ライフサイエンスコーパス: Po

1 Po fat ingestion rapidly induces insulin resistance by r

2 Po vein insulin delivery, or strategies that mimic it (i

3 Po(2+) occurrence in low-to-neutral-pH waters is attenua

4 Po(gamma) curves had the midpoint at 5.5 +/- 0.1 dyne/cm

5 (2)(1)(0)Po accumulates in the ovaries where it kills primary ooc

6 (2)(1)(0)Po also accumulates in the yolk sac of the embryo and in

7 s between environmental exposure to (2)(1)(0)Po and human health effects were identified in a literat

8 ior, biokinetics, and toxicology of (2)(1)(0)Po and identified the need for future research.

9 evaluate environmental exposure to (2)(1)(0)Po and the biological effects of low-dose exposure to it

10 The radionuclide grandparents of (2)(1)(0)Po are common in sediments, and segments of the public m

11 hronically exposed to low levels of (2)(1)(0)Po in drinking water or in food products from animals ra

12 gical and toxicological research on (2)(1)(0)Po is more than four decades old.

13 (2)(1)(0)Po is present in cigarettes and maternal smoking has sev

14 Low-level exposure to (2)(1)(0)Po may have subtle, long-term biological effects because

15 Polonium-210 ((2)(1)(0)Po) concentrations that exceed 1 Bq/L in drinking-water

16 itivity and tendency to concentrate (2)(1)(0)Po, the ovary may be the critical organ in determining t

17 r consistent with the toxicology of (2)(1)(0)Po.

18 ining the lowest injurious dose for (2)(1)(0)Po.

19 1 association with oxygen of 0.209 sec(-1) + Po(2) 2.07 x 10(-4) sec(-1)/mm Hg at 37 degrees C, and a

20 Using (31)P NMR spectroscopy, 11 Po species were detected in the mono- and diester region

21 nsP3], ATP had dramatic effects on mInsP3R-2 Po, but unlike the rInsP3R-1, this did not occur by alte

22 d Am) for long-lived polonium isotopes ((208)Po, (209)Po, (210)Po) are effectively removed during pro

23 long-lived polonium isotopes ((208)Po, (209)Po, (210)Po) are effectively removed during processing.

24 d to different amounts of (210)Po using (209)Po as a yield tracer.

25 etermined through self-deposition using (209)Po as a yield tracer.

26 (210)Po concentrations >= 0.7 pCi/L occurred almost exclusive

27 (210)Po was determined by alpha spectrometry.

28 s, lead-210 ((210)Pb) and polonium-210 ((210)Po) >= 1.0 and 0.7 pCi/L (picocuries per liter), respect

29 Polonium-210 ((210)Po) can be rapidly determined in drinking water and urin

30 Polonium-210 ((210)Po) gained widespread notoriety after the poisoning and

31 ha-emitting radon progeny Polonium-210 ((210)Po) in the olfactory epithelium, olfactory bulb, frontal

32 d a liposome sample, when compared to a (210)Po based bipolar charge equilibration device.

33 sequential determination of (90)Sr and (210)Po in food samples using ultra low-level liquid scintill

34 f stable strontium as yield tracer, and (210)Po is determined through self-deposition using (209)Po a

35 for radiocaesium, (226)Ra, (210)Pb, and (210)Po surpasses those values.

36 (210)Pb and (210)Po were detected at concentrations greater than these th

37 is 25.0 and 2.0Bqkg(-1) for (90)Sr and (210)Po, respectively.

38 three to four orders of magnitude below (210)Po-derived doses.

