ライフサイエンスコーパス: lamb

1 c efficacy of low-dose PDD/LAmB vs full dose LAmB.

2 eased expression of the outer membrane porin LamB.

3 ctions between lambda-phage and its receptor LamB.

4 Ewes were allowed to lamb.

5 mended for preserving either fresh or thawed lamb.

6 n of origin classification for South African lamb.

7 lobin from four meats: beef, pork, horse and lamb.

8 f which were deemed directly attributable to LamB.

9 sumption by plasma samples from anesthetized lambs.

10 ary artery pressure from ~15 to ~40 mm Hg in lambs.

11 o flow were measured in anesthetized newborn lambs.

12 ogressed to full term, and delivered healthy lambs.

13 lower (P < 0.05) in IUGR fetuses but not in lambs.

14 gulation of beta(2)-AR, and this persists in lambs.

15 non-esterified fatty acids (NEFAs) in young lambs.

16 s not affect barrier permeability in newborn lambs.

17 gher in supplemented samples than in control lambs.

18 s of bovine mastitis and septic arthritis in lambs.

19 er than direct interactions between multiple lambs.

20 cava (IVC) interposition grafts in juvenile lambs.

21 sed in the monocytes from repeat LPS-exposed lambs.

22 bsequent postnatal catch-up growth in female lambs.

23 increased prepubertal growth rate in female lambs.

24 ted preterm lambs compared with control term lambs.

25 minish concurrent PIV3 infection in neonatal lambs.

26 cells in the vasculature of 8-week-old shunt lambs.

27 cerol also induced pulmonary hypertension in lambs.

28 and vascular remodeling in fetal and newborn lambs.

29 eliorating infection in rodents and neonatal lambs.

30 was to our knowledge never done in neonatal lambs.

31 onitored and mechanically ventilated preterm lambs.

32 during nasal pressure support ventilation in lambs.

33 rtually abolished by increasing PaCO2 in all lambs.

34 gastrointestinal nematode burden in growing lambs.

35 Christopher John Lamb (1950-2009) made major contributions to the field o

36 sease after inoculation was high in unweaned lambs (~24 h and 2 to 3 weeks old) but much lower in old

37 B 3 mg/kg/d plus flucytosine 50 mg/kg/d, and LAmB 3 mg/kg/d plus flucytosine 100 mg/kg/d all resulted

38 B 3 mg/kg/d plus flucytosine 50 mg/kg/d, and LAmB 3 mg/kg/d plus flucytosine 100 mg/kg/d.

39 Regimens of LAmB 6 mg/kg/d alone, LAmB 3 mg/kg/d plus flucytosine 50 mg/kg/d, and LAmB 3 m

40 linical trials include LAmB 6 mg/kg/d alone, LAmB 3 mg/kg/d plus flucytosine 50 mg/kg/d, and LAmB 3 m

41 ing studies suggested that a human dosage of LAmB 3 mg/kg/d resulted in a submaximal antifungal effec

42 g tissue ET-1 levels were increased in shunt lambs (317.2+/-113.8 versus 209.8+/-61.8 pg/g, P<0.05).

43 , but over the 3-month period most of the 56 lambs (33, or 60.7%) experienced at least one episode.

44 chocardiograms on 13 fetal lambs, 8 neonatal lambs, 4 juvenile lambs, and 4 adult sheep using a blend

45 Regimens of LAmB 6 mg/kg/d alone, LAmB 3 mg/kg/d plus flucytosine 50

46 for further study in clinical trials include LAmB 6 mg/kg/d alone, LAmB 3 mg/kg/d plus flucytosine 50

47 rformed contrast echocardiograms on 13 fetal lambs, 8 neonatal lambs, 4 juvenile lambs, and 4 adult s

48 IMTG) was increased in skeletal muscle of NR lambs, a finding which may be linked to predisposition t

49 LamB accumulated in spiral patterns.

50 CADP modes induced by the evanescent guided Lamb acoustic waves and remained Landau undamped due to

51 ysiologic responses of other 132-day preterm lambs after 2 or 6 hours of CPAP 5, 8 cm H(2)O CPAP (CPA

52 r transcranial motor cortex stimulation in 6 lambs aged 1-2 days.

53 optimal dosage of liposomal amphotericin B (LAmB) alone or in combination with flucytosine is not kn

54 iques to observe the surface distribution of LamB, an abundant integral outer membrane protein in Esc

55 In newborn lambs, an aerosol of inhaled nitrite has been found to r

56 nd are expressed at similar levels in fetal, lamb and adult ovine brain.

