thi

66 ning is visible; (ii) <50% stenosis when ICA PSV is less than 125 cm/sec and plaque or intimal thicke

67 aspects of QOL are significantly impaired in PSV.

68 decreased hydrolysis of storage proteins in PSV.

69 as receptors, we examined the role of SAs in PSV binding and infection.

70 sted ventilatory assist and PSV-NIV+ than in PSV-NIV- (p < .05).

71 Thereafter, patients were ventilated in PSV and NAVA under continuous rocuronium infusion for 2

72 logy to pathways in yeast or mammals, nor is PSV ultrastructure known in Arabidopsis vegetative tissu

73 Diabetic patients had lower PSV and higher RI within CRA and TPCA (P</=0.05).

74 However, many PSV assays are nevertheless somewhat challenging and req

75 Mean PSV and VICA/VCCA increased with stenosis level (P < .01

76 Mean PSV, VICA/VCCA, and SDs were calculated for each categor

77 ts, 36 (38.7%) had proven appendicitis (mean PSV, 19.7 cm/sec; mean RI, 0.69) and 57 patients (61.2%)

78 0.69) and 57 patients (61.2%) did not (mean PSV, 7.1 cm/sec, P < .0001; mean RI, 0.50, P < .0001).

79 n the central retinal artery (CRA), the mean PSV decreased 16% (P = 0.0137), and the mean EDV decreas

80 significant differences observed in the mean PSV, EDV, or RI at 24 hours or 1 month after treatment.

81 tion of five mutation and 139 mistranslation PSVs.

82 A porcine model (PSV) was utilized to validate these metabolomic changes

83 ying stenoses as 69% or less or 70% or more, PSV and VICA/VCCA were correct in 90.6% and 90.3% of ves

84 ture of the cruciferin holocomplex, a native PSV fraction was analyzed by single particle electron mi

85 s proposed to determine whether the observed PSVs originate from mutation or mistranslation by charac

86 The advantage of PSV is that a complete experiment can be simulated relat

87 res, likely linked to a bottom-up control of PSV by the inner core's heterogeneities but with contrib

88 sured 6-8 mm, the discriminatory criteria of PSV greater than 10 cm/sec and RI greater than 0.65 yiel

89 Chosen discriminatory criteria of PSV greater than 10 cm/sec and RI greater than 0.65 yiel

90 The overall annual incidence of PSV among NHA residents was 19.8/million (95% confidence

91 ur study population, the annual incidence of PSV is slowly increasing with time and the incidence is

92 nd POB(N) were measured at various levels of PSV, ranging from 5 to 25 cm H(2)O.

93 Decreased mobilization of PSV reserves is accompanied by reductions in the free am

94 The prevalence of PSV in this cohort was estimated on December 31, 1997.

95 lation by characterizing the distribution of PSVs.

96 e demonstrate that a significant fraction of PSVs in segmental duplications overlaps with variants an

97 osynthesis is fully functional, the roles of PSVs in adult vegetative tissues are not understood.

98 Fifty-one PSV patients completed questionnaires assessing QOL (Sho

99 Optimal PSV cutoff values were less than 67 cm/sec and 39 cm/sec

100 (which targeted normal work of breathing) or PSV (which targeted a normal respiratory rate and tidal

101 d using the Respironics Vision ventilator or PSV using a Puritan-Bennett 7200ae critical care ventila

102 w lumen diameters and blood flow parameters (PSV, EDV, PI, RI).

103 There was a significant increase in PCA PSV at 1st week in Group 1 (P = 0.002).

104 endicitis exhibit significantly higher point PSV and point RI values than do patients without appendi

105 Poststenotic PSV was mildly dependent on end-organ vascular resistanc

106 d-organ vascular resistance and poststenotic PSV.

107 reported variability from using poststenotic PSV to detect hemodynamically significant renal arterial

108 We show that cPrG prevents PSV acidification in aleurone layers and prevents synthe

109 We used papillomavirus (PV) pseudoviruses (PSVs) as a model vaccine and a gene delivery vector to a

110 Taking a biochemical approach, we purified PSVs from different developmental stages.

111 We found that oral immunization with PV PSV induced minimal mucosal and systemic Abs and CTLs sp

112 rovided a basis for clinical trials using PV PSVs encoding IL-2 for vaccination of the elderly.