39 e also assessed the association between (210)Po levels and exposure parameters for urban air pollutio

40 able to detect the radiation emitted by (210)Po, an atypical clinical course prompted active consider

41 y the naturally occurring alpha-emitter (210)Po and that Fukushima-derived doses were three to four o

42 5 and from <13.6 to 233.3 Bq kg(-1) for (210)Po, (238)U, (232)Th and (40)K respectively, whereas they

43 The effective dose, from (210)Po ingested by total diet, accounts for only 5-12% of th

44 ic status also had significantly higher (210)Po levels in lungs (coefficient = -1.19; standard error

45 The olfactory bulb had higher (210)Po levels than either olfactory epithelium (p = 0.071),

46 its on radionuclides in foods including (210)Po and (90)Sr, two of the most important radionuclides f

47 radioactive alpha-particle emitter like (210)Po.

48 The mean of (210)Po activity resulted 0.40+/-0.46Bqkg(-1) with a range of

49 ent's death established the presence of (210)Po at concentrations about 10(9)-times higher than norma

50 lyses showed autolysis and retention of (210)Po at lethal doses in several organs.

51 Our findings of the deposition of (210)Po in autopsy tissues suggest that airborne radionuclide

52 Early symptoms of (210)Po poisoning are indistinguishable from those of a wide

53 on emission, raising the possibility of (210)Po poisoning.

54 ssfully applied to different amounts of (210)Po using (209)Po as a yield tracer.

55 findings show that the concentration of (210)Po was associated with anthracosis in lungs of non-smoke

56 annual effective dose due to intake of (210)Po, (238)U, (232)Th and (40)K ranged from 280 and 800 mu

57 he background activity concentration of (210)Po, a radionuclide with a high radiotoxicity.

58 ured amounts and tissue distribution of (210)Po, it was estimated that the patient had ingested sever

59 exposed to different concentrations of (210)Po-citrate.

60 ed polonium isotopes ((208)Po, (209)Po, (210)Po) are effectively removed during processing.

61 alpha-particle-emitting radiochemical ((210)Po-citrate) and 2 anticancer drugs (daunomycin and doxor

62 food products of vegetable origin, the (210)Po activity concentration follows the trend: leafy veget

63 The (210)Po activity concentration was also compared with that fo

64 The committed effective doses due to (210)Po from ingestion of honey for infants, children and adu

65 uted about 67% of the total dose due to (210)Po ingestion.

66 Exposure to (210)Po resulted initially in a clinical course that was indi

67 re determined by alpha ((235)U, (238)U, (210)Po, (232)Th and (228)Th) and gamma spectrometry ((137)Cs

68 An overlapping deficiency, Df(3R)Po(4), allowed us to map several of these groups to eith

69 e-pCa relationship for forces less than 0.50 Po (maximum Ca2+-activated force), i.e. the Hill coeffic

70 -2 s-1) and constant up to approximately 50% Po, then rising sharply to a maximum (16 +/- 0.8 s-1) in

71 currents (which in the absence of ATP have a Po of > 0.8 and are not blocked by tolbutamide).

72 in a Col-0 genetic background, but not in a Po-1 background.

73 perimentation demonstrated that some abiotic Po(v) generation is possible.

74 The flight-induced decline in absolute Po was attributed to reductions in fibre diameter and/or

75 y simply increasing the maximally achievable Po at a particular [InsP3] and [Ca2+].

76 The OM treatment increased all Po concentrations in the 0-40 cm soil depth, while NPK a

77 velocity, functional capillary density, and Po(2) in arterioles, venules, and extravascular tissue.

78 AUC) for glucagon was similar between Pe and Po, but the peak occurred earlier in Pe.

79 Pt and Po correlated poorly with total AChR protein and express

80 % (p< or =.043) of the variability in Pt and Po, respectively.

81 n Arabidopsis ecotypes Col-0 (resistant) and Po-1 (susceptible) revealed segregation of more than one

82 mpensated state, with physiological arterial Po(2).

83 espectively, and less with the associational Po and LP.

84 itions ( approximately 5 microM; channels at Po approximately 0.3) but not under diastolic Ca(2+) con

85 nnel open probability in the absence of ATP (Po(zero)) and a correlated decrease in sensitivity to in

86 Average Po(2) across the inner 50% of the retina was higher (22

87 or even more pronounced, than those between Po and ventro-posterior thalamic nucleus synapses in S1.