57 tamin D3 and 25-hydroxy-vitamin D3 (25OHD3), lamb and beef were analysed from 34 degrees S with LC-IT

58 acodynamic relationships were determined for LAmB and flucytosine administered alone.

59 Both LAmB and flucytosine produced a dose-dependent reduction

60 Levels of the outer membrane proteins LamB and OmpA in the quadruple mutant were indistinguish

61 aem iron contents in raw lean beef, chicken, lamb and pork meat samples.

62 Parameters of the Lamb and Pugh a-wave model (a(max), A, and t(eff)) for t

63 ather than the oligosaccharides preferred by LamB and related enterobacterial channels.

64 D reduced the effective dose and toxicity of LAmB and resulted in elicitation of strong parasite spec

65 n rates of infection in farm animals (during lambing and calving time).

66 t 60%, 80%, and 90% of gestation, in newborn lambs and adult sheep.

67 conduct eyeblink conditioning in preweanling lambs and demonstrates successful conditioning using the

68 pulmonary artery replacement in three young lambs and evaluated to adulthood.

69 rate two orders of magnitude higher between lambs and reproductive ewes than between any classes of

70 Systemic oxygenation was impaired in PPHN lambs and significantly improved (up to threefold) in bo

71 the feasibility of MEP recording in neonatal lambs and test its validity.

72 gher and chewier texture in sous-vide cooked lamb, and enhanced flavour scores of sous-vide samples m

73 mutants that vary in a nutrient transporter, LamB, and found evidence for both trade-offs.

74 chetypal trimeric beta-barrel OMPs, OmpF and LamB, and is dependent on POTRA 1.

75 t improved fitness on the original receptor, LamB, and set the stage for other mutations that allowed

76 and for Arg200 of the outer membrane protein LamB, and the mutant proteins were selectively labeled w

77 Undercooked meat, especially pork, lamb, and wild game meat, and soil contaminated with cat

78 13 fetal lambs, 8 neonatal lambs, 4 juvenile lambs, and 4 adult sheep using a blended mixture of sali

79 5-day (d) gestation and 140-d fetus, newborn lambs, and adult sheep, by Western immunoblot (n= 5 for

80 yearlings, ewes with lambs, and ewes without lambs, and animals with and without active infections.

81 Yearlings, ewes with lambs, and ewes without lambs showed similar group membe

82 d between contacts with yearlings, ewes with lambs, and ewes without lambs, and animals with and with

83 discriminated all the L0 lambs from the L75 lambs, and gave a correct classification score of 85.3%

84 higher in dexamethasone than placebo-treated lambs, and ZO-2 was higher in fetuses of dexamethasone t

85 osely related pine species (Pinus massoniana Lamb. and Pinus hwangshanensis Hisa) from Southeast Chin

86 Newly synthesized LamB appeared in discrete puncta, rather than evenly dis

87 Without YfgL, the levels of OmpA, OmpF, and LamB are significantly reduced, while OmpC levels are sl

88 Other OMPs, including LamB, are less affected in the Deltaskp DeltafkpA and De

89 ons 3 to 6 hours after eating beef, pork, or lamb, as well as in 13 control subjects.

90 evidence for an additional role for SecD in LamB assembly.

91 NA contamination of charcoal-grilled lamb at various stages of cooking and with various fat c

92 ses at 133 days of gestational age (dGA) and lambs at 18 days of age (dA).

93 ng highest levels of selected nutrients were lamb balti (3mg/100g iron), lamb kebab (3.2mg/100g zinc)

94 ps among environmental variables and between lamb body mass and the environmental variables.

95 variation in strength of responses of autumn lamb body mass to the NAO, to a proxy for plant growth i

96 ed local weather variables as a predictor of lamb body mass, despite the weaker mechanistic link.

97 The leptin peak in lambs born to control ewes was not clearly related to an

98 significant increase in cortisol at birth in lambs born to obese ewes related to an increase in lepti

99 e in disrupting the normal peak of leptin in lambs born to obese ewes thereby predisposing them to in

100 This peak was not present in lambs born to obese ewes.

101 In awake lambs, breathing NO at 80 ppm for 1 hour prevented the s

102 on physicochemical and sensory stability of lamb burgers, and determine the appropriate amount.