113 When aged mice were immunized with PV PSVs encoding human IL-2, specific Th cells were generat

114 e, but not other gangliosides, could restore PSV binding and infection, further confirming alpha2,3-l

115 The porcine sapelovirus (PSV) is known to cause enteritis, pneumonia, polioenceph

116 The receptor(s) for porcine sapelovirus (PSV), which causes diarrhea, pneumonia, polioencephalomy

117 y useful tool for consideration when setting PSV to unload the respiratory muscles.

118 The presence of similar PSVs also containing prolamins and large systems of intr

119 e large vacuole lumen is replaced by smaller PSVs.

120 erior ciliary (TPCA) arteries, the systolic (PSV), end-diastolic and mean blood flow velocities as we

121 l and phospholipase C), we demonstrated that PSV could recognize alpha2,3-linked SA on glycolipids as

122 lood group antigens (HBGAs), suggesting that PSVs could not use HBGAs as receptors.

123 The PSV matrix contains glycoproteins that are trafficked th

124 The PSV preparations are ideal for a global proteome analysi

125 results suggest a developmental role for the PSV in vegetative tissues.

126 oup and 6.8 days (95% CI, 5.4 to 8.8) in the PSV group (P = 0.58).

127 PAV+ group and in 28 patients (9.8%) in the PSV group (P = 0.79).

128 as 27 (interquartile range, 24 to 27) in the PSV group and 27 (interquartile range, 23 to 27) in the

129 A total of 969 patients (484 in the PSV group and 485 in the T-piece group) were included in

130 son for reintubation in 9 patients (3 in the PSV group and 6 in the T-piece group).

131 thin 24 hours in 376 patients (77.7%) in the PSV group and in 350 patients (72.2%) in the T-piece gro

132 rformed in 72 of 481 patients (14.9%) in the PSV group and in 65 of 477 patients (13.6%) in the T-pie

133 90 (29.6% in the PAV+ group and 26.6% in the PSV group), all of which were secondary outcomes, were s

134 group and 0.04+/-0.97 mg per kilogram in the PSV group.

135 o the PSV and its spatial arrangement in the PSV.

136 systolic velocity (PSV) and the ratio of the PSV in the ICA to that in the ipsilateral common carotid

137 and storage within peripheral regions of the PSV.

138 ctron microscopic observations show that the PSV preparations are homogenous, with the soluble spore

139 d ferrocene derivative, it is shown that the PSV technique can be used to recover the key chemical an

140 However, the receptor(s) that the PSV utilizes to enter host cells remains largely unknown

141 fficient transport of alpha-globulins to the PSV and its spatial arrangement in the PSV.

142 En route to the PSV, the proteins co-localize in large (>200 nm) vesicle

143 defective in trafficking of proteins to the PSV.

144 ant species, such as tomato and tobacco, the PSV contains two types of microscopically visible intra-

145 ak systolic velocity (PSV) compared with the PSV immediately upstream.

146 ophagic compartments before merging with the PSV.

147 nt of alpha-globulin and glutelin within the PSV, with the accompanying presence of numerous small al

148 The PSVs are not clathrin-coated and do not contain the SpiA

149 The PSVs contain approximately 80 proteins, and we have iden

150 In seeds of the family Brassicaceae, the PSVs lack visible crystalloids and have many small globo

151 During development the PSVs increase in size and density concomitant with an in

152 l and systemic Abs and CTLs specific for the PSVs in aged mice compared with young adult mice.

153 localized the BPEPs to structures within the PSVs, whose appearance was consistent with a diffuse net

154 Focal 2- to 2.9-times PSV elevation was associated with 75% or greater stenosi

155 cuoles for membrane proteins: a direct ER to PSV pathway, and a separate pathway via the Golgi to the

156 However, this trafficking mechanism to PSV is poorly understood.

157 2 with a defect in seed protein transport to PSV.

158 Trafficking pathways to PSVs and lytic vacuoles appear to be distinct.

159 owever, it is unclear whether trafficking to PSVs has any analogy to pathways in yeast or mammals, no

160 Total PSV, subgroups (47 Wegener's granulomatosis [WG], 12 mic

161 underwent PAV+ and the group that underwent PSV.

162 Although plants use PSV proteins during germination, before photosynthesis i

163 The protein storage vacuole (PSV) becomes acidified rapidly when aleurone cells are t

164 The protein storage vacuole (PSV) is a specialized organelle in plant seeds that accu

165 trafficking to the protein storage vacuole (PSV) is a specialized process in seed plants.

166 ith glutelin in the protein storage vacuole (PSV).