88 The extent of the biotic Po(v) production correlates exponentially with elevated

89 study conducted at Sannazzaro de' Burgondi (Po Valley), Italy, specifically aimed at optimizing the

90 binding domains increase L-type Ca2+ channel Po by a low Ca(2+)-CaM activity mechanism.

91 Bmp and CaMKII increased L-type Ca2+ channel Po in a non-additive manner, suggesting that low and hig

92 ty of NHERF PDZ1-2 to stimulate CFTR channel Po.

93 stimulatory effect of NHERF on CFTR channel Po.

94 ion ( approximately 50%) and reduced channel Po ( approximately 55%).

95 in part due to an increase in single channel Po and that the cytoplasmic tails of the beta- and gamma

96 s, has a significantly higher single channel Po compared to the wild-type channel (0.85 vs 0.60, resp

97 croM) than wild-type (Kir6.2/SUR1) channels (Po = 0.32, Ki = 28 microM).

98 roM), when compared with wild-type channels (Po = 0.3; Ki, 22 microM).

99 also significantly higher, whereas choroidal Po(2) was significantly lower in the photocoagulated ret

100 (lPPC) connects with the posterior complex (Po).

101 lowered whereas under hydrolytic conditions, Po. increases as temperature is elevated.

102 NBDs are kept at a dimerized configuration, Po is reduced by approximately 10-fold.

103 xygen tension and consequently increased CSF Po(2) resulting from administration of high Fio(2) durin

104 Mean final (d12) Po(2) was 10.64 +/- 0.77 mm Hg for the oxygenation group

105 o the conclusion that the mutation decreases Po by perturbing the gating conformational changes in CF

106 conclusion that the R117H mutation decreases Po by perturbing the gating conformational changes in CF

107 h elevated particulate Po (Po(p)): dissolved Po (Po(aq)) ratios in the cultures, consistent with effi

108 physiology to demonstrate that LP and dorsal Po cells exhibit a variety of responses to simple visual

109 responsive neurons across the LP and dorsal Po whose properties align with some of the established f

110 the open probability (Po.) is reversed, i.e. Po. increases as temperature is lowered whereas under hy

111 s in the cultures, consistent with efficient Po bioaccumulation.

112 abolished Ang II-mediated increases in ENaC Po in murine distal nephron.

113 We found that Ang II acutely increases ENaC Po, whereas prolonged exposure to Ang II also induces tr

114 Ang II actions on ENaC Po persist in the presence of saturated mineralocorticoi

115 None of the enteric caliciviruses except Po/Sapo/GIII/Cowden/80/US replicates in cell culture, wh

116 /- 22 for Pe vs. 96 +/- 29 ng/mL/180 min for Po).

117 oped less average peak Ca2+ activated force (Po) during fixed-end contractions (0.78 +/- 0.02 vs. 0.9

118 ects of both GCs on maximum isometric force (Po) were fibre-type dependent.

119 Greater Po concentrations were found, however, in the non-paddy

120 bout 22-25 pS and had a 3- to 7-fold greater Po than in 0 Ca2+o.

121 f the thalamus: the posterior nuclear group (Po), and a region located at the interface of the centra

122 us dog, insulin was infused into the hepatic Po vein or a peripheral (Pe) vein at a rate four times o

123 ry into both mode 1(low Po) and mode 2 (high Po) gating states and that these gating impairments can

124 o(2) (approximately 1% O(2)) but not at high Po(2) (approximately 21% O(2)).

125 one TRIC-B channels exhibit low Po, the high Po levels reached by multiple TRIC-B channels may provid

126 channels produced no significant changes in Po, nor did it restore the ability of RyRs to respond to

127 t, whereas the genistein-induced decrease in Po was voltage independent.

128 ls, the underlying causes of the decrease in Po were similar.