103 P>0.05) consumers' sensory acceptance of the lamb burgers.

104 d be recommended as a natural antioxidant in lamb burgers.

105 d organisms, sugar uptake is not mediated by LamB but by OprB channels.

106 t in late gestation fetal and early neonatal lambs but then disappears during the later neonatal peri

107 perone required for the assembly of OmpF and LamB, but not that of TolC and BamA.

108 ted in the bronchiolar epithelium of preterm lambs by immunostaining.

109 periments were performed in healthy mice and lambs by infusion of either murine tetrameric hemoglobin

110 perirenal adipose tissue of IUGR fetuses and lambs by measuring adrenergic receptor (AR) mRNA and pro

111 corporation patterns of an OM-porin protein, LamB, by labeling proteins only after epitope exposure o

112 and 74% lower (P < 0.05) in IUGR fetuses and lambs compared to controls, respectively, which also res

113 arteries and airways of iNO-treated preterm lambs compared with control term lambs.

114 m lambs; PVR was less in iNO-treated preterm lambs compared with term control animals.

115 Lamb contained 0.10mug vitamin D3/100g and 0.20mug 25OHD

116 SIS-ECM TVs were placed in 8 lambs; conventional bioprosthetic valves and native valv

117 ntain than was the case for cattle, and that lamb could present a greater risk to consumers than beef

118 al and protein carboxylation measured in the lamb cuts kept under protective atmosphere for up to 14

119 Five of 21 lambs delivered at 130-136 days gestation failed to keep

120 e therapeutic dose was achieved by selective LAmB delivery to APC, bypassing bystander cells, reducin

121 ping using Illumina Ovine SNP50 BeadChips on lambs descended from one carrier ram, including 19 sheep

122 tokes continuous-wave laser radiation in the Lamb-Dicke regime with sub-Doppler emission spectrum.

123 Therefore, carob in lamb diet could increase PUFA in muscle without compromi

124 The incorporation of rosemary extract in the lamb diet led to the deposition of functional levels of

125 Lamb et al first proposed the Connectivity Map to make s

126 ability of chilled-packed meat obtained from lambs fed on a diet supplemented with two different dose

127 n the medial preoptic area of the developing lamb fetus decreased during the last half of the 147-day

128 In the lamb fetus, the nascent oSDN occupies the central divisi

129 Male and female lamb fetuses were euthanized at different ages spanning

130 weekly (10 mg/kg) liposomal amphotericin B (LamB) for antifungal prophylaxis in liver transplantatio

131 Increasing the fat content of the grilled lamb from 5% to 20% caused a modest increase in total co

132 13)C/(12)C and (15)N/(14)N) of South African lambs from different regions were measured by isotope ra

133 2)C and (15)N/(14)N) of South African Dorper lambs from farms with different vegetation types were me

134 Our data suggest that resuscitation of lambs from hemorrhagic shock with autologous stored RBCs

135 t of the Longissimus lumborum (LL) muscle of lambs from seven different farms was assessed.

136 and fat of the Longissimus lumborum (LL) of lambs from six different regions were assessed.

137 values of the meat discriminated all the L0 lambs from the L75 lambs, and gave a correct classificat

138 tabase of autumn body mass of 83331 domestic lambs from the period 1992-2007 in four alpine ranges in

139 ht in a population of 752 Scottish Blackface lambs, genotyped with the 50k single-nucleotide polymorp

140 ed and both groups of control lambs; SMtb in lambs given iNO was significantly less (approximately 50

141 Four groups of nine male Romane lambs grazing a cocksfoot pasture were supplemented with

142 of total peroxides was ranked as: beef>pork>lamb>chicken.

143 NR lambs had higher mean arterial pressure (MAP; 89.0 +/- 6

144 roup, the (2 plus 7 days) repeat LPS-exposed lambs had: 1) decreased lung neutrophil and monocyte ind

145 The observational study used 20 fresh lamb heads.

146 In contrast to 4-week-old shunt lambs, immunohistochemistry revealed the emergence of ET

147 spatial distribution and dynamic movement of LamB in the outer membrane.

148 lly replaced by 24% or 35% carob pulp (n = 9 lambs in each group).

149 D), complexed with liposomal amphotericin B (LAmB) in an L. major mouse model and analyzed the therap

150 terial pressure (MAP) between DM and control lambs indicates that the compensation we have previously

151 is loss of membrane integrity results from a LamB-induced envelope stress that the cells do not suffi

152 r a median of 1.5 (interquartile range, 1-2) LamB infusions.

