ライフサイエンスコーパス: microgram

1 elicited by intracoronary nitroglycerin (200 microgram).

2 only with the highest doses (e.g., 20 and 40 microgram).

3 of deposited mass (nanograms to greater than micrograms).

4 be detected using amounts of DNA as low as 2 microgram.

5 kin varied from 1428 to 63 058 parasites per microgram.

6 digestion of sample amounts on the order of micrograms.

7 the amount of RNA required, usually tens of micrograms.

8 icle or amphetamine (0.0, 2.0, 10.0, or 20.0 microgram/0.5 microliter), and lever pressing was tested

9 s of endogenous steroids (mean cortisol 45.5 micrograms/100 ml cytosol) as well as inactivation of re

10 rogram/5 microliter, icv, n=8), prazosin (10 microgram/5 microliter, icv, n=12) or alpha-helical CRF(

11 Yohimbine (3 microgram/5 microliter, icv, n=8) pretreatment did not a

12 Pretreatment with phentolamine (30 microgram/5 microliter, icv, n=8), prazosin (10 microgra

13 r, icv, n=12) or alpha-helical CRF(9-41) (10 microgram/5 microliter, icv, n=9) prevented the decrease

14 trometry run, is compatible with nanogram to microgram amounts of cell lysate.

15 ing robust quantitative proteomic studies on microgram amounts of HCV-infected human liver tissue fro

16 otein complexes often yields nanogram to low-microgram amounts of protein, which poses several challe

17 e routine biomolecular NMR spectroscopy with microgram amounts of proteins.

18 as NMR while at the same time requiring only microgram amounts of sample.

19 Mass spectra were also obtained for microgram amounts of the pharmaceutical compounds lorata

20 es of biological small RNAs from nanogram to microgram amounts of total RNA without an amplification

21 in tRNA abundance can be quantified from sub-microgram amounts of total tRNA.

22 xpressed, the vaccine could be prepared from microgram amounts of tumor tissue.

23 Fold screening was thus achieved with microgram amounts of uniformly (2)H, (15)N-labeld OmpX a

24 Ten-microgram and 30-mug doses appeared to be toxic to the n

25 f murine RPE cells stimulated the release of microgram and nanogram levels of IL-6, MMP-3, MMP-9, and

26 Bilateral (1.5-20 microgram) and unilateral (0.01-40 microgram) RY dose-de

27 3 ng/artery, with a stent content of 71+/-10 microgram at 3 days.

28 cycling rats after sc administration of 2.5 microgram at noon of proestrus.

29 tep, avoiding serial dilution and the use of microgram balances.

30 ses judged arbitrarily to be comparable on a microgram basis.

31 ith intracoronary infusions of adenosine (32-microgram bolus), acetylcholine (54 microgram over 2 min

32 entricular (ICV) infusion of clonidine (0.03 microgram) caused an increase in NO concentration in the

33 Thus microgram comparison of all ICS could only be performed

34 sitions for all types of compounds with only microgram concentration and enantiomeric excess as low a

35 tional groups can be determined sensitively (microgram concentration) and accurately (enantiomeric ex

36 --1-mm diameter and weighing as little as 40 micrograms could be identified using this technique.

37 s of cellular proteolytic digests (e.g., 500 micrograms) could be loaded onto packed capillaries of 1

38 and that the largest IHD health benefits per microgram/cubic meter from PM2.5 air pollution control m

39 2.5 than for PM2.5 mass in general, on a per microgram/cubic meter PM2.5 basis.

40 us an IHD HR = 1.01 (95% CI: 1.00, 1.02) per microgram/cubic meter PM2.5 mass, indicated a risk rough

41 PM2.5 IHD HR = 1.05 (95% CI: 1.02, 1.08) per microgram/cubic meter, versus an IHD HR = 1.01 (95% CI:

42 One trial that used a calcitriol dose of 0.5 microgram/d noted a fall in CCr and a rise in serum crea

43 after 8 weeks of transdermal estradiol (200 microgram/d), oral conjugated estrogens (0.625 mg/d), or

44 times weekly compared with daily dosing (0.5 microgram/d); there was no rise of serum Ca over the 3-m

45 r alfacalcidol in daily doses of 0.25 to 0.5 microgram/d, and the incidence of hypercalcemia was quit

46 Median intakes of genistein (measured in micrograms/day) by African Americans and Caucasians were

47 le polymer containing 185 microgram SRL, 350 microgram DEX, or 185 microgram SRL and 350 microgram DE

48 microgram DEX, or 185 microgram SRL and 350 microgram DEX.

