ライフサイエンスコーパス: be prepared for

1 In most patients with thyroid cancer being prepared for (131)I imaging or therapy, a TSH leve

2 mates for the global poorest and richest 20% were prepared for 1990 for deaths and disability-adjuste

3 cDNAs coding full-length open reading frames were prepared for 21 ion channels (1.2-15 kb).

4 Both patients and medical staff should be prepared for a lengthy, arduous rehabilitation proces

5 nted) and black (fully-fermented) tea leaves were prepared for a structured set of samples (fermented

6 ta suggest that both promoters and enhancers are prepared for action at different stages of activatio

7 years were eligible if they were admitted or being prepared for admission to a participating paediatr

8 Na2B12H11SH), frequently referred to as BSH, were prepared for analysis by precipitation with acetoni

9 ranes, milligram quantities of Kdo-lipid IVA were prepared for analysis.

10 ve, ion correlation-based, nano-optodes have been prepared for application in vitro.

11 an, pectin, chitosan or psyllium husk powder were prepared for assessment of the best formulation aim

12 ions of unfolded and flattened visual cortex were prepared for autoradiography or cytochrome oxidase

13 Optic nerves were prepared for axon counting and other morphologic an

14 Nine additional samples were prepared for bacterial culture, after initial irrad

15 of heme on both alpha or both beta subunits, were prepared for beta W37E, beta W37A, alpha Y140G, and

16 removed 48 hours later, and frozen sections were prepared for beta-galactosidase histochemistry and

17 hosphamide (HCY) were studied in 14 patients being prepared for bone marrow transplantation with eith

18 growers) samples, each containing 40 fruit, were prepared for both kiwifruit varieties.

19 ncurred if on the preceding trial a task has been prepared for but no response required (a 'no-go' tr

20 Tissue was prepared for calbindin immunocytochemistry to identi

21 atal days 14 and 60 (P14 and P60) the brains were prepared for ChAT immunocytochemistry.

22 mechanism by which cancer cell vaccines may be prepared for clinical use.

23 Transgenes were prepared for cloning into this vector by introducti

24 The cells were prepared for combined light and electron microscopy

25 CH(2) (4), (E)-CH=CH-CH=CH(2) (5)) have also been prepared for comparison to the molecules in which t

26 inhibitor of the metalloprotease thermolysin was prepared for comparison to a known phosphinic acid i

27 Oxygenated rats subjected to global ischemia were prepared for comparison.

28 ens is described (28 and 29), and these have been prepared for conjugation to carrier protein in orde

29 Future doctrine should be prepared for contingencies in which the incidence may

30 ottis, supraglottis, glottis, and subglottis were prepared for conventional histology, immunohistoche

31 ing the additives identified and eight (40%) were prepared for crystallization trials during the firs

32 A separate portion of each flap site was prepared for descriptive histologic examination, inc

33 Northern blot analysis, and nuclear extracts were prepared for determination of NF-kappa B by electro

34 supplemented with essential nutrients, have been prepared for different tissues.

35 An iodide-doped chitosan (CT-I) solution was prepared for dipping tomatoes to coat the fresh surf

36 nships, the complete matrix of stereoisomers was prepared for each macrocycle.

37 An individualized report was prepared for each panelist; the report summarized th

38 Three biological replicates were prepared for each condition, and three experimental

39 test their essentiality, knockout constructs were prepared for each corresponding gene such that homo

40 containing nonhomologous central sequences, were prepared for each gene assayed.

41 (UTP)-labeled antisense and sense riboprobes were prepared for each sst.

42 Twenty dentin/cementum root slabs were prepared for each thickness of 0.5, 1.5, and 2.5 mm

43 Retinas from all globes were prepared for either wholemount or cryosectioning an

44 en behaviorally tested prior to their brains being prepared for electron microscopic examination.

45 th postmortem intervals of less than 4 hours were prepared for electron microscopic analysis accordin

46 Eyes were prepared for electron microscopy and AGE-specific f

47 32-month-old Brown Norway X Fischer 344 rats were prepared for electron microscopy and synapses were

48 crystals of human FVIII lacking the B domain were prepared for electron microscopy onto negatively ch

49 ent of insulin-like growth factor II (IGFII) was prepared for endocytosis by the mannose 6-phosphate/

50 Early cleavage embryos are prepared for environmental vagaries by having high l

51 (Cys227-Cys462) and TMEi4-6 (Val345-Cys462) were prepared for equilibrium dialysis experiments by ex

52 GlcN6P, 1) and five of glucosamine (GlcN, 2) were prepared for evaluation as catalytic cofactors of t

53 These compounds were prepared for evaluation as cephalosporin prodrugs c

54 Intestinal crypt fractions were prepared for ex vivo bactericidal assays.

55 rganisms and sacrificed at 24 h, and tissues were prepared for examination by light microscopy.