153 Lambs inoculated with DeltaKLP exhibited marked reductio

154 In control lambs, intratracheal lipopolysaccharides caused septic s

155 dized MEP recording and analysis in neonatal lambs is feasible, and can reliably assess neuromotor fu

156 The model based on lambs is potentially useful for training in SFE techniqu

157 d nutrients were lamb balti (3mg/100g iron), lamb kebab (3.2mg/100g zinc), mixed dhal (62mug/100g fol

158 LamB-LacZ fusion proteins have classically been used in

159 easing signal sequence hydrophobicity routes LamB-LacZ Hyb42-1 to the signal recognition particle (SR

160 -associated chaperone, trigger factor (Tig), LamB-LacZ localized to the periplasm in a SecA-dependent

161 Induction of the toxic LamB-LacZ protein fusion, Hyb42-1, leads to a lethal gen

162 retion of this hydrophobic fusion variant (H*LamB-LacZ) was reduced in the absence of fully functiona

163 ranslational lacZ fusions like malE-lacZ and lamB-lacZ42-1 causes lethal toxicity as folded LacZ jams

164 and fatty acid stability of fresh and thawed lamb leg chops, frozen stored for 3, 6 and 9months.

165 ation of Maillard reaction (MR) compounds in lamb loins was studied.

166 Forty-five lamb loins were subjected to sous-vide cooking at differ

167 induced both lipid and protein oxidation in lamb loins.

168 xin-induced clones identified in the preterm lamb lung.

169 Compared with age-matched control lambs, lung tissue ET-1 levels were increased in shunt l

170 ant genotype-by-environment interactions for lamb male body weight and parasite load, leading to a ch

171 bacterial channels, such as Escherichia coli LamB (maltoporin), has been characterized in great detai

172 Our results suggest high-dose weekly LamB may be a safe prophylactic strategy for high-risk L

173 High formate concentrations in fetal lambs may indicate a role in fetal development and sugge

174 ) models were fitted to the data to classify lamb meat and fat samples into "region of origin" (six d

175 The volatile fingerprints of South African lamb meat and fat were measured by proton-transfer mass

176 se of IRMS as a reliable analytical tool for lamb meat authentication.

177 investigated the dose-dependent response in lamb meat of stable nitrogen isotope ratio to the dietar

178 sufficient discriminative power to classify lamb meat of varying origin.

179 megranate flower, organic pear, radish leaf, lamb meat, etc.), and good results were obtained.

180 edict instrumental and sensory tenderness of lamb meat.

181 nosic acid seems to extend the shelf life of lamb meat.

182 Four term lambs, mechanically ventilated without iNO for 3 weeks,

183 ment when implanted in the IVC of a juvenile lamb model.

184 ction methods, we followed newly synthesized LamB molecules during their transit through the cell env

185 oximately five times the odds of producing a lamb mortality event of an identical contact with an inf

186 In this study, we have demonstrated that LamB moves along the bacterial surface and that these mo

187 00, 119, 133, 155, 253, and 311 bp for pork, lamb/mutton, chicken, ostrich meat, horsemeat and beef,

188 ect epicardial echocardiography in all fetal lambs (n = 13) and neonatal animals studied at one and t

189 he age range, or when considering only young lambs (n = 164).

190 However, in control lambs (n=7), ET-1 and 4 Ala ET-1 did not change pulmonar

191 In shunt lambs (n=9), exogenous ET-1 induced potent pulmonary vas

192 of the E. coli outer membrane proteins FhuA, LamB, NanC, OmpA and OmpF in a POPE/POPG (3:1) bilayer w

193 present study, low doses of BSE were fed to lambs of a range of ages (~24 h, 2 to 3 weeks, 3 months,

194 We observed a leptin peak in lambs of control ewes between days 6 and 9 of postnatal

195 conclude that the increased cortisol seen in lambs of obese sheep plays a role in disrupting the norm

196 Grilling lamb on properly prepared, ready charcoal resulted in an

197 The grilling of lamb on unready charcoal resulted in the formation of co

198 Lambs on support maintain stable haemodynamics, have nor

199 With appropriate nutritional support, lambs on the system demonstrate normal somatic growth, l

200 , we found that there are two populations of LamB--one shows very restricted diffusion and the other

201 nnual pneumonia mortality patterns: all-age, lamb-only, secondary all-age and adult-only.