49 were 55.5+/-20.3, 50.5+/-8.7, and 15.3+/-7.3 microgram/dL, respectively.

50 nts of protein, fatty acids, and cholesterol/microgram DNA also indicate smaller cells with reduced m

51 nit (95% CI: 0.5, 43.8) decreases in DPM per microgram DNA, respectively.

52 A 10-microgram dose of both, and a 1-microgram dose of one, s

53 A 10-microgram dose of both, and a 1-microgram dose of one, significantly prolonged survival

54 ility and to determine equisystemic effects (microgram dose producing equal systemic cortisol suppres

55 and antibody-mediated immune responses with microgram doses.

56 e receptor (nAChR) agonist that is lethal at microgram doses.

57 or, the best response occurring after two 30 microgram doses: one, four, four, and one person of elev

58 more than twofold increases in EBD content (micrograms EBD per gram dry tissue) in stimulated versus

59 Since serum contains 300 micrograms fibronectin per mL, the bleeding that occurs

60 ntities as small as a few nanomoles (tens of micrograms for the observed component).

61 suppression with intermittent dosing of 2.0 micrograms given either once or three times weekly compa

62 ninhydrin-positive material per day and 870 micrograms (glucose equivalents) of anthrone-positive ma

63 pient 2 hours before transplantation and 250 microgram IC into allograft.

64 tivity of about 100 picomoles per minute per microgram in the presence of Ca2+ and reaches half-maxim

65 Morphine microinjections (0.5 microgram) into accumbens shell, which caused rats to in

66 gram over 2 minutes), and nitroglycerin (200 microgram) into the left anterior descending coronary ar

67 Treatment consisted of DEVD-CHO 500 microgram IP per animal to donor and recipient 2 hours b

68 by continuous infusion of NTG for 3 days (10 microgram kg(-1). min(-1) SC) with an osmotic pump.

69 In vivo isoproterenol (0.1 microgram . kg(-1) . min(-1)) increased LVEF to maximal

70 Ac-SDKP (400 microgram. kg(-1). d(-1)) did not affect development of

71 were treated with 17beta estradiol (E2) (20 microgram. kg(-1). d(-1), S.C.) alone or combined with I

72 ytopenia, n=160) or HITTS (n=144) received 2 microgram. kg(-1). min(-1) IV argatroban, adjusted to ma

73 y the selective A(2A) antagonist ZM241385 (3 microgram. kg(-1). min(-1)).

74 ment with phorbol 12-myristate 13-acetate (4 microgram/kg body weight) before subsequent experiments

75 per minute infusion followed by a second 180-microgram/kg bolus 10 minutes later.

76 of eptifibatide would be obtained with a 180-microgram/kg bolus and a 2-microgram/kg per minute infus

77 ifibatide bolus followed by an infusion (180-microgram/kg bolus followed by 2 microgram/kg per minute

78 followed by 2 microgram/kg per minute or 250-microgram/kg bolus followed by 3 microgram/kg per minute

79 olus of eptifibatide (90 microgram/kg or 125 microgram/kg for the initial 180-microgram/kg or 250-mic

80 m/kg for the initial 180-microgram/kg or 250-microgram/kg groups, respectively) or placebo 30 minutes

81 e trial in which they received either 4 or 8 microgram/kg IL-10 subcutaneously daily for 90 days.