56 ion of ketamine with radiologist supervision were prepared for exclusive use by the pediatric interve

57 rings with outwardly pointing sulfur anchors were prepared for exploring quantum interference effects

58 hanism by which large segments of the genome are prepared for expression.

59 e propose that fibrillizing proteins need to be "prepared" for fibrillization.

60 transgenic plants from several laboratories being prepared for field trails.

61 Normal hiuman corneas were prepared for frozen sections and for culture of cor

62 Separate samples were prepared for FTIR (Fourier transform infrared) phot

63 In other cases, eyes were prepared for full-thickness eyewall sectioning or f

64 to cortistatin A), and its related analogues were prepared for further biological studies.

65 after injection, and hepatic Golgi fractions were prepared for gel electrophoresis analysis.

66 ial samples of both layers of rectus muscles were prepared for gel electrophoresis.

67 system, THz nano-metamaterial sensing chips were prepared for great enhancing of detection sensitivi

68 olated after 7 and 21 days postinduction and were prepared for gross and radiographic analysis of bon

69 d in less than 2 h once a standard curve has been prepared for H4PteGlun.

70 One group was prepared for histologic analysis, and vitreous was r

71 Animals were killed and eyes were prepared for histologic analysis.

72 month, all the rats were killed and tissues were prepared for histologic and biochemical evaluation.

73 The eyelids were prepared for histologic examination, and muscle fib

74 Tissue samples were prepared for histologic, immunohistochemical, and u

75 Clinical tissues are prepared for histological analysis and long-term sto

76 e weeks after implant placement brain tissue was prepared for histological assessment of oSDN volume

77 Lung parenchyma was prepared for histology or isolation of membrane prot

78 exposed and photographed, and tissue samples were prepared for histology and cytochemistry.

79 Globes and optic nerve segments were prepared for histology and morphometry.

80 r macroscopic examination, samples of tissue were prepared for histology, immunocytochemistry, and an

81 hat were euthanized and necropsied on day 14 were prepared for histopathologic examination.

82 respectively, and fatty acid phenacyl esters were prepared for HPLC analysis.

83 hlight the Sm-p80-based vaccine which is now being prepared for human clinical trials.

84 Hospice providers should be prepared for ICD patients, whose clinical trajectorie

85 Human cadaver eye tissue was prepared for imaging.

86 Five Fischer 344 rats that weighed 200-425 g were prepared for imaging according to an institutional

87 ateral striatum, along with the hippocampus, was prepared for immunoblotting.

88 se, rat, cat, bovine, monkey, and human eyes were prepared for immunocytochemistry and viewing by lig

89 Rats (n=8/group) were prepared for immunocytochemistry of GAD at 15 days

90 Spinal cords from other mice were prepared for immunocytochemistry using antibodies a

91 ive for 2 days to 12 weeks, and spinal cords were prepared for immunocytochemistry using antibodies a

92 2 weeks survival time, hypothalamic sections were prepared for immunocytochemistry.

93 mitted to grow longer, after which the cells were prepared for immunoelectron microscopic analyses.

94 man eyes from 5.5 to 12 weeks gestation (WG) were prepared for immunohistochemical analysis or for li

95 fter transplantation, at which time the eyes were prepared for immunohistochemical analysis.

96 rgical specimens of human ovarian carcinomas were prepared for immunohistochemical and in situ hybrid

97 After 10-14-day survival, the brains were prepared for immunohistochemistry and immunostained

98 Frozen sections were prepared for immunohistochemistry and in situ hybri

99 chemia-induced cell death, and some sections were prepared for immunohistochemistry for retinal neuro

100 The animals were perfused, and their brains were prepared for immunohistochemistry with an antibody

101 diately after exposure and paraffin sections were prepared for immunoperoxidase staining with a monoc

102 The eyes were prepared for immunostaining.

103 d samples were obtained, and the hippocampus was prepared for in vitro recordings.

104 Cryostat sections of heart and lung were prepared for in situ hybridization to elucidate the

105 re sacrificed 30 min later, and their brains were prepared for in situ hybridization to measure mRNA

106 ing up-to-date with significant improvements being prepared for inclusion within the next year and th

107 itably protected phosphoramidite derivatives were prepared for incorporation into synthetic DNAs, to

108 Transverse 6-micron corneal sections were prepared for indirect immunofluorescence localizati

109 nanogel particle (SANP) drug delivery system was prepared for injectable passive lung targeting.