129 rated that mutant channels had a decrease in Po with 0.16 +/- 0.03 versus 0.67 +/- 0.07 for wild type

130 The decrease in Po with low pHi resulted from an increase in the channel

131 de that the functional defect (a decrease in Po) of DeltaF508-CFTR is as important as the trafficking

132 prevented the genistein-induced decrease in Po, but was without effect on the genistein-induced decr

133 The increase in Po occurred within 10 min and was insensitive to the tra

134 microM Ca2+o had a 5- to 6-fold increase in Po which was accompanied by increases in both open times

135 in protocol 1 and fell faster in Pe than in Po, reaching 41 +/- 3 vs. 67 +/- 2 mg/dL (P < 0.01) by 6

136 the single channel currents had an increased Po compared to negative potentials which was associated

137 ogue 1-oleoyl-2-acetyl-sn-glycerol increased Po, but phorbol 12,13-dibutyrate, which stimulates prote

138 Previous measurements showed increased Po(2) in the preretinal vitreous of rabbits and pigs (bu

139 .2DeltaN14 may be explained by the increased Po.

140 Thus, they increased Po in the slow-twitch fibre bundles without significantl

141 the boutons made in each area by individual Po axons, as well as in functionally-relevant parameters

142 the MC versus the S1 branches of individual Po cell axons that innervate both areas.

143 at high altitude because of the low inspired Po(2), which is caused by the reduced barometric pressur

144 oelectrodes were used to record intraretinal Po(2) profiles from healed photocoagulation lesions in a

145 ur main result that HONO in the investigated Po Valley region is mainly from a gas-phase source that

146 fied as the prevalent class of enzyme-labile Po, followed by labile monoester- and diester-P.

147 However, high-level Po(v) generation in these cultures is predominantly biot

148 relationships between MEKC retention and log Po/w.

149 mutation impedes entry into both mode 1(low Po) and mode 2 (high Po) gating states and that these ga

150 acic aorta from both rabbit and mouse at low Po(2) (approximately 1% O(2)) but not at high Po(2) (app

151 d, although lone TRIC-B channels exhibit low Po, the high Po levels reached by multiple TRIC-B channe

152 odel provided a better discrimination of low Po(2) than the tissue-to-plasma ratio or the k(3) of the

153 We also show that subgroups of LP/Po cells integrate signals from both eyes in various way

154 inhibitory peptide equalized TG and WT LTCC Po and eliminated EADs, whereas a peptide antagonist of

155 y underlie their highly differential maximal Po observed in cell-attached patches.

156 nnels was 0.13 +/- 0.02, with a half-maximal Po potential (Vo) of -28.7 +/- 1.4 mV for control record

157 Retigabine increased mean maximal Po to 0.38 +/- 0.04 and produced a hyperpolarising shift

158 ylinositol (4)5-kinase increased the maximal Po of both Kv7.2 and Kv7.2/7.3 channels studied in on-ce

159 on of muscarinic agonist reduced the maximal Po of Kv7.2/7.3 channels isolated in on-cell patches.

160 affinities that correlate with their maximal Po in on-cell mode.

161 Mean Po and open times were reduced in resistant isolates.

162 The minimum Po(2) was also significantly higher, whereas choroidal P

163 was calibrated in water phantoms at multiple Po(2) and temperature conditions (n = 10) and in ex vivo

164 ic Ca(2+) conditions ( approximately 100 nM; Po < 0.01).

165 Whereas normal Po(2)s were maintained at the inner and outer border of

166 l portions of the posterior thalamic nuclei (Po), multisensory processing of information related to a

167 Thalamocortical posterior nucleus (Po) axons innervating the vibrissal somatosensory (S1) a

168 medial pulvinar (PM), and posterior nucleus (Po).

169 igated the mouse Posterior thalamic nucleus (Po) cell axons that simultaneously innervate motor and s

170 ucleus (CL), and posterior thalamic nucleus (Po).