82 t of rabbits 24 hours earlier with CCPA (100 microgram/kg IV bolus) or IB-MECA (100 or 300 microgram/

83 ed either a second bolus of eptifibatide (90 microgram/kg or 125 microgram/kg for the initial 180-mic

84 m/kg or 125 microgram/kg for the initial 180-microgram/kg or 250-microgram/kg groups, respectively) o

85 Ethinyl estradiol at a dose of 1 microgram/kg per day induced a significant elevation of

86 tained with a 180-microgram/kg bolus and a 2-microgram/kg per minute infusion followed by a second 18

87 fusion (180-microgram/kg bolus followed by 2 microgram/kg per minute or 250-microgram/kg bolus follow

88 nute or 250-microgram/kg bolus followed by 3 microgram/kg per minute) for 18 to 24 hours.

89 g) and 72-hour infusion of eptifibatide (2.0 microgram/kg per minute, n=48) or placebo (n=50).

90 ndomly assigned to an intravenous bolus (180 microgram/kg) and 72-hour infusion of eptifibatide (2.0

91 Low doses of LPS (0.1 microgram/kg) elicited a similar response profile, but h

92 the selective A(2A)AR agonist CGS 21680 (100 microgram/kg) had no effect; (2) the delayed cardioprote

93 expected, TPR rose less (P<0.05) with PE (5 microgram/kg) in old monkeys (34+/-3%) than in young mon

94 ar response profile, but higher doses (2-100 microgram/kg) provoked COX-2 expression in a progressive

95 icrogram/kg IV bolus) or IB-MECA (100 or 300 microgram/kg) resulted in an approximately 35% to 40% re

96 llenged intravenously with IL-1beta (1.87-30 microgram/kg) showed a marked increase in the number of

97 Daniplestim administered at 2.5 microgram/kg/d is tolerable and active when combined wit

98 aniplestim at doses ranging from 0.1 to 3.75 microgram/kg/d plus G-CSF 10 microgram/kg/d.

99 rom 0.1 to 3.75 microgram/kg/d plus G-CSF 10 microgram/kg/d.

100 Treated seedlings exuded 950 micrograms (leucine equivalents) of ninhydrin-positive m

101 active fractions are rapidly purified at the microgram level and individual compounds are rescreened

102 ase of sugar chains by hydrazinolysis at the microgram level, labeling with fluorescent tag AA, and p

103 At the low microgram level, we found that the consecutive use of en

104 delivery of BP-1-102 furnishes micromolar or microgram levels in tumor tissues and inhibits growth of

105 opeptides, 1693 and 1842, respectively, from microgram levels of peptide samples.

106 Twenty-five micrograms lipopolysaccharide in 50 muL sterile saline o

107 d 24 hr) and dose-dependent (concentrations [micrograms/liter] corresponding to the trough [15], peak

108 lenes), in the low milligrams/liters to high micrograms/liters concentration range.

109 Delta(9)-THC (15-30 microgram/microliter intracerebellar) resulted in a sign

110 ol, it is possible to obtain highly purified microgram-milligram quantities of the TpsA protein of in

111 ependent), and sodium nitroprusside (5 to 20 microgram/min; endothelium-independent) were measured by

112 y when estimated secretion rates exceeded 50 micrograms/min or when phlorizin was given.

113 e and during isoproterenol infusion (0.9-2.6 micrograms/min) into three patients without, and 10 pati

114 sing HPLC, CL (mean +/- SD) was 14.9 +/- 3.7 microgram/ml (range 9.1 to 24.2) and CL was not correlat

115 Treatment with 10 microgram/ml cisplatin for 12 h induced apoptosis in 2 t

116 effect of CRP on MCP-1 was present even at 5 microgram/mL CRP, with stepwise increases as the CRP con

117 pplemented with 0.2% bovine serum albumin, 1 microgram/ml Escherichia coli LPS and containing various

118 cultured for 72 hours in the presence of 80 microgram/mL ferric ammonium citrate displayed an increa

119 Co-incubation of cells with 10 microgram/ml high density lipoprotein (HDL) prevented ox

120 ed by Etest, was 32 microgram/ml versus >256 microgram/ml in 70 ermB(+) isolates.

121 d eNOS activation in cells incubated with 10 microgram/ml oxLDL (10-15 thiobarbituric acid-reactive s

122 m inhibitory concentrations (MIC) in the low microgram/mL range.