110 ) with cHyp attached as a pendant side chain was prepared for intratracheal delivery with bioinactive

111 Whole mounts of retinas were prepared for isolectin immunohistochemistry, and pr

112 body to the ambient air and its contents and is prepared for it as the first line of defense.

113 , two CMBR anisotropy satellite missions are being prepared for launch early in the next century.

114 l, 2-benzimidazoyl, and 2-pyridyl components were prepared for ligand acceleration of the copper-cata

115 The retina from an 80-year-old patient donor was prepared for light and electron microscopy, includin

116 FAs were performed after surgery, and tissue was prepared for light microscopy (LM) and scanning elec

117 Following extraction, the tooth was prepared for light microscopy and sectioned in the m

118 The spinal cord was prepared for light microscopy at intervals from 1 to

119 Fellow eyes were prepared for light and electron microscopic evaluat

120 Ganglia and corneas were prepared for light and electron microscopic immunoc

121 At the end of the experiment, retinas were prepared for light microscopy or immunocytochemical

122 Thus, sections were prepared for light microscopy to determine whether

123 Maculas were prepared for lipid-preserving electron microscopy (

124 and bridged through a uranyl oxo-group, have been prepared for Ln = Sc, Y, Ce, Sm, Eu, Gd, Dy, Er, Yb

125 After cell or tissue samples have been prepared for lysis, the described protocol can be c

126 Samples are prepared for mass spectrometric analysis by heat-ass

127 Aortic endothelial cells were prepared for measurement of mRNA or activity for ni

128 Flies can be prepared for measurements in minutes and imaged for u

129 ed arginine quantification, and supernatants were prepared for metabolomic analysis.

130 euthanasia 2-4 wk after serum transfer, paws were prepared for micro-computed tomography and histolog

131 the ground floors, and these services should be prepared for more extensive performances.

132 ference laboratory, where touch preparations were prepared for N-myc evaluation.

133 The films were blindly rated, and sections were prepared for neuropathological analysis from the sa

134 y protected versions of the deoxynucleosides were prepared for oligonucleotide synthesis following st

135 Eyes were prepared for optical measurements by bonding a PMMA

136 The samples were prepared for paraffin histologic analysis and secti

137 ized version of this antibody (huAb A33) has been prepared for Phase I and II clinical studies in pat

138 form of the enzyme in which the active site is prepared for phosphoryl transfer.

139 m which in vivo m2 selective derivatives may be prepared for potential use in positron emission tomog

140 d anti-ThCr(2)Si(2)-type structure (I4/mmm), were prepared for RE = La, Nd, Sm, Gd, Ho, and Er.

141 me time period, other patients at our center were prepared for RRA by hormone withdrawal.

142 The same type of sensor was prepared for Salmonella (SAL) by immobilizing antibo

143 Lens capsule tissue was prepared for scanning electron microscopy (SEM) usin

144 All samples were prepared for scanning electron microscopy evaluatio

145 to oxirane acrylic beads, an affinity column was prepared for selective removal of RNases from aqueou

146 period of incubation, extracts of rat lenses were prepared for separation of [14C]-glutathione by hig

147 DNA is prepared for sequencing by mechanical shearing, adapt

148 nd third EQA studies, standardized protocols were prepared for serological and molecular typing of GB

149 ing gene reassembly as well as how the genes are prepared for shuffling (PCR amplification versus res

150 ed glassy carbon electrode (poly(AHNSA)/GCE) was prepared for simultaneous determination of caffeine

151 ucting molecularly imprinted polymers (MIPs) were prepared for simultaneous chronoamperometry (CA) an

152 3)O(4)-Au core-shell nanoparticles (Au-MNPs) were prepared for simultaneous fast concentration of bac

153 -r), BALB/c (EAE-r), and B10.PL (EAE-s) mice were prepared for stereological and immunohistochemical

154 control mice were sacrificed, and mandibles were prepared for stereomicroscopy and histology.

155 and a list of optimized oligonucleotides to be prepared for subsequent gene synthesis.

156 role, many such substrates and analogs have been prepared for subsequent evaluation.

157 on at 35.0 degrees C while the recipient was being prepared for surgery.

158 e applied wIRA for 20 minutes while patients were prepared for surgery.

159 Full-thickness tissue blocks from the macula were prepared for TEM or for QFDE.

160 ed enzyme, a series of site-directed mutants were prepared for testing the roles of active site resid

161 O-protonation of substituted benzoic acids) are prepared for the first time by controlled hydration

162 ee) synthetic streptonigrin intermediates to be prepared for the first time.

163 mpletion of perception so that the brain can be prepared for the next target.