202 oli host genotypes that expressed either the LamB or OmpF receptor.

203 were fed concentrates with 60% barley (n = 8 lambs), or concentrates in which barley was partially re

204 In contrast, mortality restricted to lambs peaked in summer when ewes and lambs were concentr

205 l scrapie can transmit laterally from ewe to lamb perinatally or between adult animals.

206 The haem iron content in beef (A-age), lamb, pork and chicken are 77%, 81%, 88% and 74% respect

207 fresh weight basis in raw lean beef (A-age), lamb, pork and chicken average 1.58, 1.64, 0.81 and 0.78

208 fresh meat samples were collected from beef, lamb, pork and chicken to investigate their hydroperoxid

209 due to frequent high mortality outbreaks in lambs, probably due to association with chronically infe

210 tion between total 25(OH)D and the number of lambs produced that survived their first year of life, a

211 r labeling resulted in divergence of labeled LamB puncta, consistent with a spatial pattern of OM gro

212 similar in iNO-treated and untreated preterm lambs; PVR was less in iNO-treated preterm lambs compare

213 Eight premature lambs received mechanical ventilation for 3 weeks, four

214 by the interaction between the virus and the LamB receptors, and by the spatial organization of the r

215 onary myeloperoxidase activity was higher in lambs resuscitated with stored than with fresh RBCs (11

216 est values in TP for chicory, green lettuce, lamb's lettuce, mizuna, red chard, and red lettuce, were

217 en leafy vegetables (chicory, green lettuce, lamb's lettuce, mizuna, red chard, red lettuce, rocket,

218 4), birch (Bet v 4), turnip rape (Bra r 1), lamb's quarter (Che a 3) and olive (Ole e 3, Ole e 8) sh

219 .30, ranging from -0.53 for a beef, pork, or lamb sandwich to 0.99 for diet soda.

220 0.12) or between the thickness of human and lamb Schneiderian membranes.

221 ampylobacter isolates obtained from multiple lambing seasons on different farms in Iowa, Idaho, South

222 ced transparency in a cavity, the collective Lamb shift, vacuum-assisted generation of atomic coheren

223 sical effects such as Casimir forces and the Lamb shift.

224 , which govern phenomena such as cooperative Lamb shifts, superradiant decay rates, Van der Waals for

225 The lambs show normal growth, increasing body weight by 366%

226 Yearlings, ewes with lambs, and ewes without lambs showed similar group membership patterns, but dire

227 ployed to demonstrate that both the PhoA and LamB signal peptides appear to recognize a common set of

228 tions of a signal peptide corresponding to a LamB signal sequence (modified to enhance aqueous solubi

229 ar in iNO-treated and both groups of control lambs; SMtb in lambs given iNO was significantly less (a

230 resting screening tool to quickly categorise lamb steaks in good (i.e. tender) and bad (i.e. tough) b

231 y, inflammation, and platelet activation) in lambs subjected to severe hemorrhagic shock and that con

232 tic regression to relate those covariates to lamb survival.

233 edly attenuated, since all DeltaKLP-infected lambs survived infection.

234 membranes derived from other portions of the lamb thalamus, including the sector involved in hypoxic

235 We show that fetal lambs that are developmentally equivalent to the extreme

236 rect classification score of 85.3% comparing lambs that ate alfalfa with those that did not.

237 The lambs that failed had less than 1.9 micromol/kg Sat PC i

238 e genotype at codon 141 of the PRNP gene, as lambs that were LF heterozygotes had a longer mean incub

239 ble mutants show that elevated expression of LamB, the outer membrane porin responsible for maltose u

240 In awake, instrumented lambs, the thromboxane analogue U-46619 was intravenousl

241 e (C19H22O3) described for the first time in lamb tissues, along with carnosol, carnosic acid, rosman

242 sition and antioxidant capacity in different lamb tissues.

243 PDD was shown to escort LAmB to APCs in vivo, enhanced the drug efficacy by 83%

244 ssembly process, most likely the delivery of LamB to the YaeT assembly complex in the outer membrane.

245 uantify the surfactant necessary for preterm lambs to breathe successfully on a CPAP of 5 cm H(2)O (C

246 of endogenous Sat PC is required for preterm lambs to breathe successfully with CPAP.