123 Incubation with 100 microgram/mL recombinant human CRP induced a 7-fold incr

124 were inhibited, determined by Etest, was 32 microgram/ml versus >256 microgram/ml in 70 ermB(+) isol

125 Flagellin (1 microgram/ml) induces IkappaBalpha degradation, NF-kappa

126 Positive IgG (350 microgram/mL) inhibited I(Ba)-alpha(1C) by 50.6+/-4.7% (

127 Actinomycin D (2 microgram/mL) or cycloheximide (10 micromol/L) did not i

128 Saline or LC (100 microgram/mL) was infused into a Langendorff-perfused, i

129 ram/ml), phosphatidylethanolamine (64 +/- 20 microgram/ml), or choline-containing phospholipid (1,580

130 related with phosphatidylserine (3.8 +/- 1.7 microgram/ml), phosphatidylethanolamine (64 +/- 20 micro

131 oline-containing phospholipid (1,580 +/- 280 microgram/ml).

132 ncentration was increased to 10, 50, and 100 microgram/mL.

133 , in strains containing the irgA promoter (5 microgram/ml/OD(600)).

134 nder the control of the tac promoter (2 to 5 microgram/ml/unit of optical density at 600 nm [OD(600)]

135 hin at concentrations ranging from 0.9 to 14 micrograms/ml [corrected] in their milk were produced.

136 appears to be achievable with as little as 3 micrograms/ml [corrected] of lysostaphin in milk.

137 on (7-fold, P < 0.01) was at the level of 50 micrograms/ml of A.a. extract.

138 f inhibition of SHP-2 and PTP1B required 100 micrograms/ml sodium stibogluconate, demonstrating diffe

139 When Gln was added to the medium (292 micrograms/ml) fibroblast proliferation was stimulated,

140 conate inhibited 99% of SHP-1 activity at 10 micrograms/ml, a therapeutic concentration of the drug f

141 At higher doses (approximately 300 microgram/mouse), flagellin induces shock, characterized

142 when injected systemically (approximately 10 microgram/mouse), induces systemic inflammation characte

143 m/mouse), rmIL-1 beta (positive control; 0.1 microgram/mouse), or their vehicle (0.1% bovine serum al

144 rmMIP-1 beta (20 pg/mouse), rmIL-18 (0.01-1 microgram/mouse), rmIL-1 beta (positive control; 0.1 mic

145 approach, 1H NMR spectra can be acquired for microgram (nanomole) quantities of trace impurities in a

146 Three hundred twenty-three thousandths of a microgram of bFGF were incorporated per polymer.

147 ctase activity and contain 33% less iron per microgram of chlorophyll than wild-type chloroplasts.

148 Up to 50 microgram of DNA per injection were used without adverse

149 the amount of 5-methyl-2'-deoxycytidine per microgram of DNA with percent relative standard deviatio

150 r gave >100-fold more transformants (>10,000/microgram of DNA) than did the spectinomycin resistance

151 arbored high concentrations of transgene per microgram of DNA.

152 we have recovered up to 50 transformants per microgram of DNA.

153 yielding several thousand transformants per microgram of input DNA or conjugation mixture.

154 f the order of 10(4)-10(5) transformants per microgram of insert, which is the same order of magnitud

155 Each microgram of orally consumed 25-hydroxyvitamin D3 was ab

156 by CSG-coated stents containing 42.0 or 21.0 microgram of paclitaxel

157 nts with paclitaxel (42.0, 20.2, 8.6, or 1.5 microgram of paclitaxel per stent), CSG-coated stents wi

158 <0.007) with stents containing 42.0 and 20.2 microgram of paclitaxel per stent, respectively, versus

159 of Na(+) channels; TI cell Na(+) uptake, per microgram of protein, is approximately 2.5 times that of

160 One microgram of purified CPB, in the presence of TI, was fo

161 The proposed method requires less than ten microgram of sample and is applicable for optimizing syn

162 anograms per milliliter and as nanograms per microgram of total IgA or IgG.