167 Membranes of protein storage vacuoles (PSV) are marked by the presence of alpha-tonoplast intri

168 ge proteins inside protein storage vacuoles (PSVs) instead of the ER.

169 ins in specialized protein storage vacuoles (PSVs) within seeds and vegetative tissues.

170 finally stored in protein storage vacuoles (PSVs).

171 were identified as protein storage vacuoles (PSVs).

172 Protein sequence variants (PSVs) are a type of product-related variant in which err

173 isms (SNPs) or paralogous sequence variants (PSVs) separated by several kilobases.

174 ntify reliable paralogous sequence variants (PSVs) that differentiate repeat copies.

175 and leverages paralogous sequence variants (PSVs)-sequence differences between paralogous sequences-

176 ith an evaluation of paleosecular variation (PSV) over the past 10 Myr.

177 n children with primary systemic vasculitis (PSV).

178 ned pre-procedural peak systolic velocities (PSV) and end-diastolic velocities (EDV) in the contralat

179 The range of CCA peak systolic velocities (PSVs) and end diastolic velocities (EDVs) and velocity r

180 (c) ICA peak systolic velocity (PSV) and presence of plaque on gray-scale and/or color D

181 non-angle-corrected peak systolic velocity (PSV) and resistive index (RI) values were compared betwe

182 olic velocity (EDV), peak systolic velocity (PSV) and resistive index (RI).

183 ICA peak systolic velocity (PSV) and the ratio of the PSV in the ICA to that in the

184 higher elevation of peak systolic velocity (PSV) compared with the PSV immediately upstream.

185 The range of peak systolic velocity (PSV) measurement (maximum minus minimum) averaged 20 cm/

186 ms) with and without peak systolic velocity (PSV) thresholds (determined with receiver operating char

187 acceleration (ESA), peak systolic velocity (PSV), end diastolic velocity (EDV), and waveform morphol

188 nges observed in the peak systolic velocity (PSV), end diastolic velocity (EDV), or resistive index (

189 Peak systolic velocity (PSV), end-diastolic velocity (EDV), resistive index (RI)

190 8 ml/kg under pressure support ventilation (PSV) and under sedation.

191 re severe with pressure support ventilation (PSV) breaths than with intermittent mandatory ventilatio

192 Pressure support ventilation (PSV) is almost universally employed in the management of

193 ntilation than pressure-support ventilation (PSV) is unclear.

194 use of either pressure-support ventilation (PSV) or a T-piece.

195 applied using pressure support ventilation (PSV).

196 coordinate fusion of the prespore vesicles (PSVs) with the plasma membrane at the terminal stage of

197 irus 2 (SARS-CoV-2) spike pseudotyped virus (PSV) assays are widely used to measure neutralization ti

198 rameters from purely sinusoidal voltammetry (PSV) experiments, investigating the redox reactions of a

199 intima outside the stent (peri-stent volume, PSV) and volume of neointima within the stent (intrasten

200 ins in a clinically selected population when PSV criteria are used.

201 Whether PSV trials may result in a shorter time to tracheal extu

202 th cANCA 3.3 [1.0-10.8]), drug allergy (with PSV 3.6 [1.8-7.0], with WG 4.0 [1.8-8.7], and with cANCA

203 during working lifetime was associated with PSV (2.2 [1.2-3.8]) and with WG (2.7 [1.3-5.7]).

204 index year was significantly associated with PSV (OR 2.3 [95% CI 1.2-4.6]), with WG (2.7 [1.2-5.8]),

205 Fifty children with PSV, 17 children with nonvasculitic inflammatory disease

206 Compared with PSV delivered with the Puritan-Bennett 7200ae, PAV is as

207 lvent exposure during working lifetime (with PSV 2.7 [1.1-6.6], with WG 3.4 [1.3-8.9], and with cANCA

208 A 4.7 [1.9-11.7]), and allergy overall (with PSV 2.2 [1.2-3.9], with WG 2.7 [1.4-5.7]).

209 spontaneous-breathing trials performed with PSV did not result in significantly more ventilator-free

210 to undergo partial ventilatory support with PSV but were not yet ready for liberation from ventilati

211 onal silica exposure in the index year (with PSV 3.0 [1.0-8.4], with CSS 5.6 [1.3-23.5], and with ANC

212 nal solvent exposure in the index year (with PSV 3.4 [0.9-12.5], with WG 4.8 [1.2-19.8], and with cla