ライフサイエンスコーパス: Po

1 Po and merosin are required for normal myelination in th

2 Po fat ingestion rapidly induces insulin resistance by r

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

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 0.03 Po, 0.59 +/- 0.03 Po, and 0.65 +/- 0.02 Po were 197 +/- 35 ms, 184 +/- 35 ms, and 179 +/- 22 ms.

20 half-times for relaxation from 0.36 +/- 0.03 Po, 0.59 +/- 0.03 Po, and 0.65 +/- 0.02 Po were 197 +/-

21 axation from 0.36 +/- 0.03 Po, 0.59 +/- 0.03 Po, and 0.65 +/- 0.02 Po were 197 +/- 35 ms, 184 +/- 35

22 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

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

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

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

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

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

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

29 (210)Po was determined by alpha spectrometry.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

60 ates from steady-state forces less than 0.50 Po was also observed when bundles of fibers were bathed

61 -2 s-1) and constant up to approximately 50% Po, then rising sharply to a maximum (16 +/- 0.8 s-1) in

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

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

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

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

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

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

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

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

70 % (p< or =.043) of the variability in Pt and Po, respectively.

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

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

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

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

75 ith dATP, Vu was 25% greater than control at Po and was elevated at all P > 0.15Po, whereas Po was un

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

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

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

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

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

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

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

83 stimulatory effect of NHERF on CFTR channel Po.

84 During inactivation, channel Po was greater at hyperpolarized rather than depolarized

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

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

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

88 these (Ca2+-free) conditions, single-channel Po showed both voltage-dependent and voltage-independent

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

108 /- 22 for Pe vs. 96 +/- 29 ng/mL/180 min for Po).

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

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

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

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

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

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

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

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

117 The channels maintained their high Po in patches excised in inside-out mode into a Ca2+-fre

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

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

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

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

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

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

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

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

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

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

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

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

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

131 .2DeltaN14 may be explained by the increased Po.

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

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

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

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

136 ed times and only two closed states, and its Po was less affected by hyperpolarization.

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

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

139 relationships between MEKC retention and log Po/w.

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

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

142 o) long open time behaviour to extremely low Po, short open time channel activity.

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

144 found when the channel was gating in the low Po mode.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

161 n calcium-ascending protocols (54% vs. 3% of Po, the force at pCa 6.0) (force hysteresis); the levels

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

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

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

165 e accounted for by the voltage dependence of Po.

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

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

168 3 currents was due to a strong inhibition of Po and a moderate suppression of single channel conducta

169 Potentiation of Po by increased luminal Ca2+ occurred irrespective of wh

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

201 5 mM increased the open channel probability (Po) of native RyRs in SR vesicles, but not of purified R

202 se normally had a very low open probability (Po < 0.1), which, however, showed a dramatic and reversi

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

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

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

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

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

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

209 lationship between channel open probability (Po) and Vj was well described by a Boltzmann relationshi

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

211 conductance and decreased open probability (Po) compared with those of human CFTR.

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

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

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

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

216 channel density (N) and/or open probability (Po) increase as [Na+]o decreases.

217 switch from sustained high open probability (Po) long open time behaviour to extremely low Po, short

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

219 enantiomers increased the open probability (Po) of human CFTR, suggesting that bromotetramisole may

220 With FMRFamide, the open probability (Po) of the channel was 0.06 at 0.3 microM and 0.76 at 30

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

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

223 >/=5 microM) increased the open probability (Po) of very active ("high-activity") RyR1 of SkM reconst

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

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

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

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

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

229 and regulates the channel open probability (Po).

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

231 inetics and relatively low open probability (Po).

232 radual increase in channel open probability (Po).

233 d increased single channel open probability (Po).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

255 s studies have shown that isometric tension (Po) decreases linearly in the logarithm of [Pi] for [Pi]

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

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

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

259 the peak isometric twitch (Pt) and tetanic (Po) tensions, as well as fatigability during 5 secs of n

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

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

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

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

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

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

266 ected by respiratory distress located in the Po Valley.

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

268 The magnitude of the Po increase was a function of both the duration and the

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

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

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

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

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

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

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

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

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

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

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

280 and voltage-independent components in their Po/V relationship) show points of resemblance to those e

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 and was elevated at all P > 0.15Po, whereas Po was unchanged.

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

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

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

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

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

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