163 cutoff value of 0.9 fg of perforin mRNA per microgram of total RNA, and with a sensitivity of 79 per

164 utoff value of 0.4 fg of granzyme B mRNA per microgram of total RNA.

165 granzyme B, 1.2+/-0.3 vs. -0.9+/-0.2 fg per microgram of total RNA; P<0.001).

166 n (perforin, 1.4+/-0.3 vs. -0.6+/-0.2 fg per microgram of total RNA; P<0.001; and granzyme B, 1.2+/-0

167 The mean (+/-SD) increases (per microgram of vitamin D compound) in serum 25(OH)D concen

168 Ten micrograms of BrdU was injected intravitreally on day 3.

169 nic strength can be obtained using only 3-15 micrograms of DNA samples.

170 Fifty micrograms of estrogen did not further increase the magn

171 f picrotoxin, but not by microinjection of 5 micrograms of flumazenil or 200 ng of PK 11195.

172 inearity of detector signal as a function of micrograms of free acid added were demonstrated in the p

173 ams of DNA in a bacterium are amplified into micrograms of high molecular weight DNA suitable for DNA

174 s, and specific activity (ELISA activity per micrograms of Ig) of pre-boost serum IgG and IgM anti-TN

175 F/mg of protein as well as nanograms of iron/micrograms of LF were determined.

176 Micrograms of LF/mg of protein as well as nanograms of i

177 Hundreds of micrograms of nanoparticles/kg tissue (ppb) were found i

178 Observed levels ranged from a nanogram to micrograms of NCA.

179 ry j 2 equivalent to that in several tens of micrograms of pollen.

180 an detect subtle stability differences using micrograms of protein in 2 microL volumes within minutes

181 sify a broad set of kinase inhibitors, using micrograms of protein, without the need for protein modi

182 ng mechanisms to be characterized using just micrograms of protein.

183 Our method requires only micrograms of sample and should therefore broaden the ap

184 optimized control of amplification to create micrograms of specific amplicons without TIPs from down

185 Thirty micrograms of the agonist isoproterenol significantly de

186 ed ribonucleosides are quantified in several micrograms of tRNA in a 15-min LC-MS run.

187 milligrams of vitamin B-6 and 10 additional micrograms of vitamin B-12 were associated with 2% lower

188 Two puffs (total dose, 200 microgram) of fluticasone propionate (n = 47) or placebo

189 n a subgroup that received higher doses (>30 microgram) of intracoronary adenosine during pressure me

190 d to prepare substantial quantities (tens of micrograms) of active tubulin by in vitro folding of mou

191 interval both rapidly and with tiny amounts (micrograms) of compound.

192 t method for labeling large quantities (e.g. micrograms) of target RNA for microarray analysis.

193 transdermal patches of 17beta-estradiol (100 microgram) or placebo in a 12-week, double-blind, placeb

194 sine (32-microgram bolus), acetylcholine (54 microgram over 2 minutes), and nitroglycerin (200 microg

195 d collected samples of ERM hyphae (up to 116 micrograms) over the following 29 days.

196 te healing in the higher-dose (42.0 and 20.2 microgram) paclitaxel-containing stents consisting of pe

197 f large sample quantities (typically several micrograms), particularly for highly sulfated GAG ions.

198 ion when soot concentrations were in the low microgram per cubic meter range.

199 g mutant RebH Y455W and RebF also accumulate microgram per gram fresh-weight quantities of 12-chloro-

200 In multivariable models, each microgram per gram increase in hair Hg was associated wi

201 nts were found in the samples at levels from microgram per gram to milligram per gram levels.

202 with a lower adult height (-0.1 cm for each microgram per kilogram of body weight) (P=0.007).

203 taining BTEX and chlorinated contaminants at microgram per liter concentrations.

204 ratio (OR) was 1.37 for each ln-transformed microgram per liter increase in ln-transformed SigmaAs c

205 mination of complex chemical mixtures at the microgram per liter level, using antibody-functionalized

206 ples, even those containing MC-LR in the sub-microgram per liter range (e.g. 0.5 mug/L), could be det

207 Detection limits are currently in the sub-microgram per liter range.

208 ing BDE-47 was down to the part-per-billion (microgram per liter) level.