247 s were performed in chronically instrumented lambs to study states of alertness, glottal muscle elect

248 In contrast, all lambs treated with recombinant human SP-D were physiolog

249 MEPs were also measured in one lamb undergoing Neuro-Muscular Blockade (NMB) and anothe

250 Eighteen fetal lambs underwent in utero placement of an aortopulmonary

251 All lambs underwent serial echocardiography, measuring annul

252 n humans based on measurements made in fetal lambs using radioactive microspheres and provide prelimi

253 ygenator circuit connected to the fetus of a lamb via an umbilical cord interface that is maintained

254 zed the therapeutic efficacy of low-dose PDD/LAmB vs full dose LAmB.

255 The classification of the origin of the lamb was achieved by examining the calculated and record

256 In the selected LT recipients, LamB was administered weekly until hospital discharge af

257 tode resistance and body weight in Blackface lambs was evaluated comparing genome-wide association (G

258 RE in iNO-treated lambs was less than 40% of RE measured in preterm contro

259 bles the third-order quasi-symmetric (QS(3)) Lamb wave mode with a high quality factor (Q) characteri

260 A Lamb wave resonator utilizing the QS(3) mode exhibits a

261 Thirty weaned lambs were assigned randomly to three homogeneous groups

262 Lambs were born naturally, and fed to appetite throughou

263 All lambs were born without musculoskeletal, neurological, o

264 cted to lambs peaked in summer when ewes and lambs were concentrated in nursery groups.

265 Hearts from 0-61 d postnatal lambs were dissected or enzymatically dissociated.

266 Anesthetized lambs were embolized with intravenous injections of auto

267 Thirty-two lambs were fed with barley straw supplemented by a conce

268 iously exposed populations when outbreaks in lambs were followed by lower rates of pneumonia-induced

269 free hemoglobin continued to be infused, the lambs were given inhaled NO gas (20 ppm), inhaled sodium

270 Male Comisana lambs were individually stalled and, for 56 days, were f

271 Radial alveolar counts of iNO-treated lambs were more than twice that of preterm control anima

272 ings of the parameters in all 4 limbs of all lambs were obtained.

273 Preterm lambs were randomly assigned to receive intratracheal ae

274 Methods: After C-section delivery, lambs were randomly assigned to treatment with SOD (2.5-

275 Lambs were resuscitated with autologous RBCs stored for

276 A total of 12 3-month-old lambs were studied for a period of 3 or 8 months.

277 Lambs were subjected to 2 hours of hemorrhagic shock by

278 Lambs were treated similarly with 0.25 mg/kg-dexamethaso

279 polysaccharide instillation, preterm newborn lambs were treated with surfactant and ventilated for 5

280 es in lung, vein, and artery of hypertensive lambs were unchanged relative to controls after 2 days o

281 Twenty-six PPHN lambs were ventilated for 24 h with 100% O(2) alone (n =

282 Lambs were ventilated with progressively increasing leve

283 after the host evolved reduced expression of LamB, whereas certain other host mutations prevented the

284 Increases in exhaled NO gas were observed in lambs while breathing the nitrite aerosol ( approximatel

285 In lambs with acute pulmonary hypertension, BAY 41-2272 is

286 and enhances alveolar development in preterm lambs with chronic lung disease.

287 minant member of the pneumonic lung flora in lambs with early lesions of bronchopneumonia.

288 AR results, we challenged a second cohort of lambs with exogenous adrenaline at 21 dA.

289 inhaled sodium nitrite by aerosol to newborn lambs with hypoxic and normoxic pulmonary hypertension.

290 In 1-month-old lambs with increased pulmonary blood flow, we have demon

291 Oral treatment of neonatal lambs with JNJ-53718678, or with an equally active close

292 Six newborn lambs with PPHN (induced by antenatal ductal ligation) w

293 th vasoconstriction and oxidation in newborn lambs with PPHN.

294 00% O(2) compared with nonventilated newborn lambs with PPHN.

295 treatment improves oxygenation in premature lambs with RDS and prevents the development of pulmonary

296 , and pulmonary hemodynamics in 46 premature lambs with RDS.

297 In preterm lambs with respiratory distress syndrome, cerebral blood

298 bolus surfactant administration in premature lambs with respiratory distress syndrome.

299 In preterm lambs with severe respiratory distress syndrome, aerosol

300 ificantly decreased in arteries from ligated lambs without associated changes in SOD protein expressi