164 (1H-Tetrazol-5-yl)-allenes have been prepared for the first time, and their reactivity t

165 The key tetracycle, which has been prepared for the first time, is a versatile interme

166 Eu-doped Gd2O2SO4 hollow spheres have also been prepared for the property modification and practica

167 ension emerging from the first capture stage is prepared for the second capture stage for further enr

168 matter any member of the celastroid family, was prepared for the first time through chemical synthes

169 anobelts with varied Ni, Co, and Mn contents was prepared for the first time.

170 The report was prepared for the FTC by Carol Regueiro, MD, a medica

171 tematic Reviews and Meta-Analyses guidelines was prepared for the inclusion and exclusion criteria.

172 the existing methods, as a ready-to-go assay was prepared for the microtiter plate format.

173 A synthetic standard was prepared for the putative nucleoside cross-link remn

174 ature review and the recommendations therein were prepared for the AGA Institute Clinical Practice an

175 rature review and the recommendations herein were prepared for the American Gastroenterological Assoc

176 ature review and the recommendations therein were prepared for the American Gastroenterological Assoc

177 ature review and the recommendations therein were prepared for the American Gastroenterological Assoc

178 ature review and the recommendations therein were prepared for the American Gastroenterological Assoc

179 ature review and the recommendations therein were prepared for the American Gastroenterological Assoc

180 ature review and the recommendations therein were prepared for the American Gastroenterological Assoc

181 ature review and the recommendations therein were prepared for the American Gastroenterological Assoc

182 Columns containing immobilized lipoproteins were prepared for the analysis of drug interactions with

183 Novel disposable electrochemical DNA sensors were prepared for the detection of a target DNA sequence

184 Two cationic rhomboid shaped molecules were prepared for the first time (55-70%) by the treatme

185 and cell cytotoxicity, a set of cyclic PEIs were prepared for the first time and compared to a set o

186 212Pb@C60 and its malonic ester derivatives were prepared for the first time by allowing the 212Pb t

187 h biologically interesting functional groups were prepared for the first time.

188 olymers incorporating the triptycene subunit were prepared for the molecular-level design of low diel

189 25%, 50%, 75%, 85% and 100% iron saturation were prepared for the purpose of evaluating Chromametry,

190 r nicotinamide adenine dinucleotide (NAD(+)) were prepared for the sensing event, by which the betaHB

191 Patients were prepared for the transplantation of allogeneic hema

192 ecombinant IpaB/IpgC and IpaC/IpgC complexes were prepared for their first detailed in vitro analysis

193 A novel, covalently closed bubble substrate was prepared for this study, which topo IIIalpha fully r

194 uct (BS1.5H), expressed in Escherichia coli, were prepared for this work.

195 Orbital structures and the brain stem were prepared for tracer detection and immunohistochemis

196 illed after 6, 18, and 24 months, one retina was prepared for transmission electron microscopy; the o

197 Patients were prepared for transplantation with busulfan, cycloph

198 Anesthetized (isoflurane) cats were prepared for traumatic brain injury, and then rando

199 Retinal cryosections were prepared for TUNEL analysis to determine the time c

200 Reciprocal subtractive libraries were prepared for two strains of Flavobacterium psychrop

201 Corneas were prepared for ultrastructural morphometric analysis

202 Highly active enzyme formulations can be prepared for use in nonaqueous media.

203 Specific polymeric biomaterials can be prepared for use in varied medical applications (e.g.

204 more efficient n-type Cu(2)O electrodes will be prepared for use in various photoelectrochemical and

205 kyl chains or soybean trypsin inhibitor have been prepared for use in HPLC separations in the reverse

206 Fluorescent analogs of UDP-Glc have been prepared for use in our studies of the clostridial

207 lopment of the bacteria, which are currently being prepared for use in clinical trials in patients wi

208 A rhodamine B/benzidine conjugate was prepared for use as the nanopistons for movement in

209 he human carcinoembryonic antigen (CEA) gene were prepared for use as a preclinical model for immunot

210 Semiconductor nanocrystals were prepared for use as fluorescent probes in biologica

211 tic index, bifunctional derivatives of SN-38 were prepared for use in antibody-based targeted therapy

212 Synthetic peptide antigens were prepared for use in enzyme-linked immunosorbent ass

213 s-Tetrazine based molecules were prepared for visible-light-driven organic transform

214 Each part of the retina was prepared for Western blot analysis of tyrosine-phosp

215 4))(2) and Pd(diphosphine)(2) complexes have been prepared for which the natural bite angle of the di

216 with murine ductal carcinoma in situ (DCIS) were prepared for XFM.