209 our with 50 pg mass detection limit from low microgram per milliliter samples.

210 y concentration (MIC(meropenem)) less than 1 microgram per milliliter], and sterilization of aerobica

211 ent in the flue gas at levels of picogram to microgram per normalized cubic meter.

212 high concentrations of organic aerosol (>25 micrograms per cubic meter) was attributed to the format

213 dust events with concentrations exceeding 20 micrograms per cubic meter.

214 ation concentrations of 10(-4.5) to 10(-0.5) micrograms per cubic metre).

215 (saturation concentration less than 10(-4.5) micrograms per cubic metre).

216 (down to 25 mum) and good detection limits (micrograms per gram level).

217 The oceanic upper mantle contains 50 to 200 micrograms per gram of water (H2O) dissolved in nominall

218 Peanut protein in household dust (in micrograms per gram) was assessed in highly atopic child

219 PG, detection limits of the order of tens of micrograms per liter (10(-11) M) are attained.

220 uggest that GCs could cause effects in lower micrograms per liter concentrations that could be enviro

221 g L(-1) in major Swiss rivers and by several micrograms per liter in receiving water bodies with a hi

222 atural log-transformed DDT plasma levels (in micrograms per liter) and DDE (in micrograms per liter)

223 levels (in micrograms per liter) and DDE (in micrograms per liter) to identify predictors for each gr

224 U-Cd concentrations (micrograms per liter) were measured in 24-hr urine sampl

225 pounds in water at concentrations of tens of micrograms per liter.

226 c compounds down to a concentration level of micrograms per liter.

227 m hydrocarbon concentrations in excess of 50 micrograms per liter.

228 animal sera containing low nanograms to low micrograms per milliliter of PEGylated product with or w

229 rp endpoints with sensitivity to ODSH in the micrograms per milliliter range for plasma samples.

230 7) with PHMB concentrations of 50 and 0 ppm (micrograms per milliliter) for 24 hours at room temperat

231 Geometric mean concentrations (in micrograms per milliliter) of beta C-specific immunoglob

232 l fluid contains all major lipid classes (in micrograms per milliliter), as well as lipoproteins and

233 esults by species, expressed as MIC50/MIC90 (micrograms per milliliter), were as follows: C. albicans

234 d fluorescein, with accuracy on the scale of micrograms per square centimeter, onto glass, Tegaderm,

235 ted contributed the same color intensity per microgram protein as bovine serum albumin.

236 y isolated pentose monosaccharide using only microgram quantities and a commercial instrument and com

237 This peptide was lethal to mice at low microgram quantities and it induced serious symptoms inc

238 s are available from natural sources only in microgram quantities as mixtures.

239 s are available from natural sources only in microgram quantities as mixtures.

240 surface antigen (HBsAg), which is present in microgram quantities in the serum of chronic HBV patient

241 ctrometry to quantify specific activities of microgram quantities of 14C-labeled proteins.

242 class of columns is reported that uses only microgram quantities of active support and that provides

243 le source were used to determine the mass of microgram quantities of biomolecules.

244 The assay requires only microgram quantities of DNA and is capable of detecting

245 s of these three lesions with the use of low-microgram quantities of DNA from cultured human skin fib

246 Some molecular analyses require microgram quantities of DNA, yet many epidemiologic stud

247 on, we have developed a method for isolating microgram quantities of drusen and Bruch's membrane for

248 te 2D separation techniques, we fractionated microgram quantities of E. coli protein extract by seven

249 rs a unique capability for the sequencing of microgram quantities of HS oligosaccharide mixtures by L

250 Because MPAX requires only microgram quantities of material and is not limited by p

251 The first method, suitable for microgram quantities of material, relies on the separati

252 characterization of an intact molecule with microgram quantities of material.

253 oduct and can therefore generate the desired microgram quantities of message-derived material from 10

254 Nanogram to microgram quantities of organic material deposited on th

255 lete solution NMR structure determined using microgram quantities of protein demonstrates the utility

256 ke molecules is the requirement for at least microgram quantities of purified protein.