171 magnitude, respectively, greater amounts of Po(v) compared to the other organisms tested.

172 ong main roadsides and in vegetated areas of Po river plain.

173 Intriguingly, the composition of Po was remarkably stable after 194-years of paddy manage

174 e accounted for by the voltage dependence of Po.

175 The other resistance-determining genes of Po-1 can function, however, as they successfully conferr

176 nd RyR2 (sheep) with a maximal inhibition of Po (Emax) to 52 +/- 4% of control only after adding phys

177 3 currents was due to a strong inhibition of Po and a moderate suppression of single channel conducta

178 drolysis data, we proposed that recycling of Po in vegetative biomass residues is an important mechan

179 of the voltage-sensors; and 3), reduction of Po without impaired voltage-sensor movement.

180 ly large differences between the synapses of Po versus ventral posteromedial thalamic nucleus axons i

181 ncreased the probability of channel opening (Po) sixfold, which was associated with an increase in th

182 The probability of opening (Po) of the channel is further augmented at positive pote

183 ative potentials the probability of opening (Po) was low and the open time distributions were describ

184 buted to reductions in fibre diameter and/or Po per fibre cross-sectional area.

185 ponse properties of cells in the mouse LP or Po.

186 of intratumoral partial pressure of oxygen (Po(2)).

187 troretinography (ERG) and preretinal oxygen (Po(2)) measurements were obtained 3 to 5 days before sur

188 Total extractable organic P (Po) concentrations ranged from 504 to 1643 mg kg(-1) and

189 xtent (46%, 0.09+/-0.03 versus 0.14+/-0.02 P/Po x ML/sec) during half-maximal Ca2+ activations.

190 - myocytes (0.15+/-0.01 versus 0.19+/-0.03 P/Po x ML/sec) during maximal Ca2+ activations.

191 uptake capacity reaching >14 mmol g(-1) at P/Po of 0.4.

192 t a very low relative saturation pressure (P/Po) of 0.02.

193 ates exponentially with elevated particulate Po (Po(p)): dissolved Po (Po(aq)) ratios in the cultures

194 s and properties of soil organic phosphorus (Po) largely drive ecosystem productivity with increasing

195 evated particulate Po (Po(p)): dissolved Po (Po(aq)) ratios in the cultures, consistent with efficien

196 exponentially with elevated particulate Po (Po(p)): dissolved Po (Po(aq)) ratios in the cultures, co

197 In high-pH environments, aqueous polonium (Po) is poorly sorbed, occurring as dihydrogen polonate (

198 Thin-layer polonium (Po) sources for alpha spectrometry counting can be rapid

199 The production of volatile polonium (Po(v)), a naturally occurring radioactive element, by pu

200 We hypothesized that portal (Po) vein insulin delivery would lessen hypoglycemia.

201 Here, we present POSSUM ( Po sition- S pecific S coring matrix-based feat u re gen

202 (Med), ventral posterior (VP) and posterior (Po) nuclei.

203 l (VM), ventral lateral (VL), and posterior (Po) thalamic nuclei.

204 stablished multisensory features: posterior (Po), suprageniculate (Sg), limitans (Lim), and medial pu

205 gher-order neurons located in the posterior (Po), lateral posterior (LP), and lateral dorsal (LD) nuc

206 At positive potentials Po and the longer mean open time were greatly increased.

207 DeltaF508-CFTR targeting) and potentiator ("Po", normalizing DeltaF508-CFTR channel gating) activiti

208 Preretinal Po(2) in the posterior vitreous was measured 30 minutes

209 rug application; the lower the prestimulated Po, the higher the potentiation.

210 Maximal open probabilities (Po) of Kv7.2-Kv7.4 homomultimers and of Kv7.2/7.3 hetero

211 5 mM increased the open channel probability (Po) of native RyRs in SR vesicles, but not of purified R

212 pproximately 13-fold lower open probability (Po ), were found with the R117H mutation that is associa

213 pproximately 13-fold lower open probability (Po ).