257 DNA, ligations can be amplified to generate microgram quantities of repeat containing DNA.

258 mbers of embryonic genes and the gap between microgram quantities of RNA required by typical microarr

259 Microgram quantities of the metabolites of interest were

260 (BoNT) is the most toxic protein known, with microgram quantities of the protein causing severe morbi

261 method for isolating high-quality YAC DNA in microgram quantities should be valuable for functional a

262 ctural analysis of large soluble proteins in microgram quantities, an increasingly powerful method th

263 ecially useful for samples only available in microgram quantities.

264 s of starting material could be amplified to microgram quantities.

265 of SAXS to molecules that can be produced in microgram quantities; for typical proteins, 10-20 muL of

266 ion/10(6) unmodified nucleobases using a low-microgram quantity of DNA.

267 ne, vinyl chloride, and nitromethane) in the microgram range in mainstream smoke from 1R5F and 3R4F r

268 o 10 ng of human genomic DNA input is in the microgram range, reaching over a thousand-fold amplifica

269 nthetic estrogen dosages in the milligram to microgram range.

270 exhibiting high binding affinity (IC(50) in microgram ranges), provide unequivocal evidence that AuN

271 effect that was attenuated by leptin (2 or 4 microgram/rat, i.c.v.; two infusions, given 21 hr and 20

272 nM) showed full antiovulatory potency at 250 microgram/rat.

273 lded analogues that blocked ovulation at 250 microgram/rat.

274 p(3), Lys(8)] bridge, was fully active at 50 microgram/rat.

275 competitive BDZ antagonist ZK 93426 (ZK) (7 microgram) reversed the RY-induced suppression on EtOH-m

276 l (1.5-20 microgram) and unilateral (0.01-40 microgram) RY dose-dependently reduced EtOH-maintained r

277 When microgram(s) of RNA are taken for RT reaction, reverse t

278 ngs revealed that estradiol benzoate (EB; 25 microgram, s.c.) decreased the hyperpolarizing response

279 sible to identify thousands of proteins from microgram sample quantities in a single day and to quant

280 n efficiencies of 2D methodologies using low-microgram sample quantities.

281 The method scales from low to high microgram sample quantity and is amenable to full automa

282 and 9.8 ng/mug (nanogram fusion protein per microgram sample) for batches 1 and 2, respectively.

283 mated multistep syntheses at the nanogram to microgram scale, could be generalized to a range of radi

284 easy-to-establish 2D bottom-up strategy for microgram-scale phosphoproteomics, based on electrostati

285 SCX/RP-LC-MS render its future promising for microgram-scale-phosphoproteomics in biological, biomedi

286 The i.n. administration of 100 microgram sIL-4R before allergen challenge significantly

287 In contrast, i.p. delivery of 100 microgram sIL-4R inhibited only the influx of eosinophil

288 185 microgram SRL, 350 microgram DEX, or 185 microgram SRL and 350 microgram DEX.

289 ed with a nonerodable polymer containing 185 microgram SRL, 350 microgram DEX, or 185 microgram SRL a

290 55, P<0.05) at the highest level tested (187 microgram/stent versus control).

291 p-coated with paclitaxel (0, 0.2, 15, or 187 microgram/stent) by immersion in ethanolic paclitaxel an

292 e drug discovery demands the availability of microgram to gram quantities of high-quality protein enc

293 dy sequences will be available in 3-4 d, and microgram to milligram amounts of antibodies are produce

294 ively large amounts of sample are available (microgram to milligram quantities).

295 d are log-normally distributed, ranging from micrograms to 10s of kg.

296 amino acid containing proteins from tens of micrograms to tens of milligrams per liter in yeast.

297 sIL-4R (0.1-100 microgram) was administered by either i.n. or i.p. route

298 tion after sublingual nitroglycerin (NTG, 25 microgram) were measured by using high-resolution ultras

299 d (1:1) to receive phVEGF-2 (total dose, 200 microgram), which was administered as 6 injections into

300 protocol takes 4-16 h to produce nanogram to microgram yields, depending on the complexity of the rea