214 Delta33 showed an enhanced open probability (Po = 0.6 at -60 mV) and a reduced ATP sensitivity (Ki, 8

215 KATP channels had a higher open probability (Po = 0.7) and a lower ATP sensitivity (Ki = 196 microM)

216 ases the intrinsic channel open probability (Po(0)), thereby indirectly producing a marked decrease i

217 ctance, maximal achievable open probability (Po) and the [Ca2+] required for activation and inhibitio

218 l (Vr) of +10 mV and a low open probability (Po) at negative patch potentials.

219 IRK1 open probability (Po) decreased sharply with hyperpolarization due to an i

220 The mean maximal open probability (Po) for single KCNQ2/3 channels was 0.13 +/- 0.02, with

221 L- and N-type Ca2+ channel open probability (Po) in cell-attached patches that contained a single cha

222 do not change the channel open probability (Po) in the absence of ATP, supporting the involvement of

223 er of channels (N) and the open probability (Po) of a channel).

224 porated into bilayers, the open probability (Po) of channels from Tric-a KO mice was markedly lower t

225 of red cell membranes, the open probability (Po) of the Gardos channel is markedly reduced when the t

226 onists, the single-channel open probability (Po) of the phenylalanine 508-deleted cystic fibrosis tra

227 >/=5 microM) increased the open probability (Po) of very active ("high-activity") RyR1 of SkM reconst

228 minal Ca(2+) dependence of open probability (Po) over the physiologically relevant range (0.05-1 mM C

229 (P-dATP), can increase the open probability (Po) to approximately 0.7, implying that the gating defec

230 evel, i.e., an increase in open probability (Po), and second, these C-terminal regions of beta- and g

231 At low open probability (Po), the reciprocal of the slope in the ln(NPo)-voltage

232 to CFTR and increases its open probability (Po).

233 and regulates the channel open probability (Po).

234 , but a large reduction in open probability (Po).

235 d increased single channel open probability (Po).

236 wed us to obtain a maximum open probability (Po,max) value for the extrasynaptic receptors (Po,max =

237 perature dependence of the open probability (Po.) is reversed, i.e. Po. increases as temperature is l

238 ase L-type Ca2+ channel opening probability (Po) by inducing mode 2 gating.

239 activate EADs, and LTCC opening probability (Po) was significantly higher in TG than WT cardiomyocyte

240 igh baseline channel open-state probability (Po, at pH 7.4) with a strong inward rectification.

241 ic (L596A/G/W/Q/K) reduces open probability [Po; loss-of-function (LOF)], likely due to altered inter

242 Land reclamation promoted Po accumulation in both paddy and non-paddy topsoils (de

243 Immobilization reduced Pt, Po, fatigability, muscle mass, and fiber cross-sectional

244 L596I raises Po [gain-of-function (GOF)], apparently by placing its m

245 include mean arterial pressure, heart rate, Po(2), Pco(2), pH, and base excess.

246 ,max) value for the extrasynaptic receptors (Po,max = 0.72).

247 yperoxia increased the average inner retinal Po(2) (P(IR)) in the detached retina to a level higher t

248 After lesions, inner retinal Po(2) could also be maintained above zero, even in the a

249 ence for a chronic increase in inner retinal Po(2) in lesioned areas during air breathing.

250 used to collect spatial profiles of retinal Po(2) in both the attached and detached retina.

251 o the luminal side of purified channels, RyR Po increased significantly; however, the channels still

252 mice marked differences between MC versus S1 Po synapses in (1) bouton and active zone size, (2) neur

253 Schafmeister, Po, and Verdine (another study) introduced a method usin

254 The findings that individual dura-sensitive Po, LP, and LD neurons project to many functionally dist

255 We hypothesized that soil Po would initially increase with paddy management and th

256 T channel had indistinguishable steady-state Po values, ATP dose-response relationships and single-ch

257 One strain (Po/SaV/MI-QW19/2002/US) was most closely related to huma

258 hat yields less than 50% of maximal tension (Po).

259 conformation of Hb to tissue oxygen tension (Po(2)) and thereby provide a basis for the graded vasodi

260 a dense paddy plough pan hindered long-term Po accumulation in the paddy subsoil.

261 The Po(2) measurements were compared with spatially register

262 educed by increasing temperature, as are the Po values of inside-out patches of Chinese hamster ovary

263 Detachment did not change the Po(2) at the border between the avascular and vasculariz

264 aint significantly increased CRH mRNA in the Po (39%) and the CM-VPMpc (32%).

265 Herein, we demonstrate that ALW in the Po Valley, Italy, is also anthropogenic but is driven by

266 with chemical tracers at a rural site in the Po Valley, Italy.

267 ected by respiratory distress located in the Po Valley.

268 However, unlike channels from WT mice, the Po of SR K(+) -channels from Tric-a KO mice increased as

269 ics indicated that Ca2+ and ATP modulate the Po predominately by facilitating extended bursting activ

270 reased those in the lateral extension of the Po nucleus.

271 eserved in brackish Holocene deposits of the Po Plain, Italy.

272 acterize the suburban and rural areas of the Po Valley and of other many populated environments.

273 In the detached retina, the Po(2) at the border between the retina and the fluid lay

274 a large body of evidence indicates that the Po(2)-coupled allosteric transition from R (oxy)-state t

275 s with cloned RPS2 alleles revealed that the Po-1 allele of RPS2 can function in a Col-0 genetic back

276 s the latch bond in a tug-of-war to tune the Po of TRPV4.

277 However, when the Po was decreased (by ATP), tolbutamide was unable to blo

278 The authors sought to determine whether the Po(2) in the eye regulates lens growth.

279 equence in Bay of Hangzhou (China) for their Po composition using solution (31)P-NMR after NaOH-EDTA

280 bT2 resembled the wild-type channel in their Po and ATP sensitivity.

281 to rises of luminal [Ca] by increasing their Po.

282 Hb, and 7.5 g/dL with HES, leading to tissue Po(2) of 19, 8, and 5 mm Hg respectively.

283 dolateral part of PPC (PtP) also projects to Po but can be distinguished from lPPC based on architect

284 At least 4 weeks after treatment, Po(2)-sensitive microelectrodes were used to record intr

285 rature gradients, and ambient air on vitreal Po(2) values.

286 If uncorrected, vitreal Po(2) would be significantly overestimated (P < .001).

287 Vitreous Po(2) was imaged in three human volunteers (age range, 2

288 In vivo human vitreous Po(2) maps were spatially heterogeneous, with a whole vi

289 Measurement of vitreous Po(2) with MR imaging has the potential to be used to st

290 ging protocol to image quantitative vitreous Po(2) noninvasively and evaluated effects from vitreal m

291 atially heterogeneous, with a whole vitreous Po(2) of 16.7 mm Hg +/- 6.5 (eye closed).

292 polonide (DMPo) as the predominant volatile Po compound in culture headspace of the yeast.

293 For drinking water, Po in 10 mL samples was directly coprecipitated onto the

294 The main inputs of CL were Po and MGpd, with secondary inputs from MGad, MGm, and m

295 ble to those observed before disuse, whereas Po/CSA and unloaded shortening velocity reached a higher

296 at, although PPC subareas are connected with Po and medial LP, the medial and lateral secondary visua

297 rapid rundown following patch excision with Po decreasing from near 1.0 to near 0.

298 otential new genogroup of porcine SaVs, with Po/SaV/OH-JJ681/00/US as the representative strain.

299 or epinephrine was greater with Pe than with Po (67 +/- 17 vs. 36 +/- 14 ng/mL/180 min).

300 lucose fell faster with Pe insulin than with Po insulin, reaching 56 +/- 3 vs. 70 +/- 6 mg/dL (P = 0.